Comprehensive Coordination Chemistry Index

COMPREHENSIVE COORDINATION CHEMISTRY The Synthesis, Reactions, Properties & Applications of Coordination Compounds Edi...

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COMPREHENSIVE COORDINATION CHEMISTRY

The Synthesis, Reactions, Properties & Applications of Coordination Compounds

Editor-in-Chief: Sir Geoffrey Wilkinson, FRS Executive Editors: Robert D. Gillard & Jon A. McCleverty

Pergamon An imprint of Elsevier Science

COMPREHENSIVE COORDINATION CHEMISTRY IN 7 VOLUMES

PERGAMON MAJOR REFERENCE WORKS comprehensive Inorganic Chemistry (1973) Comprehensive Organic Chemistry (1979) Comprehensive Organometallic Chemistry (1982) Comprehensive Heterocyclic Chemistry (1984) International Encyclopedia of Education (1985) Comprehensive Insect Physiology, Biochemistry & Pharmacology (1985) Comprehensive 13iotechnology (1985) Physics in Medicine & Biology Encyclopedia (1986) Encyclopedia of Materials Science & Engineering (1986) World Encyclopedia of Peace (1986) Systems & Control Encyclopedia (1987) Comprehensive Coordination Chemistry (1987) comprehensive Polymer Science (1988) Comprehensive Medicinal Chemistry (1 989)

COMPREHENSIVE COORDINATION CHEMISTRY The §ynthesis, Reactions, Properties & Applications of Coordination Compounds

Volume 7 Indexes

EDITOR-IN-CHIEF

SIR GEOFFREY WILKINSON, FRS Imperial College of Sczence & Technology, Univerrity of London, UK EXECUTIVE EDITORS

ROBERT D. GILLARD

JON A. McCLEVERTY

University College, Curdifl, ZJK

University of Rirrninghrsm, U K

PERGAMON PRESS OXFORD. NEW YORK * BEIJING . FRANKFURT S A 0 PAUL0 SYDNEY TOKYO . TORONTO

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Pergarnon Press, Headington Hill Hall, Oxford OX3 OBW, England

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Pergamon Press Canada, Suite No. 271,253 College Street, Toronto. Ontario M5T 1R5, Canada Copyright @ 1987 Pergamon Books Ltd. All Rights Reserved. ?Vopart of this publicarion may be rcproduced, stored in a retrieval system OT transmirtedin any furin o r b j an); means: electronic, rlrc/rostutic, rnagneric tape,

mechanicol, pholocopying, recording or otherwise, upithout permission in writingfrom fhrpublishers. First edition 1987 Library of Congress Cataloging-in-PublicationData Comprehensive coordination chemistry. Includes bibliographies. Contents: v. 1. Theory and background - v 2. Ligands - v. 3 Main group and early transition elements - [etc.] 1. Coordination compounds. I. Wilkinson, Geoffrey, Sir, 192111. Gillard, Robert D. 111. McCleverty, Jon A. OD474.Ch.5 1987 541.2'242 86-'123'19 British Library Cataloguing in Publication Data Comprehensive coordination chemistry: the synthesis, reactions, properties and applications of coordination compounds. 1. Coordination compounds. I. Wilkinson, Geoffrey, 192111. Gillard, Robert D. III. McCIevcrty, Jon A. 541.2'247 OD474

ISBN 0-08-035950-7 (vo~.7) ISBN 0-08-026232-5 (set)

Printed in Great Britain by A. Wheaton & Co. Ltd., Exeter

Contents Preface

vii

Contents of All Volumes

ix

Index of Review Articles and Specialist Texts

1

Cumulative Subject Index

73

Cumulative Formula Index

255

V

Preface Since the appearance of water on the Earth, aqua complex ions of metals must have existed. The subsequent appearance of life depended on, and may even have resulted from, interaction of metal ions with organic molecules. Attempts to use consciously and to understand the metalbinding properties of what are now recognized as electron-donating molecules or anions (ligands) date from the development of analytical procedures for metals by Berzelius and his contemporaries. Typically, by 1897, Ostwald couid point out. in his ‘Scientific Foundations of Analytical Chemistry’, the high stability of cyanomercurate(I1) species and that ‘notwithstanding the extremely poisonous character of its constituents, it exerts no appreciable poison effect’. By the late 19th century there were numerous examples of the cornplexing of metal ions, and the synthesis of the great variety of metal complexes that could be isolated and crystallized was bcing rapidly developed by chemists such as S . M. Jorgensen in Copenhagen. Attempts to understand the ‘residual affinity’ of metal ions for other molecules and anions culminated in the theories of Alfred Werner, although it is salutary to remember that his views were by no means universally accepted until the mid-1920s. The progress in studies of metal complex chemistry was rapid, perhaps partly because of the utility and economic importance of metal chemistry, but also because of the intrinsic interest of many of the compounds and the intellectual challenge of the structural problems to be solved. If we define a coordination compound as the product of association of a Bronsted base with a Lewis acid, then there is an infinite variety of complexing systems. In this treatise we have made an arbitrary distinction between coordination compounds and organometallic compounds that have metal-carbon bonds. This divisim roughly corresponds to the distinction -which most but not all chemists would acknowledge as a real one - between the cobalt(II1) ions [ C O ( N H ~ ) ~ ] ~ + and [ C O ( ~ ~ - C ~ HAny ~ ) ~species ] * . where the number of metal-carbon bonds is at least half the coordination number of the metal is deemed to be ‘organometallic’ and is outside the scope of our coverage; such compounds have been treated in detail in the companion work, ‘Comprehensive Organometallic Chemistry’. It is a measure of the arbitrariness and overlap between the two areas that several chapters in the present work are by authors who also contributed to the organometallic volumes. We have attempted to give a contemporary overview of the whole field which we hope will provide not only a convenient source of information but also ideas for further advances OR the solid research base that has come from so much dedicated effort in laboratories all over the world. The first volume describes general aspects of the field from history, through nomenclature, to a discussion of the current position of mechanistic and related studies. The binding of ligands according to donor atoms is then considered (Volume 2) and the coordination chemistry of the elements is treated (Volumes 3 , 4 and 5 ) in the common order based on the Periodic Table. The sequence of treatment of complexes of particular ligands for each metal follows the order given in the discussion of parent ligands. Volume 6 considers the applications and importance of coordination chemistry in several areas (from industrial catalysis to photography, from geochemistry to medicine). Volume 7 contains cumulative indexes which will render the mass of information in these volumes even more accessible to users. The chapters have been written by industrial and academic research workers from many countries, all actively engaged in the relevant areas, and we are exceedingly grateful for the arduous efforts that have made this treatise possible. They have our most sincere thanks and appreciation. We wish to pay tribute to the memories of Professor Martin Nelson and Dr Tony Stephenson who died after completion of their manuscripts, and we wish to convey our deepest sympathies to their families. We are grateful to their collaborators for finalizing their contributions for publication. Because of ill health and other factors beyond the editors’ control, the manuscripts for the vii

...

VI11

Prefuce

chapters on Phosphorus Ligands and Technetium were not available in time for publication, However, it is anticipated that the material for these chapters will appear in the journal Polyhedron in due course as Polyhedron Reports. We should also like to acknowledge the way in which the staff at the publisher, particularly Dr Colin Drayton and his dedicated editorial team, have supported the editors and authors in our endeavour to produce a work which correctly portrays the relevance and achievements of modern coordination chemistry. We hope that users of these volumes will find thcm as full of novei information and as great a stimulus to new work as we believe thcm to be. JON A. McCLEVERTY

ROBERT D. GILLARD

Cardiff

Birmingham

GEOFFREY WILKINSON London

Contents of All Volumes Volume 1 Theory & Background

1.1 1.2 2 3 4 5 6

General Historical Survey to 1930 Development of Coordination Chemistry Since 1930 Coordination Numbers and Geometries Nomenclature of Coordination Compounds Cages and Clusters Isomerism in Coordination Chemistry Ligand Field Theory Reaction Mechanisms

7.1 7.2 7.3 7.4 7.5

Substitution Reactions Electron Transfer Reactions Photochemical Processes Reactions of Coordinated Ligands Reactions in the Solid State

8.1 8.2 8.3 9 10

Electrochemistry and Coordination Chemistry Electrochemical Properties in Aqueous Solutions Electrochemica1 Properties in Non-aqueous Solutions Quantitative Aspects of Solvent Effects Applications in Analysis Subject Index Formula Index

Complexes in Aqueous and Non-aqueous Media

Volume 2 Ligands

11 12.1 12.2 13.1 13.2 13.3 13.4 13.5 13.6 13.7 13.8 14 15.1 15.2 15.3 15.4 15.5 15.6 15.7 COC 7--A.

Mercury as a Ligand Group ZV Ligands Cyanides and Fulminates Silicon, Germanium, Tin and Lead Nitrogen Ligands Ammonia and Amines Heterocyclic Nitrogen-donor Ligands Miscellaneous Nitrogen-containing Ligands Amido and Imido Metal Complexes Sulfurdiimine, Triazenido, Azabutadiene and Triatomic Hetero Anion Ligands Polypyrazolylborates and Related Ligands Nitriles Oximes, Guanidines and Related Species Phosphorus, Arsenic, Antimony and Bismuth Ligands Oxygen Ligands Water, Hydroxide and Oxide Dioxygen, Superoxide and Peroxide Alkoxides and Aryloxides Diketones and Related Ligands Oxyanions Carboxylates, Squarates and Related Species Hydroxy Acids ix

____

Contents of All Volumes

X

15.8 15.9

Sulfoxides, Amides, Amine Oxides and Related Ligands Hydroxamates, Cupferron and Related Ligands Sulfur Ligands

16.1 16.2 16.3 16.4 16.5 16.6 17 18 19 20.1 20.2 20.3 20.4 21.1

21.2 21.3 22

Sulfides Thioethers Metallothio Anions Dithiocarbamates and Related Ligands Dithiolenes and Related Species Other Sulfur-containing Ligands Selenium and Tellurium Ligands Halogens as Ligands Hydrogen and Hydrides as Ligands Mixed Donor Atom Ligands Schiff Bases as Acyclic Polydentate Ligands Amino Acids, Peptides and Proteins Complexones Bidentate Ligands Multidentate Macrocylic Ligands Porphyrins, Hydroporphyrins, Azaporphyrins, Phthalocyanines, Corroles, Corrins and Related Macrocycles Other Polyaza Macrocycles Multidentate Macrocyclic and MacropolycyclicLigands Ligands of Biological Importance Subject Index Formula Index

Volume 3 Main Group & Early Transition Elements 23 24 25.1 25.2 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40

Alkali Metals and Group IIA Metals Boron Aluminum and Gallium Indium and Thallium Silicon, Germanium, Tin and Lead Phosphorus Arsenic, Antimony and Bismuth Sulfur, Selenium, Tellurium and Polonium Halogenium Species and Noble Gases Titanium Zirconium and Hafnium Vanadium Niobium and Tantalum Chromium Molybdenum Tungsten Tsopolyanions and Heteropolyanions Scandium, Yttrium and the Lanthanides The Actinides Subject Index Formula Index

Volume 4 Middle Transition Elements 41

42 43

Manganese Technetium Rhenium

Contents of All Volumes Iron

44.1 44.2 45 46 47 48

49

Iron(I1) and Lower States Iron(II1) and Higher States Ruthenium Osmium Cobalt Rhodium Iridium Subject Index Formula Index

Volume 5 Late Transition Elements 50 51 52 53

Nickel Palladium Platinum Copper 54 Silver 55 Gold 56.1 Zinc and Cadmium 56.2 Mercury Subject Index Formula Index

Volume 6 Applications 57 58 59 60

61.1 61.2 61.3 61.4 61.5 62.1 62.2 63 64 65 66

Electrochemical Applications Dyes and Pigments Photographic Applications Compounds Exhibiting Unusual Electrical Properties Uses in Synthesis and Catalysis Stoichiometric Reactions of Coordinated Ligands Catalytic Activation of Small Molecules Metal Complexes in Oxidation Lewis Acid Catalysis and the Reactions of Coordinated Ligands Decomposition of Water into its Elements Biological and Medical Aspects Coordination Compounds in Biology Uses in Therapy Application to Extractive Metallurgy Geochemical and Prebiotic Systems Applications in the Nuclear Fuel Cycle and Radiopharmacy Other Uses of Coordination Compounds Subject Index Formula Index

Volume 7 Indexes

67

Index of Review Articles and Specialist Texts Cumulative Subject Index Cumulative Formula Index

Index of Review Articles and Specialist Texts REG DAVIS School of Chemical and Physical Sciences, Kingston Polytechnic, Penrhyn Road, Kingston-upon- Thames, KTI ZEE, UK

AIMS AND SCOPE

The aim of this index is to provide a comprehensive listing of reviews concerning all aspects of coordination chemistry, covering the period 1945 to early 1986. Only those reviews in English (including translations from sources in German and Russian) have been included. Reviews listed have all been published in primary journals or review journals and periodicals. There has been no attempt to cite individual textbooks, as the author’s access to all the relevant texts could not be guaranteed. Reference to such texts will have been made at appropriate points in the foregoing chapters. LAYOUT AND ACCESS

As it is likely that many reviews will pertain to more than one area of coordination chemistry, the following indexing system has been used. All references are collected in a numbered and titled Main Index list, which is completely unclassified in any other way. Within each entry is given the number of pages devoted to that review and the number in parentheses following each entry is the number of references cited in each case. Entry into this Main Index is provided by 22 Acccss Tables, each of which is subdivided into sections devoted to specific topics. Further subdivision has also been carried out for topics that are very prolific. Thus, by way of example, in the table devoted to Complexes According to Element (Transition Elements) there are seven subdivisions for iron covering general reviews, those devoted to iron(II), iron(III), higher oxidation states, hemoglobin and myoglobin, hemes, hemoproteins and porphyrin complexes, and other biochemical aspects. Some of these entries are cross-referenced to the tables of Complexes According to Ligand, Biological and Medical Aspects, and Metal-containing Enzymes. The Access Tables have been laid out in a manner that parallels the foregoing chapters. The first three tables provide listings according to element and ligand. Tables 4 to 18 and 20 correspond to the chapters of Volumes 1 and 5 . Table 13 covers ligand synthesis. Two additional tables cover physical techniques for the study of complexes and thermochemistry. The final table is entitled Special Topics and includes aspects that defied inclusion under earlier headings and these aspects are listed purely in alphabetical order. ANNUAL SURVEYS

General surveys of advances in coordination chemistry appear in ‘Annual Reports’, The Royal Society of Chemistry, London, Section A. More specialized reports were published in the form of the ‘Specialist Periodical Reports: Inorganic Chemistry of the Transition Elements’, The Chemical Society, London (Volumes 1-6), which reviewed the literature published between 2971 and 1976, and the ‘Specialist Periodical Reports: lnorganic Chemistry of the Main Group Elements’, The Chemical Society, London (Volumes l-S), which reviewed the literature published between 1971 and 1976. Both these series have now been discontinued. Annual reviews of both transition element and main group chemistry are now published periodically in Coord. Chem. Rev. and the details of those which have appeared to date are given below.

1

index of Review Articles und Specialist Texts

2

Main Group Chemistry Review for 1978. Coord. Chem. Rev., 1979,30. Main Group Chemistry Review for 1979. Coord. Chem. R e v . , 1981,34. Main Group Chemistry Review for 1980. Coord. Chem. R e v . , 1982,40. Main Group Chemistry Review for 1981. Coord. Chem. Rev. 1983,49. Main Group Chemistry Review for 1982. Coord. Chem. Rev., 1984,56. Main Group Chemistry Review €or 1983. Coord. Chem. Rev., 1985, 66. Transition Metal Chemistry Review for 1979 (part A). Coord. Chem. R e v . , 1981, 35; (part B), Coord. Chem. Rev., 1981,37. Transition Metal Chemistry Review for 1980 (part A). Coord. Chern. R e v . , 1982, 41; (part E). Coord. Chem. Rev., 1982,4S. Transition Metal Chemistry Review for 1981 (part A). Coord. Chem. Rev., 1983, 51; (part B), Coord. Chem. Rev., 1984,57; (part C), Coord. Chem. Rev., 1985,67. Transition Metal Chemistry Review for 1982 (part A). Coord. Chern. R e v . , 1984,58. Transition Metal Chemistry Review for 1983 (part A). Coord Chem. Rev., 1985,62. ~

Other relevant annual survey publications which contain information on coordination complexes are listed below. All are published by the Royal Society of Chemistry (London) in the Specialist Periodical Reports series. Electron Spin Resonance. Volumes 1-6 (1971-1982). Electronic Structure and Magnetism of Inorganic Compounds. Volumes 1-7 (1970-1980). Electrochemistry. Volumes 1and 2 (196&1970). Inorganic Biochemistry. Volumes 1-3 (1977-1980). Inorganic Reaction Mechanisms. Volumes 1-7 (1969-1979). Mass Spectrometry. Volumes 1-6 (1968-1980). Molecular Spectroscopy. VoIumes 1-5 (1970-1976). Molecular Structure by Diffraction Methods. Volumes 1-6 (1971-1977). Nuclear Magnetic Resonance. Volumes 1-13 (1970-1983). Organometallic Chemistry. Volumes 1-12 (1973-1982). Photochemistry. Volumes 1-14 (1948-1982). Spectroscopic Properties of Inorganic and OrganometalIic Compounds. Volumes 1-16 (1967-1982).

Arrangement of the Access Tables 1 2 3 4 5 6 7 8 9 10 11 12 13 14

15 16 17 18 19 20 21 22

Complexes According to Element (Main Group Elements) Complexes According to Element (Transition Elements) Complexes According to Ligand Historical Survey General Coordination Chemistry, Coordination Numbers and Geometries Clusters, Metal-Metal Bonding and Polynuclear Complexes Complex Formation: Thermodynamic Relationships Isomerism and Huxionality Ligand Field Theory Bonding in Complexes Reaction Mechanisms Solvents and Solvation Ligand Synthesis Analytical Chemistry Electrochemistry, Electrochemical Applications and Electrical Properties Use of Complexes in Synthesis and Catalysis Biological and Medical Aspects Metal-containing Enzymes Physical Techniques for the Study of Complexes Photochemistry and Related Topics Thermochemistry Special Topics

3 4 9 14 15 15 16 17 17 17 18 18 19 19 19 19 20 21 23 24 24 24

Index of Review Articles and Specialist Texts

Table 1

Complexes According to Element (Main Group Elements)

1.1

Alkali Metals (see also Tables 3.39 and 17.5) 1,80,392,435,462,537,545,587,673,674,1545

1.2

Lithium (see also Tables 3.39 and 17.5) 1333

1.3

Sodium (see also Tables 3.39 and 17.5) 1133,1164,1224,1333

1.4

Potassium (see also Tables 3.39 and 17.5) 1133,1224,1333

1.5

Croup 1IA Metals (see also Tables 3.39 and 17.5) 80,282,392,435,587,673,674,675,1545

1.6

Beryllium 282,540,1535

1.7

Magnesium General (see also Table 3.39) 282,496,870 Biochemical aspects (see also Tables 17.5 and 17.6) 4'17,462,496,547,667,1087, 1157,1224, 1332,1339

1.8

Calcium (see also Tables 3.39 and 17.5) 282,462,668, 714,850.851, 1224, 1339, 1341

1.9

Strontium (see also Table 3.39) 282

1.10

Barium (see also Table 3.39) 282

1.11

Boron 88,416,435,497,507:539, 1251,1264, 1424, 1432,1451,1352, 1547, 1613

1.12

Aluminum 142,147,539,544,606,722, 1258,1264,1432,1450, 1487, 1507

1.13

Gallium 155,347,722,1432

1.14

Indium 7,347,722,1432

1.15

Thallium 289,318,347: 722, 1415,1432,1538

1.16

Silicon 539,540,722,1100,1562,1621,1630

1.17

Germanium 202,349,540,722,725,1100,1233,1562,1621

1.18

Tin 26,62,175,220,248,275,491,848,964,977, 1100,1523,1562,1621

1.19

Lead (see also Table 17.16) 466,497,722.725: 1100, 1538,1562

1.20

Phosphorus 214,648,722,1100,1606,1621,l662

1.21

Arsenic (see also Table 17.16) 214,540,722,1100,1558,1621,1662

1.22

Antimony 214,497,722,1100,1662

3

Index of Review Articles and Specialisl Texts

4 1.23

Bismuth 214,497,722,1100,1621,1662

1.24

Sulfur 540,1621,1665

1.25

Selenium 614,1080,1231,1621

1.26

Tellurium 173,944,1080, 1180,1231,1621

1.27

Polonium 158,1194

1.28

Halogenium Species 497,523,626,883,1080,1200, 1237,1423, 1434

1.29

Chlorine 1414,1423,1434

I.30

Bromine 1180, 1294, 1423, 1434

1.31

Iodine 497,559,883,1080, 1180, 1200,1237, 1423, 1434

1.32

Noble Gases 210,738,806,1080,1463,1625

1.33

Xenon 210,1180, 1463

1.34

Complexes of Organic and Ammonium Cations 1347

1.35

Complexes of Neutral Molecules 1348

Table 2

Complexes According to Element (Transition Elements)

2.1

Scandium 57,262,301,1095, 1554

2.2

Yttrium 57,89,207,262,1095,1554

2.3

Lanthanum 89,207,262, 1095, 1554

2.4

Lanthanides (see also Table 17.12) 2, 45, 57, 74, 89, 96, 130, 207,251.271, 630, 640, 641, 642, 653, 686, 687, 688, 729, 754, 889, 907. 985,1151, 1232,1278, 1350,1410,1554,1567,1635

2.5

Cerium 207

2.6

Neodymium 45,207

2.7

Praseodymium 45,207

2.8

Samarium 45,207

2.9

Europium 45,207,262, 1604

2.10

Gadolinium 207

index of Review Articles and Specialist Texts

5

2.11

Terbium 45

2.12

Dysprosium 45,207

2.13

Holmium 207

2.14

Erbium 207

2.15

Thulium 45

2.16

Ytterbium 45,207

2.17

Actinium 207

2.18

Actinide.7 (see also Table 17.16) 45,163,174,244.3?9,442,632,640,641,642,655,686,68?, 689,754,808,877,898: 911,928,1142. 1151,1187,1635

2.19

Thorium 45,262, 1413, 1425

2.20

Protactinium 45,133.1203,1480

2.21

Uranium 45,107,262,436, 616,729, 1180,1181,1413,1453,1511

2.22

Neptunium 869

2.23

Plutonium 45,329,616,1413

2.24

Americium 45,616

2.25

Curium 45

2.26

Berkelium 45,1556

2.27

Californium 45

2.28

Einsteinium 45

2.29

Fermium 45

2.30

Mendelevium 45

2.31

Titanium 49, 176,218,436, 802.811,1171,1481, I 1554,1582

2.32

Zirconium 49, 128,218,26h.285,802, 81 1, 1095, 1228, 1468, 1481, 1554

2.33

Hafnium 45, 128,218,262,285.811,1482,1554,1582

2.34

Vanadium 49,99, 104,208,214,218,384,387,436,540, 584,610,684.706,802, 1216, 1444, 1527,1554,1670, 1 L71

Index of Review Articles and Specialist Texts

4

Niobium 49, 104,214,218,256,802,811, 1171,1216, 1269, 1274, 1554, 1669

2.35 2.36

.

Tantalum 49, 104,214,218,256,802,811,1215, 1269,1274, 1554, 1571

2.37

Chromium (General) 91,171,218,408,439,802,878, 1458, 1527,1554,1593

2.38

Chromium(0) 146

2.39

Chromium(111) 192,345,408,432,489,515: 519,839,937,939,940,1001,1651

2.40

Chromium-(IV)and -(V) 513,1574,1618,1696

2.41

Chromium (VI) 436,491,513,540,612,684

2.42

Molybdenum (General} 91,218,312,386,498,499,505,565,802,811,819,833,1458,1554,1593

2.43

Molybdenum(0) 146,312

2.44

Molybdenum (1V ) 499,708,833

2.45

Molybdenum(V) 436,708,827,833,1213, 2585

2.46

Molybdenum (VI) 436,684,833,1585

2.47

Molybdenum (Biochemical Aspects) (see also Tables 3.50, 17.8 and 18) 86,333,351,458,505,525,560,579,646,694,713,844,876,980,1094,1155,1332,1403,1539,1691

2.48

Molybdenum (Clusters and Metal-Metal Bonds) (see also Table 6) 498,816,819,1073,1094, 1171,1598

2.49

Molybdenum (High Coordination Numbers) (see also Tables 5.12-5.14) 499,708, 1581

2.50

Tungsten (General) 41,91,139,218,232,312,565, 802,811,819, 1458,1554, 1593

2.51

Tungsten(0) 146,312,590,839

2.52

Tungsten(V1) 436,684, 1180

2.53

Tungsten (Clusters and Metal-Metal Bonds) (see also Table 6) 816,819,1073,1094,1171,1598

2.54

Heteropoly anions 41,75,436,665,1256,1283,1306,1338

2.55

Manganese (General) 109,296,621,887,895,932,1087,1238,1435,1467,1554

2.56

Manganese(ZZ) 895,913,1527

2.57

Manganese(III) 294,342,895

2.58

Manganese (Higher Oxidution States) 294,513,684,895,1431

2.59

Technetium 136,169,173,590,618,684, 811,846,963,1185,1199,1345,1645

Index of Review Articles and Specialist Texts

7

2.60

Rhenium 92,181,218,381: 498: 684,811,932,1196,1277,1292,1554

2.61

Iron (General) 262,275,438,449,568,872, 1094, 1152, 1184, 1281, 1430, 1554

2.62

Iron (II) 259,350,394,717,1217, 1527

2.63

Iron (III) 99,292,406,606,650,842,1454,1530,1584

2.64

Iron (Higher Uxidatiun States) 513,571, 1249

2.65

Iron (Hemoglobin and Myoglobin) (see also Tables 3.53 and 17.7) 82, 400, 404, 415, 418, 437, 457, 566, 607, 649, 658. 667, 704. 715, 719, 776, 987, 1092, 1132, 1137, 1157,1167,1307,1332,1634

2.66

Iron (Hemes, Hemoproteins and Porphyrin Complexes) 82, 400. 404, 415, 418, 437, 532, 568, 607, 631. 649, 650, 667, 704, 719, 776, 810, 830, 935. 1020, 1040,1041,1061,1092,1157,1167,1307,1332.1361,1362,1427,1639

2.67

Iron (Other Biochemical Aspects) (see also Tables 17 and 18) 320,399,41)0,401,4Wl, 40h,411,423,424,425,438,445,446,447,448,449,450,451,452,45(1,457, 480,481,485,487,532,560,568,577,613,650,459,6hO, 667,669,670,693,715,723,844,852,863, 875,887,891,920,987,1063,1079,1094,1114,1141, 1143, 1144, 1267,1298, 1305,1340,1369,1378, 1426,1437,1464, 1478,1624,1676, 1677

2.68

Ruthenium (General) 72,112,262,284.805,872,873, 1120, 1315, 1534,1554,1589, 1615

2.69

Rutheniurn(II) (see also Table 16) 330,590,601,605.840.968,1408

2.70

Ruthenium ( I l l ) 590,1530

2.71

Ruthenium (Higher Oxidation States) 684,966

2.72

Osrniun 112,284,684.805,X72,966,1208, 1315, 1365,1534.1554,1589,1652

2.73

Cobart (General) (see also Tables 3.79 and 17.10) 13,532,994,1005, 1049,1096,1165,1287, 1508,1554

2.74

Cobalt(1I) 193,259,288.311,398.613,628,941,1101.1113,1217,1255,1527,1679

2.75

CobaIt (III) 129,276,295,300, 322,343,432,433, 489,564.571,594,711,838,861,896, 1001, 1355, 1452, 1466, 1490,1509,1510,1530, 1575,1591, 1654

2.715

Cobalt (Higher Oxidation States) 513,571

2.77

Rhodium (see also Table 16) 72,112,228,234,284,380,590,805,822,839,966,988,1001,1315,1529,1537,1554,1589

2.78

Iridium 72, 112,284: 590, 805,966, 1083, 1315,1537, 1554, 1589

2.79

Nickel (General) 273, 5001532,650,1417>1554,1673

2.80

Nickel@) and -(I) 355,919.921

2.81

Nickel(II) 159, 178,259,270,288,311,388,389,603,950,1028,111311217,1255,1471,1527

2.82

Nickel-(III) and -(IVj 513,571,921,936

~

Index of Review Articles and Speciulia Texts

8 2.83

Pulladium {General) 112,159,273,284,500,532,680,755,805,1315,1537,1554,1589,1653

2.84

Palladium-(0) and -(I) 355,847,884,919, 1309,1537, 1646

2.85

Palladium (II) 388, 389,500,1471,1537,1571

2.86

Palladium (Higher Oxidation States) 847,966

2.87

Platinitm (General) 112,159,273,284,500,557,680,755,805,965,992,1069,1315,1381,1402,1537,1554,1589,1653, 1661

2.88

Platinum-(0) and -(I) 355,847,884,919,1537, 1646

2.89

Platinum (II) 354,388,389,489, 1471, 1493. 1500,1505,1514,1526,1537,1591,1698

2.80

Platinum (Higher Oxidation Statesj 298,590,847,966,1393,1583

2.91

Platinum (Antitumour Corn ounds) (see also Table 17.14) 459,466, 578,696, 1069, 1266, 1327

2.92

Copper (General) 539,650,680,925, 1554

2.93

CoFPer(I) 119,500,577,650

2.94

Copper(II) 205,328,332,494,577,584,600,606, 683,692,709,724,734, $34,886,901,905,929,946,950,976, 1113,1154,1527,1707

2.95

Copper(lI1) 513

2.96

Copper (Biochemical Aspects) (see also Tables 17 and 18) 437,457,466,486,577,602,652,667,671,715,723,885,920,924,1123,1378,1437,1464,1675

2.97

Silver 200,680,728,1000,1554

2.98

Gold 50,555,643,680,884,1301, 1471,1544,1554

2.99

Zinc (General) 63,282,532,650,651, 1554

2.100 Zinc (Biochemical Aspecrs) (see also Tables 17 and 18) 63,398,455,532,579,620, 650,651,671,828, 1019,1033, 1102,1136, 1367 2.101

Cadmium (see also Table 17.16) 282,466,497,1443,1554

2.102 Mercury (General) (see also Table 17.16)

134,466, 1554,1621

2.103

Mercury(I) 829

2.104 Mercury (II) 250,282,497,751,884,1470,1538,1577

,I.

Index of Review Articles and Specialist Texts Table 3

9

Complexes According to Ligand

3. I

A lkoxides 44,122,375,565,804,819,1118,1226,1401,1483,1494,1515, 1589

3.2

Amido 565,1055,1483

3.3

Amino 36,81,260,262,330,1509,1525,1526

3.4

Amine N-Oxides 265,353,354,726

3.5

Amino Acids (see also Tables 3.102 and 17.4) 4,93,1492,1521.1522,1571,1640

3.6

Amino Alcohols 501

3.7

Aminocarboxy Into 537,1001,1253,1272

3.8

Ammine 36,51,60S, 720,840

3.9

Aqua 192, 396,212,306,405,833,838,1690

3.10

Tertiary Arsines 118, 154,510,604,722,945, 1002, 1109,1621.1662

3.11

Aryldiazenato f Aryldiazo) 536

3.12

Azido 260,681

3.13

A z o and Diazo 81,1330

3.14

Azoles 334,1252

3.15

Bipyridyl (see Table 3.47)

3.16

Borazines 855

3.17

Boron-containing Compounds 531,855,893,956.1127,1363,1449,1547,1613

3.18

Carboranes 531,893, 1009,1076,1261, 1287, 1448,1613, 1649

3.19

Carbonato and Bicarbonato 106,260,343,1390,1511

3.20

Carbon Dioxide 561,1279,1390,1668

3.21

Carbon Disuljide and Carbon Oxysuljide (see also Table 3.20) 561,599,860,949,1656

3.22

Carbonyl (Carbon Monoxide; General) (see also Table 3.131) 428, 550, 607, 801, 813, 830, 882, 992, 994, 1096, 1150. 1151, 1153, 1186, 1203, 1238, 1281, 1428, 1534,1537, 1551

3.23

Carbonyl (Structure and Bonding) 391,502,906,1166,1220

3.24

Carbonyl (Synthesis) 801,1223

Index of Review Articles und Specialist Texts

10 3.25

Carbonyl (Reactivity) 841,990,994,996,1056,1161, 1372,1491,1550,1551,1568

3.26

Carbonyl (Reaction Mechanism) 146,428, 1153, 1491

3.27

Carbonyl (Clusters) (see also Table 6) 990,992,1120,1165,1238,1334,1365,1495,1508,1534,1537,1550,1646

3.28

Carbonyl (Derivatives) 312,1037,1096,1281,1458,lh40

3.29

Carbonyl (Physical and Spectroscopic Properties) (see also Table 19) 132,428,550,882, 1150,1335, 1336, 1551

3.30

Carbonyl (Photochemistry) (see also Table 20) 94,1110,1578

3.31

Carboxylic Acids and Carboxylato (see also Table 3.140) 19,71,120,260,494,509,905,922,988,1511,1524,1535,1561,1618

3.32

Catecholate and Quinolate 844,933

3.33

Chelates 221,582,750,993,1108,1310,1373,1633,1692

3.34

C?xelatingAlkenes (with As, 0, P,S and Se Donors) 680,918,945

3.35

Citrate 1088,1229

3.36

Compartmental Ligands (see Table 3.78)

3.37

Corrins and Corroles (see Table 3.79)

3.38

Crown Ethers, Cryptunds and Pudunih 435, 537, 545, 587, 672, 673. 674, 675. 810, 1066, 1135, 1164, 1333, 1346, 1347, 1348, 1349, 1351, 1353,1354,1356,1357.1358,1359, 1406,1545,1549,1567, 1605,1629

3.38

Cyanato 117,307,886

3.40

Cyano 145,260,370,388,389,426,564,583,685,710,727,1184,1201

3.41

Cyanogen, Cyanogen Halides and Hydrogen Cyanide 974

3.42

Cyclometalled Complexes 718,918,945, 1021, 11.59, 1501

3.43

Dialkylamido and Disilylamido (see Table 3.2)

3.44

Diarnino 300,821,1030, 1525

3.45

Diazenes 81,1330,1377

3.46

Diazo (see Table 3.13)

3.47

Diimines (Bipyridyl, Terpyridyl and 1,lO-Phenanthroline) 131,260,314,350,377,717,82G,821,824,989,1418,1498,1577

3.48

Diimines (Other Ligands) 81,118,377,394

3.4Y

(3-Diketonares(see also Tables 3.54,3.87 and 19.12) 30,309,341,348,378,396.493,853, 1093,1111, 1129,1511

3.50

Dinitrogen (see also Tables 2.42-2.47 and 17.8) 86,98,351,458,525,812,876,958. 1003.1011, 1025, 1124.1148.1155,1240, 1260,1370,1403,1455

Index of Review Articles and Specialist Texts

11

3.51

Dioximes 711,785,896

3.52

Dioxygen (see also Tables 2.65-2.67, 17.7 and 18) 82,97,166,284,415,607,649,719,830,837,913,916,941,986,1006,1050,1054,1060,1072,1089, 1101,1145, 1157,1266,1307,1392,1399,1639,1650

3.53

Dithiocarbamates and Monothiocarbamates 647,747,748,998,999,1436,1658

3.54

Dithio-p-diketonates (see also Tables 3.50 and 3.88) 237,238,304,1499

3.55

Dithiolato 14,20,60,64,238,240,500,506,1013

3.56

Ethylenediamine (see Table 3.44)

3.57

Ethylenediarninetetraacetate (edta) (see Table 3.7)

3.58

Ferrocene-based Ligands 1311

3.59

Flavins 844

3.60

Fluorides see also Table 3.65) 47,73, 39 ,397.414, 440,441,442,573,462,703,754,805,823, 1173,1181, 1276,1292,1404, 1456, 1460,1557

1

3.60a Fluorosulfate 1603 3.61

Fulminato 307

3.62

Germanium Donor Ligands 135,872,884,1344,1505,1621

3.63

Gluconato 206

3.64

Gold Donor Ligands 884

3.65

Halides (see also Table 3.60) 57,58,67,68, 108,163,223,347,379,664,734,807,811,866, 1042, 1158,1166, 1173

3.66

Hydrazido 565,1004,1222

3.67

Hydrido 49, 59, 72, 149, 191: 235,239, 245,260,269,435, 539,567,825,953,1078, 3096, 1166,1302,1308, 1501, 1520, 1580,1614

3.68

Hydroxornic und Thiohydroxamic Acids 267,745,746,881,1285

3.69

Hydroxyl 317

3.70

Imidazoles and Pyrazoles 93,100

3.71

Imido 909,1536

3.72

Imino Alcohols 501

3.73

Intramolecular Coordination of Main Group Elements 1271

3.74

Isocyanides 52,291,917, 1528

Index of Review Articles and Specialist Texts

12 3.75

Lead Donor Ligands 135,872,884,1505

3.76

Macrocyclic Ligands (General) (see also Tables 2.65-2.67 and 3.39) 95,276,367,435,535,702,810,1075,1548,1549,1607

3.77

Macrocyclic Ligands (Compartmental Ligands) 551,858,1284,1549,1692

3.78

Macrocyclic Ligands (Corrins and Corroles) (see also Table 17.10) 810,1156,1160,1312,1409

3.79

Macrocyclic Ligands (Phthalocyanines) 150,810,895,915,1206,1485

3.80

Macrocyclic Ligands (Porphyrins) (see also Tables 2.65-2.67) 296,313,532,568,631, 650, 667.704,810,895,935, 1020,1040,1041.1061,1092,1147,1291,1295, 1307,1361,1362,1385,1427,1467,1474,1549,1570,1582,1631,1640,1666

3.81

Macrocyclic Ligands (Other N Donors) 81,95,118,276,300,367,542,588.730,1293,1360,1549

3.82

Macrocyclic Ligands (0Donors) (see also Table 3.39) 95, 1360,1549

3.83

Macrocyclic Ligands (SDonors) 238,1549

3.84

Macrocyclic Ligands (N,0 and N , S Mixed Donors) 300,502,1549

3.85

Mercury Donor Ligands 884,1627

3.86

Monothiocarbamates (see Table 3.54)

3.87

Monothio-p-diketonates 237,238,303,304,1499

3.88

Nitrato 27,79,1.53,521,803,867,928,1205,1511,1553

3.85,

Nitrido 287,970,1174.1621

3.90

Nitriles 857,962,1209

3.91

Nitrito 260,727,943

3.92

Nitro 260,727

3.93

Nitrosyl (Nitrogen Monoxide) (see also Table 3.136) 31,84,370,536,586, 596: 873,916.991, 1045, 1068, 1166, 1190,1503, 1519

3.94

Nucleic Acids, Nucleosides and Nuckotides (Including D N A and R N A ) (see also Tables 17 and 18) 77, 103, 252, 253, 410, 449, 452, 453, 461, 462, 463, 467, 468, 483. 537,578, 660, 661, 1059, 1069, 1440, 1617, 1640

3.95

Oxalacetato 454

3.96

Oxalato 198,260,821, 1511

3.97

Oximato 501,580,1533,1540

3.98

Oxo and Oxides 54,319,358,436,568,591.635,684,708,970,1115,1162,1173,1213,1404,1557,lh21,1690

3.99

Oxo Ethers 118

Index of Review Articles and Specialist Texts

13

3.100 Oxyanions 203 3.101 Peptides (see also Tables 17.2-17.4) 1387,1492, 1571.1640 3.102 Perchlorates 574,1553,1559 3.103 Peroxides 11,151,708,861, 1179 3.104 Phosphines and t-phosphites (General) 87,154,286,355, 722,918,1018, 1037,1086, 1116, 1163,1170, 1226, 1321, 1560,1577 3.105 Phosphines (Chelates) 118, 124, 510,563.604,699, 847, 1002, 1032, 1109, 1564, 1610 3.106 Phosphates, Phosphonates, Phosphine Oxides and Phosphine SulJides 260,544, 1433, 1513. 1564,1658 3.107 s-Phosphites and Phosphinites 880,1484 3.108 O t h v Phosphuru Donor Ligands I177,1396,14XS, lh21,lb62 3.109 Pnictides 412

3. I10 Polypyrazoly lhorares 100,1029 3.111 Pyridine and Pyridyl-containing Ligands (Excluding Bipyridyis) 324,824, 1500 3.111a Quinones

1632

3.112 Schiff Bases 33,238,279,293, 336,383.522,535.628,709,786,800, 1284,1289,1435,1445,1549 3.113 Selenides 274,412,591,664,684,1375,1621 3.114 Selenium Donor Ligands 1207,1322, 1384,1497,1542,1564, 1621 3.115 Selenocyanates and SeIenohalides 58,66,117.307,727.871,913,1234, 1300 3.116 Silicon Donor Ligands 135,201,872,884, 1106.1344, 1505, 1621

3. I1 7 Stihines 154,722,1074 3.118 Sulfdo 238,274,412,432,492,500,591,664,684,872,970,1094,1175,1375,1621,1665 3.119 SulJinates and Sulfonates 1131,1603 3.120 Sulfoxides 17,56 3.121 Sulfur Dioxide 623,817,916 3.122 Sulfur Donor Ligaxds (see also Tables 3.133-3.135,3.137 and 3.138) 118, 237, 238. 500, 582, 700, 883, 910, 1207, 1226, 1273, 1322, 1384, 1391, 1497, 1521, 1524, 1542, 1564,1572 3.123 Superoxides 487

Index of Review Articles and Specialist Texts

14 3.124 Tartrates

338,1229

3.125

Tellurides 412,664,944,1621

3.126

Tellurium Donor Ligan& 1207,1384,1542, 1621

3.127 Tellurohulides 58,66,871 3.128 Tetrapuoroborates 823 3.129 Tetrahydroborates 88,507,539,1251,1264 3.130 Tetrathiooxalates 599 3.131

Thiocarbonyl and Selenocarbonyl (Curbon Monosulfide and Carbon Monoselenide) 860,949,1062

3.132

Thiocyanates and Thiohalides 58,66,117,307,727,871,914, 1486, 1497

3.133 Thioethers 118,438 3.134

Thiohydroxamine Acids (see Table 3.69)

3.135

Thiolato 434,500,1499

3.136 Thionitrosyls and Risulfiir Dinitride (see also Table 3.93) 1400,1659,1660

3.137

Thiosemicarbazides and Thiosemicarbazones 700,1576

3.138 Thioureas and Ureas 357,369,1674 3.139 Tin Donor Ligands 135,872,884,1505, 1531, 1621 3.140 TriJluoroacetato 120 3.I41

Ureas (see Table 3.138)

3.142 Water (see Tables 3.9 and 3.70) 3.143 Xanthates 747,748,1438,1658 3.144

Ylides 979

Table 4 4.1

Historical Perspectives 264,278,576,697,732,797.818

Historical Survey

Index of Review Articles and Specialist Texts Table 5

General Coordination Chemistry, Coordination Numbers and Geometries

5.I

Coordination Chemistry (General)

5.2

coordination Numbers (General)

5.3

15

1117,1183 1125,1624

Two and Three Coordination 43,69,862.864,870

5.4

Four Coordination (General) 43,236,600,1002,1289

5.5

Square Planar Complexes 8,43,69. 190, 865, 1600

5.6

Tetrahedral Complexes 37,39,69

5.7

Five Coordination 43,69,217,236,259,277,288,311,363,407,600,683,848,1034,1212,1459,1543,155X

5.8

Six Coordination (General) 255,283,340

5.9

Octahedral Complexes 37,39,69,331,340.488,600,683.724

5.10

Trigonal Prismatic Complexes 283

5.11

Tetragonal Complexes 344,364,901

5.12

Seven Coordination 43,246,254,499,708, 3225, 1581

5.13

Eight Coordinalion 28,39,249,382,4(19,708,864,1215

5&14 Nine, Ten, Eleven, Twelve and Fourteen Coordination 39,231,864,1215 5.15

Outer Sphere Complexes 365,1235,1242,1288,1314,1573, 1602 b

Table 6 6.I

Clusters, Metal-Metal Bonding and Polynuclear Complexes

Clusters (General) 55, 83, 85, 126, 219, 500, 553, 558, 636, 814, 972, 1171, 1211, 1215, 1495, 1508, 1537, 1 5 U , 1550, 1586,1596,1641,1644, 1646, 1652,1661

6.2

Clusters (Main G ~ u Elements) p 497,553,1605

6.3 6.4

Clusters (Halide- and Alkoxide-containing) 218,498,819,1647

Clusters (Hydride-, Carbide- and Suljide-containingj 233,245,492,756,1537,1647

6.5

Clusters (Mixed Metals) 1091

6.6

Clusters (Spectroscopy and Mugnetism) 102,517,756

6.7

Clusters (Bonding, Electronic Structure and Fluxionality) 116,517,814,934, 1172: 1544, 1642, 1643, 1644,1699

~

Iridex of Review Articles and Specialist Texts

16 6.8

Clusters (Catalysis and Analogies to Metal Surfaces) 1168,1376,1495,1586

6.9

Clusters (Ligand Free) 894,1379

6.10

Metal-Metal Bonding (General) 23,218,228,229,371,494,500.524,562,563,1095,1150,1243,1371,1587

6. I 1

Melal-Metal Bonding (illziltiple) 241,498,520,533,819,1014, 1070, 1071, 1073, 1095, 1459,1620. 1700

6.12

Metal-Metal Bonding (Singic) 618,819, 1578

6.13

Metal-Metal Bonding (Spectroscopy and Magnetism) 102,508,517, 1504

6.14

Metal-Metal Bonding (Bonding) 371,517,533

6.15

Metal-Metal Bonding (Reactirify) 3,229,816,1578, 1598,1609, 1620

5.16

Binuclear Ligand Bridge Compkxes 6, 13,24,25,71,51h, 1158.1594. 1664

6.17

Mixrd Vulmce Complexes

24. 25, 137, 168,230,640, 832. 1565,1566, 1597 6.18

Polymeric Complexes 323, 337, 390, 406, 493. 523. 551, 563. 735,798, 843, 995, 1182, 1230, 1244, 1247, 1268, 1316. 1412, 1484,1485,1585,1594,1653

6.19

One-dimensional Compoiinds and Conductors 258,524,557,836,931.951.1122,1362,1402, 1698

6.20

Starkrd ConiplexeT 500, 619

6.21

Supported Corripkxe Y 552,558,721,995

Table 7 7.1

7.2

Complex Formation: Thermodynamic Relationships

Complex Formation (General) 185, 1473 Complex Formation (Kinetics and iVfechunism) M Y , 1221,1420,1607,1638

7.3

Slnbility Constants (Genrnil) 321,360,573,676, 739,744,1188. 1219

7.4

Stability Constants (Multicomponent Systems) 339,952

7.5

Stability Constants (Methods of Determination and Calculation) 308,633,765,888, 1411

7.6

Thermodynamic Data 91,212, 321,360, 405: 573,593, 672, 676,926, 1219, 1607, 1615

7.7

Solvation Energies 679

7.8

The Chelate &flea 1002

7.9

Hard nnd Soft Acids wid Buses 409,413,419,420,421: 422: 676.678,942,1119,1246,1318,1324

Index of Review Articles uad Specialist Texts Table 8

17

Isomerism and Ftuxionality

8.1

Isomerism (General) 488,902,976, 1084, 1416,1552

8.2

Linkage Isomerism 359,727,1225

8.3

Stereoisomerism and Optical Isomerism (General) 32, 187,221,570,666,799, 809,861,902,904, 957.1082, 1130, 123h, 1245, 1248. 1262, 1328, 1462, 1498

8.4

Separation of komer.7 352,897

8.5

Racemization 488,821, 1084,1416

8.6

Absolute Configuration 403,585,957,1015

8.7

Conformational Properties 182,213,403,488.821,959, 1030, 1084, 1328, 1542

8.8

Fluxionality (SCC also Tables 6.6 and 19.14) 85,428,814,929,1024, 1046,1153,1297, 1326, 1542, IS43 Table 9

Ligand Field Theory

9.I

Ligand Field Theory (General) 363,427,602,609,624,634,682,690,692,849,866,890,983. 1134, 1192,1193, 1407,1197. i608

9.2

Crystal Field Effects 53,589,682, 1004,1077

9.3

Nephelauxeric Series 42,393

9.4

Jahn-Teller Effect 37,39,344,597,600,627,683,724,901, 1398,1706

9.5

Spin-Orbit Coupling 39,43,53 Table 10

Bonding in Complexes

10.1

Bonding (General) 69,257,391,548,549,635,655,923,1419,1.587

70.2

Covalent Bonding 21,655,657,664,923

10.3

Multiple Bonds and Back-bonding (see also Tables 3.23: 4.10 and 21.2) 520

10.4

The Concept of Valence (see also Table 6.16) 528,548,663

10.5

Charge Distribution, Electron Density Distribution and WaIsh Diagrams 69,1166,1405.1697

10.6

Ionic Radii 398,697

10.7

Molerular Orbital Theory Ca:nlculations 316,391,495,504,569,634,638,690,704,835,X90,1031,1178, 1461,1517

10.8

Angular Overlcip Mefhod 69,549,624,682,890.1407,1566

Inde.u of Review Articles and Speciahf Texts

18

Table 11

Reaction Mechanisms

11.1

Mechanisms (Substitution Reactions) 8, 146, 162, 349, 575, 593, 603.711,809, 813, 840, 861,865, 874, 908, 996,1028, 1056, 1084,1112, 1121,1198,1389,1416, 1447,1466. 1491,1493,1509,1510.1530.1570,1600,1667,1690,1694

11.2

Mechanisms (Hydrolysis and Solvation) 306,908, 1026,1416, 1509, 1510. 1592, 1695

11.3

Mechanisms (Racemization) 1084,1416

11.4

Mechanisms (Iromenzation) 1084,1416

11.5

Mechanisms (Redox Reactions and Electron Transfer) 3,9,10,11,68,99,138, 167,170,194, 195,197,326,433.434,575,594.595,598,677,715,809,831, 835, 875, 1007, 1017, 1048. 1067, 1103, 1176, 1197, 1374, 1394, 1446. 1472, 1546, 1570, 1588,1595, 1601,1616

11.6

Mechanisms (Use of Isotopic Labelling) 1429,1496

11.7

Kinetics 12,263,273,306,471, 575,595,813, 861, 1530

11.8

Trans Effect 40,129,530,809,942,947, 1263, 1422, I510

11.9

Cis Effect

129,530,942,947,970,1263

11.10 Trans Influence 268,707,942,947,1263 11.11 Cis Influence 942,947, 1263

Table 12

Solvents and Solvation

12.1

Solvents and Solvation (General) 903,948, 1553, 1655

12.2

Non-aqueous Solvents (General) 34,113, 185,691,948,1128.1191, 1270.1318

12.3

Non-aqueous Solvents (Acetonitrile) 744

12.4

Non-aqueous Solvents (Ammonia) 36, 51, 541, 1202, 1421, 1605

12.5

Non-aqueous Solvents (Uimethy 1 SulfoxidP) 17,739

12.6

Non-aqueous Solvents (Oxides of Nitrogen and Nitric Acid) 79

12.7

Non-aqueous Solvents (Sulfuric Acid) 165,1477

12.8

Donor-Acceptor Theory 419,678,698,826.942,948.1128, 1318,1446

12.9

Solvento Complexes 310,372,490,691,755,865,948.954

12.IO

Solubility Mea.rurements 356

Index vf Review Articles and Specialist Texts Table 13

Ligand Synthesis

13.1

Ligand Synthesis (General) 281

13.2

Template Synthesis 70,281, 346,367,522, 535,542,800, 810,1465 Table 14

19

Analytical Chemistry

14.1

Spectrophotometric Anulysis 740,743,784,785,790

14.2

Complexing Agents for Analytical Applications 742,777,780,785,786,789,796,1227,1250,1349,1357,1395

14.3

Solvent Extraction 48,160,262, 376,705,740,743,746,757,758,759,760, 761,762,767,768,769,771,772,773,955, 978,1058, 1195,1356, 1373,1561

14.4

Chromatography (General) 352,1343

14.5

Ion Exchange Chmmnfography 743,763,764,770,795,897,1479,1541

14.6

Gas-Liquid Chromatography of Complexes 743,1275, 1320

14.7

Other Chromatographic Techniques 766,892,1442

14.8

Nuclear Magnetic Resonance Shift Reagents (see Table 19.12) Table 15

Electrochemistry, Electrochemical Applications and Electrical Properties

15.1

Electrochemistry (General) 209,1036,1282,1299,1552

15.2

Redox Potentials (see also Table 22.19) 91, 104, 109, 112,212,326,958,971, 1007, 1475

15.3

Polarography 38,741,1210,1254,1255

15.4

Complexes as Electrocatalysts 752,1291

15.5

Inorganic Electrosynthesis 224

15.6

One-dimensional Conductors (see Table 6.18) Table 16

Use of Complexes in Synthesis and Catalysis

16.1

Stoichiometric Reactions of Coordinated Ligands 84,148,238,281,346,434,546,820, 860,883,989, 1111, 1241,1538

16.2

Catalysis (General) 234,235,260, 366, 380,527,755, 822, 841,908, 954,995, 1083, 1096, 1306, 1376, 1408, 1569, 1631, 1639,1650,1668

16.3

Catalysis (Water-splitting Reactions) 601,968, 1098, 1290, 1313, 1569, 1590, 1595

16.4

Oxidative Additiun Reactions 975,1006,1010,1027,1064,1301

Index uf Review Articles and Specialist Texts

20 16.5

Insertion Reactions 1161,1372 ~~

Table 17

Biological and Medical Aspects

17.1

Biological Aspects (General) 737,1489,1627,1692

17.2

Metalloprotein Complexes (General) 425,461,462,543,556,611,613,614,666,1022, 1303,1516, 1539, 1617

17.3

Metalloprotein Complexes (Redox Reactions) 216,715, 1546, 1701

17.4

Metallopep tide Complexes 1387,1571

17.5

Ion Transport and Ionophores 1,453,545,556,672,674,850, 1133,1333,1351,1352,1364,1626,1627,1663

17.6

Photochemistry, Photosynthesis and Chlorophyll 76,417,496,547,621,667, 887, 1087,1152,1332

17.7

Oxygen Transport and Storage {see also Tables 2.65-2.67) 82,415,418,437,607,649,719, 1157, 1307,1332, 1516

17.8

Nitrogen Fixation and Nitrogenuse 86,351,458,525,560,646,694,879,980,1094,1155,1332,1403,1648,1691

17.9

Iron-Sulfur Proteins (Ferredoxins, Rubredoxin) 320,406,411,424,438,560,669,715,891,1038, 1063,1144,1516,1590

17.10 Vitamin BI2(see also Tables 2.73, 2.74 and 3.79) 204, 215, 484, 532, 542, 554, 695, 997, 1005, 1052, 1107, 1156, 1160, 1366, 1409, 1506, 1516, 1575, 1591,1599

17.11 Phosphorylation 462,661 17.12 Heavy Metal Replacement in Enzymes 398,453,477,483,617,656,850,868,1099,1367, 1386, 1388, 1410,1679 17.13 Metallotherapy 101,169,406,456, 555,618,846 17.14 Anticancer Compounds (see also Table 2.91)

456,459,578,582,696,1069, 1296,1327,1489,1522

17.15 Antiarthritis Compounds 555,643 17.16 Antibiotic Compoundr 392,453,456,545,582,672,673,674,850,1327,1351 17.17 Metal Uptake by Plants and Organisms

927,1331,1539,1678 17.18 Metals as Nutrients

606,645,927,1672 17.19 Metal Toxicity and Chelation Therapy

466,606,612,632,927,1327,1539, 1673 17.20 Radiopharmaceuticals

169,618,846 17.21

The Application of Spectroscopic and Other Technique.s in Zizorganic Biochemistry (see also Table 19) 2,453,469,470,471,472,473,474,475,476,477,478,479,579,828,879,885,980,1676,1691,1693

Index of Review Articles and Specialist Texts Table 18 18.1

Acid Phosphatases 448

18.2

Aconitase 579

18.3

Alcohol Dehydrogenase 398,579,651

18.4

Aldehyde Oxidase 694,980

18.5

Aldolase 579

18.6

Alkaline Phosphatases 398,579

18.7

6-Aminolevulinate Dehydratase 644

18.8

Ascorbate Oxidare 652

18.9

A TPase 482,661,850,851,1332; 1339

Metal-containingEnzymes

18.10 Azurin 885 18.11 Carbonic Anhydrase 398,455,579,620.651,828.1136,1367,1628 18.12 Carboxypeptidrtse 398,579,651,1019,1033,1102, 1628, 1680 18.13 Catalase 1123,1648

18.14 Catechol Dioxygeaase 446,844,987,1683 18.15 Ceruloplasmin 652, 924 18.16 Chloroperoxidase 723 18.17 Chromatin 462 18.18 Cytochrome,$ (General) 667,715,875, 1478.1516 18.19 Cytochrome P-450 399,485,723.1141. 1267. 1298. 1305, 1341,1342, 1368 18.20 Cytochrome c Oxidase (see also Table 18.36) 457,577,667.723,920,!378,1437,1464,1648 18.21 Diamine Oxidase 887,1675 18.22 Dioxyganases (sec also Table 18.14) 1340 15.23 Enterobactin 659,669, 1364 18.24 Ferritin 406,451,452,670, 1143, 1426, 1688,1689 COC 1--8

21

Index of Review Articles and Specialist Texts

22

18.25 Formate Dehydrogenase

980,1691 18.26 GTPase

461 18.27 Hemocyanin

437 18.28 Hemerythrin

437,450,480,481, 568,669,863, 1369,1687 18.29 Hemoglobin and Myoghbin (see Table 2.65) 18.30 Hemoproteins (see Table 2.66)

18.31 Horseradish Peroxidase 457,667,723 18.32

Hydrogenase 1353,1590

18.33 Isomerases 579,1599 18.34 Monooxygenases (see Table 18.19)

1267,1648

18.35

Nitrate Reductase 694,980,1691

18.36

Oxidases - Copper-containing (see.also Table 18.20) 457,486,577,602,1123,1648,1675

18.37

Peroxidases (see also Table 18.31) 723

18.38

Phosphatases (see Tables 18.1 and 18.6)

18.39 Phosphoglucomutase 398 18.40 Phosphovitin

444,1681

18.41 Plastocyanin 577,652,885,1601 18.42 Protein Kinase

462 18.43 Pyruvate Kinase 579 18.44 Ribonucleotide Reductase

449,613,660, 1686

18.45 Siderophores 425,447,659,669, 1079,1623: 1684.1702,1703,1704,1705 18.46 Sulfite Oxidase 694,980, 1691 18.47 Superoxide Dismutase 487,887,1035,1104 18.48

Transferrin 4@6,423,445,659,669, 852, 987, 1682

18.49 Uieroferrin 448,987, 1685

18.50 Xanthine Dehydrogenase 694,980

index of Review Articles and Specialist Texts

23

18.51 Xanthine Oxidase 579,694,844,980, 1691 18.52 Urease 1674 18.53 Lipoxygenases 1677

Table 19

Physical Techniques for the Study of Complexes

19.1

Circular Dichroism and Magnetic Circular Dichroism 295,325,368,478,967,1532, 1563

19.2

Conductivity 302,1317

19.3

Dipole Moments 78, 1166

19.4

Electron Spin Resonance 127,184,299,327,453,474,511,584,h15,879,890, 1691

19.5

Electronic Spectroscopy 15, 16, 18, 24, 25: 37, 39, 43.46, 68, 217,223, 257, 290,407,408,479, 589,592,641,653, 454,684, 716,843,866, 889, 890.912, 1042, 1134, 1146, 1169, 1293, 1469, 1497, 1502

19.6

Magnetic Meusuremenfs 6,21, 35, 73, 179,227, 243, 315,323, 337, 390,493: 503, 512,514,664,706,717,730,834, 845, 946, 1051,1081, 1189.1217,1284,1385,1512,1527, 1584,1594,1608

19.7

Mass Spectrometv 90,114,678,1008,1138.1218,1555

19.8

Mossbauer Spectroscopy 29,123,152.220.257.261,275,401,815,942,1012,1518,1531,1676

19.9

Neutron Diffraction 144,257

19.10 Neutron Scattering 608,657 19.11 Nuclear Magnetic Resonance (General) 65, 113, 115, 157, 226. 256, 257, 286, 299, 306, 373, 428, 490, 538,959, 964, 965, 1097, 1382, 1383, 1439,1523,1554, 1593 19.12 Nuclear Magnetic Resonance (Shift Reagents) 2,96,429,529,853,981,1140,1257,1636 19.13 Nuclear Magnetic Resonance (Other Paramagnetic Complexes) 113,430,431,1016,1126, 1259 19.14 Nuclear Magnetic Resonance (Fluxional Molecules) 225,428, 1016,1097 19.15 Nuclear Magnetic Resonance (Biological Applications) (see also Table 17.17) 2,453,472,473,579,828, 885 19.16 Nuclear Quadrupole Resonance 143,257,402,712,854,1044,1319 19.17 Optical Rotatory Dispersion 361,368 19.I8 Photoelectron Spectroscopy (Vacuum Ultraviokt) 121,242,286,445, 625,686,1657,1658 19.19 Photoelectron Speclroscopy (X-Ray) 257,581,639,731,910,1337,1658 19.20 Vibrational Spectroscopy (General and Infrared Spectroscopy) 5,22,37,39,43,102,132,286,335,347,476,508,534,736,912,1004,1139,1149,1150,1336

Index of Review Articles and Specialist Texas

24 1 9.21

Vibrational Spectroscopy (Raman Spectroscopy) 222,374,475,534,629,736,1622

19.22 Vibrational Spectroscopy (Matrix Isolation) 5,61,550,882,894,984. 1039,1057, 1376, 1611, 1612 19.23

Vibrational Spectroscopy (Force Constants) 267,297,385,576,720,733,1053

19.24 X-Ray Absorption Spectroscopy, X-Ray Absorption Edge Spectroscopy and Extended X-Ray Absorption Fine Structure (EXAFS) 247,280,4hY,980,1090,1619, 1691 19.25 X-Ray Diffraction 470,585,753,1397,1405,1441,1587 Photochemistry and Related Topics

Table 20 20.1

Photochemistry (General) 76,94, 111, 170, 239,305, 362, 432,434,526, 590, 601, 616, 701, 774, 839,895,925,930, 937,938, 939,960,961,968,983,1098, 1110, 1214,1265,1290,1313,1329,1371,1490,1570,1602,1609, 1611, 1612

20.2

Flush Photolysih 859

20.3

Excited States 489,701,839,1043,1047

20.4

Water-splitting Reactions (see Table 16.3)

20.5

Photochromism, Photoluminescence and Chemiluminescence 105,211,601,622,774,1410 Table 21

Thermochemistry

21.1

Thermochemical Data 57,67,89, 104, 109, 112,982,975, 1335, 1436, 1525, 1037

21.2

Metal-Ligand Bond Strengths 575,1653 Table 22

22.1

Chemiluminescence (see Table 20.5)

22.2

Complexes with Large Counterions 360

22.3

Free Radical Complexes and Reactions 171,443,813,916,1304

22.4

Heterocations 140

22.5

High Pressure reactions 572,637,821,900

22.6

Intercalation Compounds 598

22.7

Lewis Acid Behaviour of Complexes 108,751

22.8

Lewis Base Behaviour of Complexes 260,1023,1286,1380

Special Topics

Index of Review Articles and Speciulist Texts 22.9

25

Metal Atom Vapour Synthesis 61,125,984,1280

22.10 Orbital Symmetry Rules 1323 22.11 Oscillatory Reactions 775,1579 22.12 Protonation 4Complexes (see Table 22.8) 22.13 Pulse Radiolysis 1065 22.14 Pyro Compounds 591 22.15 Radiation Chemistry 856 22.16 Solvated Electrons 541,856,1545 22.17 S in Labelling 8% 22.18 Thermochromism 110,973 22.19 Ultrasonic Irradiation of Complexes 263 22.20 Unstable Oxidation States 1065,1299 22.21 Antiferromagnetism 1584 22.22 Zintl Anions 1605

MAIN INDEX 1. Alkali metal ion transport and biochemical activity. P. B. Chock and E. Titus, Prog. Inorg. Chem., 1973.18.287-382 (450). 2. Lanthanide ions a$ n.m.r. chemical shift probes in biological systems. J. A. Glasel, Prog. Inorg. Chem., 1973, 18,383-413 (44). 3. Oxidation-reduction and related reactions of metal-metal bonds. T. J. Mever. Proa. Inore. ., Chem.. 1975,19,1-50 (381). 4. Transition metal complexes containin tridentate amino acids. S. T. Chow and C. A . McAuliffe, Prog. Inorg. Chem., 1975,19,51-103 t240). 5. Cryogenic inorganic chemistry: a review of metal-gas reactions as studied by matrix isulation infrared and Raman spectroscopic techniques. G. A. Ozin and A. Vander Voet, Prog. Inorg. Chem., 1975,19,105-172 (303). 6. The structural and magnetic properties of first row transition metal dimers containing hydroxo, substituted hydroxo and halogeno bridges. D. J . Hodgson, Prog. Inorg. Chem., 197.5, 19, 173-241 (248). 7. Coordination chemistry of indium. D. G. Tuck and A. Carty, Prog. Inorg. Chem., 1975, 19, 243-337 (579). 8. The intimate mechanism of re lacement in ds square planar complexes. L. Cattalini, Prog. Inorg. Chem., 1970, 13,263-327 (139f 9. Non-bridging ligands in electron transfer reactions. J. E. Earley, Prog. Znorg. Chem., 1970, 13, 243-262 (76). 10, Replacement as a prerequisite to redox processes. E. Chaffee and J. 0. Edwards, Prog. Imrg. Chem., 1970,13,205-242 (114). 11. Recent develo ments in the redox chemistry of peroxides. S. B. Brown, P. Jones and A. Suggett, Prop. Znora. &em.. 1970.13.159-204 (135). 12. Fasi'metal>omplex reactions.' K. Kustin, Prop. Znorg. Chem., 1970, 13,107-158 (190). 13. The formation, structure and reactions of binuclear complexes of cobalt. A. G . Sykes and J. A. Weil, Prog. inorg. Chern., 1970, 13,l-106 (466). 14. Structural systematics of 1,l- and 1,2-dithiolatochelates. R. Eisenberg, Prog. Znorg. Chem., 1970, 12,295-369 (173). 1

1

,

I

Y

I n d e x of Review Articles and Specialist Texrs

26

15. Spectroscopy of 3d-complexes. J. E. Ferguson, Prog. Inorg. Chem.. 1970,12,259-293 (384). 16. Electron transfer spectroscopy. C. K. Jorgensen, Prog. Inorg. Chem.. 1970,12,101-158 (222). 17. Dimethylsulfoxide in inorganic chemistry. W. L. Reynolds, Prug. Inorg. Chem., 1970, 12, 1-99 (470). IS. Absorption spectra of crystals containing transition metal ions. N. S. Hush and R. J. M. Hobbs, Prog. Znorg. Chem.. 1968, 10,259-486 (456). 19. Complexes of some simple carboxylic acids. C. Oldham, Prog. Inorg. Chem., 1968, 10, 223-258 (305).

20. Metal 1,Zdithiolene and related complexes. J. A. McCleverty, Prog. Inorg. Chem., 1968, 10, 49-221 (1 88). 21. Covalence and the orbital reduction factor, k , in magnetochemistry. M. Gerloch and 9. R. Miller, Prog. Inorg. Chern., 1968,10, 1-47 (35). 22. Vibrational spectra of transition metal complexes and the nature of the metal-ligand bond. D. W. James and M. J. Nolan, Prug. Inorg. Ckem., 1968,9, 195-275 (198). 23. Metal-metal bonds in transition metal compounds. M. C. B a r d , Prog. Znurg. Chem., 1968,9,1-159 (899). 24. Intervalence transfer absorption, part I: qualitative evidence for intervalence transfer absorption in

inorganic systems in solution and in the solid state. G. C. Alien and N. S. Hush, Prog. Znurg. Chem., 1967,8,357-389 (116). 25. Intervalence transfer absorption, part 11: theoretical considerations and spectroscopic data. N. S. Hush, Prog. Inorg. Chem., 1967,8,391-444 (44). 26. The chemistry of bivalent tin. J . D. Donaldson, Prog. Znorg. Chem . 1967,8,287-356 (268). 27. Complexes containing the nitrate ion. C. C. Addison and D. Sutton. Plug. Inurg. Chem., 1967, 8, 195-286 (389).

28. Eight coordination chemistry. S. J. Lippard, Prog. Inorg. Chem., 1967,8, 109-193 (381). 29. Chemical applications of Mossbauer spectroscopy. R. H. Herber, Prog. Inorg. Chem., 1967,8,1-41 (108).

30. Metal P-ketoenolate complexes. J. P. Fackler, Prog. Inaorg. Ckem.. 1966,7,363-425 (414). 31. Nitric oxide compounds of transition metals. B. F. G. Johnson and J. A . McCleverty, Prog. Znorg. Chem., 1966,7,277-359 (264). 32. The Cotton effect in coordination compounds. R. D . Gillard, Prog. Inorg. Chem., 1966,7,215-276 (164). 33. Metal complexes of Schiff bases and 0-ketoamines. R. H. Holm. G. W. Everett and A. Chakravorty, Prog. Znorg. Chem.. 1966,7,83-214 (371). 34. The coordination model for non-aqueous solvent behaviour. R. S . Drago and K. F. Purcell, Prog. Inorg. Chem., 1964,6,271-322 (125). 35. The magnetic properties of transition metal complexes. B. N . Figgis and J. Lewis, Frog. horg. Chem., 1964,6,37-239 (67U). 36. Reactions of metal halides with ammonia and aliphatic amines. G. W. A. Fowles, Prog. Invrg. Chem., 1964,6,1-36 (88). 37. The coupling of vibrational and electronic motions in degenerate electronic states of inorganic complexes, part I : state of double degeneracy. A. D. Lichr, Prog. Inorg. Chern., 1962,3,281-314 (25). 38. Polarographic behaviour of coordination compounds. A. A . Vlcek, Prog. Inurg. Chem., 1963, 5. 211-384 (191). 39. The coupling of vibrational and electronic motions in degenerate electronic states in inorganic com-

plexes, part 11: states of triple degeneracy and systems of lower symmetry. A. D. Liehr, Prog. Znorg. Chem., 1962,4,455-540 (52). 40. The trans effect in metal complexes. F. Basolo and R. G. Pearson, Prog. Znorg. Chem., 1962, 4. 381-453 (106). 41. Isopolytungstates. D. L. Kepert, Prog. Inorg. Chem., 1962,4,19%274 (216). 42. The nephelauxetic series. C. K. Jorgenson, Prog. Znorg. Chem., 1962.4,7>124 (104). 43. The coupling of vibrational and electronic motions in degenerate and non-degenerate electronic

states of inorganic and organic molecules, part SIT: non-degenerate electronic states. A. D. Liehr, Prog. Inorg. Ckem., 1963,5.385-430 (30). 44. Metal alkoxides. D. C . Bradley, Prog. Zriorg. Chem., 1960,2,303-361 (130). 45. Unusual oxidation states of some actinide and lanthanide elements. L. B. Asprey and B. B. Cunningham, Prog. h o r g . Chem., 1960,2,267-302 (245). 46. Intensities of spectral bands in transition metal complexes. C. J. Ballhausen, Prog. Inorg. Chem., 1960,2,251-265 (27).

47. Some fluorine compounds of the transition metals. R. D. Peacock, Prog. Inorg. Chem., 1960, 2, 193-249 (190). 48. Extraction of inorganic compounds into organic solvents. R. M. Diamond and D. G. Tuck, Prog. Inorg. Chem., 1960,2,109-192 (325). 49. Hydride compounds of the titanium and vanadium group elements. G. E. Toogood and M. G. H. Wallbridge, Adv. Znorg. Chem. Radiochem., 1982,25,267-340 (200).

50. Compounds of gold in unusual oxidation states. H. Schmidbaur and K. C . Dash, Adv. Znorg. Chem. Radiochem., 1982,25,23%266 (124). 51. Metal-ammonia solutions. W. L.Jolly, Prug. Inorg. Chem., 1959,1,235-281 (174). 52. Isocyanide complexes of metals. L. Malatesta, Prog. Inorg. Chem., 1959,1,283-379 (117). 53. The effect of inner orbitai splittin on the thermodynamic properties of transition metal compounds and coordination complexes. P. t e o r g e and D. S . McClure, h o g . Innorg. Ckem., 1959, 1,381-463 (36).

Index of Review Articles and Specialist Texts

27

54. The structure of mixed metal oxides. R. Ward, Prog. Inorg. Chem., 1959,1,465-536 (216).

55. Transition metal molecular clusters. B. F. G. Johnson and J. Lewis, A d v . Inorg. Chem. Radiochem., 1981,24,225-355 (262). 56. The coordination chemistry of sulphoxides with transition metals. J. A. Davies, Adv. Inorg. Chern. Radiochem., 1981,24, 11C187 (498). 57. Lanthanide, yttrium and scandium trihalides: preparation of anhydrous materials and solution thermochemistry. J. Burgess and J. Kijowski, A d v . Inorg. Chern. Radiochern., 1981,24,57-114, (320). 58. Solid state chemistry of thio-, seleno- and telluro-halides of representative and transition elements. J. Fenner, A. Rabenau and G . Trageser, Adv. Inorg. Chem. Radiochem., 1980,23,329-425 (434). 59. Hydride complexes of the transition metals. H. D. Kaesz and R. B. Saillant, Chem. Rev., 1972, 231-281 (395). 60. 1,l-Dithiolato complexes of the transition elements. R . P. Burns, F. P. McCullough and C . A. McAuliffe, Adv. Inorg. Chem. Radiochem., 1980,23,211-280 (442). 61. Transition metal vapour cryochemistry. W. J. Power and G. A. Ozin, Adv. Inorg. Chern. Radiochern., 1980,23,80-175 (203). 62. Recent advances in or anotin chemistry. A. G. Davies and P. J. Smith, Adv. Inorg. Chern. Radiochem., 1980,23, 1-77 t566). 63. Some aspects of the biochemistry of zinc. R. H. Prince, Adv. Inorg. Chern. Radiochem., 1979, 22, 349440 (332). 64. 1,2-Dithiolene complexes of transition metals. R. P. Burns and C. A. McAuliffe, Adv. Znorg. Chern. Radiochern., 1979,22,303-348 (209). 65. Correlations in nuclear magnetic shielding, part I. J . Mason, Adv. Inorg. Chern. Radiuchern., 1976, 18,197-228 (99). 66. Thio-, seleno- and teliuro-halides of the transition metals. M. J. Atherton and J. H. Holloway, Adv. Inorg. Chern. Rudiochem., 1979,22,171-198 (41). 67. Lattice energies and thermochemistry of hexahalornetallate(1V) complexes, AZMX6,which possess the antifluorite structure. H. D. B . Jenkins and K . F. Pratt, Adv. Inorg. Chem. Radiochem., 1979, 22, 1-111 (81). 68. Reorganisation energies of optical electron transfer processes. R. D. Cannon, Adv. faorg. Chem. Radiochern., 1978,21 179-230 (155). 69. A new look at structure and bonding in transition metal complexes. J. K . Burdett, Adv. Inorg. Chern. Radiochern., 1978,21,113-146 (73). 70. Template reactions. M . De Sousa Healey and A. J. Rest, Adv. Inorg. Chem. Radiochem., 1978,21, 1-40 (143). 71. Structures and physical properties of polynuclear carboxylates. J. Catterick and P. Thornton, A d v . Inorg. Chem. Radiochem., 1977,20,291-362 (315). 72. Hydride complexes of ruthenium, rhodium and iridium. G. L. Geoffroy and J. R. Lehman, Adv. Inorg. Chem. Radiochem., 1977,20,190-290 (340). 73. Ferrimagnetic rnateriais:A. Tressaud and J. M. Dance. Adv. Inorg. Chem. Radiochern., 1977, 20, 133-188 (205). 74. Recent advances in the chemistry of the less common oxidation states of the lanthanide elements. D. A. Johnson, Adv. Inorg. Chem. Radiochem., 1977,20, 1-133 (599). 75. Isopolymolybdates and isopol tungstates. K. H. Tytko and 0. Glemser, Adv. Inorg. Chem. Radiochern., 1976, 19,239-315 (2167. 76. Aspects of organotransition metal photochemistry and their biological significance. E. A. Koerner von Gustorf, L. H. G . Leenders, I. Fischler and R. N. Perut2, Adv. Inorg. Chem. Radiochem., 1976, 19,65-183 (632). 77. Structure of binary complexes of mono- and poly-nucleotides with metal ions of the first transition group. H. Pezzano and F. Podo, Chem. Rev., 1980,80: 365401 (389). 78. Dielectric behaviour and molecular structure of inorganic comulexes. S. Sorriso. Chern. Rev.. 1980. 80,313-327 (240). 79. Dinitrogen tetroxide, nitric acid and their mixtures as media for inorganic reactions. C. C . Addison, Chem. Rev.. 1980.80.21-39 (178). 80. Coordination chemistry of alkali and alkaline earth cations. 3’.S. Poonia and A. V. Bajaj, Chem. Rev., 1979,79,389-445 (773).

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81. Or anometallic intramolecular-coordination compounds containing a nitrogen donor ligand. I. 8 m a e . Chem. Rev., 1979.79,287-321 (227). 82. Synthetic oxygen carriers related to biological systems. R. D. Jones, D. A. Summerville and F. Basolo, Chem. Rev.. 1979,79, 139-179 (412). 83. Clusters and surfaces. E. L. Muetterties, T. N. Rhodin, E. Bond, C . F. Brucker and W. R. Pretzer, Chem. Rev., 1979,79;91-137 (295). 84. Reactions of nitric oxide coordinated to transition metals. J. A . McCleverty, Chern. Rev., 1979,79, 53-76 (172).

85. Mechanistic features of metal cluster rearrangements. E. Bond and E. L. Muetterties, Chem. Rev., 1978,78,639458 (139).

86. Recent advances in the chemistry of nitrogen fixation. J . Chatt, J. R. Dilworth and R. L. Richards, Chem. Rev., 1978,78,589-625 (2YY). 87. Steric effects of phosphorus ligands in organometallic chemistry and homogeneous catalysis. C. A . Tolman, Chem. Rev., 1977,77, 313-348 (298). 88. Covalent transition metal lanthanide and actinide tetrahydroborate complexes. T. J. Marks and J. R. Kolb, Chem. Rev., 1977,77,263-293 (213). 89. Thermodynamic properties of yttrium, lanthanum and the lanthanide elements and ions. L. R. Morss, Chem. Rev.. 1976,76,827-841 (149).

Index of Review Articles and Specialist Texts 90. Energetics of the ionisation and fragmentation of metal chelates in the mass spectrometer. J . B. Westmore, Chem. Rev., 1976,76,695-715 (133). 91. Chromium, molybdenum and tungsten: thermodynamic properties, chemical equilibria and standard potentials. 1. DelIien, F. M. Hall and L. G. Hepler, Chem. Rev., 1976, 76, 283-310 (400). 92. Recent advances in the chemistry of rhenium. G. Rouschias, Chern. Rev., 1974,74,531-566 (548). 93. Interactions of histidine and other imidazole derivatives with transition metal ions in chemical and biological systems. R . J. Sundberg and R. B. Martin, Chem. Rev., 1974,74,471-517 (517). 94. The photochemistry of metal carbonyls. M. Wrighton, Chem. Rev., 1974,74,401-430 (273). 95. The synthesis and ion binding of synthetic multidentate macrocyclic compounds. J. J. Christensen, D. J . Eatough and R. M. Izatt, Chem. Rev., 1974,74,351-384 (217). 96. Lanthanide shift reagents for n.m.r. spectroscopy. A. F. Cuckcrill, G. L. 0. Davies, R. C. Harden and D. M. Rackham, Chem. Rev., 1973,73,553-588 (488). 97. The dioxygen ligand in mononuclear group VI11 transition metal complexes. J. S. Valentine, Chem. Rev., 1973,73,235-245 (101). 98. Dinitrogen complexes of the transition metals. A. D. Allen, R. 0. Harris, B . R. Loescher, J . R . Stevens and R. N. Whitely, Uhem. Rev., 1973,73,11-20 (130). 99. Aqueous electron transfer reactions: vanadium(V) as reductant compared to iron(I1). D. R. Rosseinsky, Chem. Rev., 1972,72,215-229 (116). 100. The coordination chemistry of pyrazole-derived ligands. S. Trofimenko, Chem. Rev., 1972, 72, 497-509 (179). 101. Metals, ligands and cancer. D. R . Williams, Chem. Rev., 1972,72,203-213 (108). 102. Vibrational spectra of intra- and inter-metal and semimetal bonds. E. Maslowsky, Chem. Rev., 1971,71,507-524 (248). 103. Sites and thermodynamic quantities associated with proton and metal ion interaction with ribonuc-

leic acid, deoxyribonucleic acid and their constituent bases, nucleosides and nucleotides. R. M. Izatt, J. J. Christensen and J. H. Rytting, Chern. Rev., 1971, 71, 439-481 (229). 104, Thermochemistry and oxidation potentials of vanadium, niobium and tantalum. J. 0. Hill, I. Cr. Worsley and L. G. Hepler, Chem. Rev., 1971,71,127-137 (129). 105. Photoluminescence of transition metal coordination compounds. P. D. Fleischauer and P. Fleischauer, Chem. Rev., 1970,70,19%230 (219). 106. The chemistry of metal carbonato complexes. K.V. Krishnamurty, G. M. Harris and V. S. Sastri, Chem. Rev., 1970,70, 171-197 (329). 107. The chemistry of uranium(V). J. Selbin and J. D. Ortego, Chern. Rev., 1969,69,657-671 (132). 108. Quantitative aspects of the Lewis acidity of covalent metal halides and their organo-derivatives. D. P. N. Satchell and R . S . Satchell, Chem. Rev., 1969,69,251-278 (175). 109. Thermochemistry and oxidation potentials of manganese and its compounds. T. A. Zordan and L. G. Hepler, Chem. Rev., 1968,68,737-745 (81). 110. Thermochromism of inorganic compounds. J. H. Day, Chem. Rev., 1968,68,649-657 (54). 111. Photochemistry of transition metal coordination compounds. A, W. Adamson, W. L. Waltz, E. Zinato, D. W. Watts, P. D. Fleischauer and R. D. Lindholm, Chem. Rev., 1968, 68, 541-585

(42). 112. Thermochemistry and oxidation potentials of the platinum group metals and thcir compounds. R. N. Goldberg and L. G. Hepler, Chem. Rev., 1968,68,229-252 (212). 113. N.m.r. studies of ions in pure and mixed solvents. J. F. Hinton and E. S. Amis, Chem. Rev., 1967, 67,367-425 (366). 114. Some applications of mass spectroscopy in inorganic and organometallic chemistry. J. M. Miller and G. L. Wilson, Adv. Inorg. Chern. Radiochem., 1976,18,229-285 (301). 115. Correlations in nuclear magnetic shielding, part 11. J. Mason,Adv. Inorg. Chem. Radiochern., 1979, 22,199-237 (180). 116. Structural and bonding patterns in cluster chemistry. K . Wade, Adv. Inorg. Chem. Radiochern., 1976,18,1-66 (220). 117. Coordination chemistry of cyanate, thiocyanate and selenocyanate ions. A. H. Norbury, A h . Inorg. Chem. Radiochem., 1975, 17: 232-386 (825). 318. Complexes of open chain tetradentate ligands containing heavy donor atoms. C. A. McAuliffe, Adv, Inorg. Chem, Radiochem., 1Y75, 17, 165-187 (58). 129. Copper(1) complexes. F. H. dardine, Adv. Inorg. Chem. Radiochern., 1975, 17, 116163 (362). 120. Inorganic compounds containing the trifluoroacetate group. C. D. Garner and B. Hughes, Adv. Inorg. Chem. Radiochem., 1975,17,1-47 (272). 121. Vacuum ultraviolet photoelectron spectroscopy of inorganic molecules. R. L. De Kock and D. R. Lloyd, Adv. Inorg. Chem. Radiochem., 1974, 16,66107 (187). 122. Metal alkoxides and dialkylamides. D. C. Bradley, Adv. Inorg. Chem. Radiochem., 1972, 15, 259-322 (235). 123. Mossbauer spectra of inorganic compounds: bonding and structure. G. M. Bancroft and R. H. Platt, Adv. Inorg. Chem. Radiochem., 1972, 15,59-258 (577). 124. Transition metal complexes containing bidentate phosphine li ands. W. Levason and C. A. McAuliffe, Adv. Inorg. C h m . Radiochem., 1972, 14, 172-253 (3153. 125. Low temperature condensation of high temperature species as a synthetic method. P. L. Timrns, Adv. Inorg. Chern. Radiochem., 1972,14,121-171(143). 121% Transition metal clusters of r-acid ligands. R. D. Johnston. Adv. Inorr. Chem. Radiochem., 1970, 13,471-533 (412). 127. E.s.r. spectroscopy of transition metal complexes. B. A. Goodwin and J. B . Raynor, A d v . Inorg. Chem. Radiochem., 1970,13,136-362 (735). L

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128. Zirconiuni and hafnium chemistry. E. M. Larson. Adv. Inorg. Chem. Radiochem., 1970, 13, 1-133 (611). 129. Cis- and trans-effects in cobalt(II1) complexes. J. M . Pratt and R. G. Thorp, Adv. Inorg. Chem. Radiochern., 1969, 12,375427 (181). 130. Preparation of anhydrous lanthanon halides. M. D. Taylor. Chem. Rev., 1962,62,503-511 (112). 131. The chemistry of complexes containing 2,2’-bipyridyl. 1,lO-phenanthroline or 2,2‘,6’,2”-terpyndyl as li ands. W. R. McWhinnie and J. D. Miller, Adv. Inorg. Chem. Radiochem., 1969, 12, 135-215 (7477. 132. Vibrational spectra of transition metal carbonyl compounds. L. M. Haincs and M. H. B. Stiddard, A d v . Inorg. Chem. Radiochem., 1969,12,5>133 (340). 131. Some recent preparative chemistry- of protactinium. D. Brown, Adv. Inorg. - Chrm. Radiochem., , 1969,12,i-si (138). 134. Some general aspects of mercury chemistry. H. L. Roberts, Adv. Inorg. Chem. Radiochem., 1968, 11.309-339 (621. 135. Transition nietal complexes with group IVB elements. J . F. Young, Adv. Inorg. Chern. Radiochem., 1968,1I, 92-152 (254). 136. Technetium. K. V. Kotegov, 0. N. Pavlov and V. P. Shvedov, Adv. Inorg. Chern. Radiochem., 1968. 11. 1-90 1273). 137. Mixed valence chemistry- a survey and classification. M. B. Robin and P. Day, Adv. Inorg. Chem. Radiochem., 1967.10,24&422 (820). 138. Further advances in the study of the mechanisms of redox reactions. A. G. Sykes, Adv. Inorg. Chem. Radiocliem., 1967, 10, 153-245 (425). 139. The inorganic chemistry of tungsten. R. V. Parish, Adv. Inorg. Chern. Radiochem., 1966, 9 , 315-354 (293). 140. I’Ieterocations. A . A . Woolf, Adv. Inorg. Chern. Radiochem., ‘I966,9,217-314 (345). 141. Stereoselectivity in coordination compounds. J . H. Duniop and R.D. Gillard, Adv. I n t i g . Chem. Radiochem.! 1966,9,185-215 (97). 142. The chemistry of complex aluminohydrides. E. C. Ashby, Adv. Inorg. Chem. Radiochem., 1966,8, 283-335 (155). 143. Nuclear quadrupole resonance and its applications in inorganic chemistry. M. Kubo and D. Nakamura, Adv. Inorg. Chem. Radiochem., 1966,8?257-283 (78). 144. Neutron diffraction and its ap lications in inorganic chemistry. G. E. Bacon, Adv. Inorg. Chem. Radiochem., 1966,8,225-256 b4). 145. Transition metal cyanides and their complexes. B. M. Chadwick and A. G. Sharpe, Adv. Inorg. Chem. Radiochem.. 1966,8,83-176 (544). 146. Substitution products of group VIB metal carbonyls. G. R. Dobson, I. W. Stolz and R. K. Sheline, Adv. Inorg. Chem. Radiochern., 1966,8, 1-82 (398). 147. Organoaluminum compounds. R. Koster and P. Binger, Adv. Inorg. Chern. Radivchem., 1965, 7, 263-348 (326). 148. Reactions of chclated organic ligands. U. Fernando, Adv. Inorg. Chem. Radiochem., 1965, 7, 185-261 (210). 149. Hydride complexes of the transition metals. M. L. H. Green and D. J. Jones, Adv. lnorg. Chem. Radiochern., 1965,7,115-183 (273). 150. The phthalocyanines. A. B. P. Lever, Adv. Inorg. Chem. Radiochern., 1965,7,28-114 (382). 151. Peroxy compounds of the transition metals. J. A. Connor and E. A. V. Ebsworth, Adv. Inorg. Chem. Radiochem. 1964,6,280-381 (595). 152. The Mossbauer effect and its application in chemistry. E. Fluck, Adv. Inorg. Chern. Radiochem., 1964,6,433489 (58). 153. Anhydrous metal nitrates. C. C. Addison and N. Logan, Adv. Inorg. Chem. Radiochem., 1964,6, 72-142 (255). 154. Complexes of the transition metals with phosphines, arsines and stibines. G . Booth, Adv. Inorg. Chem. Radiochtm., 1964,6,1-69 (460). 155. The chemistry of gallium. N. N. Greenwood, Adv. Inorg. Chem. Radiochern., 1963, 5 , 91-134 (310). 156. The stabilisation of oxidation states of the transition metals. R. S. Nyholm and M. L. Tobe, A d v . Inorg. Chem. Radiochem., ‘1963,5 , 1-40 (67). 157. The use ot’n.rn.r. in inorganic chemistry. E. L. Muetterties and W. D. Phillips, Adv. Inorg. Chem. Radiochem., 1962,4,231-292 (139). 158. The chemistry of polonium. K. E. Bagnall, Adv. Inorg. Chem. Radiochem., 1962,4,198-229 (137). 159. Recent advances in the stereochemistry of nickel, palladium and platinum. J. R. Miller, Adv. Inorg. Chem. Radiochem., 1962,4, 133-195 (270). 160. Solvent extraction of inorganic species. Y. Marcus, Chem. Rev., 1963,63, 139-170 (465). 161. The general, selective and specific formation of com lexes by metallic cations. G. Schwarzenbach, Adv. Inorg. Chem. Radiochem., 1961,3,257-285 (707. 162. Mechanisms of substitution reactions of metal complexes. F. Basolo and R. G. Pearson, Adv. Inorg. Chern. Radinchem.. 1961,3, 1-89 (132). 163. Halides of the actinide elements. J. J . Katz and I Sheft, Adv. Inorg. Chem. Radiochern., 1960, 2, 1Y5-236. 164, Prope.rties of organic solutions of heavy metal soaps. N. Pilpel, Chem. Rev., 1943, 63, 221-234 (101j. 165. The sulphuric acid solvent system. R. J. Gillcspic and E. A. Robinson, Adv. Inorg. Chem. Radiochem., 1959.1,385423 (87). ~

COC 7-6.

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146. Synthetic reversible oxygen carrying chelates. L. H. Vogt, H. M. Faigenbaum and S. E. Wiberley, Chem. Rev., 1963,63.269-277 (52). 167. Mechanisms of redox reactions in simple chemistry. H. Taube, Adv. Inorg. Chem. Radiochem., 1959,1,1-53 (144). 168. Mixed valence complexes of &-d6 metal centres. C. Creutz, Prug. Znorg. Chem., 1983, 30, 1-73 (149). 169. Technetium chemistry and technetium radiopharmaceuticals. E. Deutsch, K. Libson, S. Jurisson and L. F. Lindoy, Prog. Inorg. Chem., 1983,30,75-139 (279). 170. Structural and photochemical probes for electron transfer reactivity. J. F. Endicott, K. Kumar, T. Ramasami and F. P. Rotzinger, Prog. Inorg. Chem., 1983,30, 141-187 (185). 171. Homolytic and free radical pathways in reactions of organochromium complexes. J. H. Espenson , Prog. Inorg. Chem., 1983,30,189-212 (85). 172. Mechanistic aspects of the photosubstitution and photoisomerisation reactions of dh-metal cornplexes. P. C. Ford, D. Wink and J. Dibenedetto, Prog. Inorg. Chem., 1983.30,213-271 (182). 173. Oxides and oxyacids of technetium. W. A. Dutton and W. C. Cooper, Chem. Rev., 1966, 66, 657-675 (144). 174. The coordination chemistry of rhe actinides. A. E. Comyns, Chem. Rev., 1960,60, 115-147 (584). 175, Organotin compounds. R. K. Ingham, S. D. Rosenberg and R. H. Gilman, Chem. Rev., 1960,60, 459-539 (924). 176. The organic chemistry of titanium. I. Shiihara, W. T. Schwarz and H. W. Post, Chem. Rev., 1961, 61, 1-30 (423). 177. Coordination compounds of unsaturated 1 ,2-dithiols and dithioketones. G. N. Schrauzer, Transition Met. Chem. ( N . Y . ) , 1968,4,229-335 (87). 178. Electronic structure and stereochemistry of nickel(I1). L. Sacconi, Transition Met. Chem. ( N .Y . ) , 1968,4,1.99-298 (296). 179. The nature of the transition between high spin and low spin octahedral complexes of the transition metals. R. L. Martin and A. H. White, Transition Met. Chem. ( N . Y . ) ,1968,4, 113-198 (115). 180. Paramagnetic relaxation in solutions. W. B. Lewis and L. 0 . Morgan, Transition Met. Chem. ( N . Y . ) , 1968,4,33-112 (140). 181. The spectra of rhenium(4+) in cubic crystal fields. P. B. Dorain, Transition Met. Chem. (N.Y.), 1968,4,1-31 (27). 182. Conformation of coordinated chelates. A. M. Sargeson, Transition Met. Chem. ( N . Y . ) , 1966, 3, 303-343 (46). 183. Fluorescent lifetimes of trivalent rare earth transition metal chemistry. G. E. Peterson, Transition Met. Chem. (N.Y.), 1966,3,202-302 (173). 184. E.s.r. spectroscopy of transition metal complexes. B. R. McGarvey, Transition Met. Chern. ( N .Y . ) , 1966,3,89-201 (288). 185. Equilibria of complexes in non-aqueous solvents. L. I. Katzin, Transition Met. Chem. ( N . Y . ) , 1966, 3,57-88 (58). 186. Electronic structure of some organometallic molecules. D. A. Brown, Transition Mer. Chem. ( N . Y . ) ,1966,3, 1-55 (150). 187. Optical activity of inorganic and organic compounds. A. D. Liehr, Transition Met. Chem. ( N . Y . ) , 1966,2, 166-338 (66). 18s. Transition metal ions as reagents in metallo-enzymes. A. F. Dennard and R. J. P. Williams, Transition Met. Chem. ( N . Y . ) ,1966,2,116134 (35). 189. Reactions of ligands coordinated to transition metals. J. P. Collman?Transition Met. Chem. ( N . Y . ) , 1966,2,1-114 (303). 190 Electronic struction of square planar metal complexes. H. B. Gray: Transition Met. Chem. (N.Y.). 1965. 1.24G-287 (69). 191. Hydride com lexks of the transition metals. A. P. Ginsburg, Transition Met. Chem. ( N . Y . ) , 1965, I , 112-237 (331p. 192. Aqueous chemistry of chrornium(II1). J. E. Earley and R. D. Cannon, Transition Met. C h e m ( N . Y . ) , 1965,1,34-109 (364). 193. Electronic structure and stereochemistry of cobalt(l1). R . L. Carlin, Tramition Met. Chem. ( N . Y . ) , 196S, 1, 1-32 (61). 194. Theory of electron transfer reactions: insights and hindsights. N. Sutin. Prog. Inorg. Chem., 1983, 30,441-498 (148). 195. Excited state electron transfer. T. J. Meyer, Prog. Inorg. Chern., 1983,30, 389440 (104). 196. Aquo complexes of metal ions. J. P. Hunt and H. L. Friedman, Prog. Inorg. Chem., 1983, 30, 359-387 (110). 197. Mechanisms of electron transfer reactions: the bridge activated complex. A. Haim, Prog. Inorg. Chem., 1983,30,273-358 (196). 198. The chemistry of metal oxalate complexes. K. V. Krishnamurty and G. M. Harris, Chem. Rev., 1961,61,213-240 (456). 199. Complex compounds of biguanides and guanylureas with metallic elements. P. Ray, Chem. Rev., 1961,61,313-359 (188). 200. Higher oxidation states of silver. J. A . McMillan, Chem. Rev., 1962,62,6580 (194). 201. Some aspects of silicon-transition metal chemistry. B. J . Aylett, Adv. Inorg. Chem. Radiochem., 19K2,25, 1-133 (458). 202. Organogermanium chemistry. D. Quane and R. S. Boltei, Chem. Rev., 1963,63,403-442 (221). 203. Structure and reactivity of oxyanions of the transition metals. A. Carrington and M. C. R. Symons, Chem. Rev., 1963,63, 443-460 (115). I

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204. The chemistry of the vitamin B12 group. R. Bonnett, Chem. Rev., 1963,63,573-605 (293). 205. Copper(I1) complexes with subnormal magnetic moments. M. Kato, H. B. Jonasson and J. C. Fanning, Chem. Rev., 1964,64,99-128 (197). 206. Metal gluconate complexes. D.T. Sawyer, Chem. Rev., 1964,64,633-643 (140). 207. Coordination chemistry of yttrium and the rare earth metal ions. T. Moeller, D. F. Martin. L. C. Thompson, R. Ferrus, G. R. Feistel and W. J. Randell, Chem. Rev., 1965,65,1-50 (651). 208. The chemistry of oxovanadium(V). J. Selbin, Chem. Rev., 1965,65,153-175 (396). 209. The isoelectronic points of solid oxides, solid hydroxides and aqueous hydroxo complex systems. G. A. Parks, Chem. Rev., 1965,65, 177-198 (131). 210. The chemistry of xenon. J. G. Malm, H. Selig, J. Jortner and S. A. Rice, Chern. R e v . , 1965, 65, 199-236 (183). 211. Phototropy (or photochromism). R. Exelby and R. Grinter, Chem. Rev., 1965,65,247-260 (187). 212. Electrode potentials and hydration energies: theories and correlations. D. R. Rosseinsky, Ckem. Rev., 1965,65,467-490 (221). 213. Conformational aspects of chelate rings. R. D. Gillard and H. M. Irving, Chem. Rev., 1.965, 65, 603-616 (132). 214. Addition compounds of the group V pentahalides. M. Webster, Chem. Rev., 1966, 66, 87-118 (575). 215. Chemistry of vitamin B12 and related inorganic model systems. D. G. Brown, Prog. Inurg. Chem., 1973,18,177-286 (268). 216. Metalloporphyrin redox reactions. L. E. Bennett, Prug. Inorg. Chem., 1973, 18, 1-176 (750). 217. Stereochemical and electronic structural aspects of five coordination. J. S. Wood, Prog. Inorg. Chern., 1972,16,227-486 (566). 218. Halides and oxyhalides of the early transition series and their stability and reactivity in non-aqueous media. R. A. Walton, Prng. Inorg. Chem., 1972,16, 1-226(65). 219. Transition metal cluster compounds. R. B. King, Prog. Inorg. Chem., 1972,15,287-473 (383). 220. The interpretation of '%n Mossbauer spectra. R. V. Parish, Prug. Inorg. Chem., 1972,15,101-200 (142). 221. The stereochemistry of his chelate metal(I1) complexes. R. H. Holm and M. J. O'Connor, Prog. Inorg. Chem., 1971: 14,241-401 (559). 222. Single crystal and gas phase Raman spectroscopy in inorganic chemistry. G. A. Ozin: Prog. Inorg. Chem., 1971,14,173-239 (169). 223. Electronic spectroscopy of high temperature open-shell polyatomic molecules. D. M. Gruen, Prug. Znorg. Chem., 1971,14>119-172 (148). 224. Inorganic electrosynthesis in non-aqueous solvents. B. L. Laube and C. D. Schmulbach, Prog. Inorg. Chem., 1971,14,65-118 (451). 225. Studies of dynamic organometallic compounds of the transition metals by means of N.M.R. K. Vrieze and P. W. N. M. van Leewen, Prog. Inorg. Chem., 1971,14, 1-63 (181). 226. N.M.R. of metal nuclides. Part 1: the main group elements. J . J. Dechter, Prog. Inurg. Chem., 1982,29,285-385 (335). 227. Magnetochemistry - advances in theory and experimentation. C. J. O'Connor, Prog. Inorg. Chem., 1982,29,203-283 (271). 228. The chemistry, structure and metal-metal bonding in compounds of rhodium(I1). T. R. Felthouse, Prug. Inurg. Chern.. 1982: 29,73-166 (353). 229. Chemical reactions of metal-metal bonded compounds of the transition elements. M. H. Chisholm and I. P. Rothwell, Frog. Znorg. Chem., 1982,29,1-72 (238). 230. A dynamic model for mixed valence compounds. K. Y. Wong and P. N. Schatz, Prog. Inorg. Chem., 1981,28,369-449 (98). 231. Aspects of the stereochemistry of nine-, ten- and twelve-coordination. M. C. Favas and D. L. Kepert, Prog. Inorg. Chem., 1981,28,309-367 (78). 232. The coordination chemistry of tungsten. Z . Dori? Prug. Znorg. Chem., 1981,28,239-307 (346). 233. Metal carbide clusters. M. Tachikawa and E. L. Muetterties, Prog. Inorg. Chem., 1981,28,203-238 (69). 234. Chlorotris(triphenylphosphine)rhodium(I): its chemical and catalytic reactions. F. H. Jardine, Prog. Inorg. Chem., 1981,28,63-202 (650). 235. Heterolytic activation of hydrogen by transition metal complexes. P. J. Brothers, Prog. Inorg. Chem., 1981,28,1-61(168). 236. Aspects of the stereochemistry of four- and five-coordination. M. C. Favas and D. L. Kepert, Prog. Znorg. Chem., 1980,27,325-463 (602). 237. Dithiolium salts and dithio-p-diketone complexes of the transition metals. T. N. Lockyer and R. L. Martin, Prog. Znorg. Chem., 1980,27,223-324 (198). 238. Some aspects of the reactivity of metal ion-sulphur bonds. C. G. Kuehn and S. S. Isied, Prog. Inorg. Chern., 1980,27,153-221(317). 239. Photochemistry of transition metal hydride complexes. G . L. Geoffroy, Prog. Inorg. Chem., 1980, 27, 123-151 (58). 240. The chemistry of dithioacid and 1 ,l-dithiolate complexes, 1968-1977. D. Coucouvanis, Prug. Inorg. Chem., 1979,26,301-469 (645). 241. Metal-metal bonds of order four. J. L. Templeton, Prog. Inorg. Chern., 1979,26,211-300 (255). 242. U.V. photoelectron s ectroscopy in transition metal chemistry. A. H. Cowley, Prog. Znorg. Chern. 1979,26,45-160 (2917.

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Index of Review Articles and Specialist Texts 243. A local view of magnetochemistry. M. Gerloch, Prog. Inorg. Chern., 1979,26, 1-43 (48). 244. Chemistry and spectroscopy of f-element organometallics: Part 11. the actinides. T. J. Marks, Prog. Inorg. Chern, 1979,25, 22>333 (410). 245. The hvdrido-transition metal cluster comolexes. A. P. Humuhries and H. D. Kaesz. Proa. Znora. Chern: 1979,25,145-222 (244). 246. Aspects of the stereochemistry of seven coordination. D. L. Kepert, Prog. Inorg. Chern., 1979,25, 41-144 (192). 247. X-ray abso;ption spectroscopy: a new structural method and its applications to bioinorganic chemistry, S. P. Kramer and K. 0 . Hodgson, Prog. Inorg. Chem., 1979,25,1-39 (71). 248. Structural tin chemistry. J. A. Zubieta and J. J . Zuckerman, Prog. Inorg. Chern., 1978,24,251475 (751). 249. Aspects of the stereochemistry of eight coordination. D. L. Kepert, Prop. Inorg. C'hern., 1978, 24, 179-249 (133). 250. The coordination chemistry of mercuric halides. P. A. W. Dean, Prog. fnorg. Chern., 1978, 24, 109-178 (334). 251. Chemistry and spectroscopy of f-element organometallics: Part I, the lanthanides. T. J. Marks. Prog. Inorg. Chern., 1978, 24,51-107 (201). 252. Metal ion interactions with nucleic acids and nucleic acid derivatives. L. G. Marzilli, Prog. Inorg. Chern., 1977,23,255-378 (337). 253. The stereochemistry of metal complexes of nucleic acid constituents. D. J. Hodgson, Prog. Inorg. Chern., 1977,23,211-254 (175). 254. Seven coordination chemistry. M. G. B. Drew, Prog. Inorg. Chem.. 1977,23, 67-210 (652). 255. Aspects of the stercochemistry of six Coordination. D. L. Kepert, Prog. Znorg. Chern., 1977, 23, 1-65 (258). 256. Applications of C-13 n.m.r. in inorganic chemistry. M. H. Chisholm and S. Godleski, Prog. Inorg. Chern., 1976,20,299436 (240). 257. Thc study of electron distribution in inorganic solids: a S U T V ~of~ techniques and results. B. C . Tofield, Prog. Inorg. Chern., 1976,20. 153-228 (228). 258. One dimensional inorganic complexes. J. S. Miller and A. J. Epstein, Prog. Inorg. Chem., 1976,M, 1-151 (581). 259. Five-coordination in iron(I1): cobalt(I1) and nickel(I1) complexes. R. Morassi, I. Bertini and L. Sacconi, Coord. Cheni. Rev., 1973,11,343-402 (33). 260. Acid catalysed reactions of transition metal complexes. P. J. Staples, Coord. Chern. Rev., 1973, 11, 277-342 (181). 261. Partial quadrupole splittings in inorganic chemistry. G. M. Bancroft, Coord. Chem. Rev., 1973, 11, 247-262 (53). 262. The extraction of metal ions from aqueous sulphate media by alkylamines. R. W. Cattrall and S. J. E. Slater, Coord. Chern. Rev., 1973, 11,227-245 (64). 263. The application of ultrasound absorption to reaction kinetics. N. P u d i c and M. M. Farron, Coord. Chern. Rev., 1973, 11, 189-226 (109). 264. Alfred Werner's research on structural isomerism. Ci. E. Kaufman, Coord. Chem, Rev., 1973, 11, 161-'19Y (279). 265. Metal complexes of aromatic amine W-oxidcs. N. M. Karayannis: L. L. Pytlcwski, and C . M. Mikulski, Coord. Chern. Rev.: 1973, 11,93-159 (447). 266. The structural chemistry of zirconium compounds. T. E. MacDermott, Coord. Chern. R e v . , 1973, 11,l-20 (121). 267. A study of force fields for tetrahedral molecules and ions. L. 3. Basile, J . R., Ferraro, P. La Bonville and M. C. Wall, Coord. Chenr. Rev., 1973,11,21-69 (111). 268. The trans influence: its measurement and significance. T. G. Appleton, H. C. Clark and L. E. Manzer, Coord. Chem. Rev.. 1973,10, 335-422 (302). 269. Transition metal hydrides. J. P. McCue, Cuord. Chrm. Rev., 1973,10,265-333 (287). 270. Stcric and electronic factors influencing the structure of nickel(I1) comolexes. E. Uhlie, . Coord. Chem. Rev., 1973,10,227-264 (152). 271. Complexes of lanthanide ions with N-donor ligands. J. €I. Forsberg, Coord. Chern. Rev., 1973, 10, 195-226 (129). 272. A descriptive introduction to analysis of the vibrational spectra of solids. D. M. Adams, Coord. Chern. Rev., 1973,lO. 183-193 (8). 273. Kinetics of nickel? palladium and platinum complexes. A. Peloso, Coord. Chern. Rev., 1973, 10, 123-181 (305). 274. Thio- and seleno-compounds of the transition metals with do configuration. E. Diemann and A . Muller, Coord. Chern. Rev., 1973,10,79-122 (222). 275. Magnetically perturbed Mossbauer s ectra of iron and tin coordination compounds. W. M. Reiff, Coord. Chern. Rev., 1973: 10,37-77 638). 276. Kinetics and mechanisms of substitution reactions of octahedral macrocyclic amine complexes. C. K. Poon, Coord. Chem. Rev., 1973, 10, 1-35 (130). 277. The geometry of pentacoordinated complexes. B. F. Hoskins and F. D. Williams, Coord. Chem. Rev., 1972,9,365-388 (82). 278. Alfred Werner's research on polynuclcar coordination Compounds. G. 3.Kauffman, Coord. Chem. Rev., 1972,9,339-363 (115). 279. N,N-Ethylenebis~salicyIidcneiminato)-transition metal ion chelates. M. D. Hobday and T. D. Smith, Coord. Chem. Rev., 1972,9?311-337 (223). 280. X-ray absorption edge spectrometry (XAES) as applied to coordination chemistry. U. C. Srivastava and H. L. Nigam, Coord. Chern. Rev., 1972,9,275-310 (135). ,

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281. Ligand design and synthesis. D. St. C. Black and A. J. Hartshorn, Coord. Ckem. Rev., 1972: 9. 219-274 (363). 282. Infrared spectra and geometry of group I1 metal dihalides. I. Eliezer and A. Reger, Coord. Ckem. Rev., 1972,9, 189-200 (36). 283. Trigonal prismatic versus octahedral stereochemistry in complexes derived from innocent ligands. R. D. Wentworth. Coord. Chem. Rev.. 1972.9.171-187 (34). 284. Chelating dioxygen com ounds of the' platinum metals. 'V.'J. Choy and C. J. O'Connor, Coord. Ckem. Rev., 1972: 9 14c170 (86). 285. The chemistry of d'l complcxes of niobium, tantalum, zirconium and hafnium. D.A. Miller and K.D. Bereman, Coord. Chem. Rev., 1972,9, '107-143 (9.5). 286. Spectroscopic studies of metal-phosphorus bonding in cnordination complexes. J. G. Vcrkade, Coord. Ckem. Rev., 1972,9, 1-106 (308). 287. Transition metal nitrido complexes. W . P. Griffith, Coord. Ckem. Rev., 1972,8,369-396 (100). 288. The influence of geometry and donor atom set on the spin state of five coordinate cobalt(I1) and nickel(I1). L. Sacconi, Coord. Chem. Rev., 1972,8, 351-367 (117). 289. The coordination chemistry of thallium(1). A. G. Lee, Coord. Chem. Rev., 1972,8,29&349 (398). 290. Spin-forbidden electronic transitions in transition metal complexes. L. L. Lohr, Coord. Chem. Rev. 1972,8,241-259 (74). 291. Isocyanide insertion and related reactions. Y. Yamamoto and H. Yamazaki, Coord. Ckem. Rev., 1972,8,225-239 (47). 292. Some aspects of the coordination chemistry of iron(II1). S. A. Cotton, Coord. Ckem. Rev. 1972,8, 18.5-223 (263). 293. Structural aspects of metal complexes with some tetradentate Schiff bases. M. Calligaris, G. Nardin and L. Randaccio: Coord. Chem. Kev., 1972,7,385403 (56). 294. Higher oxidation state chemistry of manganese. W. Levason and C. A. McAuliffe, Coord. Ckem. Rev., 1972,7,353-384 (294). 295. Bonding effects in circularly dichroic cobalt(II1) complcxes. L. T. Katzin and I. Eliezer, Coord. Ckem. Rev., 1972,7,331-343 (20). 296. Manganese porphyrin complexes. L. J. Boucher, Coord. Ckem. Rev., 1972,7,289-329 (112). 297. A study of force fields for octahedral hexahalogen molecules. P. La Bonville, J. R. Ferraro, M. C . Wall and L. J. Basile, Coord. Chem. Rev., 1972,7, 257-287 (42). 298. Platinum(I1) catalysed substitution of platinum(1V) complexes. W. R. Mason, Coord. Ckem. Rev., 1972,7,241-255 (41). 299. Magnetic resonance methods in the study of the elcctronic structure of transition metal complcxes. D. R. Eaton and K. Zaw, Coord. Chem. Rev., 1971,7,197-227 (189). 300. Complexes of cobalt(II1) with flexible tetradentate ligands. G. R. Brubaker, D. P. Schaefer, J. H. Worrell and J. I. L.rgg, Coord. Ckem. Rev., 1971,7, 161-195 (102). 301. The coordination chiinistry of silicon. G. A. Melson and R. W. Stotz, Coord. Ckem. R e v . , 1971,7, 133-160 (225). , , 302. The use of conductivity measuTements in organic solvents for characterisation of coordination compounds. W. J. Gearg, Coord. Chem. Rev., 1971,7,81-122 (377). 303. Monothio-P-diketoner and their metal complexes. S. E . Livingstone. Coord. Ckem. Rev., 1971, 7, 59-80 (73). 304. Metal complexes of thio-P-diketones. M. Cox and J. Darken. Coord. Chem. Rev., 1971, 7, 2%58 (99). 305. Solid state photochemical reactions of transition metal coordination compounds. E. L. Simmons and W. W. Wendlandt, Coord. Chem. Rev., 1971,7. 11-27 (88). 306. Water exchange kinetics in labile aquo and substituted aquo transition metal ions by means of "0 n.m.r. studics. J. P. Hunt, Coord. Chem. Rev., 1971,7,1-10 (29). 307. Infrared spectra oE complexes of the thiocyanate and related ion>. R. A. Bailey, S. L. Kozak. T. W. Michelson and W. N . Mills, Coord. Chem. Rev., 1971,6,407445 (90). 308. Some su gested calculation procedurcs and the variation in results obtained from different calcuiation metkods for evaluation of concentration stability constants of metal ion complexes in aqueous solution. A . M. Bond. Coord. Cherri. Rev.. 1971.6.377405 (431. 309. Optical and geometrical isomerisation of i-diketonate compfexes. J. J. Fortman and R. E. Sievers, Coord. Chem. Rev.. 1971.6.331-375 (122). 310. Solvent coordination numbers of metal ions in solution. S. F. Lincoln, Coord. Ckem. Rev., 1971,6, 309-329 (133). 311. The stereochemistry of five coordinate nickel(I1) and cobalt(I1) complexes. P. L. Orioli. Coord. Ckem. Rev., 1971,6,285-308 (76). 312. Steric effects in substituted halocarbonyls of molybdenum and tungsten. R. Colton, Coord. Ckem. Rev.,1971,6,269-284 (29). 313. The coordination chemistry of metalloporphyrins. P. IIambright, Coord. Ckem. Rev., 1971, 6, 247-268 (145). 314. The steric effect in bis(2J-bipyridyl) and bis(1,IO-phenanthroline) metal compounds. E. D. McKenzie, Coord. Chem. Rev., 1971,6, 187-216 (145). 315. Paramagnetic anisotropy. W. De W. Horrocks and b4De W. Hall, Coord. Ckem. Rev., 1971, 6 , 147-186 (70). 316. Molecular orbital calculations for transition metal compounds. D. R. Davies and G. A. Webb, Coord. Chem. Rev., 1971,6,95-146 (267). ~

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lndex of Review Articles and Speciulisr Texts

317. Hydroxyl ion as a ligand. V. Baran, Coord. Chem. Rev., lY71.5,65-93 (216). 318. Coordination complexes of the thallium(1ll) halides and their behaviour in non-aqueous media. R. A. Walton, Coord. Chem. Rev., 1971,6, 1-25 (167). 319. Transition metal oxo complexes. W. P. Griffith, Coord. Chem. Rev., 1970,5,459-517 (307). 320. Structural studies on iron-sulphur proteins. J. C. M. Tsibris and R. W. Woody, Coord. Chem. Rev., 1970,5,417458 (155). 321. The thermodynamics of metal complex and ion pair formation. G. H. Nancollas, Coord. Chem. Rev., 1970,5,379-415 (144). 322. AsDects of the chemistrv of cobalt(II1) in aaueous uerchlorate solution. G. Davies and B. Warn' quht, Coord. Chem. Re;., 1970,5,349-378 (85). 323. Magnetic exchangc in polynuclear metal complexes. E. Svrin, Coard. Chern. Rev., 1970,5,313-347 (230). 324. The coordination behaviour of some chelating ligands containing non- or weakly-conjugated 2-pyridyl groups. W. R. McWhinnie, Uoord. Chrm. Rev., lY70,5,293-311 (91). 325. Some applications of C.D. measurements to problems in metal ion complexes, using nickel(I1) and lanthanides as examples. L. I. Katzin, Coord. Chem. Rev., 1970,5,279-292 (12). 326. The role of complexes in metal ion oxidations in solution. A. McAuley, Coord. Chem. Rev., 1970, 5,245-273 (139). 327. E.p.r. studies of exchange coupled metal ions. G. F. Kokoska and R. W. Duerst, Coord. Chem. Rev., 1970,5,209-244 (186). 328. The electronic properties and stereochemistry of mononuclear complexes of the copper(I1) ion. B. J. Hathaway and D. E. Billing, Coord. Chem. Rev., 1970,5. 143-207 (183). 329. Aqueous coordination chemistry of plutonium. J. M. Cleveland. Coord. Chem. Rev., 1970, 5 , 101-137 (125). 330. Properties and reactions of ruthenium(I1) amine complexes. P. C. Ford, Coord. Chem. Rev., 1970, 5,75-99 (67). 331. The mechanism of octahedral complex formation by labile metal ions. D. J. Hewkin and R . H. Price, Coord. Chem. Rev., 1970,5,45-73 (177). 332. Copper(I1) ammonia complexes. B. J. Hathaway and A. A. G. Tomlinson, Cuord. Chew. Rev., 1970,5, 1-43 (82). 333. Biochemical asDects of molvbdenum coordination chemistrv. 3. T. SDence. Coord. Chem. Rev.. 1969,4,475-498 (74). 334. Complex compounds of l,5-disubstituted tetrazoles. A. I. Popov, Coord. Chem. Rev., 1969, 4, 463-474 (36). 335. Far infr&ed spectra and lattice vibrations of inorganic complex salts. I. Nakagawa, Coord. Chem. Rev., 1969,4,423462 (35). 336. Schiff base metal complexes as ligands. E. Sinn and C . M. Harris, Coord. Chem. Rev., 1969, 4, 391-422 (144). 337. The magnetic pro erties of polynuclear transition metal complexes. P. W. Ball, Coord. Chem. Rev., 1969.4.361-383 ?lSOI. 338. Stereochemistry of t;rtrato(4-) bridge binuclear complexcs. R. E. Tapscott, R. L. Belford and I. C. Paul, Coord. Chem. Rev., 1969,4,323-359 (145). 339. The stabilitv of mixed comdexes in solution. Y. Marcus. Coord. Chem. Rev.. 1969. 4. 273-322 (236). 340. Stereochemical changes during octahedral substitution reactions. R. D. Archer, Coord. Chem. Rev., 1969,4,243-272 (148). 341. Carbon bonded fi-diketone complexes. D. Gibson, Coord. Chem. Rev., 1969,4,225-240 (30). 342. Some aspects of the chemistry of manganese(II1) in aqueous solution. G. Davies, Coord. Chem. Rev., 1969,4,199-224 (101). 343. Carbonato complexes of cobalt(II1). C, R. P. Mac-Coll, Coord. Chem. Rev., 1969, 4. 147-198 (198). 344. The effect of axiaI ligands on ground state properties of complexes with orbitally degenerate ground terms. G. A. Webb, Coord. Chem. Rev., 1969,4, 107-145 (151). 345. Electronic spectra of quadrate chromium(II1) complexes. J. R. Perumareddi, Coord. Chem. Rev., 1969,4,73-105 (108). 346. Reactions involving metal complexes of sulphur ligands. L. F. Lindoy, Coord. Chem. Rev., 1969,4, 41-71 (223). 347. Metal-halogen stretching vibrations in coordination complexes of gallium, indium and thallium. A. J. Carty, Coord. Chem. Rev., 1969,4,29-39 (32). 348. Divalent transition metai P-keto-enolate complexes as Lewis acids. D. P. Graddon, Coord. Chem. Rev., 1969,4,1-28 (117). 349. Coordination chemistry of germanium. A. A. Lavigne, J. M. Tancrade and R. M. Pike, Coord. Chem. Rev., 1968,3,497-508 (68). 350. Some aspects of the chemistry of bis(2,2'-bipyridyl) and bis( 1,lO-phenanthroline) complexes of iron(I1). E. Koni , Coord. Chem. Rev., 1968,3,471-495 (81). 351. The activation ofmolecular nitrogen. R. Murray and D. C. Smith, Coord. Chem. Rev., 1968, 3, 429470 (172). 352. Chromatography of coordination complexes. L. F. Druding and G . B. Kaufman, Coord. Chem. Rev., 1968,3,409-428 (158). 353. The coordination chemistry of aromatic amine N-oxides. R. G. Garvey, 3. H. Nelson and R. 0. Ragsdale, Coord. Chem. Rev., 1968,3,375-407 (136). 354. Pyridine N-oxide complexes of platinum(I1). M. Orchin and P. J. Schmidt, Coord. Chem. Rev., 7968,3,345-373 (43). I

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355. The coordinative reactivity of phosphine com lexes of platinum(O), palladium(0) and nickel(0). R. Ugo. Coord. Chem. Rev., 1968,3,319-344 &2), 356. Solubility measurements and complex formation in solution. L. Johansson, Coord. Chem. Rev., 1968,3,293-318 (82). 357. Metal complexes of hvdroxamic acid analogues. S . Mizukami and K. Nagato, Coord. Chern. Rev., 1968,3,26?-278 (56).* 358. Oxygen bonding in coordination compounds. B. Jezowska-Trzebiatowska, Coord. Chern. Rev., 1968.3.255-266 (44). 359. Linkage isorneriim in metal complexes. J. L. Burmeister, Coord. Chem. Rev., 1968. 3. 225-245 (110).360. Stabilisation of metal complexes by large counter ions. F. Basolo, Coord. Chetn. Rev., 1968, 3, 213-223 (541. 361, O.R.D. i n d the Pfeiffcr effect in coordination compounds. S. Kirschner, N. Ahmad and K. Magnell, Coord. Chem. Rev., 1968,3,201-206 (11). 362. Some aspects of the photochemistry of coordination compounds. A. W. Adamson, Coord. Chem. Rev., 1968,3, 169-188 (47). 363. Ligand field interpretation of some cases of pentacoordination, C. Furlani, Coord. Chem. Rev., 1968,3, 141-167 (58). 364. The electronic spectra of tetragonal metal complexes - analysis and significance. A. B. P. Lever, Coord. Chem. Rev., 1968,3,119-140 (31). 365. Chemistry of outer sphere complexes. M. T . Beck, Coord. Chem. Rev., 1968,3,91-115 (84). 366. Catalytic functions of metal ions and their complexes. E. I. Ochiai, Coord. Chem. Rev., 1968, 3, 49-89 ( 130). 367. Macrocyclic coordination compounds formed bv condensation of metal amine complexes with aliphatic carbonyl compounds. N. F. Curtis, Coord. Chem. Rev., 1968,3,3-47 (78). 368. The O.R.D. and C.D. of coordination compounds. S . Kirschner, Coord. Chern. Rev., 1967, 2, 461494 (193). 369. Donor properties of 1-amidino-0-alkylureas. R. L. Dutta and A. Syamal, Coord. Chem. Rev., 1967,2,441-459 (55). 370. The nitroprusside ion. J. H. Swinehart, Coord. Chem. Rev., 1967,2,385-402 (100). 371. Bonding in coordination compounds containing a metal-metal bond. B. J. Bulkin and C. A. Rundell, Coord. Chem. Rev., 1967,2,371-384 (85). 372. Coordination chemistry of certain transition metal ions: the role of the solvent. V. Gutmann, Coord. Chem. Rev., 1967,2,239-256 (39). 373. The uses of n.m.r. in the study of ligand substitution processes. T. R. Stengle and C. H. Langford, Coord. Chem. Rev., 1967,2,349-370 (44). 374. Raman s ectroscopic studies in coordination chemistry. R. E. Hester, Coord. Chem. Rev. 1967,2, 3'19-347 1;04). 375. Metal oxide alkoxide (trialkylsilyloxide) polymers. D. C. Bradley, Coord. Chem. Rev., 1967, 2, 299-318 (25). 376. Metalkchloride complexes studied by ion-exchange and solvent extraction methods, Part I and Part 11. Y. Marcus, Coord. Chem. Rev., 1967,2, 195-238 (228) and 257-297 (239). 377. Complexes of iron(II), cobalt(I1) and nickel(l1) with a-diimine and related bidentate ligands. L.F. Lindoy and S . E. Livingstone, Coord. Chem. Rev., 1967,2, 173-193 (251). 378. 1,3-Diketo compounds of the non-metallic elements. R. M. Pike, Coord. Chem. Rev., 1967, 2, 163-172 (22). 379. The coordination chemistry of the actinide halides. K. W. Bagnall, Coord. Chem. Rev., 1967, 2, 145-162 (225). 380. Reactions and catalytic properties of rhodium complexes in solution. B. R. James, Coord. Chem. Rev., 1966, 1,505-524 (160). 381. Recent advances in the coordination chemistry of rhenium. J. E . Fergusson, Coord. Chem. Rev., 1966,1,459-503 (287). 382. Eight coordination in the transition series. R. V. Parish, Coord. Chem. Rev., 1966, 1,43%458 76). 383. Recent aspects of the stereochemistry of Schiff-base metal complexes. S. Yamada, Coord. C em. Rev., 1966, I ?415-437 (65). 384. The coordination chemistry of vanadium. D. Nicholls, Coord. Chern. Rev., 1966,1,379-414 (168). 385, The si nificance of force constants of general quadratic valence force fields: application to A U ( C N ~ ~PtClZ-, -: AuCL-, AuBr4- and AU(CN)~CI~-. L. H. Jones, Coord. Chem. Rev., 1966,1, 351-378 (15). 386. Coordination compounds of molybdenum. P. C. H. MitchelI, Coord. Chern. Rev., 1966, 1,315-350 1180). 387. Oxovanadium(1V) complexes. J. Selbin, Coord. Chern. Rev., 1966, 1,293-314 (103). 388. Electronic spectra and structural pro erties of complex tetracyanides of Pt, Pd and Ni. M. L. Moreau-Colin, Strucf. Bonding (Berliny, 1972, 10, 167-140 (33). 389. Vibrational spectra and structural propertics of corn lex tetracyanides of Pt, Pd and Ni. S. JeromeLerutte, Struct. Bonding (Berlin), 1972, 10, 153-166 r35). 390. On the general theory of magnetic susceptibilities of polynuclear transition metal compounds. J. S. Griffith, Struct. Bonding (Berlin), 1972, 10,87-126 (43). 391. Spectra and bonding in metal carbonyls: part A, bonding. P. S. Braterman, Struct. Bonding (Berlin), 1972, 10, 57-86 (110). 392. Kinetics and mechanism of alkali ion complex formation in solution. R. Winkler, Srruct. Bonding (Berlin), 1972, 10,l-24 (38). I

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Index of Review Articles and SpPcialist Texts 393. The nephelauxetic effect: calculation and accuracy of the interelectronic repulsion parameters I, cubic high spin d2, d3, d7 and d8 systems. E. Konig, Struct. Bonding (Berlin), 1971,9, 175-212 (64). 394. Iron(I1) diimine and related complexes. P. Krumholz, Struct. Bonding (Berlin), 1971, 9, 139-174 (233). 395. The electronic spectra of the hexafluoro-complexes of the first row transition series. G. C. Allen and K. D. Warren, Struct. Bonding (Berlin), 1971,9,50-138 (137). 396. Structure and bonding in inorganic derivatives of P-diketones. D. W. Thompson, Struct. Bonding (Berlin), 1971,9,27-47 (69). 397. Absorption spectra and ligand field parameters of tetragonal 3d-transitional metal fluorides. D. Oelkrug, Struct. Bonding (Berlin), 1971, 9,1-26 (91). 398. Cobalt(l1) in metalloenzyrnes; a report of structure-function rclationships. S. Lindskog, Struct. Bonding (Berlin), 1970: 8, 154196 (142). 399. The chemical nature and reactivity of cytochromc P-450. H. A . 0 . JTill. A. Riider and R. J. P. Williams, Struct. Bonding (Berlin), 1970,8,124-151 (72). 400. Structural studies of hemes and hemoproteins by n.m.r. spectroscopy. K. Wiithrich, Struct. Bonding (Berlin), 1970,8,55-121 (124). 401. Iron electronic configurations in proteins: studies by Mossbauer spectroscopy. A. J. Bearden and W. R. Dunham, Struct. Bonding (Berlin),1970,8,2-52 (196). 402. The application of N.Q.R. spectra to the study of transition metal compounds. W. van Bronswyk. Struct. Bonding (Berlin), 1970, 7, 87-113 (120). 403. The absolute configuration of transition metal complexes. R.D. Gillard and P. R. Mitchell, Struct. Bonding (Berlin), 1970,7,4&86 (165). 404. The spectra of ferric haems and haemoproteins. D. W. Smith and R. J. P. Williams, Struct. Bonding (Berlin), 1970,7,1-45 (138). 405.Ionic radii and enthalpy of hydration of ions. D. F. C. Morris, Struot. Bonding (Berlin), 1968, 4, 63-82 (61); Appendix, Struct. Bonding (Berlin), 1969,6, 157-159 (4). 406. Polynuclear complexes of iron and their biological implications. T. G. Spiro and P. Saltrnan, Strucf. Bonding (Berlin), 1949, 6: 11&156 (170). 407. Spectra of 3d five coordinate complexes. M. Ciampolini, Slruct. Bonding (Berlin), 1969, 6, 52-93 (86). 408. Ligand field spectra and chemical bonding in Cr3+-containing oxidic solids. D. Reinen, Struct. Bonding (Berlin), 1969, 6 , 30-51 (34). 409. Thermodynamics of complex formation between hard and soft acceptors and donors. S. Ahrland, Struct. Bonding (Berlin),1968: 5,118-149 (103). 410. Reaction of some transition metals with nucleic acids and their constituents. U. Weser, Sfruct. Bonding (Berlin), 1968, 5 , 4 1 4 7 (108). 411. Biochemical aspects of Fe-S linkages in non-aqueous heme iron proteins with special reference to Andrenodoxin. T. Kimura, Struct. Bonding (Berlin), 1968,5,230 (72). 412. Crystal chemistry of the chalcogenides and pnictides of transition elements. F. Hulliger, Struct. Bonding (Berlin), 19h8,4,83-229 (532). 413. Relations between softness, covalent bonding, ionicity and electric polarizability. C. K. Jorgensen. Struct. Bonding (Berlin), 19h7, 3, 106-115 (39). 414. Structural chemistry of octahedral fluorocomplexes of the transition elements. D. Babel, Strcrct. Bonding (Berlin), 1967,3,1-87 (348). 415. Reversible oxygenation of metal complexes. E. Bayer and P. Schretzmann, Struct. Bonding (Berlin), 1967,2,181-250 (247). 416. Chemistry and structure of some borate olyol compounds of biochemical interest. U. Weser, Struct. Bonding (Berlin), 1967, 2, 16G180 477). 417. Chlorophyll triplet states. G. M. Maggiora and L. L. Ingraham, Struct. Bonding (Berlin), 1967, 2, 12C1.59 (23). 418. The physics of hemoglobin. M. Weissbluth, Strut. Bonding (Berlin), 1967,2, 1-125 (60). 419. The classification of acceptors and donors in inorganic reactions. R. J. P. Williams and J . D. Hale: Struct. Bonding (Berlin), 1966, I, 249-281 (16). 420. Electric polarizability, innocent ligands and spectroscopic oxidation states. C. K. Jorgensen, Struct. Bonding (Berlin), 1966,1, 234-248 (46). 421. Displacement reactions and the concept of soft and hard acids and bases. Struct. Bonding (Berlin), 1966,1,221-233 (19). 422. Factors contributing to (b)-behaviour in acceptors. S. Ahrland, Shuct. Bonding (Berlin), 1966, 1, 207-220 (24). 423. The transferrins. R. E. Feeney and S. K. Komatsu, Struct. Bonding (Berlin), 1966,1,149-206 (141). 424. The chemistry and function of ferredoxin. B. B. Buchanan, Struct. Bonding (Berlin), 1966, 1, 109-148 (115). 425. Naturally occurring non-porphyrin iron compounds. J. B. Neilands, Struct. Bonding (Berlin),1966, 1,59-108 (151). 426. The ambident nature of cyanide. D. F. Shriver, Strucr. Bonding (Berlin), 1966, 1,32-58 (114). 427. Recent pro ress in ligand field theory. C. K. Yorgensen, Struct. Banding (Berlin),1966, I , 3-31 (49). 428. Dynamic n.m.r. spectroscopy of metal carbonyls. S. Aime and L. Milone, Prog. Nucl. Magn. Reson. Spectrosc., 1978,Il, 383-210 (143). 429. Paramagnetic lanthanide shift reagents in n.m.r. spectroscopy; principles methodology and applications. J. Reuben, Prog. Nucl. Magn. Reson. Spectrosc., 1973,9,3-70 (280). 430. N.m.r. of paramagnetic systems. E. De Boer and H . Van Willigen, Prog. Nucl. Magn. Reson. Spectrosc., 1967,2,111-161 (121).

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431. N.m.r. of paramagnetic molecules. D. R. Eaton and W. D. Phillips, A d v . Magn. Reson., 1965, 1, 103-148 (121). 432. The photochemistry of cobalt 111) and chromium(II1) complexes in solution. D. Valentine, A d v . Photochem., 1968,6.123-192 151). 433. Re-examination of the CO(NH~);+’~+self-exchange rate. D. Geselowitz and H. Taube. A h . Inorg. Bioinorg. Mech., 1982: 1,391-407 (54). 434. Mechanistic aspects of transition metal complexes containing coordinated sulphur. E. Deutsch, M. J. Roof and D. L. Nosco, A d v . Inorg. Bioinorg. Mech.. 1982, 1,269-389 (296). 435. Rates and mechanisms of reactions for elements in groups 1-111. J. C. Lockhart, A d v . Znorg. Bininorg. Mech., 1982, 1. 217-268 (140). 436. Substitution reactions of oxo-metal complexes. K. Saito and Y. Sasaki, A d v . Inorg. Bzuinorg. Mech., 1982, 1, 178-216 (176). 437. Functional properties of the biological oxygen carriers. A. G. Sykes, A d v . Inorg. Bioinorg. ~ W e c h . , 1982,1, 121-178 (169). 438. Oxidation-reduction and substitution reactions of iron sulphur centres. F. Armstrong, A d v . Imrg. Bioinorg. Mech., 1982, 1.65-120 (167). 439. Reactions and reaction mechanisms of organo-chromium(1II) complexes. J. H. Espenson, A d v . Inorg. Bioinorg. Mech., 1982, 1, 1-63 (153). 440. Transition metal pentafluorides and related compounds. R. D. Peacock, A d v . Fluorine Chem.. 1972,7,113-145 (172). 441. Transition metal fluorides and their complexes. A. G. Sharpe, A d v . Fluorine Chem., 1960, 1,29-67 (251). 442. Fluorides of the actinide elements. N. I-Iodge,A d v . Fluurine Chem., 1961,2, 138-182 (231). 443. Free radical reactions in the presence o f rnctal ions: reactions of nitrogen compounds. G. Sosnovsky and D. J. Rawlinson, Adv. Free-Radical Chenz., 1972: 4,203-284 (160). 444. Phosvitin. G. Tarborsky, A d v . Inorg. Biochem., 1983,4,23&279 (214). 445. Transferrin: a perspective. N. D. Chasteen, A d v . Inorg. Biochem., 1983,5,201-233 (9U). 446. The catechol dioxygcnases. L.. Que, A d v . Inorg. Biochem., 1983,5, 167-199 (130). 447. Siderophores. J. B. Neilands, A d v . Inorg. Biochem., 1983,5: 138-166 (57). 448. Uteroferrin and the purple acid phosphates. B. C. Antanaitis and .’l Aisen, A d v . Znorg. Biochem., 1983,5, 111-136 (74). 449. Ribonucleotide reductase. B. M. Sjoberg and A. Grasland, A d v . Inorg. Biochem., 1983, 5, 87-110 (85). 450. The chemistry of hemerythrin. R. F. Wilkins and P. C. Harrington, A d v . Inorg. Biochem., 1983,5, 52-85 (162). 451. The spatial structure of horse spleen apoferritin. D. W. Rice, G. C. Ford, J. L. White! J. M. A. Smith and P. M. Harrison, A d v . Inorg. Biochem.?1983: 5,39-50 (18). 4.52. Ferritin: structure, function and regulation. F. C. Theil, A d v . Inorg. Biochem., 1983, 5, 1-38 (137). 4.53. N.m.r. and e.p.r. investigation of bi-metalloenzymes. J. J . Villafranca and F. M. Rauschel, Adv. Inorg. Biochem., 1982, 4, 289-3’19 (5.1). 454. The cnzymatic and non-enz .matic decarboxylation of oxalace.tate. D. L. Lenssing, Adv. laorg. Biochem., ‘1982,4,171-200 (Sf. 455. Carbonic anhydrase. S. Linkskog, A d v . Inorg. Dimhem., 1982,4, ll&170 (272). 456. Bleomycin. J. C. Dabrowiak, A d v . Inorg. Biochem.: 1982,4,7&113 (122). 457. Peroxidases. H. B. Dunford, A d v . Inorg. Biochem., 1982,4,41-68 (254). 458. Bioinorganic chemistry of nitrogenase. M. J. Nelson, P . A. Lindahl and W. H. Orme-Johnson, A d v . Znorg. Biochem.? 1982, 4, 1-40 (148). 459. The mechanism of action of antitumour platinum coordination compounds. J. J. Roberts, A d v . Znorg. Biochem.; 1981,3,273-332 (141). 460. The binding of metals to t-RNA. M. M. Teeter, G. J. Quigley and A. Rich, A d v . Inorg. Biochem., 1981,3,234-272 (59). 461.. Cation control of equilibrium and rate processes in initiation of protein synthesis. M . GrunhergManago, H. B . Iloa: P. Douzou and A. Wishnia, Adv. Innrg. Biochem., 1981,3,193-232 ( 7 8 ) . 462. Metal ion effects on nuclcar protein phosphorylation. M. 0. J. Olson, A d v . Inorg. Biouhem., .1981, 3, 167-191 (123). 463. Intrinsic metals in RNA polyrnerasc. F. Y. H. Wu and C. W. Wu, A d v . Znorg. Binchem., 1981, 3: 143-166 (87). 464. The role of metal ions in the fidelity of DNA and RNA synthesis. L. A. Loeb and A. S. Mildvan, A d v . Inorg. Biochem., 1981,3, 126-142 (66). 465. The role of metal ions in the mechanism of DNA and RNA polymerases. A. S. Mildvan and L. A. Loeb, A d v . Inorg. Biochem., 1981,3, 103-123 (79). 466. Heavy metals in the cell’s nucleus. S. E. Bryan, A d v . Znorg. Biochem., 1981,3,87-101 (53). 467. Metal complexes of nucleic acid derivatives and nucleotides: binding sites and structures. L. G. Marzilli, A d v . Znorg. Biochem., 1981,3,48-85 (138). 468. The effect of metal ions on the structure and function of nucleic acids. G. L. Eichorn, A d v . Inorg. Biochem., 1Y81.3,2-46 (147). 469. On thc resolution of metal-ligand distances in metalloporphynns by EXAFS. B. M. Kincaid and R. G. Shulrnan, Adv. Znorg. Biochem., 1980,2,303-309 (11). 470. X-ray diffraction. W. N. Lipscomb, A d v . Inorg. Biochem., .1980, 2,265-302 (81). 471. Kinetic approach. G . S. Harnmes, A h . Inorg. Biochem., 1980,2,237-263 (59). 472. Nuclear magnetic relaxation rates. A. S. Mildvan, 3. Granot, G. M. Smith and M. N. Liebrnan, A d v . Inorg. Biochem., 1980,2,211-236 (44). 473. High resolution n.m.r. L. Lee and B. D . Sykes, A d v . Inorg. Biochem., 1980,2,183-210 (68).

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Electron paramagnetic resonance. G. Palmer, A d v . Inorg. Biochem. 1980,2, 153-182 (54). Raman spectroscopy. D. F. Shriver, A d v . Inorg. Biochem., 1980,2, 117-151 (87). Infrared spectroscopy. W. S. Caughey, A d v . Inorg. Biochern.? 1980,2,95-115 (43). Metal ions as donors and acceptors of fluorescence. B. Holmquist, A d v . Inorg. Biochem., 1980, 2, 75-93 (49). 478. Circular dichroism and magnetic circular dichroism. B. L. Vallee and B. Holmquist, A d v . Znorg. Biochem., 1980,2,27-74 (94). 479. Electronic absorption spectroscopy. H. B. Gray, A d v . Znorg. Biochem., 1980,2,1-25 (68). 480. Hemerythrin: a review of structural and s ectroscopic properties. J. S. Loehr and T. M. Loehr, A d v . Inorg. Biochem., 1979: 1,235-252 (547. 481. Hemerythrin and myohemerythrin: a review of models based on X-ra crystallographic data. R . E. Stenkamp and L. H.Jenson, A d v . Inorg. Biochem., 1979,1,219-233 482. The structure of (Na' K+)-ATPase: implications for the mechanism of Na and K transport. C. M. Grisham, A d v . Inorg. Biochem., 1979.1, 193-218 (105). 483. Chromium(II1) and cobalt(II1) nucleotides as biological probes. W. W. Cleland and A. S . Mildvan, A d v . Inorg. Biochem., 1979, 1, 163-191 (39). 484. B12-dependent methyl transfer reactions. Y. T. Fanchiang, W. P. Ridley and J. M. Wood, A h . Inorg. Biochem., 1979, I ? 147-162 (45). 485. Cytochrome P-450 and other heme-containing oxygenases. J. T. Groves, A d v . Inorg. Biochem., 1979,1,119-145 (109). 486. The copper containing oxidases. B. Reinhammar, Adv. Inorg. Biochem., 1979,1,92-118 (76). 487. Superoxide and superoxide dismutase. I. Fridovich, A d v . h o r g . Biochem., 1979, 1,67-90 (245). 488. Kinetics and mechanisms of isomerisation and racemisation processes of six coordinate chelate cornplexes. N. Serpone and D. G. Bickley, Prog. Inorg. (:hem., 1972,17,391-566 (359). 489. Excited states of metal complexes and their reactions. P. D. Fleischauer, A. W. Adamson and G.Satori, Prog. Inurg. Chem., 1972,17, 1-56 (171). 490. N.m.r. cation solvation studies. A. Fratiello, Prog. Inorg. Chem., 1972, 17,57-92 (88). 491. Chromium(V1) oxidations of inorganic substances. J. K. Beattie and G. P. Haight, Prog. Znorg. Chem., 1972,17,94-145 (86). 492. Synthesis, structure and properties of some organometallic sulfur cluster compounds. P. J. Vergamini and G. J. Kubas, Prog. Znorg. Chem., 1976,21,261-282 (40). 493. Structural and magnetic studies of polynuclear transition metal 0-polyketonates. M. D. Glick and R. L. Lintvedt, Prog. Inorg. Chern., 1976,21,233-260 (51). 494. Structure and metal-metal interactions in copper(I1) carboxylate complexes. R. J. Doedens, Prog. Znorg. Chem., 1976,21,209-231 (70). 495. M. 0. theory, chemical bonding and photoelectron spectroscopy for transition metal complexes. R. F. Fenske, Prog. Inorg. Chem., 1976,21,179-208 (62). 496. Structural studies related to photosynthesis: a model for chlorophyll aggregates in photosynthetic organisms. C. E. Strouse, Prog. Inorg. Chrm., 1976,21,159-177 (31). 497. Homopolyatomic ions of the post-transition elements - synthesis, structure and bonding, J. D. Corbett, Prog. Znorg. Chem., 1976,21, 129-158 (61). 498. Ligand induced redox reactions of low oxidation state rhenium halides and related systems in nonaqueous solvents. R. A. Walton, Prog. Inorg. Chem., 1976,21, 105-127 (81). 499, Seven and eight coordinate molybdenum complexes and related molybdenum(1V) oxo complexes with cyanide and isocyanide ligands. S. J. Lippard, Prog. Inorg. Chem., 1976,21,91-103 (44). 500. Multinuclear d8--d" metal ion complexes with sulphur-containing ligands. J. P. Fackler, Prog. Znorg. Chem., 1976,21,55-90 (73). 501. Polynuclear complexes with aminoalcohols and iminoalcohols as ligands: 0-bridged and hydrogen bonded species. J. A . Bertrand and P. G. Eller, Prog. Inorg. Chem., 1976,21,29-53 (54). 502. Metal carbonyls - some new observations in an old field. F. A. Cotton, Prog. Inorg. Chem., 1976, 21, 1-28 (36). 503. Chemical applications of magnetic anisotropy studies on transition metal complexes. S. Mitra, Prog. Inorg. Chem., 1977,22,31&408 (160). 504. The derivation and application of normalised spherical harmonic Hamiltonians. J. C . Donini, 53. R. Hollebone and A. B. P.Lever, Prog. Inorg. Chem., 1977,22,22&307 (76). 505. Coordination and bioinorganic chemistry of molybdenum. E. I. Stiefei, Prog. Inorg. Chem., 1977, 22,1-223 (860). 506. The chemistry of dithioacid and 1,1-dithiolate complexes. D. Coucouvanis, Prog. Inorg. Chem., 1970, 11,233-371 (516). 507. Metal tetrah droborates. B. D. James and M. G. H. Wallbridge, Prog. Inorg. Chem., 1970, 11, 101-231 (6164;. 508. Vibrational spectra and metal-metal bonds. T. G. Spiro, Prog. Znorg. Chem., 1970, 11, 1-51 (145). 509. Stereochemistrv of a-hvdroxvcarboxvlate comDlexes. R . E. TaDscott, Transition Met. Chem. ( N . Y . ) , 1982,s; 253-429'(429): 510. 3-d metal complexes with tripodal polytertiary hosphines and arsines. L. Sacconi and F. Mani, Transition Met. Chem. ( N . Y . ) . 1982.8. 179-252 h 6 ) . 511. E.s.r. spectra of metai complexes 'of the first 'transition series in low symmetry environments. A. Bencini and D. Gatteschi, Transition Met. Chem. ( N . Y . ) ,1982,8,1-178 (587). 512. Magnetic anisotropy. S. Mitra, Transition Met. Chem. (N.Y.), 1972,7, 184-337 (345). 513. Preparation and properties of high valent first row transition metal oxides and halides. C. Rosenblum and S. L. Holt, TransifionMet. Chem. ( N .Y . ) ,1972,7,87-182 (303). 514. Magnetic phase transitions at low temperatures. J. E. Rives, Trunsition Met. Chem. ( N . Y . ) , 1972,7, 1-86 (235).

474. 475. 476. 477.

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39

515. Amine complexes of chromium(II1). C. S. Garner and D. A. House, Transition Met. Chern. ( N . Y . ) , 1970,6,59-295 (923). 516. Theory of bridge bonding and the structure of binuclear coordination compounds. B . JezowskaTrzebiatowska and W. Wojciechowski, Transition Met. Chem. ( N .Y.),1970,6, 1-58 (203). 517. Metal-metal exchange interactions. G. F. Kokoszka and G. Gordon, Transition Met. Chem. ( N . Y . ) , 1969,5, 181-277 (260). 518. Cop er complexes. W. E. Hatfield and R. Whyman, Transition Met. Chem. ( N . Y . ) , 1969,5,47-179 (7507. 519. The's ectra of chromium(TT1) complexes. L. S. Forster. Transition Met. Chem. ( N . Y . ) ,1969, 5 , 1 4 5 858). 520. Multiple bonding and back coordination in inorganic compounds. L. D. Pettit, Q. Rev.. Chem. SOC.,1971,25, 1-29 (105). 521. Structural aspects of coordinated nitrate groups. C. C. Addison, N. Logan, S . C. Wallwork and C. D. Garner. 0.Rev.. Chern. SOC..1971.25.289-322 (851. 522. Metal-ion control in the synthesis o f Schiff base complexes. L. F. Lindoy, Q. Rev., Chem. Sou., 1971,25,379-391(42). 523. Halogen and interhalogen cations. R. J. Gillespie and M. J. Morton, Q. Rev., Chem. Soc., 1971,25, 553-570 (50). 524. Metal-metal interactions in transition metal complexes containing infinite chains of metal atoms. T. W. Thomas and A . E. Underhill, Chem. SOC. Rev., 1972, I ?99-120 (70). 525. Nitrogen fixation. J. Chatt and G. J. Leigh, Chem. SOC.Rev.: 1972, 1, 121-144 (37). 526. The photochemistry of transition metal coordination compounds - a survey. W. L. Waltz and R. G. Sutherland, Chern. SOC.Rev., 1972,1,241-258 (75). 527. The 16- and 1BeIectron rule in organometallic chemistry and homogeneous catalysis. C. A . Tolman, Chem. Soc. Rev., 15172, l , 337-353 (90). 528. Valence in transition metal complexes. R. Mason, Chem. Snc. Rev., 1972,1,431-444 (52). 529. Lanthanide shift reagents in n.m.r. spectroscopy. B . C. Mayo, Chem. SOC. Rev., 1473- 2, 49-74 (152). 530. The cis- and trans- effects of ligands. F. R. Hartley, Chem. SOC. Rev., 1972,2,163-179 (102). 531. Metalloboranes and metal-boron bonding. N. N. Greenwood and I. M. Ward, Chem. SOC.Rev.. 1974,3,231-271 (57). 532. Porphyrins and related ring systems. A. W. Johnson, Chem. SOC.Rev., 1975,4,1-26 (54). 533. Quadruple bonds and other multiple metal to metal bonds. F. A. Cotton, Chem. SOC.Rev., 1975,4, 27-53 (127). 534. Vibrational infrared and Raman spectroscopy in inorganic chemistry. I. R. Beattie, Chem. Soc. Rev., 1975,4, 107-152 (140). 535. Transition metal complexes of synthetic macrocyclic ligands. L. F. Lindoy, Chem. SOC.Rev., 1975, 4,421-441 (93). 536. Coordination chemistry of aryldiazonium cations: aryldiazcnato (arylazo) complexes of transition metals and the aryIdiazenato-nitrosyl analogy. D. Sutton, Chem. SOC.Rev., 1975, 4, 443-470 (89). 537. Alkali metal complexes in aqueous solution. D. Midgley, Chern. Sou. Rev., 1975,4, 549-568 (126). 538. N.m.r. and the periodic table. R.K. Harris, Chem. SOC.Rev., '1976,5, '1-22 (81). 539. The functional group selectivity of complex hydride reducing agents. E. R. H. Walker, Chem. SOC. Rev., 1976,5,23-50 (64). 540. Inorganic pyro-compounds, M,[(X207)b]. G. M. Clark and R. Morley, Chem. SOC.Rev., 1976, 4, 269-295 (144). 541. Solutions of metals: solvated electrons. M. C. R. Symons: Chem. SOC.Rev., 1976,5,337-358 (91). 542. Post-B12problems in corrin synthesis. A. Eschenmoser, Chem. SOC. Rev., 1976,5,377-410 (63). 543. The binding of heavy metals to proteins. T. L. Blundell and J. A . Jcnkins, Chern. Sou. Rev., 1977.6, 139-171 (87). 544. The chemistry and binding properties of aluminium phosphates. J. H. Morris, P. G. Perkins, A . E, A. Rose and W. E. Smith, Chem. SOC. Rev., 1977.6,173-194 (176). 545. Across the living barrier. D. E. Fenton, Chem. SOC. Rev., 1977, 6, 325-343 (73). 546. Metal-ion-promoted reactions of organo-sulphur compounds. D. P. N. Satchell, Chem. Suc. Rev., 1977,6.345-371 (65). 547. N.m.r. spectral change as a probe of chlorophyll chemistry. J. K. M. Saunders, Chem. SOC. Rev., 1977,6,467387 (58). 548. Bond valences - a simple structural model for inorganic chemistry. I. D. Brown: Chem. SOC. Rev., 1978,7,359-376 (42). 549. Molecular shapes. J. K. Burdett, Chem. SOC. Rev., 1978,7,507-526 (57). 550. Fe(CO)+ M. Poliakoff, Chem. SOC.Rev., 1978,7,527-540 (25). 551. Compartmental ligands: routes to homo- and hetero-dinuclear complexes. U . Castellato, P. A . Vigato, D. E. Fenton and M.Vidali, Chern. SOC.Rev., 1979,8,199-220 (62). 552. Transition metal oxide chelates of carbohydrate-directed macromolecules. J. F. Kennedy, Chern. SOC.Rev., 1979,8,221-257 (108). 553. Ring, cage and cluster compounds of the main group elements. R. J. Gillespic, Chem. SOC. Rev., 1979,8,315-352 (41). 554. Vitamin BI2-retrospect and prospect. A. W. Johnson, Chern. SOC.Rev., 1.980,9, 125-141 (75). 555. The chemistry of the guld drugs used in the treatment of rheumatoid arthritis. D. H. Brown and W. E. Smith, Chern. SOC. Rev., 1980,9,217-240 (107).

Index of Review Articles and Specialist Texts

40

556. On first looking into nature’s chemistry. Part I, the role of small molecules and ions: the transport of the elements. Part 11. the role of large molecules, especially proteins. R. J. P. Williams, Chem. SOC. Rev., 1980,9,281-324 (9) and 325-364 (46). 557. One-dimensional metallic complexes. A. E. Underhill and D. M. Watkins, Chem. SOC.Rev., 1980, 9,429-448 (62). 558. The relationship between metal carbonyl clusters and supported metal catalysts. J. Evans, Chem. .. SOC. Rev., 1981; 10,159-180 (94). 559. Arvliodine(II1) dicarboxvlates. A . Varvodis. Chem. SOC.Rev.. 1981. 10. 377407 (127). 560. M&l clustkrs’in biolok: quest for a synvthetic re resentation of the catalytic site of‘nitrogenase. R. H. Holm, Chem. Soc. Rev., 1981,10,455-490 637). S61. Reactivities of carbon disulphide, carbon dioxide and carbonyl sulphide towards some transition metal systems. J. A. Ibers, Chem. Snc. Rev., 1.982, 11, 57-73 (78). 562. Synergic interplay of experiment and theor in studying metal-metal bonds of various orders. F. A. Cotton, Chem. SOC. Rev.: 1983. 12,35-51 8 9 ) . 563. Chemistry of bis(dipheny1phosphino)methane. R. J. Puddephatt, Chem. SOC. Rev., 1983, 12, 99-127 (151). 564. The synthesis of mononuclear cyanocobalt(II1) complexes. M. G. Burnett, Chem. SOC. Rev., 1983, 12,267-280 (111). 565. Alkoxy, amido, hydrazido and related compounds of molybdenum and tungsten. J. A. McCleverty, Chem. SOC.Rev., 1983.12.331-360 (69). 566. E.S.R. of haemoglobin and myoglobin. L. C. Dickinson and M. C. R. Symons, Chem. SOC. Rev., 1983,12,387-414 (93). 567. Hydrido complexes of the transition metals. D. S. Moore and S. D . Robinson, Chem. Soc. Rev., 1983,12,415-452 (218). 568. Binuclear oxo-bridged iron(II1) complexes. K. S. Murray, Cuord. Chem. REV.,1974,12,1-35 (241). 569. Current methods in MO theory for inorganic systems and their future developmenl- an interpretative view. P. G. Burton: Coord. Chem. Rev., 1974, 12, 37-71 (76). 570. Alfred Werner’s research on o tically active coordination compounds. G . 13. Kauffman, C o d . Chem. Rev., 1974,12, 105-149 676). 571. Higher oxidation state chemistry of iron, cobalt and nickel. W. Levason and C. A. McAuliffe, Coord. Chem. Rev., 1974, 12: 151-184 (398). 572. High pressure coordination chemistry. E. Sinn, Coord. Chem. Rev., 1974. 12, 185-220 (238). 573. Simple electrostatic correlations of fluoride complexes in aqueous solution. G. Hefter, Coord. Chem. Rev., 1974,12,221-239 (74). 574. The role of the perchlorate ion as a ligand in solution. L. Johansson, Coord. Chem. Rev., 1974, 12, 241-261 (88). 575. Empirical approach to ligand cffccts on the kinetics of substitution and redox reactions. V. Gutmann and R. Schmid, Coord. Chem. R e v . , 1974,12,263-293 (YO).

576. Normal coordinate treatment of lanthanide hexahalide anions (Ln&’-). M. Choca, J. R. Ferraro and K. Nakarnoto, Coord. Chem. Rev., 1974,12,295-307 (25). 577. Models for coppcr-protein interaction based on solution and crystal structure studies. K.Osterberg, Coord. Chern. Rev.. 1974,12,30’+347 (130). 578. Transition metal complcxcs in cancer chemotherapy. M. J. Cleare, Coord. Chem. Rev., 1974, 12, 349-405 (158).

579. Magnetic resonance studies on metal-enzymes. P. J. Quilley and G. A. Webb, Coord. Chem. Rev., 1974,12,407-430 (101). 580. Structural chemistry of transition metal complexes of oximes. A. Chakravorty, Coord. Chem. Rev., 1974, 13, 1-46 (298). 581. The application of X-ray photoelectron spectroscopy to inorganic chemistry. W. J. Jolly, Coord. Chem. Rev., 1974, 13,47-81 (119). 582. Metal complexes of sulphur-nitrogen chelating ligands. M. A. Ali and S. E. Livingstone, Coord. Chem. Rev., 1974,13,101-132 (194). 583. Cyanide phosphine complexes of transition metals. P. Kigo and A. Turco, Coord. Chem. Rev., 1974,13,133-172 (151). 584. Thc determination of structural ptopcrties of dimeric transition metal ion complexes from e.p.r. spectra. T. D. Smith and J . R. Pilbrow, Coord. Chem. Rev., 1974: 13,173-278 (186). 585. Absolute configurations of metal complexes determined by X-ray analysis. Y. Saito, Coord. Chem. Rev., 1974,13,305-337 (52). 586. Principles of structure, bonding and reactivity for metal nitrosyl complexes. J. H. Enemark and R. D. Feltham, Coord. Chem. Rev., 1974,13,339406 (126). 587. Coordination compounds of alkali and alkaline earth metals with covalent molecules. P. N. Kapoor and R. C. Mehrotra, Coord. Chern. Rev., 1974,14,1-27 (120).

588. Thermodynamics and kinetics of the transition metal complexes of tripodal amines. S. G. Zipp, A , P. Zipp and S.K. Madan, Coord. Chem. Rev., 1974,14,29-45 50). 589. Vibronic spectra of coordination compounds. C. D . Flint, Coord. C em. Rev., 1974,14,47-66 (45). 590. Photochemistry of hexacoordinate complexes of the heavier transition metals. P. C. Ford, 3. D. Petersen and R. E. Ilintze, Coord. Chem. Rev., 1974, 14,67-105 (109). 591. Vibrational spectra of transition metal chalcogen compounds. K. H. Schmidt and A . Muller, Coord. Chem. Rev., 1974,14,115-179 (326). 592. The application of diffuse reflectance spectroscopy to the chemistry of transition metal coordination compounds. E. L. Simmons. Coord. Chem. Rev,, 1974, 14, 181-196 (81). 593. Activation parameters and reaction mechanism in octahedral substitution. T. W. Swaddle, Coord. Chem. Rev., 1974,14,217-268 (231).

k

Index of Review Articles and Specialist Texis

41

594. A phenomenological model for redox reactions in solution: application to aquocobalt(II1) systems. I. Bodek and G. Davies, Coord. Chem. Rev., 1974,14.269-285 (40). 595. The mechanistic assignment of terms in empirical rate laws for complexation and redox reactions of metal ions in aqueous solution: acid dependences in perchlorate media. G. Davies, Coord. Chem. Rev.. 1974.14.287-303 (36). 596. Synthetic methods in transiiion metal nitrosyl chemistry. K. G. Caulton, Coord. Chem. Rev.. 1975, 14,317-355 (253). 597. The Jahn-Teller effect in crystal chemistry and spectroscopy. I. B. Bersuker, Coord. Chem. Rev., 1975,14,357-412 (105). 598. Intercalation chemistry: electron/ion transfer rcactions. R. Schollhorn, Comments Inorg. L'hern., 1983,2,271-292 (48). 599. Facts and fantasy on tetrathio oxalate-activation and condensation of carbon disulphidc. E. Hoyer, Comments lnorg. Chem., 1983,2,261-270 (22). 600. Cu2+ a chameleon in coordination chemistry. D. Reinen, Commenrs Inorg. Chem., 1983, 2, 227-i46 (44). 601. Transition metal complexes as mediators in photochemical and chemiluminescence reactions. V. Balzani and F. Bolleta, Comments Inorg. Chern.. 1983,2,211-226 (33). 602. On the relationship between protein-forced ligand fields and the properties of 'blue' copper centres. H. B. Gray and B. G. Malmstrom, Comments Inorg. Chem., 1983,2,203-209 (14). 603. Mechanisms of ligand replacement in octahedral nickel(I1) complexes - an update. R. G . Wilkins, Comments lnorg. Chem.?1983,2, 187-201 (54). 604. Reactions involving transition metal ions and tripodal phosphines and arsines. F. Mani and L. Sacconi, Comments Inorg. Chem., 1983,2, 157-186 (73). 605. Ruthenium aqua ions - their comparison to ruthenium ammines. P. Bernhard, H. Lehmann and A. Ludi, CornmentltsInorg. Cheni., 1983, 2, 145-156 (22). 606. Kinetic studies of colloidal metal complex species relevant to natural waters. C. €1. Langford and M. K. S. Mak, Comments Inorg. Chem., 1983,2: 127-143 (21). 607. On carbon nionoxide and dioxygen binding by iron(I1) porphyrinato systems. G. B. Fameson and J. A. Ibers, Conmenis Inoug. Chem., 1983,2,97-126 (100). 608. Neutron scattering: some recent applications to inorganic chemistry. H. Fuess, Cumments Inorg. Chem., 1982,2,3947 (49). 609. Theoretical aspects of transition metal chemistry. L. G. Vanquickenborne, Comments Inorg. Chem., 1982,2.2>38 (37). 610. The new biochemistry of vanadium. K. Kustin and I. G . Macara, Comments Inorg. Chem., 1982,2, 1-22 (72). 611. Metal ions in enzymic catalysis. J. E. Coleman, Prog. Binorg. Chem., 1.971,1, 159-344 (503). 612. Metabolism of carcinogen chromate by cellular constituents. P. 11. Connctt and K . E. Wetterhani, Struct. Bonding (Berlin), 1983, 54, 94-124 (121). 613. The ribonucleotide reductrtscs - a unique group of metalloenzymes essential for cell proliferation. M. Lammcrs and H. Follmann, Struct. Bonding (Berlin), 1983.54,27-91 (354). 614. Selenium biochemistry. Chemical and physical studies. J. D. Odom, Struct. Bonding (Berlin), 1983, 54,l-26 (288). 615. Electron nuclear double resonance of transition metal complexes with organic ligands. A. Schweiger, Struct. Bonding (Berlin), 1982, 51>1-119 (294). 616. Uranyl photophysics. C. K. Jorgensen and R. Reisfeld, Sfruct. Bonding (Berlin), 1982, 50, 122-171 (256). 617. The chemistry of lanthanide ions in solution and in biological systems. R. J. P. Williams. Struct. Bonding (Berlin),1982.50,81-119 (71). 618. The chemistry of technetium: toward improved diagnostic agents. M. J. Clarke and P. H. Fackler, Struct. Bunding (Berlin), 1982, 50, 58-78 (178). 619. Stacked metal complexes: structures and properties. J. A . Ibers, L. J . Pace, J . Martinsen and B. M. Hoffman, Struci. Bonding (Berlin), 1082,50, 1-55 (212). 620. Carbonic anhydrase: an insight into the zinc binding site and into thc activc cavity through metal substitution. I. Bertini, C. Luchinat and A. Scozzafava, Struct. Bonding (Berlin), 1982, 48, 46-92 (296). 621. The role of manganese in photosynthesis. J. Livorness and T. D. Smith, Struct. Bonding (Berlin), 1982,48, 1-44 (223). 622. Chemical luminescence analysis of inorganic substances. A . P. Golovina, V. K. Runov and N. B. Zorov, Struct. Bonding (Berlin),1981, 47, 54-119 (746). 623. Structure and bonding of transition metal-sulphur dioxide complexes. R. R. Ryan, G. J. Kubas, D. C. Moody and P. G. Eller, Struct. Bonding (Berlin), 1981: 46,4&100 (210). 624. The context and application of ligand field theory. M. Gerloch, J. H. Harding and R . G . Woolley, Struct. Bonding (Berlin), 1981, 46, 2-46 (60). 625. Breakdown of one-electron pictures in photoelectron spectra. G. Wendin, Struct. Bonding (Berlin), 1981,45, 1-123 (214). 626. Polyhalogeo cations. J. Sharnir, Strucf. Bonding (Berlin). 1979, 37,143-210 (148). 627. Local and cooperative Jahn-Teller interactions in model structures. D. Reinen and C. Friebel, Struct. Bonding (Berlin),1979, 37, 1-60 (136). 628. The electronic structure of cobalt(I1) complexes with Schiff bases and related ligands. C. Daul, C. W. Schlapfer and A. von Zelewsky, Struct. Bonding (Berlin),1979,36,129-171 (76).

Index of Review Articles and Specialisi Texts

42

- review of the theory and of applications in inorganic chemistry. R. J. H. Clark and R. Stewart, Struct. Bonding (Berlin), 1979,36, 1-80 (110).

629. The resonance Raman effect

630. Complexes of the lanthanides with neutral oxygen donor ligands. D. K. Koppikar, P. V. Sivapullaiah, L. Ramakrishnan and S. Soundararajan, Struct. Bonding (Berlin), 1978,34, 135-213 (406). 631. Cis, trans and metal effects in transition metal porphyrins. J. W. Buchler, W. Kokisch and P. D. Smith, Struct. Bonding (Berlin), 1978,34,80-134 (158). 632. Chemistry of plutonium and the transuranics in the biosphere. R. A. Bulman, Struct. Bonding (Berlin), 1978,34,39-77 (198). 633. Measurement of complexing constants by radiochemical methods. S. Hubert, M. Hussonnois and R. Guillaumont, Struct. Bonding (Berlin), 1978,34, 1-18 (29). 634. Molecular orbital bonding concepts in polyatomic molecules: a novel pictorial approach. D . K. Hoffman, K. Ruedenberg and J. G. Verkade, Struct. Bonding (Berlin), 1977,33,57-96 (14). 635. Optical electronegativity and nephelauxetic effect in oxide systems. J . A. Duffy, Struct. Bonding (Berlin),1977,32, 148-166 (33). 636. Recent results in the chemistry of transition metal clusters with organic ligands. H. Vahrenkamp. Struct. Bonding (Berlin),1977,32,2-56 (408). 637. Application of the functional approach to bond variations under pressure. V. Gutmann and H. Mayer, Struct. Bonding (Berlin), 1976,31, 50-66 (58). 638. Paradoxical violations of Koopman’s theorem with special reference to the 3d transition elements and the lanthanides. R. Ferreira, Struct. Bonding (Berlin),1976,31, 1-22 (73). 639. Deep-lying valency orbitals and problems of degeneracy and intensities in photo-electron spectra. C . K. Jorgensen, Struct. Bonding (Berlin), 1976,30,142-192 (224). 640. Spectroscopy of homogeneous mixed valence rare earth compounds. M. Campagna, G. K. Wertheim and E. Bucher, Struct. Bonding (Berlin), 1976,30. 99-140 (76). 641. Excited states and energy rransfer from donor cations to rare earths in the condensed phase. R. Reisfeld, Struct. Bonding (Berlin), 1976,30,65-97 (74). 642. A systematic correlation of the properties of thef-transition metal ions. S . P. Shina, Struct. Bonding (Berlin), 1976,30, 1-64 (98).

643. The biological chemistry uf gold: a metallo-drug and heavy atom label with variable valency. P. J . Sadler, Srruct. Bonding (Berlin), 1976,29, 17G214 (142). 644. The 8-aminolevulinate dehydratases: molecular and environmental properties. A. M. Cheh and J . B . Neilands, Struct. Bonding (Berlin), 1976, 29, 125-169 (164). 645. The uptake of elements bv biological svstems. J. J. R. Frausto da Silva and R. J. P. Williams, Struct. Bonding (Berlin), 1976,29>6 7 - R l (40). 646. The molecular basis of bioloeical dinitroeen ” fixation. W. G. Zumft. Struct. Bonding (Berlin). ,, 1976. 29,3-65 (347).

u

v

\

647. Dithiocarbamates of transition group elements in ‘unusual’ oxidation states. J. Willemse, J. A. G a s , J. J. Steggerda and C. P. Keijzers, Struct. Bonding (Berlin),1976,28,83-126 (195). 648. Structural and banding aspects in phosphorus chemistry - inorganic derivatives of oxohalogeno phosphoric acids. K. Dehnicke and A. F. Shihada, Struct. Bonding (Berlin), 1976,28,52-82 (119). 649. Reversible oxygenation. K. W. E.rskine and B. 0 . Field, Scruct. Bonding (Berlin), 1976, 28, S 5 0 (282). 650. Kinetics and mechanism of metalloporphyrin formation. W. Schneider, Struct. Bonding (Berlin), 1975,23,123-166 (65). 651. Mechanisms of zinc ion catalvsis in small molecules and enzymes. M. F. Dunn. Struct. Bonding (Berlin), 1975,23,61-122 (190). 652. Copper proteins. Systems containing the ‘blue’ copper centre. 3. A. Fee, Struct. Bonding (Berlin), 1975.23. 1-60 (227). 653. Radiative and nokradiative transitions of rare-earth ions in glasses. R. Reisfeld, Struct. Bonding (Berlin), 1975,22, 123-175 (56). 654. The intensities offjftransitions. R. D. Peacock, Struct. Bonding (Berlin), 1975,22,83-122 (113). 655. Partially filled shells constituting anti-bonding orbitals with higher ionisation ener y than their bonding counterparts. C. K . Jorgensen, Slrucl. Bonding (Berlin), 1975,2X. 49-81 (1307. 656. Lanthanide ions as structural probes in biological and model systems. E. Nieboer, Struct. Bonding (Berlin), 1975,22, 1.-47 (235). 657. The study of covalency by magnetic neutron scattering. B. C. Tufield, Strucl. Bonding (Berlin), 1975,21,1-87 (156). 658. Mossbauer spectroscopy in heme proteins. A. Trautwein, Struct. Bonding (Berlin), 1974, 20, 101-167 (115). 659. The electronic state of iron in some natural iron compounds: determination by Mossbauer and E.S.R. spectroscopy. W. T. Oosterhuis, Struct. Bonding (Berlin). 1974: 20,59-99 (66). 660. The enzymatic reduction of ribonucleotides, H. P. C. Hogenkamp and G. N. Sando, Strucf. Bonding (Berlin), 1974,20,2>58 (158).

661. The role of divalent cations in the mechanism of enzyme catalysed phosphoryl and nucleotidyI transfer reactions. A. S. Mildvan and C. M. Grisham, Struct. Bonding (Berlin), 1974,20, 1-21 (88). 662. The electronic spectra of the hexafluoro complexes of the second and third transition series. G. C. Allen and K. D. Warren, Slruci. Bonding (Berlin), 1974, 19, 105-165 (94). 663. Considerations of the valence concept. A. Kjekshus and T . Kakke, Struct. Bonding (Berlin). 1974, 19,45-83 (37). 664. Relationships between covalency. interatomic distances and magnetic properties in halides and chalcogenides. R. D. Shannon and H. Vincent, Struct. Bonding 1974, 19, 1 4 3 (50). 665. Some aspects of heteropolymolybdates and heteropolytungstates. T. J. R. Weakley, Struct. Banding (Berlin), 1974, 18, 131-176 (237).

Index of Review Articles and Specialist Texts

43

666. Optical activity in conjugated proteins. G. Blauer, Strucf. Bonding (Berlin), 1974, 18, 6S129 (393). 667. The oxidation states and reversible redox reactions of metalloporphvrins. . . _ J. H. Furhrhop, Struct. Bonding (Berlin), 1974, 18, 1-67 (221). 668. Calcium-binding proteins. F. L. Siegel, Struct. Bonding (Berlin), 1973, 17,221-268 (209). 669. Metal-polypeptide interactions: the conformational state of iron proteins. M . Llinas, Struct. Bonding (Berlin), 1973, 17, 135-220 (320). 670. Ferritin. R. R. Crichton, Struct. Bonding (Berlin),1973,17,67-134 (238). 671. Structural asDects and biochemical functions of ervthrocuorein. U. Weser. Struct. Bondina - (Berlin), . 1973,17, 1-85 (226). 672. Thermodynamics of cation-macrocyclic compound interaction. R. M. Izatt, D. J. Eatough and J. J. Christensen, Struct. Bonding (Berlin),1973, 16, 161-189 (53). 673. Specificity for alkali and alkaline earth cations of synthetic and natural or anic complexing a ents in membranes. W. Simon, W. E. Morf and P. C. Meier, Srruct. Bonding- (EBerZin), 1973, 16, 1S160 , (123). 674. Structures of organic complexes with alkali metal ions. M. R . Truter, Struct. Bonding (Berlifi), 1973.16.71-111 (107). 675. Design of organ& complexing agents strategies towards properties. J.-M. Lehn, Struct. Bonding (Berlin), 1973,16, 1 4 9 (165). 676. Thermodynamics of the stepwise formation of metal ion complexes in aqueous solution. S . Ahrland, Struct. Bonding (Berlin), 1973, 15, 167-188 (86). 677. Redox properties: changes effected by coordination. V. Gutmann, Struct. Bonding (Berlin), 1973, 15,141-166 (56). 678. Quantitative evaluation and prediction of donor-acceptor interactions. R. S. Drago, Struct. Bonding (Berlin), 1973,15,73-139 (86). 679. Structural radii. electron cloud radii, ionic radii and solvation. E. C . Baughan, Struct. Bonding_ (Ber. lin), 1973, 15,5>71(49). 680. Metal complexes of chelating olefin-group V ligands. D. I. Hall, J. II. Ling and R. S. Nyholm, Struct. Bondina (Berlin). 1973. 15, 1-51 (66). 681. Structural chemi‘stry of azide. U. Muller,>St;uct. Bonding (Berlin), 1973,14,141-172 (82). 682. Two symmetry parameterizations of the angular overlap model of the ligand field. Relation to the crystal field model. C. E. Schaffer, Struct. Bonding (Berlin), 1973, 14, 69-110 (33). 683. The evidence for ‘out-of-plane’ bonding in axial complexes of copper(I1) ion. B. J. Hathaway, Struct. Bonding (Berlin), 1973, 14, 49-67 (41). 684. Electronic spectra of tetrahedral oxo-, thio- and seleno-complexes formed by elements of the beginning of the transition groups. A. Muller, E. Diemann and C. K . Jorgensen, Struct. Bonding (Berlin), 1973, 1 4 , 2 3 4 7 (122). 685. Structural chemistry of polynuclear transition metal cyanides. A. Ludi and H. U. Giidel, Struct. Bonding (Berlin), 1973.14, 1-21 (71). 686. The inner mechanism of rare earths elucidated by photoelectron spectra. C. K. Jorgensen, Sfruct. Bonding (Berlin),1973. 13,199-253 (176). 687. The crystal chemistry of rare-earth silicates. J. Felsche, Struct. Bonding (Berlin), 1973, 13, 99-197 (90). 688. Spectra and energy transfer of rare earths in inorganic glasses. R. Reisfeld, Struct. Bonding (Berlin), 1973, 13,53-98 (79). 689. Structural systematics in actinide fluoride complexes. R. A . Permman, R. R. Ryan and A. Rosenzweig, Struct. Bonding (Berlin), 1973,13, 1-52 (174). 690, Real irreducible tensorial sets and their application to li and field theory. S. E. Harnung and C. E. Schaffer, Struct. Bonding (Berlin),1972, 12,257-295 (267. 691, Phenomenological approach to cation-solvent interactions. U. Mayer and V. Gutmann, Struct. Bonding (Berlin). 1972.12. 113-140 (102). 692. Ligandufiild splhtings in copper(I1) iompounds. D. W . Smith, Struct. Bonding (Berlin), 1972, 12, 49-1 12 (220). 693. Evolution of biological iron binding centres. J. B. Neilands, Struct. Bonding (Berlin), 1972, 11, 145-170 (112). 694. Molybdenum-containing enzymes. R. C. Bray and J. C. Swann, Struct. Bonding (Berlin), 1972, 11, 107-144 (115). 695. The chemistry of vitamin-BI2-enzymes. J. M . Wood and D . G. Brown, Struct. Bonding (Berlin), 1972,11,47-105 (146). 696. The chemistry of complexes related to cis-Pt(NH&CIz. An anti-tumour drug. A . J . Thomson, R. J. P. Williams and S. Resolva, Struct. Bonding (Berlin), 1972, 11, 1-46 (90). 697. Alfred Werner’s research on geometrically isomeric coordination compounds. C . B. Kaufmann, Coord. Chem. Rev., 1975, 15, 1-92 (564). 698. Empirical approach to molecular interactions. V. Gutmann, Coord. Chem. Rev., 1975, 15,207-237 (75). 699. Transition metal complexes of cyclic phosphines and their derivatives. D. G. Holah, A. N. Hughes and K. Wright, Coord. Chem. Rev., 1975,15,239-278 (91). 700. Transition metal complexes of thiosemicarbazide and thiosemicarbazones. M. J. M. Campbell, Coord. Chcrn. Rev.,1975, 15, 279-319 (98). 701. Quenching and sensitisation processes of Coordination compounds. V. Balzani, L. Moggi, M. F. Manfrin, F. Bolletta and G. S. Laurence, Coord. Chem. Rev., 1975, 15,321-433 (216). 702. Problems of complex formation with macrocyclic ligands. S. L. Davydova and N. A. Plate, Coord. Chem. Rev., 1975,16,195-225 (130).

f

44

Index qf Review Articles and Specialist Texts

703. The electronic spectra of the hexafluoro complexes of the transition metals. G. C. Allen and K. D. Warren, Coord. Chem. Rev., 1975, 16,227-244 (30). 704. The status of molecular orbital calculations on porphyrins and their complexes. S. J. Chantrell, C . A. McAuliffe, R. W. Mann and A. C. Pratt, Coord. Chem. Rev., 1975,16,259-284 (111). 705. Chelating reagents in solvent extraction processes: the present position. A. W. Ashbrook, Coord. Chem. Rev., 1975,16,285-307 (74). 706. Spin-spin coupling in oxovanadium complexes. A. Syamal, Coord. Chem. Rev., 1975, 16, 309-339 (101). 707. The mutual influence of ligands in transition metal coordination compounds with multiple metalligand bonds. E. M. Shustorovich, M. A. Porai-Koshits and Y . A . Buslaev, Coord. Chem. Rev., 1975,17, 1-98 (345).

708, Structural aspects of rnulybdenum(1V) molybdenum(V) and rnolybdenum(V1) complexes. B. Spivack and Z. Dori, Coord. Chem. Rev., 1975, 17,99-136 (117). 709. The conformation of Schiff-base complexes of copper(I1): a stereo-electronic view. H. S. M a s h andT. N. Waters, Coord. Chem. Rev., 1975,17, 337-176 (127). 710. Cyanide complexes of the early transition metals. W. P. Griffith, Coord. Chem. Rev., 1Y75, 17, ~

177-247 (359). 711. Kinetics and mechanism of substitution reactions in cobalt(II1) trans-dioximes. A. V. Ablov and N. M. Samus, Coord. Chem. Rev., 1975,17,253-279 (64). 712. Anomalous temperature variation of n.q.r. frequencies and bonding in metal complexes. D. Nakamura, R. Ikeda and M. Kubo, Coord. Chem. Rev., 1975,17,281-316 (136). 713. Mechanism for the reactions of molybdenum in enzymes. R. A. D . Wentworth, Coord. Chem. Rev., 1976, 18, 1-27 (136). 714. Calcium in biological systems. R. H. Kretsinger and D. 3 . Nelson, Coord. Chem. Rev.? 1976, 18, 29-124 (450). 715. Electron transfer proteins. G. R. Moore and R. J. P. Williams, Coord. Chrm. Rev., 1476, 18, 125-197 (262). 716, Hypersensitivity in the elcctronic transitions of lanthanide and actinide corn lexes. D. E. Hentie, R. L. Fellows and G. R. Chnppin, Conrd. Chem. Rev., 1976, 18,199-234 (897. 717. Spin transitions in six-coordinate iron(I1) complexes. H. A . Goodwin, Coord. Chem. Rev., 1976, 18,293-325 (139). 718. Cyclometallated compounds. J. Dehand and M. Pfeffer, Coord. Chem. Rev., 1976, 18, 327-352 (114). 719. Inorganic oxygen carriers as models for biological systems. G. McL.endon and A. E. Martell, Coord. Chem. Rev., 1976: 19, 1-39 (235). 720. Vibrational spectra and force constants of pure ammine complexes. K. H. Schmidt and A. MuIler. Coord. Chem. Rev., 1976, 19,41-97 (220). 721. Ion binding in charged polymers. J. A. Marinsky, Coord. Chem. Rev. 1976, 19, 125-171 (65). 722. Phosphorus, arsenic and antimony complexcs of thc main group elcments. W. Levason and C. A. McAuliffe, Coord. Chem. Rev., 1976, 19, 173-185 (88). 723. On the function and mechanism of action of peroxidases. H. B. Dunford aad J. S. Stillman, Coord. Chem. Rev., 197A,19, 187-251 (46X). 724. Plasticity of the coordinatiun sphere of copper(I1) complexes, its manifestation and causes. J. Gazri, I. B. Bersuker, J. Garaj, M.Kabesova, J. Kohout, H. Ldngfelderova, M. Melnik, M. Serator and F. Valach, Coord. Chem. Rev., 1976,19,253-297 (220). 725. The structural chemistry of bivalent germanium, tin and lead. P. G. Harrison, Coord. Chern. Rev. 1976,20,1-36 (194). 726. Coordination complexes of the N-oxides of aromatic diimines and diazines. N. M. Karayannis, A. N. Speca, D. E. Chasan and L.. L. Pytlewski, Coord. Chern. Rev.: 1976,20,37-80 (365). 727. Linkage isomers: their preparation and reactions. R. J. Balahura and N. A. Lewis, Coord. Chem. Rev., 1976,20,109-153 (188). 728. Heterocyclic and macrocyclic amine complexes of silver(I1) and silver(II1). H. N. Po, Coord. Chem. Rev., 1976,20, 171-195 (92). 729. Systematic features in the structural chemistry of the uranium halides, oxyhalides and related transition metal and lanthanide halides. J. C. Taylor, Conrd. Chem. Rev., 1976,20, 197-273 (205). 730. Magnetic interaction in metal complexes with bridging nitrogen-heterocyclic ligands. M. Inoue and M. Kubo, Coord. Chem. Rev., 1976,21,1-27 (110). 731. The X-ray photoelectron spectroscopy of metal halides and their complexes: halogen binding energies and their correlation Rith structure. R. A. Walton, Coord. Ciiem. Rev., 1976,21,63-91 (112). 732. Marcel Deleuine’s research on coordination comDounds. G. B. Kaufman. Coord. Chem. Rev.. 1976,21,181-219 (214). 733. Some principles of normal coordinate analysis of transition metal complexes. N. Mohan, S. J. Cyvin and A. Muller. Coord. Chem. Rev.. 1976.21.221-260 (911. 734. Chlorocuprates(I1). D. W. Smith, Coord.’ Chem. Rev. ,‘19?6,21,93-158 (302). 735. Inorganic polymers. B. R. Currell and M. J. Frazer. RZC Rev.: 1969,2,13-40 (78). 736. infrared and Raman spectra of inorganic compounds. H. E. Hallam, RIC Rev., 1968, I , 39-61 (16). 737. Role of transition metal ions in biological systems. R. J . P. Williams, HlC Rev., 1968, 1, 13-38 (50). 738. Recent advanccs in the chemistry of noble gas compounds. N. K. Jha, RIC Rev., 1971,4, 147-171 (193). 739. Formation constants of metal complexes in non-aqueous solvents, part 111: DMSO. R. C.Kapoor, J. Kishan and B. S. Agarwal, Rev. Anal. Chem., 1982,6,241-259 (81). 730. Solvent extraction and spectrophotometric methods for the determination of some toxic metal ions. Y . K. Agrawal and G. I).Mehd, Rev. Anal. Chem., 1982,6,1&5-239 (328). ~

Index of Review Articles and Specialist Texts

45

741. Analytical polarographic separation of Cu(I1)-Cd and Cu(I1)-Ni by differential complexation with salicylic acid and iminodiacetic acid. V. K. Chitale and K. S. Pitre, Rev. Anal. Chem., 1982, 6 , 177-184 ( 5 ) . 742. Amperometric titration of trace amounts of Sm3+ and Gd3+ with methyl thymol blue. S. C. Lavale and K. S. Pitre, Rev. Anal. Chem., 1982,6,169-176 (13). 743. The analytical chemistry of thorium. D. E. Ryan, R. R. Brooks and H. F. Zhang, Rev. Anal. Chem., 1981,5,281-318 (380). 744. Formation constants of metal complexes in non-aqueous solvents, I - acetonitrile. R. C . Kapoor and J. Kishan, Rev. Anal. Chem., 1981,5,257-280 (96). 745. Ilydroxamic acids and their analytical applications. Y . K. Agrawal, Rev. Anal. Chem., 1980,5,3-28 (116). 746. Hydroxamic acids: reagents for the solvent extraction and spectrophotometric determination of metals. Y . K. Agrawal and S. A. Patel, Rev. Anal. Chern., 1980, 4,237-278 ('167). 747. Determination of xanthates, dithiocarbamates and organotrithiocarbamates. B. C. Verma and S. Kumar, Rev. Anal. Chem., 1978,4, 6'1-80 (99). 748. Metal xanthates and dithiocarbamates. R. J. Magee, Rev. Anal. Chem., 1973,1,335-337 (204). 749. The use of ion exchangers in analytical chemistry. J. Inczedy, Rev. Anal. Chem., 1972, 1, 157-174 (135). 750. Inorganic cyclic compounds. I. Haidus, Rev. Inorg. Chem., 1983,5,8-121 (666). 751. Lewis acidity of mercury(I1) compounds. D. P. Graddon, Rev. Znorg. Chem., 1982, 4, 211-283 (162). 752. Electrocatalysis on transition metal chelates. J. A. R. Van Veen and J. F. Van Baar, Rev. Inorg. Chem., 1982,4,29%327 (89). 753. X-ray diffraction studies on the structures of metal complexes in solution. H. Ohtaki, Rev. Zqorg. Chem., 1982,4,103-177 (223). 754. The crystal chemistry of A&Fh and A2RF5compounds with A=alkali and R=rare earth elements. 0. Greis, Rev. Inorg. Chem., 1982,4,87-101 (5.5). 755. Synthetic and catalytic intermediates of palladium(I1) and platinum(I1). F. R. Hartley and J. A. Davies, Rev. Inorg. Chenl., 1.982,4,27-43 (60). 756. Recent advances in the vibrational spectroscopy of metal cluster complexes. I. A. Oxton, Rev. Znorg. Chem., 1982,4, 1-26 (107). 757. Solvent extraction from aqueous-organic media, J. Hala, Ion Exch. Solvent Extr., 1981, 8?369-410 (127), 758. Solvent extraction of elements of the platinum group. L. M. Gindin, Zon Exch. Solvent Extr., 1981, 8,311-368 (326). 759. Extraction with solvent impregnated resins. A . Warshawsky, Zon Exch. Solvent Extr., 1981, 8, 229-310 (102). 760. Metal extraction with hydroxyoximes. R. J. Whewell and C . Hanson, Zon Exch. Solvent Extr., 1981, 8, 1-93 (220). 761. Solvent extraction in the separation of rare earths and trivalent actinides. B. Weaver, Ion Exch. Solvent Extr., 1974,6, 1OC-277 (538). 762. Application of the solubility concept in liquid-liquid extraction. H. M. N. IT. Irving, lon Exch. Solvent Extr., 1974,6. 14CL187 (61). 763. Application of ion e.xchange to element separation and analysis. R. W. E. Strelow, Zon Exch. Solvent Extr., 1973,5! 121-206 (220). 764. New inorganic ion exchangers. A. Clearfield, G. H. Nancollas and R. H. Blessing, Zon Exch. Solvent Extr., 1973.5, 1-119 (304). 765. Equations for the evaluation of formation constants of complexed ion species in cross-linked and linear polyelectrolyte systems. J. A. Marinsky, Zon Exch. Solvent Extr., 1973,4,227-243 (18). 766. Ligand exchange chromatography. H. F. Walton, Zon Exch. Solvent Extr., 1973,4,121-153 (58). 767. N.M.R. studies of oreanoDhosDhorus extractants. W. E. Stewart and T. H. Siddall, Zon Exch. Solvent Extr., 1973,3, 8T-110(51)'. 768. Solvent extraction with sulphonic acids. G. Y. Markovits and G. R. Choppin, Ion Exch. Solvent Extr.. 1973.3.51-81 (57). 769. Extraction of metals by'carboxylic acids. D , S. Nett and M. 3 . Jaycock, lon Exch. Solvent Extr., 1973,3,1-50 (160). 770. Ion-exchange studies of complex formation. Y. Marcus, Ion Exch. Solvent Extr., 1966, 1, 101-138 (63). 771. Solvent extraction of protactinium. R. Guillaumont and C. Miranda, Solvent Extr. Rev., 1971, 1, 105-149 (150). 772. Extraction of polonium. W. W. Schulz, Solvent Extr. Rev., 1971,1,151-184 (58). 773. Kinetics of metal extraction by organophosphorus acids. C . F. Coleman and J. W. Roddy, Solvent Extr. Rev., 1971: 1, 63-91 (58). 774. Luminscence kinetics of metal complexes in sohtion. T. J. Kemp, Prog. React. Kinet., 1981, 10, 301-398 (256). 775. Homogeneous liquid phase inorganic oscillatory reactions. D. 0. Cooke, Prog. React. Kinet., 1978, 8, 185-229 (184). 776. The rates of reaction of some haem compounds. Q. H. Gibson, Prog. Renct. Kinet., 1964, 2, 319-335 (67). 777. Aromatic ortho-dihydroxy compounds as reagents for inorganic analysis. B. W. Bundesinsky and K. E. Curtis, Chelates Anal. Chem., 1976,5, 16S292 (398). 778. Edta and other aminopolycarboxylic acids as chromogenic agents. F. Bermejo-Martinez, Chelates Anal. Chem., 1976.5,l-161 (266).

46

Index of Review Articles and Specialist Texts 779. The application of chelates to flame analytical techniques. J. W. Robinson, P. F. Lott and A. J. Barnard, Chelates Anal. Chem., 1972,4, 233-275 (171). 780. 2-Pyridylazo compounds in analytical chemistry. S. Shibata, Chelates Anal. Chern., 1972, 4. 1-232 (241). 781. Electroanalytical methods in the study of chelation reactions. M. Kopanica and J. Zyka, Chelates Anal. Chem., 1972,3,151-209 (196). 782. Amperometric titrations involving chelates and chelating agents. J. Dolezal, K. Stulik and J. Zyka, Chelates Anal. Chem., 1972,3,57-150 (300). 783. Extractive titrations involving chelates and chelating agents. A. Galik, Chelates Anal. Chem. 1972, 3, 1-55 (86). 784. Chelates and chelating agents in the analytical chemistry of niobium and tantalum. E. Lassner and R. Puschel, Chelates Anal. Chern., lY69,2,213-340 (311). 785. Selectivity and analytical applications of dimethylglyoxime and related dioximes. K. Burger, Chelates Anal. Chem., 1969, 2, 179-212 (95). 786. Analytical applications of Schiff bases. E. Jungreis and S. Thabet, Chelates Anal. Chem., 1969, 2 , 149-177 (66). 787. Chelating agents as metal precipitants: advances, 196C-1965. F. H. Firsching, Chelates Anal. Chem., 1969,2,117-148 (203). 788. Electrometric titrations with two polarizable electrodes involving chelating agents. K. Stulik and F. Vydra, Chelates Anal. Chern. 1969,2,93-115 (70). 789. Monoarylazo and bis(ary1azo) derivatives of chromotropic acid as photometric reagents. B. Budesinsky, Chelates Anal. Chern., 1969,2, 1-91 (178). 790. Chelates and chelating agents in the analytical chemistry of molybdenum and tungsten. R. Piischel and E. Lassner, Chelates Anal. Chern., 1967,1,265-356 (326). 791. Chelates in inorganic polarographic analysis: applications. M. Kapanica, J. Dolezal and J . Zyka, Chelates Anal. Chern. 1967, 1, 179-264 ('187). 792. Chelates in inorganic polarographic analysis: fundamentals. M. Kapanica, J. Dolezal and J. Zyka, Chelates Anal. Chern., 1947, 1, 145-177 (113). 793. The thermal dissociation of chelating agents anqchelates of analytical interest. W. W. Wendlandt, Chelates Anal. Chern., 1967,1,107-143 (65). 794. Conductometric and high frequency impedimetric titrations involving chelates and chelating agents. F. Vydra and K. Sulik, Chelates Anal. Chern., 1967, 1, 81-105 (70). 795. Chelating ion-exchange resins. E. Blasius and B. Brozio, Chelates Anal. Chem., 1967, 1, 49-79 (149). 796. Xylenol orange and methylthymol blue as chromogenic reagents. E. Budesinsky, Chelates Anal. Chern., 1967, 1, 15-47 (124). 797. An outline of the history of analytical methods based on complex formation. F. Szabadvary and M. T. Beck, Chelates Anal. Chern., 1971, 1, 1-14 (69). 798. Coordination polymers. J . C. Bailar, Prep. Inorg. React., 1964, 1, 1-27 (44). 799. Optically active coordination compounds. S. Kirschner, Prep. Inorg. React., 1964, 1,29-57 (140). 800. Metal derivatives of ketimine and aldimine compounds. D. F. Martin, Prep. Znorg. React., 1964, 1, 59-75 (48). 801. Metal carbonyls. J. C. Hileman, Prep. Znorg. React., 1964, 1,77-120 (140). 802. Halide and oxyhalide complexes of elements of the titanium, vanadium and chromium sub-groups. G. W. A. Fowles, Prep. Znorg. React., 1964,1,121-140 (51). 803. Anhydrous metal nitrates. C. C . Addison and N. Logan, Prep. Inorg. React., 1964,1, 141-164 (62). 804. Metal alkoxides. D. C. Bradley, Prep. Inorg. React., 1965, 2,169-186 (54). 805. Fluorine compounds of the platinum metals. N. Bartlett, Prep. Inorg. React., 1965,2, 301-339 (77). 805. Compounds of xenon. E. H. Appelman and J. G. Malm, Prep. Znorg. React., 1965,2,341-350 (21). 807. Metal halides in low oxidation states. J. D. Corbett, Prep. Inorg. React., 1966,3, 1-33 (141). 808. Compounds of the actinides. B. B. Cunningham, Prep. Inorg.Reacl., 1966,3,79-121 (104). 809. The application of reaction mechanisms to the synthesis of coordination compounds. J. L. Burmeister, Prep. Inorg. React., 1968,5, 1-43 (211). 810. Complexes of macrocyclic ligands. L. F. Lindoy and D. H. Busch, Prep. Inorg. React., 1971,6,1-61 (173). 811. Metal-metal halogen compounds of the transition metals. J. E . Fergusson, Prep. Znorg. React., 1971,7,93-163 (353). 812. Complexes of dinitrogen. G. J. Leigh, Prep. Znorg. React., 1971: 7, 165-193 (86). 813. Bimolecular substitution and oxidation reactions of 17-electron pentacoordinate metal carbonyl radicals. A. Po&,Transition Met. Chem. (Weinheim, Ger.),1982, 7, 65-69 (41). 814. Structures and fluxional behaviour of transition metal cluster carbonyls. R. E. Benfield and B. F. G. Johnson, Transition Met. Chem. (Weinheim, Ger.), 1981, 6, 131-144 (90). 815. Conversion electron Mossbauer studies of compounds containing iron. F. J. Berry, Transition Met. Chem. (Weinheim, Ger.), 1979,4,209-218 (60). 816. Prospects for dinuclear transition metal chemistry illustrated by recent advances in the chemistry of dimolybdenurn and ditungsten. M. H. Chisholm, Transition Met. Chem. (Weinheim, Ger.), 1978,3, 321-333 (91). 817. Sulphur dioxide complexes of the platinum metals. D. M. P . Mingos, Transition Mer. Chem. (Weinheirn, Ger.), 1978,3, 1-15 (83). ~

~

Index of Review Articles and Specialist Texts

47

818. Nikolai Semenovich Kurnakov, the reaction (1893) and the man (1860-1941). A ninety-year retrospective view. G. B. Kauffman, Polyhedron, 1983.2,855-863 (39). 819. Metal-metal bonds and metal-carbon bonds in the chemistry of molybdenum and tungsten alkoxides. M. H. Chisholm, Polyhedron, 1983,2,681-721 (90). 820. The reactions of nucleophiles with complexes of chelating heterocyclic imines; a critical survey. E. C. Constable, Polyhedron, 1983,2,551-572 (185). 821. Mechanisms in the racemization of optically active coordination complexes in the solid state. P. O'Brien, Polyhedron, 1983,2,233-2&3 (54). 822. Carbonylhydridotris(triphenylphosphine)rho~ium(I).F. H. Jardine, Polyhedron, 1982: 1, 569405 1'11

<\

(L.511.

823. Formation of fluoride-containing coordination compounds by decomposition of transition-metal tetrafluortiborates. J . Reedijk, Comments Znorg. Chem., 2982,1,379-389 (34). 824. Bipyridine radical ions. C. Creutz, Comments Inorg. Chem., '1982, 1,293-311 (38). 825. The Bronsted acidity of transition metal hydrides. I<. G. Pearson and P. C. Ford, Comments Inorg. Chem., 1982,1,279-291(33). 826. The impact of the donor-acceptor concept. V. Gutmann and R. Resch, Comments Inorg. Chem., 1982,1,265-278 (44). 827. On the interpretation of the electronic spectra of complexes containin the molybdenyl ion. J . R. Winkler and H. B. Gray, Comments Znorg. Chem.. 1981,1,257-263 (125. 828. The investigation of coordinated water in paramagnetic metalloproteins through N.M.R. spectroscopy. I. Bertini, Comments Znorg. Chem., 1981,1,227-243 (68). 829. Dimercury(1)-nitrogen compounds and other addition compounds of the Hg-H$+ ion. K. Brodersen, Comments Znorg. Chem., 1981, I, 207-225 (57). 830. An explanation of the relative oxygen and carbon monoxide affinities of some iron(I1 porphyrin complexes. T. Hashimoto and F. Basolo, Comments Inorg. Chem., 1981, 1,199-205 (181. 831. The redox behaviour of transition metal complexes with soft ligands. E. Uhlig, Comments Inorg. Chem., 1981,1,169-182 (43). 832. Theory and experiments on valence delocalisation in mixed-valence cornpounds. P , Day, Comrnenfi Znorg. Chem., 1981,1,155-167 (23). 833. The aquo ions of molybdenum. D. T. Richens and A . G. Sykes, Comments Znorg. Chem.. 1981,1, 141-153 (43). 834. Effect of bridge geometry on exchange coupling in ligand bridged copper(I1) dimers and chains. W. E. Hatfield, Comments Znorg. Chem., 1981, 1, 105-121 (80). 835. Application of molecular orbital theory to electron transfer reactions of metal complexes in solution. J. K. Burdett, Comments Znorg. Chem., 1981, 1 , 8 5 1 0 3 (7). 836. One dimensional inorganic conductors. H. J. KeHer: Comments Znorg. Chem., 1981, 1 , 7 1 4 4 (29). 837. Coordination and activation of dioxygen. R. S. Drago, B. B. Corden and A. Zombeck, Comments Inorg. Chem,, 1.981, 1, 53-70 (36). 838. On the role of the high spin state in the water exchange reaction of hexaaquocobalt(J1T). J. R. Winkler, S. F . Rice and H. B. Gray, Comments Znorg. Chem., 1981, 1,47-~51(4). 839. Assigning reactive excited states in inorganic photochemistry. A. W. Adamson, Commenrs .Tnorg. Chem., 1981, 1 , 3 3 4 5 (56). 840. Substitution reactions of ruthenium ammines. H . Taube, Comments Znorg. Chem., 1981, 1. 17-31 (55). 841. Oxidation of carbon monoxide by metal ions and homogeneous catalysis of the water gas shift reaction and related processes. J . Halpern, Comments Znorg. Chem., 1981, 1,3-15 (42). 842. Hydrolysis of iron(II1) - chaotic olation versus nucleation. W. Schneider, Comments Inorg. Chem., 1984,3,205-223 (38). 843. Singly and doubly excited states of exchange-coupled dimers. H. U. Gudel, Comments Inorg. Chem., 1984,3,18%204 (28). 844. Electrochemical effects of metal ion coordination to non-innocent biologically important molecules. M. J. Clarke, Comments Znorg. Chem., 1984,3,133-151 (57). 845. Ferrorna netically coupled dinuclear complexes. 0. Kahn, Comments Inorg. Chem., 19&4, 3, 105-132 $30). 846. Recent advances in technetium chemistry: bridging inorganic chemistry and nuclear medicine. E. Deutsch and K. Libson, Comments Znorg. Chem.,1984,3,83-103 (30). 847. Odd oxidation states of palladium and platinum. A. L. Balch, Comments Znorg. Chem.. 1984, 3, 51-67 (53). 848. Aspects of pentacoordinate tin compounds. A. Tzschach and K. Jurkschat, Comments Znorg. Chem., 1983,3,35-50 ( 5 5 ) . 849. Quantitative comparison of the symmetry components of a ligand field: illustrations of the orthonormal operators formalism. M. Brorson, T. Damhus and C. E. Schaffer, Comments Znorg. Chem., 1983,3, 1-34 (29). 850. Lanthanide ion probes of biomolecular activity. W. D. Horrocks, Adv. Znorg. Biochem., 1982, 4, 201-261 (259). 851. The structure and mechanism of the sarcoplasmic reticulum Ca2+-ATPase:a bioinorganic perspective. E. M. Stephens and C. M. Grisham, Adv. Inorg. Biochem., 1982,4,263-288 (151). 852. Human serotransferrin: structure and function. N . D. Chasteen, Coord. Chem. Rev., 1977,22,1-36 (178). 853. Metal chelates of fluorinated 1,3-diketones and related compounds. K. C. Joshi and V . N . Pathak, Coord. Chem. Rev., 1977,22,37-122 (401). 854. N.Q.R. in coordination compounds. L. Ramakrishnan, S . Soundararjan, V. S. S. Sastry and J. Ramakrishnan?Coord. Chem. Rev., 1977,22?123-182 (273).

48

Index of Review Articles and Specialist Texts 855. Metal derivativcs of the borazines. J. J. Lagowski, Coord. Chem. Rev., 1977,22, 185-194 (37). 856. The radiation chemistry of metal ions in aaueous solution. G. V. Buxton and R. M. Sellers, Coord. Chem. Rev., 1977,22,i95-273 (303). 857. Oreanonitrile comdexes of transition metals. B. N. Storhoff and H. C. Lewis. Coord. Chem. Rev.. 1977,23, 1-29 (156). 858. Transition metal complexes of binucleating ligands. U. CaseIlato, P. A. Vigato and M. Vidoii, Coord. Chem. Rev.. 1977.23.31-117 (184). 859. Flash uhotolvsis of coordination compounds. Z. Stasicka and A. Marchai. Coord. Chem. Rev.. 1977,23,1311181 (271). 860. Thiocarbonyl and related complexes of the transition metals. P . V. Yaneff, Coord. Chvrn. Rev., 1977.23.183-220 (1081. 861. Sterdochernistry ind reaction rates of anionopentaaminc complexes of cobalt(I1T) and chromium(i1i). D. A . House, Coord. Chem. Rev., 1977,23,223-322 (451). 862. Three coordination in metal complexes. P. G. Eller, D . C. Bradley, M. B. Hursthouse and D. W. Meek, Cloord. Chem. Rev., 1977,24, 1-95 (306). 863. Structural chemistry of hemerythrin. D. M. Kurtz, D. F. Shriver and I. M. Klotz, Coord. Chem. Rev., 1977,24,145-178 (70). 864. Structures of high coordination complexes. M. G. B. Drew, Coord. Chem. Rev., 1977, 24, 179-275 (295). 865. Solvent paths and dissociate intermediates in substitution reactions of square planar complexes. R. 3. Mureinik, Coord. Chem. Rev., 1978,25, 1-30 (133). 866. Ligand field parameters and spectra of first row transition metal dihalides in the solid state. D. R. Rosseinsky and I. A. Dorrity. Cuord. Chem. Rev., 1978,25,3147 (109). 867. A review of platinum metal nitrato complexes. P. C. Critchlow and S. D . Robinson, Coord. Chern. Rev., 1978,25, 69-102 (193). 868. Substitution-inert metal ions as probes of biological function. J. I. Legg, Coord. Chrrn. Rev.,1978, 25.103-132 (84). 869. Aqueous coordhation chemistry of neptunium. S. R. Patil, V. V. Rarnakrishnan and M. V. Ramaniah, Coord. Chem. Rev.; 1Y78.25, 133-171 (216). 870. Three coordinate magnesium. A . G. Pinkus, Coord. Chem. Rev.: 1978,25,173-197 (117). 871. The sulphido-, seleno- and telluro-halides of the transition elements. D. A. Rice, Coord. Chern. Rev., 1978,25,199-227 (102). 872. Group IVB derivatives of the iron triad carbonyls. A. Bonny: Coord. Chem. Rev., 1978, 25, 229-273 (145). 873. Nitrosyl complexes of ruthenium. F. Bottomley, Coord. Chem. Rev., 1978,26,7-32 (154). 874. New coordination chemistry of saturated ligands. H. Taube, Coord. Chem. Rev., 1978, 26, 33-45 (31). 875. The cytochromes of higher plants and algae. D. B. Knaff, Coord. Chem. Rev., 1978, 26, 47-70 (112). 876. Properties of the system: transition metal compound-magnesium. Fixation and activation of NZ, COz, C O , HZand related molecules. P. Sobota and E. Jezowska-Trzebiatowska, Coord. Them. Rev.,'1978, 26,73-84 (20). 877. Actinide comulexes with carboxylic acids. U. Casellato, P. A. Vieato and M. Vidali. Coord. Chem. Rev., 1978,26, 85-159 (276). 878. Stereochemistry of chromium complexes: a bibliographic listing. I. D. Brown, Coord. Chem. Rev., 1978.26. 161-206 (2291. 879. Interaction of spinlabeis with transition metals. S. S. Eaton and G. R. Eaton, Coord. Chrm. Rev., 1978,26,207-262 (218). 880. Metal complexes of substituted phosphinites and secondary phosphites. D. M. Roundhill, R. P. Sperline and W. B. Beaulieu, Coord. Chem. Rev., 1978,26,263-279 (73). 881. Donor properties of hydroxamic acids. B. Chaterjee, Coord. Chem. Rev.,1978,26,281-303 (48). 882. Matrix isolation studies on transition metal carbonyls and related species. J. K. Burdett, Coord. Chern. Rev.,1978,27, 1-58 (212). 883. Oxidation and other products from the reaction of thiones and phosphine sulphides with metaI salts and halogens. E. W. Ainscough and A. M. Brodie, Coord. Chem. Rev.. 1978,27,59-86, (103). 884. Reactions of zerovalcnt platinum and palladium complexes with organometallic compounds of nontransition metals. V. I. Sokulov and 0. A. Reutov, Cuord. Chem. Rev.,1978,27,89-107 (SO). 885. Blue copper proteins: n.m.r. investigations. E. L. Ulrich and J . L. Markley, Coord. Chem. Rev., 1978,27, 109-140 (117). 886. Cyanato-copper(I1) complexes with nitrogen organic ligands: preparation, properties and structure. J. Kohout, M. Hvastijova and 3. Gazo, Coord. Chem. Rev., 1978,27, 141-172 (116). 887. The chemistrv of biological manganese. G. D. Lawrence and D. T. Sawver, Coord. Chem. Rev., 1978,27, 1731193 (100); 888. Computer evaluation of complex equilibria. F. Gaizer, Coord. Chem. Rev., 1979, 27, 195-222 (163). 889, Absorption spectra and structure of lanthanide coordination compounds in solution. K . B. Yatsimirskii and N. K . Davidenko, Cuord. Chern. Rev., 1979,27,223-273 cobalt(I1). Y. Nishida 890 Splitting ofd-orbitals in square planar complexes of cop er(TI), nickel and S. Kida, Coord. Chem. Rev., 1979,27,275-298 (947. 891 Iron-sulfur centres of the chloroplast membrane. R. Malkin and A. J. Bearden, Coord. Chem. Rev.. 1979.28. 1-22 173). 892. Thin'layer and filter paper chromatography of metal complexes and some non-metal elements. R. L. Dutta, R. K. Ray and G. a. Kauffman, Coord. Chem. Rev., 1979,28,23-45 (93). ",

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index of Review Articles and Specilrlist Texts

49

893. Metal sandwich complexes of cyclic, planar and pyramidal ligands containing boron. R. N. Grimes, Coord. Chern. Rev., 1979,28,47-96 (132). 894. Cobalt, nickel and copper naked metal clusters and olefin chemisorption models. G. A. Ozin, Coord. Chem. Rev.. 1973.28,117-146 (45). 895. Photochemistrv of manganese complexes. A. Harriman. Coord. Chem. Rev., 1979, 28, 147-175 (125). 896. Kinetics and mechanisms of substitution reactions of cobalt(II1) rrans-dioximes, in non-aqueous media. N. M. Samus and A. V. Ablov, Coord. Chem. Rev., 1979,28, 177-203 (47). 897. Chromatographic resolution of metal complexes on Sephadex ion exchangers. Y. Yoshikawa and R. Yamasaki, Coord. Chem. Rev., 1979,28,205-229 (98). 898. Actinide complcxcs with chelating ligands containing sulfur and amidic nitrogen donor atoms. U. Casellato, M. Vidali and P. A . Vigato, Coord. Chem. Rev.. 1979,28,231-277 (181). 899. Crystal field aspects of the vibrational spectra of metal complexes. D. A. Thornton, Cuord. Chem. Rev., 1984.55, 113-149 (66). 900. Vibrational studies of solid inorganic and coordination complexes at high pressures. J. R. Ferraro, Coord. Chem. Rev., 1979,29,1-66 (324). 901. Six coordinate copper complexes with 811 < g _ in the solid state. I. Bertini, D. Gatteschi and A. Scozzafava, Coord. Chem. Rev., 1979,29,67-84 (10). 902. Isomerism in complexes of bidentate ligands with enantiotopic donor atoms. R . E. Tapscott, J. D. Mather and T. F. Them, Coord. Chem. Rev., 1979,29,87-127 (254). 903. Correlations among solvent polarity scales, dielectric constant and dipole moment, and a means to

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reliable predictions of polarity scale values from current data. T. R. Ciriffiths and D. C . Pugh. Coord. Chem. Rev., 1979,29, 12Y-211 (130). Y04. Oatical activity of coordination compounds. H, P. Jensen and F. Woldhve, Coord Chem. Rev . 1@79,29,210-?35 (185). 905. Mono-, bi-, tetra- and poly-nuclear copper(I1) halogenouarboxylates. M . Mclnik. Conrd. Chem. Rev.. 1 9 8 1 . 3 6 . 1 4 (1671. 906. v,-bridging carbonyl systems in transition metal complcxcs. R. Colton and M. J . McCormick, Coord. Chem. Rev., 1980,31, 1-52 (162). 907. Coordination chemistry of lanthanides with emphasis on derivatives with Ln--0-C bonds. R.C. Mehrotra, P. N. Kapoor and J. M. Batwara, 1980,31,67-91 (203). 908. Initial state and transition state solvation in inorganic reactions. M. J. Blandamer and J. Burgess. Coord. Chem. Rev., 1980,31,93-121 (78). 909. Transition metal complexes containing organoimido (NR) and related ligands. W. R. Nugerrt and B. L. Haymore, Coord. Chem. Rev., 1980,31,123-175 (192). 910. The X-ray photoelectron spectra of metal complexes of sulphur-containing ligands: sulphur 2p-binding energies. R . A. Walton, Coord. Chern. Rev., 1980, 31, 183-220 (88). 911. Some aspects of the bioinurganic chemistry of the actinides, R. A. Bulrnan, Coorcl. Chern. Rev., 1980,31,221-250 (100). 912. Vibrational fine structurc in the electronic spectra of transition metal compounds: an experimental survey. M. Cicslak-Golanka, A. Bartecki and S. P. Sinha. Coord. Chem. R e v . , '1980, 31, 251-288 (351). 93 3. Dioxygen reactivity-structure correlations in manganese(I1) complexes. W. M. Coleman and L. T. Taylor, Coord. Chem. Rev., 1980,32, 1-31 (122). 914. Bimetallic tetrathiocyanates and selenocyanates as Lewis acids. P. P. Singh, Cuord. Chern. Rev., 1980,32,33-65 (108). 915. Some new developments in the chemistry of metallophthalocyanines. K. Kasuga and M. Tsutsui, Coord. Chem. Rev.. 1980,32,69-95 (129). 916. Free radical reactions of transition metal svstems. R. S. Drago. Coord. Chem. Rev.. 1980. 32, 97-110 (35). 917. Zerovalent transition metal complexes of organic isocyanides. Y. Yamamoto, Coord. Chem. Rev., 1980.32.193-233 (172). 918, Organometallic irhinolecular coordination compounds' containing a phosphorus donor ligand. I. Ornae, Coord. Chem. Rev., 1980,32, 235-271 (168). 919. Synthesis of electron-rich nickel triad complcxcs. E. Uhlig and D. Walther, Cuurrl. Chern. Rev., 1Y80,33,3-53 (182). 920. Structure and function of copper proteins. H. Beinert, Coord. Chem. Rev., 1980,33,55-85 (95). 921. Monovalent, trivalent and tetravalent nickel. K. Nag and A. Chakrovorty, Coord. Chem. Rev., 1980,33,87-147 (316). 922. Relationships between the carbon-oxygen stretching frequencies of carboxylato complexes and the type of carboxylate coordination. G. B. Deacon and R. J. PhiIlips, Coord. Chem. Rev., 1980, 33, 227-250 (177). 923. The interpretation of reactivity in chemical and biological systems with the E and C model. R. S. Drago, Cuord. Chem. Rev., 1980,33,251-277 (52). 924. Caeruloulasmin: the eniematic comer motein. S. H. Laurie and E. S. Mohammed, Coord. Chem. Rev., lY'80,33,779-312 ('189). 925. Photochemical properties of copper complexes. G. Ferraudi and S. Muralidharan, Cnovd. Chem. Rev.. 1981. 36. 4-588 11151. 926. Activation volumes of the reactions of transition mctal compounds in solution. D. A. Palmer and H. Kelm, Coord. Chew. Rev., 1981,36,89-152 (225). 927. Metal tolerant plants. M. E. Farago, Coord. Chem. Rev., 1981,36, 155-182 (275). 928. Actinide nitrate complexes. U. Casellato, P. A. Vigato and M. Vidali. Coord. Chem. Rev., 1981, 36,183-265 (247). Y

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50

Index of Review Articles and Specialist Texts 929. The stereochemistry and electronic properties of fluxional six-coordinate copper(I1) complexes. B. Hathaway, M. Duggan, A. Murphy, J. Mullane, C. Power, A. Walsh and B. Walsh, Coord. Chem. Rev., 1981,36,267-324 (132). 930. Multiple state emission and related phenomena in transition metal complexes. M. K. DeArmond and C. M. Carlin, Coord. Chem. Rev., 1981,36,325-355 (89). 931. Structural and conductivity aspects of one-dimensional transition metal complexes. J. R. Ferraro and K. B. Mertes, Coord. Chem. Rev., 1981,36,357-371 (29). 932. Coordination chemistry of the manganese and rhenium fragments, (C5H5)M(C0)2.K. G . Caulton, Coord. Chem. Rev.,1981,38, 1-43 (138). 933. Transition metal complexes of o-benzoquinone, o-semiquinone and catecholate ligands. C. G. Pierpont and R. M. Buchanan, Coord. Chem. Rev., '1981,38,45-87 (72). 934. Electronic structures of transition metal cluster complexes. M. C. Manning and W. C. Trogler, Coord. Chem. Rev., l Y & l l 38,89-138 (406). 935. Structural aspects and coordination chemistry of metal porphyrin complexes with emphasis on axial ligand binding to carbon donors and mono- and di-atomic nitrogen and oxygen donors. P. D. Smith, B. R. James and D . H. Dolphin, Coord. Chem. Rev., 1981,39>31-75 (170). 936. Synthesis and reactivity of nickel(II1) complexes. R. I. Haines and A. McAuley, Coord. Chem. Rev., 1981,39,77-119 (89). 937. Advances in the photochemistry and photophysics of chromium(II1) polypyridyl complexes in fluid media. M. A. Jamieson, N . Serpone and M. Z. Hoffmann, Coord. Chem. Rev., 1981,39, 121-179 (119). 938. The mechanisms of hotoreactivity of coordination compounds: limiting cases of decay on a specific nuclear coordinate bosenco) or via random coordinate selection (dercos). B . R. Hollebone, C. H. Langford and N. Serpone, Coord. Chem. Rev., 1981,39, 181-224 (95). 939. Chrornium(TI1) photochemistry and photophysics. A . D. Kirk, Coord. Chem. Rev., 1981, 39, 225-263 (163). 940. Fluoro-diamine complexes of chromium(II1). J. W. Vaughn, Coord. Chem. Rev., 1981,39,265293 (69). 941. Recent developments in the studies of molecular oxygen adducts of cobalt(I1) com ounds and related systems. T. D. Smith and J. R . Pilbrow, Coord. Chem. Rev., 1981,39,295-383 637). 942. A ligand's eye view of coordination. R. V. Parish, Coord. Chem. Rev., 1982,42,1-29 (51). 943. Transition metal nitrite complexes. M. A. Hitcheman and G. L. Rowbottom, Coord. Chem. Rev., 1982,42,55-132 (265). 944. The ligand chemistry of tellurium. H. J. Gysling, Coord. Chem. Rev., 1982,42,133-244 (398). 945. Organometallic intramolecular coordination com ounds containing an arsine donor ligand. I. Omae, Coord. Chern. Rev., 1982,42,245-257 (44p. 946. Study of the relationship between the structural data and magnetic interaction in cxo-bridged binuclear copper(I1) compounds. M. Melnik, Coord. Chem. Rev., 1982,42,259-293 (147). 947. Equatorial-axial interactions in complexes as a manifestation of mutual influencc of ligands. J. Gazo, R. Boca, E. Jona, M. Kabesova, L. Macaskova, J. Sima and P. Pelikan, Coord. Chem. Rev., 1982,43,87-131 (106). 948. Structural variability in solutions. V. Gutmann, G. Resch and W. Linert, Coord. Chem. Rev., 1982, 43, 133-164 (80).. 949. Novel coordination cornmunds formed from CS7 and heteroallenes. H. Werner, Coord. Chem. Rev., 1982,43,165-185 (33). 950. The conformation and interconversion of Schiff base complexes of nickel(I1) and copper(I1). S. Yamada and A. Takeguchi. Coord. Chem. Rev.. 1982.43. 187-204 (27). 951. Structural, conductivity i n d spectroscopic aspects 'of one-dimensionai transition metal Complexes. J. R. Ferraro, Coord. Chem. Rev., 1982,43,205-232 (50). 952. Principles of concentration distributions in multicomponent equilibrium systems. I. Nagypal and M. T. Beck, Courd. Chern. Rev., 1982,43,233-250 (14). 953. Transition metal complexes with bridging hydride ligands. L. M. Venazi, Coord. Chem. Rev., 1982, 43,251-274 (40). 954. A discussion of the different typcs of solute-solute and solute-solvent interactions acting in homogeneous catalysis by transition metal complexes. E. Cesarotti, R.Ugo and L. Kapan, Coord. Chem. Rev., 1982,43,275-208 (47). 955. Liquid-liquid extractions of metal ions by chelating ligands. E. Uhlig, Coord. Chem. Rev., 1982,43, 299-312 (38). 956. CIoso borate anions as a means of synthesising new coordination compounds. I. A. Zakharova, Coord. Chem. Rev.. 1982,43,313-324 (20). 957. Utilization of the Pfeiffer effect and outer-sphere complexation for the prediction of absolute configurations of optically active metal complexes. S . Kirschner and I. Bakkar, Coord. Chem. Rev., 1982,43,325-335 (27). 958. Ligand effects. J. Chatt, Coord. Chem. Rev., 1982,43,337-347 (4). 959. Conformational analysis of chelate ring systems by n.m.r. C. J. Hawkins and J. A. Palmer, Coord. Chem. Rev., 1982,44, 1-60 (150).. 960. The ligand field photosubstitution reactions of d6 hexacoordinate metal complexes. P. C. Ford, Coord. Chem. Rev., 1982,44,hl-82 (44). 961. Metal phthalocyanines and porphyrins as photosensitizers for reduction of water to hydrogen. J. R. Darwent, P. Douglas, A. Harriman, G. Porter and M. C. Kichoux, Coord. Chem. Rev., 1982,44, 83-126 (91). 962. The coordination chemistry of acrylonitrile. S. J. Bryan, P. G. Huggett, K. Wade, J. A. Daniels and J. R. Jennings, Coord. Chern. Rev., 1982,44, 149-189 (315).

Index of Review Articles and Specialist Texts

51

963. Crystal structures of technetium compounds. G. Bandoli, U. Mazzi, E. Roncari and E. Deutsch, Coord. Chem. Rev., 1982,44,191-227 (106). 964. l19Sn n.m.r. in coordination chemistry. R. Hani and R. Geanangel, Coord. Chem. Rev., 1982,44, 229-246 (66). 965. Platinum-195 n.m.r. P. Pregosin, Coord. Chem. Rev., 1982,44,247-291 (122). 966. The chemistry of ruthenium, osmium, rhodium, iridium, palladium and platinum in the higher oxidation states. D. J. Gulliver and W. Levason, Coord. Chem. Rev., 1982,46, 1-127 (1131). 967. Circular dichroism of transition metal complexes. R. D. Peacock and B. Stewart, Coord. Chem. Rev., 1982,46,129-157 (43). 968. Photophysics, photochemistry and solar energy conversion with Ru(bipy)3*+ and its analogues. K. Kalyanasundaram, Coord. Chem. Rev., 1982,46,159-244 (360). 969. Disulphur complexes. A . Miiller, W. Jaegermann and J. H. Enemark, Coord. Chem. Rev., 1982, 46,245-280 (147). 970. Stereochemical aspects of reactions of complexes of d) transition metals with multiply bonded ligands. Y. V. Kokunov and Y. A. Buslaev, Coord. Chem. Rev., 1982,47,15-40 (120). 971. Trends in redox potentials of transition metal complexes. H. L. M. Van Gaal and J. G. M. Van der Linden, Coord. Chem. Rev., 1982,47,41-54 (29). 972. Electrochemistry of transition metal clusters. P. Lemoine, Coord. Chem. Rev., 1982, 47, 55-88 (109). 973. Thermochromic phase transitions in transition metal salts. D. R. Bloomquist and R. D. Willett, Coord. Chem. Rev., 1982,47,125-164 (75). 974. The coordination chemistry of hydrogen cyanide. cyanogen and cyanogen halides. B . Corain, Coord. Chem. Rev.: 1982, 47, 165-200 (111). 975. Thermochemistry of the oxidative addition reaction. J. U. Mondal and D. M. Blake, Coord. Chern. Rev., 1982,47,205-238 (80). 976. Structural isomerism of copper(I1) compounds. M. Melnik, Coord. Chem. Rev., 1982,47,239-261 (150). 977, Organostannate(1V) complexes. J. W. Nicholson, Coord. Chem. Rev., 1982,47,263-282 (79). 978. Solvent extraction Dromrties of ditertiarvDhosDhine dioxides. T. S. Lobana and S. S. Sandhu, Coord. Chem. Rev.: 1982,47,283-300 (1205. 979. The coordination chemistry of ylides. W. C. Kaska, Coord. Chem. Rev., 1983,48,1-58 (193). 980. Modelling the molybdenum centres of the molybdenum hydroxylases. J. T. Spence, Coord. Chem. Rev., 1983,48,5%32 (67). 981. N.m.r. studies of coordination complexes using lanthanide shift reagents. L. F. Lindoy, Coord. Chem. Rev.. 1983.48.83-100 (38). 982. Thermochemistry’of gaseous tcansition metal complexes of group V and VI ligands. P. M. Burkenshaw and C . T. Mortirner, Coord. Chem. Rev., 1983,48, 101-155 (110). 983. Ligand field models and the photochemistry of coordination compounds. L. G. Vanquickenborne and A. Ceulemans, Coord. Chem. Rev., 1983,48,157-202 (179). 984. Taking metal atom chemistry out of the cold. G. A. Ozin, M. P. Andrews, L. F. Nazar, H. X. Huber and C. G. Francis, Coord. Chem. Rev., 1983,48,203-242 (41). 985. Chiral lanthanide compounds. H. G. Brittain, Coord. Chem. Rev., 1983,48,243-276 (179). 986. Dioxygen activation in transition metal com Iexes in the light of molecular orbital calculations. R. Boca, Coord. Chern. Rev., 1983,50,1-72 645). 987. Metalloproteins with phenolate coordination. L. Que, Coord. Chem. Rev., 1983,50,73-108 (181). 988. Rhodium(I1) carboxylates. E. 3. Boyar and S. D. Robinson, Coord. Chem. Rev., 1983,50,1G9-208 (211). 989. Covalent hydration and pseudobase formation in transition metal polypyridyl complexes: reality or myth? N. Serpone, G. Ponterini, M. A. Jamieson: F. Bolletta and M. Maestri, Coord. Chem. Rev., 1983,50,209-302 (229). 990. A possible mechanism for the reactions of electrophiles with polynuclear transition metal carbonyls and related complexes. A. R. Manning, Coord. Chem. Rev., 1983,51,41-67 (41). 991. Transition metal nitrosyls in organic synthesis and in pollution control. K. K. Pondey, Coord. Chem. Rev., 1983,51,69-98 (143). 992. Platinum carbonyls and their use in homogeneous catalysis. I-€. C. Clark and V. K . Jain, Coord. Chem. Rev., 1984.55, 151-204 (288). 993. Molecular mechanics calculations in coordination chemistry. G. R. Brubaker and D. W. Johnson, 1984,53, 1-36 (80). 994. Cobalt carbonyl radicals and radical reactions of cobalt carbonyl. G. Palyi, F. Ungvary, V. Galamb and L. Marko, Coord. Chem. Rev., 1984,53,37-53 (90). 995. Coordination and redox chemistry of some macromorecular systems. A. Skorobogaty and T. D. Smith, Coord. Chem. Rev., 1984,53,55-226 (783). 996. Reagent and catalyst induced substitution reactions of metal carbonyl complexes. M. 0. Albers and N. J. Coville, Coord. Chem. Rev., 1984,53,227-259 (153). 997. Towards the unification of coenzyme Blz-dependent diol dehydratase stereochemical and model studies: the bound radical mechanism. R. G. Finke, D. A. Schiraldi and B. J. Mayer, Coord. Chem. Rev., 1984,54,1-22 (40). 998. Electrochemistry and redox behaviour of transition metal dithiocarbamates. A. M. Bond and R. L. Martin, Coord. Chem. Rev., 1984,54,23-98 (182). 999. Monothio- and monoseleno-carbamate complexes. B. J. McCormick, R. Bereman and D. Baird, Coord. Chem. Rev., 1984,54,9-130 (96). 1000. Mechanistic aspects of reactions involving A (11) as an oxidant. E. Mentasti, C. Baiolchi and J. S. Coe, Coord. Chem. Rev., 1984,54,131-157 8 3 ) .

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Index of Review Articles and Specialist Texts

1001. Optical activity of cobalt(III), chromium(II1) and rhodium(II1) complexes with aminopolycarboxylate, edta-type and related ligands. D. J. Radanovic, Coord. Chern. Rev., 1984,54, 159-261 (195). 1002. An investigation of the chelate effect: the binding of bidentate phosphine and arsine chelates in square-planar transition metal complexes. D. M. A. Minahan, W. E. Hill and C. A. McAuliffe, Coord. Chem. Rev., 1984,55,31-54 (153). 1003. Geometric and electronic factors of dinitrogen activation on transition metal complexes. P. Pelikan and R. Boca, Coord. Chem. Rev., 1984,55,55-112 (190). 1004. The coordination chemistry of substituted hydrazines. J. R.Dilworth, Coord. Chem. Rev., 1976,21, 29-62 ( 172). 1005. Organocobalt chemistry of vitamin Bl2 model compounds (cobaloximes). G. N. Schrauzer, Acc. Chem. Res., 1968,1,97-103 (40). 1006. Patterns of organometallic reactions related to homogeneous catalysis. J. P. Collman, A M . Clzrm. Res., 1968, 1, 13&143 (86). 1007. Free energies, barriers and reactivity patterns in oxidation-reduction reactions. N Sutin, Acc. Chem. Res., 1968, I, 225-231 (39). 1008. Mass spectra of some organometallic molecules. J. Lewis and B. F. G. Johnson, Acc. Chem. Res., 1968,1,245-256 (35). 1009. The chemistry of the polyhedral species derived from transition metals and carboranes. M. F. Hawthorne, Acc. Chem. Res., 1968, 1,281-288 (40). 1010. Reversible activation of covalent molecules by transition metal complexes. The role of the covalent molecule. L. Vaska, Acc. Chem. Res., 1968, 1, 335-344 (51). 1011. Inorganic nitrogen fixation. Nitrogen compounds of the transition metals. A. D. Allen and F. Bottomley, Acc. Chem. Res., 1968, 1 , 360-365 (40). 2012. High-pressure Mijsshauer resonance studies with iron-57. H. G. Drickamer, R. W. Vaughan and A. R. Champion, Acc. Chem. Res., 1969,2,40-47 (40). 1013. Coordination compounds with delocalised ground states. The transition metal derivatives of dithioketones and ethylene(l,2)dithiolates (metal dithiencs). CJ. N. Schrauzer, Acc. Chem. Res., 1969,2,72-80 (36). 1014. Strong homonuclear metal-metal bonds. F. A. Cotton, Acc. Chem. Res., 1969,2,240-247 (49). 1015. The application of exciton theory to the determination of the absolute configuration of inorganic complexes. B. Bosnich, Acc. Chem. Res., 1969,2,266-273 (21). 1016. Application of isotropic shifts to the investigation of structures and structural equilibria of metal complexes. R. H. Holm, Acc. Chem. Res., 1969,2,307-316 (38). 1017. Organic molecules as bridging groups in electron transfer reactions. H. Taube and E. S. Gould, Acc. Chem. Res., 1969,2,321-329 (51). 1018. Chemical consequences of fluorocarbon phosphines. A. B. Burg, Acc. Chem. Res., 1969,2,353-360 (61). 1019. Structure and mechanism in the enzymatic activity of carboxy e tidase A and relations to chemical sequence. W. N. Lipscomb, Ace. Chem. Res., 1970,3, 81-89 667. 1020. The structure of porphyrins and metalloporphyrins. E. B . Fleischer. ACC.Chem. Res., 1970, 3: 105-112 (41). 1021. Intramolecular aromatic substitution in transition metal complexes. G. W. Parshall, Acc. Chem. Res., 1970,3,139-144 (51). 1022. On the discriminating behaviour of metal ions and ligands with regard to their biological significance. H. Sigel and D. B . McCormick, Acc. Chem. Res., 1970: 3,201-208 (66). 1023. Transition metal basicity. D. F. Shriver, Acc. Chem. Res., 1970,3. 231-238 (68). 1024. Stereochemically non-rigid structures. E . L. Muetterties, Acc. Chem. Res., 1970,3,266-273 (65). 1025. Design and development of an organic-inorganic system for the chemical modification of molecular nitrogen under mild conditions. E. E. van Tamelen, Acc. Chem. Res., 1970,3,361-367 (25). 1026. Base hydrolysis of octahedral complexes. M. L. Tobe, Acc. Chem. Res., 1970,3,377-385 (44). 1027. Oxidative-addition reactions of transition metal complexes. J . Halpern, Acc. Chem. Res., 1970, 3, 386392 (66). 1028. Mechanisms of ligand replacement in octahedral nicket(I1) complexes. R. Cr. Wilkins, Acc. Chem. Res., 1970,3,40&416 (93). 1029. Polypyrazolylborates, a new class of ligands. S. Trofimenko?Acc. Ckem. Res., 1971,4,17-22 (37). 1030. Conformational analysis of tris(ethy1enediamine) complexes. J. K . Beattie, Acc. Chem. Res., 1971, 4,253-259 (31). 1031. Persistence of atomic orbitals in complexes and other comDounds. C. K . Jorgensen, Acc. Chem. Res., 1971,4,307-315 (50). 1032. Some recent studies on poly(tertiary phosphines) and their metal complexes. R. B. King, Acc. Chem. Res.. 1972.5. 177-185 (32). 1033. Carboxypeptidase A: a rnechanisiic analysis. E. T. Kaiser and B. L. Kaiser, Acc. Chem. Res., 1972, 5,219-224 (43). 1034. Spectroscopy and structure of pentacoordinated molecules. R. R . Holmes, Acc. Chem. Res., 1972, 5,296-303 (73). 1035. Superoxide radical and superoxide dismutase. I. Fridovich, Acc. Chern. Res., 1972,5,321-326 (60). 1036. Or anometallic electrochemistry. R . E. Dessy and L. A. Bares, Acc. Chem. Res., 1972, 5,415-421 (367. 1037. Stereochemical studies of metal carbonyl-phosphorus trifluoride complexes. R. J. Clark and M. A. Busch, Acc. Chem. Re.r. 1973, 6,246-252 (34). 1038. Iron-sulphur coordination compounds and proteins. S. J. Lippard, Acc. Chem. Res., 1973, 6, 282-288 (42). I

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1039. Transition metal atom inorganic syntheses in matrices. G . A. Ozin and A. Van der Voet, Acc. Chem. Res., 1972,6, 313-318 (44). 1040. The biochemical significance of porohvrin n-cation radicals. D. DolDhin and R. H. Felton. Acc. . Chem. Res., 1974,7,26-32 (71). 1041. Novel metalloporphyrins - syntheses and implications. D . Ostfeld and M. Tsutsii, Acc. Chem. Res., 1974,7,52-58 (75). 1042. On the interpretation of the optical spectra of hexahalogen complexes of 4d and 5d transition metal ions. P. C. Jordan, Acc. Chem. Res., 1974,7,202-208 (34). 1043. Relaxation of excited states in transition-metal complexes. M. K . DeArmond, Acc. Chem. Res., 1974,7,309-315 (39). 1044. Cobalt-59 N.Q.R. spectroscopy. T. L. Brown, Acc Chem. Res., 1974,7,40&415 (48). 1045. The coordination chemistry of nitric oxide. R . Eisenberg and C. D. Meyer, Acc. Chern. Res., 1975, 8,2&34 (56). 1046. Solid-state pressure effects on stereochemically nonrigid structures. J. R. Ferraro and G. J, Long, Acc. Chem. Res.. 1975,8, 171-179 (57). 1047. Spectroscopic investigations of excited states of transition metal complexes. G. A . Crosby, Acc. Chem. Res., 1975,8,231-238 (53). 1048. Role of the bridging ligand in inner-sphere electron transfer reactions. A. Haim, Acc. Chem. Res., 1975,8,264-272 (80). 1049. Mechanism of Cobalamin-dependent rearrangements. B . M. Babior, Acc. Chem. Res., 1975, 8 , 376-384 (35). 1050. Synthetic oxygen carriers of biological interest. F. Basolo, B. M. Hoffman and J. A . Ibers, Acc. Chem. Res., 1975, 8,384392 (7.5). 1051. Magnetism and magnetic transitions of transition metal compounds at low temperatures. R. L. Carlin, Acc. Chem. Res., 1976,9,67-74 (36). 1052. The vitamin B12coenzyme. R. H. Abeles and D. Dolphin, Acc. Chem. Res., 1976,9, 114-120 (57). 1053. Interpretation of potential constants: application to study of bonding forces in metal cyanide complexesand metal carbonyls. L. I-I. Joncs and B. I. Swanson, Acc. Chem. Res., 1976,9,128134 (27). 1054. Dioxygen metal complexes; towards a unified view. L. Vaska, Acc. Chem. Res., 1976, 9 , 175-183 .

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1055. Trinsition metal dialkyiamides and disilylamides. D. C. Bradley and M. H. Chisholm, Acc. Chern. Res.. 1976.9.273-280 (108). 1056. Trends in reactivity fo; ligand-exchange reactions of octahedral metal carbonyls. G. R. Dobson, Acc. Chem. Res., 1976,9.30&306 (48). 1057. Metal atom matrix chemistry. Correlation of bonding with chemisorbed molecules. G . A . Ozin, Acc. Chem. Res., 1977,10,21-26 (32). 1058. Chemical kinetics and mechanisms in solvent extraction of copper chelates. D. S. Flett, Acc. Chem. Res., 1977,10,99-104 (21). 1059. Stereoselectivity in the binding of transition metal chelate complexes to nucleic acid constituents: bonding and non-bonding effects. L. G. Marzilli and T. J . Kistenmacher, Acc. Chew. Res., 1977, 10. 146-152 (29). 1060. Synthetic m6dds for the oxygen-binding hemoproteins. J. P. Collman, Acc. Chem. Res., 1977, 10, 265-272 (107). 1061. Trends in metalloporphyrin stereochemistry. W. R. Scheidt, Acc. Chem. Res., 1977, 10, 339-345 (45). 1062. Transition metal thiocarbonyls and selenocarbonyb. I. S . Butler, Acc. Chem. Res., 1977, 10, 359-365 (73). 1063, Svnthetic approaches to the active sites of iron-subhur proteins. R. H. Holm. Acc. Chem. Res., 1977,10,427-434 (74). 1064. Mechanisms of oxidative addition of organic halides to group 8 transition metal complexes. J . K. Stille and K. S. Y . Lau, Acc. Chem. Res., 1977, 10,434442 (49). 1065. Complexes of cations in unstable oxidation states in aqueous solutions as studied by pulse radiolysis. D. Meyerstein, Acc. Chem. Res., 1978,11,43-48 (95). 1066. Cryptates: the chemistry of macropolycyclic inclusion complexes. J. M. Lehn, Acc. Chem. Res., 1978, 11,49-57 (82). 1067. Optical and thermal electron transfer in metal complexes. T. J. Meyer, Acc. Chem. Res., 1978, 11, 94-100 (47). 1068. Electrophilic behaviour of coordinated nitric oxide. F . Bottomley, Acc. Chem. Res., 1978, 11, 158-163 (64). 1069. Platinum complexes: probes of polynucleotide structure and antitumour drugs. S. J. Lippard, Acc. Chem. Res., 1978,11,211-217 (56). 1070. Discovering and understanding multiple metal to metal bonds. F. A. Cotton, Acc. Chem. Res., 1978, 11,225-232 (87). 1071. Electronic spectra and photochemistry of complexes containing uadruple metal-metal bonds. W. C. Trogler and H. B . Gray, Acc. Chem. Res., 1978,11~232-239143) 1072. Electronic spectra of metal-dioxygen complexes. A . B. P. Lever and H. B. Gray, Acc. Chem. Res., 1978,11,348-355 (67). 1073. Chemistry of compounds containing metal to metal triple bonds between molybdenum and tungsten. M. H. Chisholm and F. A. Cotton, Acc. Chem. Res., 1978, 11,356-362 (66). 1074. Coordination chemistry of organostibines. W. Levason and C. A, McAuliffe, Acc. Chern. Res., 1978, 11, 36S368 (61). 1075. Distinctive coordination chemistry and biological significance of complexes with macrocyclic ligands. D. H. Busch, Acc. Chem. Res., 1978,11,392-490 (61). coc 7

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Index of Review Articles und Specialist Texts

1076. Structure and stereochemistry in metalloboron cage compounds. R. N. Grimes, Acc. Chem. Res., 1978, 11,42W72 (58). 1077. The ligand polarisation model and the spectra of metal complexes. A complementation of the crystal field. S. F. Mason, Acc. Chem. Res., 1979,12,55-61(30). 1078. Structures of transition metal hydride complexes. R. Bau, R. G. Teller, S. W. Kirtley and T. F. Koetzle, Ace. Chem. Res., 1979, 12, 176-183 (63). 1079. Coordination chemistry and microbial iron transport. K. N. Raymond and C. J. Carrano, Acc. Chem. Res., 1979,12. 183-190 (45). 1080. Recent developments in the chemistry of some electronegative elements. K. Seppelt, Ace. Chem. Res., 1979,12,211-216 (63). 1081. New transparent ferromagnets. P. Day, Acc. Chem. Res., 1979,12,23&243 (59). 1082. Optical induction in organo-transition metal compounds and asymmetric catalysis. H. Brunner, Acc. Chem. Res., 1979.12,250-257 (85). 1083. Iridium compounds in catalysis. R. Crabtree, Acc. Chem. Res., 1979,12,331-338 (30). 1084. Role of activation volume in the elucidation of reaction mechanisms in octahedral coordination complexes. G. A. Lawrance and D. R. Stranks, Acc. Chem. Res., 1979, 12,403-409 (50). 1085. Photoinduced electron-transfer reactions of metal complexes in solution. D. G. Whitten, Am. Chem. Res., 1980, 13,83-90 (105). 1086. Alkylaminobis(difluorophosphines): novel bidentate ligands for stabilizing low metal oxidation states and metal-metal bonded systems. R. B. King, Acc. Chem. Res., 1980, 13,243-248 (41). 1087. A role for manganese in oxygen evolution in photosynthesis. K. Sauer, Acc. Chem. Res., 1980, 13, 249-256 (44). 1088. Citrate conformation and chelation: enzymatic implications. J. P . Glusker, Ace. Chem. Res., 1980, 13,345-352 (84). 1089. Spin-pairing model of dioxygen binding and its application to various transition metal systems as well as hemoglobin cooperativity. R. S. Drago and B. B. Corden, Acc. Chem. Res., 1980, 13, 353-360 (39). 1090. Chemical ap lications of extended X-ray absorption fine structure (EXAFS) spectroscopy. B. K. Teo, Acc. Cfem. Res., 1980, 13,412-419 (36). 1091. Synthesis, molecular dynamics and reactivity of mixed-metal clusters. G . L. Geoffroy, Acc. Chem. Res., 1980, 13,469-476 (29). 1092. Synthetic models for hemoproteins. T. G. Traylor, Acc. Chem. Res., 1981,14, 102-109 (70). 1093. Metalla-fi-diketones and their derivatives. C. M. Lukehart, Acc. Chem. Res., 1981, 14, 109-116 (43). 1094. Fe-M-S complexes derived from MS-: anions (M=Mo. W) and their possible relevance as analogues for structural features in the Mo site of nitrogenase. D. Coucouvanis, Acc. Chem. Res., 1981, 14,201-209 (57). 1095. Extended metal-metal bonding in halides of the early transition metals. Y. D. Corbett, Acc. Chern. Res., 1981,14,239-246 (48). 1096. HCO(CO)~, the quintessential catalyst. M. Orchin, Acc. Chcm. Res., 1981, 14,259-266 (54). 1097. Determination of structural and dynamic aspects of organometallic and coordination chemistry by phosphorus-31 n.rn.r. spectroscopy. D. W. Meek and T. J. Mazanec, Acc. Chem. Res., 1981, 14, 266-274 (69). 1098. Artificial Dhotosvnthesis: water cleavage into hydrogen and oxvgen by visible light. - M. GratzeI, Acc. Chem. Res.: 1981, 14,376-384 (541. 1099. Lanthanide ion luminescence probes of the structure of biological macromolecules. W. De W. Horrocks and D. R. Sudnick. Acc. Chem. Res., 1981.14.384-392 (871. 1100. Metalloid porphyrins and phthalocyanines. P. Sayer, M. Gouterman and C. R. Connell, Acc. Chem. Res., 1982,15,73-79 (69). 1101. Formation and stabilities of cobalt dioxygen complexes in aqueous solution. A. E. Martell, Aec. Chem. Res., 1982, IS, 155-162 (68). 1102. Acceleration of reactions by enzymes. W. N. Lipscomb, Acc. Chem. Res., 1982,15,232-238 (67). 1103. Nuclear, electronic and frequency factors in electron transfer reactions. N. Sutin, Acc. Chem. Res., 1982,15,275-282 (78). 1104. Chemistry of the imidazolate-bridged bimetallic centre in the Cu-Zn superoxide dismutase and its model compounds. K. G. Strothkarnp and S. J. Lippard, Acc. Chem. Res., 1982,15,318-326 (66). 1105. The Mossbauer effect and its significance in chemistry. E. Fluck, W. Kerler and W. Neuwirth, Angew. Chem., Int. Ed. Engl.. 1963,2,277-287 (25). 1106. Recent developments of metal silyls of the type M(SiR3),. E. Wiborg, 0. Strecher, H. J. Andrasheck, L. Kreuzbichler and E. Staude, Angew. Chem., Int. Ed. Engl., 1963,2,507-515 (24). 1107. New chemical and biochemical developments in the vitamin BI2field. K. Bernhauer, 0. Muller and F. Wagner, Angew. Chem., Int. Ed. Engl., 1964,3,200-211 (133). 1108. Structure and specificity of organic chelating agents. E. Bayer, Angew. Chem., Int. Ed. Engl., 1964, 3,325-332 (36). 1109. Complexes of tetradentate ligands containing phosphorus and arsenic. L. M. Venanzi, Angew. Chem., Int. Ed. E @ . , 1964,3,453-460 (27). 1110. Photochemical substitutions on metal carbonyls and their derivatives. W. Strohmeier, Angew. Chem., Int. Ed. Engl., 1964,3,73&737 (68). 1111. Reactions of metal acetylacetonates. J. P. Collman, Angew. Chern., Int. Ed. Engl., 1965,4132-138 (31). 1112. Exchange rates of ligands in complex ions. R. G. Pearson and M. M. Anderson, Angew. Chem., Inl. Ed. Engl., 1965,4,281-287 (27). -

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1113. Colour centres in alkali borate glasses containing cobalt, nickel and copper. R. Juza, H. Seidel and J. Tiedemann, Angew. Chem., Int. Ed. Engl., 1966,5,85-94 (44). 1114. Problems of iron metabolism with special reference to biochemical, physiological and clinical aspects. W. Keiderling and H. P. Wetzel, Angew. Chem., Int. Ed. Engl., 1966,5,633-641(82). 1115. Some recent developments in the chemistry of transition metal oxo-cations. J. Selbin, Angew. Chem., Inr. Ed. Engl., 1966,5,712-722 (184). 1116. Trifluoro hosphine complexes of transition metals. T. Kruck, Angew. Chem., Int. Ed. Engl., 1967, 6.53-67 /&I). 1117. Hieher coorhination numbers of the twical elements. R. F. Hudson. Annew. Chem., h t . Ed. E n d . 196y7,6,749-756 (57). 1118. Siloxane compounds of the transition metals. F. Schindler and H. Schmidbaur, Angew. Chem., Znt. Ed. End.. 1967.6.683-694 (149). 1119. The co"ncept of hard and 'soft'acids and bases as applied to multicentre chemical reactions. B. Saville, Angew. Chem., rut. Ed. Engl., 1967,6,92%939 (84). 1120. Dodecacarbonyltriruthenium. M . I. Bruce and F. G. A. Stone, Angew. Chem., Int. Ed. Engl., 1968,7,427-432 (74). 1121. Kinetic studies on substitution reactions of carbonyl metal complexes. H . Werner, Angew. Chem., Int. Ed. Engl., 1968,7,93@941 (106). 1122. Planar complexes containing metal-metal bonds. K . Krogmann, Angew. Chem., Znt. Ed. Engl., 1969,8,35-42 (50). 1123. Catalase and peroxidase activity of Cu2+ complexes. H. Sigel, Angew. Chem., Znt. Ed. Engl., 1969, 8, 167-177 (97). 1124. Non-enzymatic activation of molecular nitrogen. G. Henrici-Olive and S . Olive, Angew. Chem., Znt. Ed. Engl., 1969,8,650-654 (47). m e ,. Anaew. Chem., Int. Ed. End.. 1125. The coordination number - an 'inorganic chameleon'. R. H o.. 1970,9,25-34 (25). 1126. Magnetic resonance of paramagnetic com lexes. H. J. Keller and K. E. Schwarzhaus, Angew. Chem.. Int. Ed. End.. 1970.9. 196205 (677. 1127. Metal-boron comp&ds --'problems and perspectives. G. Schmid, Angew. Chem., Znt. Ed. Engl., 1970,9,819-830 (89). 1128. The ionisation (heterolysis) of covalent compounds as a coordination chemical phenomenon. V . Gutmann, Angew. Chem., Znt. Ed. Engl., 1970,9,843-860 (116). 1129. Bond character of @diketone metal chelates. B. Bock, K. Flatau, H. Junge, M. Kuhr and H. Muses,Angew. Chem., Int. Ed. Engl., 1971, 10,225-235 (114). 1130. Optical activity from asymmetric transition metal atoms. H. Brunner, Angew. Chem., Int. Ed. Engl., 1971, 10,249-250 (88). 1131. Subhinato comulexes. G. Vitzhum and E. Lindner. Annew. Chem.. Znt. Ed. End., 1971,. 10,. 313-326 (128). * 1132. The present position of hemoglobin research. G. Buse, Angew. Chem., Int. Ed. Engl., 1971, 10, 663-673 173). 1133. Active t r h i p o r t of Na' and K+ through animal cell membranes. W. Schoner, Angew. Chem., Znf. Ed. Engl., 1971,10, 882-889 (175). 1134. Application of ligand field spectroscopy to problems of chemical bonding in solids. D . Reinen, Angew. Chem., Znt. Ed. Engl., 1971,10,901-909 (30). 1135. Macrocvclic Dolvethers and their comulexes. C. J. Pedersen and H. K. Frendsdorf, Angew. Chem., Int. Ed.>Engi.,i972, 11,1625 (45). 1136. Metal ion function in carbonic anhydrase. R. H. Prince and P. R. Woolley, Angew. Chem., Int. Ed. E n d . . 1972. 11.408417 (58). 1137. G e k t i c as 'ects of hemoglobin synthesis. B. Schmidt, Angew. Chem., Int. Ed. Engl., 1972, 11, 576-583 ( 6 5 . 1138. Decomposition of organometallic complexes in the mass spectrometer. J. Milller, Angew. Chem., Int, Ed, Engl., 1972, 11,653465 (112). 1.139. Metal isotope effects on metal-ligand vibrations. K. Nakarnoto, Angew. Chem., Int. Ed. Engl., 1972,11,666-674 (37). 1140. Shift reagents in n.m.r. s ectroscopy. R. von Amrnon and R. D. Fischer, Angew. Chem., Int. Ed. Engl., 1972, 11,675-692 f169) 1141. Enzymatic hydroxylations with molecular oxygen. V. Ullrich, Angew. Chem., Int. Ed. Engl., 1972, 11,701-712 (134). 1142. The loose connection between electron configuration and the chemical behaviour of the heavy elements (transuranics). C . K. Jorgensen, Angew. Chem., Znt. Ed. Engl., 1973,12, 12-19 (73). 1143. Structure and function of ferritin. R. R. Crichton, Angew. Chem., Znt. Ed. Engl., 1973, 12, 57-65 (90). 1144. Iron-sulphur proteins: structural chemistry of their chromophores and related systems. R. Mason and J. A. Zubieta, Angew. Chem., Int. Ed. Engl., 1973, 12,390-399 (101). 1145. Activation of molecular oxygen. G. Henrici-Olive and S. Olive, Angew. Chem., Int. Ed. Engl., 1974,13,29-38 (74). 1146. Electronic transitions in transition metal compounds at high pressure, H. G. Drickamer, Angew. Chem., Int. Ed. Engl., 1974, 13,3947 (34). 1147. The reactivit of the porphyrin ligand. J. H. Fuhrhop, Angew. Chem., Int. Ed. Engl., 1974, 13, 321-335 (1037. 1148 Dinitrogen-transition metal complexes: synthesis, properties and significance. D. Sellmann, Angew. Chem., Znt. Ed. E&., 1974,13,639-649 (86).

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Index of Review Articles and Speciulisl Texts

1149. Isolation and reaction of metal atoms in matrices. G. C. Pimente.1,Angew. Chenz., Int. E d . E n d . . 1975,14,199-206 (73). 1150. Transition metal atoms in the synthesis of binuclear complexes. E. P. Kundig, M. Moskvits and G . A. Ozin. Anaew. Chem.. Int. Ed. Enal.. 1975. 14.292-303 (46). 1151. Spectral evidenck for lanth&oid and accnoid carbonyl compokds. R.K. Sheline and J. L. Slater, Angew. Chem., Int. Ed. E@., 1975,14,309-313 (20). 1152. The flipping of CO ligand groups in metal carbonyl compounds and its frequency in Fe(CO)5. R . K . Sheline and H. Mahnke, Angew. Chem., Int. Ed. Engl., 1975, 14,314-321 (25). 1253. Sulphur atoms as ligands in metal complexes. H. Vahrcnkamp, Angew. Chem., Int. Ed. Engl., 1975,14,322-329 (121). 1154. Ternary Cu2+ complexes: stability, structure and rcactivity. H. Sigel, Angew. Chem., h t . Ed. Engl., 1975, 14, 39+402 (86). 1155. Non-enzymatic simulation of nitrogenase reactions and the mechanism of biological nitrogen fixation. G. N. Schrauzer, Angew. Chem., Int. Ed. Engl., 1975, 14,514-522 (36). 1156. New developments in the field of vitamin B12: reactions of the cobalt atom in corrins and vitamin BIZ model compounds. G. N.Schrauzer, Angew. Chem., Int. Ed. Engl., 1976,15,417-426 (67). 1157. Molecular complexes and oxygen adducts of tetrapyrrole pigments. J. H. Fuhrhop, Angew. Chem., Int. Ed. Engl., 1976, 15.648-659 (76). 1158. Gaseous chloride complexes with halogen bridges - homo-complexes and hetero-complexes. H. Schafer, Angew. Chem., Znt. Ed. Engl., 1976, 15,713-727 (167). 1159. Cyclometalation reactions. M. I. Bruce, Angew. Chem.. In[. Ed. Engl., 1977, 16,73-86 (157). 1160. New developments in the field of vitamin BI2: enzymatic reactions dependent u on corrins and coenzyme BI2, G. N. Schrauzer, Angew. Chem., Int. Ed. Engl., 1977.16,233-244 69). 1161. Synthetic and mechanistic aspects of inorganic insertion reactions. Insertion of carbon monoxide. F. Calderazzo,Angew. Chem., Int. Ed. Engl., 1977, 16,299-311 (121). 1162. Oxometallates with planar coordination. H. Muller-Buschbaum, Artgew. Chem., Int. Ed. Engl., 1977,16,674-687 (73). 1163. The versatility of tertiary phosphane ligands in coordination and organometallic chemistry. R. Mason and D. W. Meek,Angew. Chem., Int. Ed. Engl., 1978,17,183-194 (138). 1164. Sodium-23 n.m.r. spectroscopy. P. Laszlo, Angew. Chem., hnt. Ed. E@., 1978,17,254-266 (225). 1165. Tetrahedral carbonylcobalt clusters. G. Schmid, Angew. Chem., Int. Ed. Engl., 1978, 17. 392400 (42). 1166. The distribution of charge in complex compounds. J. Chatt and G. J. Leigh, Angew. Chem., Int. Ed. Engl., 1978,17,400-407 (59). 1167. Hemoglobin - an inspiration for research in coordination chemistry. J. W. Buchler. Angew. Chem., Int. Ed. Engl.; 1978,17,407423 (127). 1168. A coordination chemist’s view of surface science. E. L. Muetterties. Angew. Chem., Ina. Ed. Engl., 1978,17,545-558 (60). 1169. Polarised low-temperature crystal spectra of inorganic complexes. P. Day, Angew. Chern., Int. Ed. Enal.. 1980. 19.29C301 (361. 1170. Trhethylphosphaw coiplexes of nickel, cobalt and irun - model compounds for homogeneous catalysis. H. F. Klein, Angew. Chem., Int. Ed. Engl., 1980, 19,362-375 (108). 1171. Trinuclear clusters of the early transition elements. A. Muller, R. Jostes and F. A. Cotton, Altgew. Chem., Int. Ed. Engl., 1980,19,875-882 (57). 1172. Condensed metal clusters. A . Simon, Angew. Chem., Int. Ed. Engl., 1981,20, 1-22 (225)1173. Recent progress in oxo- and fluoro-metalate chemistry. R. Hoppe, Angew. Chem., Int. Ed. Engl., 1981,20,63-87 (223). 1174. The transition metal-nitrogen multiple bond. K. Dehnicke and J . Strahle, Angew. Chem., Znt. Ed. Engl., 1981,20,413-426 (124). 1175. Transition metal thiometalates: properties and significance in complex and bioinorganic chemistry. A. Muller, E. Diemann! R. Jostes and H. Bogge, Angew. Chem., Int. Ed. EngI., 1981,20,934-955 (227). 1176. ETC: a mechanistic concept for inorganic and organic chemistry. M. Cahnon and M. L. Tobe, Angew. Chern., Int. Ed. Enggl., 1982,21, 1-23 (311). 1177. Transition metal complexes with cyclo-triphosphorus (q3-F3) and tetrahedro-tetraphosphorus (q’-P4)ligands. M. Di Vaira and L. Sacconi, Angew. Chern., Inr. Ed. Engl., 1982,21,33&342 (41)). 1178. Building bridges between inorganic and organic chemistry (Nobel lecture). R. Hoffmann, Angew. Chem., Int. Ed. Engl., 1982,21,711-724 (42). 1179. Oxygen transfer from inorganic and organic peroxides to organic substrates: a common mechanism. H. Mimoun, Angew. Chem., Int. Ed. Engl., 1982,21,734-750 (145). 1180. Stabilisation of unusual oxidation and coordination states by the ligands OSF5, OSeFs and OTeFj. K. Seppelt, Angew. Chem., Int. Ed. Engl., 1982, 21,877-888 (138). 1181. The chemistry of uranium fluorides. I. V. Tananaev, N . S . Nikolaev, Y . A. Luk’yanychev and A. A . Opalovskii, Russ. Chern. Rev. (Engl. Transl.), 1961,30, 654671 (175). 1182. Polymeric coordination compounds. 1. Haiduc, Russ, Chem. Rev. (Engl, Transl.), 1961,30,498-526 (483). 1183. The present state and future development of coordination chemistry. A. A. Grinberg, Russ. Uhem. Rev. (Engl. Trmsl.), 1%1,30,334-338 (64). 1184. Sodium nitroprusside and its use in analysis. V. N. Bernshtein and V . G. Belikov, Russ. Chern. Rev. (Engl. Transl.), 1961,30, 227-236 (297). 1185. Technetium. A. N. Murin, V. D. Nefedov, Y. A. Ryukhin and M. A. Toropova, Russ. Chem. Rev. (Engl. Transl.), 1961,30,107-115 (85). i

Index of Review Articles and Speciaht Texts

57

“emistry of the metal carbonyls. J. S. Anderson, Q. Rev., Chem. SOC., 1947,1,331-357 (98). Clhemistry of the transuranic elements. M. W. Lister. Q. Rev., Chem. SOC.,1950,4,20-44 (91). The stabilities of complex compounds. A. R. Burkin. Q. Rev., Chem. SOC.,1951,5,1-21(40). 1Magnetism and inorganic chemistry. R. S. Nyholm, Q. Rev., Chem. SOC.,1953,7,377-406(138). The chemistry of the nitrosyl group (NO). C. C. Addison and J. Lewis, Q. Rev., Chem. Soc., 1955, 9 , 115-149 (166). 1191. Reactions in some non-aqueous ionising solvents. V. Gutmann, Q. Rev., Chem. SOC., 1956, 10, 151462 (135). 1192. Ligand field theory. J. S. Griffith and L. E. Orgel, Q. Rev., Chem. SOC., 1958,11,381-393 (41). 1193. [norganic stereochemistry. R . J. Gillespie and R. S. Nyholm, Q. Rev., Chem. SOC., 1958. 11, 339-380 (39). 1194. The chemistry of polonium. K. W. Bagnall, Q. Krv., Chem. Soc., 1957,11,3&48 (79). 1195. Liquid-li uid extraction in inorganic chemistry. F. S. Martin and R. J. W. Holt, Q. R e v . , Chem. SOC.,1953, 13,327-352 ( 7 2 ) 1196. An outline of rhenium chemktry. A. A. Woolf, Q. Rev., Chem. Soc., 1961,15,372-391 (94). 1197. Mechanisms of electron transfer and related processes in solution. J. Halpern, Q. Rev., Chem. Soc., 1961,15,207-236 (91). 1198. Kinetics and mechanism of replacement reactions of coordination compounds. R. G. Wilkins, Q. Rev., Chem. SOC.,1962.16,316-342 (141). 1199. An outline of technetium chemistry. R. Colton and R. D. Peacock, Q. Rev., Chem. Soc., 1962,16, 299-315 (117). 1200. Halogen cations. J. Arotsky and M. C. R. Symons, Q. Rev., Chem. SOC.,1962,16,282-297 (44). 1201. Cyanide complexes of thc transition mctals. W. P. Griffith, Q. Rev., Chem. SOC., 1962, 16, 18R207 (106). 1202 Inorganic reactions in liquid ammonia. G. W. A. Fowles and D. Nicholls, Q. Rev,, Chem. SOC., 1962,16, 1 9 4 3 (92). 1203. Protactinium. D. Brown and A. G. Maddock, Q. Rev., Chem. Soc., 1963,17,289-341(303). 1204. The metal carbonyls. E. W. Abel, Q. Rev., Chem. Soc., 1963,17,133-159 (144). 1205. Inorganic nitrates and nitrato-compounds. B. 0. Field and C. J. Hardy, Q. Rev., Chem. SOC.,1964, 18,361-388 (95). 1206. Semiconductivity of the phthalocyanines. C. J. Hoffman, Q. Rev., Chem. SOC., 1964, 18, 113-121 (22). 1207. Metal complexes of ligands containing sulphur, selenium or tellurium as donor atoms. S. E. Livingstone, Q. Rev., Chem. Soc., 1965, 19,386425 (303). 1208. Osmium and its compounds. W. P. Griffith, Q. Rev., Chem. Soc., 1965,19,254-273 (111). 1209. The reactions of metal halides with alkyl cyanides. R. A. Walton, Q. Rev., Chem. SOC., 1965, 19, 126-143 (128). 1210. The study of complexed metal ions by polarographic methods. D. R. Crow and J . V. Westwood, Q. Rev., Chern. Sac., 1965,19.57-76 (75). 1211. Transition metal compounds containing clusters of metal atoms. F. A. Cotton, Q. R e v . , Chem. Soc., 1966,20,38%401 (43). 1212. Penta-coordination. E. L. Muettertie4 and R. A. Schunn, Q. Rev., Chem. SOC., 1966,20, 245299 (316). 1213. Oxo-species of molybdenum(V) and (VI). P. C. H. Mitchell, Q. Rev., Chem. SOC., 1966, 20, 103-118 (72). 1214. Photochemical behaviour of transition metal complexes. E. L. Wehry, Q. Rev., Chem. Soc., 1967, 21,213-230 (45). 1215. Molecular polyhedra of high coordination number. E. L. Muetterties and C. M. Wright, Q . Rev., Chem. Soc., 1967,21,109-194 (404). 1216. Isopoly-vanadates, -niobates and -tantalates. M. T. Pope and B. W. Dale, Q. Rev., Chem. Suc., 1968,22,527-548 (65). 1217. Iron, cobalt and nickel Complexes having anomalous magnetic moments. E. K. Barefield, D. H. Busch and S. M. Nelson, Q.Rev., Chem. Soc., 1968,22,457498 (134). 1218. Mass s ectra of organometallic compounds. D.B. Chambers, F. Glockling and J. C. R. Light, Q. Rev., 8hem. Soc., 1968,22,317-337 (51). 1239. Some recent studies in the thermodynamics of metal complex formation. G. Geech, Q. Rev., Chem. SOC.,1969,23,41&429 (56). 1220. The chemistry of transition metal carbonyls: structural considerations. E. W. Abel and F. G. A. Stone, Q. Rev., Chem. SOC., 1969,23,325-371(209). 1221. Kinetics and mechanism of metal ion complex formation in solution. A. McAnley and J. Hill, Q. Rev., Chem. SOC.,1969,23,18-36 (113). 1222 The reactions of hydrazine with transition metal complexes. F. Bottomley, Q. Rev., Chem. SOC.. 1970,24,617-638 (132). 1223. The chemistry of transition metal carbonyls: synthesis and reactivity. E. W. Abel and F. G. A. Stone, Q. Rev., Chem. SOC.,1970,24,498-552 (360). 1224. The biochemistry ofsodium, potassium, magnesium and calcium. R. J. P. Williams, Q . Rev., Chem. SOC.,1970,24,331-365 (50). 1225. The coordination of ambidentate ligands. A. H. Norbury and A. 1. P. Sinha, Q. Rev., Chem. Soc., 1970,24,69-94 (218). 1226. Transition metal complexes of some perfluoro-ligands. R . S. Nyholm, Q. Rev., Chem. Suc., 1970, 24,l-19 (33). 1227. Use of N-benzoyl-N-phenylhydroxylaminein analytical chemistry. I. P. Alimann, F. P. Sudakov and B. G. Golovkin, Russ. Chem. Rev. (Engl. Transl.), 1962,31,466-474 (47).

1186. 1187. 1188. 1189. 1190.

I

58

Index of Review Articles and Specialist Texts

1228. The chemistry of aqueous solutions of zirconium salts (does the zirconyl ion exist?). A. S. Solovkin and S.V. Tsvetkova, Russ. Chem. Rev. (Engl. Transl.), 1962,31,655-669 (161). 1229. Metal complexes of hydroxy-acids. I. V. Pyatnitskii, Russ. Chem. Rev. (Engl. Transl.), 1963,32, 44-58 (278). 1230. Chelate polymers. V. V. Rode, E. G. Rukhadze and A. P. Terent’ev. Russ. Chem. Rev. (Engl. Transl.), 1963,32,66&-682 (162). 1231. New aspects of the chemistry of complexes of selenium and tellurium. D. I. Ryabchikov and 1. I. Nazarenko, Russ. Chem. Rev. (Engl. Transl.), 1964,33,55-64 (145). 1232. Halides of rare earth eIements in a lower state of oxidation. G. I. Novikov and 0. G. Polyachenok, Russ. Chem. Rev. (Engl. Transl.), 1964,33,342-350 (86). 1233. Complex compounds of germanium and its state of oxidation. V. A. Nazarenko and A. M. Andrianov, Russ. Chem. Rev. (Engl. Transl.), 1965,34,547-558 (259). 1234, Metal selenocyanates and their properties. A. M. Golub and V. V. Skopenko, Rwls. Chem. Rev. (Engl. Transl.), 1965,34,901-908 (95). 1235, Outer-sphere interaction in aqueous solutions of complex compounds. V. E. Mironov, Russ. Chem. Rev. (Engl. Transl.), 1966,35,455-469 (123). 1236. 0 tically active chelate compounds. G. V. Panova, E. G. Rukhadze and A. P. Terent’ev, Russ. Clem. Rev. (Engl. Transl.), 1966,35,687-695 (134). 1237. Alkali metal fluorohalogenates. A. A. Opalovskii, Russ. Chem. Rev. (Engl. Transl.), 1967. 36, 71 1-725 (154). 1238. The chemistry of manganese carbonyl. K. N. Anisimov, A . A. Ioganson and N. E. Kilobova, Russ. Chem. Rev. (Engl. Transl.), 1968,37,184-197 (229). 1239. Catalysis and coordination interaction. M. I. Siling and A . I. Gel’bshtein, Russ. Chem. Rev. (EngI. Transl.), 1969,38,24%260 (210). 1240. Complexes of molecular nitrogen. Y. G . Borod’kov and A . E. Shilov, Russ. Chem. Rev. (Engi. Transl.), 1969,38,355-374 (121). 1241. Types of reactions undergone by coordinated ligands and the factors influencing the change in their reactivity. Y. N. Kukushkin, Russ.Chem. Rev. (Engl. Transl.), 1970,39,169-178 (93). 1242. Outer sphere corn [exes of tervalent cobalt. V. E. Mironov, RWS. Chem. Rev. (Engl. Transl.), 1970,39,319-333 532) 1243. Metal-metal bonds andcovalent atomic radii of transition metals in their m-complexes and polynuclear carbonyls. B . P. Biryukov and Y. T. Struchkov, Russ. Chem. Rev. (Engl. Transl.), 1970, 39, 789-798 (56). 1244. Synthesis and chemical reactions of metal-containing macromolecules. S. L. Davydova, N. A. Plate and V. A. Kargin, Run. Chem. Rev. (Engl. Transl.), 1970.39, 1082-1098 (111). 1245. Factors determining the optical activity of coordination compounds. V . V. Dunina, E. G. Rukhadze and A. P. Terent’ev, Russ. Chem. Rev. (Engl. Transl.), 1971.40,551-562 (124). 1246. The principle of hard and soft acids and bases and the problem of competitive coordination in complex compounds. A . D. GarnovskiI, D. A. Osipov and S. B. Bulgarevich, Rum. Chem. Rev. (Engl. Transl.), 1972,41,341-359 (441). 1247. Metallopolymers. E . M. Natanson and M. T. Bryk, Rws. Chem. Rev. (Engl. Trans/.), 1942, 41, 671686 (175). 1248. Some applications of the optical activity of coordination compounds. V. V. Dunina, E. G. Rukhadze and A. P. Terent’ev, Russ. Chem. Rev. (Engl. Transl.), 1972,41,862-877 (225). 1249. Oxygen compounds of iron (VI, V, IV). I. G. Kokarovtseva, I. N. Belyaev and L. V. Semenyakov, Russ. Chem. Rev. (Engl. Transl.), 1972,41,929-937 (108). 1250. Analytical chemistry of metal complexes with nitrogen-containing ligands of the 2,2’-bipyridyl ty . A. T. Pilipenko and E. R. Falendysh, Russ. Chem. Rev. (Engl. Transl.), 1972,41,991-1008 (249y 1251. Covalent tetrahydroborates. K. N. Semenenko, 0. V. Kravchenko and V. B. Polyakova, Russ. Chem. Rev. (Engl. Truplsl.), 1973,42,1-13 (114). 1252. Advances in the coordination chemistry of azoles. A. D. Garnovskii, 0. A. Osi ov, L. I. Kuznet!(S.) sova and N. N. Bogdashev, Rws. Chem. Rev. (Engl. Transl.), 1973,42,89-110 O 1253. The use of p.m.r. in the study of complexones. N. A. Kostromina, Russ. Chent. Rev. (Enagl. Transl.), 1973,42,261-277 (99). 1254. Polarographic catalytic currents of complexes of metals in catalysis by a ligand. Y. I. Tur’yan, Rms. Chem. Rev. (Engl. Traml.), 1973,42,427437 (168). 1255. Polarographic behaviour of cobait(II), nickel(I1) and iron(I1). V. N. Pavlov and V. V. Bondar, Russ. Chem. Rev. (Engl. Trmsl.), 1973,42,438-451 (93). 1256. Double molybdates and tungstates of the rare earth and alkali metals. A. A. Maier, M. V. Provotorov and V. A. Balashov, Russ. Chem. Rev. (Engl. Transl.), 1973,42,822-833 (82). 1257. Paramagnetic shift reagents in n.m.r. spectroscopy. I. Y.Slonim and A. K. Bulai, Russ. Chem. Rev. (Engl. Transl.), 1973,42,904-921(348). 1258. Structure and behaviour of aluminate ions in solution. N. I. Eremin, Y. A. Volokhov and V. E. Mironov, Russ. Chem. Rev. (Engl. Transl.), 1974,43,92-106 (154). 1259. Parama etic reagents for the investigation of the structures of organic ligands. V. K. Vornov, Russ. C f k . Rev. (Engl. Transl.), 1974,43,171-183 (109). 1260. Fixation of nitrogen in solution in the presence of transition meta1 complexes. A. E. Shilov, Russ. Chem. Rev. (Engl. Traml.), 1974,43,37&398 (161). 1261. Metallocarboranes. L. I. Zakharkin and V. N. Kalinin, Russ. Chem. Rev. (Engl. Transl.), 1974,43, 551-573 (142). 1262. Enantioselective effects in coordination compounds. V. A. Davankov, A. A. Kurganov and S. V. Rogozhin, Russ. Chem. Rev. (Engl. Transl.), 1974,43,764-780 (307).

~

lndex of Review Articles and Specialist Texts

59

1263. Mutual influence of li ands in complexes. Y . N. Kukushkin, Russ. Chem. Rev. (Ens!. Transl.), 1974,43,804-820 (166f 1264. Application of the n.m.r. method in the study of simple and complex hydrides of light metals. G. N. Boiko, Y. I. Malov and K. N. Semenenko, Russ. Chem. Rev. (Engl. Transl.), 1975,44, 1-8 (101). 1265. Energy transfer between organic molecules and transition metal ions. V. L. Ermolaev, E. G. Sveshnikova and T. A. Shakhverdov, Russ. Chem. Rev. (Engl. Transl.), 1975,44,26-40 (110). 1266. Activation of molecular oxygen on interaction with transition metal complexes. A. V. Savitskii and V. I. Nelyubin, Russ. Chem. Rev. (Engl. Trunsl.), 1975,44, 110-121 (124). 1267. Mono-oxygenase enzymes and their simulation. A. A. Akhrem, D. I. Metelitsa and M. E. Sknrko, Russ. Chem. Rev. (Engl. Transl.), 1975,44,398-412 (193). 1268. Coordination polymers with inorganic main chains. S. V. Vinogradova and 0. V. Vinogradova Rum. Chem. Rev. (Engl. Transl.), 1975,44,510-521 (125). 1269. Applications of heteroligand complexes in the analytical chemistr of niobium and tantalum. S. V. Elinson, Russ. Chem. Rev. (Engl. Transl.), 1975,44,707-717 (1313. 1270. The solvation of inorganic substances and complex formation in non-aqueous solutions. A. M. Golub, Russ. Chem. Rev. (Engl. Transl.), 1976,45,479-500 (358). 1271. Intramolecular coordination in organic derivatives of non-transition elements. A. K. Prokof ev, Russ. Chem. Rev. (Engl. Transl.), 1976,45,519-543 (331). 1272. Methods of synthesis of aminopolyacetic acids. V. G. Yashunskii and 0. I. Samoilova. Russ. Chern. Rev. (Engl. Transl.), 1976,45,777-791 (203). 1273. Dithiocarboxylic acids, their esters and metal dithiocarboxylates. E. Jansons, Russ. Chem. Rev. (En 1. Transl.), 1976,45,1035-1051 (350). 1274. Niogates and tantalates of tervalent elements. A. M. Sych and A. M. Golub, Russ. Chem. Rev. (Engl. Transl.), 1977,46,210-225 (147). 1275. Gas chromatographic analysis of metals as volatile chelates. D. N. Sokolov, Russ. Chem. Rev. (Engl. Transl.), 1977,46,38&393 (78). 1276. Reactions of organic compounds with higher fluorides off- and d-elements of groups V and VI. V. T. Orekhov, Rms. Chem. Rev. (Engl. Transl.), 1977,46,42@435 (169). 1277. Present state of the chemistry of rhenium. V. I. Spitsyn, A. F. Kuzina and A. A. Oblova, Russ. Chem. Rev. (Engl. Trunsl.), 1977,46, 1030-1039 (129). 1278. Some aspects of the coordination chemistry of the lanthanides. V. T. Panyushkin, Y. A. Afanas’ev, A. D. Garnovskii and O.A. Osipov, Russ. Chem. Rev. (Engl. Trunsl.), 1977,46,1109-1131(484). 1279. The interaction of carbon dioxide with transition metal complexes. I. S. Kolomnikov and M. K. Grinorvan. Russ. Chem. Rev. ( E n d . Transl.). 1978.47.334-353 (306). 1280. ‘ i e h i o n s of transition metalgin the atomic state.’G. A . Domrachev and V. D. Zinov’ev, Russ. Chem. Rev. (Engl. Transl.), 1978,47,354-367 (100). 1281. Dinuclear iron carbonyl complexes with nitrogen containing bridges. A. N. Nesmeyanov, M. I. Rybinskaya and L. V. Rybin, Russ. Chem. Rev. (Engl. Transl.), 1979,48,213-227 (123). 1282. Electrochemistry of metal chelates in non-aqueous media. G . K. Budnikov and T. V. Troepo1’skaya, Russ. Chern. Rev. (Engl. Transl.), ‘1979,48,449-462 (100). 1283. Extraction of heteropol compounds and its ap lication in inorganic analysis. E. N. Dorokhova and I. P. Alimaria, Rws. Clem. Rev. (Engl. Transfi, 1979,48,502-516 (211). 1284. Dinuclear and polynuclear complexes with azomethine ligands and their magnetic properties. V. A . Kogan, V. V . Zelentsov, 0.A. Osipov and A. S . BUT~OV, Russ. Chem. Rev. (Engl. Transl.), 1979, 48,645-656 (112). 1285. Hydroxamic acids and their metal complexes. Y. K. Agrawal, Russ. Chem. Rev. (Engl. Transl.), 1979,48,94%963 (123). 1286. The basicity of transition metal complexes in reactions with aprotic acids. B. V. Lokshin, A. G . Ginzburg and E. B. Nazarova, Russ. Chem. Rev. (Engl. Transl.), 1980,49,115-130 (136). 1287. Cobalt complexes of carboranes. E. V. Leonova: R u n . Chem. Rev. (Engl. Transl.), 1980, 49, 147-171 (229). 1288. Outer-sphere interactions in solutions of labile complexes. Y. A. Makashev and V. E. Mironov, Russ. Chem, Rev. (Engl. Transl.), 1Y80, 49, 631-644 (203). 1289. Stereochemistry of four coordinate chelate compounds of Schiff bases and their analogues. G. V. Panova, N . K. Vikulova and V. M. Potapov, Russ. Chew. Rev. (Engl. Trunsl.), 1Y80,49, 655467 (188). 1290. Possible approaches to the development of photo-catalytic solar energy converters. K. I. Zamaraev and V. N. Parmon, Russ. Chem. Rev. (Engl. Transl.), 1980,49,695-717 (408). 1291. Electrocatalysis on metalloporphyrins. M. R. Tarasevich and K , A. Radyushkina, Russ. Chem. Rev. (Engl. Transl.j, 1980,49,718-730 (132). 1292. Rhenium fluorides. E. G. Rakov, A. S. Dudin and A. A. Opalovskii, Russ. Chern. Rev. (Engl. Trunsl.), 1980,49,95&967 (152). 1293. The spectra and structure of transition metal complexes with tetradentate macrocyclic ligands. K. B. Yatsimirskii and Y. D. Lampeka, Russ. Chem. Rev. (Engl. Trunsl.), 1980,49,1003-1020 (191). 1294. Heptavalent bromine compounds. V. V. Gavrilov and V. K. Isupov, Russ. Chem. Rev. (Engl. Trunsl.), 1980,49,104+1055 (80). 1295. The formation, structure and pro erties of extracomplexes of or hyrins B D. Berezin and 0. I. Koifman, RLLSS. Chern. Rev. (En& Transl.), 1980,49, 1188-12!3 (245). . . 1296. The chemistry of anti-tumour platinum complexes. A. I. Stetsenko, M. A. Presnov and A. L. Konovalova, Rum. Chem. Rev. (Engl. Transl.), 1981,50,35%367 (131). 1297. Metallotropic tautomeric transformations of the o,o type in organometallic and complex com-

pounds. L. A. Fedorov, D. N. Kravtsov and A. S. Peregudov, Russ. Chem. Rev. (Engl. Transl.), 1981,50,682-700 (221).

60

Index of Review Articles and Specialist Texts

1298. Cytochrome P-450 - an effective catalyst of the oxidation of organic compounds by peroxides. D. I. Metelitsa, Russ. Chem. Rev. (Engl. Transl.), 1981,50,1058-1073 (147). 1299. Metal ’ ‘ ual and unstable states of oxidation and the steps of electrochemical reactions. B. G. s. Chem. Rev. (Engl. Transl.), 1981,50,1119-1133 (162). tes. V. V. Skopenko, G. V. Tsintsadze and E. 1. Ivanova, Russ. Chem. Rev. 1300. Metal (Engl. Transl.), 1982,51,21-30 (156). 1301. The oxidation-reduction reactions of gold complexes. V. P. Dyadchenko, Russ. Chem. Rev. (Engl. Trunsl.), 1982,51,265-271 (66). 1302. Monometal hydrido-corn lexes of transition metals. G. L. Soloveichik and B. M. Bulychev, Russ. Chem. Rev. (Engl. Tram/?),1982.51.286302 (160). 1303. The interaction of metals with proteins. M. G. Bezrukov, A. M. Belousova and V. A. Sergeev, Russ. Chem. RPV.(Engl. Traml.), 1982,51,397406 (132). 1304. The unpaired electron in transition metal complexes. E. R. Milaeva, A. 2. Rubezhov, A . I. Prokofev and 0. Y. Okhlobystin, R u s ~Chem. Rev. (Engl. Trunsl.), 1982,51,942-960 (201). 1305. Activation of oxygen by cytochrome P-450 and other hemoproteins. D. I. Metelitsa, Rum. Chem. Rev. (Engl. Transl.), 1982,51, 1042-1059 (184). 1306. Heteropolyacids in catalysis. I. V. Kozhevnikiv and K. I. Matveev, Russ. Chem. Rev. (Engl. Transl.), 1982,51,1075-1088 (182). 1307. Metal complexes of porphine and azaporphine compounds as catalysts of reactions involving oxidation of molecular oxygen. N. S . Enikolopyan, K. A. Bogdanova and K. A. Askarov, Russ. Chem. Rev. (Engl. Transl.), 1983,52, 13-26 (161). 1308. Bimetallic transition metal hydride complexes. G. L. Soloveichik and B. M. Bulychev, Russ. Chem. Rev. (Engl. Transl.), 1983,52,43-60 (191). 1309. Palladium(1) complexes in coordination chemistry and catalysis. 0. N. Temkin and L. G. Bruk, Russ. Chem. Rev. (Engl. Truml.), 1983,52,117-137 (163). 1310. Steric aspects of the formation of metal chelate complexes. V. G. Dashevskii, A. P. Baranov and M. I. Kabachnik, Russ. Chew. Rev. (Engl. Trunsl.), 1983,52,152-167 (105). 1311. Heterometallic ferrocene-based transition metal compounds. P. N. Gaponik, A. I. Lesnitovich and Y. G . Orlik, Russ. Chem. Rev. (Engl. Trunsl.), 1983,52,168-183 (293). 1312. The structure and reactivity of octadehydro-corrins and corroles. T. A. Melent’eva, Russ. Chem. Rev. (Engl. Trunsl.), 1983,52,641-661 (87). 1313. Molecular photocatalytic systems for solar energy conversion: catalysts for the evolution of hydrogen and oxygen from water. K. I. Zamaraev and V. N. Parman, Russ. Chem. Rev. (Engl. Transl.),

1983,52,817-836 (114). 1314. Thermodynamics of the formation of outer-sphere complexes in solution. V. E. Mironov and A. IS. Pyartman, Russ. Chem. Rev. (Engl. Transl.), 1983,52,837-849 (144). 1315. Platinum metal fluorides. A . V. Dzhalavyan, E. Ci. Rakov and A. S. Dudin, Russ. Chern. Rev. (Engl. Transl.), 1983,52,9&972 (185). 13 16, Metal-containing monomers: advances in polymerisation and copolymerisation., A. D. Pomogailo and V. S. Savost’yanov, Russ. Chem. Rev. (Engl. Transl.), 1983,542,975992 (215). 1317. Conductance of electrolytes in organic solvents. B. Kratochvil and €1. L. Yeager, Top. Curr. Chem., 1972,27, 1-58 (150). 1318. Ionic and redox equilibria in donor solvents. V. Gutmann, Top. Curr. Chem., 1972, 27, 59-115

(124). 1319. Crystal field effectsin n.q.r. A. Weiss, Top. Curr. Chem., 1972,30, 1-76 (167). 1320. Gas chromatography of inorganic compounds. H. Russel and G. Tolg, Top. Curr. Chem., 1972,33, 1-74 (629). 1321. The chemistry of phosphine. E. Fluck, Top. Curr. Chem., 1973,35,1-64 (493). 1322. Transition metal dithio- and diseleno-phosphate complexes. J. R. Wasson, G. M. Woltermann and H. J. Stoklosa, Top. Curr. Chern., 1973,35,66-129 (428). 1323. Orbital symmetry rules for inorganic reactions from perturbation theory. R. G. Pearson, Top. Curr. Chem., 1973,41,75-112 (53). 1324. Continuum effects indicated by hard and soft acid-base (Lewis acids) and bases. C. K. Yorgenscn, Top. Curr. Chem., 1975,56,146 (210). 1325. Stereochemistry of the reactions of optically active organometallic transition metal compounds. H . Brunner, Top. Cum Chem., 1975,56,68-90 (74). 1326. Dynamics of intramolecular metal-centred rearrangement reactions of tris-chelate complexes. L. H. Pignolet, Top. Curr. Chem., 1975.56,93-137 (85). 1327. Medicinal chemistry. D. D. Perrin, Top. Curr. Chem., 1976,64, 183-217 (192). 1328. Diastereoisomerism and diastereoselectivity in metal complexes. K. Bernauer, Top. Curr. Chem., 1976,65, 1-35 (134). 1329. Mechanistic aspects of the photochemical reactions of coordination compounds. M. S. Wrighton, Top. Curr. Chem., 1976,65,38-104 (196). 1330. Complexation and activation of diazenes and diazo compounds by transition metals. A. Albini and H. Kirsch, Top. Curr. Chem., 1976,65, 106-145 (119). 1331. Interactions between metal ions and living organisms in sea water. K. Kustin and G . C. McLeod, Top. Curr. Chem., 1977,69, 1-37 (136). 1332. Inorganic metabolic gas exchange in biochemistry. G. Renger, Tup. Curr. Chem., 1977, 69,39-90 (216). 1333. Complex formation of monovalent cations with biofunctlonal ligands. W. Burgermeister and R. Winkler-Oswatitsch, Top. Curr. Chern., 1977,69,91-196 (327).

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1334. Tetranuclear carbonyl clusters. P.Chini and B. T. Heaton, Top. Curr. Chem., 1977,71,1-70 (253). 1335. Thermochemical studies of organo-transition metal carbonyls and related compounds. J. A. Connor, Top. Curr. Chem., 1977,71,72-110 (122). 1336. The vibrational spectra of metal carbonyls. S. F. A. Kettle, Top. Curr. Chem., 1977, 71, 111-148 (79). 1337. Inorganic ap lications of X-ray photoelectron spectroscopy. W. L. Jolly, Top. Curr. Chern., 1977, 71, 15G182 829). 1338. Heteropoly compounds of molybdenum and tungsten. G . A. Tsigdinos, Top. Curr. Chem., 1978, 76,l-64 (275). 1339. The sarcoplasmic calcium pump. W. Hasselbach, Top. Curr. Chem., 1979,78,1-56 (201). 1340. Oxygenases and dioxygenases. M. Nozaki, Top. Curr. Chem., 1979,78,147-186 (226). 1341. Vitamin D and calcium metabolism. H. F. DeLuca. H. E. Paaren and H . K. Schnoes, Top. Curr. Chem., 1979,83, 1 4 5 (413). 1342. Cytochrome P-450 and biological hydroxylation reactions. V. Ullrich, Top. Curr. Chem., 1979,83, 68-104 (166). 1343. Chromatography in inorganic trace analysis. G. Schwedt, Top. Curr. Chem., 1979, 85, 159-212 (345). 1344. Chemical and stereochemical properties of compounds with silicon- or germanium-transition metal bonds. E. Colomer and R. J. P. Corriu, Top. Curr. Chem., 1981,96,79-107 (68). 1345. The analytical chemistry of technetium. K. Schwochau, Top. Curr. Chem., 1981,96,109-147 (155). 1346. Crown-type compounds - an introductory overview. E. Weber and F. Vogtle, Top. Curr. Chem., 1981,98, 1-41 (80). 1347. Concept, structure and binding in complexation. D. 3 . Cram and K.N. Trueblood, Top. Curr. Chem., 1981,98,43-106 (61). 1348. Complexation of uncharged molecules and anions by crown-type host molecules. E;. Vogtle, H. Sieger and W. M.Muller, Top. Curr. Chem., 1981,98, 107-161 (130). 1349, Analytical applications of crown compounds and cryptands. E. Blasius and K. P. Janzcn, Tup. Curr. Chem., 1981,9S, 163-189 (99). 1350. Chemistry and spectroscopy of rare earths. C. K . Jorgensen and R. Reisfield, Top. Curr. Chem., 1982,100, 127-167 (265). 1351. Structural chemistry of natural and synthetic ionophores and their complexes with cations. R. Hilgenfeld and W. Saenger, Top. Curr. Chem., 1982,101,l-82 (346). 1352. Dynamic aspects of ionophore mediated membrane transport. G . R. Painter and B. C. Pressman, Top. Curr. Chem., 1982,101,83-110 (105). 1353. Bioorganic modelling. Stereoselective reactions with chiral neutral ligand complexes as model systems for enzyme catalysis. R. M. Kellogg, Top. Curr. Chern., 1982, 101, 111-145 (93). 1354. Phase-transfer catalysed reactions. F. Montanari, D. Landini and F. Rolla, Top. Curr. Chem., 1982, 101,147-200 (295). 1355. Modern syntheses of cobalt(II1) complexes. M. Shibata, Top. Curr. Chem., 1983, 110,l-116 (77). 1356. The solvent extraction of metal ions by crown compounds. Y. Takeda, Top. Curr. Chem., 1984, 121, 1-38 (113). 1357. Crown compounds as alkali and alkaline earth metal ion selective chromogenic reagents. M. Takagi and K . Ueno, Top. Curr. Chem., 1984,121,39-65 (37). 1358. Photocontrol of ion extraction and ion transport by photofunctional crown ethers. S. Shinkai and 0. Manabe, Top. Curr. Chem., 1984,121,67-104 (101). 1359. Macroheterocyclic ligands on polymers. J. Smid and R. Sinta, Top. Curr. Chem., 1984, 121, 105-156 (194). 1360. Synthesis and metal complexes of azamacrocycles with pendant arms having additional ligating groups. T . A. Kaden, Top. Curr. Chem., 1984,121,157-179 (54). 1361. Bridged, capped and fenced porphyrins. J. E. Baldwin and P. Perlmutter, Top. Curr. Chem., 1984, 101,181-220 (164). 1362. Porphyrinic molecular metals. B. M. Hoffman and J. A. Ibers, Acc. Chem. Res., 1983, 16, 15-21 (44). 1363. The role of metals in borane clusters. R. N. Grimes, Acc. Chem. Res., 1983,16,22-26 (30). 1364. Macrocyclic carbonyl compounds as structural models for natural ion carriers. A. Shanzer, J. Libman and F. Frolow, Acc. Chem. Res., 1983, 16,60-67 (48). 1365. Chemistrv of triosmiurn carbonvl cluster compounds and its implications for catalysis. R. D. Adams, Acc. Chem. Res., 1983,16,67-?2 (27). 1366. The electrochemistry of vitamin BIZ. D. Lexa and J. M. Saveant, Acc. Chem. Res., 1983, 16, 235-243 (57). 1367. Cobalt(I1) as a probe of the structure and function of carbonic anhydrase. I. Bertini and C. Luchinot, Acc. Chem. Res., 1983,16,272-279 (57). 1368. Chemical mechanisms of catalysis by cytochromes P-450: towards a unified view. F. P. Guengerich and T. L. Macdonald, Acc. Chem. Res., 1984,17,9-16 (68). 1369. Binuclear oxygen carriers: hemerythrin. I. M. KIotz and D. M. Kurtz, Acc. Chem. Res., 1984, 17, 16-22 (57). 1370. The organic chemistry of dinitrogen. FI. M. Col uhoun, Acc. Chem. Res., 1984, 17,2%28 (36). 1371. Nonhomolytic cleava e pathways in the photo%emistry of metal-metal bonded carbonyl dimers. A. E. Stiegman and R. Tyler, Acc. Chem. Res., 1984,17,61-66 (36). 1372. Carbonyl insertion reactions of sauare-Dlanar complexes. G. K. Anderson and R. J. Cross, Acc. Chem. Res., 1984,17,67-74 (59). 1373. Kinetics and mechanism of metal chelation processes via solvent extraction techniques. H. Freiser, Acc. Chem. Res., 1984,17, 126-131 (40).

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1374. Redox reactions between metal complexes. H . Taube, Angew. Chem., Int. Ed. Engl., 1984, 23, 32%339 (100). 1375. Thio- and seleno-compounds of the main group elements - novel inorganic oligomers and polymers. B. Krebs, Angew. Chem., Inr. Ed. Engl., 1983,22,113-134(252). 1376. Catalysis by molecular metal clusters. E. L. Muetterties and M. J. Krause, Angew. Chem., Int. Ed. Engl., 1983,22,135-148(106). 1377. The versatile chemistry of 1,4-diazines: organic, inorganic and biochemical aspects. W. Kairn, Angew. Chem., Int. Ed. Engl., 1983,22,171-190(217). 1378. Structure and evolution of the ‘atmungsferment’ cytochrome c oxidase. B. Kadenbach, Angew. Chem., Int. Ed. En E., 1983,22,275-283 (142). 1379. Ligand-free metal cfusters. G. A . Ozin and S. A. Mitchell, Angew. Chem., Int. Ed. Engl., 1983,22, 674-694 (140). 1380. Electron rich half-sandwich complexes - metal bases par excellence. H. Werner, Angew. Chem., Int. Ed. Engl., 1983,22,927-949(170). 1381. Complexes of the platinum metals containing weak donor ligands. J. A . Davies and F. R. Hartley, Chem. Rev., 1981,81,79-90(159). 1382. Nitrogen n.m.r. spectroscopy in inorganic, organometallic and bioinorganic chemistry. J. Mason, Chem. Rev., 1981,81,206-227 (199). 1383. AR ring contributions to 31P n.m.r. parameters of transition metd-phosphorus chelate complexes. P. E. Garron, Chem. Rev., 1981,81,22%266 (93). 1384. Coordination chemistry of thioethers, selenoethers and telluroethers in transition metal complexes. S. G. Murray and F. R. Hartley, Chem. Rev., 1981,81,365-414(748). 1385. Spin state/stereochemical relationships in iron porphyrins: implications for the hemoproteins. W. R. Scheidt and C. A. Reed, Chem. Rev., 1981,81,543-555(111). 1386. Manganese(I1) as a magnetic relaxation probe in the studies of biomechanisms and of biomacromolecules. N. Niccolai, E. Tiezzi and G. Valensin, Chem. Rev., 1982,82,359-384(281). 1387. Coordinating properties of the amide bond. Stability and structure of metal ion corn lexes of peptides and related ligands. H. Sigel and R. B. Martin, Chem. Rev., 1982,82,385-426(f09). 1388. Terbium(II1) and europium(II1) ions as luminescent probes and stains for biomolecular systems. F. S. Richardson, Chem. Rev., 1982,82,541-552(69). 1389. Ligand substitution reactions at low-valent four-, five- and six-coordinate transition metal centres. J. A. S. Howell and P. M. Burkinshaw, Chem. Rev., 1983,83,557-599(468). 1390. The chemistry of metal carbonato and carbon dioxide complexes. D. A. Palmer and R. Van Eldik, Chem. Rev., 1983,83,651-731(628). 1391.Dialkyldithiophosphate derivatives of the non-transition elements. R. C. Mehrotra, G. Srivastava and B. P. S. Chauhan. Coord. Chem. Rev.. 1984.55.207-259 (210). . Thermodynamics of oxygen binding in natural and‘ synthetic‘dioxygen complexes. E. C. Nieder1392. hoffer, J. H. Timmons and A. E . Martell, Chem. Rev., 1984,84,137-203 (599). 1393. Synthesis and characterisation of platinum(1V)-ethanolamine complexes. M. S. Masoud, G. Y . Ali and A. F. Abdul Moneim, Rev. Inorg. Chem., 1983,5,207-218(22). 1394. Kinetics and mechanism of the outer sphere electron transfer reactions between complex ions. E. D. German, Rev. Inorg. Chem., 1983,5,123-184 (132). 1395. Analytical applications of substituted cinnamohydroxarnic acids in spectrophotometry and solvent extraction of metal ions. Y. K. Agrawal and R, K. Jain, Rev. Anal. Chem., 1982,6,49-64(71). 1396. Comdexinc modes of the DhosDhole moietv. F. Mathev. ,, J . Fischer and J. H . Nelson. Struct. Bonding (berfinx 1983,55,15$201(116). 1397. Crystal structure non-rigidity of central atoms for Mn(II), Fe(II), Fe(III), Co(II), Co(III), Ni(II), Cu(I1) and Zn(I1) com lexes. F. Valach, B. Koren, P. Swy and M. Melnik, Struct. Bonding (Berfin),1983,559,102-151 r72). 1398. The role of vibronic coupling in the interpretation of spectroscopic and structural properties of biomolecules. M. Bacci, Struct. Bonding (Berlin), l983,55,67-99 (169). 1399. The structure and reactivity of dioxygen complexes of the transition metals. M. H. Gubelmann and A. F. Williams, Struct. Bonding (Berlin), 1983,55,1-65 (529). 1400. Transition-metal thionitrosyl and related complexes. H. W. Roesky and K. K. Pandey, Adv. Inorg. Chem. Radiochem., 1983,26,337-356(69). 1401, Transition metal alkoxides. R. C. Mehrotra, Adv. Inorg. Chem. Rndiochem., 1983, 26, 26s33.5 (174). 1402. One-dimensional inorganic platinum-chain electrical conductors. J. M. Williams, Adv. Inorg. Chem. Radiochem., 1983,26,235-268(107). 1403. The chemistry of nitrogen fixation and models of the reactions of nitrogenase. R. A. Henderson, G. J. Leigh and C. J. Pickett, A d v . Inorg. Chem. Radiochem., 1983,27, 197-292 (360). 1404. Preparations and reactions of inorganic main-group oxide fluorides. J. H. Holloway and D. Laycock, Adv. Inorg. Chem. Radiochem., 1983,27,157-195 (342). 1405. Electron densitv distributions in inorganic comDounds. K. Toriumi and Y . Saito. Adv. Inorg. Chem. Radiochem., 1983,27,27-81(94). 1406. Alkali and alkaline earth metal cryptates. D. Parker, Adv. Inorg. Chem. Radiochem., 1983, 27, 1-26 (1.50). 1407. The fbcdonal roup in ligand field studies: the empirical and theoretical status of the angular overla model. M. 8erloch and R. G. Woolley, Prog. Inorg. Chem., 1984,31,371-446(87). 1408. d e chemical and catalytic reactions of dichlorotris(triphenylphosphine)ruthenium(II) and its major derivatives. F. H. Jardine, Prog. Inorg. Chem., 1984,31,265-370(357). 1409. B I 2and related organocobalt chemistry: formation and cleavage of cobalt-carbon bonds. P. J. Toscan0 and L.G. Marzillo, Prog. Inorg. Chem., 1984, 31,105204 (677).

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1410. Lanthanide ion luminescence in coordination chemistry and biochemistry. W. De W. Horrocks and M. Albin, Prog. Inorg. Chem., 1984,31,1-104(432). 1411. Investigation of complex formation in solution by the distribution method. A. P. Zozulya and V. M. Peshkova, Russ. Chem. Rev. (Engl. Transl.), 1960,29,101-118(264). 1412. Polymeric chelate complexes. A. A , Berlin and N. G. Matveava, Rws. Chem. Rev. (Engl. Transl.), 1960,29,119-128(83). 1413. Progress in the analytical chemistry of uranium, thorium and plutonium. V. I. Kuznetsov, S.B . Savvin and V.A. Mikhailov, Russ. Chem. Rev. (Engl. Transl.), 1960,29,243-267(925). 1414. Physico-chemical properties of chlorine trifluoride. Y. D. Shishkov and A . A. Opalovskii, Russ. Chem. Rev. (Engl. Transl.), 1960,29,357-364 (93). 1415. The analytical chemistry of thallium. A. I. Busev and V. G . Tiptsova, Russ. Chem. Rev. (Engl. Transl.), 1960,29,479-488(280). 1416. Stereochemistry and reaction mechanism of hexavalent inorganic complexes. F. Basolo, Ckem. Rev., 1953,52,459-527(274). 1417. The stereochemistry and valence states of nickel. R. S. Nyholm, Chem. Rev., 1953,53, 263-308 (212). 1418. Chelate complexes of 1,lO-phenanthroline and related compounds. W. W. Brandt, F. P.Dwyer and E. C. Gyarfas, Chem. Rev., 1954,54,959-1017(303). 1419. The molecular volume as a criterion of bond type in coordination compounds. R. W. Parry, Chem. Rev., 1950,46,507-516(21). 1420. On the tendency of metal ions toward complex formation. J. Bjerrum, Chem. Rev., 1950, 46, 381-401 (161). 1421. Reactions of inorganic substances with solutions of metals in liquid ammonia. G. W. Watt, Chem. Rev,, 1950,46,28-315(165). 1422. The trans effect in complex inorganic compounds. J. V. Quagliano and L. Schubert, Chem. Rev., 1952,50,201-260(157). 1423. The halogen fluorides. H. S. Booth and J. T. Pinkston, Clam. Rev., 1947,41,421-439(36). 1424. Coordination compounds of boron bromide and boron iodide. D. R. Martin, Chem. Rev., 1948,42, 581-599 (33). 1425. The analytical aspects of thorium chemistry. T. Moeller, G . K. Schweitzer and D. D. Starr, Chem. Rev., 1948,42,63-105(263). 1426. Ferriton: its properties and significance for iron metabolism. S. Granick, Chem. Rev., 1946, 38, 379-403 (58). 1427. The properties of metalloporphyrins. R. J. P. Williams, Chem. Rev., 1956,56,299-328(101). 1428. Bond hybridization and structure in the metal carbonyls. J. W. Cable and R. K. Sheline, Chem. Rev., 1956,56,1-26 (91) 1429. Isotope tracer investigations of mechanism and structure in inorganic chemistry. D. R. Stranks and R. G. Wilkins, Chem. Rev., 1957,57,74>866 (503). 1430. Oxidations by ferricyanide. B. S. Thyagarajan, Chem. Rev., 1958,58,439-460(110). 1431. Kinetics and mechanism of oxidation by permanganate. J . W . Ladbury and C. F. Cullis, Chem. Rev., 1958,58,403-438 (146). 1432. Stability relationships among analogous molecular addition compounds of group 111 elements. F. G. A. Stone, Chepn. Rev., 1958,58,101-129(109). 1433. Metal com lexing by phosphates. J. R. Van Wazer and C. F. Callis, Chem. Rev., 1958, 58, 1011-1046 h36). 1434. Halogen fluorides and other covalent fluorides. H. C. Clark, Chem. Rev., 1958,58,869-894(149). 1435. Manganese Schiff base complexes. H. Connors, C. A. McAuliffe and J. Tames, Rev. Inorg. Chem., 1981,3,199-257(168). 1436. The thermochemistry of metal dithiocarbamate complexes and related compounds. J. 0. Hill and R. J. Magee. Rev. Inorg. Chern., 1981,3,141-197(137). 1437. The mechanism of reduction of dioxy en by fully reduced cytochrome oxidase. Correlation of room and low temperature studies. G. M. &ore, Rev. lnorg. Ckem., 1980,2,343-360(52). 1438. Inorganic xanthates. G . Winter, Rev. Inorg. Chem., 1980,2,253-342(211). 1439. Recent applications of metal ion n.m.r. in coordination chemistry. P. L. Rinaldi, G . C. Levy and G. R. Choppin, Rev. Inorg. Chem., 1980,2,5>92 (91). 1440. Electrochemistry of transition metal complexes with flavins, nucleosides and their constituent bases. M. J . Clarke, Rev. Inorg. Chem., 1980,2,27-51(56). 1441. On the structure of concentrated ionic solutions by X-ray diffraction techni ues. R. Caminiti. G . Licheri, G. Piccaluga, G. Pinna and M. Magini, Rev. Inorg. Chem., 1979,1,136385 (83). 1442. High performance liquid chromatography in organometallic and coordination chemistry. H . Veening and B. R. Wilteford, Rev. Inorg. Chem., 1979,1,282-302(55). 1443. The stereochemistry of the coordination compounds of cadmium(I1). D. G. Tuck, Rev. Inorg. Chem., 1979,1,209-243(173). 1444. Preparation, structures and properties of vanadium(I1) halides and complex halides. C. Cros, Rev. Inorg. Chem., 1979,1,165-204(93). 1445. Metal chelates of pyridine-2-aldehyde-2’-pyridylhydrazone(paphy) and related ligands. C . F. Bell, Rev. Inorg. Chem., 1979,1,133-161(46). 1446. The donor-acceptor approach to solvent effects on the rates of redox reactions between different metal complexes. R. Schmid, Rev. Inarg. Chem., 1979,1,117-131 (48). 1447. Substitution reactions of square planar complexes involvmg polydentate ligands. R. J. Muremik, Rev. Inorg. Chem., 1979,1,l-50(123). 1448. Carboranes. R. E.Williams, Prog. Boron Chem., 1970,2,37-118(201).

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64

1449. The chemistry of polyhedral borane ions. L.J. Todd, Prog. Borun Chem., 1970,2,1-35 (81). 1450. Molten salt chemistry of the haloaluminates. C. R. Boston, Adv. Molten Salt Chem., 1971, 1, 129-163 (284). 1451. Some aspects of the coordination chemistry of boron. T. D . Coyle and F. G. A. Stone, Prog. Boron Chem., 1964,1,83-166 (360). 1452. The chemistry of compounds which contain boron-boron bonds. R . J. Brotherton, Prog. Boron Chem., 1964,1,1-81(189). 1453. Reactions and comparative reactivity of uranium hexafluoride. P. W. Wilson, Rev. Pure Appl. Chem., 1972,22, 1-12 (56). 1454. The hydrolysis of iron(II1). R. N . Sylva, Rev. Pure Appl. Chem..lY72,22,115-132 (82). 1455. A survey of dinitro en complexes of the transition metals. J. E. Fergusson and J. L. Love, Rev. Pure Appl. Chem., f970,20,33-50 (93). 1456. Chemical reactivity of higher fluorides of the transition metals. T. A. O’Donnell, Rev. Pure Appl. Chem., 1970,20,159-174 ( 5 6 ) . 1457. The design of quinquedentate chelating agents. F. Lions. Rev. Pure Appl. Chem., 1969, 19, 177-190 (14). 1458. Substituted halocarbonyls of the group VI transition metals. M. W. Anker, R. Colton and I. B . Tomkins, Rev. Pure Appl. Chem., 1968, 1 8 , 2 3 4 0 (77). 1459. Quadruple bonds and other multiple metal-metal bonds. F. A . Cotton, Rev. Pure Appl. Chem., 1967,17,25-40 (26). 1460. Fluorides of the heavy transition metals. J. FT. Canterford, R. Cnlton and T. A. O’Donnell, Rev. Pure Appl. Chem., 1967, 17, 12S132 (58). 1461. Semi-empirical calculation of the electronic structures of complexes. F. A . Cotton, Rev. Pure Appl. Chem., 1966,16,175-184 (39). 1462. Optical inversions in the reactions of cobalt complexes. 3 . C. Bailar, Rev. Pure Appl. Chem.. 1966, 16,91-101 (16). 1463. Noble gas chemistry. G. J . Moody and J . D. R. Thomas. Rev. Pure Appl. Chem., 1966, 16, 1-24 (168). 1464. Chemical structure and reaction mechanisms of cytochrome c oxidase. R. Lemberg, Rev. Pure A D D Chem.. ~. 1965.15.125-136 (1321. 1465. Eifect of chelation o n the synthe‘sis of or anic macrocycles. D. St. C. Black and E. Markham, Rev. Pure Appl. Chem., 1965, 15, 109-124 (927. 1466. Bimolecular nucleophilic substitutions of octahedral cobalt complexes. S. C. Chan and J. Miller, Rev. PureAppl. Chern., 1965, 15, 11-22 (21). 1467. Coordination chemistry of manganese and porphyrins. M. Calvin, Rev. Pure Appl. Chem., 1965,15, 1-10 (9). 1468. Structural aspects of zirconium chemistry. A . Clearfield, Rev. Pure Appl. Chem., 1964, 14,91-108 (94). 1469. Spectra of transition metal ions in crystals. J. Ferguson, Rev. Pure Appl. Chern., 1964,14,1-14 (59). 1470. Chemistr of halomercurate(I1) complexes. G. B. Deacon, Rev. Pure Appl. Chem., 1963, 13, 189-210 J60). 1471. Spin-paired complexes of Ni(II), Pd(II), Pt(I1) and Au(II1); with higher covalency. C. M. H a m s and S . E. Livingstone, Rev. Pure Appl. Chem., 1962,12, 16-31 (96). 1472. Recent advances in electron transfer reactions. R. T. M. Fraser, Rev. Pure Appl. Chem., 1961, 11, 6 4 7 7 (62). 1473. The chemistry of inner complexes. B. 0. West, Rev. Pure Appl. Chem., 1960, 10,207-242 (123). 1474. The ionisation and coordination behaviour of porphyrins. J. N. Phillipe, Rev. Pure Appl. Chem., 1960,10,35-60 (72). 1475. The oxidation-reduction potentials of metal complex ions. D. D. Perrin. Rev. Pure Appl. Chem., 1959,9,257-285 (111). 1476. Moltensalts. H . Bloom, Rev. Pure Appl. Chem., 1959,9,13%168 (114). 1477. Electrolytes in sulphuric acid. R. J. Gillespie, Rev. Pure Appl. Chern., 1959, 9,1-32 (59). 1478. The cytochromes. R. K . Morton, Rev. Pure Appl. Chem., 1958,8, 161-220 (289). 1479. Some applications of ion exchange in the study of complexes. J. E. Salmon, Rev. Pure Appl. Chern., 1956,6,24-39 (58). 1480. The chemistry of protactinium. G . L. Miles. Rev. Pure Appl. Chem., 1952,2,163-173 (54). 1481. Systematic chemistry of the transition elements - recent chemistry of titanium, zirconium and hafnium. F. K . McTaggart. Rev. Pure Appl. Chem., 1951,1, 152-170 (31). 1482. High temperature coordination chemistry of group VIII. K. E. Johnson and J. R. Dickinson, Adv. Molten Salt Chem., 1973,2, 83-198 (284). 1483. Organometallic coordination polymers involving alkoxo- and alkylamido-bridges. D. C . Bradley, Inorg. Macromol. Rev., 1970, 1,141-157 (59). 1484. Polymeric metal phosphates. P. Block, Inorg. Macromol. Rev,, 1970,1,115-125 (49). 1485. Synthesis and properties of polymeric phthalocyanines and their metal derivatives. A. A , Berlin and A . I . Sherle, Inorg. Mucromol. Rev., 1971,1,235-270 (128). 1486. The chemistry of thiocyanate melts. D. H. Kerridge, Adv. Molten Salt Chem., 1975, 3, 249-273 (881.

1487. Organic reactions in molten tetrachloroaluminate solvents. H. L. Jones and R. A. Osteryoung, Adv. Molten Salt Chem., 1975,3, 121-176 (135).

Index of Review Articles and Specialist Texts

65

1488. Double bonding between the heavier main-group elements: from reactive intermediates to isolable molecules. A. H. Cowley, Polyhedron, 1984,3.389-432 (116). 1489. Metal chelates as probes of biological systems. C. F. Meares and T. G . Wensel, Acc. Chem. Res., 1984,17,202-209 (64). 1490. Photochemistry of cobalt(II1) complexes. V. Balzani, L. Moggi, F. Scandola and V. Carassiti, Inorg. Chim. Acta, Rev.. 1967, 1, 7-34 (111). 1491, Substitution reactions of metal carbonyl compounds. D. A. Brown, Inorg. Chim. Acta, Rev., 1967, 1 , 3 5 4 7 (76). 1492. Stereoselectivity and reactivity in complexes of amino-acids and peptides. R. D. Gillard, Inorg. Chim. Acta, Rev., 1967, 1,69-86 (102). 1493. Anomalies in ligand exchange reactions for platinum(I1) complexes. D. S. Martin, (norg. Chim. Acta, Rev., 1967, 1,87-97 (40). 1494. Alkoxides and alkylalkoxides of metals and metalloids. R. C. Mehrotra, Inorg. Chim. Acta, Rev., 1967,1,99-112 (315). 1495. The closed metal carbonyl ctustcrs. P. Chini, Inorg. Chim. Acta, Rev., 1968, 2, 31-51 (223). 1496. The double isotope label technique and inorganic reaction mechanisms. J. 0. Edwards and P. D. Fleischauer, Inorg. Chim. Acta, Rev., 1968, 2, 53-63 (35). 1497. Spectra and electronic structure of com lexes with sulphur-containing ligands. C. K. Jorgensen, Inorg. Chirn. Acta, Rev., 1968,2, 65-88 695). 1498. The electronic spectra and optical activity of phenanthroline and dipyridyl metal complexes. S . F. Mason, Inorg. Chim. Acta, Rev., 1968, 2,89-109 (84). 1499. Thiol and thio-b-diketone derivatives of the elements. R. C. Mehrotra, V. D. Cupta and D. Sukhani, Inorg. Chim. Acta, Rev., 1968, 2, 111-121 (241). 1500. Pyridine complexes of platinum(I1). M. Orchin and P. J . Schmidt, Inorg. Chim. Acfa,Rev., 1968, 2, 123-135 (61). 1501. The effect of ligand and metal hardness on the formation of hydrido- and organometallic complexes by the p-interaction. R. J . Cross, Inorg. Chim.Acta, Rev., 1969, 3,75-79 (52). 1502. Cooperative effects in the clectronic spectra of inorganic solids. P. Day, Inorg, Chirn. Acta, Rev., 1969,3,81-97 (84). 1503. Electrophilic reactivity and structure of the coordinated nitrosyl group. J. Masek, Inorg. Chim. Acta, Rev., 1969.3,99-108 (36). 1504. Spectroscopic studies of metal-metal bonded compounds. K . L. Walters and W. M. Risen, Inorg. Chim. Acta, Rev., 1969,3,129-154 (196). 1505. Complexes of platinum(I1) with Group IV donor ligands. U. Belluco, G. Deganello, R. Pietropaolo and P. Uguagliati. Inorg. Chim. Acta, Rev., 1970, 4,7-39 (149). 1506. Extension of the ‘model’ approach to the study of coordination chemistry of vitamin BIZgroup a m pounds. A. Bigotto, G. Costa, G. Mastroni, G . Pellizer, A. Puxeddu, E. Reisenhofer, L. Stefani and G. Tauzher, Inorg. Chim. Acta, Rev., 1970,4,4149 (43). 1507. Synthesis and reactions of aluminium hydride derivatives. S. Cucinella, A. Mazzei and W. Marconi, Inorg. Chim. Actlt, Rev., 1970,4,51-71 (183). 1508. Methinyltricobalt enneacarbonyl compounds; preparation, structure and properties. G. Palyi, F. Piacenti and L. Marko, Inorg. Chirn. Acta, Rev., 1970,4, 1oP-121 (94). 1509. Mechanisms of substitution of octahedral cobalt(II1) amine corndexes. C. K . Poon, Znorn. Chirn. Acta, Rev., 1970.4. 123-144 (131). 1510. Trans activation and limiting SN1mechanisms for substitution reactions of cobalt(II1) complexes in aaueous solution. J. E. Bvrd and W. K. Wilmarth, Inora. Chim. Acta. Rev.. 1971.5,7-18 (422). Degetto and E. Tondello, Inorg. Chim. 1511. Uianyl chelate complex&. L. Cattalini, U. Croatto. Acta, Rev., 1971,5, 1 9 4 3 (268). 1512. Magnetic exchange in transition metal complexes VI: aspects of exchange coupling in magnetic cluster compounds. A. P. Ginsberg, Inorg. Chim. Acta, Rev.. 1971,5,45-68 (83). 1513. Neutral organophosphorus chalcogenide-metal salt interactions: addition and decomposition products. N. M. Karayannis, C. M. Mikulski and L. L. Pytlewski, Inorg. Chim. Acta, Rev., 1971, 5, 6%105 (479). 1514. Electronic spectra for coordination complexing of platinum(l1). D.S. Martin, Inorg. Chim. Acta, Rev., 1971,5.107-125 (50). 1515. Chemistry of double alkoxides of various elements. R. C. Mehrotra and A . Mehrotra, inorg. Chim. Acta, Rev., 1971,5.127-136 (48). 1516. Catalysis by metallo-enzymes: the entatic state. R. J. P. Williams, Inorg. Chim. Acta, Rev., 1971, 5, 137-155 (52). 1517. Molecular orbital theory of transition metal complexes. D. A. Brown, W. J. Chambers and N. J. Fitzpatrick, Inorg. Chim. Acta, Rev., 1972,6,7-30 (193). 1518. The application of Mossbauer spectroscopy in the study of mixed ligand complexes. K. Burger, Inorg. Chirn. Acta, Rev., 1972,6,31-46 (125). 1519. Recent developments in transition metal nitrosyl chemistry. N. G . Connelly, Znorg. Chim. Acta. Rev., 1972,6,47-89 (395). 1520. Hydrido coin lexes of rhenium: synthesis and reactivity, D . Giusto, Inorg. Chim. Acto, R e v . , 1972, 6,91-101 (61f 1521. Metal complexes of sulphur-containin amino-acids. C. A. McAuliffe and S. G. Murray, Inorg. Chim. Acta, Rev., 1972,5,103-121 (198) 1522. Anti-cancer drug design involving com lexes of amino-acids and metal ions. D. R. Williams, Inorg. Chim. Acta, Rev. 1972,6, 123-133 (967. 1523. Application of “‘Sn chemical shifts to structural tin chemistry. P. J. Smith and L. Smith, Inorg. Chim. Acta, Rev., 1973,7, 11-33 (73). 1

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Index of Review Articles and Specialist Texts

1524. Pseudo-allyl metal carbonyl complexes. T. Inglis, Inorg. Chim. Acta, Rev., 1973,7,3542 (43). 1525. Thermochemistry of metal-polyamine complexes. P. Paoletti. L. Fabrizzi and R. Barbucci, Inorg. Chim. Acta, Rev., 1973,7,43-68 (100). 1526. Monodentate amine complexes of platinum(I1). K. P. Beaumont and C. A. McAuliffe, Znorg. Chim. Acta, 1974,8, 105-127 (166). 1527. The physical properties of some transition metal compounds of the ABX3 type. J. F. Ackerman, G. M. Cole and S . L. Holt, Inorg. Chim. Acta, 1974, 8, 323-343 (96). 1528. Recent advances in the chemistry of isocyanide complexes. F. Bonati and G. Minghetti, Inorg. Chim. Acta, 1974, 9,95-112 (238). 1529. The system p-dichlorotetracarbonyldirhodium-tertiary phosphines. P. Uguagliati, G. Deganello and U. Belluco, Znorg. China.Acta, 1974,9,203-207 (21). 1530. Rate parameters for ligand replacement processes in octahedral complexes of metals in oxidation state three. J. 0. Edwards, F. Monacelli and G. Ortaggi, Znorg. Chim. Acta, 3974,11,47-104 (368). 1531. Mossbauer spectroscopy of mono-organotin(1V) derivatives. R. Barbier, L. Pellerito, N. Bertazzi and G. C . Stocco, Inorg. Chim. Acta, 1974, 11, 173-183 (66). 1532. Contributions to the Pfeiffer effect. P. E. Schipper, Znorg. Chim. Acta, 1975, 12,199-204 (25). 1533. Oxime and hydroxytamine derivatives of metals and metalloids. R. C. Mehrotra, A. K . Rai, A. Singh and R. Bohra, Inorg. Chiin. Acta, 1975, 13,91-103 (170). 1534. Advances in platinum metal carbonyls and their substituted derivatives, I. Ruthenium and osmium carbonyls. S. C. Tripathi, S. C. Srivastava, R. P. Mani and A. K . Shrimal, Inorg. Chim. Acta, 1975. 15,249-290 (327). 1535. Chemistry of beryllium-h-oxoacetato complexes. A. I Grigor’ev and V. A. Sipachev, Inorg. Chim. Acta, 1976, 16,269-279 (55). 1536. Organic azides and isocyanates as sources of nitrene species in organometallic chemistry. S. Cenini and G. La Monica, Inorg. Chim. Acta, 1976,18,27%293 (86). 1537. Advances in platinum metal carbonyls and their substituted derivatives, 11. Rhodium, iridium, palladium and platinum carbonyls. s. C. Tripathi, s. C . Srivastava, R. P. Mani and A. K. Shirmal, Inorg. Chim. Acta, 1976, 17,257-290 (463). 1538. Com arative reactions of nitrogen compounds with the isoelectronic series, mercury(II), thallium&II) and lead(1V) acetates. Principles of oxidation reactions. R. N. Butler, Chem. Rev., 1984, 84.249-276 (307’1. 1539. Synthetic aspect; of Cu-Mo-S systems and their possible relevance to copper-molybdenum antagonism. s. Sarker and s. B. S. Mishra, Coord. Chem. Rev., 1984,59,239-264 (80). 1540. Transition metal hydroxyoxime complexes. M. E. Keenery and K. Osseo-Asare, Coord. Chem. Rev., 1984,59,141-201(313). 1541. Coordination chemistry of chelating resins and ion exchangers. S. K. Sahni and J. Reedijk, Coord. Chem. Rev., 1984,59, 1-139 (685). 1542. The stereodynamics of metal complexes of sulphur, selenium and tellurium containing ligands. E. W. Abel, S. K. Bhargava and K. G. Orrell, Prog. Znorg. Chem., 1984,32,1(250). 1543. Five-coordinated structures. R. R. Holmes, Prog. Inorg. Chem., 1984,32,119 (352). 1544. Homo- and hetero-nuclear cluster compounds of gold. K. P. Hall and D. M. P. Mingos, Prog. Inorg. Chem., 1984,32,237 (225). 1545. Electrides, ne atively charged metal ions and related phenomena. J. L. Dye, Prog. Inorg. Chem., 1984,32,327 8337). 1546. Lon range electron transfer in peptides and proteins. S . S. Isied, Prog. Inorg. Chem., 1984,32,443 (1877. 1547. The polyhedral metalloboranes, Part I: metalloborane clusters with seven vertices and fewer. J. D. Kennedy, Prog. Inorg. Chem., 1984,32,519 (312). 1548. The specification of bonding cavities in macrocyclic ligands. K. Hendrick, P. A. Tasker and L. F. Lindoy, Prog. Inorg. Chem., 1985,33, l(146). 1549. Inclusion complexes of molecular transition metal hosts. T. J. Meade and D. H. Busch, Prog. fnorg. Chem., 1985,33,59 (331). 1550. Novel reactions of metal carbonyl cluster compounds. R. D. Adams and 1. T. Horvarth, Frog. Inorg. Chem., 1985,33,127 (200). 1551. Ion pairing effects on transition metal carbonyl anions. M. Y.Darensbourg, Prog. Znorg. Chem., 1985,33,221 (138). 1552. Structural changes accom anying metal complex electrode reactions. W. E. Geiger, Prog. Inorg. Chem., 1985,33,275 (1787. 1553. Spectroscopic studies of ion-ion-solvent interaction in solutions containing oxyanions. D. W. James, Prog. Inorg. Chem., 1985,33,353 (118). 1554. N.m.r. of metal nuclides, Part 11: the transition metals. J. J. Dechter, Prog. Inorg. Chem., 1985, 33, 393 (578). 1555. Fast atom bombardment mass spectrometry and related techniques. J. M. Miller, Adv. Inorg. Chem. Radiochern., 1984,28, l(118). 1556. The chemistry of berkelium. J. R. Peterson and D. E, Hobart, Adv. Inorg. Chern. Radiochem., 1984,28,29 (240). 1557. Preparations and reactions of oxide fluorides of the transition metals, the lanthanides and the actinides. J. H. Holloway and D. Laycock, Adv. Inorg. Chem. Radiochem., 1984,28,73 (278). 1558. Compounds of pentacoordinated arsenic(V). R. Bohra and H.W. Roesky, Adv. Inorg. Chem. Radiochem., 1984,28,203 (204). 1559. Perchlorate ion complexes. N. M. N. Gowda, S. €3. Naikar and G . K. N. Reddy, Adv. Inorg. Chem. Radiochem., 1984,28,255 (162).

Index of Review Articles and Specialist Texts

67

1560. Trifluorophosphine complexes of transition metals. J. F. Nixon, Adv. Inorg. Chem. Radiochem., 1985,29, l(368). 1561. Solvent extraction of metal carboxvlates. H. Yamada and M. Tanaka. Adv. Inorg. Chem. Radiochem., 1985,29,143 (159). 1562. Where are the lone-pair electrons in subvalent fourth group compounds? S. W. Ng and J. J. Zuckerman. Adv. Inora. Chem. Radiochem.. 1985.29.297 (178). 1563. Bioinorganic afplications of m.c.d. spectroscopy: copper, rare earth ions, cobalt and non-heme iron systems. D. M. Dooley and J. H. Dawson, Coord. Chem. Rev., 1984,60, 1 (176). 1564. The coordination chemistry of secondary phosphine chalcogenides and their conjugate bases. B. Walther, Coord. Chern. Rev., 1984,60,67 (1 10). 1565. Mixed valence molecules: electronic delocalisation and stabilisation. D. E. Richardson and H. Taube, Coord. Chem. Rev., 1984,60, 107 (40). 1566. The angular overlap model for the description of the paramagnetic properties of transition metal complexes. A . Benici, C. Benelli and D. Gatteschi, Coord. Chem. Rev., 1984,60,131 (204). 1567. Rare earth complexes with neutral macrocyclic ligands. J. C. G. Bunzli and D. Wessner, Coord. Chem. Rev., 1984,60,191 (186). 1568. Trimethylamine N-oxide: a versatile reagent for organometallic chemistry. T. Y. Luh, Coord. Chem. Rev., 1984.60,255 (171). 1569. Photocatalytic systems with light-sensitive coordination compounds and possibilities of their spectroscopic sensitization - an overview. H. Hennig and D . Rehorek, Coord. Chem. Rev., 1985,61,1 (281). 1570. Kinetics and mechanisms of metalloporphyrin reactions. D. K. Lavallee, Coord. Chem. Rev., 1985, 61,55 (219). 1571. Complex formation between palladium(I1) and amino aads, peptides and related ligands. L. D . Pettit and M. Bezer, Coord. Chem. Rev., 1985,61,97 (90). 1572. Complexes of heterocyclic thione donors. E. S. Raper, Coord. Chern. Rev., 1985,61, 115 (310). 1573. Outer sphere coordination of organic molecules to electrically neutral metal complexes. V. M. Nekipelov and K. I. Zamarawu, Coord. Chem. Rev., 1985,61,185 (136). 1574. Chromium(V) coordination chemistry. M. Mitewa and P. R. Bontchev, Coord. Chem. Rev., 1985, 61,241 (264). 1575. Organocobalt BI2models: axial ligand effects on the structure and coordination chemistry of cobaloximes. N. Bresciani-Pahor, M. Forcohin, L. G . Marzirli, L. Randaccio, M. F. Summers and P. J. Toscano, Coord. Chem. Rev., 1985,63, l(263). 1576. Transition metal complexes of semicarbazones and thiosemicarbazones. S. Padhye and G. B. Kauffman, Coord. Chern. Rev., 1985,63,127 (110). 1577. Coordination chemistry of organomercury(I1) involving phenanthrolines, bipyridines, tertiary hoshineslarsines and some related ligands. T. S . Lobana, Coord. Chem. Rev., 1985,63, 161 (186f. 1578. hotochemical disproportionation of metal-rnetal bonded carbonyl dimers. A. E. Stiegman and D. R. Tyler, Coord. Chew. Rev., 1985,63,217 (59). 1579. Transition metal coordination compounds in oscillatin chemical reactions. K. B. Yatsimirskii and L. P. Tikhonova, Coord. Chem. Rev., 1985,63.241 (93). 1580. Transition metal polyhydride complexes. G. G. Hlatky and R. H. Crabtree, Coord. Chem. Rev., 1985,65, 1 (292). 1581. Seven coordination in molybdenum chemistry: analysis of oligonuclear structures. M. Melnik and P. Sharrock, Coord. Chem. Rev., 1985,65,49 (91). 1582. Recent developments in the studies of titanium and vanadium porphyrins with special emphasis on oxygen adducts, low valent metalloporphyrins and related systems of sulphur and selenium. R. Guilard and C. Lecomte, Coord. Chem. Rev., 1985,65,87 (76). 1583. The preparation and properties of compounds containing Pt(II1). J. D. Woolins and P. F. Kelly, Coord. Chem. Rev., 1985,65, 115 108). 1584. The A2[FeX5H20)] series of anti erromagnets. R. L. Carlin and F. Palacis, Coard. Chem. Rev., 1985,65,141{36). 1585. Structural and electronic properties of some polymolybdates reducible to molybdenum blues. R. I. Buckley and R . J. H. Clark, Coord. Chem. Rev., 1985,6S, 167 (104). 1586. Selective metal-ligand interactions in heterometallic transition metal clusters. E. Sappa, A. Tiriplochi0 and P. Braunstein, Coord. Chem. Rev., 1985,65,219 (218). 1587. X-ray diffraction and the charge distribution in transition metal complexes. P. Coppens, Coord. Chem. Rev., 1985,65,285 (56). 1588. Quantum mechanical effects in inorganic and bioinorganic electron transfer. T. Guarr and G. McLendon, Coord. Chem. Rev., 1985,68, l(227). 1589. Alkoxo derivatives of the platinum metals. R. C. Mehrotra, S. S. Agarwal and Y. P. Singh, Coord. Chem. Rev., 1985,68, 101 (81). 1590. Hydrogenase and its application for photoinduced hydrogen evolution. I. Okura, Coord. Chem. Rev., 1985,68,53 (141). 1591. Reactions of alkylcobalamins with platinum complexes. Y. T. Fanchiang, Coord. Chem. Rev., 1985, 68.131 (761. 1592. Metal-ion catalysed aquation of transition metal complexes. R. Banerjee, Coard. Chrm. Rev., 1985.68. 145 (1181. \---I 1593. Then.m.r. properties of chromium, molybdenum and tungsten compounds. M. Minelli, J. H . Enemark, R. T. C. Brownlee, M. J. O’Connor and A. G. Wedd, Coord. Chem. Rev., 1985, 68, 169 (201). 1594. Intramolecular ferromagnetic interactions in polynuclear metal complexes. C. J. Cairns and D. H. Busch, Coord. Chem. Rev., 1986,69, l(174). i

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68

Index of Review Articles and Specialist Texts

1595. Interfacial electron transfer in colloidal metal and semiconductor dispersions and photodecomposition of water. K. Kalyanasundaram, M. Gratzel and E. Pehzzelti. Cuord. Chem. Rev., 1986, 69,57 (338). 1596. Cluster complexes containing opened transition metal polyhedra. M. 0. Albers, D. J. Robinson and N. J. Coville, Coord. Chem. Rev., 1986,69, 127 (357). 1597. The chemistry and spectroscopy of mixed-valence compounds. R. J. H. Clark, Chem. SOC. Rev., 1984,13,219 (91). 1598. Reactions involving the triple bond in dimolybdenum and ditungsten hexa-alkoxides and C-€, C-N and C-0 triple bonds. M. H . Chisholm, D. M. Hoffman and J. C. Huffman, Chem. Soc. Rev., 1985,14,69 (62). 1599. The B12-dependent isomerase enzymes: how the protein controls the active site. J. M. Pratt, Chem. SOC.Rev., 1985,14, 161 (50). 1600. Ligand substitution reactions of square planar molecules. R. J. Cross, Chern. SOC. Rev., 1985, 14, 197 (100). 1601. Structure and electron transfer reactivity of the blue copper protein, plastocyanin. A. G. Sykes, Chem. SOC. Rev., 1985, 14,283(117). 1602. ‘Second-sphere’ photochemistry and photophysics of coordination compounds. V. Balzani. N. Sabbatini and F. Scandola, Chem. Rev., 1986,86,319 (173). 1603. Coordinated trifluoromethanesulphonate and fluorosulphate. G. A. Lawrance, Chem. Rev.. 1986. 86, 17 (221). 1604. Chemistry and thermodynamics of europium and some of its simpler inorganic compounds and aqueous species. J. A. Rand, Chem. Rev., 1985,85,555 (343). 1605. Polyatomic zintl anions of the post-transition elements. J. D. Corbett, Chem. Rev., 1985, 85, 383 (117). 1606. Synthesis and reaction chemistry of stable two-coordinate phos horus cations (phosphenium ions). A. H. Cowley and R. A. Kemp. Chem. Rev., 1985,85,367 (1007. 1607. Thermodynamic and kinetic data for cation-macrocycle interaction. R. M. Izatt, J. S. Bradshaw, S. A. Nielsen, J. D. Lamb, 3. J. Christensen and D. Sen, Chem. Rev., 1985,85,271(340). 1608. The nature of spin state transitions in solid complexes of iron(I1) and the interpretation of some associated phenomena. E. Konig, G. Ritter and S. K. Kulshreshtha, Chem. Rev., 1985, 85, 219 (91). 1609. Photochemistry of metal-metal bonds. T. J. Meyer and J . V. Caspar, Chem. Rev., 1985, 85, 187 (113). 1610. Transition metal-mediated phosphorus-carbon bond cleavage and its relevance to homogeneous catalyst deactivation. P. E. Gorrou, Chem. Rev., 1985,85, 171(109). 1611. Photochemistry of small molecules in low temperature matrices. R. N. Perutz, Chem. Rev., 1Y8.5, 85,97 (278). 1612. Photochemical reactions involving matrix-isolated atoms. R. N. Perutz, Chem. Rev., 1085, 85, 77 (187). 1613, Electrochemistry of boron compounds. J . H. Morris, M. H. Gysling and D. Reed, Chem. Rev., 1985,85,51 (202). 1614. The transition metal-hydrogen bond. R. G. Pearson, Chem. Rev., 1985,85,41(72). 1615. Chemistry and thermodynamics of ruthenium and some of its inorganic compounds and aqueous species. J. A. Rard, Chem Rev., 1985,85,1(480). 1616. Bound and unbound radical intermediates in inorganic electron-transfer reactions. E. S. Gould, Acc. Chem. Res., 1985, 18,22 (57). 1617. Nucleoside sites for transition metal ion binding. R. B. Martin, Acc. Chem. Res., 1985,18,32 (35). 1618. Reductions of carboxylate-bound chromium(V). E. S. Gould, Acc. Chem. Res., 1986,19,66 (SO). 1619. Application of x-ray absorption spectroscopy to the studies of structure and bonding of metal complexes in solution. T. K . Sham, Acc. Chem. Res., 1986, 19, 99 (40). 1620. The 2 rr4 triple bond between molybdenum and tun sten atoms: develo ing the chemistry of an inorganic functional group. M. H . Chisholm, Angew. $hem., Int. Ed. Eng?, 1986,25,21(70). 1621. Multiple bonds between transition metals and ‘bare’ main group elements: links between inorganic solid state chemistry and organometallic chemistry. W. A. Herrmann, Angew. Chem., lrzt. Ed. Engl., 1986,25,56 (115). 1622. Resonance Raman spectroscopy and its application to inorganic chemistry. R. J. H. Clark and T. J. Dines,Angew. Chem., Int. Ed. Engl., 1986,25,131(191). 1623. Complexation of iron by sideropfiores. A review of their solution and structural chemistry and biological function. K. N. Raymond, G. Muller and B. F. Matzanke, Top. Curr. Chem., 1984, 123, 49

(227). 1624. The problems of the two-electron bond in inorganic compounds; analysis of the coordination number, N . C. K: Jorgensen, Top. Curr. Chern., 1984,124, l(12S). 1625. Cationic and anionic complexes of the noble gases. H. Selig and J. H. Holloway, Tup. Curr. Chem., 1984,124,35 (172). 1626. Active transport of ions using synthetic ionophores derived from macrocyclic pol ethers and related compounds. M. Okahara and Y . Nakatsuji, Top. Curr. Chem., 1985,128,37 (773. 1627. Macrocyclic polyamines as biological cation and anion complexones - an application to calculi dissolution. E. Kimura, Top. Curr. Chem., 1985,128,113 (85).

index of Review Articles and Specialist Texts

69

1628. Micellar models of zinc enzymes. W. Tagaki and K. Ogino, Top. Curr. Chem., 1985,128,143 (43). 1629. High pressure synthesis of cryptands and complexing behaviour of chiral cryptands. J. Jurczak and M. Pietraszkiewicz, Top. Curr. Chem., 1986,130, 183 (49). 1630. Molecular and electronic structures of penta- and hexa-coordinate silicon compounds. S . N. Tandura, M. G. Voronkov and N. V. Alekseev, Top. Curr. Chem., 1986,131,99 (1008). 1631. Metalloporphyrins as catalysts of chain transfer in radical polymerisation and stereoselective oxi-

dation. L. Karmilova. G. V. Ponomarev, B. R. Smirnov and I. M. Bel’yovskii, Russ. Chem. Rev. (Engl. Transl.), 1984,53, 132 (44). 1632. The structure and stereochemistry of paramagnetic metal complexes of o-quinones. M. J. Kabachnik, N. N. Bubnov. S. P. Solodovnikov and A. I. Prokof‘ev, Russ. Chem. Rev. (Engl. Transl.), 1985.53.288 (56). , 1633. Organometalfic &elate complcxcs of the v-T and v-n type. N. J . Rybinskaya and V. V. Krivykh, Russ. Chem. Rev. (Engl. Transl.), 1984,53,476 (267). 1634. The oxidation of haemoglobin. A. E. Myshkin, Russ. Chem. Rev. (Engl. Transl.), 1984, 53, 606 (121). 1635. Thequantum chemistry of unusual oxidation states of the lanthanides and actinides. V. I. Spitsyn and G. V. Ionova, Russ. Chem. Rev. (Engl. Transl.), 1984,53,725 (138). 1636. The use of lanthanide shift reagents in the analysis of the microstructure of olymers by nmr spectroscopy. Y. E. Shapiro, Russ. Chem. Rev. (Engl. Transl.), 1984,53,817 (57f 1637. The high temperature microcalorimetry of inorganic substances. N. D. Topor and Y. L. Suponitskii, Russ. Chem. Rev. (Engl. Transl.), 1984,53,827 (423). 1638. The temperature jump method and its application to the study of com lex formation. V. I. Pogonin and A. K. Chibisov, Russ. Chem. Rev. (Engl. Transl.), 1984,53,929 818). 1639. Catalysis by metalloporphyrins of reactions involving oxidation by molecular oxy en and oxygencontainingmmpounds. N.S. Enikolopyan, K . A. Bogdanova, L. V. Karmilova a n f K . A. Askarov, Russ. Chem. Rcv. (Engl. Transl.), 1985,54,215 (188). 1640. Metal carbonyl complexes with ligands of biologicai origin. A. A. loganson, Russ. Chem. Rev. (Engl. Transl.), 1985,54,277 (124). 1641. Three-membered metallocycles (trinuclear clusters). S. P. Gubin, Russ. Chem. Rev. (Engl. Transl.), 1985,54,305 (169). 1642. The structure of cluster compounds of transition metals and the limits of applicability of the electron 1~~

counting rules for polyhedral molecules. Y. L. Slovokhotov and Y. T. Struchkov, Russ. Chem. Rev. (Engl. Transl.), 1985,54,323 (150). 1643. The electronic structure of transition metal cluster complexes with weak- and strong-field iigands. G. P. Kostikova and D. V. Korol’kov, Russ. Chem. Rev. (Engl. Transl.), 1985,54,344 (137). 1644. Estimation of the stability of clusters with the aid of the theory of the electron dcnsity functional. Y. A. Borisov, Rim. Chem. Rev. (Engl. Transl.), 1985,54,361 (104). 1645. The chemistry of cluster compounds of technetium. V. 1. Spitsyn, A. F. Kuzina, A. A . Oblova and S. V. Kryuchkov, Rum. Chem. Rev. (Engl. Trans!.), 1985,54,373 (106). 1646, Phosphinc palladium and phosphine platinum carbonyl cluster compounds. N. K . Eremenko, E. Ci. Mednikov and S. S . Kurasov, Russ. Chem. Rev. (Engl. Transl.), 1985,54,394 (69). 1647. Cluster transition metal chalcogcnidc halides. V. E. Fedorov, A . V. Mishchenko and V . P. Fedin, Russ. Chem. Rev. (Engl. Transl.), 1985, 54,408 (102). 1648. The modelling of biological catalysts. A. P. Purmal and L. A. Nikolaev, Russ. Chern. Rev. (Engl. Transl.), 1985,54,466 (124). 1649. Metallocarboranes: structural studies in recent years. A. I. Yanovskii, Russ. Chem. Rev. (Engl. Transl.), 1985.54.515 (78). 1650. Activation of molecular oxygen by metal complexes and its role in the mechanism of liquid phase oxidation. I. P. Skibida, Russ. Chem. Rev. (Engl. Transl.), 1985, 54,875 (119). 1651. Chromium(lI1) and the glucose tolerance level. J. Barrett. P. O’Brien and J. Pedrosa de Jesus. Polyhedron. 1985,4, 1(170). 1652. Reactions of triosmium clusters with organic compounds. K. Burgess, Polyhedron, 1984, 3. 1175 (223). 1653. Plathum-ligand and palladium-ligand bond energies. C. T. Mortimer, Rev. lnorg. Chew., 1983, 6, 233 (50). 1654. The stereochemistry of optically active derivatives of Werner’s hexol complex. Y . Shimura, Rev. lnorg. Chem., 1984,6,149 (59). 1655. Preferential solvation of ions in binary mixed solvents. S. Janardhanau and C. Kalidas, Rev. Znorg. Chem., 1984,6, 101, (91). 1656. The chemistry of carbonyl sulphide (COS) and its interaction with transition metal complexes. K. K. Pandey and H. L . Nigam, Rev. Znorg. Chem., 1984,6,69, (111). 1657. Gas phase U.V. photoelectron spectroscopy as a tool for the investigation of electronic structures of coordination compounds. C. Cauletti and C. Farlani, Comments Znorg. Chem., 1985, 5,29 (95). 1658. Photoelectron spectroscopy of metal dithiocarbamate, xanthate and dithiophosphate complexes. J. 0 . Hill, R. J . Magee and J. Liesegang, Comments Inorg. Chem., 1985,5,1(63). 1659. The preparation and structure of complexes containing simple sulphur-nitrogen ligands. P. F. Kelly and J. D. Woollins, Polyhedron, 1986,5,607 (159). 1660. Coordination compounds of disulphur dinitride. K. Dehnicke and U. Muller, Transition Met. Chem. (Weinheim, Oer.),1985, 10,361 (50). 3661. Homonuclear cluster compounds of platinum. D. M. P. Mingos and R. W. M. Wardle. Transition Met. Chem. (Weinheim, Ger.), 1985, 10,441 (76). 1662. Phosphorus, arsenic, antimony and bismuth multiply bonded systems with low coordination number -their role as complex ligands. 0. J. Scherer, Angew. Chem., Znt. Ed. Engl., 1984,24,924 (85).

70

index of Review Articles and Specialist Texa

1663. Mechanisms of biological ion transport-carriers, channels and pumps in artificial lipid membranes. P. Lauger, Angew. Chem.,Znt. Ed. Engl., 1985,24,905 (265). 1664. Dinuclear complexes with predictable magnetic properties. 0. Kahn, Angew. Chem., Znt. Ed. Engl., 1985,24,834 (88). 1665. Transition metal polysulphides: coordination compounds with urely inorganic chelate ligands. M. Draganjac and T. B. Rauchfuss, Angew. Chem., Znt. Ed. Eng?, 1985,24,742 (129). 1666. Complexation and demetalation reactions of porphyrins. D. K. Lavailee, Comments Znorg. Chem., 1986,5,155 (45). 1667. Mechanistic information from the effect of pressure on thermal and photochemical substitution reactions. R. van Eldik, Comments Inorg. Chem., 1986,5, 135 (33). 1668. Catalytic fixation of carbon dioxide by metal complexes. S. lnoue and H. Koinama, Rev. Znorg. Chem., 1984,6,291 (53). 1669. Niobium coordination compounds: classification and analysis of crystallographic and structural data. C . E. Holloway and M. Melnik, Rev. Inorg. Chem., 1985,7,162 (198). 1670. Vanadium coordination compounds: classification and analysis of crystallographic and structural data. C. E. Holloway and M. Melnik, Rev. Znorg. Chem., 1985,7,75 (185). 1671. Tantalum coordination compounds: classification and analysis of crystallographic and structural data. C. E. Holloway and M. Melnik, Rev. Znorg. Chem., 1985,7, 1 (161). 1672. Vanadium: a versatile biochemical effector with an elusive biological function. D. W. Boyd and K. Kustin, Adv. Znorg. Biochem., 1984,6,311 (291). 1673. Perspectives on the mechanism of nickel carcinogenesis. M. Costa and J. D. Heck, Adv. Znorg. Biochem., 1984,6,285 (53). 1674. Urea and urease. R. K. Andrews, R. L. Blakeley and B. Zerner. Adu. Znorg. Biochem., 1984, 6, 246 (162). 1675. Copper amine oxidases; structure and function. B. Mondovi and P. Riccio, A d v . Znorg. Biochem., 1984,6,225 (116). 1676. Mossbauer studies on iron proteins. B . H. Huynh and T. A. Kent, Adv. Znorg. Biochem., 1984,6, 164 (178). 1677. Lipoxygenases, non-heme iron containing enzymes. G. A. Veldink and J. F.G. Vliegenthart, A d v . Znorg. Biochem., 1984,6,139 (67). 1678. Elucidation of the structure and metal sequestering properties of metallothionein by n.m.r. D. C. Dalgarno and I. M. Armitage, A d v . Znorg. Biochem., 1984,6, 113 (84). 1679. High spin cobalt(I1) as a probe for the investigation of metalloproteins. I. Bertini and C. Luchinat, Adv. Znorg. Biochem., 1984,6,71 (145). 1680. Structure and mechanism of carboxypeptidase. A . M. W. Makinen, G. B. Wells and S. 0. Kang, Adv. Znorg. Biochem., 1984,6, l(196). 1681. Phosvitin. G. Taborsky, A d v . Znorg. Biochem., 1983,5,236 (214). 1682. Transferrin: a erspective. N. D. Chasteen, Adu. Znorg. Biochem., 1983,5,202 (90). 1683. The catechol bi)oxygenases. L. Que, Adv. Znorg. Biochem., 1983,5,167 (130). 1684. Siderophores. J. B. Neilands, A d v . Znorg. Biochem., 1983,5, 138 (57). 1685. Uteroferrin and the purple acid phosphatases. B. C. Antanaitis and P. Aisen, Adv. Inorg. Biochem., 1983,5, 111 (74). 1686. Ribonucleotide reductase. B. M. Sjoberg and A. Graslund, Adv. Znorg. Biochem., 1983,5, 88 (85). 1687. The chemistry of hemerythrin. R. G . Wilkins and P. C. Harrington, Adv. Znorg. Biochem., 1983,5, 52 (162). 1688. The spatial structure of horse spleen apoferritin. D . W. Rice, G. E. Ford, J. L. White, J. M. A. Smith and P. M. Harrison, Adv. Znorg. Biochem., 1983.5,39 (18). 1689. Ferritin: structure, function and regulation. E. C. Theil, A d v . Inorg. Biochem., 1983,5,1 (137). 1690. Oxygen-18 exchange studies of a ua and oxo ions. H. Gamsjager and R. K. Murmann, Adv. Znorg. Bioinorg. Mech., 1983,2,318 (223). 1691. Molybdenum enzymes: a survey of structural information from EXAFS and EPR spectroscopy. S. P. Cramer, Adv. Znorg. Bioinorg. Mech., 1983,2,260 (137). 1692. Do binucleating ligands have a biological relevance? D. E. Fenton, Adv. Znorg. Bioinorg. Mech., 1983,2,188 (264). 1693. Rapid reaction techniques and bioinorganic reaction mechanisms. R.G . Wilkins, Adv. Znorg. Bioinorg. Mech., 1983,2,139 (288). 1694. Substitution reactions of divalent and trivalent metal ions. T. W. Swaddle, Adv. Znorg. Bioinorg. Mech., 1983,2,96 (243). 1695. Base hydrolysis in transition-metal complexes. M. L. Tobe, Adv. Znorg. Bioinorg. Mech., 1983,2, 1 (269). 1696. Chemistry of tetra- and penta-valent chromium. K. Nag and S. N. Bose, Struct. Bonding (Berlin), 1985,63, 153 (278). 1697. Com lementary spherical electron density model. D. M. P. Mingos and J. C. Hawes, Struct. Bonding (ierlin), 1985,63, l(93). 1698. Spectroscopic properties of the quasi-one-dimensional tetracyanoplatinate(I1) compounds. G. Gliemann and H. Yersin, S~rucf.Bonding (Berlin), 1985,62,88 (181). 1699. Developments in transition metal cluster chemistry - the way to large clusters. G. Schmid, Struct. Bonding (Berlin), 1985,62,5 1 (132). 1700. Metal-metal multiple bonds in dinuclear clusters. F. A . Cotton and R.A. Walton, Struct. Bonding (Berlin), 1985,62,1 (188). 1701. Redox reactions of sulphur-containing amino-acid residues in proteins and metalloproteins. U.Weser, Struct. Bonding (Berlin), 1985,61, 146 (48).

Index of Review Articles and Specialist Texts

71

1702. Phytosiderophores: structures and pro erties of mugineic acids and their metal complexes. Y. Sugiura and K. Nomoto, Strucr. Bonzng (Berlin), 1984,58, 107 (50). 1703. Lysine analogues of siderophores. A . Chimiak and J. B. Neilands, Struct. Bonding (Berlin), 1984, 58,89 (20). 1704. Siderophore mediated absorption of iron. R. C. Hider, Struct. Bonding (Berlin),1984,58,25 (324). 1705. Methodology of siderophores. J. B. Neilands, Strucf. Bonding (Berlin),1984,58, 1(82). 1706. Calculations of the Jahn-Teller coupling constants for dx systems in octahedral symmetry via the angular overlap model. K. D. Warren, Struct. Bonding (Berlin), 1984,57, 119 (20). 1707. A new look at the stereochemistry and electronic pro erties of complexes of the copper(I1) ion. E.J. Hathaway, Struct. Bonding (Berlin), 1984,57,55 68).

,-'

Cumulative Subject Index JOHN NEWTON David John (Services), Farnham Royal, Slough, UK"

This index contains over 25 000 entries to the 6562 text pages of Volumes 1-6. The index covers general types of coordination complex, specific coordination complexes, general and specific organic compounds where their synthesis or use involves coordination complexes, types of reaction (insertion. oxidative addition, etc.), spectroscopic techniques (NMR, IR, etc.), and other topics involving coordination complexes, such as medicinal and industrial applications. Entries where the oxidation state of a metal has been specified occur after all the entries for the unspecified oxidation state. and the same or similar entries may occur under both types of heading. Thus cyanide appears under Chromium complexes: Chromium(0) complexes, Chromium(1) complexes, etc. More specific entries, such as Chromium, hexacyano-, may also occur. Similar ligands may also occur in different entries. Thus a carboxylic acid-metal complex may occur under Carboxylic acid complexes, under entries for specific carboxylic acids, and under the specific metal. Coordination complexes may also be listed in the Cumulative Formula Index.

73

A A 23187 calcium transport, 3,66 Abelsonite structure, 6,850 Abscesses imaging techniques radiopharmaceuticals, 6,992 Absolute configuration, 1,195 amine metal complexes, 2,26 Absorptiometry, 1,549-552,557 Acetaldehyde disproportionation catalysts, 6,304 hydration metal catalysis, 6,474 oximes metal complexes, 2,270 reactions catalysts, 6,303 synthesis ruthenium catalysts, 6,298 Acetaldehyde, aminocobalt(II1) complexes, 6, 188 Acetals benzaldehyde methyl 8-quinolyl hydrolysis, metal catalysis, 6,440,464 cyclic oxidative cleavage, 6,348 hydrolysis metal catalysis, 6,464 metal complexes hydrolysis, 1,428 Acetamide metal complexes, 2,490 Acetamide, N-methylmetal complexes, 2,494 Acetic acid allyl ester hydroesterification, 6,286 carbonylation catalysts, ruthenium complexes, 6,268 2,4-dinitrophenyl ester hydrolysis, cobalt hydroxide catalysis, 6,434 manufacture cobalt catalysts, 6,386 metal complexes, 2,436,438 geochemistry, 6,867 methyl ester carbonylation, 6,267,278 4-nitrophenyl ester hydrolysis, cobalt hydroxide catalysis, 6,434 organometallic ligands, 2,442 synthesis, 1,28 Monsanto process, 6,272 from methanol, 6,278 vinyl ester asymmetric hydroformylation, 6,266 Acetic acid, (carboxymethyl)iminobis(ethyieneimino)tetrametal complexes equilibrium data, 2, 788

stability, 2, 787 Acetic acid, cyanoethyl ester hydrolysis, metal catalysis, 6 , 450 hydrolysis metal catalysis, 6.450 Acetic acid, N-(cyanomethy1)iminodisynthesis, 2,779 Acetic acid, truns-cyclohexanediaminetetrametal complexes, 1,554 Acetic acid, tram-l,2cyclohexylenediiminotetrametal complexes, 2,786 Acetic acid, 1,2-diaminocyclohexanetetraalkaline earth metal complexes, 3,32 Acetic acid, ethylenebis[(carboxymethyl)iminoethyleneiminoltetrametal complexes equilibrium data, 2,788 stability, 2, 787 Acetic acid, ethylenebis(oxyethy1eneimino)tetrametal complexes stability, 2, 786 Acetic acid, ethylenediaminetetra-, 4,253 acid-base equilibria, 2,779 in analysis, 1, 522 complexes Composition, 2,783 coordination numbers, 2,783 solid state structure, 2,783 cyclic derivatives complexes, 2,785 in electroplating, 6, 14 heteroatom derivatives metal complexes, 2,786 homologs binuclear complexes, 2,784 complexes, 2,784 complexes, stability constants, 2,784 protonated complexes, 2,784 masking, 1,558 mercury( II) complexes photographic emulsion stabilizers, 6,98 metal complexes, 1,554 equilibrium constants, 2, 784 formation, 2,781 hydrolytic, 2,783 photographic developer, 6,98 stability constants, 2,782 methyl derivatives complexes, 2,785 phenyl derivatives complexes, 2,785 synthesis, 2,778 Acetic acid, ethylenenitrito[( hydroxyethyl)nitrilo]triiron(II1) complexes, 2,788 Acetic acid, hexamethylenediamine tetrasynthesis, 2,779 Acetic acid, irninodichelating resins mineral processing, 6,824 metal compIexes, 1,554; 2,788

74

75

Cumulative Subject Index

color photography, 6,109 Acetic acid, iodoinhibitor binding dehydrogenases, 5,1016 Acetic acid, mercaptophotographic stabilizer, 6, 103 Acetic acid, nitrilotrimetal complexes stability, 2, 789 stability constants, 2,789 titrimetry, I , 554 synthesis, 2,778 Acetic acid, octamethylcnediarninetetrasynthesis, 2,779 Acetic acid, pentamethylenediamhetetrametal complexes equilibrium constants, 2,784 Acetic acid, tetramethylenediamine tetrametal complexes equilibrium constants, 2,784 synthesis, 2,779 Acetic acid, trimethylenediaminetetrametal complexes equilibrium constants, 2,784 synthesis, 2,779 Acetic anhydride manufacture, 6,330 bicarbonylation of methyl acetate, 6.273 Acetoacetic acid ethyl ester bromination, 1,419 Acetobacterium woodii carbon monoxide dehydrogenase nickel, 6,645 Acetogenic bacteria carbon monoxide dehydrogenase nickel, 6, 645 Acetohydroxamic acid metal complexes spectroscopy, 2,506 Acetohydroxamic acid, N-phenylas metal precipitants, 2,506 metal complexes, 2,507 2-Acetonaphthalene, a-diethylamjnoasymmetric hydrogenation catalysts, rhodium complexes, 6,257 Acetone oximes metal complexes, 2,270,798 synthesis ruthenium catalysts. 6,298 Acetone, acetylantiviral activity, 6,771 deprotonation metal complexes, 1,419 dianion metal complexes, 2,369 hydrogen bonds, 2,365 ions metal complexes, 2,369 metal complexes alcoholysis, 2, 379 C-q', 2,367 C q 3 ,a-bonded, 2,367 charge transfer complexes, 2,386 dienediolate ligands, 2,369 electrochemical synthesis, 2,375 reactions, 1,422 standard enthalpies of formation, 2,366 reactions with metal surfaces, 2,395 reaction with amines aza macrocycles from, 2, 902

tautomers reactions with iron(III), 2,367 trivalent metal complexes polymorphs, 2,371 zinc complexes, 5,967 Acetone, dibenzoylacetylmetal complexes, 2,399 Acetone, hexafluoroacetylmetai complexes decomposition, 2,385 Acetone, selenoylLiquid-liquid extraction, 1,544 Acetone, thenoyltrifluoroliquid-liquid extraction, 1,544 Acetone, trifluorothenoylin analysis, 1,523 Acetonitrile electrochemistry in, 1,493 exchange reactions, 1,286 hydrolysis metal catalysis: 6,449 leaching copper, 6,786 ligand exchange reactions, 2,261 metal complexes hydrolysis, I , 428 reactions catalysts, 6,304 Acetonitrile, aminometal complexes reactions, 6,451 prebiotic systems, 6,871 Acetonitrile, ethylenediaminetetrasynthesis, 2,778 Acetonyl phosphonate metal complexes, 6,473 Ace tophenone, o-rnercaptometal cornpiexes, 2,654 Acetoxylation allylic alkenes, 6,366 aromatic compounds palladium catalyzed, 6,368 dienes palladium catalysts, 6,367 palladium catalyzed, 6,365-368 Acetylacetone alkali metal complexes, 3,25,30 complexes, 1 , 2 2 liquid-liquid extraction, 1,543 Acetylacctone, hexafluorothiometal complexes gas chromatography, 1,560 Acetylactone, trifluorothiomctal complexes gas chromatography, 1,560 Acetylation metal complcxes, 1,421 Acetylene arylation catalysts, palladium complexes, 6,302 carbonylation catalysts, nickel complexes, 6,279 hydroesterification catalysts, palladium complexes, 6,289 re actions catalysts, 6,298 reduction vanadium(I1) complexes, 3,471 Acetylene, bis(diphenylphosphin0)-, 2,993 Acetylene, cyanoprebiotic systems, 6, 871 Acetylene, diphenyl-

Acetylene

Acetylene hydrogenation catalysts, rhodium complexes, 6,243 Acetylene, phenylreduction catalysts, rhodium complexes, 6, 244 Acetylenedicarboxylic acid dimethyl ester cycloaddition reactions, 1,458 Acetyl phenyl phosphate hydrolysis metal catalysis, 6,443 Acetyl phosphate hydrolysis metal catalysis, 6,443 Acid alizarin black SN metallochromic indicator, 1,556 x-Acidity of ligands for technates, 6,979 Acid phosphatases, 2,773 Acid salts, 3, 2 Aconitase, 6,475,632 Acoustic emission diazine metal complexes, 2,80 Acrylic acid asymmetric hydrogenation rhodium complexes, 6,251 ethyl ester hydrogenation, 6,244 hydrogenation catalysts, iridium complexes, 6, 246 methyl ester hydroformylation, 6,261 Acrylic acid, 2-acetoxyethyl ester asymmetric hydrogenation, 6,256 Acrylic acid, methyl ester carbonylation, 6,271 Acrylic acid, a-phcnylasymmetric hydrogenation catalysts, rhodium complexes, 6,250 Acrylonitrile hydrolysis metal catalysis, 6,450 metal complexes, 2,263 Actinide complexes, 3,1129-1220 applications, 6, 1024 coordination numbers, 3,1131 cupferron, 2,510 dimethyl sulfoxide IR spectra, 2,490 geometry, 3, 1131 kinetic stability, 3, 1130 phosphines SHAB theory, 1040 phthalocyanines, 2, 864 steric effects, 3, 1130 thiocyanates, 2,236 Actinide(II1) complexes, 3, 1131-1136 amides, 3,1133 ammines, 3,1131 antipyrine, 3,1134 aqua, 3,1133 aromatic hydroxy acids, 3,1134 carbonates, 3,1134 carboxylates, 3,1134 N,N-diethyldithiocarhamates, 3, 113.5 N,N-dimethylformamide, 3,1134 ethers, 3, 1134 halogens, 3,1135 hydrides, 3, 1135 hydroxides, 3,1133 p-ketoenolates, 3, 1134

Cumulative Subject Index

76

mixed donor atom ligands, 3,1136 multidentate macrocyclic ligands, 3, 1136 nitriles, 3, 1133 nitrogen ligands, 3, 1131 oxides, 3,1133 oxoanions, 3, 1134 oxygen ligands, 3,1133 pyridines, 3, 1133 pyrimidones. 3,1134 selenides, 3, 1135 sulfato, 3, 1134 sulfides, 3,1135 sulfur ligands, 3,1135 tellurides, 3, 1135 tribromides, 3,1135 trichlorides, 3, 1135 trifluorides, 3,1135 triiodides, 3: 1135 Actinide(1V) complexes, 3, 1136-1178 alcohols, 3, 1146 aldehydes, 3,1151 aliphatic amines, 3: 1137 aliphatic hydroxy acids, 3,1159 alkoxides, 3, 1147 amides, 3, 1161 amine oxides, 3,1165 ammines, 3, 1137 aqua, 3,1144 aromatic amines, 3>1137 aromatic hydroxy acids, 3, 1159 arsine oxides, 3,1170 arsines, 3,1144 aryl oxides, 3, 1147 2,2’-bipyridyl?3, 1139 carbamates, 3, 1159 carbonates, 3: 1155 carboxylates chelating, 3, 1155 carboxylic acid hydrazides, 3, 1164 catecholates, 3,1150 complexones, 3, 1175 crowu ethers, 3.1178 cryptands, 3,1178 cupferron, 3,1170 cyanides, 3,1136 2,6-diacetylpyridine bis(p-methoxybenzoyl hydrazone), 3,1177 dialkylamides, 3, 1141 diamines, 3, 1137 diarylamides, 3, 1141 dicarboxylates, 3,1157 dipyridylamines, 3, 1140 dipyridylethanes, 3+1140 disclenocarbamatcs, 3, 1173 dithiocarbamates, 3, 1172 dithiolates, 3,1172 dithiophosphinates, 3,1173 esters, 3, 1151 ethers, 3,1150 ethylenediamine, 3, 1137 halides, 3, 1173 halogeno, 3, 1173 hexafluoroacetonylpyrazolides, 3, 1177 hydrazines, 3: 1137 hydrides, 3, 1175 hydrogen, 3,1175 hydroxamates, 3>1170 8-hydroxyquinolines, 3,1177 hyroxides, 3,1146 imidazole, 3,1140 isonitriles, 3, 1136 isoquinoline, 3,1139 P-ketoenolates, 3, 1148

77 ketones, 3,1151 monocarboxylates, 3,1153 monothiocarbamates, 3, 1172 nicotine, 3,1138 nitrates, 3, 1151 nitriles, 3, 1143 nitroalkanes, 3, 1159 nitrogen ligands, 3,1137 oxalates, 3, 11.56 oxides, 3,1146 oximes, 3, 1143 oxohalides, 3,1173 peroxides, 3, 1146 1,lO-phenanthroline, 3, 1140 phenols, 3,1146 phosphates, 3,1152 phosphines, 3, 1144 phosphine selenides, 3, 1173 phosphorus oxides, 3,1165 phthalocyanine, 3, 1178 piperazine, 3, 1141 piperidine, 3, 1139 PolypyrdZOl-l-yl borates, 3,1142 pyrazine, 3, 1140 pyridine, 3, 1139 pyrrolidines, 3, 1338 quinoline, 3, 1139 quinones, 3,1150 Schiff bases, 3, 1175 selenates, 3, 11.53 selenides, 3,1173 selenites, 3, 11.53 selenocyanates, 3, 1142 silyl oxides, 3,1147 sulfates, 3, 1152 sulfides, 3, 1170 sulfur oxides, 3, 1170 tellurates, 3, 1153 tellurides, 3, I I73 tellurites, 3, 1153 tcrpyridyl, 3,1140 tetracarboxylates, 3,1159 tetrahalides, 3, 1173 thiocarboxamides, 3, 1172 thiocyanates, 3, 1142 thioethers, 3, 1172 thiohydroxamates, 3,1172 thiols, 3, 1171 thioureas, 3, 1172 triazenes, 3, 1142 tropolonatcs, 3, 1148 ureas, 3,1143,1164 Actinide(V) complexes, 3, 117S1187 alcohols, 3, 1180 aliphatic amines, 3, 1179 aliphatic hydroxyacids, 3, 11S3 alkoxides, 3, 1181 amides, 3,1183 amines, 3,1179 aqua, 3,1179 aromatic hydroxy acids, 3,1183 arsenates, 3,1182 arsenic ligands, 3, 1179 aryl oxides, 3,11S1 2,2'-bipyridyl, 3, 1179 carbonates, 3,1183 carboxylates chelating, 3, 1183 complexones, 3, 1187 dihydroazirine, 3, 1179 diphenyl diselenide, 3,1185 diphenyl ditelluride, 3,1185 dithiocarbamates, 3,1184

Cumulative Subject Index

Actinide(V1) complexes

esters, 3,1182 ethers, 3,1182 halogeno, 3,1186 hydroxides, 3, 1180 8-hydroxyquinolines, 3,1187 iodates, 3, 1182 isoquinoline, 3, 1179 P-ketocnolates, 3, 1182 ketones, 3,1182 mixed donor atom ligands, 3, 1187 monocarboxylates, 3,1182 1&naphrhyridine, 3, 1179 nitrates. 3,1182 nitriles, 3, 1179 oxalates, 3, 1183 oxides, 3,1180 oxohalides, 3,1185, 1186 pentahalides, 3, 1185 1,lO-phenanthroline, 3,1179 phenazine, 3,1179 phosphates, 3,1182 phosphine selenides, 3, 1185 phosphine sulfides, 3,1185 phosphorus oxides, 3,1184 phthalazine, 3, '1.179 polycarhoxylates, 3, 1183 pyrazine, 3: 1179 pyrazole, 3,1179 pyridine, 3,1179 quinoline, 3,1179 selenates, 3, 1182 silyl oxides, 3, 1181 sulfates, 3, 1182 sulfur oxides, 3, 1184 thiocarboxylates, 3, 1184 thiocyanates, 3,1179 thiols, 3, 1184 thiourea, 3,1184 trichlortiacryloyl chloride, 3, 1183 tropolonatcs, 3,1182 Actinide(V1) complexes, 3,1187-1215 alcohols, 3, 1193 aldehydes, 3, 1196 aliphatic amines, 3; 1187 aliphatic hydroxyacids, 3, 1202 alkoxides, 3, 1194 amides, 3,1204 amine oxides, 3,1206 amino acids, 3,1212 ammines, 3,1187 aqua, 3,1192 aromatic amines, 3, 1187 aromatic hydroxy acids, 3, 1203 arsenates, 3, 1197 arsenic oxides, 3,1207 aryl oxides, 3,1194 2,2'-bipyridyl, 3, 1190 4,4'-bipyridyl, 3, 1190 carbamates, 3,1202 carbonates, 3,1201 carboxylates chelating, 3, 1198 carboxylic acid hydrazides, 3, 1205 catecholates, 3, 1195 complexones, 3,1213 crown ethers, 3,1214 CryptdndS, 3: 1214 cupferron, 3,120g cyanates, 3,1191 cyanides, 3, 1187 diamines, 3,1189 dicarboxylates, 3,1201 dioxo

Actinide(V1) complexes

Cumulative Subject Index

seven-coordination, 3,1131 dipyridylalkanes, 3, 1190 di-2-pyridylamine, 3, 1190 dithiocarbamates, 3,1209 dithiolates, 3,1210 dithiophosphinates, 3, 1210 esters, 3, 1196 ethers, 3,1195 ethylenediamine, 3, 1189 hexacarboxylates, 3,1202 hexahalides, 3,1210 hydrazines, 3, 1188 hydroxamates, 3,1208 hydroxides, 3,1193 8-hydroxyquinoline, 3, 1213 imidazole, 3,1190 isonitfiles, 3, 1187 isoquinoline, 3, 1190 P-ketoenolates, 3, 1195 ketones, 3,1195 5-methylpyrazole, 3, 1191 monocarboxylates, 3,1198 monothiocarbamates, 3,1209 nitrates, 3, 1196 nitriles, 3, 1191 nitroalkanes, 3, 1202 nitroarenes, 3, 1202 oxalates, 3, 1201 oxides, 3, 1193 oximes, 3,1192 oxyhalides, 3,1211 peroxides, 3, 1193 1,lO-phenanthroline, 3,1190 phosphates, 3,1197 phosphites, 3, 1197 phosphorus oxides, 3,1207 phthalocyanine, 3, 1214 piperidine, 3,1190 pyrazine, 3,1191 pyridinc, 3,1189 quinoline, 3, 1190 quinones, 3, 1195 Schiff bases, 3, 1212 selenates, 3, 1197 silyl oxides, 3, 1195 sulfates, 3, 1197 sulfur oxides, 3, 1207 superoxides, 3,1193 superphthalocyanine, 3,1214 tellurites, 3, 1197 thiocyanates, 3, 1191 thioureas, 3, 1210 triazenes, 3, 1191 tropolonates, 3, 1195 uranates, heptafluoro-, 3, 1211 urea, 3, 1205 xanthates, 3, 1210 Actinide(VI1) complexes, 3, 12141215 Actinide ions , hydrolysis, 6,886 Actinides carboxylic acid complexes recovery from nuclear fuel waste, 6,960 dissolution reprocessing irradiated nuclear fuel, 6, 927 in environmental waters, 6,961 extraction 9 !% nuclear fuel processing, 6, Purex process, enthalpy change, 6,952 hydroxides, 6,887 irradiated nuclear fuel separation, 6,925 lifespan, 6,883

magnetic properties, 1,263 in natural waters computer simulation, 6,962 occurrence, 6,883 oxidation states, 3, 1130 Purex process, 6,945 recovery from nuclear fuel waste, 6,960,961 recovery from nuclear fuel waste, 6,959 Actinometry chemical, 1,409 Actins, 2: 973 alkali metal complexes, 3?64 cation transport, 6,554 Activators mineral processing, 6.782 Acylates y,-ligands electrophilic attack. 2,343 Acylation 1,3-diketonemetal complexes, 6,204 metal-catalyzed, 6,439 metal complcxcs, I, 419 a-A cy Ioin oximes metal complexes, 2,797 Acyl transfer reactions metal catalysis, 6,471 Adamantanc metal complexes structure, 2,301 Adamantanoid cages, 1, 151 Adenine cadmium complexes, 5 : 957 metal complexes, 2, 92 zinc complexes, 5, 956,957 Adenochrome iron complexes, 2,969 Adenosine diphosphate magnesium chelates, 6,579 metal complexes. 6,445 Adenosine-2’-monop hosphate lanthanide complexes NMR,3,1103 Adenosine-3 ‘monophosphate lanthanide complexes NMR,3,1103 Adenosine-5’-monophosphate lanthanide complexes NMR,3,1104 Adenosine phosphates metal complexesl 2; 977; 6,445 Adenosine 5’-triphosphate alkali metal complexes, 2,977; 3,34 dephosphorylation, 2,978 hydrolysis chrornium(TT1) complexes, 6,447,448 cobalt(II1) complexes, 6,447,448 magnesium chelates, 6,579 metal complexes isomers, 1,203 polyammonium macrocyclic complexes, 2,950 vanadyl complexes, 3,568 Adenylate cyclase activation magnesium ions, 6,584 vanadium, 6,666 Adipic acid manufacture cobalt catalysts, 6 : 385 Adiponitrile synthesis by hydrocyanation of butadiene, 6,297

79 Adriamycin, 6,729 Adsorption chelates oxide minerals, 6.782 inorganic complexes geochemistry, 6,850 Advanced Gas Cooled Reactor, 6,883 Aequorin calcium, 6. 595 Aerobactin, 6,675 animal infections, 6, 679 iron complexes, 2,972 structure, 6,678 Aerobic carboxydobacteria terminal oxidases, 6,698 Aggregation reactions cluster synthesis, 1, 171 Aging trace elements and, 6,773 Agrobactin, 6,676 Alamine-336 liquid-liquid extraction, 1,548 Alane, 3,123 amine adducts, 3,107 phosphine adducts, 3, 111 Alane, alkoxy-, 3, 124 Alane, amino-, 3, 109 Alane, imino-, 3, 109 Alanine ethyl ester hydrolysis, metal catalysis, 6.421 metal complexes, 6.858 prebiotic systems, 6,872 stereoselectivity, 2,755 ore formation, 6, 869 @-A1anin e metal complexes prebiotic systems, 6,872 Alanine, levo-dihydroxyphenylmanufacture, 1,28 Albrittonite structure, 6,847 Albumins copper complexes, 6,671 blood, 2,965 metal complexes, 2,770 trace metal complexes, 2,975 zinc transport, 6,672 Alchemists' gold, 5, 1048 Alcohol dehydrogenase, 5,1008 binding of substrate, 6,609 coenzyme binding, 6,608 mechanism kinetics, 6,610 metal for zinc substitution, 6, 609 model systems for metal catalysis, 6,475 zinc, 6,608 zinc-carbonyl mechanism, 5,1003 Alcohols amino polynuclear complexes, 2,794 carbonylation catalysts, palladium complexes, 6,280 imino polynuclear complexes. 2.794 oxidation chromium-oxo complexes, 6.351 copper catalysts, 6,393 palladium catalysts, 6,371 permanganate, 6,355 ruthenium tetroxide. 6,357

Cumulative Subject ladex

Alkali metal complexes

oxidative carbonylation palladium catalyzed, 6,'369 oxycarbonylation copper catalysts, 6,395 reactions with metal atom vapors, 2,337 with metal halides, 2,337 with metals, 2,336 thiol-substituted metal complexes, 2,804 Aldehyde dehydrogenase activators potassium ions, 6,562 Aldehyde oxidase molybdenum, 6,658 Aldehydes hydrogenation catalysis, rhodium complexes, 6,241 catalysis, ruthenium complexes, 6,232, 235 reactions with metal alkyls, 2,341 Aldolase zinc-carbonyl mechanism, 5,1003 Aldol condensations amino acid metal complexes, 6,466 amino acids metal catalysis, 6,468 crossed, 6,217 Aldol reactions amino acids metal complexes, 1,424 Alginates metal complexes geochemistry, 6,868 Aliquat-336 liquid-liquid extraction, 1,548 Alizarin, 6,35 history, 1 , 2 met2llochromic indicator, I , 557 Alizarin complexan metallochromic indicator, 1,557 Alizarin fluorine blue metallochromic indicator, 1,557 Alkali metal alkoxides physical properties, 2,345 reactions filth metal halides, 2,338 Alkali metal complexes, 3, 1-70 acid anions, 3,30 acid salts, 3: 30 amides, 2,162,493 arsines, 2, 1005 bipyridyl, 3, 13 crown ethers cavity size, 3,38 cryptates, 2,938 alkali metal transport, 3,55 cyanides synthesis, 2 , 9 diacetamide, 3,15 l,Zdiaminoethane, 3,11 1,3-diketones, 2,375 1,2-&methoxyethane, 3, 14 ethylene glycol, 3,14 hexamethylphosphoramide, 3 , 6 hydration energies, 3 , 3 ionic radii, 3, 3 macrocyclic complexes, 2,920,928 organometallic compounds, 3, 10 phenacylkojate, 3,15 o-phenanthroline, 3,13 phosphine oxides, 3 , l S phosphines, 2,991

Alkali metal complexes

Cumulative Subject Index

phosphoramides, 3, 15 polyamines, 3,12 polyethylene polyamines, 3,11 Schiff bases, 3,28 solvates, 3,s stibines, 2. 1008 thiourea, 3 , 6 tri-n-octykphosphine oxide, 3 , 6 triphcnylphosphine oxide, 3 , 6 Alkali metal fluoroboratcs, 3,101 Alkali metal ions enzyme activators, 6,559 structure stabilizers, 6,562 Alkali metal phenoxides reactions with metal halides, 2, 338 Alkali metals coordination numbers, 3 , 3 ionic potentials, 3, 3 ionic size, 3 , 3 solvation by dimethyl sulfoxide, 2,488 Alkaline earth metal complexes, 3,6-10 amides, 2,493; 3 , 9 anions, 3, 10 cations diacetamide, 3, 15 c r o u ~ethers ~ cavity size, 3, 38 diacetamide, 3, 15 1.3-diketones, 2,375 1,2-dimethoxyethane, 3, 14 hydration energies, 3 , 3 ionic radii, 3 , 3 macrocyclic complexes, 2,920. 928 organometallic, 3, 10 phenacylkojate, 3,15 o-phenanthroline, 3,13 phosphinc oxidcs, 3, 15 phosphoramidcs, 3, IS Schiff bases, 3,28 Alkaline earth metals coordination numbers, 3 , 3 ionic potentials, 3, 3 ionic size, 3 , 3 Alkaline phosphatase, 2,774 mechanism, 6,612 metal substitution, 6,611 structure, 6,611 zinc, 5,1006; 6,610 Alkanes dehydrogenation catalysts, 2,711 hydroxylation cobalt catalysts, 6, 388 iron catalysts, 6,282,380,383 manganese catalysts, 6,377 vanadium-alkyl peroxide catalysts, 6,341 vanadium-peroxo complexes, 6,333 oligomerization carbonyl nickel complexes, 5,lO oxidation manganese(II1) salts, 6,376 permanganate, 6,356 Alkanes, bis(diphenylphosphin0)-, 2 993 Alkanesulfonic acid, mercaptophotographic fixer, 6, 100 Alkenes acetalization, 6,365 ace toxylation palladium catalysts, 6,365-368 activated hydrogenation, 6,236,237,243

allylic acetoxylation palladium catalysts, 6, 366 amination, 2,182 arylation catalysts, palladium complexes, 6,301 palladium catalysts, 6. 371 asymmetric hydrogenation catalysts, 6,250 catalysts, rhodium complcxcs, 6,256 carhonylation isornerixatiun, 6,286 cyclic oxidation, 6,349 epoxidation alkyl hydroperoxide catalysts, 6,343,344 chromium-oxo complexes, 6,352 iodosylbenzene, 6,377 iron catalysts! 6,380, 381 molybdenum catalysts, 6,330 sodium hypochlorite, 6.378 vanadium-alkyl peroxide catalysts, 6, 341, 342 hydrocarboxylation catalysts, palladium complexes, 6,285 hydroesterification catalysts, platinum cornplexcs, 6,291 hydroformy lation catalysis, rhodium complexes, 6,260 hydrogenation catalysts, iridium complexes, 6,246 catalysts, ruthenium complexes, 6,232 nitrosyl rhodium complexes, 2,106 Wilkinson’s catalyst, 6,239 lanthanide shift reagents, 3, 1104 oligomerization nickel(0) complexes. 5 , 16 oxidation cobalt catalysts, 6,384,387 copper catalyst’s,6,390 manganese(II1) salts, 6,375 osmium-oxo compounds, 6,358 osmium tetroxide, 4,590 palladium chloride catalysts, 6, 363 palladium-nitro complex catalysts, 6,373 permanganate, 6;355 selenium dioxide; 6,360 oxidative cleavage ruthenium tetroxide, 6,357 oxidative coupling palladium catalysts, 6,371 oxycarbonylation palladium catalyzed, 6 : 368 polymerization tcmplatc reactions. 1: 447 prochiral asymmetric epoxidation, 6,381 reactions for metal catalysis. 6,475 with metal alkoxides, 2,354 with metal hydrides, 2,707 reduction with formic acid, catalysts, 6, 303 terminal hydrogenation, 6,234,238,242,243 selective oxidation, 6,347 Alkenyl acetate epoxidation, 6 +383 Alkoxides amino polynuclear complexes, 2,794 ligands organometallic chemistry, 2,355 perfluoro metal, 2,343

80

81 Alkylation acetylacetone metal complexes, 6,205 amines catalysts, rhodium complexes, 6,277 catalysts rhenium complexes, 6,298 coordinated nitrogen atoms macrocycles, 1,444 coordinated sulfur and nitrugen, 1,417 P-diimine metal complexes, 6, 169 1,3-diketone metal complexes, 6,203 Alkyl complexes metal hydroxides chemistry, 2,358 Alkyl halides reduction vanadium(I1) complexes, 3, 469 Alkylidene complexes metal hydroxides chemistry, 2,357 Alkylidyne complexes metal hydroxides chemistry, 2, 357 Alkyl peroxides do metal oxidation catalysts, 6, 341-346 Alkylperoxo complcxcs catalysts oxidation, 4,341-350 Group VI11 metal oxidation catalysts, 6,347-350 Alkyne complexes metal hydroxides chemistry, 2,357 Alkynes allylic dihydroxylation sclcnium dioxide, 6,360 carbonylation catalysts, palladium cornplcxcs, 6,288 hydrogenation catalysts, rhodium complexes, 6, 242 oxidation copper catalysts, 6,390 ruthenium tetroxide, 6,358 oxidative carbonylation catalysts, palladium complexes, 6,289 reactions niobium(II1) complexes, 3: 661 osmium tetroxide, 4,590 tantalum(II1) complexes, 3,661 with mctal hydridcs, Z1 709 Allcnc reactions catalysts, 6.307 reactions with carbon dioxide catalysts, palladium complexes, 6,296 Allogons, 1,206 Alloisoleucine epimerization geochemistry. 6,866 Allothreonine epimerization geochemistryl 6, 866,867 metal complexes prebiotic systems, 6, 872 Alloys electroplating, 6, 13 Allylaminc cyclization carbonylation and, 6,277 Allysum nickel uptake, 6,648 Alteromonas haloplanktis

Cumulative Subject In.dex

Aluminum complexes

enzyme activators sodium ions, 6,559 Alumina, 3, 112 dissolution, 6,787 slag viscosity, 6 , 833 Aluminates stability. 6,787 structure. 6,788 Aluminates, fluoro-, 3, 121 Aluminates, heptachlorodi-, 3, '123 Aluminates, tctrahalo-, 3, 122 Aluminohydrides, 3, 124 Ahminosilicates ion exchange resins, 6,814 metal complexes geochemical melts, 6,855 Aluminoxanes, 3,113,114 Aluminum cumulative toxicity, 3, 118 gravimetry, 1,528,529 hydrometallurgy, 6,787 reactions with phenols, 2,336 removal Alzheimcrk discase, 6,770 Thorcx process, 6,957 Aluminum?alkylalkuxides synthesis from, 2,342 Aluminum, bis(acetonitri1e)trinitratostructure, 1,28 Aluminum, tribromotris(tribromostibine)structure, 1,28 Aluminum, trichlorobis(tetrahydrofuran)structure, 1,45 Aluminum; trichlorotris(trimethy1amine)structure, 1,28 Aluminum, tris(acety1acctonato)-, 3,114 structure, 1,65 Aluminum, tris(tropolona1o)-, 3, 115 Aluminum alkoxides physical properties, 2,345 synthesis, 2,336 Aluminum borohydride phosphine adducts, 3,111 Aluminum bromide, 3,121 Aluminum chloride, 3, 121 Aluminum complexes, 3, 105-142 acetylacetone synthesis, 2,378 alkoxides, 3, 113 alkoxyhydrides, 3, 114 amides, 2,164 structure, 2, 171 amido, 3, I O Y amines, 3, IU7 ammincs, 3,107 aqua, 3,112 arsenates, 3, 115 ATP, 3,116 azides, 3,110 borates, 3, 115 borohydrides, 3,125 bromates, 3,117 carbonates, 3.115 carboxylates, 3, 117 chlorates, 3, 117 crown ethers, 3,119, 126 cyanates, 3, 110 cyanides, 3, 106 dialkyl sulfides, 3, 120 1,3-dikclones ligand exchange reactions, 2,381 dimethyl sulfoxide, 3,119

Aluminum complexes edta, 3,126 ethers, 3,118 fluorides, 3,120 fluorophosphato, 3,116 germyl, 3,107 hexafluoroacetylacetone isomerization, 2,382 hydrides, 3,123 hydroxides, 3,112 imido, 3,109 iodates, 3, 117 P-ketoenolates, 3,114 metalla-P-diketones, 3,115 mixed halides, 3,121 mixed oxides, 3,112 molybdates, 3, 116 nitrates, 3, 115 nitriles, 3,111 oxides, 3, 112 oxy anions, 3,115 perchlorates, 3, 117 periodates, 3, 117 phosphates, 3, 115 phosphines, 3,111 phosphorus oxychloridc, 3,114 phthalocyanines, 2,863; 3, 126 porphyrins, 2,821; 3,126 Schiff bases, 3, 125 selenates, 3, 116 selenides, 3,120 silicates, 3, 115 silyl, 3,107 silyl phosphine, 3,112 sulfates, 3, 116 sulfides, 3,120 tellurates, 3,116 tellurides, 3,120 thiocyanates, 3, 110 tungstates, 3, 116 Alurninum(II1) complexcs citric acid, 2,476 fulvic and humic acids, 6,859 minerals, 6,846 naphthoic acid, 2,483 Aluminum compounds catalysts alkene epoxidation, 6, 346 Aluminum fluorides minerals, 6,846 Aluminum halides antimony halide complexes, 3,112 2,2'-bipyridyl, 3, 108 bismuth halides complexes, 3,1 12 morpholine adducts, 3, 108 1,lO-phenanthroline adducts, 3,108 2,2':6',2"-terpyridyl, 3, 108 Aluminum hydroxide, 3,112 Aluminum hydroxyfluorides minerals, 6, 846 Aluminum iodide, 3,121 Aluminum isopropoxide, 3,114 complexes, 3,108 Aluminum methoxide, 3, 114 Aluminum nitride, 3,104 Aluminum phosphide, 3, 111 Aluminum trihalides pyridine adducts, 3,108 Aluminum trisoxinate in gravimetry, 1,524 liquid-liquid extraction, 1,545 Alzheimer's disease aluminum removal, 6,770

CumulativeSubject Index Amavadin, 3,548,568 Amberlite LA 2 solvent extraction palladium and platinum, 6, 809 Americium breeder reactor fuels Purex process, 6,955 reprocessing, 6,954 Purex process, 6,946,950 sequestering agents, 6,962 Americium(II1) complexes carbonates recovery from nuclear fuel waste, 6,961 cupferron, 2,510 humic acid stability, 6,961 salicylic acid crystal structure, 2,481 Americium ions recovery from nuclear fuel waste, 6,960 Amex process, 6,911 uranium ore processing, 6, 903 Amide oximcs mctal complexes, 2.274 Amides amino metal complexes, 1,440 amino acids hydrolysis, catalyzed, 6, 425 hydrolysis, metal-cataiyzed, 6,431 carboxylic acids hydrolysis, metal-catalyzed, 6,437 a-keto synthesis by double carbonylation, 6,284 metal complexes hydrolysis, 1,428 as solvents, 2,490 synthesis by carbonylatiun, 6,284 toxicity, 2,491 Amidines heterobinuclear complexes bridging ligands, 2,202 metal complexes, 2,195-206,275 bridging ligands, 2,198,200 chelate bonded, 2,203 insertion reactions. 2, 197 monodentate, 2, 196 NMR, 2,197 reactions, 1,424 spectroscopy, 2,196 Amido complexes, 2,161-184,487-501 bond lengths, 2,490; 493 0-bridging, 2,491 carbon-hydr0ge.n bond activation, 2, 183 elcctronic spectra, 2, 169 homoleptic prototypal structures, 2, 170 insertion reactions, 2, 180 IR spectroscopy, 2,169,493 ligand field parameters, 2,494 ligand to metal n-bonding, 2,176 6-mercapto, 2,655 metal-nitrogen bond reactivity, 2, 179 metal-nitrogen bond rotational barrier, 2, 177 metathetical exchange reactions, 2, 181 molecular complexities, 2, 168 molecular structure, Z1170 NMR, 2,169,493 photoelectron spectroscopy, 2, 178 polynuclear structure, 2, 173

82

83

CumulativeSubjecl Index

properties, 2, 168 reactions, 2,179 with acidic hydrogen-containing molecules, 2,179 with metal carbonyls, 2, 181 solid state structure, 2, 170 spectator ligands, 2,179 stretching wave numbers, 2,493 structure, 2,176 synthesis, 2,162-168 thio N-substituted, 2,804 volatilities, 2, 168 Amidoximes metal complexes, 2,797 Amination alkenes, 2,182 Amine oxidases, 6,700 copper, 6,655 Amines alkylation catalysts, rhodium complexes, 6,277 base metal salts solvent extraction, 6,802 coordinated secondary alkylation, 1,417 cyclic complexation, thermodynamics, 2,911 metal complexes, 2,23-59 reactions, 2,24 stoichiometry, 6,802 molybdenum Complexes solvent extraction, 6,806 N-oxides metal complexes, 2,494 metal complexes, bridging, 2,496 oxycarbonylation copper catalysts, 6,395 reactions with dicarbonyl compounds aza macrocyclcs from, 2,902 reactions with monocarbon$ compounds aza macrocycles from, 2,900 secondary carbonylation, 6,268 iron complexes, solvent extraction, 6,803 oxycarbonylation, 6,395 solvent extraction, platinum group metals, 6, 808 zinc complexes, extraction, 6,804 solvent extraction platinum group metak. 6,807 tertiary cobalt complexes, solvent extraction, 6,804 molybdenum complexes, sotvent extraction, 6,806 in photochemical hydrogen production from water, 6, 510 selective oxidation, 6,346 selectivity series, metal extractions, 6,802 solvent extraction, 6,805 solvent extraction, platinum, 6,808 tungsten complexes, solvent extraction, 6, 806 vanadium complexes, sotvent extraction, 6,805 tertiary oxides alkene epoxidation, iron catalysts, 6,282 in thorium ore processing, 6.915 tungsten complexes solvent extraction, 6,805 uranium complexes solvent extraction, 6 , go4 Amino acids cadmium complexes, 5,938 amides hydrolysis, 6,414 hydrolysis, metal-catalyzed, 6,425 chirality metal complexes, 2,741

Aminomethylation

complexes linkage isomers, 1,186 copper complexes blood plasma, 2,965 esters hydrolysis, 1,428; 6,414,416 metal complexes, 2,757 esters, metal complexes hydrolysis, stereoselectivity ,6,424 formation nitrile metal complexes in, 2,265 hydrolysis catalysis by labile metal ions, 6,414 ionization constants, 2, 741 metal complexes, 2,73%774 animal fluids, 2,964 asymmetric synthesis, stereoselectivity and, 2,754 bidentate coordination, 2,740 biology, 6,546 a-C-H bond activation, 2,756 formation, 2,752 formation constants, 2,742 geochemistry, 6,866 geometrical isomerism, 2,753 methylene activation, 1,424 monodentate coordination, 2,740 naturally occurring, 2,964 occurrence, 2,962 optical isomerism, 2,753 optical resolution, stereoselectivity and, 2,754 oxidation, 2,758 prebiotic systems, 6,871 reactions, 6,466 reactivity, 2, 755 reduction, 2,758 stereochemistry, 2,753 stereoselectivity, 2,753 stereoselectivity, asymmetric synthesis and, 2,754 stereoselectivity, optical resolution and, 2, 754 structures, 2,744 tridentate chelation, 2,746

mono esters, hydrolysis, 6,416 prebiotic systems, 6,872 racemization metal complexes, 2,757 reactions osmium tetroxide, 4,590 Schiff bases metal complexes, 2,751,752 synthesis metal catalysis, 6,468 ternary metal complexes, 2,751 formation, 2, 750 thioethers metal complexes, 2,557 zinc complexes, 5,938 a-Amino acids amides metal complexes, 6,214 carboxylate derivatives metal complexes, 6,212-216 esters hydrolysis, metal complexes, 6,212 metal complexes reactions, 6,206-212 synthesis imine chelates, 6 , 187 Aminolysis mechanism, 2,266 Aminomethylation catalysis transition metal complexes, 6,274

Amino peptidases

Cumulative Subject Index

Amino peptidases zinc, 6,606 Amino sugars metal complexes geochemistry, 6,867 Ammonia in alcohol reactions with metal halides. 2,338 from dinitrogen, 2,101 in electroplating, 6,14 hydrometallurgy, 6,786 liquid solvent, 1,27 metal complcxes, 2,23-59 bond distances, 2,26 oxidation Nitrosornonas europaea, 6,727 Ammonium chloride structure, 1,5 Ammonium ions macromonocyclic complexes, 2,943 Ammonium ions, alkylaffinity series inorganic anions, 6,802 platinum group metal comptexes affinity series, 6,808 in reprocessing irradiated nuclear fuel, 6,929 Ammonium ions, methyltriphenyh gravimetry, 1,534 Ammonium ions, tetradecyldimethylbenzylliquid-liquid extraction, 1,548 Ammonium molybdate, 3,1257 Ammonium nitrate, hydroxylas plutonium(1V) reductant Purex process, 6,949 Amphotericin B metal complexes, 2,973 a-Amylase zinc, 6,607 Anabaena spp. ribonucleotide reductase, 6,(a2 Analysis iron complexes, 4,1180 Analytical separations metal sulfides, 2,526 Anation, 1,307 dissociative mechanism, 1,310 mechanism, 1,309 solid state, 1,468 Ancylite structure, 6,848 Andersonite, 6,890 structure, 6,848 Anderson structure, 3,1044 1,4-Androstadiene-3,17-dione hydrogenation catalysis, ruthenium complexes, 6,232 Anemia iron complexes, 6,763 Angiotensin metal complexes, 2,968 Angular overlap model, 1,225 crystal field theory and, 1,228 halogen-metal bonding, 2,677 magnetism, 1,269 f-orbital, 1, 231 regular octahedron, 1,227 tetrahedron, 1,227 Anhydrides hydrolysis mctal catalysis, 6,463 zinc hydroxides, catalysis, 6,443 Aniline carbonylation

catalysts, palladium complexes, 6,ZW metal complexes, 2,59 Aniline, N-(benzaldehyd0)metal complexes structure, 2,719 Aniline, p,p'-methylenedialkali metal complexes, 3,14 Aniline, pyridylazometal complexes color photography, 6,108 Aniline, N-2-pyridylmethylenehydrolysis metal catalysis, 6, 460 Aniline, N-(saliqla1dchydo)photochromism, 2,718 Aniline N-salicylidenehydrolysis metal catalysis. 6,460 Aniline, N-sulfinylmetal complexes, 2,804 Anils circular dichroism, 2,717 malondiaidehyde metal complexes, 6,83 ORD, 2,717 thermochromisrn, 2,717 Animals infections microbial iron wansport, 6,679 Anion exchange resins mineral processing, 6,815,817,820 Anionic complexes macrocycles, 2,921,948 Antamanide alkali metal complexes, 3,64 metal complexes, 2,970 Anthracene oxidation copper catalysts, 6,391 rhodium complex catalysts, 6,349 An thram ycin synthesis by carbonylation, 6.285 Anthranilate synthase-phosphoribosyltransferase Salmonella ryphimurium, 6,582 Anthranilic acid in gravimetry, 1,530 metal complexes, 2,795 synthesis by carbonylation, 6,280 Anthraquinone, 2-acetoxy-1-hydroxysynthesis, 6,%? Anthraquinone, 1,4-dIhydroxymetal complexes dyes, 6 , & 6 Anthraquinone I ,5-dihydroxymetal complexes dyes, 6,86 Anthraquinone, 1,s-dihydroxymetal complexes dyes, 6,86 Anthraquinone, I-hydroxycalcium aluminum chelate compound, 1,2 metal complexes dyes, 6,86 Antiarthritis drugs labelled goid compounds, 6,969 metal complexes, 6,758 Antibiotic M139163,2,974 Antibiotics ionophoric, 6,553 metal complexes selective binding, 6,552 ~

84

85

Cumulative Subject Index

transition metal ions, 6,728 Antibodies labelling radiopharmacology, 6,972 radiolabelling, 6,995 Anticancer drugs labelled platinum complexes, 6,969 metal complexes, 6,756 Anticoagulants blood calcium, 6,591 Anticuboctahedra twelvc-coordinate compounds, 1, IM Antifoggants photographic emulsions, 6,97 Antimicrobial effects copper([) bipyridyl metal complexes, 2,90 Antimonate, hexabromostructure, 1,73 Antimonate, hexachloroelectron pair, 1,37 structure, 1,73 Antimonate, hexafluoro-, 3,276 Antimonate, tris(cthy1 dithiocarbonate)electron pair, 1, 37 Antimonates, 3,265 Antimonic acids, 3,265 Antimony, 3,237-294 biology, 3,277 carcinogenicity, 3, 278 coordination number, 3,256 determination silver diethyldithiocarbamate, 5, 818 electronic structure. 3,256 in medicine, 3,278 pharmacology, 3,278 teratogenicity, 3,278 toxicology, 3,277 Antimony, biphenyltriphenyistereochemistry, 1,M Antimony, di-~-d-tartarato(4)-bisdipotassium trihydrate, 3,278 Antimony, (0-ethylxanthato)bis(quinolin-E-olato)-, 3,267 Antimony, pentafluorolone electron pair structure, 1, SO Antimony, pentamethyl'H NMR, 1,41 Antimony, pentaphenylbond lengths, 3,270 stereochemistry, 1.4(1 structure, 1,3Y Antimony, pentatolylstereochemistry, 1,40 Antimony, (pheny1enedioxy)triphenylaqua(pheny1enedioxy) triphenylantimonate stereochemistry, 1.46 Antimony, triphenylbiscatecholate hydrate, 3,270 Antimony, triphenylcatecholate-, 3,270 Antimony, tris(diethy1dithiocarbamate)-, 3,266 Antimony, tris(dipheny1dithiophosphinato)-, 3,267 Antimony, tris(dipheny1dithiophosphonium)stereochemistry, 1, 82 structurc, 1,82 Antimony, tris(ethy1dithiocarbonato)stereochemistry, 1,82 structure, 1,82 Antimony, tris(oxa1ato)stereochemistry, I, 82 structure, 1,82 Antimony, tris(1-pyrro1idinecarbodithioato)-, 3, 266 Antimony complexes, 3,259 COC 1-D

acetylacetone rearrangement, 2,383 catenation, 3,262 cupferron, 2.512 double bonds, 3,261 Group IV ligands, 3,259 Group V ligands, 3,259 halogen, 3,270 nitrogen Jigands, 3,259 organooxy; 3.264 organosulfur ligands, 3,265,269 pentacoordinate, 3,269 phthalocyanines, 2,864 porphyrins, 2,822 sulfur ligands, 3,265 Antimony(II1) complexes cyclic, 3,262 oxo acids, 3,263 oxyfluoro, 3,264 tartaric acid, 2,479 Antimony(V) complexes organohalo, 3,257 orgmotrihdu, 3,258 triaryl diketones, 2,377 Antimony heterocycles transition metal complexes, 2, 1041 Antimony ligands, 2,989-1061 bonding, 2,103&1041 x bonding, 2,1033-1039 trigonal bipyramidal complexes, 2, 1036 Antimony oxides toxicologyl 3,277 Antimony oxoacids, 3,265 Antimony oxoiodides, 3,265 Antimony oxychlorides, 3,264 Antimony oxyhalides, 3,264 Antimony pentachloride, 3,272 toxicology, 3, 278 Antimony pentafluoride, 3,272 Antimony phosphite, 3,263 Antimony pseudohalides, 3,276 Antimony spots, 3,278 Antimony tribromide stereochemistry, 1,36 Antimony trichloride, 3,270,276 geometry, 1,36 stereochemistry, 1,36 Antimony trifluoride, 3,270 geometry, 1,36 stereochemistry, 1,36 Antimony trihalides, 3,270,272 mixed chloride/fluorides, 3,274 stereochemistry, I , 36 Antimony triiodidc sulfur complex stereochemistry, 1,36 Antistain agents photography, 6,104 Antiviral chemotherapy, 6,771 Apatite packing, 6,598 weathering, 6,868 Apatite, hydroxycalcium deposition as, 6, 597 packing, 6,598 AplasmornyGn, 3,96; 5,839 Apocarbonic anhydrase zinc(I1) complexes, 6,419 Apocarboxypeptidase zinc(I1) complexes, 6,419 Apoferritin, 6,667 iron deposition, 6, 668 oxidation, 6,669

Apoferritin

Apometallothioneins Apome tallothioneins metal binding models, 6, 673 Apoplastocyanin structure, 6,650 Aquadioxo cations, 2,296 Aquapentaammine complexes structure, 1, 8 Aquaspirillum magnetotacticum magnetotactic, 6,680 Aquation, 1,24 1 Arco-Oxirane process, 6,327 Arencdiazonium salts carhnylation, 6,290 Arenes hydrogenation catalysis, cobalt complexes, 6.238 oxidation copper catalysts, 6,391 oxidative coupling palladium catalysts, 6, 371 Arenesulfonic acids in nickcl elcctroplating, 6, 11 Argentate, tetrafluoropotassium salt history, 1,21 Arginine metal complexes, 2,750 Armeria maritima copper accumulation, 2,964 Aromatic compounds acetoxylation palladium catalysts, 6.368 oxidation manganese(II1) salts, 6,376 oxidative carbonylation palladium catalysts, 6,369 reversible one-electron redox potentials. 1,496 Aromatic hydrocarbons acetoxylation palladium catalysts, 6, 365-368 hydroxylation iron catalysts, 6,380 Aromatization iridium catalysts, 4, 1160 Arsazine, lO-chloro-S,lO-dihydro-. 3.256 Arsenates, tetraphenylgravimetry, 1, 534 Arsenic, 3,237-284 biology, 3,255 determination silver diethyldithiocarbamate, 5,818 environmental, 3, 255 in medicine, 3,255 oxidation states, 3,239 tolerancc lower marine life, 3,256 toxicity, 3,255 trace element, 3,256 uses, 3.239 ylides, 3,239 Arsenic, chlorobis(trifluoromethy1)(trimethylsily1)aminobis-, 3,242 Arsenic, dichlorobis(trifluoromethy1){bis(trimethylsilyl)amino}-, 3. 242 Arsenic, pcntaphcnylstereochemistry, 1,40 Arsenic acid esters, 3,245 oxaorganic compounds, 3,245 Arsenic chloride complex anions, 3,253

Cumulative Subject Index

86

Arsenic complexes amides structure, 2, 175 coordinated open-chain, 3,244 Group VI ligands, 3,245 Group V ligands, 3.240 germanium ligands, 3.240 halogen, 3,250 nitrogen ligands, 3,230 oxygen ligands, 3,245 phosphorus ligands. 3.243,244 phlhalocyanines, 2. 864 porphyrins, 2,822 selenium ligands? 3.249 silicon ligands. 3.239 structures: 3,239 Arsenic(II1) complexes, 3,240 diselenocarbamate, 3.250 tartaric acid, 2,479 Arsenic(V) complexes, 3,242 Arsenic(V1) complexes haloselenocarbamate, 3.250 selenium ligands. 3,250 selenocarbamate. 3,2SO Arsenic compounds catalysts alkene epoxidation, 6 . 332 Arsenic halides. 3,250,252 mixed, 3,253 reactions, 3.252 Arsenic heterocycles transition metal complexes, 2, 1041 Arsenic ligands, 2: 989-1061 bonding, 2,1030-1041 n bonding, 2: 1033-1039 macrocyclic, 2,1010 trigonal bipyramidal complcxcs, 2 , 1036 Arsenic cixyflutirides. 3;254 Arsenic pentachloride, 3,253 Arsenic pentafluoride. 3,252 Arsenic pseudohalides, 3.252 Arsenic sulfates, 3,246,247 bond lcnths and angles, 3.247 Arsenic triastatinc. 3,251 Arsenic tribromide stereochemistry, 1: 36 Arsenic trichloride, 3.252 stereochemistry, I? 36 Arsenic tricyanide, 3,252 Arsenic trifluoride stereochemistry. 1 , 3 6 Arsenic trihalides stereochemistry, 1: 36 Arsenic triiodide, 3,251 stereochemistry. 1.36 Arsenic triisocyanate, 3, 252 Arsenic triisotbioqanate, 3,252 Arsenotungstates, 3,1042 Arsine, alkylamino-, 3,240 Arsine, alkylbis~(dimethylarsino)propyl]-,2,1007 Arsine, alkylenebis(dipheny1-, 2, 1006

cis-,2,1006 trans-, 2, 1006 Arsine, bis(dimethy1arsino-o-pheny1ene)methyl-,2,1006 Arsine, (o-bromup~enyl)dichloro-,2,1005 Arsine, but-3-enylbis(3-dimethylarsinopropyl)-,2, 1010 Arsine, (chloroa1kyl)dichloro-, 2, 1005 Arsinc, 2-chloroethylbis(3-dimethylarsinopropyl)-,2,1010 Arsine, 3-chloropropylbis(but-3-cnyl)-,2,10'10 Arsine, dialkylamino-, 3,241 Arsine, dialkvlaminodiffuoro-, 3,242 Arsine, dichlbrophenyl-, 2 , 1005 Arsine, difluoroethylenebis(dimethy1-,2,1006

87

Cumulative Subject Index

Arsine, diiodomcthyl-, 2, 1004 Arsine, dimethyl-, 2. 1006 Arsine, 3-dimethylarsinopropylbis(but-3-enyl)-,2, 1010 Arsine, dimethylphenyl-, 2>1006 Arsine, diphenylchloro-, 3,256 Arsine, diphenylcyano-, 3,256 Arsine, ethylenebis(dichlor0-: 2, 1005 Arsine, ethylenehis(dimethy1-. 2, 1006 Arsine, ethylenebis(dipheny1-, 2, 1006 Arsine, ethylidynetris(methylenebisdimethy1-, 2, 1007 Arsine, ethylmethylphcnylcomplcxcs inversion, 1, 199 Arsine, iododimethyl-, 2, 1 [:)OS Arsine, methyldiphenyl-, 2, 1006 Arsine, o-phenylenebis(dichlor0-. 2, 1005 Arsine, o-phenylenebis(dimethy1-, 2, 1006 metal complexes, 2,499 Arsine, o-phenylenebis(dimethylaminopropy1-,2, 1007 Arsine, o-phenylenebis(methyIpheny1-,2, 1006 Arsine, silyl-, 3, 239 Arsine, tributyl-, 2, 1006 Arsine, triethyl-, 2, 1006 Arsine, trifluorohaloethylenebis(dimethyl-,2, 1006 Arsine. trimethyl-, 2, 1005, 1006 oxide metal complcxcs, 2,499, 500 in prawns, 3,256 Arsine, trimethylenebis(dimethyl-.2. 1006 Arsine, triphenyl-, 2, 1006 oxide metal complexes, 2, 500 sulfide metal complexes, 2,644 Arsine, tris(diethy1dithiocarbamato)stereochemistry, I, 81 structure, 1, 82 Arsine, trisilyl-, 3, 239 Arsine, vinylidenehis(dimethy1cis- and rruns-, 2 , 1004 Arsines, 2, 1004 macrocyclic, 2,999 multidentate, 2, 1007 oxides metal complexes, 2,497,500 tertiary, 2, 1005 Arsonic acid, methylgeochemistry, 6, 868 Arsonic acid, phenylgeochemistry, 6, 868 Arsonium ions, tetraphenq-lliquid-liquid extraction, 1- 548 Arsorane spirocyclic, 3,246 Arsorane, 2-acetyl-3,4,5triphenylcyclopentadienetriphenyl-,3,239 Arsphenamine syphilis treatment, 6,756 Arthrobactin structure, 6,678 Arylation alkenes catalysts, palladium complexes, 6,301 Aryl bromidcs carbonylation catalysts, cobalt complexes, 6.270 Aryl complexes metal hydroxides chemistry, 2. 358 Aryl halides reduction vanadium(I1) complexes. 3,469 Ascorbate oxidase, 6, 699

Aza macrocycles

cytochrome oxidases, 6,683 spectra, 6,652 Ascorbic acid copper(I1) dioxygen complexes, 5,717 iron complexes naturally occurring, 2,963 in photochemical nitrogen production from water. 6. 508 in photoproduction of hydrogen from water, 6,512 Asparagine mctal complexes. 2, 749 prebiotic systems, 6,871 L-Asparagine, glycylmetal complexes, 2,764 Aspartate transcarbamylase zinc, 6,606 Aspartic acid metal complexes, 2,749; 6,858 naturally occurring, 2,964 prebiotic systems, 6,871 terbium complexes, 3, 1108 Aspartic acid. p-carboxysynthesis metal catalysis, 6,468 r.-Asparric acid, glycylmctal complexes, 2,764 Aspartic acid, p-hydroxycalcium complexes biology, 6, 546 Asphalts structure, 6,856 Asymmetric induction directed aldol reaction, 6,219 Asymmetric synthesis carbonyl compounds metal chelates and, 6,221 Asymmetry, I 182 AI’P synthesis elcctron transfer, 6, 714 zinc complexes, 5,956,957 ATPase F, activation, 6,581 proton translocating activation, 6, 581 ATP synthase activation magnesium ions, 6,581 Atacamite, 6, 855 Atomic absorption spectroscopy mctal complexes biology, 6,550 Atomic spectroscopy, 1,231-234 Atrupisomers, 1 200 Aurintricarboxylic acid beryllium(I1) complexes, 2,482 Aurocyanides dissolution, 6$784 Auto trophic bacteria in oxidative leaching of uraniferous ores, 6,900 Autunite structure, 6,892 Azacycln hexanes metal complexes, 2,81 7-Azaindole metal complexes, 2,93 zinc complexes, 5,957 Aza macrocycles addition reactions, 2,907 alkylation, 2. 906 binuclear, 2.907 bora-substituted I

Aza macrocycles

Cumulative Subject I a d a

synthesis, 2,905 complexes structure, 2,907 complex formation reaction kinetics, 2,909 constrictive effect, 2, 909 coordination chemistry, 2, 899 hydrogenation, 2,906 magnetic properties, 2,908 metal complexes acid dissociation, 2, 909 metal ion oxidation-reduction, 2.913 substitution reaction, 2, 911 modification, 2,905 oxidative dehydrogenation, 2, YO5 reaction kinetics, 2,909 spectroscopy, 2,908 substitution, 2,906 synthesis, 2,900 metal ion promoted, 2,900 Azamethine dyes color photography, 6,110 Azaporphyrins, 2,856-870 demetallation, 2,858 fused benzene rings, 2,859 metallation, 2, 858 NMR, 2,857 photochemistry, 2,858 reactions, 2,858 redox chemistry, 2, 859 spectra, 2,857 synthesis, 2,857 8-Azapurine metal complexes, 2,93 Azepines metal complexes, 2, 81 Azetidines metal complexes, 2 , 8 1 Azides metal complcxes, 2,225-238 molecular geometry, 2,226 synthesis from, 2, 167 Azidinone, 1,3-di-r-butylreaction with Grignard reagents, 2,725 Azines metal complexes thermodynamic template reactions, 6, 180-184 Aziridine carbonylation catalysts, palladium complexes, 6,290 metal complexes, 2, 81 zinc complexes, 5,951 Azirine, 2-arylcarbonylation catalysts, rhodium complexes, 6,277 Azobenzcne metal complexes structure, 6,41 Azobenzene, 2,2'-dihydroxychromium complexes geometrical isomerism, 6, 69 Azobenzene, o-hydroxycopper complexes dyes, 6,42 Azobenzene, 2-hydroxy-5-methyl-2'carboxymethyleneoxymetal complexes dyes, 6,75

88

Azo compuunds o-amino-o '-hydroxydiaryl transition metal complexes, 6,57 bidentate dyes, 6; 42 o,o'-diaminodiaryl cobalt complexes, 6,58,60 o,o'-dihydroxydiaryl coppcr complcxes. 6: 55,57 p k ,647 o- halogeno-o'-hydrtixydiaryl copper complexes, 6,5S hexaden tate metal complexes, 6 , 7 6 o-hydroxy-0'-acetylaminodiaryl coppcr(I1) complexes, 6,56 o-h ydroxydiaryl oxidative coupling, 6, 54 metal complexes bonding, 6,41 dyes, 6 , J o

o-methoxy-0'-hydroxydiaryl demethylative coupling, 6,53 pentadentate metal complexes, 6,76 tctradcntaie metal complexes, 6 , 7 5 tridentate hetero donor atoms, metal complexes, 6,73 metal complexes, 6:46 metal complexes; isomerism, 6,73 tridentate o-aminodiaryl copper complexes, 6,57 Azo dyes, 1,29; 6 , 3 6 diffusion transfer system photography, 6,106 metal complexes silver dye-bleach process, 6 , 105 tridentate heterocyclic nitrogcn donor, 6,74 Azc-hydrazone tautomerism, 6,58 tridentate azo crirnpound metal complexes, 6,63, 71 Azoles metal complexes, 2,76 Azomethines electronic spectra, 2,717 metal complexes dyes, 6,83 Azopyrazolone o-hydroxyarylchromium complex geometrical isomerism, 6, 70 cobalt complexes stability, 6, 52 Azoresorcinol, arylnitrosnmetal complcxes dyest 6?85 Azoresorcinol, pyridylmetal complexes dyes, 6,74 Azurins, 6,651,652 copper(I1) complexes, 2 , 772; 5, 721 electron transfer reactions, 6,653 NMR, 6,652 Raman spectra, 6,652 spectra, 6,652 thioether complexes, 2.557 Azurite structure, 6, 849

.

BAL -see Propan-l-ol.2,3-dimercaptoBacillus cereus calcium transport, 6,572 Bacillus megaterium calcium efflux, 6,570 calcium transport, 6,572 sporulation zinc transport. 6. 572 Bacillus spp. sodium ions, 6,559 sporulation calcium transport, 6,571 Bacillus subtilis manganesc transport. 6,570 sporulation manganese transport, 6, S70 tumbling calcium, 6,595 Bacillus thuringiensis molybdenum uptake. 6,681 Bacitracin, 6,729 Backwashing in reprocessing irradiated nuclear fuel, 6.,932 Bacteria chemotaxis calcium, 6,595 photosynthetic reaction centres, 6,591 Bacteriochlorins, 2.851 Bacteriochlorophyll a-pruteins, 6,591 Bacterioferritin, 6,680 Bacteriorhodopsin photosynthesis, 6,589 Band intensities spectral, 1,249 selection rules, 1,244 Band widths spectral, 1,246 temperature effects, 1,248 Barbiturates metal complexes, 6,773 Barbituric acid metal complexes, 2,798 Barbituric acid, methyl-5-nitrosozinc complexes, 5,958 Barium Purex process, 6,940 Barium, pentakis(diacetamide)stereochemistry, 1, 99 Barium alkoxides synthesis, 2,336 Barium complexes cryptands, 3,53 phthalocyanines. 2,863 porphyrins, 2,820 pyridine oxide, 3, Y urea, 3 , 9 Barium meal, 6,756 Bathocuproine absorptiometry, 1,550 Bathophenanthroline

absorptiometry, 1,550 Bathophenanthrolincdisulfonicacid electrodcs, 6,25 Bayldonite, 5,960 Bayleyite structure, 6, 848 Beauveracin alkali metal complexes, 3,63 Becium hombiei copper accumulation, 2,964 Bentonite minerals prebiotic systems, 6,872 Benzaldehyde, 2-amino('i-diiminemetal complcxcs from, 6, 172 self-condensation aza macrocycles from, 2,900 Benzaldehyde, 0-aminoself-condensation, 4,257 Benzaldehyde, 2-amino-5-methylP-diimine metal complexes from, 6, 173 Benzamide, o-mercaptometal complexes, 2,655 Benzamide oximes metaI complexes, 2,274 Benzamidine, N , "-diphenylmetal complexes, 2,275 Benzene hydroxylation copper catalysts, 6,391 vanadium-alkyl peroxide catalysts, 6,341 Benzene, alkyloxidation cobalt catalysts, 6,384 Benzene, 1,2-diaminoreactions with dicarbonyl compounds aza macrocycles from, 2,902 Benzene, divinylion exchange resins, 6,816 Benzene, iodosyloxidation iron catalysts, 6,381 manganese catalysts, 6,377 Benzene, l-(methylphenylarsin0)-2-(methyIphenylphosphine)complexes chirality, 1, 199 Benzene, nitrohydrogenation catalysis, cobalt complexes, 6,237 reduction catalysts, palladium complexes, 6,248 catalysts, ruthenium complexes, 6,269 Benzcne, 4 mcthylthionitrosometal complexes, 2,804 Benzene dioxygenases, 6,708 Benzene-l,3-disulfunic acid, 4,5-dihydroxyan tifoggants photographic emulsions, 6,98 Benzenedithiolates metal complexes, 2,605

89

Benzenemethanethiol

Cumulative Subject Index

Benzenemethanethiol, a-(selenylmethy1ene)metal complexes, 2,809 Benzeneselenic acid metal complexes, 2,807; 5,977 Benzenesulfonic acid, 3,4-dihydroxyantifoggants photographic emulsions, 6, 98 Benzene-4-sulfonic acid, l-hydroxy-2-(2-hydroxy-6-sulfol-naphthylazo)-6-(2-hydroxy-l-nap hthy1azo)metallochromic indicator, 1.556 Benzenetetrathiols metal complexes, 2,606 Benzenethiol, 2-aminometal complexes, 2,799 Benzenethiol, o-hydroselenometal complexes, 2,809 Benzil asymmetric hydrogenation catalysts, cobalt complexes, 6,257 Benzimidazole metal complexes, 5,949 Benzimidazole, 2-guanidiniummetal complexes, 2,283 Benzimidazole, 2-(o-hydroxyphenyl)mercury determination, 1,532 Benzimidazolc, 2-mercaptogold(1) complexes photography, 6,102 metal complexes, 2, 802 Benzimidazole, 2-(2-pyridyi)metal complexes, 2,93 Benzimidazoles metal complexes, 2,78,85 PK,, 2,77 Benzimidic acid, thioesters hydrolysis, metal catalysis, 6,456 5,6-Benzocinnoline metal complexes structurc, 6,41 Benzo-5-crown-5 alkali metal complexes cavity shape and size, 3.51 Benzo-15-crown-5 alkali metal complexes, 3,40 1.4-Benzodiazepine synthesis by carbonylation, 6,285 Benzohydroxamic acid dioxouranium complexes, 2,507 metal complexes, 2,506,507 metal precipitant, 2,506 Benzohydroxamic acid, N-methylmetal complexes, 2,506 Benzohydroxamic acid, N-phcnylmetal complexes, 2,507 reactions with carboxylic acids. 2 , 507 metal precipitant, 2,506 titanium complexes, 2,506 Benzohydroxamic acid, N-(o-tolyl)metal precipitant, 2,506 Benzohydroxamic acid, N-m-tolyl-p-methoxymetal complexes, 2,506 Benzoic acid manufacture cobalt catalysts, 6,386 Benzoic acid, dihydroxyberyllium(l1) complexes, 2,481 Benzoic acid, 2,3-dihydroxyminerals weathering, 6,868 Benzoic acid, o-iodoxy-, 3,318 Benzoic acid, mercapto-

lithographic printing plates, 6, 101 Benzoic acid, o-mercaptoesters metal complexes, 2,655 thioesters metal complexes, 2,655 Benzoic acid complexes linkage isomers, 1, 186 a-Benzoin oximes metal complexes, 2,273,798 tx-Benzoin oximc in gravimetry, 1,530 Benzonitrile hydrolysis metal catalysis, 6,449 metal complexes structure, 2,262 Benzophenone, o-mercaptometal complexes. 2,654 Benzoquinoline zinc complexes. 5,953 Benzoquinone metal complexes spectra, 2,397 Benzoquinone. 3,s-di-&butylcobalt complexes, 2,398 Benzoquinone dioximates metal complexes non-integral oxidation states, 6 , 144 Benzoselenophene, 2-(2-pyridyl)metal complexes, 2: 807 Benzothiazole zinc complexes, 5,981 Benzothiazole, hydroxyin gravimetry, l , 531 Benzothiazole, rnercaptoin gravimetry, 1,534 Benzothiazole, 2-mercaptocadmium complexes liquid-liquid extraction, 1,547 Benzothiazole-2-thiol metal complexes, 2,802 Benzotriazoles metal complexes, 2,78 PK,, 2,77 zinc complexes, 5,950 Benzoxazole metal compiexes, 5,951 Benzoxazole; 2-(o-hydroxyphenyl)cadmium determination, 1,531 Benzylamine, a-methyl-N,N-dimethylcomplexes chirality, 1 , 199 Benzylamine oxidase, 6,700 Benzyl complexes metal hydroxides chemistry, 2,358 a-monooxime, 2,272 Benzyl halides carbonylation catalysts? cobalt complexes, 6,270 Benzylideneimine Schiff bases metal complexes, 2,721 Berbine synthesis by carbonylation? 6,285 Berry pseudorotation, 1,39 Berry twist copper(I1) complexes, 5,607 Beryllates, fluorocomplexes, 3, 10

90

91 Beryllates, tetrachloroalkali metal complexes, 3?10 Beryllium analysis, 1, 523 gravimetry, 1,529 Beryllium, alkylalkoxy synthesis, 2,340 Beryllium, his(trifluoroacety1acetone)gas chromatography, 1,560 Beryllium acetate basic, 2,304 complexes, 3, 8 Beryllium borohydride ammine complexes, 3 , 8 Beryllium carboxylatcs basic, 3,31 Beryllium complexes, 3.3 acetylacetone solvolysis, 2, 378 amides, 2, 164 amines, 3 , 7 anionic, 3, 10 1,3-diketones sulfur dioxide complexes, 2,392 hydrates, 3 , 6 phthalocyanines, 2,863; 3,59 polycarboxylic acid, 3 , 3 3 porphyrins, 2,820 Schiff bases, 3 , 2 8 Beryllium(I1) complexes hydroxysalicylic acid, 2, 481 naphthoic acid, 2,483 salicylic acid, 2, 482 Beryllium dichloride ether complexes, 3 , 8 Beryllium difluoride ammine complexes, 3 , 7 Beryllium dihalides sulfide cornplcxes, 3, 10 Beryllium halides amine complexes, 3 , 8 ammonia complexes, 3 , 7 carbonyl complexes, 3 , 9 Beryllium nitrate basic, 3,32 Berzelius's conjugate theory. 1 , 4 1,l'-Bibismolane, 3,284 Bicapped pentagonal prisms repulsion energy coefficients. 1,34 twelve-coordinate compounds. 1, 100 Bicapped square antiprisms repulsion energy coefficients, 1, 33, 34 ten-coordinate compounds, 1.98 Bidentates mixed donor atoms, 2,79>809 nitrogen-oxygen ligands, 2*793 amine group donors, 2.794 hydroxylamine group donors, 2,797 N heterocyclic donors, 2,795 oxime group donors, ZI797 nitrogen-sulfur ligands, 2>799 amine donor groups, 2,799 N heterocyclic donors, 2 , SO0 selenium-nitrogen ligands, 2,806 selenium-oxygen ligandsl 2,807 selenium-sulfur ligands, 2.808 sulfur-oxygen ligands, 2, 804 thioetber donnr groups?2,805 thiol group donors, 2: 804 Bifurandiones synthesis, 6,272 Biguanide, phenylin colorimetry, 2,284

Cumulative Subject lndex

2,2'-Biquinolyl

Biguanides metal complexes, 2,284 Biguanidine metal complexes, 2.281 2,2'-Bi-2-imidazolinyl metal complexes, 2. 89 2,2'-Biimidazolyl metal complexes, 2,82,89 1,l'-Binaphthyl, 2,2'-bis(diphenylphosphino)complcxes atropisoiners, 1,200 1,l'-Binaphthyl, 2,2'-dilithio-, 1,200 Binding groups metals biology. 6.546 Bioinorganic chemistry, 1.28 Biological membranes cation transport, 6,552 BioIogy coordination compounds in, 6,541-730 dioxygen, 6,681-711 Biomethylation, 6 , 868 Biophenylation, 6,868 Biotin sulfoxide reductase molybdcnum cofactor, 6,663 Biphenyl! 4,4'-diamino-3,3'dicarhoxymetal complexes, 5,939 Biphenyl, 6,6'-dirnethyL2,2'-diaminocomplexes atropisomers, 1 . 200 2.2'-Biphenyldiamine metal complexes, 2,.59 Bipyramidal structure skew-trapezoidal, 1,58 4,4'-Bipyrazolyl polymers metal complexcs, 2,90 4,4'-Bipyridinium, N-(benzylpolyviny1)-W-mcthylin photochemical hydrogen production from water, 6 , 505 4,4'-Bipyridiniurn, poly(N-vinylhenzyl-~-n-butyI)in photochemical hydrogen production from water, 6, 505 4,4'-Bipyridinium, poly(N-vinylbenzyl-N'-n-propyl)in photochemical hydrogen production from water, 6, 505 4,4'-Bipyridinium, polyvinyl-N-acetate-N'methylin photochemical hydrogen production from water. 6, 505 Bipyrid yl electrode modification, 6,25 metal complexes, 5, 958 in photochcmical production of hydrogen from watcr, 6,506 2,2'-Bipyridyl in analysis, 1, 523 complexes history-,I, 21 liquid-liquid extraction, 1,544 metal complexes absorptiometry, 1,549 rearrangement, 1,458 uranium complexes structure, 1,94 2.2'-Bipyridyl, 4-rnethyl-4'-vinylelectrochemical polymerization, 6,25 electropolymerization, 6, 16 Bipyrid yls bis[N-oxide) metal complexes, 2,496 metal complexes, 2 , 89,90,93 steric effects, 2.W 2,2'-Biquinolyl

2,2‘-Biquinolyl

Cumulutive Subject Index

in analysis, 1,523 copper complexes absorptiometry, 1,549 2,2’-Biquinolyl, 4,4’-diphenylabsorptiometry, 1,550 Bis(chlorophylls), 3,58 Bis (dithiolenes) metal complexes symmetrically substituted, 2,600 s-vnthesis,2,597 Bismuth, 3,237-294 biology, 3,292 pharmacology, 3,292 toxicology, 3,293,294 Bismuth, amminebis(trich1oro)-, 3,282 Bismuth, chlorotriphenyl(8quinoIinolato)-, 3,280 Bismuth, dichlorotriphenyl-, 3,280 3,288 Bismuth, isopropylxanthogenatodiphenyl-; Bismuth, triamminetrichloro-, 3,282 Bismuth, trichlorotris(3-sulfanilamido-6meth0xypyridazine)-, 3,293 Bismuth, tris(dipropy1dithiophosphonato)structure, 1,82 Bismuth, tris(dipropy1dithiophosphonium)stereochemistry, 1,81 Bismuthate, hexabromostructure, 1,73 Bismuthate, hexachlorostructure, 1,73 Bismuthate, hexaiodostructure, 1,73 Bismuthate, diphenylbis(triRuoroacetato)tetraphenyl bismuthonium salts, 3,279 Bismuthate, tetrakis(ethy1dithiocarbonato)stereochemistry, 1,94 Bismuthate, tetrathiocyanatorubidium salt structure, 1,44 Bismuth-azide bonds, 3,283 Bismuth complexes carbon ligands, 3,279 germanium ligands, 3,280,281 Group IV ligands, 3,279 Group V ligands, 3,282 Group VI ligands, 3,284 halogen, 3,290 nitrogen ligands, 3,282 organosulfur ligands, 3,285 oxygen ligands, 3,284 phthalocyanines, 2,864 porphyrins, 2,822 silicon ligands, 3,280 sulfur ligands, 3,284 tin ligands, 3,281 Bismuth(II1) complexes, 3,282 Bismuth(V) complexes, 3,283 Bismuth halides, 3,290 crystal structure, 3,291 Bismuth heterocycles transition metal complexes, 2, 1041 Bismuthine, alkylamino-, 3,282 Bismuthine, alkylxanthogenato-, 3,288 Bismuthine, alkylxanthogenatodimethyl-, 3: 289 Bismuthine, bis(diethy1thiocarbamato)methyl-, 3,288 Bismuthine, bis(diorganodithiocarbamat0)organo-, 3,289 Bismuthine, bis(organothi0)-, 3,287 Bismuthine, dithio-, 3,285 Bismuthine, organodithiocarbamato-, 3,288 Bismuthine, thio-, 3,285 Bismuthine, triphenyl-, 2,1009 Bismuthine, tris(organothi0)-, 3,287 Bismuthine azides organo-, 3,283

Bismuthines, 2,1008; 3, 281 tin, 3,281 Bismuth ligands, 2 ; 989-1061 bonding, 2,1030-1041 n bonding, 2,1033-1039 trigonal bipyrarnidal complexes, 2, 1036 Bismuth line, 3,294 Bismuthotungstates, 3: 1042 Bismuth pentafluoride, 3: 292 Bismuth tribromide, 3, 291 Bismuth trichloride, 3,290 Bismuth tritluoride. 3,290 Bismuth triiodide, 3, 292 Bismuth trioxide, 3,284 2,2’-Bisphenol metal complexes color photography, 6,109 Bis(trimethy1ene)triamine metal complexes, 2,49 4,4’-Bi-1,2,4-triaz01yl metal complexes, 2, 89 polymers metal complexes, 2,90 Blastocladiella emersonii cation transport, 6,559 sporulation calcium transport, 6, 572 Bleaching photography, 6,99 Bleomycins, 6,728 indium-111 complexes tumor lmaging techniques, 6, 992 labelled in medicine, 6,968 mechanism, 6,729 metal complexation biological activity, 6,771 metal complexes, 2,969 structure, 6,728 Blomstrand-J~rgensenchain thcory, 1 , 6 Blood coagulation calcium, 6,591 Bloodlbrain barrier brain imaging techniques technetium complexes, 6,991 technetium complexes, 6.985 Blood plasma amino acids copper complexes, 2,965 metal complexes, 2,965 Blue copper electron transfer proteins, 6,712-717 Blue copper oxidases, 6,699 Blue copper proteins, 2,557; 6,649 Blue electron transfer proteins, 6,649,652 spectroscopy, 6, 651 Bluc oxidases copper, 6,654: 655 Blueprint process, 6 . 124 Blue proteins model studies, 6,653 BolCite structure, 6,847 Bond dissociation Si=Cr, 3,184 Bond energies Group IVB elements, 3,185 Bonds antimony-antimony, 3,263 antimony-halogenl 3,271 antimony-metal, 2,103&1041 arscnicGroup IV, 3,239 arsenic-Group V, 3,240 arsenic-halogen, 3,251

92

93

Cumulative Subject index

angles, 3,251 lengths, 3,251 arsenic-metal, 2, 103C-1041 arsenic-nitrogen, 3,240 bismuth-bismuth, 3: 284 bismuth-metal, 2, 103C-1041 bismuth-selenium, 3; 290 bismuth-silicon, 3,280 bismuth-sulfur angles, 3,285 lengths, 3,285 bismuth-tellurium, 3, 290 carbon-hydrogen activation, alkoxy ligands, 2, 359 carbon-nitrogen tungsten complexes, 3, 1013 chromium-chromium, 3, 749 double pnictide ligands, 2, 1045 energies metal ion-water complexes, 2: 309 transition metal-ammonia complexes, 2,26 gold-gold, 5 , 899 iron-germanium, 4,1189 iron-lead, 4,1189 iron-tin, 4,1189 lengths metal-nitrogen, 2 , 2 6 metal-alkyl oxygen insertions, 2. 341 metal-metal double halogen bridged complexes, 2,683 metal alkoxides, 2, 349 triple halogen bridged complexes, 2.683 metal-phosphine, 2. 1039 metal-sulfide, 2,523 mctal-sulfur, 2,516 molybdcnum-carbon, 3,1405 molybdenum comp1rxe.s metal-metal, 3, 1301-1322 molybdenum-molybdenum. 3. 1301, 1317 molybdenum-molybdenum double, 3,1316 length, 3, 1317 molybdenum-molybdenum quadruple, 3,1308 activation energy for rotation, 3,1308 electronic structure, 3, 1308 IR spectroscopy, 3,1308 length, 3,1308 NMR spectroscopy, 3: 1309 UV spectroscopy. 3, 1308 molybdenum-molybdenum triple, 3,1301, 1310-1315 cleavage, 3,1315-1322 oxidative addition, 3, 1315 reaction with alkynes, 3, 1315 reaction with CO, 3, 1315 rcaction with cyanamidc. 3, 1315 reaction with diazomethane, 3, 1315 multiple, 2, 1048 phosphorus-nitrogen, 2.1051 palladium-sulfur, 5 , 1131 phosphorus-metal, 2, 10342-1041 phosphorus-transition metal, 2,1039 soft and hard acids and bases, 2,1040 platinum-carbon stability, 5,393 pnictide-transition metal, 2, 1030 double, 2, 1052 rhodium-rhodium, 4,903 cleavage, 4,950 triple pnictide ligands, 2, 1046 n-Bonds antimony ligands, 2, 1033-1039 COC 1-D'

Borane complexes

arsenic ligands, 2,1033-1039 bismuth ligands, 2, 1033-1039 metal-oxygen metal alkoxides, 2,351 phosphines basicity, 2: 1030 phosphorus ligands, 2,1033-1039 Bone chronic cadmium poisoning, 5,1000 diagnostic imaging techniques radiopharmaceuticals, 6,985 imaging pharmaceutical agents, 6,968 imaging agent technetium-99,6,976 radioactivity accumulation radiopharmacology, 6,971 Boramycin alkaline earth metal complexes, 3,68 Borane electrophilicity, 3, 82 Borane, l-alkenylcarbonylation catalysts, palladium complexes, 6,289 RoTane. alkoxyLewis acidity, 3,82 Borane, alkylthiocomplexesl 3,88 Borane, aminoLewis acidity, 3,82 synthesis, 2, 164 Borane, carboxyamine complexes, 3, 84 Borane, cyanatocomplexes, 3- 88 Borane, cyanoamine compiexes, 3, 84 Borane, fluoroalkoxycomplexes, 3, 88 Borane, halogenocomplexes, 3, S688 nitrogen donors, 3,87 oxygen donors, 3,86 stoichiometry, 3,85 syntheses, 3,&4 relative acidities, 3, 82 Borane? 1-methylbenzylaminocyanohydropyrrolyi-,3 ,8 4 Borane, thiocyanatohalogenohydro-, 3,88 Borane, trialkoxyamine complexes, 3,88 Borane, triarylguanidine complexes, 2,283 Borane, trifluaro-

complexes Lewis acids, 3,87 van der Waals complexes, 3,84 Borane complexes aminecarboxy-, 3,84 aminehalogeno-, 3,84 amines, 3,82,101 B-N bond polarity, 3,82 preparation, 3,83 reactions, 3, 83 bonds B-?I, 3,88 s o ,3 , 8 8 B S , 3 ,8 8 ITbonds, 3,82 carbon monoxide, 3,84 chiral boron, 3,84 dimethyl sulfide, 3, 84 enthalpy of dissociation, 3,82

Borane complexes halogenohydro, 3.84 hydro, 3 , 8 3 monocyano, 3,84 NMR, 3,83 neutral, 3,81-90 stability, 3, 81 relative stabilities, 3, 82 Borate, tetraphenylin gravimetry, 1,534 Borates B-C bonds, 3,97 B-N bonds, 3,97 B-0 bonds, 3,94 B-P bonds, 3,97 B-Si bonds, 3 , 9 1 oxo acid anion complexes, 3, Y6 Borates, alkoxo-, 3,94 Borates, amidotrihydro-, 3,92 Borates, aryloxo-, 3,94 Borates, carboxylato-, 3,96 Borates, catechol, 3,95 Borates, chlorosulfato-, 3,97 Borates, dicarboxylato-, 3,96 Borates, dipyrazol-I-yl-, 3, 92 Borates, halogeno-, 3,92 Borates, halogcnohydro-, 3.90 Borates, hydro-, 3,90 Borates, hydrohydroxo-, 3 , 9 0 Borates, hydropyrazol-I-yl-, 3, 92 Borates, hydroxo-, 3,94 Borates, hydroxycarboxylato-, 3.96 Borates, inositol, 3,95 Borates, monoalkyl-, 3,92 Borates, monophosphido-, 3,92 Borates, peroxohydroxo-, 3,94 Borates, polyol, 3,95 Burates, pyrrol-I-yl-, 3,92 Borates, sulfato-, 3,97 Borates, tetrabromo-, 3,92 Borates, tetrachloro-, 3, 92 Borates, terrafluoro-, 3,YZ minerals, 6, 847 Borates, tetrahalogenomixed, 3,93 ltB NMR, 3,92 Borates, tetraiodo-, 3, 92 Borates, tetranitrato-, 3,96 Borates, tetraperchlorato-, 3 , 9 7 Borates, tripyrazol-1-yl-, 3,92 Borax, 3,101 Borazines metal complexes, 2 , S l structure, 2, 176 Boric acid, fluoro-, 3, 101 Bornite brines, 6,853 Boromycin, 3,96 Boron, 3,81-101 as ligand, 3,99 Boron, alkylalkoxides synthesis from, 2.342 Boron complexes acetylacetone, 2,370 anionic, 3,9C!-97 antibiotics, 3, 101 applications, 3,101 cationic, $97 chelates, 3,89 1,3-diketones synthesis, 2,317 porphyrins, 2,821 pyridine oxide, 2,496 Boron(II1) complexes

Cumulative Subject Index salicylic acid, 2,482 Boron compounds catalysts alkene epoxidation, 6,332,345 Boron halides dimethyl sulfoxide complexes. 2,488 Boron trialkoxides physical properties, 2,345 Bovine erythrocyte superoxide dismutase copper(I1) cornplcxes, 5,724 Braggitc, 5. 1099 Brain diagnnstic imaging techniqucs radiopharmaceuticals, 6,990 Brass electroplating, 6,13 Breeder reactor fuels dissolution, 6,927 reprocessing, 6,934,954 Breeder reactors, 6; 885 Brevibacteriurn ammoniagenes manganese, 6,587 Bridge groups, 1 22 Bridging ligands double hydroxide, 2,299 p-H,OZ-: 2,305 hydroxides, 2,296: 298 p2-hydroxides, 2,298 p3-hydroxides, 2,300 oxides, 2,296,298.301 double, 2: 302 triple, 2,302 p2-oxides, 2: 301 ps-oxides, 2>302 p4-oxides, 2.304 p.,-oxides, 2,304 p6-oxides, 2,304 trifurcated hydroxide, 2, 300 triple hydroxide, 2,299 water: 2,296,298 Briggs, Samuel Henry Clifford, 1, 14 Brighteners, 6,5 Brincs inorganic complexes, 6 , $53 metal complexes geochemistry, 6,852 Bromates effective bond length ratios, 1,37 stereochemistry, 1,37 Bromates, dinitrato-, 3,319 Bromination acetylacetone chromium(I1) complexes, 6,203 fi-diketone complexes, 1,420 8-hydroxyquinoline metal complcxcs, I, 418 N-macrocycles, 1,416 pyruvic acid metal ions. 1,420 Bromine anions BrF,-, 3,316 Bromine cations BrF4+, 3,315 BrF,+, 3,316 Br3+, 3,314 ClF2',3,314 Bromine complexes single bridges, 2,680 Bromine(II1) compounds, 3, 317 [Br(OSO,F)],', 3,320 Bromine fluorosulfate, 3,320 Bromine htxafluoroantimonate, difluoro-, 3,313 Bromine perchlorate, bis(quino1ine)-, 3, 319 Bromine tetrafluoroborate, bis(quinuc1idine)-, 3,319

94

95

Cumulative Subject Index

Bromine trifluoride, 3,313.314 Bromopyrogallol red metallochromic indicator, 1; 556 Brush plating, 6 , s Bryostatin 1,2,974 Bufflex, 6,911 Bufflex process uranium extraction, 6,821 Butadiene dimerization-carbonylation, 4,288 hydrocyanation catalysts, nickel complexes, 6,297 hydrogenation catalysts, cobalt complexes, 6.236 catalysts, iridium complexes, 6,247 1,3-Butadiene reactions with carbon dioxide catalysts, nickel complexes, 6.295 1,3-Butadiene, l-phenylhydrogenation catalysts, cobalt complexes, 6,236 trans-Butadienetetrathiolates metal complexes, 2,606 I-Butanal hydrogenation catalysts, iridium cornplexcs, 6,246 Butane, 2,3-diaminometal complexes, 2,34 Butane, ruc-pp'-diaminodphenylalkali metal complexes. 3, 14 Butane, 2,3-O-isopropylidene-2,3-dihydroxy-l,4bis(dipheny1phosphino)rhodium complexes asymmetric hydrogenation, 6,251 Butane-l,3-dione, 4,4,4-trifluoro-l-(selen-2-yl)liquid-liquid extraction, 1,544 Butane-2,4-dione, 1 , l .l-trifluoro-4-(2-thenoyl)in uranium ore processing, 6,910 1,2,3,4-Butanetetrarninc metal complexes, 2 , 5 6 2-Butanone, 4-alkoxycarbonylation

Butyric acid

catalysts, rhodium complexes, 6,273 15,17-Butanoporphyrins metal complexes geochemistry, 6,864 Butene asymmetric carbonylation catalysis by palladium complexes, 6,293 asymmetric hydroformylation catalysts, platinum complexes, 6,266 2-Butene, 1,4-diacetoxysynthesis tellurium catalysts, 6,367 I-Butene. 2,3-dimethylasymmetric hydroformylation catalysts, platinum complexes, 6,266 Butene, hexacyanometal complexes, 2,263 But-S-en-2-one, l,l,l-trifluoro-4-(2-thieny~)-4-mercaptoliquid-liquid extraction, 1,544 Butex process, 6,938 But-2-yne-l,4-diol hydrogenation catalysts, iridium complexes, 6,248 3-Butp-1-01 dehydrogenase inhibition, 5,1017 Butyric acid metal complexes geochemistry, 6,867 Butyric acid, aminoore formation, 6,869 Butyric acid, 4-aminoethyl ester hydrolysis, metal catalysis, 6,421 Butyric acid, 2,4-diaminometal complexes, 2,750 Butyric acid, 2-hydroxymetal complexes NMR, 2,467 Butyric acid, 4-hydroxymetal complexes NMR. 2; 467

C Cadaverine coppcr(I1) complexes, 2, 44 Cadmium, 5,925-1022 acute poisoning, 5,1000 binding to metallothioneins, 6 , 673 chronic poisoning, 5, 1000 gravimetry, 1,532 masking, 1,538 metallothioneins, 5, 1021 poisoning therapy, 5,1001 toxicology, 5,999 Cadmium, bis(hydroxybenzuaio)tris(pyridine)structure, 1,78 Cadmium, dinitratotripyridinestructure, I , 78 Cadmium, dithiocyanatohis(pyridine)gravimetry, 1,534 Cadmium, tris(acety1acetone)potassium salt structure, 1 , 65 structure, 1,65 Cadmium, tris(diethy1dithiocarbamatojtetrabutylammonium salt structure, 1,62 Cadmium, tris[4,4,4-trifluoro-1-(2-fur$)-113butanedionelstructure, 1,65 Cadmium complexes acetylacetone, 2,372 alcohols, 5, 964 amides, 5,944 amine oxides, 5,964 amines, 5,933 amino acids, 5, 938 1.4-aminobutyne-2-tetraacetate-5,946 applications, 6, 1024 azides, 5,931 azo compounds, 5,948 biology, 5, 1001 bis(2-dimethylaminoethyl)methylamine,5, 936 carboxylates, 5,968 corrins, 2, 885 cyclic aminrs, 5,990 cyclic ethers, 5,990 ciS-l,2-cyc~ohexdnediaminetetraacelic acid, 5, 947 trans- 1,2-cyclohexylenedinitrilotetraacetic acid, 5,947 1,4-diaza-1,3-butadiene, 2, 211 diketones, 5,967 equilibrium constant solvent effect, 1,516 Z ,Z-ethanediamine, 5,933 ethers, 5,964

hydrazoncs, 5.910 hydroxidcs, 5; 960 hydroxylamine, 5,931 imides, 5,944 iminodiacetic acid, 5,946 industrial uses, 5 . 998 ketones, 5.964 kinetics, 5: 996 macrocyclic. 5: 990 malonic acidt 2: 444 multinuclear, 5,988 nit.ratcil5. 962 NMR,5,926

NQR,5,926 organosullur oxides, 5.964 oximcs. 5, 940 oxygen ligands, 5,960 phoqphates. 5.962 phosphine oxides, 5,964 phosphine selenides, 5,980 phosphine sulfides, 5, 980 phosphorus ligands, 5>959 photoelectron spectroscopy, 5,929 phthalocyanines, 2,868 porphyrins, 2 . 842 1,2-propanedidrninc, 5,935 pseudohalides, 2,235 pyridine oxide, 2,496 reactivity. 5, 996 salicylaldiminc: 5: 942 sclenium hcterocyclcs, 5.980 SUlldlO,5. 963 sulfur heterocycles, 5,980 sulfur ligands, 5: 972 thioacids, 5.976 thioamides, 5.976 thioethers, 5.972 thiols. 5: 972 tris(2-~minoethyl)amine,5,937 tris(2-dimethylaminoethyl)amine,5,938 vibrational spcctroscopy, 5, 929 water, 5.960 X-ray diffraction, 5,929 Cadniium(1) cnnipkxes, 5 , 989 Cadmium halides, 5, 981 molten state coordination, 5,981 solution chemistry, 5,893 Cadmium hydrides, 5,931 ammonia, 5,931 Cadmium pseudohalides, 5,981 solid state, 5,985 Cage compounds in gravimetry, I , 525 Cage nicchanisrn photochemistry, I, 393 Cages. 1, 135 formaticin kinetic metal temppate reactions, I,453 geometrical structure, 1: 138 synthesis, 1, 171

ethylcncbis[N,N'-(2,6-dicarboxy)pipcridine]5,946 ethylenediaminedisuccinic acid, 5.947 ethylenediatnine-N.N'-diacetic acid, 5,946 EXAFS, 5,929 formate, 5,968 fulvic and humic acids, 6,860 hydrazides. 5,944 hydrazine, 5,931 ~

96

97 Cahn, lngold and Prelog notation, 1 , 128 Calcein metallofluorescent indicator, l I558 Calcein blue metallofluorescent indicator. 1: 558 Calcichrome IREA metallochromic indicator, 1, 556 Calcification, 6, 596 Calcineurin, 6,574 Calciphorin, 6,569 Calcites porphyrin ligands, 6,850 Calcium binding groups biology, 6,546 biology, 6,546,562-598 trigger, 6,594 blood coagulation, 6,591 cells regulator, 6,565 colorimetry biology, 6,550 efflux sarcoplasniic reticulum; 6.567 enzymes activator, 6,5Y1,5Y3 masking, 1,538 mobilization, 6, 596 transport mitochondria, 6,568 plants, 6,572 uptake intestines, 6,596 Calcium, heptaaquadecaiodide stereochemistry, 1,72 Calcium, tetraaquabis(picrate)structure, 1,8Y Calcium, tetrakis(methano1)dinitratostructure, I, XY Calcium alkoxides synthesis, 2,336 Calcium-binding proteins, 6,564,572,596 intestinal, 6,576 structure, 6,573 Calcium carbonate calcium deposition as; 6,597 Calcium complexes acetylacetone, 2, 372 amides, 2,164 amino acids, 3,33 arsine oxides, 3, 9 biology, 6, 549 bipyridyl, 3, 13 crown ethers, 3,39 dimethylphthalate, 3, 16 enzyme stabilization, 6,549 hydrates, 3,7 ionophores, 3,66 malonic acid, 2,444 peptides, 3,33 phosphines, 3,9 phthalocyanines, 2,863 porphyrins, 2,820 proteins, 2,770 pyridine oxide, 3,9 Schiff bases, 3,29 urea, 3,9 Calcium(I1) complexes maleic acid conformation, 2,475 mandelic acid, 2,474

Cumulative Subject Index

Capped trigonal prisms

Calcium deposition biology, 6, 597 Calcium ions binding to proteins, 6,563 biology structure stabilizers, 6,564 coordination compounds biology. 6, 563 enzyme activator, 6,565 phosphate ester hydrolysis, 6,443 probes?6,563 transport mammals, 6,568 microbes. 6,569 Calcium'magnesium ATPase sarcoplasmic reticulum calcium pump, 6,566 Calcium phosphate calcium deposition as, 6, 597 Calcium pump, 6,565 Calcium salis electrolyte balance, 6,771 Calclactite structure, 6 , 848 Calcoii mctallochromic indicators, I , 556 Caldopentarnine metal complexes, 2,S7 Calelecrrin, 6. 578 Calixarenes alkali metal complexes, 3,57 classification, 2,919 metal ion complexes, 2,936 synthesis, 2.925 Calmagire metallochromic indicator, 1,556 Calmodulin, 6,572,574,578 binding targct cnzymcs: 6, 574 clcavagc, 6, 574 neurotransmitters, 6,595 structure: 6,573 Tetrahymena, 6,574 Cal-red metallochromic indicators, 1,556 Calsequestrin. 6, 577 calcium binding, 6,566 Camphor, formylSchiff bases metal complexes, 2,732 NMR, 2,732 X-ray analysis, 2,732 Camphor, (+)-(hydroxymethylene)amino acid Schiff bases metal complexes, 2,752 Camphorquinone dioximes metal complexes, 2,271,798 Cancer depression and, 6,773 CANDU reactor, 6, 883 Capped octahedra repulsion energy coefficients, 1,33,34 scven-coordinate compounds, 1,69 Cappcd pentagonal antiprisms eleven-coordinate compounds, 1,99 repulsion energy coefficients, 1,34 Capped square antiprisms nine-coordinate compounds, 1, Y5 repulsion energy cocfficients, 1,34 Capped trigonal prisms repulsion energy coefficients, 1,34

Capped trigonal prisms

Cumulative Subject Index

scven-coordinatc compounds, I , 69 Carbamates synthesis by carbonylation, 6,277 Carbamic acid metal complexes, 2,450 bridging coordination, 2,450 chelate coordination, 2,450 reactivity, 2,451 synthesis, 2,451 unidentate, 2,450 Carbamic acid, diethyldithiometal complexes gas chromatography, 1,560 liquid-liquid extraction, 1,547 Carbamoselenothioic acid metal complexes, 2,808 Carbamoyl-phosphate synthetase activators sodium ions, 6,561 Carbaplatinaboranes conformation, 5,374 Carbazide, diphenylin chromium(II1) analysis, 1, 523 liquid-liquid extraction, 1,545 reaction with fatty acid metal salts thermography, 6,121 Carbarides metal complexes, 2, 798 Carbitol, dibutyl in reprocessing irradiated nuclear fuels, 6,935 Carboalkoxylation, 6,286 Carbodiimides insertion reactions metal alkoxides, 2,354 Carbohydrates alkaline earth metal complexes, 3,24 metal complcxes naturally occurring, 2,984 Carhanates leaching uranium, 6,788 minerals, 6, 848 Carbon dioxide alkali metal complexes, 3, 16 insertion reactions metal alkoxides, 2,354 metal complexes, 2,451 carbon atom coordination, 2,452 oxygen atom coordination, 2,453 side-on coordination, 2,452 reactions catalysts, 6,293-296 Carbon diselenide metal complexes, 2,664 Carbon disulfide in gold electroplating, 6, 11 as ligands, 2,580 metal complexes, 2,579491 +bonded, 2,580 bridging between two metals, 2.582 end-on bonded via S, 2.580 Carbon electrodes potential range aqueous solution, 1, 480 Carbonic acid metal complexes, 2,446 bridging, 2,448 chelate coordination, 2,447 reactivity, 2,448 synthesis, 2,448 unidentate, 2,447 rhodium complexes

hydroformylation catalysts, 6.262 Carbonic anhydrascs, 6,474 carbon dioxide hydration kinetics, 6,601 cobalt(II), 6>602 inhibitors. 6,602 mechanism, 6: 602 structure, 6,640 zinc, 6, 6M11001, 1004 zinc-carbonyl mechanism, 5, 1003 zinc deficiency and, 6,764 Carbon monoxide binding hemes, 6,698 estimation copper(1) complexes, 5, 566 exchange reactions, 1,288 ligands history, 1,21 metal complexes for hydrogenation, 2,342 reactions metal alkoxides, 2, 355 reduction catalysts. ruthenium complexes, 6,269 vanadium(l1) complexes, 3,471 Carbon monoxide dehydrogenase acetogenic bactcria nickel, 6,645 nickel, 6, 645 Carbon monoxide oxidase molybdenum. 6.662 Carbonylation asymmetric catalysts, 6,292 catalysts transition metal complexes, 6,267-293 copper(1) complexes in, 5,568 Carbonyl complexes substitution reactions, I, 288 Carbonyl compounds by alcohol oxidation chromium-xo complexes, 6,351 asymmetric hydrogenation catalysts, 6,257 aza macrocycles from: 2,900 coordinated reactions, 6,202 hydrations metal catalysis, 6,474 reactions with amines reactions with diaza compounds diaza macrocycles from, 2,904 reductions for metal catalysis, 6, 475 synthesis by alkene oxidation palladium chloride catalysts, 6,363 Carbonyl sulfide as ligands, 2: 580 metal compfexes, 2,579-591,806 reactivity; 2,583 Carboxylates metal complexes basic, 2, 302 solvent extraction, 6,790 Carboxylation ketone complexes, 1,450 Carboxylic acids esters hydrolysis, metal-catalyzed, 6,437 iton(II1) complexes solvent extractions, 6, 791 metal complexes, 2,43j-456

98

99

Cumulutive Subject index

bridging, 2, 439 geochemistry, 6,867 magnetic susceptibility. 2,437 naturally occurring, 2.961 NMR, 2,437 paddlewheel systems, 2.440 reactivity, 2,442 structures, 2, 436 symmctrical chclatc coordination: 2,438 synthesis, 2,442 midentate coordination. 2,438 nickel and cobalt complexes solvent extraction, 6,790 nomenclature, 2 . 462 organometallic ligands, 2,442 polynuclear complexes. 2* 442 rhodium complexes hydroformylation catalysts. 6: 262 solvent extraction metals, 6,789 synthesis homolytic liquid-phase processes. 6, 327 trinuclear complexes, 2 , 4 4 1 Carboxypeptidasc A, 5,1U04 hydrolysis mechanism, 6,463 mcchanism, 5. 1004 models, 6,415 structure, 5 , 1002 Carboxypeptidases amino acid residues chemical modification. 6. 605 mechanism, 6,605 structure, 6,603 zinc, 5 , 1001, 1004; 6, 603 zinc-carbonyl mechanism, 5.1003 Cardiovascular system chronic cadmium poisoning. 5 . 1000 Carnosine cobalt( 11) complexes kidney, 2,966 metal complcxcs. 2. 762 Carnotitc, 6,891 structure, 6, 892 Casey. Evans, Powell descriptors, 1.124 Cassiterite, 6, 855 Catalases. 4,263,264; 6.682.703,706. 982 imaging systems, 6, 126 Catalysis, 1, 28 activation small molecules, 6: 299-307 copper(I1) complexes, 5 : 7163-720 heterogeneous metal sulfides, 2, 526 homogeneous hydrogenation, 2, 70Y transition metal hydrides in. 2! 709 Lewis acid coordinated ligand reaction, 6.411 photochemical reactions, 1, W8 Catapinands anionic complexes, 2,950 classification, 2,920 Catechol, 3,5-di-f-butylmolybdenum complexes, 2. 398 Catecholate siderophores iron, 6,634 Catecholdiacetic acid in gravimetry. 1, 525 Catechol dioxygenases. 4: 230; 6, 707 iron, 6,634 Catechols antifoggants

Cerium(I1f) complexes

photographic emulsion stabilizers, 6, 98 metal complexes, 2,398

oxidative cleavage copper catalysts, 6, 393 reactions osmium tetroxide, 4,590 sequestering agents actinides, 6. 962 Catenands classilicatiun. 2, Y20 metal ion cornplcxcs, 2, 940 Cation concentration gradicnts biology metal cornplcxcs, 6, 551 Carion exchange resins, 6, 815 mineral processing, 6, 817 Cationic complexes molecular macrocycles, 2.921,943 Cations hydrolysis. 6,413 transport biology. 6,552 Catoptromers -.yee Enantiomers Cell division calciuni. 6.595 Cell membranes alkali mctal transport, 3, 54 Cclls labelled diagnostic nuclear medicine, 6,994 Cellulose dyes. 6.38 metal complexes: 2, 984 Cell walls transition metal binding, 6, 680 Cementation dcctrochemical basis, 6, 829 mineral proccssing, 6, 828, 829 Ccntrifug.d 1 contactors actinides Purex process, 6, 952 Centrifuging reprocessing irradiated nuclear fuels, 6, 935 Cephalosporins hydrolysis metal catalysis, 6 , 461 Cerate, tetrakis(dimethy1dithiophosphonium)stereochemistry. 1. 94 Cerate, Letrakis(pheny1enedioxy)stereochemistry, 1,94 Ceric ammonium nitrate, 3, 1114 Ceric sulfate, 3, 1.1 14 Cerium oxidation statc, IV solvent extraction, 1,523 Purex process, 6, 941 Cerium-144 recovery. 6. 959 Cerium, pentacarbonatostereochemistry, 1,99 Cerium, tetrakis(acety1acetone)-, 3, 1114 stereochemistry, 1,94 Cerium complexes retrakisldibcnzoylmethanate), 3, 1114 tctrapositive oxidation state, 3, 1 I I3 tetrapositive oxidation state catechol, 3, 1115 tetrapositive oxidation statc hydratcd ions. 3, 1113 organic oxyaniotis, 3, 1114 Cerium(II1) complexes cerium(1V) system water cleavage. 6,495 cupferron

Cerium(IL1) complexes thermal stability, 2,510 peptides hydrolysis, 6,425 Cerium(1V) complexes fluorides, 3,1115 peptides hydrolysis, 6,425 Cerium tetraalkoxides physical properties, 2,347 Ceruloplasmin, 6,656,672,699,700 copper complexes, 2,772,975 blood, 2,965 cytochrome oxidases, 6,683 ferroxidase activity, 6,671 labelled in medicine, 6,968 mechanism, 6,656 oxidase activity, 6,656 spectra, 6,652 structure, 6,656 Cesium leaching from Synroc, 6,961 Purex process, 6,940 Cesium auride, 5,863 Cesium complexes crown ethers, 3,40 porphyrins, 2,820 Cesium ions recovery from nuclear fuel waste, 6,959 Chalcocite brines, 6,853 Chalconatrite structure, 6,849 Chalcones thiol adducts photographic stabilizer, 6, 103 Chalcopyrite brines, 6,853 Icaching, 6,786 Charge control agents electrophotography, 6,123 Charge density wave, 6,135 Chelate effects cone angle concept, 2,1012 Chelating agents, 6,768 heavy metal poisoning, 6,767 Chelating resins mineral processing, 6,814,815, 823 Chemical analysis, 1 , 521-561 modified electrodes, 1,488 Chemical reactivity excited state, 1, 393 Chemiluminescence, 1,396 electrogenerated, 6,26 Chevrel phases, 3,1321 Chirality, 1, 182,190,193 Chiraphos, 1,200 Chitin uranium complexes geochemistry, 6,868 Chlamydomonas reinhardii swimming speed calcium, 6,595 Chloraluminite, 6,855 Cbloranilic acid in gravimetry, 1,533 Chlorates effective bond length ratios. 1,37 stereochemistry, 1,37 Chlorella spp. nitrate reductase, 6,664

Cumulative Subject Index

100

Chlorella vulguris nitrate reductase structure, 3: 1438 Chlorides electrooxidation, 1.488 gravimetry, 1: 533 leaching copper, 6.786 Chlorin, octaethyliron(I1) structure. 6,625 Chlorination platinum ammine complexes, 1,416 Chlorine cations CIF2+,3,314 ClF,+, 3, 316 Chlorine complexes bridge systems, 2: 678 single bridges, 2,680 six-coordinate, 2,687 Chlorine trifluoride, 3.314 structure, 1,45 Chlorins, 2.851 iron, 6,625 spectra, 2, 851 Chlormagnesite, 6,855 Chlormanganokalite structure, 6.846 Chlorocruorins, 6,6S9 Chloromethylation acetylacetone metal complexes, 6,205 Chloromethyl compounds toxicity, 4, 1270 Chloroperoxidase, 6,705 Chlorophylls, 2,982 alkaline earth metal complexes, 3,58 geochemistry, 6.863 photosynthesis, 6 , 590 Chloroplatinic acid, 5,489 catalyst hydrosilylation, 5, 357 Chlorosis iron complcxes, 6,763 Choline antimony analogue, 3,279 Chorioallantoic membrane calcium transport, 6,568 Chromatography optical resolution, lI26 radiochemical purity technetium-99,6,976 Chrome axurol S metallochromic indicator, 1,556 Chromium biology, 6,665 dissolution in acids, 3,716 electroplating, 6 , 7 , 8 electrowinning, 6>831,832 extraction cation exchange resins, 6,817 liquid-liquid extraction, 1,541 microorganisms, 6,681 oxidation states, 3,701 tolerance Leptospermum scoparium, 2,963 Chromium-51 red blood cell labelling, 6,994 Chromium, alkylcarboxylatodichlorofatty acids vesicular imaging systems, 6, 126 Chromium, his( 1,2-ethanediamine) bis(isothiocyanat0)photochemistry reactivity, 1,398

101

Cumulative Subject index

Chromium, bis( 1,2-rthanediamine)difluorophotochemistry, 1 , 3 9 3 Chromium, bis( 1,2-ethanediamine)oxalatocoordination isomerism, 1. 183 Chromium, diamminetetrakis(isothiocyanato)photoaquation chemical actinometer. 1.409 photochemistry reactivity, 1, 398 Chromium, dichlorobis( I ,?-ethanediamine)raccmization solid state, I , 467 thermal ver.sii.s photochemical rcactions, 1, 399 Chromium, dichlorutetrakis(amine)ligand field photochemistry, 1, 399 Chromium, dihalobis( 1.2-ethanediamine). hydrate photoaquation, 1,471 Chromium, heptafluoro-, 3,927 Chromium, heptakis(pentanenitri1e)bis( hexafluorophosphonate)structure, 1 , 7 2 Chromium, hexaamminchexacyanocobaltate coordination isomerism. 1 . 183 trioxalatoaluminum reactions, 1.27 Chromium, hexaaquaelectron transfer, 1.367 with hexaaquachromium, 1,370 with pentaamineisonicotinamidoruthenium,1,367 with pentaaquahydrovychromium, 1,370 isomerism, 1, 183 trichloride isomerism, 1, 183 Chromium, hexacyano-, 3,7U3,777 hexaamminecobaltate coordination isomerism. 1: 183 ligand field photochemistry+ 1:398 photochemistry excited states. 1.398 production, 3,704 Chromium, hexatluoro-. 3.427 Chromium, hexahalo-. 3. 889 Chromium, hexaiodo->3.766 Chromium, hexakis(dimethy1 sulfoxide)photoanation, 1,399 Chromium, (r-oxalatodireduction by chromium(lI), 1,378 Chromium, oxodipert,xupyridylstructure, 1, 24 Chromium, oxohalo-. 3- 935 Chromium, oxybis(dioxygeo)(p4.ridine)structure, 1, 61 Chromium, pcntaammincaquatrihalide ligand exchange, 1,469 water exchange, 1 , 2 9 2 Chromium, pentaamminechlorophotochemistry, 1 , 3 9 3 Chromium, pentaamminecyanophotochemistry, 1,393 Chromium, pentaammineisothiocyanatoabsorption spectrum, 1 387 Chromium, pentaammineselrnatoaquation, 1 , 2 9 2 Chromium, pentaamminethiocyanobase hydrolysis. I 504 Chromium, peniaaquachlorodichloride hydrate hydrate isomerism. 1- IS3 Chromium, pentaaquahydroxy~

I

electron transfer with hexaaquachromium, 1,370 Chromium. pentaaquamaleatoelectron transfer, 1,374 Chromium, pentafluoro-, 3,927 Chromium, pentahalo-, 3,766 Chromium. u-sulfatodireduction by chromium(II), 1, 378 Chromium. te traammineaquahromoreactions, 1 , 2 7 c.hromium. tetraaquadichlorochluridc dihydrate hydratr isomerism, I , 183 Chromium, lelrabromosolvated, 3.758 synthesis, 3,763 Chromiuml tetrachloroantiferromagnetic, 3, 761 ferromagnetic magnetic properties, 3,7559 optical properties, 3,759 structure,3,759 solvated, 3.758 synthesis. 3, 750 Chromium. tetrachlorooxytetraplienylarsenate stereochemistry, 1 , 4 4 Chromium, tetrahalo-, 3,889 Chromium, tetrakis(di0xygen)stereochemistry, 1 , 9 4 Chromium, triamminediperoxystructure. 1 . 7 8 Chromium, tricyanodiperoxystructure, 1, 78 Chromium, tritluoroelectronic spectra, 3, 757 magnetic properties, 3,757 structurcs. 3.757 synthesis: 3: 756 Chromium, trihaluclcctronic spectra, 3,764 magnetic properties, 3, 764 structure. 3, 764 synthesis, 3. 763 Chromium. tris(acety1acetone)structure. 1.65 Chromium. tris(bipyridy1)ligand field photochemistry, 1,398 photochemistry exciled states, 1, 398 Chromium tris(.3,.5-di-r-hutyIquinone)structure. 2 , 397 Chromiuml tris( 1,2-ethanediamine)pentacy anonickelate isomers, 1,207 photochcmistry reactivity, 1 , 398 photolysis. 1.397 reactions, 1 , 2 7 trichloride deamination, 1,470 trihalide deamination, 1,469 photochemical reactions, 1,471 trithiocyanate dcaminatiun, 1,470 Chromium. Iris( hexafluoroacety1acetonato)optical isomerism, 1, 28 Chromium. tris(oxa1ato)racemization solid state. 1,466 strychnine salt I

Chromium

Chromium

Cumulative Subject Index

racemization, 1,466 Chromium, tris( 1,lo-phenanthro1ine)ligand field photochemistry, 1,398 Chromium, tris(trifluoroacety1acetonato)isomerism, 1,28 Chromium, (q6-benzene)tricarbonylstereochemistry nomenclature, 1,131 Chromium complexes, 3,699-948 acetylacetone complex formation, 2,386 exchange reactions, 2,380 amidines, 2,276 bridging ligands, 2,198 chelating ligands, 2,203 anionic oxo halides, 3,944 applications, 6,1014 azo dyes, 6,41 biological effects, 3,947 carbamic acid, 2,450 paddlewheel structure, 2,451 carboxylic acids, 2,438 trinuclear, 2,441 carcinogenicity, 3,947 corroles, 2,874 crystal structures, 3,702 cyanides, 3,703 1,4-diaza-1,3-butadiene, 2,209 1,3-diketones ligand exchange reactions, 2,381 dimethyl sulfoxide, 2,488 eiectroplating, 6 , 4 , 5 geometric isomerism, 1,11 mixed oxidation state(II1 and VI) oxo. 3,945 mutagenicity, 3,947 neutral 1,3-diketones, 2, 402 NMR, 3,943 oxalic acid, 2,446 oxo oxidation catalysts, 6,351-354 peroxo oxidation, 6,333-396 phthalocyanines, 2,865 porphyrins, 2, 825 pseudohalides, 2,229,230 salicylic acid electrophotography, 6, 123 spectroscopy, 3,943 structures, 3, 943 triazines bridging ligands, 2,198 chelating ligands, 2,203 tridentate azo compounds geometrical isomerism, 6 , h 8 No-Np isomerism, 6,66 tridentate azo dyes synthesis, 6,46 trifluoroacetylacctone gas phase isomerization, 2,382 irradiation, 2,384 Chromium(0) complexes, 3,702 alkyl isocyanides, 3,704-709 aryl isocyanides, 3,704-709 2,2’-bipyridyl, 3,709 electrochemistry, 3,713 electronic spectra, 3,712 ESR spectra, 3,712 IR spectra, 3,712 magnetic properties, 3,710 synthesis, 3,709 cyanides, 3,703 Ruorophosphine, 3,714 germanium ligands, 3,709 I

isocyanides crystallography, 3, 708 spectroscopy, 3,708 synthesis, 3,707 magnetic behavior, 1,273 1,lO-phenanthroline, 3.709 electrochemistry, 3,713 electronic spectra, 3, 712 ESR spectra. 3- 712 IR spectra, 3,712 magnetic properties, 3,710 synthesis. 3,709 quinones, 3,716 tertiary phosphines dinitrogen, 3: 713 2,2‘:6‘,2”-terpyridyl, 3, 709 electrochemistry, 3,713 electronic spectra. 3,712 ESR spectra, 3?712 IR spectra, 3,712 magnetic properties, 3,710 synthesis, 3,709 tris(bipyridy1) NMR, 3,711 trjs(1, I0-phenanthroline) NMR, 3,711 Chromium(1) complexes, 3,702 alkyl isocyanides, 3,704-709 aryl isocyanides, 3,704-709 2,2‘-bipyridyl, 3,709 electrochemistry, 3,713 electronic spectra, 3,712 ESR spectra, 3,712 IR spectra, 3,712 magnetic properties. 3, 710 synthesis, 3,709 cyanides, 3,703 Buorophosphinel 3,716 isocyanides crystallography, 3, 708 electrochemistry, 3,709 spectroscopy, 3,708 synthesis, 3,707 magnetic behavior, I , 272 1,lO-phenanthroline. 3,709 electrochemistry, 3, 713 electronic spectra, 3,712 ESR spectra, 3,712 IR spectra, 3, 712 magnetic properties, 3,710 synthesis, 3,709 2,2’:6’,2”-terpyridyl, 3,70Y electrochemisty, 3,713 electronic spectra, 3,712 ESR spectra, 3: 712 IR spectra, 3,712 magnetic properties, 3,710 synthesis, 3,709 tertiary phosphines dinitrogen, 3,713 tris(bipyridy1) NMR, 3,711 Chromium(I1) complexes, 3.716-927 acetates. 2,440 aqueous solutions, 3,752 acctylacetone, 2,371 adenine, 3,726 alcohols, 3, 737 alkoxides, 3,737 alkyl isocyanides, 3,704-709 amines bidentate, 3,720 polydentate, 3, 721

102

103

Cumulative Subject Index

amino acids, 3,768 2-aminobenzenethiol, 3.769 2-aminomethylpyridine. 3, 726 8-aminoquinoline, 3, 726 ammines, 3,718 magnetic properties, 3, 718 spectroscopy, 3, 718 structures, 3, 718 synthesis, 3, 71.8 aqua, 3,735 arsenic ligands, 3,732 arsinc oxides, 3, 753 aryl isocyanidcs, 3.704-709 aryl oxides, 3,737 2,2'-bipyridyl, 3, 726 biurets, 3,739 bromides, 3,75&766 carbonates, 2,448 CdrbOraneS, 3,731 carboxylates, 3, 740 magnetic properties. 3, 752 mass spectra, 3, 752 structures, 3,748 synthesis, 3,745 chlorides, 3,75%766 chlorosulfates, 3,740 complexones, 3: 708 coordination numbcrs, 3, 701 corrins, 3,770 dehydration, 3. 717 dialkylamines synthesis, 3,729 1,2-diamino-2-methylpropane,3,720 1,2-diaminopropanel 3,720 1,3-diaminopropanel3,720 diethylenetriamine, 3,721 N,N-dimethylethylenediamine,3,720 NN-dimcthylcthylcncdiamine, 3,720 dimethyl sulfoxidcl 3.753 rne.so-5,12-dimethyl-114~8, 11-tetraazacyclotctradccane 3, 770 dinuclear photoelectron spectroscopy, 3, 750 disilamides synthesis, 3, 729 dithiocarbamates, 3,754 double sulfates hexahydrates, 3, 736 ethane-1,2-dithiol, 3,755 ethylenediamine. 3,720 fluorides, 3,756 glucose tolerance. 3,904 glutathione, 3, 905 halidcs, 3,755-766 anhydrous, 3,755

rnrs0-5,7,7,12,~4,~4-hexamethy1-1,4,8,11tetraazacyclotetradecane, 3,770 hydrates, 3, 735 hydrazines, 3,729 hydrides, 3,766 hydrogen, 3,766 hydroxy acids, 3,753 imidazoles, 3, 726 inner-sphere electron transfer: 3,716 iodides, 3. 75tk766 isocyanidcs crystallography, 3,708 electrochemistry, 3, 709 spectroscopy, 3,708 synthesis, 3. 707 Jahn-Teller distortion, 3. 701 p-ketoamines. 3,766 p-ketoenolates, 3,738

Chromium(II1)complexes

low-spin, 3. 703 magnetic behavior. 1,272 mandelic acid, 2,474 monohydrogenphosphate, 3,740 nicotinic acid. 3, 725,904 nitriles, 3,732 oxo anions. 3*740 1,lU-phcnanthrolinc, 3,726 o-phcnylcncbis(dimcthylarsinc),3, 734 phosphinato. 3,740 phosphine oxides, 3,753 phusphitcs, 3.740 phosphorus ligands, 3,732 phthalocyanines, 3,770 polyazamacrocycles, 3.770 polyprazolylborates, 3,731 porphyrins. 3,770.91 1 dioxygen adducts. 2, 325 pyrazoles, 3,722,726 pyridines, 3, 722 Schiff bases, 3, 766 polymeric. 3, 767 saccharin. 3,725 spectra, 1.252 stereochemistry, 3, 772 sullato, 3, 740 sulfur ligands, 3, 754 synthesis, 3,716,717 non-aqueous solutions, 3,717 by reduction of chromium(II1) solutions, 3, 716 solutions? 3,716 1.4,8.Il-tetraazacyclopentadecane,3, 770 1.4,8,12-tetraazacyclotetradecane,3,770 tetrahydrofuran, 3,739 1.4.8,1l-tetramethyI-l,4,8,1 I-tetraazacyclotetradecane. 3.770 tetranuclear electronic spectra, 3, 751 thiocyanate Grunwald-Winstein analysis, 1 , 505 thiocyanates, 3, 729 thiourca, 3.755 tricyanomethides, 3, 709 triethylenetetramine, 3,722 tripod ligands tetradentate, 3,734 tris(2-dimethylaminoethyl)amine,3,722 urea. 3,739 Chromium(II1) complexes, 3,701 acetates. 3,869 acetylacetonates, 3, 861 phase chcrnistry. 3,863 physical studics, 3,862 alcoholates, 3, 860 al koxides, 3, 860 alkyl, 3,779 alkylamines, 2,28 alkyl isocyanides, 3,704-709 amides. 3, 835,852 amines bidentate, 3,789-806 monodentate, 3, 787 amino acids, 3,902-908 hydroxy-bridged, 3,903 solution studies, 3,903 ammines, 3. 78(&787 polynuclear, 3,783 anilines: 3,788 antimony ligands. 3,852 aqua, 3,856 arsenic ligands, 3,852,901 aryl, 3.779 aryl isocyanides, 3,704-709

Chrorniurn(lI1) complexes azides, 3, 843 azo, 3,833 azo dyes electrophotography, 6 , 124 biguanides, 2,284; 3, 850 bipyridyls. 3,816 bis(oxalato), 3, 871

1,6-bis(2’-pyridyl)-2,5-diazahexane,3,812 borates, 3,869 camphorates, 3,862 carboxylates, 3, 869 catecholates, 3, 865,866 citrates, 3. 874 complexones, 3, 908 corrins, 3,911 cyano binuclear, 3,777 multinuclear, 3,777 tetranuclear, 3, 777 cyanoamines, 3,775 cyanoamrnines, 3,775 2,6-diacetyIpyridine, 3, 899 diamines aliphatic, 3,788 bidentate, 3, 797 diarnrnines, 3,781 cis-dicyanobis(ethylenediamine), 3: 794 diethylenetriamine, 3,806 P-diketonates chcmical reactivity, 3, 861 NMR, 3,864 optical activity, 3, 863 dimethylfuran, 3,875 dimethyl sulfoxide, 3,874 disulfido. 3,876 dithiocarbamates, 3, 883 1,l-dithiolates, 3,883 1,2-dithiolates, 3,883 dithiophosphates, 3, 883 doublet excited states reactions, I, 400 emission rules, 1,395 ethanolamine, 3,897 ethylenediamine, 2,31,33; 3,789-806 ammonolysis, 3,795 fluoro. 3,796 polynuclear, 3, 799 thiolato, 3, 796 ethylenediamine-N,N’-diacetato, 3.910 ethylenediaminetetraacetic acid, 3,908 guanidine, 2,283 halides, 3, 889 dimeric, 3,890 solution chemistry, 3,891 hexaammines, 3,783 hexafluoroacetylacetone, 2, 372 hexamines aliphatic, 3, 787 hydrazines, 3,834 hydroxamates, 3,866 hydroxy polymeric, 3,857 hydroxy acids, 3,873 aliphatic, 3,873 aromatic, 3,874 hydroxylamines, 3, 834 8-hydroxyquinoline, 3,8YY imidazoles, 3,821 irninoacetic acid, 3,910 isocyanates, 3,842 isocyanides, 3,779 crystallography, 3,708 electrochemistry, 3,709

Cumulative Subject Index spectroscopy, 3,708 synthesis. 3: 707 isoselenocyanates. 3, 842 isothiocyanates. 3* 837 P-ketoamines. 3,892-897 0-ketoenolates, 3* 861 ligand field states reactivity, 1?397 magnetic behavior, 1.272 malonaldehyde. 3. 861 malonatcs, 3, 873 2-mcrcaptoctbyIaminc, 3, 900 mixed-ligand reactivity, 1 . 398 monothio 0-diketonates, 3,901 nitrates, 3,867 nitriles. 3. 8-16 nitrilotriacetic acid, 3. 911 nitrito isomerism, 1. 184 nitrosyls. 3 . 823 alkoxido, 3: 830 amido, 3.830 arsines, 3, 826 azido, 3. 8L3 chalcogcns, 3, S26 cyano, 3,823 hydroxylamines, 3,823 isocyanides, 3.826 macrocycles, 3: 831 nitriles, 3.826 phosphines, 3.826 pyridinecarboxvlates, 3 pyridines, 3%823 N-thiocyanato, 3,823 organometallic, 3,897 oxalates, 3, 870 oxides, 3; 859 hydroxides, 3.859 N-oxides, 3,874,875 1’-oxides, 3,874,876 oximes, 3, 849 pentaammines, 3,783 pcn tamines aliphatic, 3,787 perchlorates, 3.869 peroxides, 3,859 phenanthrolines, 3, 816 phosphates, 3,868 phosphinates, 3: 868 phosphoric acid. 3,867 phosphorous acid, 3 ; 867 phosphorus ligands, 3,852 photosubstitution reactions, I , 399 stereomobility, I , 399 picolinic acid, 3,899 polyamines open chain, 3 , 8 6 8 1 5 polypyrazolylborates, 3,845 porphyrins, 3,911,913 I ,3-propylenediaminetetraaceticacid, 3, 910 pyrazines, 3,822 pyrazoles, 3: 822 pyridines, 3,815 l-(2-pyridyl)ethylamine di-p-hydroxo-, 3; SO5 l-(2-pyridyl)ethylene, 3,803 l-(2-pyridyl)methamine, 3,803 di-p-hydroxo-, 3,805 quinones, 3,865 reactivity, 1,297 Schiff bases, 3,892497 selenium ligands, 3.889

104

~

3 05

Cumulative Subject Index

o-semiquinoncs. 3. 865 spectra, 1,252 squarates, 3, 873 squaric acid, 2,455 sulfato, 3, 867 sulfides binary, 3,882 ternary, 3,882 sulfoxides, 3, 874 tartrates, 3, 873 tcllurium ligands, 3,88Y terpyridyls, 3, 816 tetraammines, 3,781 tetraethylenepentamine, 3.814 tetrahydrofuran, 3, 865, 867 tetramethylguanide. 3.850 tetramines, 3. 812 aliphatic, 3, 788 tetranitrosyls, 3, 832 thiobis(ethylenenitri1o)tetraacetic acid, 3, 911 thiocyanates bridged, 3,838 linkage isomers, 3: 841 thioethers, 3,876 thioglycolic acid, 3.901 thiolates, 3, 876 thionitrosyls, 3, 832 thiourea, 3,888 triamines aliphatic, 3, 788 2,2',2"-triaminotriethylamine. 3, 811 triammines, 3>781 triazinides, 3, 845 tridentate azo compound chromium complex synthesis from, 6,49 triethylenetetramine, 3, 808 trifluoromethylsulfatc. 3: 867 tris(oxalato), 3, 870 urea, 3,852, 86.5, $67 Chrornium(1V) complexes, 3,701, 927 alkoxides, 3. 928 alkyls, 3, 928 amides, 3,930 chloro, 3,927 cyano, 3,927 ffuoro, 3,927 halo, 3,927 peroxo, 3,945 porphyrins, 3,916 Chromium(V) complexes, 5701,931-938 cyclarn, 3,918

Citric acid

hexafluoro, 3, 938 organoimido, 3,945 peroxo, 3,945 Chromium dioxide, 3,928 Chromium fluoride, 3,932 Chromium oxide applications, 6, 1014 Chromium salts aquated kridenhte azo compound chromium complex synthesis from, 6,47 azo dyes, 6 . 3 6 Chromium lelrafluoride, 3, 927 Chromium trichloride hexahydrate hydrate isomerism, 1,183 Chromium trioxide, 3,941 Chromogrannin A, 6,578 Chrornyl bromide. 3,940 Chromyl chloride, 3,940 Chromyl halides, 3,933,935,938 Chromyl nitrate: 3,940 Chromyl perchlorate, 3,940 Chugaev's rule of rings, 1, 14 Chugacv's salts, 5,381 Cigarette smoking cadmium toxicity, 5, 1000 Cimetidine metal complexes, 2,801 Cinnabar: 5: 1069 Cinnamic acid methyl ester hydrogenation, 6,250 synthesis, 6,285 reduction catalysts. rhodium complexes, 6,245 Cinnamic acid, a-acetamidoasymmetric hydrogenation catalysts, rhodium complexes, 6,250,25 1 rncchanisms, 6,253 Cinnamic acid, u-acylaminoasymmetric hydrogenation rhodium complexes, 6,251 Cinnamic acid, o-mercaptohydrometal complexes, 2,655 Cinnamic acid, (E)-&methylasymmetric hydrogenation catalysts, 5 , 251 Cinnamic 6-carboxypicolinic monoanhydride hydrolysis metal catalysis, 6,463 5,4-dimethyl-l,4,8.11-tetraazacyclotetradeca-4,6,11,13-Cinnamic picolinic anhydride tetraenates. 3?924 hydrolysis halogens, 3, 932 metal catalysis, 6,463 5,7,7,12.14,14-hexamcthyl-1,3,8~11C-;seffect, 1, 317 tetraazacyclotetradecanc, 3,920 Cisplatin -see Platinum, cis-dichlorodiamminemagnetic behavior, 1,271 Cis-trans isomerization, I , 467 oxides, 3,936 Citrate lyase peroxides, 3, 936, 945 activation phthalocyanines, 3. 924 magnesium ions, 6,584 polyazamacrocycles, 3.91E-924 Citratotellurates, 3, 303 porphyrins, 3,916 Citric acid salen, 3, 917 ionization, 2,465 spectra, 1,251 isomerization tertiary n-hydroxycarhoxylates, 3,936 aconitase, 6,475 1,4,7,10-tetraazacycIndecaii~, 3,921 metal complexes, 2,476,963 1,4,6-triazacyclononanc, 3,924 crystdl structure, 2,476 tris(k-hydroxo) 3.924 geochemistry, 6,867 Chromium(V1) complexes, 3, 70.1, 938 naturally occurring, 2, 962 chloro, 3,940 KMR, 2,467 L-cysteine, 3,948 mincrals fluoro, 3,940 weathering, 6,868 glutathione, 3,947 moIybdenum(V1) complexes ~

Citric acid

Cumulative Subject ladex

IR spectra, 2,469 protonation, 2,465 zinc transport, 6,672 Citric acid, fluoroabsolute configuration, 2,478 Citric acid, hydroxycrystal structure, 2,478 Clathrates amines, 2,25 Claus’s ammonia theory, 1, 5 Clay electrode modification, 6,23 Clay minerals ruthenium oxide support catalysts, hydrogen production from water, 6,523 Cleanex process, 6,959,960 Clostridium thermoaceticurn carbon monoxide dehydrogenase nickel, 6,645 Cluster complexes metal alkoxides, 2,349 selenium, 2,667 tellurium, 2,671 Clusters, 1, 135 cubanoid MO bonding theory, 1,152 geometrical structure, 1, 138 gold-silver alloy, 1, 170 irowsulfur redox potentials, 1,513,515 metal-metal bonding, 1, 169 nomenclature, I , 124,133 polyhedra, 1, 138 synthesis, 1, 171 Coals energy resource, 6,488 structure, 6,856 Cobalamin, 2,983 Cobalamin, adenosyl-, 2,984; 6,637 coenzyme, 6,640 Cobalamin, cyanolabelled in medicine, 6,968 microorganisms, 6,681 Cobalamin, methyl-, 2,984; 6,637 cofactor, 6,642 Cobalamins, 6,637 reactions, 6, 639 Cobaloxime, alkyldegradation, 1,447 Cobaloximes, 6,638 Cobalt analysis, 1,522 biochemistry, 6,637-643 deficiencies metal complexes, 6,766 extraction cation exchange resins, 6,817 hydrometallurgy, 6,786 liquid-liquid extraction, 1,538 masking, 1,538 microorganisms, 6,681 powder mineral processing, 6, 829 precipitation hydrolysis, 6,827 recovery chelating resins, 6,825 transport, 6,672 Cobalt, (acetonitri1e)trinitratostereochemistry, 1,82 Cobalt, y-amido-yforrnatobis(tctraarnmine)reduction

106

by chrorniurn(IT), 1,376 Cobalt, amminechlorobis(dioximine)solvolysis, 503 Cobalt, amminechlorobis( 1,2-ethanediamine)isomerism, I , 25 Cobalt, aquabis(l,2-ethanediamine)sulfatoreactions, 1,27 Cobalt, aquiichlorobis(l.2-ethanediamine) racemization solid state, I , 467 Cobalt, aquahalotctraamminedihalide anation, 1,469 Cohalt , aquapentaarnrnine-, I , 3 Cobalt, aquapentacyanoanation? 1.310 isomerization, 1,186 Cobalt, aquatetracyanosulfitoanation, 1,310 Cobalt, bis(dimethy1glyoxime)isocyano-,1, 186 Cobalt, bis( 112-ethanediamine)bis(isothiocyanato)chloride ionization isomerism, 1, 183 Cobalt, bis(l,2-ethanediamine)halo(pyridinc)dihalide anation, 1,469 Cobalt, bis(l,2-ethanediaminc)nitritothiocydnatoisomerization, 1, 365 Cobalt, bis( 1.2-ethsnediamine)( 1,lO-phenanthroline)racemization, 1.466 Cobalt, bis(l,2-ethanediamine)(phenyl phosphate)structure, 1,203 Cobalt, bis( I ,2-ethanediamine)phosphatostructure, 1,203 Cobalt, bis( 1,2-ethanediamine)pyrophosphatostructure, I , 202 Cobalt, bis-phydroxooctaamminedireduction by chromium(II), 1, 378 Cobalt, hrornobis(l.2-etbanediamine)nitrosolvolysis, 1,505 Cobalt, bromobis(l,Z-ethanediamine)(pyridine)dibromide ligand exchangc 1,469 Cobalt, bromochlorobis(l.2-ethanediamine)hydrate thiocyanate aquation-anation, 1,469 Cobalt, cis-chloroamminebis(1,2-ethanediamine)optical isomerism, 1, 12 Cobalt, chlorobis(l,2-ethanediamine)solvation, 1,503 Cobalt, ChlOFObiS(1,2-ethanediamint)isothiocyanatothiocyanate ionization isomerism, 1,183 Cobalt, chlorobis(l,2-ethanediamine)nitrochloride ionization isomerism, 1, 183 Cobalt, chloropentaammine-, 1 , 3 chloride preparation, 1 , 7 , 8 Cobalt, R-a-cyanoethylbis(dimethylg1yoximato)racemization, 1,470 Cobalt, diacetatobis(methylirnidazoly1)angular parameters, 1,59 Cobalt, dimminebis( dimethylg1yoxime)decomposition, I , 186 Cobalt, diarnminediaquadinitrosostructure: I, 26 Cobalt, diamminedichloro(172-ethanediamine)hydrate thiocyanate isomerization, 1:469 reactions, 1,27 Cobalt, diaquabis(dimethylg1yoxymethylato)~

Cumulative Subjecs Index

107

electron transfer, 1,366 Cobalt, diaquabis(1,Z-ethanediamine). trihalide anation, 1,469 trinitrate anion exchange, 1,469 Cobalt, dibromobis(1,2-ethanediamine)bromide halogen exchange, 1,468 synthesis, 1,469 ch1orid e halogen exchange, 1,468 isomerization, 1,467 Cobalt, dibromobis(l,2-propancdiamine)chloride hydrate halogen exchange, 1,468 Cobalt, dibromotris(difluoropheny1phosphine)structure, 1,45 Cobalt, dibromotris(dipheny1phosphine)structure, 1,45 Cobalt, dicarbonyl-q5-cyclopentadienylexchange reactions, 1,290 Cobalt, dichlorobis(N,N’-dimethyl-1,2-ethanediamine)chloride hydrate isomerization, 1,468 Cobalt, dichlorobis(l,2-ethanediamine)base hydrolysis, I , 304 chloride anation, 1,469 halogen exchange, 1,468 chloride hydrate isomerization, 1,468 isomers, 1,191 nitrate preparation, 1,469 nitrite ionization isomerism, 1.183 racemization solid state. 1,467 solvolysis, 1,505 stereoisomers, 1,190 Cobalt, dichlorobis( 1Jpropanediamine)bromide hydrate halogen exchange, 1,468 chloride hydrate dehydration-dehydrochlorination, 1,468 isomerization, 1: 468 isomerization, 1,467,468 Cobalt, dichlorobis( 1,3-propanediamine)conformation, 1,197 Cobalt, dichloro(l,10-diamino-4,7-dithiadecane)configuration, 1,159 Cobalt, dichloro(triethy1enetetramine)chirality, 1,194 isomerization, 1,467 isomers, 1,201 Cobalt, diisothiocyanatobis(triethy1phosphine)structure, 1,24 Cobalt, dinitratobis( trimethylphosphine oxide)angular parameters, 1,57 structure, 1,57 Cobalt, dinitratobis\tris(dimethyiamino)phosphine oxide]angular parameters, 1,57 Cobalt, (1,2-ethanediamine)bis( 1,lO-phenanthro1ine)racemization, 1,466 Cobalt, N,N’-ethylenebis(salicy1ideniminato)complexes with bis(hexafluoroacetylacetone)copper, 2,

387 Cobalt, ethylenedinitrilotetraacetatoreaction with hexacyanoferrate. 1,376 Cobalt, ethylmalonatopentaamminereactions

Cobalt

with hexaaquachromium, 1,377 Cobalt, glycinato(triethy1enetetramine)isomers, 1,202 Cobalt, hexaammine-, 1,3 chloride structure, 1.5,7 electron transfer, 1,365 history, 1 , 2 oxalate history, 1,3 1-(2-pyridylazo)-2-naphthol clectron recording system, 6,127 solvents, 1 26 structure, 1,7 Cobalt, hexaamminetrifluoroacetatophotothermography, 6,119 Cobalt, nitropentaammine-, 1,3 Cobalt, octacarbonyldiexchange reactions, 1,289 GIbalt , pentaammineelectron transfer, 1,373 in isomerization of pentaamminethiocyanatocobait, 1, 465 reduction, I , 375,378 structure, 1,8 Cobalt, pentaammineaquaelectron transfer, 1,371 trichloride ligand exchange, 1,469 trihalide ligand exchange, 1,469 photochemical reactions, 1,471 water exchange, 1,292 Cobalt, pentaamrnineaspartatoreduction electron transfer, 1,374 Cobalt, pentaamminebenzoatoreduction electron transfer, 1,374 Cobalt, pentaarnrninechlorodichloride ligand exchange, 1,469 electron transfer, 1,365 hydrolysis, 1,510 sulfate structure, I , 8 Cobalt, pentaamminecyanoisomerization, 1,186 Cobalt, pentaamminehydroxythiocyanate isomerization, 1,185 Cobalt, pentaammineisonicotinamidoelectron transfer, 1,373 with hexaaquachromium, 1,369 reduction by chromiurn(II), 1,375 CobaIt, pentaammineisothiocyanato-, 1,185 reduction by hexaaquachromium, 1,376 solubility, 1,185 Cobalt, pentaamminemaleatoelectron transfer, 1,374 reduction by hexaaquachromium, 1,374,376 Cobalt, pentaammine(Nmethy1isonicotinoato)reduction electron transfer, 1,374 Cobalt, pentaamminemolybdateaquation, 1,291 Cobalt, pentaamminenitratothiwyanate isomerization, 1,185 Cobalt, pentaamminenitrilotriacetato-

Cobalt

Cumulative Subject Index

electron transfer with hexaaquairon, 1,369 Cobalt, pentaamminenitritoisomerization, 1,465 iinkage isomerization reactions, 1 365 Cobalt, pentaamminenitrodichloride linkage isomerism, 1,184 photochemical reactions, 1,471 Cobalt, pentaammine-0-(pyrazinecarbony1ato)electron transfer with chromium(II), 1,373 Cobalt, pentaammineparaformylbenzoatoreactions with chromium(II), I , 377 Cobalt, pentaamminepentacyanocyano bisisomerization, 1,186 Cobalt, pentaamminepentacyanoisocyanobisisomerization, 1,186 Cobalt, pentaamminethiocyanato-, l 1185 base hydrolysis, 1,504 charge transfer transition, 1,471 isomerization, 1,185 linkage isomerization, 1,465 labelling studies, 1,465 solubiiity, 1, 185 thiocyanate ligand cxchangc, 1,468 Cobalt, pentaamminc(thiosu1fato)linkage isomers, 1, 186 Cobalt, pentacyanoelectron transfer, 1,366 Cobalt, pentakis(nitrosoto1yI)stereochemistry, 1,40 Cobalt, pentakis(trideuteroamrnine)reduction, 1,375 Cobalt, p-peroxobis(pentaammine)cyclic voltammetry, 1,482 Cobalt, tetraamminestructure, 1 , 8 Cobalt, tetraammine(aden0sine triphosphate)isomers, 1,203 Cobalt, tetraammineaquahydroxyreactions, 1,27 Cobalt, tetraamminedichloroisomerization, 1,182,201,467 Cobalt, tetraamminedihydroxycobalt(II1) salt structure, 1, 184 Cobalt, tetraamminepyrophosphatostructures, 1,202,203 Cobalt, tetraammine(sarc0sine)chirality, 1,198 Cobalt, triamminestructure, 1, &-lo Cobalt, tricarbonatoreactions, 1,22 Cobalt, tricarbonylnitrosoexchange reactions, 1,290 Cobalt. trichloroequilibrium constant, 1,517 Cobalt, trichlorobis(triethy1phosphine)structure, 1,45 Cobalt, trichlorotris( 1,2-ethyIenediamine)conformation, 1,197 Cobalt, (triethy1enetetramine)isomerism, 1,200,201 Cobalt, trinitratostructure, I , 67 Cobalt, tris(acety1acetone)structure, I , 62,65,67 Cobalt, tris(bipyridy1)structure, 1 , 6 4

10s

Cobalt, tris(dimcthy1 dithiophosphat0)structure, 1,67 Cobalt, tris(dithiooxa1ato)structure, 1,68 Cobalt, tris(1,Z-ethanediamine)conformation. 1.25, 197 polarography; 1; 481 racemization, 1, 466 solid state, 1,466.467 reactions, 1, 27 redox potential, 1,514 structure, I, 67 Cobalt, tris(ethy1dithiocarbonaio)structure, I , 67 Cobalt, tris(oxa1ato)racemization solid state; I, 467 structure, 1: 68 Cobalt, tris(1,lO-phenanthro1ine)racemization, 1,466 structure, 1,64 Cobalt, tris(l,2-propanediamine)complexes structure, 1; 25 conformation, 1,25 nomenclature, 1, 129 stereonotation, 1: 129 Cobalt, tris(pyrro1idinedithiocarbamato)gravimetry, I , 535 Cobalt, tris(tetraamrnine-p-dihydroxocoba1t)optical isomerism, 1,13 Cobalt, tris(tetramerhy1enediamine)structure, I , 67 Cobalt ammines configuration, 1, l G 1 3 history, 1 , 3 structure, 1,7710 Cobaltate, diamminediaquadicyanostructure, 1 ,2 6 synthesis, l1 22 Cobaltate, (1,2-ethanediamine)('l,2-propanediaminc)dinitritosynthesis, 1 ,2 2 Cobaltatel hexacyanodiscovery, lI3 Cobalt complexes. 4,635-882 acety laceto ne pyridine complexes, 2, 386 structure, 2,388 tetranuclear, 2,371 ADP, 4,760 amides, 2,491; 4,682 amidines chelating ligands, 2,205 amines base hydrolysis, 2.28 applications, 6,1018 arsenates, 4: 774 arsenic ligands, 4,767-775 ATP, 4,760 azo dyes, 6,41 structure, 6,42 bipyridyl, 4,691 bis(dimethylglyoximato), 6,638 bis(dithiolates)? 4,876 boron ligands. 3,99 cage compounds in hydrogen production from water, 6, SO7 carboxylates, 4,790 catalysts asymmetric hydrogenation, 6,257 carbon dioxide reactions, 6,294 carbonylation, 6,269

109

Cumulative Subject Index

hydroformylation, 6,259 hydrogenation, 2,711;6,236 oxidation, 6,384-389 corrins, 2,884 corroles, 2,874 cyanates, 4,679 cyanides reduction, 4,646 synthesis, 2,9

1,4-diaza-1,3-butadiene, 2,210 1,3-diketones ligand exchange reactions, 2,381 dimethyl sulfoxide, 2,488 stoichiometry, 2,488 dipyrazolyl ketone, 2,256 disulfides, 4,829 1,2-dithiolates, 4,871 1,3-dithiolenes, 4,880 geometric isomerism, 1, 11 guanidine, 2,283 hexaammine reduction, 1,333 imaging processes photography, 6,11.3 nitriles, 4,674 nitrito, 4,666 nitro, 4,666 oxidation catalysts, 6,372 nitrosyl, 4,657 bonding, 4,663 reactivity, 4,664 structure, 4,663 synthesis, 4,657 nitrosyl insertion reactions, 2: 115 oximes, 2,271 oxygen ligands, 4,775829 peptides, 4,682 peroxo, 4,775,784,785 binuclear, 2,323 phenanthroline, 4,691 phosphinates, 4,767 phosphine oxides, 4,767 phosphines, 4,701 dinitrogen, 4,709 hydrides, 4,704 nitrosyl, 4,711 phosphinites, 4,746 phosphites, 4,704,746,766 phosphoamidates, 4,766 pbosphonates, 4,766 phosphonites, 4,746 phosphoramides, 4,767 phosphorus ligands, 4,699-767 photographic devcloper. 6,99 photothermography, 6, 118,119 phthalocyanines, 2 , 867 in oxygen production from water, 6,534 polypyrazolylborates, 2,252 porphyrins, 2,837 reactions, 2,845 properties, 4,637 pseudohalides, 2,231,232 putrescine crystal structure, 2,44 pyrophosphates, 4,760 reactions, 4,637 Schiff bases, 6,638 selenates, 4,880 selenites, 4,880 selenium ligands, 4,B O selenocyanates, 4,679 selenophosphinates, 4,869 sepulchrates, 1,22

silyl, 4, 655 structure, 4,637 sulfenates, 4,833 sulfides, 4:829,849 sulfinates, 4:833 sulfur ligands, 4,829-880 trans effect, 4,856 superoxo, 4,775,776,781 mononuclear, 2,323 reactions, 2,329 structure, 6,319 synthesis, 4,637 terpyridyl, 4, 691 thiocyanates, 4,679 thiolates, 4,833 metal binding, 4,847 thionitro, 4,858 thionitrosyl, 4,858 thiophosphinates, 4,869 triamines, 2,50 triazines chelating ligan&, 2,205 tridentate azo compounds N,.-N@ isomerism, 6, 66 tridcntate a20 dyes synthesis, 6 , 5 0 trifluoroacetylacetone flash photolysis, 2,384 triphosphates. 4,760 tris(l,2-dithiolates), 4,876 ureas, 4,682 urylene, 2,286 Cobalt(0) complexes arsenic ligands, 4,769 bipyridyl, 4,691 carbon disulfide, 4,646 cyanides, 4,646 phenanthroline, 4,691 phosphines, 4,718 bidentate, 4,728 rnultidcntate, 4,738 tridentate, 4,738 phosphinites, 4,747 phosphites, 4,747 phosphonites, 4,747 terpyridyl, 4,691 Cobalt( -I) complexes arsenic ligands, 4,769 bipyridyl, 4,691 cyanides, 4,646 phenanthroline, 4,691 phosphines bidentatt, 4,728 monodentate, 4,718 mulridentate,4,738 tridentate, 4,738 phosphites, 4,747 phosphites, 4,747 phosphonites, 4,747 terpyridyl, 4,691 CobaltII) complexes arsenic ligands, 4,769 bipyridyl, 4,691 carbon dioxide, 2,452;4,637 cyanides, 4,647 formato, 4,791 magnetic properties, 1,274 peroxo dioxygen, 2,318 phenanthroline, 4,691 phosphines, 4,722 bidentate, 4,735 multidentate, 4,744

Cobalt(1) complexes

Cobdt(T) complexes

Cumulative Subject Index

tridentate, 4,744 phosphinites, 4,747 phosphites, 4,747 phosphonites, 4,747 terpyridyl, 4,691 Cobalt(I1) complexes acetylacetone, 2,371 arsenic ligands, 4,769 bipyridyl, 4,691 carbonates, 4, 811 carnosine kidney, 2,966 citric acid crystal structure, 2,477 cyanides, 4,648 dioximes, 2,271 dioxygen mononuclear, 2,320 dithiocarbonates, 4,868 ethers, 4,828 formazans dyes, 6,78 hexafluoroacetylacetone, 2.377 histidine, 2,747 hydroxy oximes, 2,273 imidazole, 4,693 magnetic properties, 1,273 maleic acid, 2,476 nitroaminoguanidine, 2, 283 oxalic acid, 2,444 oximes, 2,270 phenanthroline, 4,691 phosphines, 4,724 bidentate, 4,736 multidentate, 4,745 tridentate, 4,745 phosphinites, 4,749 phosphites, 4,749 phosphonites, 4,749 in photochemical nitrogen production from water, 6, 509 porphyrins dioxygen adducts, 2,326 purine, 4,683 pyrazine, 4,683 pyrazole, 4,693 pyridine, 4,683 reduction vanadium(I1) complexes, 3,472 Schiff base reaction with oxygen, 1,515 selenenates, 4,881 seleninates, 4,881 selenolates, 4,881 selenophosphinates, 4, 870 spectra, 1,254 squaric acid, 2,455 sulfides, 4,849 terpyridyl, 4,691 tetrazole, 4,693 thiophosphinates, 4,870 thiosemicarbazones, 4,857 triazine, 4,683 triamle, 4,693 trithiocarbonates, 4,868 Cobalt(II1) complexes acyclic tetramines isomerism, 1,200 alkenedithiolates, 4,869 alkyl monocarboxylates, 4, 792 amides, 4,682 amines, 2,25,55 structure, 2,25

110

amino acid esters hydrolysis, 6,427 amino acids, 6,213 oxidation, 2,758 ammine reduction, 1,332 arsenic ligands, 4.773 aryl monocarboqlates, 4,792 biguanide, 2,284 bipyridyl, 4,692 bis(l,2-diaminoethane) cyclization, 6, 189 carbonates, 4,811 carboxylates quadridentate, 4,803 quinquedentate, 4, 808 sexidentate, 4,808 synthesis, 4,790 tridentate, 4,803 chlorites, 4,825 chloroamine aquation, 1,509 chromates, 4,825 citrates, 4,803 citric acid crystal structure, 2,477 cyanatcs, 4,679 cyanides, 4,652 synthesis, 2: 9 dibenzocorromins, 6, 176 dicarboxylates, 4>800 dicarboxylic acids, 2: 443 dioximes, 2: 271 dipeptides, 2,766 disulfides, 4,855 1,l-dithio acids, 4,860 dithiocarbamates, 4, 864 dithiocarbimates, 4,869 dithiocarboxylatcs, 4,864 1,l-dithiolates, 4,860,868,869 ethylenediamine, 2,33 formato, 4,791 hydroxy acids IR spectra, 2,469 hydroxycarboxylates, 4,802 IR spectra, 2,469 imidazole, 4,697 imines, 6,185 iodates, 4,825 iodine polyoxyanions 4,826 isothiocyanates, 4,858 ligand field states reactivity, I, 400 magnetic behavior, 1,273 malates, 4,803 maleic acid conformation, 2,467 molybdates, 4,825 molybdenum polyoxyanions, 4,826 niobium polyoxyanions, 4,826 nitriles, 4, 674 nitrosyl, 2, 104 one-coordinated alkylamine, 2,28 orthophosphates, 4,750 halides, 4: 753 oxyanions, 4,811 peptides, 4,682 perchlorates, 4,825 perrhenates, 4,825 phenanthroline, 4,682 phosphate ester hydrolysis, 6,446 phosphates, 4,750 phosphines, 4,726 ~

111 bidentate, 4,736 phosphinites, 4,749 phosphites, 4,749 phosphonites, 4,749 photography image amplification, 6,117 purine, 4,687 pyrazine, 4,687 pyrazole, 4,697 pyridine, 4,687 reactivity, 1,293 reduction, 1,24 salicylates, 4,802 salicylic acid, 2,482 selenates, 4,817 selenenates, 4,881 seleninates, 4,881 selenites, 4,820 selenocyanates, 4,679 selenolates, 4,881 selenophosphinates, 4,871 spectra, 1,253 sulfamides, 4,858 sulfates, 4,817 sulfenates, 4,835 mixed bidentates, 4,839 monodentate, 4,835 quadridentate. 4,847 sexidentate, 4 , 847 tridentate, 4,847 tris(bidentate), 4,837 sulfides, 4,849 bidentate, 4,850 multidentate, 4,852 sulfinates, 4,835 mixed bidentates, 4,839 monodentate, 4,835 quadridentate, 4,847 sexidentate, 4,847 tridentate, 4,847 tris(bidentate), 4,837 sulfites, 4,820 sulfonamides, 4,858 sulfones, 4,849 bidentate, 4,850 multidentate, 4,852 sulfoxides, 4,849 bidentate, 4,850 multidentate, 4,852 tartaric acid NMR, 2,468 structure, 2,471 tartrates, 4,803 tellurates, 4,817 tcrpyridyl, 4,692 tetrazola te isomerization, 1, 186 tetrazole, 4,697 thiocyanates, 4,679 thiolates, 4,835 mixed bidentates, 4,839 monodentate, 4,835 quadridentate, 4,847 sexidentate, 4,847 tridentate, 4,847 tris(bidentate), 4,837 thiophosphinates, 4,871 thioselenocarbamates, 4,&j4 thiosemicarbazides, 4,857 thiosulfates, 4,817 thioxanthates, 4,866 tnalkylphosphine dithio acids, 4,867

Cumulative Subject Index

Conalbumin

triazine, 4,687 triazole, 4,697 l,l,l-tris(aminornethyl)ethane,6,191 tris(l,2-diaminoethane), 6,190 tungstates. 4,825 tungsten polyoxyanions, 4,826 two-coordinated alkylamine, 2,28 ureas, 4,682 water decomposition, 6,493 xanthates, 4,866 Cobalt(1V) complexes magnetic behavior, 1,272 Cobalt hydridcs catalysts water cleavage, 6,495 Cobalt hydroxide amino acid ester hydrolysis, 6,434 in electrochemical production of oxygen from water, 6,

534 Cobalticyanide discovery. 1 , 3 Cobaltitungstates, 3,1042 Cobalt(I1) salts catalysts oxygen production from water, 6,517 Colrinamides reactions, 6,639 Coboglobin, oxyESR, 6,686 Coccoliths calcium deposition, 6,597 Coenzyme BIZ,2,887 Coenzyme M, 6,643 Cofactor M reductase molecular weight, 6,645 Collagenase zinc, 5 , 1006 Collcctors cationic Rotaticm, 6, 783 mineral processing, 6,780,781 Colloids labelled diagnostic nuclear medicine 6,994 Colorimetry calcium biology, 6,550 Color photography metallized dyes, 6,106 Columnar stacked structures, 6, 34 Column chromatography amine metal complexes, 2,25 Complex anions nomenclature, 1,122 Complex cations nomenclature, 1,121 Complex formation, 1,307 associative mechanism, 1,310 rate law, 1,307 Complexometric titrations, 2,782 Complexones, 2,777-791 applications, 2,790 macrocyclic, 2,789 metal complexes titrimetry, 1,554 metallochromic, 2,789 pK, 2,786 Computer modelling solvent extraction reprocessing irradiated nuclear fuels, 6,935 Conalbumin animal infections, 6,679

Concanavalin Concanavalin, 2,773 Concanavalin A, 6,572 manganese, 6,587 Concentration mineral processing flotation, 6,780 Concerted electron transfer oxidases, 6,683 Cone angle concepts, 2,1012-1028 chelate effects, 2, 1012 definitions, 2,1015 models, 2, 1015 phosphincs chiral, 2, 1014 polydentate, 2, 1013 solubility effects, 2, 1014 use, 2,1028 Cone angle factor, 2, 1019 Cone angles computer generated, 2,1020 estimation mathematical, 2, 1018 X-rays, 2, 1022 Configuration cobalt ammines, I , I C 1 3 X-ray diifraction, 1, 16 Conformational analysis, 1, 197 Control processes biology calcium, 6,591 Cooley's anemia treatment chelating agents, 6,768 Coordination numbers geometries and, 1,31-101 Coordination polymers electrical conductivity, 6, 151 Coordinative unsaturation catalysis transition metal Complexes, 6,230 Copper analysis, 1,522 antagonism molybdenum, 6,657 antiarthritis drugs, 6, 759 biochemistry, 6,648-656 biological systems, 5,535 biological transport, 5,721 deficiencies metal complexes, 6,765 dimethylglyoxime complex. 1.525 dodecametallic complexes cuboctahedron, 1,167 electronic configuration, 5,534 electroplating, 6 , 9 acid baths, 6,lO extraction cation exchange resins, 6,817 leaching, 6,785 metabolism metallothioneins, 6,673 microorganisms, 6,681 occurrence, 5,534,720 oxidation states, 5,535 pIants ethylene effect, 6,656 precipitation mineral processing, 6,828 properties, 5,534 recovery chelating resins, 6,825 removal Wilson's disease, 6,769

Cumulative Subject index solvent cxtraction o-hydroxyoximes. 6.799 storage metallothioneins, 6,672 microorganisms. 6.681 tolerance Armeria maritima,2.964 Becium homblei, 2,964 toxicity, 5,534 transport, 6,671 Copper-64 myambutol complexes hepatohiliary system imaging techniques, 6. !NO Copper, bis( acety1acetonc)spectrum, 1,230 Copper, bis(A',N-diethylethylenediamine)dichlorate thermochromism, 1,470 Copper, bis(g1ycinato)hydrate isomerization, 1,468 Copper, bis(hexafluoroacety1acetone)complex with N - N ethylcnebis(salicylideniminato)cobalt, 2,387 Copper, diarnrninestructure, 1 1 4 copper, (ethyl valinate-N,N-diacetat0)diaquastructure, 6,421 Copper, hexadecakischloropentakis-, 1, 137 Copper, hexakis(imidazo1e)dinitrate structure; 1: 53 Copper, hexakis(pyridine 1-oxide)diperchlorate structure: I, 53 Copper, hexakis(2-pyridone)diperchlorate structurc, I , 53 Copper, tetraamminehistory, 1, 2 Copper. tris( 1 .%-ethanediarnine)salts structure, 1,66 sulfate structure, 1,66 Copper, tris(ethy1ene glycol)sulfate structure, 1,66 Copper, tris(l,1,1.5,5,5-hexafluoroacetylacetone)salts structure, 1, 66 Copper, tris(octarnetby1pyrophosphoramide)diperchlorate structure, 1,66 Copper, tris( 1 JO-phcnanthro1ine)salts structure, 1,6h Copper blue proteins, 5,721 Copper(I1) carboxylates structure, 6,791 Copper chloride Cu3Cl3, 1,28 Copper complexes, 5,533-750 acet ylacetone hydrolysis, 2,379 photoreduction, 2,384 amid i nes bridging ligands, 2,201 amine oxides bridging, 2,496 amino acids blood plasma, 2,965 amino oximes, 2,274

112

113 antiarthritis drugs, 6 , 759 anticancer drugs, 6,758 applications, 6,1022 binuclear models, 6,654 biology, 6,549 carhoxylic acids binuclear, 2, 441 catalysts hydrogenation, 6.250 corrins, 2,885 corroles, 2,875 cupferron, 2, SOY cyanides structure, 2,8 1,4-diaza-1,3-butadiene, 2: 211 dithiocarbamates, 2, 585,586 electron transfer Franck-Condon barrier, 6,653 fulvic and humic acids, 6,860 fungicides, 6, 1023, 1025 hexafluoroacetylacetone amine complexes, 2,387 formation constants, 2,387 nitroxide complexes, 2,388 octahedral ctlordinaticm, 2, 387 imidazole, 5, 5Y2 malonic acid magnetochemistry? 2,445 organic transport, 6,869 oxalic acid, 2,444 oxidation catalysts, 6, 389 oxyanions EXAFS spectroscopy, 2,422 D-penicillamine, 5,592 peroxo oxidation catalysts, 6.340 photography physical development. 6. 116 phthalocyanines, 2,868 polypyrazvlylborates, 2.254 biological applications, 2,255 porphyrins, 2,841 proteins, 2,772 pseudohalides, 2,233: 234 pyridine oxide, 2,495 salicylaldimine: 5, 942 salicylic acid crystal structure, 2,481 thioethers, 2,557 triazines bridging ligands, 2: 201 triazole, 5, 592 tridentate, azo dycs synthesis, 6,53 tridentate azo compounds Na-NO isomerism, 6 , 6 j Wilson's disease, 2,959 Copper(0) complexes, 5,535 Copper(1) complexes, 5,535-591 acetonitrile, 5, 583 alkenes, 5,538,582 stereochemistry, 5,568 amidines, 2,275 amines, 5,583 ammonia, 5,583 aqueous solution chemistry, 5 : 536 arsine ligands, 5,5&3 atmospheric oxidation, 5,538 binuclear stereochemistry, 5,551-556 biological, 5, 580

Cumulative Subject Index

Copper(1) complexes

bromides, 5,585 carbon disulfide, 5,584 carbon ligands. 5,582 carbon monoxide, 5,582 stereochemistry, 5,566 carbonyl, 5,538 chlorides; 5,584 copper(I1) mixed oxidation states, 5, 586591 biological, 5,591 cyanides, 5: 582 synthesis, 2,9 d"l

photorcactivity, 1,407 diamines. 5,583 disproportionation, 1,512 1,l-dithiolates. 2,585 dodecanuclear stereochemistry, 5,562 fluorides, 5,584 halide ligands, 5,584 hexanuclear stereochemistry, 5,562 hydrogen ligands, 5,585 infinite chains stereochemistry, 5, 563 iodidcs, 5: SXS ligands, 5,582486 mercury ligands, 5,582 mixed ligands, 5,586 mixed metal stereochemistry, 5,572 molecular orbital calculations, 5,575 mononuclear five-coordinate, 5,547 four-coordinate, 5,542 square coplanar, 5,542 stereochemistry, 5, S3Y-551 tetrahedral, 5,542 three-coordinatc, 5,547 trigonal pyramidal, 5,542 two-coordinate, 5, 547 nitrogen ligands, 5,582 octanuclear stereochemistry, 5,562 organic sulfides, 5,584 oxides, 5,584 oxyanions, 5,584 oxygen ligands, 5,584 pentanuclear stcreochcmistry, 5,561 phosphine ligands, 5,583 physical development photography, 6, 113 polynuclear thio, 2,566 redox properties, 5,576 Schiff bases, 5,586 selenium ligands, 5,584 sheets stereochemistry, 5,563 spectroscopy, 5,572-576 EXAFS, 5,574 IRI 5,575 MLTC bands, 5,575 NMR, 5,574 Raman, 5,575 stereochemistry, 5,538-572 stibine ligands, 5, 584 sulfides, 5,584 sulfurdiimine reactivity, 2, 194 sulfur dioxide, 5,584 sulfur ligands, 5,584 synthesis, 5,536538

Copper(1) complexes

Cumulative Subject Index

tellurium ligands, 5,584 tetranuclear butterfly configuration, 5,558 linear, 5,557 rectangular, 5,557 square planar, 5,557 stereochemistry, 5,557-561 tetrahedral, 5,558 thioacetamide, 5,584 thiocyanates, 5,583,584 thiourea, 5,584 three-dimensional lattices stereochemistry, 5,563 trinuclear stereochemistry, 5,556 tris(pyrazolyl)borates, 5, 583 water, 5,584 Copper(I1) complexes acetates, 2,440; 5,740 acetonylacetone, 5,740 albumin, 2,975 amino acid ester complexes, 6,419 6-amino imines, 6, 163 4-aminosalicylic acid, 2,481 ammines, 5,730 antiferromagnetism, 5,657,661 aqua, 5,735 azides, 5,733 benzamide oxime, 2,274 biguanide polarography, 2,284 biological model compounds, 5,726 2,2’-bipyridyl, 5,734 bonding functions, 5,714 2,2’-bipyridylamine, 5,734 2,2’-bipyrimidinyl, 5,735 bis(1,l -dialkylcthylenediaminc) thermochroism, 2,43 his(salicy1aldoximato) structure, 6, 800 bond angles, 5,595 bond lengths, 5,595 bromides, 5,741 carbonates, 5,718,740 carbon ligands, 5,729 catalysis, 5,716720 chlorides, 5,741 coordination number, 5,594 copper(1) mixed oxidation states, 5,586591 biological, 5,591 croconic acid, 2,455 crystal-field calculations, 5,654 cyanates, 5,733 cyanides, 5,729 cyclic voltammetry, 5,685 dq photoreactivity, 5,407 diamine, 2,31 diethylenetriamine, 5,734 diethyl ether, 5,739 difluoro-3,3’-(trimethylenedini trilo)bis(2-butanone oximato)borate, 5, 735 1,3-diketones ternary complexes, 2,387 dimeric ferromagnetic, 5 , 658 paramagnetic, 5,658 dinuclear, 5,718; 6,160 asymmetric bridging, 5,627 bent, 5,621 flexibility, 5,629 four equivalent bridges, 5,634

monatomic bridging, 5,628 nonequivalent bridging, 5,625 organic bridging, 5>632 planar, 5,621 polyatomic anion short ligand bridging, 5,626 redox properties, 5,687 stereochemistry, 5,619-634 three short bonding rigid ligands, 5,633 tridentate Iigands, 5,625 two bridging ligands, 5,626 dioxane, 5,739 dioxygen, 5,716 dipeptide Schiff bases, 2,766 dissociation kinetim, 5,682 distortion isomers, 5,707 DNA, 2,979 double ligand bridges, 5, 640 electronic properties, 5,652-716 electronic spectra, 5,656,674-678 charge-transfer bands, 5,677 charge-transfer transitions. 5 , 674 combination and overtone vibrations of ligands, 674 internal ligand transitions, 5,674 intervalency charge-transfer transitions, 5,674 polarized single-crystal spectra, 5, 674 pure d - d transitions, 5,674 reflectance spectra, 5,674 solution, 5,673 static stereochemistry, 5,700 energy levels angular overlap method, 5,713 CAMMAG programme, 5,713 crystal field theory, 5,712 effective symmetry, 5,713 extended Hiickel calculations, 5,712,716 ligand field theory, 5,712 molecular orbital calculations, 5 , 716 molccuhr orbital theory, 5,712 theoretical calculations, 5,711-716 X , technique, 5.713 equilibrium curisrant solvent effect, I. 516 equilibrium studies, 5 ; 681 ESR spectroscopy, 5655,662-672 fingerprinting, 5,667 fluxional stereochemistry, 5,669 reversed, 5,66il static stereochemistry, 5,667 temperature variable stereochemistry, 5,667 1,2-ethanediarnine, 5,734 EXAFS spectroscopy, 5,689 Frank-Condon principle, 5,683 ferromagnetism, 5, 657 five-mcmbcred rings magnetic exchange, 2,83 fluorides, 5,741 fluxional electronic spectra, 5,703 formazans dyes, 6,78 glycolic acid, 2: 472 guanidine, 2,283 halogen ligands: 5. 741 hexafluoroacetyIacctone,2,372 hexanuclear stereochemistry, 5,638 histidine, 2,747 hydrated zeolites, 5,720 hydrazone, 6, 181 hydrogen ligands, 5,744 hydroxides. 6,442

114

115

Cumulative Subject Index

hydroxy, 5,739 2-hydroxy-3-naphthoic acid, 2,483 hydroxy oximes, 2,273 IR spectroscopy, 5,688 Irving-Williams series stability, 5,680 imidazole, 5,734 imine oximes, 2,273 iodides, 5,741 Jahn-Teller effect, 5,655,690-698 cooperative, 5,690,703 first order, 5,696 noncooperative, 5,690,703 observation, 5,698-711 pseudodynamic, 5,698 second order, 5,690,693,698 kinetic exchange, 5,658 kinetics, 5,680-688 lactic acid, 2,473 large planar molecules, 5,642 ligands, 5,729-744 ligand substitution reactions, 5,680 linear chain structures., 5.643 . low temperature X-ray crystallography, 5,669 magnetic interactions nonmagnetically dilute systems, 5 , 657 magnetic properties, 1,274;5,65%2 maleic acid crystal structure, 2,475 malononitrilodithiol, 5,741 mercury ligands, 5,729 methoxy, 5,739 mixed copper(II1) complexes, 5,744-745 mixed donor chelate ligands, 5,744 mixed metal, 5,652 mononuclear bicapped square pyramidal, 5,614 &distorted octahedral, 5 : 611 compressed tetrahedral, 5,606 eight-coordinate, 5,612 electron diffraction, 5,596 elongated tetragonal, 5,601-604 EXAFS spectroscopy, 5,596 five-coordinate, 5,606-609 linear, 5,612 neutron diffraction, 5,5% nine-coordinate, 5,612 octahedral, 5,596-600 powder profile analysis, 5,596 rhombic coplanar, 5,605 rhombic octahedral, 5,601404,610 seven-coordinate, 5,612 single-crystal X-ray crystallography, 5,596 square coplanar, 5,605 stereochemistry, 5,59G619 temperature variable, 5 , 616 tetragonal, 5,610 trigonal octahedral, 5,596-600 naphthoic acid, 2,483 nitrates, 5,740 nitrites, 5,733,740 nitroaminoguanidine, 2,283 nitrogen ligands, 5,730 Orgel diagrams, 5,654 one-dimensional chains, 5,64&647 optical activity, 5,678 magnetic circular dichroism, 5,678 natural circular dichroism, 5,678 organic sulfides, 5,741 oximes, 2,270,272 physicochemical studies, 2,272 oxyanions, 5,740 oxygen ligands, 5,735 peptides, 2,768

Copper(1II) complexes

perchlorates, 5,740 1,lO-phenanthroiine, 5,734 phenoxy, 5.739 phosphate hydrolysis, 6,444 phosphorus ligands, 5,735 photoacoustic spectroscopy, 5,687 photochemistry, 5,749 phthalocyanines, 5,735,744 physical development photography, 6,113 plasticity effect, 5,685,690 polyaza macrocycles rcdox properties, 5,687 polynuclear cyclic voltammetry, 5,690 ESR spectroscopy, 5,669,690 magnetic interactions, 5,716 magnetic susceptibility, 5,690 zero-field splitting parameters, 5,669 nuclear hyperfine splitting patterns, 5,672 potential exchange, 5,658 pseudo compressed stereochemistry, 5,693 pyranne, 5,734 pyridine, 5,734 pyridine oxide, 5,739 redox properties, 5,68&688 rcduction stabilization, 5,594 Schiff bases adsorbed on optically transparent thin-layer electrodes, 5,688 single-crystal ESR spectroscopy, 5,664 six-coordinate, 1,53 Mexican hat model, 5,698 spectra, 1,255 static distortion, 5,654 static elongated rhombic octahedral stereochemistry, 5, 693 static stereochemistry, 5,690 stereochemistry, 5,596 electronic criterion, 5,708 structural pathway, 5,707 structure, 1,66 sulfur ligands. 5,741 synthesis, 5,594-596 tartaric acid, 2,479 temperature variable stereochemistry, 5,690 2,2’, 2"-terpyridyl , 5,735 tetraaza macrocycles, 2,909 tetranuclear stereochemistry, 5,636 tetrahedral, 5,637 thermodynamic properties, 5,680 thiocarbamates, 5,741 thiocyanates, 5,733 thiolates, 5,741 three-dimensional structures, 5,650 transport cell membranes, 5,683 triamines, 2,50 triethylenediarnine, 5,735 trinuclear stereochemistry, 5,635 twisted linear chains, 5,640 two-dimensional ligands, 5,647 photoreactivity, 1,407 Copper(II1) complexes, 5,745-749 biological, 5,749 1,l-dithiolates, 2,585 electronic properties, 5,748 IR spectroscopy, 5,749 magnetic properties, 1,274

Copper(II1)complexes mixed copper(I1) complexes, 5,744745 peptides, 2,769 phosphines SHAB theory, 2,1040 polynuclear, 5,748 stereochemistry, 5,746 synthesis, 5,745 Copper(1V) complexes, 5,750 Copper cupferronate vibration frequencies, 2,511 Copper glycinate gravimetry, I , 524 structure, 1, 13 Copper halides cubanes with Lewis bases, 1, 153 Copper(II/III) couples redox properties, 5,749 Copper(I1) ions catalysts amino acid hydrolysis, 6,415 hard acid, 5,594 Copper nitrate structure, 1,28 Copper proteins, 1,168; 5,720 models, 2,85 nonblue, 5,723 type Ill, 5,724 Copper salts cellulose dyes, 6,38 Copper(1) salts stabilization, 6,786 Copper(I1) salts ammoniacal leaching, 6,787 oxidant in chloride solutions, 6,786 Copper sulfate pentahydrate structure, 1 , 5 Copper(I1) systems biological, 5,72&729 Coprogtn iron(II1) complexes, 2, 971 Coproporphyrin I synthesis, 2,816 Coronands alkali metal complexes, 3,3,37-45 classification, 2,919 metal ion complexes, 2,928,938 Corphins, 2,855 Corrin, dehydrometal complexes, 6,198 Cortin, hexadehydrosynthesis, 6, 198 Corrin, octadehydrosynthesis, 6.197 Corrhoids. 2,983 metal complexes synthesis and reactions, 6,192-202 metal-free, 6, 641 Comns, 2,871-888 cavity metal complexes, 6,548 demetallation, 2,882 deuteration, 2,879 electrophilic reactions, 2, 879 kinetic formation kinetic template reactions, 1,451 metal complexes biology, 6,546 geochemistry, 6,862 metallation, 2, 882 NMR, 2,878 nucleophilicity, 2, 886

Cumulative Subject Index nucleophilic reactions, 2.879 oxidation, 2,879 oxidative lactamization, 2,880 oxidative Iactonization, 2,880 photochemistry, 2,887 reactions, 2,879 at metal, 2,885 rearrangements, 2, 879 redox chemistry, 2,888 spectra, 2,877 synthesis, 2,878; 6,200 Corroles: 2,871-888 demetallation, 2,874 deuteration, 2,872 hydrogenation, 2,872 metallation, 2,874 reactions, 2,872 at metal, 2,875 redox chemistry, 2,876 synthesis, 2,871 Corticotropin zinc complexes medical use, 2,966 Corynebacterium spp. diphosphate reductase, 6,642 Cotton effect anils, 2,717 bidentate Schiff base metal complexes, 2,725 hydroxy acid metal complexes, 2,470 Cotunnite, 6,855 Coumarins electroplating, 6 , 6 in nickel electroplating, 6.10 Creatine metal complexes, 2, 283 Creatine kinase activation magnesium ions, 6, 580 Creatinine metal complexes: 2,283 Crenitc structure, 6,849 Cresolphthalexone metallochromic indicator, 1,557 Creutz-Taube complex, 1,359; 2,80 Criticality reprocessing irradiated nuclear fuel, 6,925 solvent extraction, 6,940 Croconic acid metal complexes, 2,153 preparation, 2,456 Crotonic acid methyl ester hydroformylation, 6, 261 Crotonic acid, u-acetamidoasymmetric hydrogenation rhodium complexes, 6,251 [18]Crown-6 metal complexes structure, 1: 182 thermodynamics, 2, 931 [18]-Crown-6, dicyclohexylalkali metal complexes cavity shape and size,3,50 Crown ethers alkali metal complexes, 1, 22; 3, 3, 37-45, 60 classification, 2,919 formation kinetic metal tcmplatc effects, 1,441 history, 1,21 lanthanide complexes, 3,1092 metal cation complexes, 2,928 metal complexes

116

117

Cumulative Subjecl Index

sclcctivc binding- 6,S.i.l organometallic, 2, 933 phosphorus-containing, 2.998 selective ion electrode. 1, 559 synthesis, 2, 924 Cryolite, 3, 121 structure, 6,846 Cryolithionite structure, 6,846 Cryptands alkali metal complexcs, 3, 3,4,35.45,54 cavity shape and sizc. 3, 50 conformational rigidity, 3, 53 Rexihility, 3, 53 classification, 2, 920 heteropoly, 3, 1049 metal complexes selective binding. 6.551 metal ion complexes, 2.937 synthesis, 2,927 [2.2.C8]-Cryptands alkali metal complexes donor atom arrangements, 3,50 12.2.21-Cryptands alkali metal complexcs donor atom arrangenicnts: 3- 50 Cryptates alkali metal complexes stability, 3, 52 transition metal complexes. 2: 937 Crystal engineering, 2,719 Crystal field potential definition, 1,215 Crystal field splitting parameter. 2.309 Crystal field theory, I, 215-221 angular overlap model, 1,228 calculations, I , 220 generality, 1, 219 low symmetry, 1,220 ,f-orhital, I , 23 I Crystal hydrates, 2. 305.3Uh bond distances, 2, 307 Crystals molecular compounds. 1, 15 Cubanes structure hydroxide metal complexes, 2.300 metal complexes, 2,303 oxide metal complexes, 2.304 Cubes eight-coordinate compounds, 1 , 83 square antiprisms, dodccahedron and, 1,84 Cuboctahcdra twelve-coordinate compounds. 1 100 Cupfcrrun in analysis, 1. 523 in gravimetry, 1.532 liquid-liquid extraction, 1, 544 metal complexes, 2, 509-512 IR spectra, 2,511 UV spectra, 2,511 potentiometric titration with metal ions, 2, 510 uranium(1V) complexes magnetic susceptibility, 2.512 Cuprate, hexafluarotripotassium salt history, 1, 21 Cuprate, hexanitritostereochemistry. I , 53 Cuprate, tctrachlorostructure, I , 53 Cuprates, chlorocatalysts COC 7-E

Cyclic voltammetry

warm cleavage, 6,497 Cuprotungstates, 3, 1042 Curie temperature, 1,258 Curie-Weiss law, 1,258 Curium Purex process, 6.946 Curtis reaction metal template reactions, 1,449 Curvularin synthesis catalysts, palladium cornplexcs, 6,281 Cyanate complexes linkage isomers, I , 186 Cyanates metal complexes, 2,225-238 synthesis, 2,237 molecular geometry, 2,226 Cyanidation gold ores, 6, 784 Cyanides activator mineral processing, 6,782 bridging ligands, 2,s conccntration in cementation mineral processing, 6, 830 dinuclear complexes synthesis, 2 . 9 electroplating, 6.4 copper, 6 , 9 effluent disposal, 6, 14 gold, 6 , l l zinc, 6. 12 ligands, 2.7 masking, 1, 536 metal complexes, 2,7-13 bond lengths, 2 , l l elcctronic structurc, 2, 8 formation constants, 2, 11 gcochemistry, 6,868 kinetics, 2 , 8 prebiotic systems, 6, 870 Raman spectroscopy, 2, 11 reactions, 2 , 9 reduction. 2 , s replacement by other ligands, 2, l# structures, 2, 10 substituted, 2, 10 synthesis, 2 ,9 thermodynamics, 2,lO oxidation. 2 . 7 physical properties, 2, 8 Cyanine silver(1) complexes physical development, 6,114 Cyanobacteria photosynthesis, 6,589 Cyanohydrin amino acid formation prebiotic systems, 6,871 Cy anoke tones metal complexes color photography, 6,107 Cyclam metal complexes alkylation. 1,417 Cyclam, tetra-hi-methylmetal complexes isomerism, 1 204 Cyclic bonding, 1, 14 Cyclic compounds nomenclature, 1, 125 Cyclic voltammetry, 1,475,482 electrochemistry ~

Cyclic voltammetry

Cumulative Subject Index

aprotic solvents, 1,494 hydrogen or oxygen production from water coordination complex catalysts, 6,532 single electron transfer reactions chemistry following, 1,499 technetium complexes, 6,983 Cyclidenes classification, 2,920 metal ion complexes, 2,939 Cyclization free radical coordinated phosphines, 1,444 3-Cydobutene-l,2-dione, 3,4-dihydroxy -we Squaric acid Cyclodextrins classification, 2,920 1,5,9-Cyclododecatriene hydrogenation catalysts, nickel complexes, 6,248 catalysts. ruthenium compIexes. 6,232,234 Cycloheptane-1 ,2-dione dioxime in gravimetry, 1,533 1,4-Cyclohexadiene hydrogenation catalysts, iridium complexes, 4,246, 248 Cyclohexane hydroxylation cobalt catalysts, 6,388 vanadium-alkyl pcroxide catalysts, 6,342 oxidation vanadium-alkyl hydroperoxide catalysts, 6,346 Cyclohexane, phenyloxidation ruthenium-oxo complexes, 4,358 Cyclohexane-l,2-diamine Cis

-

complexes, 1,25 metal complexes, 2,34 Cyclohexane-l,2-dione monooxime metal complexes, 2,273 Cyclohexane- I ,2-dione, 4-methyldioxime nickel determination, 1,533 Cyclohexane-1,2-dione dioxime in gravimetry, 1,533 Cyclohexane-l,3,Striamine metal complexes, 2,50 Cyclohexanol oxidation iron catalysts, 6,380 Cyclohexanone hydrogenation catalysts, ruthenium complexes, 6.235 oxime nickcl complexes, 2,270 Cyclohexene hydrogenation catalysts, cobalt complexes, 6,238 catalysts, nickel complexes, 6.248 catalysts, rhodium complexes, 6.243,244 oxidation cobalt catalysts, 6,384 copper catalysts, 6,390 oxygenation manganese catalysts, 6 , 376 1,5-Cyclooctadiene carbonylation catalysts, palladium complexes, 6,287 Cyclooctene oxidation iridium-peroxo catalysts, 6,350 Cyclopentadiene

118

hydrogenation catalysts, cobalt complexes, 6,236 Cyclopentanecarboxylic acid ethyl ester bromination, 1,419 Cyclopentanecarboxylic acid, 2-oxoethyl ester halogenation, 6,473 Cyclopcntanc-l,2-diaminc metal complexes, 2,43 Cyclopentene-l -dithiocarboxylic acid, 2-aminometal complexes, 2 , 800 Cyclophane chlorophylls, 3,58 Cyclophane hemes iron complexes, 4 1261) Cyclophosphazenes metal complexes, 2,81 Cyclopropane carbonylation catalysts, rhodium complexes, 6,277 synthesis from dihalomethane, 6,305 Cyclopropane, methylenereaction with carbon dioxide catalysts, palladium complexes, 6,296 Cyclote traphosphazenc, octamethylplatinum complexcs, 2,82 Cyclotetraphosphazenes metal complexes, 2; 81 Cyclotriphosphorus complexes, 2,1058 Cyclotron radioisotope production, 6,965 Cysteamine, S-methylcobalt(II1) complexes sulfur inversion, 1, 199 Cysteine chelating agents heavy metal poisoning, 6,768 cobalt complexes electrochemical production of hydrogen or oxygen from water, 6,532 copper complexes blood, 2,966 disulfide metal complexes, 2,749 metal complexes, 2,748 binding, 2,749 oxidation, 2,758 stereoselectivity, 2,754 methyl ester, palladium(I1) complexes hydrolysis, 6,423 in photochemical hydrogen production from water, 6, 501

photographic stabilizer, 6 , 103 Cysteine, S-methylcobalt( 111) complexes sulfur inversion, 1,199 Cytidine cadmium complexes, 5,957 metal complexes, 2,796 zinc complexes, 5,957 Cytochrome a , 6,624,693 Cytochrome a 3 ,6,693 EXAFS, 6,694 Cytochrome b, 4,263; 6: 623 Cytochrome b2, 6,624 Cytochrome b,, 6,623 redox potential, 6,617 Cytochrome h , chloroplast, 6,423 Cytochrome b,,,.,, 6,679 Cytochrome bSSl,6,624

119

Cumulative Subject ladex

Cytochrome b563,6,624 Cytochrome c , 4,263; 6,619 cytochrome oxidases, 6,683 electrochemistry, 6, 622 electron transfer with transition metals, 6,621 electroreduction, 1,488 metal substitution, 6,621 model systems, 2,847 reaction kinetics, 6,621 redox potential, 6,617 tin(IV), 6,621 zinc(II), 6,621 Cytochrome cj, 6,623 Cytochrome cSs2,6,623 denaturation, 6,623 Cytochrome cSs4,6,623 Cytochrome cd,, 6,624,698 Cytochrome c' Rhodospirillum rubrum, 6,622 Cytochrome d , 6,624,697 Cytochrome f electron transfer reactions, 6,653 Cytochrome 0,6,624,697,698 Cytochrome P-450,4,263,264,1269; 6,326,682, 709 catalysis, 6,709 reactions, 2, 844

Cytochrome enzymes, 2,772 Cytochrome u3 oxidase, 6,697 Cytochrome c oxidase, 6,683 copper complexes, 2,724,772 Cytochrome oxidases, 6,624 bacterial, 6,696 concerted electron transfer, 6,683 copper, 6,654 dioxygen binding, 6,692 dioxygen uptake, 6,682 electron transfer pathways, 6,696 interaction with lipids, 6,694 proton pump, 6,692 reaction mechanisms, 6,694 structure, 6,693 Cytochrome c peroxidase, 6,705 Cytochromes, 2,982; 4,259,263,1268; 6,618 bacteria, 6,622 classification, 6,619 horse heart, 6,620 nitrogen hation, 6,728 redox potential, 6,616 axial ligands, 6,617 respiration, 6,624 Cytosine metal complexes, 2,796

Cytosine

Dapcx process, 6,909, Y1.I uranium ore processing, 6,903 Data storage surface coated electrodes, 6,30 DDPA process uranium ore processing, 6,903 Deactivation cyanides mineral processing, 6,782 Dealkylation ligands, 1,432 Deamination solid state anation, 1,46Y cis-Decalin hydroxylation iron catalysts, 6,282 Decametallic complexes, 1, 166 fused adamantanoid cages, 1,166 tetracapped octahedron, 1, 166 Decanning irradiated nuclear fuel, 6, 925-963 nuclear fuels, 6,927 Decan-5-01,6-ethoxysolvent cxtraction gold, 6,808 Decarbonylation iridium catalysts, 4, 1160 Decarboxylation carbonate complexes, 2,449 catalysis labile metal ions, 6,413 keto acids metal complexes, 1,427 @-oxoacids metal catalysis, 6,453 Decatungstates, 3, 1034 Decatungstometalates, 3,1045,1046 Decavanadates, 3,1027 1-Decene hydroesterification catalysts, cobalt complexes, 6 : 271 Decontamination factors nuclear fuel reprocessing, 6,885 Deep-sea nodules, 6,852 Deficiency diseases metal complexes, 6,760 Dehydration in amide-metal complex synthesis, 2; 491 Dehydrocorrins, 2,877 alkylation, 2, 882 hydrogenation, 2,882 Dehydrogenases carboxymethylation, 5 , 1015 cobalt substituted, S, 1012 coenzymes binding, 5, 1010 denaturation, 5,1016 half-site reactivity, 5, l o l l iron-sulfur clusters, 6, 634 inhibitors

binding, 5: 1016 substratc compctitive, 5, 1017 nickel substituted, 5,I013 structure. 3,1438; 5.1009 subunit equivalent: 5,1011 zinc, 5, 1012 Dehydrogenation amine complexes, 1,455 Dejacketing irradiated nuclear fuel, 6,925 DelCpine’s salt, 2: 303 Deltic acid metal complexes, 2,453 Dem asking in gravimetry, 1,538 Demethylation aromatic methyl ethers, 1,432 Dernethylative coppering o-methoxy-0’-hydroxydiarylazo compounds, 6 , 5 3 Denitrification, 6: 717,726 biochemistry, 6,727 Dentine phosphoproteins, 6,597 Deoxophylloer ythroetioporphyrin metal complexes geochemistry, 6.861 Deox yheinocyanin coppcr(I1) complexes, 5,720,724 Depressants mineral processing, 6,783 Dcpressivc illncss cancer and, 6,773 trace elements and, 6,773 Desferrioxamine Cooley’s anemia, 6,768 protein modification with, 6, 995 Despujolsite, 4, 104 Desulfo enzymes molybdenum: 6,659 Desulfoxanthine oxidase molybdenum, 6, A59 Deuteration enantioselective amino acids, 1,425 Deutcrium exchangc catalytic, 6,233 Dextran iron complexes, 2,985 Diace tyl monooxime metal complexes, 2,272 Diagnostic imaging techniques non-invasive gamma raysI 6,965 Dialkyl sulfides solvent extraction gold and silver, 6 , 807 palladium: 6: 807 Diamagnetism, I, 257 Diamines cobalt catalysts

120

121

Cumulative Subject Index

hydrogenation, 6,237 ligands in carbonylation, 6,274 metal complexes, 2,30, 35 1,3-Diamines oxidative dehydrogenation metal complexes, 1,455 Dianomycin alkaline earth mctal complexcs, 3, 66 cation transport, 6,554 Diamines, 2,1006 Diastereomers, 1 , 181 Diazabicyclo[2.2.2]octane metal complexes color photography, 6 , 109 1,4-Diaza-l,3-butadienc ligands, 2,206 coordination modes, 2,206 metal complexes, 2,206~216 activation, 2,213 bridging ligands, 2,208.211 chelating ligands, 2,209 formation, 2,212 occurrence, 2,208 properties, 2,208 synthesis, 2,208 monodentate complexes, 2,208 Diaza compounds reactions with carbonyl compounds diaza macrocycles from, 2,904 3.6-Diazaoctane, 1,8-diaminometal complexes structure, 1, 182 Diazapolyoxamacrobicycles synthesis, 2,926 5,15-Diazaporphyrin synthesis, 2,857 5,15-Diazaporphyrin, octahydro-, 2, 859 Diazepam metal complexes, 6.773 synthcsis by carbonylation. 6,285 Diazines macrocyclic synthesis, 2,904 metal complexes, 2 , 8 0 Diazinido complexes transition metals, 2, 13&141 bonding, 2,134 eight-coordinate, 2, 135 five-coordinate, 2, 134 four-coordinate, 2,134 geometries, 2. 134, 135 molccular orbital calculations, 2, 137 NMR, 2,139 reactions, 2, 140 seven-coordinate, 2, 135 six-coordinate, 2, 135 spectroscopy, 2, 137 structures, 2, 134,136 svnthesis. 2. 131 X-ray photoelectron spectroscopy, 2, 139 Diazo compounds photothermography, 6,121 Diazo ligands, 2, 100 Dibenzo-18-crown4 alkali metal complexes, 3,35 electronic influences, 3,54 Dibenzo-21-crown-7 in radionuclide recovery from nuclear fuel waste, 6,959 Dibenzo-24-crown-8 alkali metal complexes, 3,40

Diffusion transfer process

Dibenzo-30-crown- 10 alkali metal complexes, 3,40 Dibismuthines, 3,284 Dibismuthines, tetrakis(trimethylsily1)-. 3, 284 Diborane Lewis base complexes, 3,83 Dibutyl carbitol -see Decan-5-01,6-ethoxyDicarbonyl compounds reaction with amincs aza macrocycles from, 2,902 Dicarboxylation catalysts palladium complexes, 6,287 Dicarboxylic acids metal complexes, 2,443 bridging systems, 2,444 chelate coordination, 2,443 naturally occurring, 2,962 reactivity, 2,446 synthesis, 2,446 tetradentate bridging, 2,444 unidentate, 2,443 Dichromates, 3,941,943 relief-image-forming systems, 6, 125 Dickinson. Roscoe Gilkey, I, 16 Dicyanohemin dimerization, 6,616 Diencs acetoxylation palladium catalysts, 6,365-368 asymmetric hydroformylation catalysts, rhodium Complexes, 6,266 cationic rhodium complexes hydroformylation catalysts, 6,263 conjugated hydrogenation, 6,236 cyclic hydroformylation, 6,262 hydrogenation, 6,248 hydrocyanation catalysts, nickel complexes, 6,297 hydroesterification catalysts, palladium complexes, 6,287 hydrogen ation catalysts, cobalt complexes, 6,237 catalysts, iridium complexes, 6,246 oxycarbonyiation palladium catalyzed, 6, 368 reactions asmiurn tetroxide, 4,590 synthesis from vinyl halides, 6,306 Dielh ylenetriamine metal complexes titrimetry, 1, 553 Diethylenetriamine, N’-{2-[(2-aminoethyl)amino]ethyl} metal complexes, 2,56 Diethylenetriamine, N’-{2-[(2-aminoethyl)methylamino]ethyl}metal complexes, 2,56 Diethylenetriamine, N,N’-bis(3-aminopropyl)metal complexes, 2,56,57 Diethylenetriamine, N’,N’-ethylenebismetal complexes, 2,58 Dicthyl ether solvent extraction hafnium, 6,812 uranium, 6,810 uranyl nitrate complex solvent extraction, 6,810 Diffuse X-ray scattering Peierls distortion, 6, 135 Diffusion transfer process

Diffusion transfer process

Cumulative Subject Index

photography metallized dyes, 6, 106 silver halide, 6,101 Diglycine hydrolysis copper(I1)-catalyzed, 6,426 1,2-Dihydrazones reactions with formaldehyde metal-promoted, 6,181 template reaction with diformylphenanrhroline, 6,183 Dihydrogen evolution nitrogen fixation, 6,723 oxidative addition niobium(I1) complexes, 3,678 niobium(II1) complexes, 3,660 tantalum(I1) complexes, 3,678 tantalum(II1) complexes, 3,660 1,2-Diimines chelate rings formation, 1,445 iron( 11) complexes hydroxylation, 1,455 metal complexes, 6, 162 1.,3-Diimines macrocyclic complexes reactions, 1,422 metal complexes, 6,165-180 oxygenation, 1,457 Diketones carbon bonded q 1 ligands, 2,367 coordination chemistry, 2,365 metal complexes tridentate, 2,369 tridentate bonding, 2,368 fl-Diketones alkali metal complexes, 3 , 2 alkaline earth metal complexes, 3,25-30 anions, 2,365 bimetallic complexes, 2, 377 dithio metal complexes, 2,653 metal complexes, mass spectra, 2,654 metal complexes, reduction potentials, 2,654 metal complexes, spectra, 2,654 liquid-liquid extraction, 1,543 metal complexes complex formation, 2,386 decomposition, 2,385 displacement reactions, 2,378,386 electrophilic substitution, 1,422 free radical complexes, 2,388 ligand exchange reactions, 2,380 monodentate oxygen bonded, 2,367 photochemistry, 2,384 reactions, 1,420; 2,378; 6.20S206 rearrangements, 2,381 semi-chelating bonding, 2,367 solvolysis, 2,378 structure, 2,370 substitution reactions, 2,378 synthesis, 2,374 synthesis from metal salts, 2, 376 qz oxygen bonded, 2,367 monothio fluorinated, metal complexes, mass spectra, 2,649 metal complexes, 2,648 metal complexes, dipole moments, 2,649 metal complexes, IR spectra, 2,649 metal complexes, stability constants, 2,648 neutral metal complexes, 2,401 nitroxide metal complexes, 2,388

nonmetal complexes, 2, 370 organometallic chemistry, 2,392 carbon bonded complexes, 2,392 reactions with metal surfaces, 2,395 Schiff bases metal compiexes, IR spectra, 2,728 metal complexes: NMR, 2,728 metal complexes, X-ray analysis, 2, 730 tautomers rcactions with metal ions, 2,366 transition metal complexes, 2,370 in uranium ore processing, 6,910 Dimerization nitrile metal complexes, 2,265 Dimetallenes, 3,217 Dimethylamine ore formation, 6,869 Dimethyl carbonate alkylation copper catalysts, 6,395 Dimethyl sulfoxide hydrometallurgy, 6,785 solvent cobalt complcxes , I , 22 Dimolybdate, 3,1408 Dinitriles metal complexes, 2,262 Dinitrogen activation niobium(II1) complexes, 3,661 niobium(V) complexes, 3,617 tantalum(II1) complexes, 3, 661 tantalum(V) complexes, 3,617 conversion to ammonium, 2,101 fixation vanadium(l1) complexes, 3,473 hydrazido complexes, 2,141. reduction hydrazine in, 3,1397 vanadium(I1) complexes, 3,469 transition metai complexes, 6,718 tungsten complexes, 3, 1011-1014 reduction, 3, 1012 Dinitrogen monoxide reductase, 6,727 Dinuclear compounds symmetrical nomenclature, 1: 122 unsymmetrical nomenclature, 1,123 Dioctylamine in thorium ore processing, 6,915 a,p-Dione dioximates metal complexes electrical properties, 6, 143 non-integral oxidation state compounds, 6 , 143 nickel complexes electrical conductivity, 6, 144 structure, 6,143,144 X-ray photoelectron spectroscopy, 6,144 palladium complexes structure, 6,144 Diopside structure, 6,856 Diorganoarsinates metal complexes, 3,1054 Dioxacorroles: 2,876 Dioxasapphyrins metallation, 2,891 Dioxasrnaragdyrin synthesis, 2.889 Dioximes nickel extraction, 1,544

122

123 vic metal complexes, 2,271 Dioxygen activation, 6,682 niobium(II1) complexes, 3,661 tantalum(II1) complexes, 3,661 biology., 6,681-711 chemistry, 6,682 evolution photosynthesis, 6,591 metal complexes, 6,319 molecular orbital diagram, 2; 315 nitrogenase sensitivity, 6,725 oxidation iron catalysts, 6, 380 manganese catalysts, 6,376 physical properties, 2,316 reactivity, 6,682 transport and storage, 6,683 1,2-Dioxygenase, 4,232 Dioxygenases, 6,325,706 copper(I1) complexes, 5 ; 721 cytochrome oxidases, 6,683 extradiol, 6,707 heme, 6,708 intradiol, 6,707 non-heme, 6,706 Dioxygen complexes, 2,315-330 bonding, 2,316 reactions, 2,328, 329 transition metals, 5, 717 Dipeptides metal complexes, 2,762 synthesis asymmetric hydrogenation in, 6,256 Diphosphine disulfide, 2,991 Diphosphines, 2,992 platinum complexes catalysts, hydroformylation, 6: 264 rhodium complexes catalysts, hydroformylation, 6,261 Dipicolinic acid calcium transport microbes, 6,571 Di(picoly1)amine amides methanolysis, metal catalysis, 6,438 1,2-Diplatinavinyl complexes, 5,417 Dirhenates, nonahalo-, 4, 176 Dirhenium heptoxide, 4,197 Diselenides metal complexes, 2,662 1,4-Disilabenzene, hexamethyl-, 3, 190 Disilene, tetramesityl-, 3, 1W Disilenes Si=% x bond energy, 3.184 stability, 3, 190 Disiloxane, tetramesityl-, 3,206 Disproportionation iridium catalysts, 4, 1159 Dissolution nuclear fuels, 6,927 Distannene, 3,217 Distannoxane, 113-dichloro-,3,207 Distibine, tetraphenyl-, 2, 1008 Distibines, 2, 1008 Disulfido ligands metal complexes, 2,531-540,553 bonding, 2,539 electron transfer, 2,537 intramolecular redox reactions, 2,537 reactions, 2,537 reactions with nucleophiles, 2,538

Cumulative Subject Index

Dithioformic acid

spectroscopy, 2,538 synthesis, 2,536 qcql ligands, 2,533 q2-S2 unit, 2,532 +q2 ligands, 2,533 S-S bond distances, 2,535 Disulfur dinitride metai complexes, 2,799 Disulfur dioxide metal complexes, 2,636 Disulfur monoxide metal complexes, 2, 636 Ditclluride, di(o-aminophcnyl) copper complcxes, 2,794 Dithiacyclobutenes equilibrium with dithiodiketones, 2,599 1,5-Dithiacyclooctane metal complexes, 2,644 3,6-Dithiaoctanedioic acid photography diffusion transfer process, 6, 101 Dithiaporphyrins, 2,850 Dithietane metal complexes, 2,591 Dithioacetic acid, phenylmetal Complexes, 2,646 colours, 2: 646 Dithio anions in photochemical nitrogen production from water, 6, 510 Dithiobenzoic acid metaI complexes, 2,646 colours, 2, 646 Dithiobiuret metal complexes, 2,640 Dithiocarbamates chelating resins mineral processing, 6,826 Dithiocarbarnic acid metal complexes, 2,585 amine exchange, 1,428 photographic emulsions, 6,98 nickel poisoning, 6,768 tellurium(l1) complexes photothermography, 6,121 Dithiocarbazic acid metal complexes, 2,803 Dithiocarbimic acid metal complexes, 2,588 Dithiocarbimic acid, cyanometal complexcs, 2,808 Dithiocarboxylic acids metal complexes, 2,646 Uithiodiacetic acid metal complexes, 2,806 Dithiodiketones dithiolene metal complex synthesis from, 2,598 Dithioethers metal complexes, 2,551 Dithioformic acid alkali salts synthesis, 2,584 Dithioformic acid, arsinometaI complexes, 2,589 Dithioformic acid, azidometal complexes, 2,587 Dithioformic acid, bismuthinometal complexes, 2,590 Dithioformic acid, cyanometal complexes, 2,585 Dithioformic acid, Auorometal complexes, 2,588 Dithioformic acid, halogeno-

Dithioformic acid

Cumulative Subject Index

metal complexes, 2,590 Dithioformic acid, phosphinometal complexes, 2,589 Dithioformic acid, stibinometal complexes, 2,590 Dithiolate complexes structure, 1,63 Dithiolates formation flotation, 6,781 metal complexes, 6, 147 integral oxidation state, 6,147 non-integral oxidation state, 6, 148 I ,l-Dithiotates metal complexes, 2,585 Dithiolato complexes bipyridyl, 2,603 main group elements, 2,605 metallocenes, 2, 604 nitrogen ligands, 2,603 o-phenanthroline, 2,603 phosphines, 2,603 phosphorus ligands, 2,603 synthesis, 2,601 with other sulfur ligands, 2,602 Dithiolenes charge transfer salts, 2,623 cobalt complexes cyclopentadienyl, 2, 604 complexes isomorphic, 2,626 metal complexes, 2,595 alkylation, 2,618 bonding, 2,596 catalysts, 2, 627 conductivity, 2,622 crystal structure, 2,608 cycloaddition reactions, 2: 619 dithiocarbamato, 2,602 ESR, 2,612 electron delocalization, 2,596 electronic spectra, 2,613 IR spectroscopy, 2,566 MBssbauer spectroscopy, 2,616 magnetism, 2,622 mass spectra, 2,616 molecular structure, 2,608 multinuclear, 2,606 NMR, 2,611 one-dimensional stack, 2,622 partially reduced, 2,623 o-phenylenediamine, 2,607 photochemistry, 2,613 properties, 2,608 redox chemistry, 2,596 redox properties, 2,610 substitution, 2,618 synthesis, 2,597 synthesis, dithiodiketones, 2,598 theoretical treatments, 2, 617 X-ray photoelectron spectroscopy, 2,616 nomenclature, 2,596 selenium analogs metal complexes, 2,607 synthesis ethylenedithiolates, 2,598 tellurium analogs metal complexes, 2,607 Dithionites in antibody labelling with technetium-%, 6, 996 Dithiooxalic acid metal complexes, 2,585, 645 Dithiooxamide

124

in gravimetry, 1,534 metal complexes, 2, ROO Dithiophosphates collectors mineral processing, 6.781 Dithiophosphinic acid metal complexes, 2: 642 Dithiophosphinic acid, imino metal complexes, 2,643 Dithiuphosphonic acid rnonoalkyl metal curnplexes. 2,613 Dithizone in analysis, 1,523 in gravimetry, 1 534 masking agents, 1,546 metal complexes, 2,803 absorptiometry, 1: 550 metallochromic indicator, 1,557 selenium analogs metal complexes, 2,807 trace metal complexes absorptiometry, 1,546 Di(tridecy1)amine in thorium m e proccssing, 6, 915 Diuranatc precipitation, 6, 897 in uranium ore processing, 6, 902 l,(i-Diynes ring closure catalysis by palladium complexes, 6,289 DNA metal complexes, 2: 92 strand scission bleomycin, 2,969 structure, 2,976; 6: 562 synthais metal activators, 5 , 1008 platinum complexes and, 6,757 DNA polymerases activation magnesium ions, 6, 584 zinc, 5 , 1007 Dodecametallic complexes, 1,167 Dodecamolybdometalates, 3,1045 Dodecatantalates, 3, 1029 Dolerophane, 6 : 855 Donor numbers, 2,74 Dopamine p-hydroxylase, 6: 711 copper, 6,654 Dopa -see Phenylalanine, dihydroxyDopplerite structure, 6 , 849 Douglasite structure, 6 , 846 Down’s syndrome Alzheimer’s disease, 6,770 DPPA process, 6,911 Drugs absorption metals, 6,774 interactions with elements and vitamins, 6,773 stereoselective action, 6,774 Dwarfism zincdeficicncy, 6,599 Dyes, 6 , 3 5 9 1 photography, 6,1U4 Dysprosium, aquatris(2,2,6,6-tetramethyl-3,5heptanedione)stereochemistry: 1?81 ~

Earlandite structure, 6,849 Edge-coalesced icosahedra eleven-coordinate compounds. 1,99 repulsion energy coefficients, 1.33,34 Edta -see Acetic acid, ethylenediaminetetraEffective atomic number concept, 1,16 Effective bond length ratios non-bonding electron pairs, 1.37 Effective d-orbital set, 1:222 Egta -see Acetic acid, ethylenebis(0xyet hy1eneimino)tetraEight-coordinate compounds stcreochemistry, 1,86Y4 Electrical conductivity metal complexcs, 6, 133 tetracyanoplatinates anion-deficient salts, 6 , 136 Electrical properties metal complexes, 6,133-154 Electrocatalysis, 6, 28 Electrochemical cells, 6 , 1 Electrochemistry, 1,475477; 6, 1-33 aqueous solution, 1,479-490 hydrogen or oxygen production from water coordination complex catalysts, 6,532 metal alkoxide synthesis, 2.337 mineral processing, 6,831 reduction, 6,831 multimetallic systems, 1,485 non-aqueous solutions, 1: 493 Electrodeposition of metals, 6,l-15 mineral processing difficulty, 6,831 Electrodes clay modified, 4-23 ferrocene modified, 6-20 modified, 1,487 nafion coated, 6,15 optically transparent thin layer transmission UV-visible spectroscopy, I , 476 Prussian blue modified, 6.21 polymers on, 6, I6 polyvinylferrocene coatcd, 6 , 19 poly(4-vinylpyridine) coated, 6,17 redox centres, 6 , 17 surface modified, 6, 15-31 Electrolysis synthesis, 1,476 transition metal carbonyl complexes, 6,27 water hydrogen and oxygen production, 6,490 Electrolysis-EPR, 1,476 Electrolyte balance metal complexcs, 6,771 Electron distribution excited state, 1,393 Electronegativity, 3, 184 Group IVB elements. 3. 183 Electronic devices COC 7-E*

surlace modified electrodes, 6,29 Electron recording systems, 6,127 Electrons non-bonding pair geometry, 1,36 Electron shuttIe reactions copper(I1) complexes, 5,717 Electron spin resonance, 1,269 g value, 1,270 Electron transfer, 1,331-379 adiabatic, 1, 347 adjacent vs. remote attack, 1,376 hridging groups mechanism, 1,37-3-376 diffusion control limit, 1, 346 distance dcpendcncc, 1,345 clectronic coupling, 1,340,349,362 frequency factors, 1,346 inner sphere, 1,332,359-379 intermolecular, 1,365-379 intramolecular, 1,333,359-365 direct measurement, 1,364 inverted region, 1,356359 non-adiabatic, 1,347 optical mixed valence ions, 1,359-362 outer sphere, 1 332 cross-reactions, 1,353-356 factors, 1 , 337 preassociation, 1,349 quantum mechanics, 1,342 ratc constant expressions, 1,345 rate constants calculated and observed, 1,348 solvent effects, 1, 351 structure and, 1, 352 rime dependence, 1,346 Electron transfer catalysis hydrogen and oxygen production cyclic water cleavage, 6,523 Electron transfer chains, 6,713 Electron transfer reactions, 6,652,711 ATP synthcsis, 6,714 bipyrxzolyl metal complexes, 2,90 diazinc metal cumplexes, 2,80 intermolecular oxygen production from water, 6, 515 photochemical decomposition of water, 6,498-530 intramolecular long-distance, 6,713 ligand-based mixed valency, 1,495 mitochondria, 6,714 oxide metal complexes, 2,301 proteins, 6,653 respiration, 6 , 712 Electron transfer series, 1,493 Electron transport heme proteins, 4,263 intramolecular, 6,712 Electrophoresis technetium-99 in medicine, 6,976

125

Electrophotography

Cumulative Subject Index

Elcctrophotography, 6, 122 Electroplating addition reagents, 6 , 5 coordination compounds, 6 , 4 Electroreduction plutonium(1V) Purex process, 6,954 Electrowinning, 6, 828, 831 Elements interactions with vitamins and drugs? 6- 773 Eleven-coordinate compounds stereochcmistry, 1,99 Elitnination reactions catalysis transition metal complexes, 6,231 Elongation factor 1 zinc, 5, 1007 Elpasolite structure, 6, 846 Eluex process, 6,911 Elution gold cyanide anion exchange resins, 6? 823 Emission spectroscopy metal complexes biology, 6, 550 Enamines oxidative cleavage copper catalysts, 6,394 Enantiomers, 1, 181, 182 [leu5]Enkephalin synthesis cobalt(II1) catalysis, 6,437 Enniatins alkali metal complexes, 3,63 metal complexes, 2,969 synthetic analogues, 3,65 Enolization keto acids metal catalysis, 6,473 Entering group effect platinum complexes substitution reactions. S1 494 Enterobactins, 6,675 calcium complexes, 2, 972 gallium and indium complexes radiopharmacology, 6,971 iron complexes, 4,230 iron deficiency, 2,971 iron receptors, 6,678 Enterochelin, 6,675 Environmental effects photoreactivity. 1,394 Enzymes activators alkali metal ions, 6, 559 calcium, 6.591 magnesium and calcium ions. 6.565 magnesium ions, 6, 578 vanadium, 6,666 electron transfer active sites, 2, 525 extracellular calcium activation, 6, 593 inhihition vanadyl ions, 6,665 iron-sulfur clusters, 6,634 manganese requirements, 6,586 molybdenum, 3. 1334 oxornolybdenum, 3, 1336 zinc, 6,599 Epoxidation alkenes

126

alkyl hydroperoxide catalysts, 6,344 chromium-oxo complexes, 6,352 molybdenum catalysts, 6,330 vanadium-alkyl peroxide catalysts, 6, 342 asymmetric alkenes. 6.331 catalytic hydrogen peroxide, 6,332 cyclic pcroxymetallation mechanism, 6 , 331 Epoxides carbon ylation catalysts. rhodium complexes, 6,273 hydrogenation catalysts, rhodium complexes, 6 , 2 4 I hydrolysis metal catalysts, 6, 470 Equilibrium constants solvent effects. 1. 515 Erasable thermal recording system, 6, 127 Erbium, aquahexakis(dimethy1urea)triperchlorate structure, 1 73 Erbium? tri~(2~2,6~6-tetramethy1-3,5-heptanedione)structure: 1: 65,66 Erbium complexes acelylacetone, 2, 374 Erhiuni( 111) ctmplcxes glycolic acid. 2.472 Eriochalcite, 6,855 Eriochrome black T metallochromic indicators, 1,555 Eriochrome blue black R metallochromic indicators, 1, 556 Eriochrome cyanine R metallochromic indicator, 1, 556 Erythrocruorin, 6,689 dioxygen transport, 6,683 stability calcium ions: 6- 565 Erythrosideri te structure, 6,846 Escherichia coli calcium. 6.570 cation transport. 6 . 558 enzyme I activation, 6.582 magnesium transport, 6,569 manganese transport, 6,570 melibiose system cation coupling, 6.559 nitrate reductase, 6.664 structure, 3, 1438 potassium transport, 6, 559 rcspiration. 6.715 Essential trace elements, 6,762 mclal complexes, 6,760 Esterascs acyl transfer. 6.471 Esters amino metal complexes, hydrolysis, 1,440 amino acids hydrolysis. 6.416.427 bidentate hydrolysis, metal ion catalysis, 6,419 exchange reactions metal catalysis, 6,469 hydrolysis carboxypeptidase A , 6,463 metal complexes, 1.439 2-hydroxy acids hydrolysis, metal catalysis, 6,442 P-mercapto

127

Cumulative Subject Index

metal complexes, 2, 6S5 monoainino acids mixed ligand complexes, 6.417 polydentate hydrolysis, metal ion catalysis, 6,419 Estradiol mercury-203 complexes mammary tumor imaging techniques, 6,994 Ethane, 1,2-bis(diphenylphosphino)cis- and trans-, 2,993 Ethane, (K)-l-cyclohexyl-l,2-bis(diphenylphosphino)rhodium complexes asymmetric hydrogenation, 6,253 ‘Ethane, tetracyanometal complexes, 2,263 Ethane, tetrakis(aminomethy1)metal complexes, 2, 56 Ethane, tris[ 1,l,l-(trisaminomethy1)lcom p Iexes structure, 1,26 1.2-Ethanediamine complexes conformation, 1, 196 metal complexes configuration, 2 . 31 conformation, 2, 32 monoacetate amino acid ester complexesl 6,417 nickel complexes titrimetry, 1, 553 rhodium(II1) complexes alkylation, 1,417 1.2-Ethanediamine, N-(2-aminoethyl)metal complexes, 2, 46 1,2-Ethanediamine, N,N’-(benzaldehydo)-1,2-diphenylstructure, 2, 721 1.2-Ethanediamine. N,N’-bis(o-aminoacetophenone). liquid-liquid extraction, I . 545 1,2-Ethanediaminc, N,N’-bIs(2-aminoethyI)metal complexes, 2, 51 l,Z-Ethanediamine, N.N’-bis(3-aminopropyl)metal complexes, 2. S5 1.2-Ethanediamine, dialkylmetal complexes. 2.43 1,2-Ethanediamine, N,N-ethylenebis-imethylcomplexes isomerism, 1,25 synthesis, 2, 716 1,2-Ethanediamine. N,N,N.-e thylidynetrimethylenetrismetal complexcs. 2 , 5 8 1,2-Ethanediamine,N,N’-(salicy1aldchydo)1,2-Ethanediamine,“ V N , N .N‘-tetramethylmetal complexes, 2.43 Ethanedithiolates dithiolene metal complex synthesis from, 2,598 Ethancsulfcnic acid. 2-aminometal complcxcs, 2 , 8W Ethanetetrathiol metal complexes, 2,606 Ethanethiol, 2-aminometal complexes, 2,799. 800 Ethanol carbonylation catalysts, palladium complexes. 6 , 280 catalysts, rhodium complexes, 6,273 Ethanol, 2-aminochromium(I1) complexes, 2,794 copper(I1) complexes. 2.795 Ethanol, 2-mercaptocarbonylation catalysts, nickel complexes, 6,279 metal complexes, 2, 80.1 Ether, bis(butoxyethy1)

Europium complexes

in uranium ore processing, 6,910 Ether. dimethyl carbonylation catalysts, nickel complexes, 6,279 catalysts, rhodium complexes, 6,273 catalysts. ruthenium complexes, 6,267 Ethers synthesis metal alkaxides, 2,355 Ethyl acetate halogenation acetate-catalyzed, 6,473 Ethylaminc ore formation, 6, X69 Ethylene acetuxylation catalysts, palladium complexes, 6,365 arylation catalysts, palladium complexes, 6,301 carbonylation catalysts, iridium complexes, 6,278 hydrocyanation catalysts, palladium complexes, 6,298 hydrogenation catalysts, iridium complexes, 6, 247 1ig an ds history. 1,21 oxidation glycol acetate from, 6,366 rhodium(II1)-nitro complex catalysts, 6, 374 tellurium-oxo compounds, 6,361 oxidative carbonylation palladium catalysts, 6, 368 oxychlorination palladium catalysts, 6,370 oxycyanation palladium catalysts, 6, 370 reactions catalysts, 6,29K reactions with carbon dioxide catalysts. rhodium complexes, 6,204, reduction catalysts, rhodium complexes, 6,245 Ethylene effect plants copper, 6.656 Ethylene glycol manufacture, 6,329 synthesis by carbonylation, 6,275 palladium catalysts, 6, 370 Etioporphyrins metal complcxcs geochemistry, 6,865 synthcsis, 2. 816 Euglena gracilis zinc deficiency, 6, 584 Europium photoreduction, 1,408 Europium. dichlorohexaaquachloride structure. 1. 87 Europium, pentanitratostereochemistry, 1,99 Europium tetrakis(hexafluoroacety1acetone)stereochemistry, 1,94 Europium, tris(2.2,h,6-tetramethyl-3,S-heptanedione)photosubstitution. 1.408 Europium, tris(2,2,6,6-tetramethyl-3,5-heptanedionequinuc1idine)stereochemistry, 1, XI Europium complexes 1,3-diketones. 2.387; 3, 1081

Europium complexes

Cumulative Subject Index

dipositive oxidation state hydrated ions, 3, 1109 malonic acid, 2,444 Europium salts in photochemical nitrogen production from water, 6, 508 Evolution chelates naturally occurring, 2.960 Ewaldite snucturc, 6,848 Ewens-Bassett number. I . 112, 120 EXAFS cadmium complcxcs, 5,929 copper(I1) complexes, 5,720 molybdenum oxides, 2, 308 water-metal complexes, 2, 296 zinc complexes, 5,929 Exchange reactions solmto ions, 1,285 Excited state decay electron transfer, 1,356-359 Excited states, 1, 387

charge transfer, 1.388 ligand-to-metal, 1.403,404 rcactiviiy, 1, 402 charge-transfer-to-solvent reactivity, 1. 405 DOSENCO. 1.391 delocalized. 1: 388 intraligand, I. 388 react.ivit.yl1. 405 ligand field. I. 397 ligand field theory, I,387 metal-metal, 1. 389 proccsscsl I. 387 kinetics. I , 391 thexi. I, 389 bimolecular reactions, 1,394 types. 1. 387 Exochelin, 6.675 Exocytosis calcium, 6.595 Extractive metallurgy. 6, 779-835 classification, 6 ! 780

128

Factor F430,6,643 nickel complex, 6,546,644 Factor IX blood coagulation, 6,593 Factor VI1 blood coagulation, 6,593 Factor X blood coagulation, 6,593 Fan angle, 2,1019 Fast electron transfer, 6, 712 Fast neutrons uranium-235,6,883 , Fast reactor fucl preparation, 6 , 924 Fatty acids mctal salts reactions with carbazides. thermography, 6, 121 Feldspars inclusions, 6,869 structure, 6, 845 Fenton’s reagent, 6,379 Ferredoxin I, 6,632 Ferredoxins, 1, 142; 2,773; 4.237.238, 1240, 1241 2-iron, 4,235 redox potentials, 1 , 513 Ferribalamins, 2, 883 Ferrichrome A, 4,233. 234 Ferrichromes, 2. 970; 4,233; 6, 675: 676 calcium complexes, 2,972 Ferricyanides bleaching photography, 6, 100 oxidation by, 1,504 redox couples, 1,512 Ferricytochrome c reduction, 6,621 Ferrioxalates photography, 6, 124 physical devclopment. 6 , 1I4 photothermography, 6, 11Y Ferrioxarnine E, 6 , 678 Ferrioxarnines, 2, 9713, 971; 4, 233; 6 , 678 Ferritin, 2, 772: 6, 634, 667 EXAFS. 6,668 gallium-67 binding, 6,992 structure, 1, 137; 2,975

Ferrobacillus ferrooxidans in oxidative leaching of uraniferous ores, 6,900 Ferrocene electrode modification, 6.20 history, 1 , 3 photothermography, 6.119 stereochemistry nomenclature, 1. 131 Ferrocene, 1-acetyl-2-methylnorncnclaturc, 1, 131 Ferrocene, vinylpolymerization on two platinum electrodes. 6. 16 Ferrochelatase, 6,671 heme biosynthesis, 6, 616

Ferrocyanides stability. ti, 830 Ferrocytochrome c oxidation. 6: 621 Ferroin, 4>1203 redox indicator. 1,558 Ferrokinetics radiopharmaceutical agents, 6,968 Ferrornanganese nodules formation. 6; 570 Ferroverdin, 2,797; 4,1238 structure, 2, 272 Ferliliralion eggs

calcium, 6,595 Fihi-inogen labelled 6 995 cardiology, 6.994 deep vein thrombosis diagnosis, 6,995 Fibrinogenase zinc- 6.613 Field desorption mass spectrometry radiophamacological agents, 6,976 Filter dyes photognphy, 6, 104 Fissile material criticality reprocessing, 6 , 925 Fission energy. 6, 883 Fission products decontamination Purex process, 6 , 953 elements. 6 . 883 Purex process. 6.940 Fission reactors natural: 6*895 Five-coordinate complexes stereochemistry, 1,3>48 substitution reactions, 1,321 Five-membered rings metal complcxes, 2. 76 substituents metal complexes, 2, 82 Fixing agents photography. 6.99 Flavonols oxygenolysis cobalt catalysts, 6 , 388 Flotation mineral processing hydrophilic. 6.780 hydrophobic, 6,780 Fluorescence. I , 395 Fluorexone metallofluorescent indicator, 1, 558 Fluoridcs grwimctry! i , 553 Fluorimetry, 1,55 1 Fluorine bond formation, 2,677 participation of higher d orbitals, 2, 677 ~

129

~

Fluorine

Cumulative Subject Index

dissociation, 2,675 Fluorine bridges trifluoroxenon hexabismuthate, 3,313 Fluorine complexes bridge systems, 2,678 double bridged, 2,681 single bridged, 2,680 three-coordinate, 2,684 triple bridged, 2,683 Fluorites inclusions, 6,869 Formaldehyde hydroformylation catalysts, rhodium complexes, 6,261 Formamide metal complexes, 2,487-501 Formamide, dimethylas solvent, 2,491 electrochemistry in, 1,493 metal complexes NMR, 2,493 Formamide, diphenylmetal complexes, 2,491 Formamide, N-methylmetal complexes synthesis, 2,492 Formamidine, N , N-di-2-anthraquinonylmetal complexes, 2,275 Formamidine, N,N'-diarylmetal complexes, 2,275 Formamidine, N,N'-dibenzylmetal complexes, 2,276 Formamidine, N,N'-diisopropylmetal complexes, 2,276 Formamidinesulfinic acid technetium complexes, 6,974 Formate dehydrogenases bacteria molybdenum, 6,662,663 Formazan, l,S-bis(2-carboxyphenyl)-3-cyanocopper complexes dyes, 6,81 Formazan, 1-(2-~arboxyphenyl)copper complexes dyes, 6, 79 Formazan, 1-(2-hydroxopheny1)-3,5-diphenylcopper(I1) complexes dyes, 6,81 Formazan, 1-(2-hydroxyphenyl)copper complexes dyes, 6,79 Formazan, 1-(2-hydroxyphenyl)-3-phenyi-5-(2carhoxypheny1)copper complexes dyes, 6,81 Forrnazan, l-(2-hydroxy-5-sulfophenyl)-3-phenyl-S-(2carboxypheny1)zinc detection, 6, 83 Formazans cobalt complexes dyes, 6,81 metal complexes bidentate, 6,78 color photography, 6, 111 dyes, 6,77 tetradentate. 6. 81 tridentate, 6,79 silver dye-bleach process, 6. 105 Formic acid alkyl esters synthesis from carbon dioxide, 6,296 ethyl ester synthesis from carbon dioxide, 6,294

__

130

metal complexes, 2,436 reactions catalysts, 6,303 Formylation metal complexes, 1,421 Four-coordinate complexes planar substitution reactions, dissociative activation, 1,320 substitution rcactions, nucleophilicity, 1,312 suhstitution reactions, rate laws, 1,311 substitufioti reactions. stereochemistry, 1,318 substitution reactions, 1, 311 reactivity, non-participating ligands, 1, 315 planar d*, 1,320 Freshwater trace element complexes, 6, 851 Friend, John Albert Newton, 1, 14 a-o-Fructose alkaline earth metal complexes, 3 ,2 5 Fructose- 1,6-bisphosphatase zinc, 6,613 a-o-Fucose alkaline earth metal complexes, 3,25 Fulminate complexes linkage isomers, 1. 186 Fulminates metal complexes, 2,7-13 Fulminating silver, 5: 780 Fulminatocobaltate ions, 2. 13 Fulminic acid microwave spectrum, 2, 13 Fulvic acids isolation, 6, 857 metal complexes computer models, 2,962 geochemistry, 6 , 857-861 minerals, 6,849 naturally occurring, 2,961 stability, 6, 859 structure, 2,961 thorium(1V) complexes, 6,887 Fumarate electron acceptor respiration, 6,715 Fumarate reductase Escherichia coli respiration, 6, 716 Fumaric acid hydrogenation catalysis, ruthenium complexes, 6,236 Fungicides copper complexes, 6,1U23, '1025 Furan, tetrahydro1.3-diketone metal complexes, 2, 377 electrochemistry in, 1.493 oxidation ruthenium tetroxide, 6,358

Furan-2,5-dicarbaldehyde in imine chelate synthesis, 6, 160 Furanones synthesis by carbonylatiun, 6,274 by hydroesterification, 6,275 2-Furanylmethyleneimine,N,W-ethylenebishydrolysis metal catalysis, 6, 460 a-Furil dioximc in gravimetry, 1,533 liquid-liquid extraction, 1,544 Fusarinines, 6,676

G Gadolinium, octaaquasalts structure, 1,84 Gagarinite structure, 6, 846 a-D-Galactose alkaline earth metal complexes, 3,25 Galactose oxidase, 6,700 copper, 6,655 copper(I1) complexes, 5.723 copper(II1) cornplexcs, 5,749 Galena brines, 6, 853 depression, 6,783 djssolution, 6, 787 humic acids, 6,861 Gallium gravimetry, 1, 530 isotopes medical diagnosis, 6,969 radiopharmaceutical applications, 6,969 Gallium-67 complexes hepatobiliary system imaging techniques, 6, 990 transport, 6,671 tumor imaging techniques, 6,992 Gallium, hexakis(methano1)solvent exchange, 1,285 Gallium, tris(acety1acetone)structure, 1,65 Gallium alkoxides, 3, 133 physical properties, 2,345 Gallium bromide, 3, 139 Gallium chloride, 3, 139 Gallium complexes, 3, 105-142 amido, 3,130 aqua, 3,133 azides, 3, 131 2,2'-bipyridyl, 3, 130 carboxylato radiopharmacology, 6,970 cyanates, 3, 131 dimethyl sulfoxide, 2,488 hydroxides, 3, 133 imido, 3,130 nitriles, 3, 131 oxides, 3, 133 1,lO-phenenthroline, 3, 130 phosphines, 3, 132 phthalocyanines, 2,863 piperidine, 3, 130 porphyrins, 2,821 pyrazolyl, 3, 130 pyridine, 3,130 selenocyanates, 3, 131 terpyridyl, 3, 130 thiocyanates, 3, 131 Gallium(1) complexes. 3, 127 halides, 3, 127 oxides, 3, 127 selenides, 3, 127

sulfides. 3, 127 Gallium(II) curnplexes, 3, 127 halides? 3, 128 selenides, 3. 128 sulfides: 3, 128 tellurides. 3, 128 Gallium(II1) complexes. 3, 129 amines. 3: 129 amino acids, 3, 141 arsenates, 3, 135 borates, 3. 134 borohydrides, 3,131 bromates, 3, 135 carbonates, 3,134 carboxylate.^, 3, 135 chloratcs, 3, 135 citrates. 3, 136 cyanides, 3: 129 dithiocarbamates, 3, 138 ethers, 3: 136 fluorides, 3,138 germanates, 3, 134 hydrides, 3,140 iodates, 3, 135 /3-ketoenolates,3, 134 lactates, 3, 136 mixed halides, 3, 139 molybdates, 3,135 nitrates. 3 , 135 peptides. 3, 141 perchloratcs, 3, 135 phosphates, 3, 135 phosphites, 3; 135 phthalocyanines, 3,141 porphyrins. 3,142 evolution, 2,961 proteins. 3, 141 Schiff bases, 3, 141 salicylaldehyde, 3, 136 selenatesl 3, 135 selenides, 3. 137 silicates, 3, 134 silyl; 3, 129 sulfates, 3, '135 sulfides: 3,137 tartrates. 3, 136 tellurates, 3. 135 tellurides, 3, 137 thiophosphates, 3, 138 tropolones rearrangement, 2,382 tungstates, 3, 135 xanthates, 3, 138 Gallium iodide, 3, 139 Gallium isopropoxides synthesis electrochemistry, 2,337 Gallium trihalides, 3, 126, 130 pyridine adducts, 3, 108 Gas chromatography, 1,560 Gases

131

Gases

Cumulative Subject Index

metal complexes geochemistry, 6,854-856 Gattermann-Koch reaction, 5,568 Gelatin photography silver halides, 6,96 Gel precipitation process fast reactor fuel, 6,924 Gels metal hydroxides phosphatc cster hydrolysis, 6,448 Generator systems radioisotopes from, 6, 965 nifCenes, 6,720 Geochemistry, 6,843-873 segregation of uranium from thorium, 6.886895 Geometric isomerism cobalt ammines, 1 , 11 Geometry coordination numbers andl 1,31-101 Geoporp h yrins metal complexes spectrophotometry, 6,863 Gcrmaalkenes, 3,191 Germaarenes, 3,191 Germaimines, 3, 191 Germanate, trichloro-, 3, 195 Germanates, 3,203 Germanediol, di-t-butyl-, 3,206 Germanium elemental structure, 3, 183 Germanium-68 production, 6,965 Germanium, cyclopentadienyl-, 3, 218 Germanium, tris(acety1acetone)structure, 1, 65 Germanium alkoxides physical properties, 2,346 Germanium complexes, 3,183-223 acet ylacetone isomerization, 2,383 bivalent stereochemistry, 3, 188 coordination geometry, 3, 185 dialkyl or diaryl, 3,216 multiple bonding, 3, 188 peat, 6, 858 phthalocyanines, 2,864 porphyrins, 2,822 tetravalent, 3,205 Germanium(1V) complexes mandelic acid, 2,474 Germanium ethoxides synthesis electrochemistry, 2, 337 Germanium fluoride, 3, 193 Germanium halides, 3, 197 bivalent structure, 3,192 Lewis acidity, 3,199 Germanium iodide, 3, 194 Germanium ligands transition metal complexes, 2, 15-18 Germanium oxides structure, 3, 192,202 Germanium selenide structure, 3,202 Germanium sulfide structure, 3,202 Germanocene nomenclature, 3,217 Germanocenium ions pentamethyl, 3,218

132

Germancmes, 3, 191 Germaphosphirnines, 3,191 Germathiones, 3, 191 Germatranes, 3.212 Germylene complexes transition metals. 2. 17 Germylenes, 3, 192 structure? 3, 193 Gianellaite structure, 6, 848 Gilsonite, 6,865 Glasscs gcochcmistry. 6.855 Gluconic acid metal complexes, 2,480 6-D-Glucopyranoside. 8-quinolyl hydrolysis metal catalysis, 6,464 D-Glucopyranosides- I-thiophenyl solvolysis, metal catalysis, 6, 465 Glucose isomerases activation magnesium ions, 6,583 Glucose tolerance chromium(1II) complexcs, 3, YO4 Glucose tolerance factor chromium, 6,666 Glutamic acid metal complexes, 2,749 Glutamic acid, carboxymetal complexes biology, 6,546 L-Glutamic acid, glycylmetal complexes. 2, 764 Glutamine metal complexes, 2,749 Glutamine synthetase, 6.720 activation magnesium ions; 6,582 Glutaraldehyde protein modification with. 6,9Y5 Glutaric acid 8-(2-carboxq:quinoly1)estcr metal catalysis. 6?441 8-quinoIyl ester metal catalysis, 6,441 Glutaric acid, Z-ketometal complexes geochemistry, 6.867 minerals weathering, 6,868 Glutathione cadrnium(I1) cwrnplcxcs, 2, 968 metal complexes, 2,764 naturally occurring, 2,967 in photochcmical hydrogen production from water, 6, 501 zinc(I1) complexes, 2,968 Glutathione peroxidase, 6,682,706 selenoprotein, 6,774 Glyceric acid metal complexes, 2,480 a-Glycerophosphate hydroxide metal catalysis, 6, 448 GIycinamidc hydrolysis metal-catalyzed, 6,425,431 Glycine butyl ester hydrolysis, metal catalysis, 6,421 ethyl ester

133

Cumulative Subject Index

hydrolysis, metal catalysis, 6,421,428 ethyl ester, diacetate hydrolysis, metal catalysis, 6,121 ethyl ester, palladium(I1) complexes hydrolysis, 6,423 ethyl ester, ruthenium(II1) complexes linkage isomerism, 1, 186 metal complexes a-C-H bond activation, 2,757 geochemistry, 6,859 prebiotic systems, 6,871,872 reactivity, 2, 756 ore formation, 6,869 ruthenium(Ii1) complexes linkage isomerism, 1,186 Glycine, N,N-bis( hydroxyethyllmetal complexes, 2,788 Glycine, 2-cyclopropylsynthesis metal catalysis, 6,468 Glycine, ethylene-N,N'-bis-2-( 0-hydroxyphenyl)chelating agents iron overload, 6. 769 Glycine, glycylhydrolysis copper(T1)-catalyzed. 6,425 isopropyl ester, palladium(T1j complexes hydrolysis, 6,424 methyl ester hydrolysis, copper(I1)-catalyzed, 6,422 hydrolysis, palladium(I1)-catalyzed, 6,424 Glycine, L-histidylmetal complexes, 2, 762 Glycinecresol red metallochromic indicator. 1,557 Glycinethymol blue metallochromic indicator, 1,557 Glycobiarsol, 3,256 Glycvl acctiltc synthesis by ethylene oxidation, 6: 366 Glycolic acid met.al complexes, 2,465,472 IR spectra, 2,470 NMR spectra, 2.467 Glycols alkaline earth metal complexes, 3, 17 by alkene oxidation osmium-oxo compounds. 6.358 reactions osmium tetroxide, 4: 590 Glycoproteins metal complcxes, 2, 984 Glycosidation silver imidazole complexes: 5 , 786 Glycosides hydrolysis metal catalysis, 6,464 Koenigs-Knorr synthesis, 5,810 Glycylglycine dipeptidase models, 6,415 Glymes alkali metal complexes, 3, 17 Glyoxal bis(2-hydroxyanil) metallochromic indicator, I?557 Glyoximates metal complexes non-integral oxidation states, 6, 144 Glyoximc, N , N'-bis(4'-bcnzo( is-crown-S)diaminometal complexes, 2,274 Glyoxime, dimethylin analysis, 1, 522; 2,271 metal complexes

Gold{I) complexes

neutron diffraction, 2, 269 nickel cornpIexes, 2.269,271 nickel determination, 1, 533 Glyoxylase 1 zinc, 6, 607 Gmelin's compound history, 1 3 Goethite precipitation, 6 , 827 Gold anodic dissolution, 6, 784 clusters inetaCmetal bonding, 1, 169 deposition organic complexcs, 6,869 electroplating, 6, 11 extraction anion exchange resins, 6,822 leaching, 6,784 nonametallic clusters, 1, 165 body-centred cube, 1, 165 precipitation, 6,829 smeIting, 6.833 solvent extraction, 6, 806 toxicity, 5.877 Gold. methoxycarbonylmethylthiophotography silver image stabilizer, 6, 102 Gold clustcr complexes, 5,899 bonding, 5: 902 carbides, 5,908 mixed metal. 5,906 structure'el5.902 Gold complexes, 5,861-911 antiarthritis drugs, 6,758 labelled, 6,969 applications, 6 , 1024 bonding, 5, 867 boron bonds, 5,903 brines geochemistry, 6, 853 carbon hunded linkage isomerism, 2,392 carboranes, 5,903 geochemistry, 6, 851 Group Iv metal bonds, 5,903 main group metal bonds, 5,903 mobilization geochemistry, 6.868 organic ligands, 6,861 oxidation. 5.863 phthalocyanines, 2,868 polypyrazolylborates, 2,254 porphyrins, 2,841 pseudohalides, 2,233,234 stabilizers photographic emulsions, 6, 98 rrans influence, 5,869 transition metal bonds, 5,904 tnchlorostannate, 5,904 Gold(-I) complexes, 5 , 863 Gold(0) complexes, 5,863 Gold(1) complexes, 5,864 alkyl phosphites. 5, 882 amines, 5,880 anionic nitrogen donor ligands, 5,879 antimonides, 5, 881 antimony donor ligands, 5,881 arsenic donor ligands, 5,881 arsenides, 5,881 arsines, 5,882 azides, 5. 879 2,2'-bipyridyl, 5. 881

Gold(1) complexes

Cumulative Subject Index

bonding, 5,867 carbenes, 5,886 carbodiphosphoranes, 5,886 carbon donor ligands, 5,885 cyanides, 5,885 cyano, 6,784 structure, 6,784 N,N-dialkyldithiocarbamates, 5,878 0,O’-diisopropyldithiophosphates, 5,878 2-(dimethylphosphino)pyridine, 5,881 2-(diphenylphosphino)pyridine, 5,881 dithioacetates, 5,878 dithiocarbamates, 5,878 dithiophosphinates, 5,878 electron-deficient, 5,899 fulminates, 5,885 gold-gold bonds, 5,899 halides, 5,870 hydrides, 5,869 imidazoles, 5,881 iminoalkyl, 5,886 isocyanates, 5,879 isocyanides, 5,885 2-mercaptobenzimidazole photography, 6,102 monodentate arsines, 5,882 monodentatc phosphates, 5,882 monodentate stibines, 5,882 nitriles, 5,880 nitrogen donor ligands, 5,879 oxygen donor ligands, 5,871 phosphides, 5,881 phosphines, 5,882 phosphorus donor ligands, 5,881 polynuclear thio, 2,566 pyrazoles, 5,881 pyridines, 5,880 selenides, 5, 872 selenium donor ligands, 5,872 selenocyanates, 5,873 sensitizers silver halide light sensitivity, 6, 97 stibines, 5,882 sulfides, 5,872 sulfites, 5,873 sulfur donor ligands, 5,872 tetrathiosquarates, 5,878 thioarnides, 5,874 thiocyanates, 5,873 thioethers, 5,874 thiohydroxamic acid, 5,874 thiolates, 5,875 thiosulfates, 5,873 thiourea, 5,874 triphenylphosphine sulfide, 5,874 unsaturated thiolates, 5,878 GoldIII) complexes, 5,865, 886-889 carboranes, 5,889 dinuclear, 5,887 diselenocarbarnates, 5,888 dithiocarbamates, 5,888 maleonitriledithiolates, 5,888 mononuclear, 5,888 phthalocyanine, 5,889 reaction intermediates, 5,889 Gold(II1) complexes, 5,865 alkene dithiolates, 5, 893 amido, 5,895 ammines, 5,895 arsines, 5,897 azides, 5,894 2,2’-bipyridyl, 5,896 2,2’-biquinolyl, 5,896

bonding, 5,868 bromides, 5,889 carbon donor ligands. 5.898 chlorides, 5,889 cyanides, 5,898 cyano, 6>784 diamines, 5,895 2,3-dimercaptopropanol, 5,893 dimercaptosuccinic acid, 5,893 2,9-dimethyl-l,l0-phenanthroline, 5 , 896 diselenocarbamates, 5,894 dithiocarbamates, 5,893,894 dithiolatcs, 5,893 fluorides, 5,889 halides, 5,889 hydrides, 5,891 iodides, 5,890 isocyanides, SI898 nicotinic acid, 5,895 nitrato, 5,891 nitrogen donor ligands, 5,894 oxygen donor ligands, 5,891 penicillamine, 5,893 phenanthroline, 5 , 896 phosphines, 5,897 porphyrins, 5 , 897 pyrazoles, 5,895 pyridines, 5,895 selenides, 5,892 selenites, 5,892 selenium donor ligands, 5,892 sensitizers silver halide light sensitivity, 6,97 spectra, 1,255 stibines, 5,897 substitution reactions, 1,311 sulfides, 5: 892 sulfites, 5,892 sulfur donor ligands, 5:892 tellurides, 5,892 tellurium donor ligands, 5 , 892 2,2‘,2”-terpyddyl, 5,8Y(r thiocarbonyl, 5,892 thiocyanates, 5,892 thioethers, 5,893 thioselenocarbamates. 5.894 triarnines, 5,895 tripyrazolylborate, 5,896 tripyrazolylmethane, 5,896 Gold(1V) complexes, 5,866 Gold(V) complexes, 5,866, 898 Gold(1II) oxides, 5, S9l Graham’s ammonium theory, 1,4 Gramicidin cation transport, 6 , 553 metal complexes, 2,970 Gramicidin A dimerization, 6,553 Gravimetry, 1,524-535 Green bacteria anoxygenic photosynthesis, 6,589 Grignard reagents reactions with pyridyl thiolates, 6,219 Grimselite structurc, 6,848 Groundwaters inorganic complexes geochemistry, 6, 852 Group IV elements bivalent compounds Group IV, 3,216 Group V,3,216

134

135 Group VI, 3,216 coordination geometry, 3, 185 elemental radii, 3, 184 ionization energies, 3.326 ionization potentials. 3.326 properties, 3,326 tetravalent compounds, 3,205 Group IVB elements coordination geometries. 3. 186 Group V elements tetravalent compounds, 3.205 Group Vi elements tetravalent compounds, 3.205 Group IIA ions transport, 6,565 microbes, 6,569 plants, 6,572 Group V ligands bidentate mixed, 2,1009 mixed, 2,1009 Group I metals reactions with alcohols, 2, 336 Group I1 metals alkoxides physical properties, 2 , 345 reactions with alcohols, 2,336 Group IIA metals, 3, 1-70 Group 111 metals

Cumulative Subject Index reactions with alcohols. 2. 336 Group VI11 metals peroxo complexes oxidation, 6,335-341 Group overlap integrals angular overlap model, 1,226 Grunwald-Winstein analysis, 1, 504 Guanidine, diphenylmetal complexes, 2,283 Guanidine. lithiostructure, 2,283 Guanidine. njtroaminometal complexes, 2,283 Guanidinc, tctramcthylmetal complexes, 2,282 Guanidines metal complexes, 2,269,281 silver(1) complexes light-sensitive compounds, 6, 115 Guanidinium ions macromonocyclic complexes, 2,944 metal complexes. 2,282 Guanilate cyclase activation magnesium ions, 6, 584 Guanine cadmium complcxcs, 5,957 metal complexes, 2 , 9 3 minerals, 6,849 zinc complexes, 5,957

Guanine

H Haber proccss, 2. 116 Haernanthus spp. mitosis calcium, 6,596 Hafnates, bromo-, 3,430 Hafnates, chloro-, 3,430 Hafnates, Auoro-, 3,423 alkali metal salts, 3, 425 alkylammonium salts, 3, 427 divalent metal salts, 3,427 guanidinium salts, 3,427 hydrazinium salts, 3,427 vibrational spectra, 3, 429 Hafnates, iodo-, 3,430 Hafnium, tetrakis(tropo1one)stereochemistry, 1, 94 Hafnium bascs benzoyl hydrazones, 3,434 Hafnium chloride separation from zirconium chloride, 6; 812 Hafnium complexes, 3,363-440 alkyl alkoxy reactions, 2,358 appkations, 6,1012 coordination geometries, 3,364 oxidation states, 3,364 phthalocyanines, 2, 865 porphyrins, 2,823 pseudohalides, 2,228 tetrakis-chelate stcreochcmistry, 3,364 Hafnium(0) complexes, 3,364 2,2'-bipyridyl, 3,366 nitrogen ligands, 3,366 l,l0-phenanthroline, 3,366 Hafnium(II1) complexes, 3,366-370 arsenic ligands, 3,369 nitrogen ligands, 3, 366 phosphorus ligands, 3,369 Hafnium(1V) complexes, 3,370-400 2-acetylpyridine, 3, 373 aldehydes, 3, 403 alkaxides, 3,389 reactions, 3,390 alkyl thioglycolates, 3,439 amides! 3,414 amines, 3,371 amino acids, 3, 410 aminopolycarboxylates, 3,436 ammines, 3,371 aqueous solutions polynuclear, 3,384 Raman spectra, 3,384 arsenic ligands, 3,383 arsines, 3,383 aryloxides, 3, 3x9 N-arylsalicylaldimines, 3,437 azides, 3.379 benzoquinoline, 3,372 2,2'-bipyridyl, 3,372 bis(amido)silane, 3,375

bis(dikctonatcs), 3 , 4 U bis(trirnethylsilylamido), 3, 375 carbamates, 3,310 carbonates, 3; 410 carboxylates. 3.109 catecholates. 3,403 citric acid, 3, 422. cupferron. 2.512; 3,417 cyanates, 3,379 cyanides, 3,370 3-cyanopyridine33.373 dialkylamido, 3>375 photr~clectrouspectra. 3.375 reactions, 3.375 dichlorophosphates. 3,407 diethylenetriaminepenlaacerare, 3. 436 dithiocarbamatcs, 3,319 dithiolencs, 3,420 esters, 3>403 ethers, 3,403 ethylenediaminetetraacetate, 3, 436 fluorosulfates, 3,407 glycolic acids. 3.412 halogenoids, 3.381 hydrazine, 3,374 hydrides, 3,432 hydroborates, 3.432 hydroperoxo, 3.387 hydroxamates. 3: 417 hydroxide, 3,384 hydroxy acids aliphatic, 3,412 aromatic, 3?412 imidazoles, 3: 372 indazoles, 3.372 interhalogen-halogenoids, 3,381 interhalogenoids, 3,381 isoproxides NMR, 3,389 @-ketoenolates,3>392 kctoncs, 3>403 lactic acid, 3,412 malic acid, 3.412 mandelic acid, 3$4'13 o-mercaptophenolato,,3,421 N-methyl-p-thiotolylhydroxamato, 3,439 molybdates, 3: 408 mono(diketonates)+3.401 monothiocarbamates, 3,419 N heterocyclic ligands. 3.372 IR spectra, 3,372 nicotinamide, 3,373 nitrates?3,406 nitrilcs, 3, 382 IR spectra, 3- 382 Raman sepctra, 3: 382 nitrilotriacetate, 3.436 nitrogen ligands. 3,371 nitro ligands, 3: 374 octaethylporphinato, 3,439 oxalates. 3*411

136

137

Cumulative Subject Index

oxides, 3,384 oxoanions, 3,406 oxygen ligands, 3,384 N-oxides, 3,414 P-oxides, 3,414 perchlorates, 3,408 peroxo, 3,387 IR spectra, 3,388 Kaman spectra. 3. 388 1,10-pl~etiatitliroiinc,3 , 372 phosphincs, 3,383 phosphorus ligands. 3.383 phthalocyanines, 3,440 poly(pyrazoly1)borates. 3.381 porphyrins, 3,439 pyridine, 3,372 8-quinolinol, 3, 437 quinones, 3,403 Schiff bases, 3,434 salicylic acid. 3.413 selenates, 3, 407 selenium ligands. 3. 421 selenocyanates. 3.380 selenoxides, 3,414 sulfates, 3,407 sulloxides, 3,414 sulfur ligands, 3,418 tartaric acid, 3. 412 tetrahalides, 3,422 tetrakis(diketonates). 3,397 bromination, 3,398 ligand exchange, 3.398 mass spectra, 3.399 NMR, 3,398 volatility, 3, 399 tetra~henylporphyrin~ 3.140 .thiocyanates, 3, 380 thioethers, 3, 418 thiolates, 3, 418 thiourea, 3,421 tin-containing ligands, 3. 370 trialkysilyl oxides, 3. 380 triazenes. 3, 378 trihydroxyglutaric acid, 3.112 tris(diketonates), 3, 399 tropolonates, 3,402 urea, 3,382 water, 3, 384 Halides determination, 1,535 in eleciroplating. 6, 14 organic carbonylation. 6.28'1,282 tlallucinogenic drugs mctal complcxcs, 6, 773 Haloarsine cotnpounds, 2 , 1004 Halobacltlrium halubirim activity calcium, 6. 595 calcium transport, 6, 571 cation transport, 6,558 photosynthesis, 6 . 589 Halobacterium spp. cation concentration gradients. 6.551 Halogenation coordinated nitrogen atoms, 1 : 4 Ih 1,3-diketone metal complexes, 6 , 2 0 3 N-halosucciniinides. 1 421 1,lalogencations, 3, 319 hexafluoro, 3,316 tetrafluoro, 3, 315 Halogen complexes, 2, h75-687 bridge systems, 2.677484 ~

Heme c

asymmetry. 2,678 theoretical srudics, 2,682 double bridged, 2,681 four-coordinate, 2,686 quadruple bridged, 2,684 single bridged, 2, 680 three-coordinate. 2,684 triple bridged, 2,683 theoretical studies, 2,683 Halogen compounds hgpervalent, 3, 316 I.Ialogen(1)compounds, 3,313, 317, 319 Halogen(ll1) compounds, 3, 313, 3'17,320 Halogen(V) compounds, 3,315,318,320 hcxafluoro anions, 3, 315 HalogeniVII) compounds, 3,316 Halogenium gases oxidation states, 3, 312 Halogenium halides, 3,317 Halogenium species, 3,311-321 carbon ligands, 3, 316 coordination compounds, 3,312 coordination geonietry, 3,312 halogen ligands, 3, 313-316 nit.rogeti ligands, 3, 319 oxygen ligands, 3, 319 seleiiium ligands. 3, 321 sclcnocyanates, 3, 321 sullur ligands, 3, 321 thiocyanates, 3, 321 Halogen pentafluorides, 3, 315 Halogens bond formation, 2.677 physical properties, 2, 675 reduction vanadium(I1) complexes, 3,471 Halophosphine compounds, 2. 990 Halostibine compounds, 2, I007 Handedness origins hinlogical systcms, 6, 872 Hapto compounds nomenclalure. 1, 131 Haptonotation, 1 , 116, 117 Hdta -see Acetic acid, hexamethylenediaminetetra Heart diagnostic imaging techniques radiopharmaceuticals, 6,990 Heavy metals extraction cation exchange resins, 6,817 poisoning chelation therapy, 6,767 Heiratite structure. 6,837 Helicity, 1. 192 Hellyerite structure, 6,849 Hematein. 6.36 Hematite precipitation, 6.827 Heme biosynthesis, 6, 616,671 dioxygen carriers modcX compounds, 6,684 iodosobenzene systems reactions, 2, X44 reactions, 2, 82!> Heme a structure, 6,614 Heme b structure. 6, 614 Heme c

Heme c

Cumulative Subject Index

structure, 6,614 Heme proteins, 4,262 carbon monoxide binding, 6,698 electron transport, 4,263 Hemerythrin, 2,315; 4,253 dioxygen binding, 6,689 dioxygen transport, 6,683 iron, 6,634 structure, 2,301 Hemerythrin, deoxydioxygen binding, 6,689 Hemin ester, 4 , 1266 Hemins reactions, 2,834 Hemiporphyrazines metal complexes dyes, 6,91 Hemispherands alkali metal complexes, 3,43 Hemithio acetals, 6,457 Hemocyanin, 2,315 active site, 6,692 carbon monoxide binding, 6. 692 copper, 6,654 cytochrome oxidases, 6,683 dioxygen binding, 6,691 dioxygen transport, 6,683 stability calcium ions, 6,564 Hemocyanin, dcoxycopper complexes, 5,592 Hemocyanin, oxyEXAFS, 6,691 resonance Raman spectra, 6,692 Hemoglobin, 2,315,772,980; 4,262.1257, 1269 allosteric effector, 6, 688 artificial, 4, 100 cooperative effect, 6,687 dimeric, 6,688 dioxygcn transport, 6,683 dioxygen uptake, 6,682 giant, 6, 689 magnetic properties, 6,685,686 monomeric, 6,688 oxygen affinity, 6,685 reactions, 2,829 relaxed (R) high affinity form, 6,687 structure, 6,685 tensed (T) low affinity form. 6,687 Hemoglobin, deoxy-, 6,686 EXAFS, 6,686 Hemoglobin, nitrosyl-, 4 , 1194 Hemoglobin, oxydiamagnetism, 6,686 Hemoproteins, 4,259 dioxygen reversible binding, 6,6119 Hemorrhagic toxins zinc, 6,613 Hemosiderin, 2,975 Hepatobiliary agents technetium complexes, 6,984 Hepatobiliary system diagnostic imaging techniques technetium complexes, 6,989 Heptafluorotellurates, 3,303 Heptametallic complexes, 1 , 161 centred hexagon, 1,161 cubanoid, 1, 162 pentagonal bipyramid, 1, 161 Heptamolybdates, 3, 1030, 1376 Heptanal hydrogenation

catalysis, ruthenium complexes, 6,235 Heptane-3,5-dione metal complexes stability, 2, 366 Heptane-3,5-dione, 1,l 1,2,2.6,6,7,7,7-decafluorometal complexes gas chromatography, lI560 Heptane-4,6-dione, decaffuorometal complexes decomposition, 2 , M S Hcptanc-2,4,6-trione mctal complexes, 2,399 Heptatungstates, 3. 1033 1-Heptene hydroesterification catalysts, palladium complexes, 6,285 hydrogenation catalysts, iridium complexes, 6,246 Heptoxime liquid-liquid extraction, 1,544 Heteroallenes coordinated reactivity, 2,579 metal complexes, 2.579 Heterocyclic compounds synthesis, 5 , 1121 Heterocyclic nitrogen compounds basic pK, metal complcxes. 2,74 metal complexes. 2.73-94 steric aspects, 2,74 Heterocyclop hanes cations anionic complexes, 2,950 Heterocylic nitrogen compounds metal complexes electronic aspects. 2,74 Hctercilytic cleavage catalysis transition metal complexcs, 6,230 Heteropentalenes in hydrogen production from water, 6,508 Hcteropolyanions, 3,1023-1055 Anderson structures, 3, 1043, 1044 heteroatoms, 3. 1035 Keggin structures, 3, 1037 ligands, 3,1046 multisubstituted, 3, 1048 phosphorus(V). 3-1039 trivalent antimony?3, 1042 trivalent arsenic, 3. 1042 Heteropoly blues. 3. 1049. I052 Hetcropolymolybdatesl 3, 1256 Anderson structure, 3, 1045 Heteropolyvanadates, 3. 1041 Anderson structure. 3,1045 Heteroporphyrins, 2.850 Hexachloroselenates. 3,303 1,5-Hexadiene terminal hydrogenation, 6.242 Hexahalogenotellurates, 3,302, 303 Hexaiodoselenates, 3,303 Hexametallic complexes, 1, 156 base-centred trigonal pyramid, 1, 158 centred trigonal prism. 1, 159 concentric triangles. 1, 157 edge-bridged tetrahedron, 1, lS7 hexagonal, I , 156 hexagonal prism, 1,158 octahedra, 1. 159 pentagonal pyramid, 1,158 planar, 1 , 156

138

139

Cumulative Subjecr Index

puckered hexagon, 1,157 square two metal-edge bridges, 1,157 tetrahedra edge-linked, 1,157 Hexamethylenediamine copper(I1) complexes. 2,44 Hexamethylenetetramine complexes, 2.28; 5,937 Hexamines metal complexes, 2,58 Hexane-2,4-dione, 5-methylmetal complexes synthesis, 2,376 Hexaniobates, 3, 1028 1-Hexanol in thorium ore extraction, 6,919 1-Hexanol, 2-ethylin actinide recovery from nuclear fuel waste, 6.961 Hexaphyrin synthesis, 2,892 Hexatantalates, 3, 1029 Hexatungstates, 3, 1034 Hexavanadates, 3, 1027 1-Hexene hydrocyanation catalysts, nickel complexes, 6,296 hydro formylation catalysts, rhodium complexes, 6,261 hydrogenation catalysts, rhodium complexes, 6,241,244 catalysts, ruthenium complexes, 6,235 Hexokinase activation magnesium ions, 6,580 1-Hexyne reactions with carbon dioxide catalysts, nickel complexes, 6, 2YS Highly active waste nuclear fuel reprocessing. 6,885 High performance liquid chromatography technetium-99,6,976 High-potential proteins, 4,238 High-spin/low-spin transitions bipyridyl metal complexes, 2,90 iron complexes. 2 , 9 4 polypyridyl metal complexes, 2,91 High Temperature Gas Cooled Reactor, 6, 927 Histamine metal complexes. 2,82 Histidine copper complexes, 6,671 naturally occurring, 2,965 esters, nickel(1I) complexes hydrolysis, 6,424 metal complexes, 2,746; 5,948 naturally occurring, 2,966 reactivity, 2,756 stereoselectivity, 2,754 methyl ester hydrolysis, metal catalysis. 6,419 hydrolysis, palladium(I1)-catalyzed, 6,423 Schiff bases metal complexes, 2,753 L-Histidine, L-aspartyl-L-alanylmetal complexes, 2, 764 L-Histidine, glycylmetal complexes, 2,762 L-Histidine, glycyl-glycylmetal complexes, 2,764 Hodgkin’s disease, 6,728 Holmium, aquatris(dibenzoy1rnethane)-

Hydrazido(2--) complexes

stereochemistry, 1, 81 Holmium, pentanitratostereochemistry, 1,99 Holmium, tris(2,2,6,6-tetramethyl-3,5-heptanedione)photosubstitution, 1,408 Holmium complexes 1,3-diketones, 2,387 phenanthroline, 3,1069 Homoazaporphyrins synthesis, 2, 817 Homolytic cleavage catalysis transition metal complexes, 6,230 Homopolymolybdates, 3,1377 Homopolypeptides metal complexes, 2,764 Homoporphyrins, 2,851 synthesis, 2,817 Hormones metal complexes, 6,773 Horse liver alcohol dehydrogenase, 5,1008 Horseradish peroxidase, 4,265; 6,704 Human liver alcohol dehydrogenase, 5,1009 Human serum albumin technetium-99 lahelled lung profusion techniques, 6,994 t-lumboltine structure, 6,849 Humic acids metal complexes geochemistry, 6,857-861 minerals, 6,849 naturally occurring, 2,961 stability, 6,859 structure, 2,961 thorium(W) complexes, 6,887 FIumic materials isolation, 6, 857 Humin, 2,961 isolation, 6.857 Humus soils structure, 6, 856 Huttonite structure, 6,912 Hybanthus jioribundus nickel uptake, 6,648 Hybridization tautomerism, 2,105 Hydrates. 3 , 4 amides, 3 , 6 ammines, 3 , 4 rnetal-oxygen bond distances, 2,308 solvates, 3,4 Hydration carbonyl groups metal catalysis, 6,474 covalent coordinated heterocycles, 1,431 enthalpy, 2,309 metal ions, 2,297 Hydration numbers, 2,305,306 pressure effects, 2, 307 temperature effects, 2,307 Hydratido ligands, 2,101 Hydrazido(1-) complexes, 2,141-151 chemistry, 2, 150 structure, 2,150 synthesis, 2,145 Hydrazido(2-) complexes, 2, 141-151 bond lengths and angles, 2, 145 bridging, 2, 150 chemistry, 2, 145 electrochemical reduction, 2, 147 Group VI,2,148

Hydrazido(Z-) complexes

Cumulative Subject Index

protonation, 2, 147 reactions with gem-dihalides, 2, 146 with triethylamine, 2, 145 ’side-on’, 2, 150 structure, 2, 145 synthesis, 2, 141 terminal, ‘bent’, 2,149 terminal, linear, 2, 145 terminal, neutral, 2, 149 I5NNMR, 2,145 Hydrazine, bis( allylthiocarbamido). in gravimetry, 1, 534 liquid-liquid extraction, I , 546 Hydrazines, 2, 101 macrocyclic synthesis, 2,904 metal complexes, 2, 30 in plutonium extraction, 6, 948 Hydrazoic acid in plutonium extraction, 6,948 Hydrazones glyoxalanil metal complexes, 6,83 lithium salts reactions, 6,218 macrocyclic synthesis, 2,904 metal complexes thermodynamic template reactions, 6, 180-184 Hydrides ligands, 2,689-711 metal clusters stability, 2,694 metal complexes, 2,694 bond dissociation energies, 2; 699 bridging, 2,701 clusters, 2,692,705 diamagnetism, 2,692 dipole moments, 2,705 electron paramagnetic resonance, 2. 705 fluxionality, 2,705 isotopic perturbation of resonance, 2 , 705 loss of hydrogen, 2,707 loss of hydrogen halides, 2.707 Mossbauer spectroscopy, 2: 705 mass spectroscopy, 2,705 NMR, 2,703 polarity, 2,706 reactions. 2,706 reactions, with unsaturated organic compounds, 2, 707 spectra, 2,702 stability, 2, 693 structure and bonding. 2.700 synthesis from acids, 2,696 synthesis from molecular hydrogen, 2 , 694 synthesis from other hydrides, 2,697 rrans cffect, 2,705 trans influence, 2.705 vibrational spectroscopy, 2$702 polynuclear metal complexes bridging, 2,692 terminal complexes, 2,691 ternary complexes, 2,693 transition metal complexes photochemistry, 2,711 Hydrocarbons homolytic oxidation vanadium-peroxo complexes. 6,333 hydroxylation chromium-oxo complexes, 6,353 liquid-phase oxidation, 6.327

140

oxidation chromium-peroxo complcxcs, 6,334 cobalt catalysts, 6.384 iron catalysts, 6,379 palladium-oxo compounds, 6,361-371 vanadium-alkyl peroxide catalysts, 6, 341 Hydrocyanation alkenes nickel catalysts, 6.296 asymmetric catalysts, palladium complexes, 6,298 Hydrocyanite, 6- 835 Hydrodesulfurization molybdenum catalysts, 3, 1435 Hydroesterification catalysts platinum complexes, 6.291 1-decene catalysts. cobalt complexes, 6,271 furanone synthesis, 6, 275 1-heptene catalysts, pdladium complexes, 6, 285 Hydrofluoric acid metal extraction Irom. 1. 540 Hydroformylaliun alkcnes catalysts, rhodium cornplcxes, 6,260 asymmetric transition metal catalysts, 6, 265 catalysis plalinum(1I) complexes, 5,421 platinum hydride complexes, 5,371 transition metal complexes, 6,258-266 Hydrogen and oxygen production cyclic water cleavage. 6,523 electrochemical production from water coordination complex catalysts, 6,532 explosions, 6,489 ligands history, 1 , 2.1 metal comp[exes acidity, 2,706 mineral processing reduction, 6,829 molecular metal complexes, 2,690 photochemical production from water ruthenium(1I) complexes in, 6, 506 tris(bipyridyl)ruthenium in, 6,500,508,499-510. 502-506 photoelectrochemical production from watcr, 6,531 photoproduction of \yater metalloporphyrins, 6,510-S 13 production from water metal salt catalysts, 6, 493 thermodynamics. 6,489 tris(bipyridy1)ruthenium in, 6, 506 solar production from water, 6,489 storage. 6,489 Hydrogenases, 2.773 colloidal in photoproduction of hydrogen from water, 6,515 iron-sulfur clusters, 6,633 nickel, 6,645,646 Hydrogenation asymmetric amino acid complcxcs, 2,755 catalysts, 6.253 mechanisms, 6,233 rhodium catalysts, 6,241 transition metal catalysts, 6,250-258

141

Cumulutive Subject Index

carbon monoxide complexes, 2,342 catalysis iridium complexes, 6, 247 platinum(I1) complexes, 5,421 platinum hydride complexes, 5?354, 371 rhodium complexes, 6,245 rhodium-phosphine complexes. 6,241 transition metal complexes. 6,231-250 cobalt hydrido phosphorus complexes, 4,707 iridium catalysts, 4, 1158 platinum hydride complexes synthesis, 5,359 unsaturatcd compounds rhodium complexes, 6: 241 Hydrogen bonding intramolecular heterocyclic nitrogen compoundst metal connplexes, 2,75 Hydrogen cyanide reactions catalysts, 6, 296 Hydrogen ligands, 2,689-711 Hydrogen01ysis platinum hydride complexes synthesis, 5,359 Hydrogcn pcroxide catalytic oxidation, 6,332,334 hydrocarbon oxidation iron catalysts, 6,379 reduction vanadium(I1) complexes. 3,471 Hydrogen selenide metal complexes, 2,663 Hydrogen sulfide metal complexes, 2,516 Hydrogen telluride metal complexes, 2,670 Hydrogen transfer iridium catalysts, 4, 116U Hydrolascs zinc, 5,1002 Hydrolysis amino acid amides metal-catalyzed, 6,425 amino acid esters, 6,416 cobalt hydroxide catalysis, 6,434 metal-catalyzed, 6,427 amino acids catalysis by labile metal ions, 6.414 anhydrides in catalysis, 6,463 carboxylic acid estery metal-catalyzed, 6, 437 cations, 6,413 coordinated imines, I, 431 epoxidcs metal catalysis, 6,470 glycosides metal catalysis, 6, 46.1 imines metal catalysis, 6,460 lactams metal catalysis, 6,461 mineral processing electrowinning, 6,831 precipitation, 6,827 peptides metal-catalyzed, 6,43'1 phosphate esters metal catalysis, 6,443 sulfate esters metal catalysis, 6,465 urea

Hydroxides

metal catalysis, 6,470 Ilydrometallurgy, 6,780,783-814 Hydroperoxo complexes catalysts oxidation, 6, 341-350 Group VI11 metal oxidation catalysts, 6.347-350 structure, 6.323 Hydrophobic chelates flotation; 6,781 Hydroporphyrins, 2, 814856 basicity, 2,853 dehydrogenation, 2; 853 demetallatiun, 2, 854 deuteration. 2, 853 mass spectra, 2,852 metallation, 2, 854 NMR, 2,852 non-aromatic. 2, 855 photochemistry, 2,854 redox chemistry, 2,855 synthesis, 2, 852 HydrosiIyIarion allenes catalysts, 6,307 catalysis ch1orr)platinicacid, 5,357,489 palladium complexes, 6,300 platinum hydride complexes, 5,354,371 rhodium complexes, 6,299 Hydrosulfido complexes, 2,517 bonding, 2,519 reactivity, 2: 519 structures, 2,519 synthesis, 2,518 types, 2,518 Hydrothermal systcms metal cmnplexcs gcockemistry, 6,854 Hybroxamates metal complexes. 2, SOS-508 Hydroxamic acid in gravimetry, 1,532 liquid-liquid extraction, 1,544 Hydroxamic acid. N-methylmetal complexes, 2,507 Hydroxamic acid, phenylmeta1 complexes stability, 2,506 Hydroxamic acids colorimetric and gravimetric reagents, 2,505 metal complexes complexes wirh bases, 2,507 stability constants, 2,506 metal prccipilants, 2,506 minerds weathering, 6,868 radiolytic degradation Purex process, 6,953 reactions with silicon tetrachloride, 2, 507 in reprocessing irradiated nuclear fuels sotvent extraction, 6,940 sequestering agents actinides, 6,962 tautomerism, 2,505 in uranium ore processing, 6,910 Hydroxides metal complcxes, 2,29S310 preparation, 2,305 stability, 2, 297 metal coordination reactions, 6,442

Hydroxides

Cumulative Subject Index

metal oxides, 2,305 Hydroxy acids aliphatic metal complexes, 2,472 aromatic metal complexes, 2,480 basicity, 2,465 chirality, 2,462 conformation, 2,467 formation prebiotic systems, 6,871 ionization constants, 2,466 metal complexes, 2,461-483 chiroptical properties, 2,470 electronic spectra, 2,470 geochemistry, 6,867 IR spectra, 2,468 NMR, 2,467 structure, 2,471 Hydroxyazo dyes metallochromic indicators, 1 , 555 Hydroxylamido complexes, 2, 101 Hydroxylamine ammonia oxidation to Nitrosomonas europaea, 6,727 as plutoniurn(1V) reductant Purex process, 6,949 Hydroxylamine, 0-acetyl-N-benzoyl-N-phenylhydroxamic acids from, 2,506

142

Hydroxylamine N-benzoyl-N-phenylin gravimetry, 1; 532 liquid-liquid extraction, 1, 544 Hydroxylamine, N-cinnamoyl-N-phenylliquid-liquid extraction, 1,544 Hydroxylamine, iV,N-di-r-butylmetal complexes, 2,798 Hydroxylamine, N,N--diethylmetal complexes, 2,798 Hydroxylamine, N-methylmetal complexes, 2,798 Hydroxylamine, N-2-naphthol-N-nitrosoammonium salt --see Ncocupferron Hydroxylamine, RI-nitrosophenylammonium salt -see Cupferron Hydroxylamine ligands, 2, 101 Hydroxylamine oxido reductase, 6,727 Hydroxylases molybdenum. 6,658,662 Hydroxylation arenes vanadium-peroxo complexes, 6,333 a-diimine iron(I1) complexes, 1,455 hydrocarbons chromium-xn complexes, 6,353 Hydrozirconationl 2,342 Hvpcrcalcaemia.. 6.597 . H ypoxanthines metal complexes, 2,93 I

Icosahedra repulsion energy coefficients, 1 , 3 3 , 34 twelve-coordinate compounds, 1, 100 Image amplification photography, 6,113 Image dyes, 6,104 photography stabilization, 6 , 112 Imaging agents brain technetium complexes, 6,985 metal complexes photography, 6 , 111 myocardial technctium complcxcs, 6: 983 pyridoxylideneamine hepatobiliary, 6,979 Imaging systems enzymatic, 6, 126 non-catalytic photography, 6,124 vesicular, 6, 125 Imaging techniques diagnostic radiopharmaceuticals, 6,985 myocardial, 6, 980 Imidates metal complexes, 2,276 Imidazole, l-acetylhydrolysis cobalt catalysis, 6,436 Imidazole, 1,2-dimethylmetal complexes, 2,77 Imidazole, 4,5-diphenyl metal complexes geometrical isomerism, 6: 69 Imidazole, 2-mercapto-1methyldodecacopper complex, I , 167 metal complexes, 2, 802 Imidazole, pyridylchelating resins mineral processing, 6.825 metal complexes, t , 9 3 Imidazole-4,5-dicarbaldehgde reactions with 2-aminoethylpyridine and copper(I1) chloride, 6, 158 Imidazoles basic pK, metal complexesl 2,74 bicopper(I1) complexes, 6.654 dehydrogenase inhibitor, 5,1017 metal complexes, 2,76; 5,94S geochemistry. 6, 867 steric aspects, 2,74 pK,, 2,77 Imidazolidine-2-thione photographic stabilizer. 6, 103 lmidazolines metal complexes, 2,79, 87 Imidazoline-( lH,3H)-Z-thione

metal complexes, 2,802 Imidazolium ions macromonocyclic complexes, 2,944 Imidazo[l,5-a]pyridine metal complexes color photography, 6,108 lH-lmidazo[4,5-h]quinoline metal complexes color photography, 6, 110 Imido complexes, 2,161-184 bridging ligands, 2, 176 homoleptic structure, 2, 175 insertion reactions, 2, 180 ligand to metal x-bonding, 2, 176 metal complexes synthesis. 2,162-168 metal-nitrogen bond reactivity, 2, 179 metal-nitrogen bond rotational barrier, 2, 177 metathetical exchange reactions, 2, 181 molecular structure, 2, 170 photoelectron spectroscopy, 2, 178 properties. 2, 170 reactions, 2, 179 with acidic hydrogen-containing molecules, 2,179 with rnctal carbonyls, 2, 181 solid state structure, 2, 170 spectator ligands, 2, 179 structure, 2,176 Imine oximes metal complexes, 2,273 Imines fi-amino metal complexes, 6,162-165 chelates synthesis and reactions, 6,156-192 coordinated reduction, 1,454 formation metal catalysis, 6,458 hydrolysis metal catalysis, 6, 460 lithium salts reactions, 6, 218 metal complexes, 2,279 hydrogenation, 6, 161 hydrolysis, 1,431 kinetic template reactions, 6, 185-192 thermodynamic template reactions, 1,434; 6,156-161 Immune y-globulin labelling, 6,995 Immunoglobulin-G indiurn-113,6,995 Indazole, 6-hydroxy-7-nitrosoiron(I1) complexes dyes, 6,85 Indium gravimetry, 1,530 isotopes medical diagnosis, 6,969 liquid-liquid extraction, 1,539

143

Indium radiopharmaceutical applications 6.969 Indium-11 1 antibody labelling, 6, 995 Indium-113 antibody labelling, 6,995 Indium, pentachlorostereochemistry, 1,40 Indium complexes, 3, 153-175 carboxylato radiopharmacology, 6, '370 phthalocyanincs, 2, 863 porphyrins, 2,821 Tndium(1) complexes, 3, 154 cyanates, 3, 155 halogens. 3, 155 P-ketoenolates, 3, 155 macrocyclic ligands, 3, 155 nitrogen ligands, 3, 154 thiocyanates, 3, 155 Indium(1I) complexes, 3, 156 halogens, 3, 157 nitrogen ligands, 3, 156 oxygen ligands, 3,156 phosphorus ligands, 3,156 sulfur ligands, 3, 156 Indium(II1) complexes, 3, 157 alkoxidcs, 3, 161 amido, 3, 159 amines, 3 , '1% ammines, 3, 158 aqua, 3,160 arsenic ligands, 3, 160 azides, 3. 159 bipyridyl, 3, 159 borohydrides, 3, 166 bromates, 3, 163 bromides, 3,165 carboxylates, 3, 163 chlorates, 3,163 chlorides, 3, 165 crown cthers, 3, 167 cyanates, 3, 159 cyanides, 3, 157 cyclam, 3, 167 ethers, 3, 163 fluorides, 3, 165 fluorosulfates, 3,162 germanium compounds, 3, 158 hexafluoroacetylacetone exchange reactions, 2,380 hydrides, 3,166 hydrogen, 3, 166 hydroxides, 3, 160 8-hydroxyquinoline, 3, 166 imido, 3,159 iodates, 3, 163 iodides, 3, 165 6-ketoenolates, 3,161 macrocyclic ligands, 3,167 mixed halides, 3, 166 nitrates, 3, 162 nitriles, 3, 160 nitrites, 3, 162 orthophosphates, 3,162 oxides, 3, 160 perchlorates, 3, 163 l,KJ-phenanthroline, 3, 159 phosphorus ligands, 3,160 phthalocyanines, 3, 167 porphyrins, 3,167 pyridines, 3, 158 selenides, 3, 164 selenocyanates, 3, 159

Cumulative Subject Index silicon compounds. 3. 158 sulfates, 3, 162 sulfur compounds. 3* 164 bidentate. 3. 164 thiocyanates. 3, 159 tin compounds, 3: 158 Indolamine Z13-dioxygenase,6,708 Indole metal complexes gcocherriistry, 6, 867 oxidativc cleavage cobalt catalysrs, h, 388 3-Indoleacetic acid metal complexes, 5.950 Infections microbial iron transport, 6,679 Infrared dyes dithiolenes, 2,625 Infrared spectroscopy metal ion-water complexes, 2,309 redox potentials and, 1,498 Inner complexes, I, 13 Inorganic coniplexes aqueous solutions high temperature, 6,854 solutions geochemistry. 6.850 Inosine cadmium complexes, 5,957 zinc complexes. 5,457 Inositol hexaphosphate zinc transport. 6.599 cis-Inositol alkaline earth metal complexes, 3,24 metal complexes, 2.984 ey i-Inositol alkaline earth metal complexes, 3, 25 myo-Inositol alkalinc earth mctal cornpicxcs, 3,25 Inositol, phosphatidylhydrolysis calcium, 6, 595 Inositolpolyphosphoric acid antistain agent photography: 6.104 Insertion reactions catalysis transition metal complexes, 6,230 metal alkoxides, 2.353 Insulin, 2: 774 chromium complexes: 2,968 hexamer zinc cornplexcs, 5,999 vanadium, 6.665 zinc, 5,999 zinc complexes medical use, 2: 966 Interallogons, 1,206 Intervalence transfer electrons, 1,360 Intestines calcium uptake, 6- 596 Intramolecular reactions rate constants. 1,362 Inversion nitrogen ligands, 2,24 Iodates, dicyano-, 3, 317 Iodates, dinitrato-, 3, 319 Iodates. octafluoro-, 3,316 Iodides 13 -

structurc, l 145

144

145

Cumulative Subject Index

Iodination 8-hydroxyquinoline-5-sulfonic acid complexes, 1,418 pyruvic acid metal ions, 1,420 Iodine, chlorodiphenyl-, 3.317 Iodine, heptafluorostructure, 1 , 7 1 Iodine, pentafluorolone electron pair structure, 1 , SO Iodine, pctitafluorooxystructure, 1 , 4 9 Iodine, triphenyl-, 3, 317 Iodine anions IF,-, 3.316 IF*-, 3,316 Iodine cations, 3,319 (bipy)(INd2,3,319 bis(thiourea), 3. 321 ICI2+,3,314 IC14+,3,315 IF,+, 3,315 IF6+,3,316 PY(IZ)Z, 3,319 Iodine complcxcs singlc bridges, 2, 680 three-coordinatc, 2,685 lodine(II1) complexes fluorosulfate, 3.320 six-coordinate compounds structure, 1 , 5 3 Iodine dichloride, phenyl-, 3.317 Iodine dioxide, p-chlorophenyl-, 3,318 Iodine dioxide, phenyl-, 3: 318 lodine fluorosulfate. 3.320 Iodine halides, diphenyl-, 3, 317 Iodine heptafluoride; 3.316 Iodine pentafluoride. 3: 315 Iodine perchlorate, 3, 320 Iodine tctrafluoridc, phmpl-, 3,318 Iodine tetrafluoridc, trifluoromcthyl-, 3, 318 Iodine trifluoride, 3, 314 Iodine trifluoride. diphenyl-. 3.318 Ion exchange mineral processing, 6,813-827 in non-aqueous media. 6 : 826 in uranium ore processing, 6.82?,899 Ion exchange resins organic, 6, 814 solvent impregnated mineral processing, 6,826 1on.hydration enthalpy. 2, 309 Ionic charge nomcnclature, 1 , 120 Ionization potcntijls gas-phase solution redox potentials. I. 496 Ionizing radiations in medicine, 6, 965 Ionomycin alkaline earth metal compiexes. 3.68 Ionophores, 2,974; 3,60 A23 187 calcium transport, 6,563 carboxylic, 3, 66 carriers, 6,553 channel-forming, ti, 553 metal cation transport. 6 >554 molybdeniim c0mplexe.s. 2: Y7U neutral, 3, 62-66 non-peptide based metal complexes, 2,972 peptides

Iridium(0) complexes

metal complexes, 2,969 Ion-sensitive electrodes, 3,22; 6,26 metal complexes biology, 6,550 Ion transport crown ethers, 2, 932 Iridium, carbonylchlorobis(tripheny1phosphine)solid state reactions with hydrogen chloride, 1,470 Iridium, dihalodicarhonyl-, 6, 142 Iridium, hexachiorocatalysts water cleavage, 6,495 photoreactivity. 1, 407 Iridium, tris(acety1acetone)structure, I , 65 Iridium complexes, 4, 1097-1167 acetylacetone synthesis, 2, 376 alkylperoxo oxidation catalysts, 6,349 amidincs bridging ligands, 2,201 chelating ligands, 2, 20.5 anticancer drugs, 6 , 758 antimony ligands, 4,1164 applications, 6, l O l Y arsenic ligands, 4, 1164 boron ligands, 4, 116.5 carbon dioxide, 2,452 catalysts, 4; 1158, 1160 carbon dioxide reactions, 6,294 carbonylation, 6,278 hydroformylation, 6,259,263 hydrogenation, 2,710; 6,246,247 1,4-diaza-1,3-butadiene, 2,210 dioxy gcn reactions, 2. 328 halides, 4. 1166 halot r icarhon yl electrkal properties, 6, 151 hydrides, 4, 1166 imidatcs, 2,277 nitrogen, 4,1161 nitrosyls, 4, 1161 reaction with carbon monoxide, 2, 113 orthometallated, 2,394 oxygen ligands, 4,1164 partially oxidized, 6, 136 peroxo mononuclear, 2,318 oxidation catalysts, 6, 341 phosphorus ligands, 4,1162 phthalocyanine.s, 2; 867 porphyrin.;, 2,837 reactions, 2, 845 pseudohalides, 2,231,232 selenium ligands, 4, 1165 sulfur ligands, 4, 1165 triazines bridging ligands, 2,201 chelating ligands, 2,205 Iridium(-I) complexes, 4, 1099 nitrogen ligands, 4, 1099 nitrosyls, 4. 1099 phosphincs, 4, 1100 phosphorus ligands, 4, 1100 Iridium(C) complexes, 4, 1,100 aliphatic amines, 4, 1100 nitrogen ligands, 4. 1100 nitrosyls, 4, 1100 phosphines, 4, 1101 phosphorus Iigands, 4,1101

Iridium(1) complexes Iridium(1) complexes, 4,1101-1120 amines, 4, 1103 ammines, 4,1103 arsenic ligands, 4, 1108 azides, 4,1105 bicarbonates, 4, 1116 carbon disulfide, 4,1117 carboxylates, 4, 1116 catecholates, 4, 1115 cyanides, 4,1101 diazo compounds, 4,1105 p-diketonates, 4, 1115 dinitrogen, 4,1105 disulfur, 4, 1117 fulminates, 4,1101 halides, 4,1119 hydrides, 4, 1119 hydrogen, 4, 1119 isocyanides, 4,1101 rnultidentate macrocyclic ligands. 4, 1120 nitrogen ligands, 4, 1103 nitrosyl catecholates, 4, 1116 nitrosyls, 4, 1104 oxygen ligands, 4,1115 phosphine sulfides, 4,1118 phosphorus ligands, 4,1108 polypyrazolyl borates, 4, 1108 porphyrins, 4,1120 selenocyanatcs, 4,1105 semiquinones, 4, 1115 sulfurdiimine fluxional behavior, 2, 192 monodentate, 2, 191 sulfur dioxide, 4,1118 sulfur ligands, 4,1117 tetrazenes, 4, 1105 thiocarbamates, 4, 1117 thionitrites bonding, 2,192 tin compounds, 4,1103 triazenes, 4,1105 Vaska-type complexes electrochemical oxidation, 4, 1109 oxidative addition, 4, 1108 Iridium(I1) complexes, 4, 1120 arsenic ligands, 4, 1121 halides, 4,1123 magnetic properties, 1,273 mixed donor atom ligands, 4, 1123 multidentate macrocyclic ligands, 4, 1124 nitrogen ligands, 4, 1120 nitrosyls, 4, 1120 phosphines, 4, 1121 phosphorus ligands, 4,1121 Schiff bases, 4,1124 sulfur ligands, 4,1121 Iridium(II1) complexes, 4, 1124-1155 alkenic imines, 4, 1153 alkyl isothiocyanates, 4, 1154 alkylperoxy, 4, 1142 amines, 4,1128 ammines, 4,1128 antimony ligands, 4,1134 areneselenols, 4,1148 arsenic ligands, 4, 1134 aryl isothiocyanates, 4, 11.54 azides, 4,1133 benzo(k]quinoline, 4,11.54 benzylideneamines, 4, 1152 2,Z'-bipyridyl, 4,1130 bromides, 4, 1149 carbonates, 4, 1141 carbon diselenides, 4, 1148

Cumulative Subject Index carbon disulfides, 4, 1145 carboxylates, 4, 1141 catecholates, 4: 1140 chlorides, 4, 1149 cyanides, 4,1125 diazenato, 4,1132 diazo compounds, 4,1132 @-diketonates,4, 1140 dioxygen, 4,1138 dithiocarbamates, 4, 1145 fluorides, 4, 1148 fulminates, 4, 1124 germanium compounds, 4,1126 guanidine, 2,283 hydrides, 2,702; 4,1149 hydrogen, 4,1149 hydroxy, 4,1138 imidates, 2,278 iodides, 4, 1149 isocyanides, 4,1125 ligand field states reactivity, 1,400 magnetic properties, 1,274 mercury compounds, 4,1124 mixed donor atoms, 4,1152 multidentate macrocyclic ligands, 4,1155 nitrates, 4, 1143 nitritenitro, 4, 1143 nitrogen heterocycles, 4,1130 nitrogen ligands, 4* 1128 octaethylporphyrin. 4,1155 oxalato, 4,1142 oxygen ligands, 4,1138 peptides hydrolysis, 6,433 peroxocarbonates, 4,1141 peroxycarboxylates, 4, 1141 1,lO-phenanthroline, 4, 1130 phenyldiimides, 4, 1153 phosphines, 4- 1134 phosphorus ligands, 4,1134 polypyrazolylborates, 4, 11.34 reactivity, 1,298 selenium ligands, 4,1147 selenolato, 4, 1148 semiquinones, 4,1140 silicon compounds, 4,1126 sulfenato, 4,1146 sulfides, 4, 1145 sulfinato, 4,1146 sulfur ligands, 4, 1145 tetrazenes, 4, I153 tin compounds, 4,1126 Iridium(1V) complexes, 4, 1155 arsenic ligands, 4, 1155 bromides, 4,1157 chlorides, 4, 1157 halides, 4,1157 hydroxy, 4,1156 magnetic behavior, 1,273 nitrates, 4, 1156 oxalates, 4, 1156 oxygen ligands, 4,1156 phosphorus ligands, 4,1155 spectra, 1,254 sulfur ligands, 4,1157 Iridium(V) complcxcs, 4, 1158 fluorides, 4,1158 Iridiurn(V1) Complexes, 4, 1158 Iridium oxide colloidal catalysts, oxygen production from water, 6 , 5 19 Iridium salts

146

147

Cumulative Subject Index

sensitizers silver halide light sensitivity, 6:97 Iron ammoniacal leaching rejection, 6,786 analysis, 1,522 biochemistry, 6,614-634 biology, 6,545 deficiency metal complexes, 6,762 determination high-frequency titration with cupferron, 2 , 5 11 dissociative absorption with acetylacetone, 2,395 electroplating ethylenediaminetetraacetic acid, 6,14 intracellular release, 2,972 microbial transport, 6,679 photothermography, 6,119 plants transport and storage, 6 , 680 poisoning, 6,764 release, 6,679 into cytoplasm, 6:678 removal chromium electrolytes, 6,832 precipitation, 6,827 smelting, 6,834 storage microorganisms, 6,679 transport, 6,671 microorganisms, 6,673,675 transport and storage mammals, 6,667 Iron, aquapentachlorostereochemistry, 1,50 Iron, bis(cyclopentadieny1)- -see Ferrocene Iron, dicarbonylbis(hexahydrodithiopyridinecarboxy1ato)angular parameters, 1,57 Iron, dicyanobis(2,2'-bipyridyl)solvolysis, 1,506 Iron, diperchloratotris(1,lO-phenanthro1ine)gravimetry, 1,524 Iron, ethylenediaminetetraacetatobleaching photography, 6,100 Iron, hexaaquaelectron transfer intramolecular vibrational trapping, 1,337 with pentaamminenitrilotriacetatocobalt, 1,369 Iron, hexacyano-, 4,220,1204 bleaching photography, 6,100 history, 1 , 2 reactions with bis(ethylenedinitrilotetraacetato)cobalt, 1,376 Iron, nonacarbonylbisreaction with sulfurdiiminesl 2. 194 Iron, pentaazidostereochemistry, 1,40 Iron, pentacarbonyl13CNMR, 1,41 Iron, pent kis(pentanenitri1e)'T N&, 1,41 Iron, pentakis(trifluoroph0sphine)-

NMR,1,41 Iron, tetrdcyano(4-cyanopyridine)dissociation, 1, SO9 Iron, tricarbonyl[bis(dimethylarsenyl)phenyl]stereochemistry, 1,47 Iron, tricarbonyl[methylenebis(diphenylphosphine)]-

Iron complexes

stereochemistry, 1,47 Iron, trichlorobis(cyanopyridine)structure, 1,45 Iron, trinitrato(dinitr0gen tetroxide)structure, 1,28 Iron, tris(acety1acetone)electron recording system, 6,127 structure, 1,65 Iron, tris(bipyridy1)in photoproduction of oxygen from water, 6,516 Iron, tris(2,2'-bipyridyl)absorptiometry, 1,549 racemization. 1,456 solvoIysis, I , 506 Iron, tris(dibenzoy1methane)structure, 1,65 Iron, tris(2,3-dimercapto-2-butenedinitrile)structure, 1,63 Iron, tris(hexaAuoroacety1acetone)structure, 1,65 Iron, tris(oxa1ato)chemical actinometer, 1,409 photoreduction, 1,471 relief-imagc-forming systems, 6,125 Iron, tris(1 ,lo-phenanthro1ine)absorptiometry, 2,549 racemization, 1,466 solid state, 1,467 structure, 1, 64 Iron(II1) chloride amino acid formation prebiotic systems, 6,871 Iron complexes acetonitrile. 4,1210 acetylacetone, 2,371 amidines chelating ligands, 2,204 analysis, 4, 1180 anionic, 4; 266,267 oxidation, 6,356 applications, 6,1017 biological systems, 4,1180 biology, 6,549 boron ligands, 3,99 carbonyl tellurides, 2,669 catalysts hydrofonnylation, 6,258 hydrogenation, 6,231 oxidation, 6,379 citrates plant xylem, 2,962 coordination geometries, 4,1183 coordination numbers, 4,1182-1187 corrins, 2,883 corroles, 2,874 cyanides synthesis, 2,9 1,4-diaza-1,3-butadiene, 2,206,210,212 dimethyl sulfoxide, 2,488,490 dinitrosyldicarbonyl, 4,1188 Eormamide, 2,491 hexafluoroacetylacetone structure, 2,389 imines, 2,279,281 Mossbauer spectroscopy, 1181 nitric oxide, 4, 1187-1195 nitrosyls, 2, 107 binary, 4,1188 his(dithiolene), 4,1193 carbonyl, 4, 1188 dithiocarbamates, 4,1192 halides, 4,1193 iodide, 4,1193

Iron complexes

Cumulative Subject Index

polydentate ligands, 4, 1194 tetraphenylporphyrin, 4, 1194 organic mobilization, 6, 869 oxalic acid actinometry, 2,446 oxidation states, 4, 1182-1187 oxo oxidation catalysts, 6, 356-359 q3-l-phosphaallyl, 2,1055 phthalocyanines, 2,866 polypyrazolylborates, 2,251 biological applications, 2,255 electrochemistry, 2,257 porphyrins, 2, 829 proteins, 2,772 pseudohalides, 2,230,231 pyridine, 4,1213 superoxo structure, 6,319 thiocarbamates magnetic properties, 2,587 triazines chelating ligands, 2,204 tricarbonylnitrosyl anion, 4, 1188 urea, 2,285 urylcue, 2,286 Iron(-11) complexes, 4, 1184 Iron(-I) complexes, 4,1184 Irun(0) complexes, 4,1184, 1195 2,2’-bipyridine,4, 1195 1,2-dimethyIphosphinoethane,4, 1197 guanidine, 2,283 magnetic properties, 1, 274 nitrogen ligands, 4, 1195 phosphites, 4,1197 phosphorus ligands, 4, 1196 trifluorophosphinc, 4, 1197 triphenylphosphine, 4, 1196 Iron(1j complexes, 4, 1184, ‘I 197-1203 alkyl, 4, 1202 arsines, 4, 1197 aryl, 4. 1202 1,2-bis(diphenylphosphino)ethane.4. 1198, 1199 carbenes ESR. 4,1200 carbon monoxide, 4, I197 cyanide, 4,1201 macrocyclic ligands, 4., 1201 nitricoxide, 4, 1203 phosphorus ligands, 4:, 11% phtbalocyaninc, 4, 1201 tetraphenylporphyrin, 4, 1202 3 ,lo, 17,24-tetrasulfiinatophthalocyanine, 4,1202 tricarbonylhis(tripheny1phosphine) oxidative substitution, 4, 1245 Iron(1I) complexes, 4,1179-1270 a,a’-bipiperidine, 4, 1223, 1225 acetonitrile Mossbauer spectra, 4, 1255 acetylacetonate, 4, 1236 a-alanine, 4, 1226 alkyl cyanides, 4,1209 amines, 4, 1210 aromatic, 4, 1210 hexamines, 4, 1210 monodcntatc aromatic., 4. 1212 polyethyleneamine, 4, 1211 pyridinc, 4, 1211 amino acids, 4, 1238 o-aminobenzenethiol, 4, 1247 2-aminomethylpyridine, 4, 1226

6-amino-2-methylquinoline. 4, 1213 amminepentacyanohydrolysis, 4.1206 arsenic ligands, 1233 monodentate. 4, 1233 polydentate, 4, 1234 benzimidazole. 4,1228,1229 bipyridinc, 4,1215-1222 cyanide, 4. 1219 Mosshauer spectra, 4, 1221 spectra, 1, 3215 thermodynamic properties, 4, 1220 1.2-bisdiethylphosphinoethane,4. 1234

bis(2-dimethylaminoethyl)methylaminc,4, 1211 2.6-bis(2-diphenylphosphinocthyl)pyridine,4, 1235 bis(cthy1 dithiocarbonatc), 4, 1246 bis(methy1imidazole). 4, 1231 bis(1 ,lO-phenanthroiinej. 4, 1219 bis(thiosalicylideneiminato), 4, 1248 bromide, 4,1250 Curtis ligands, 4. E5 2 capped porphyrins nitric oxide binding, 4, 1270 chloride, 4>1249 citric acid, 2.476; 4, 1237 cubancs, 4. 1242 cyanide, 4. 120&1209 3-cyanopyridine: 4. 1213 4-cyanopyridinc. 4>1213 2-cyanopyridine R.’-oxide,4, 1237 3-cyanopyridine X-oxide. 4, 1237 4-cyanopyridine X-oxide, 4, 1237 cyclarn? 4, 1250 1,2-cyclohexanedione dioxime, 4,1231, 1232 cysteine, 4, 1248 2,6-diacetylpyridinebis(semicarbazone),4, 1238 dibenzothiazole, 4: 1229 3,5-dichloropyridine, 4, 1213 diimincs, 4: 1214-1230; 6.171 formation constani, 4, 1216 [Mikelonates, 4, ‘1236 tx-diketone dihydrazones, 4, 1224 1 ,2-diniethoxyethanel 4, 1238 1,l’-dimethyl-4,4’-bipyridine, 4, 1247 5,5’-dimethyl-2,2’-bipyridine, 4, 1221 3,5-dimethyl-1,2-dithiolinium, 4, 1246 dimethylglyoxime. 4, 1231 1,2-dimethyCmidazole, 4, 1213 2,7-dimethpl-l &naphthyridine, 4, 1211 2,9-dimethyl-l110-phenanthroline, 4, 1214 4,7-dimethyl- 1 ,lO-phenanthroline spectra, 4, 1220 2,6-dimethylpyrazine, 4, 1214 I,l-dioxane, 4, 1238 3,6-dioxaoctanc-l,8-diarnine, 4, .I260 dioximes, 2*271 dioxines, 4. 1222. I231 4,7-diphenyl-l,10-phenanthroline sulfonated, 4, 1217 2,2‘-dipyridyImethane, 4, 1226 dithio, 4, 1245, 1246 dithioacetylacetonates, 4, 1245 dithiocarbamates, 4, 1245 dithiolenes. 4, 1245, 1246 1,2-dIthiolinium, 4, 1246 ethylenediamine, 4. 1211 oxidation, 4. 1226 fluoride, 4,1249 geometry, 4, 1184 halides, 4, 1249 hexacyano. 4- 1204 1,1,1,5,515-hexafluoro-2,4-pentanedionato, 4, 1251 hydrazine. 4. 2231

248

149

Cumulative Subject Index

hydroxy oximes, 2,273 imidazole, 4, 1213 imidazoline, 4,1229 imine oximes, 2,273 iodide, 4,1250 iron(II1) system redox behaviour, 4, 1185 water cleavage, 6,494 isocyanide, 4,1208 alkylation, 4, 1209 aromatic, 4, 1209 transalkylation, 4, 1208 isoquinoline, 4, 1213 macrocyclic ligands loss, activation parameters, 4: 1259 magnetic behavior, 1, 273 methionine, 4, 1238 2-methylimidazole, 4, 1213 2-rnethyl-l,S-naphthyridine, 4, 1211 2-methyl-l,10-phenanthroline.4, 1215 minerals, 6, 846 mixed donor ligands oxygen containing, 4, 1238 mixed iron(II1) complexes, 4, 1 I87 mixed 0 , N donors tridentate, 4, 1238 mixed S,N donors, 4,1247 monodentate aromatic nitrogen donors, 4, 1214 monothiocarbamates, 4, 1245 N donor macrocycles, 4,125&1270 saturated, 4,1250 l&naphthyridine, 4, 1211 nitrosyl meso-2,3,7,8,12,13,27,28-octaethyl-5nitroporphyrinato, 4: 1194 oximes, 2,272 physicochcmical studies, 2,272 oxygcn donors, 4, 1235 partially unsaturated N donrir macrocycles, 4, 1252-1 260 pentacyano, 4. 1205 photolysis, 4, 1206 reactions. 4, 1205 l,l0-phenanthroline, 4, 1215-1222,1229 cyanide, 4,1219 formation constant; 4* 1215 spectra, 4, 1215,1220.1221 thermodynamic properties, 4: 1217 1,lO-phenanthroline N-oxide, 4. E 3 8 phenols, 4,1242 o-phenylenehis(dimethylarsine), 4,1234 phosphines, 4,1233 carbon monoxide reactions. 4, 1233 phosphites, 4, 1233 phosphorus donor, 1233 monodentate, 4, 1233 polydentate, 4, 1234 phthalocyanine, 4,126U-1266 Mossbauer spectra, 4,1264 p-picoline, 4, 1213 y-picoline, 4, 1213 porphyrins, 4,1203,1266 bis(phosphine), 4, 1268 bis(phosphite), 4, 1268 carbenes, 4, 1270 dichlorocarbenes. 4,1270 double carbenes, 4,1270 reversible oxidation, 4: 1268 porphyrins, dioxygen adducrs, 2,326 immobilization, 2,328 low temperatures, 2,326 steric hindrance, 2,326 propylenediamine, 4,1211 COC 7-F

Iron(1II) complexes

pyrazole, 4, 1213 pyrazoledione oxide, 4, 1237 pyrazole-4,5-dione oximes, 4, 1232 pyridine, 4: 1212 pyridine-2-carbalde hyde 2-pyridylhydrazone, 4,1225 pyridine macrocycles seven-coordination, 4, 1258 pyridine N-oxide, 4, 1237 pyridincnitroso, 4, 1268 pyridylimidazole, 4: 1228 quinoline, 4, 12.13 Schiff bases, 4,1233,1238,1247 polydentate, 4, 1225 spectra, 1,253 squaric acid, 2: 455 magnetic effects, 2, 456 strati-Schiff bases, 4, 1238 sulfidelnitrosyl, 4, 1243 sulfides binary, 4,1240 sulfur donors, 4,1238-1248 terpyridinc, 4, 1222,1229

1,4,8,11-tetraazacyclotetradecane,4,1251 Lelraazil macrocycles, 2,909; 4, 1257 tetraazatetrarninc, 4, 1254 tetraazatriimine, 4, 1254 tetraethylenepcntamine, 4, 1211 tetrahydrofuran, 4, 1238 meso-tetrakis(2,4,6-trimethoxyphenyl)porphyii n , 2,327 tetraphenylporphyrin, 4,1258 2-thiazole. 4; 1229 thiocyanate, 4, 1247 thiols, 4, 1241 thiosemicarbazides, 4,1248 thioxanthates, 4, 1246 3,3‘,Q-triaminotripropylamine, 4, 1211 1,2,4-triazine, 4; 1230 triazole; 4, 1213 trimethylarsine sulfidc, 4, 1240 tripyridyl-s-triazine, 4, 1229 tris-a,a‘-diimines reduction, 4,1196 tris(2,2’-bipyridine), 4, 1216 pyrolysis, 4, 1220 tris(ethy1 dithiocarbonate), 4, 1246 tris(1J0-phenanthroline), 4, 1216 trisulfides, 4, 1243 1,4,7-trithiacyclononane,4,1239 vanillin thiosemicarbazone, 4,1248 violurate, 4, 1238 water? 4, 1236 xanthates, 4. 1216 o-xylyldithiolate, 4, 1240 Iron(II1) complexes, 4,217-267 acetnhydroxamates iron-deficient anemia, 2,506 alcoholates, 4,227 amides, 4,227 amino acids, 4,253 aminocarboxylates, 4,253 aqua, 4,226 arsenic ligands, 4,226 arsine oxide, 4,228 azido, 4,222 benzohydroxamato, 4,234 structure. 2,505 2,2’-hi-?-imidazoline, 4,224 ZJ.’-bipyridine, 4,223 bis(trimethylsilyl)amine, 4,222 2.2’-bi- 1,2,3,4-retrahydropyrimidine,4,224 carbon ligands, 4,220 carboxylates, 4, 228

Iron(II1) complexes

Cumulative Subject Index

relief-image-forming-systems, 6, 125 catecholates, 4,230 chlorides, 4,247 clusters, 4,229 colour, 4,219 cyanides, 4,220 1,2-diaminoethane,4,223 dicarboxylic acids vesicular imaging systems, 6, 125 1 ,l-dicyanoethylene-2,2-dithiolate, 4,245 diketoncs, 4,229 di-2-pyridylamine, 4,225 diselenocarbamates, 4,243 dithioacetylacetates, 4,246 dithiocarbonates, 4,243 dithio-P-diketones, 4, 1246 dithiooxalates, 4,246 dithiophosphinates, 4,243 equilibrium constant solvent effect, 1,516 1,2-ethanediol, 4,1241 ethers, 4,227 fluorides, 4,247 fulvic and humic acids, 6,859 halides, 4,247 hydrolysis, 4,218 hydrolytic polymerization, 4,228 hydroxamates, 4,230 hydroxamic acids, 4,233 hydroxy oximes, 2,273 o-hydroxyoximes structure, 6, 800 iron(l1) complexes redox behaviour, 4, 1185 ironsulfur cluster compounds. 4,234 liquid-liquid extraction, 1,539 macrocyclic ligands, 4,255-265 magnetic behavior, 1,272 magnetic moments, 4,218 2-methyl-8-quinolinol electrochemistry, 4,233 minerals, 6, 846 mmed iron(I1) complexes, 4, 1187 monothio-e-diketones stability, 2,649 N,A”-bis(2-pyridylmethyl)ethylenediamine,4,225 N,N’ ,N-triacetylfusarinine, 234 N,N’-( 1,2-phenylene)bis(saIicylidenimaro), 4,232 naphthoic acid, 2,483 nitrogen ligands, 4,222-226 Mossbauer spectra, 4,223 oxygen ligands, 4,226-234 1,lO-phenanthroline,4,223 phenols, 4,230 phosphine N-oxides, 4,228 phosphorus ligands, 4,226 pyridine, 4,222 pyridine N-oxide, 4,227 2-(2’-pyridyl)imidazole,4,225 8-quinolinol electrochemistry, 4,233 quinones, 4,230 Schiff bases, 4,226,249 spin-crossover, 4,252 salicylaldimine, 4,249 semiquinones, 4,232 in slags, 6, 833 spectra, 1,253 sulfido, 4,234 sulfoxides, 4,227 sulfur ligands, 4,234-247 tartaric acid, 2,479 terpyridyl, 4,223,225

150

1,4,S,ll-tetra;tzacyclotetradecane, 4,256 thiocarbamates, 4,247 thiohydroxamic acids, 4,233,234 thiolato, 4,234 thioxanthates, 4,243 tri-2-pyridylamine, 4, 225 1,3,5-tris(213-dihydroxybenzoylaminomethyl)benzene, 4,231 tris(salicyla1doximato) structure, 6 , ROO xanthates, 4,243 Iron(1V) complexes, 4,266,1187 magnetic behavior, 1,272 phosphines SHAB theory, 2,1040 Iron(V) complexes, 4.266,1187 Iron(V1) complexes, 4,266,1187 Iron(II1) complexes, tetraphenylporphyrinatobenzenethiolatobenzenethiol-, 2,517 Iron cupferronate structure, 2,510 Iron hydroxide in electrochemical production of oxygen from water, 6, 534 Iron(I1) ions photographic developer. 6, 98 Iron rnethoxide physical properties, Z1 346 Iron-molybdenum cofactor, 3,1425 composition, 3,1425 EPR, 3,1423 extended X-ray absorption fine structure, 3, 1426 level of oxidation, 3, 1326 57FeMossbauer spectra, 3,1425 X-ray absorption near edge structure, 3,1426 Iron-molybdenum-sulfur clusters, 3,1425-1430 cubane-like crystal structure, 3,1429 electrochemistry, 3, 1429 electronic structure, 3, 1428 magnctic moments, 3, 1428 57FeMossbaucr spectra, 3, 1428 NMR, 3,1428 synthesis, 3,1426 double cubane-like bridged, 3,1428 EPR, 3,1428 NMR, 3,1427 reactions, 3, 1427 structure, 3, 1426 synthesis, 3, 1426 Iron overload chelating agents, 6, 768 Iron pivaiate basic, 2, 303 Iron proteins iron-sulfur group, 2,773 non-hcmc, 4,234 Iron(I1) sulfamate breeder reactor fuels reprocessing, 6,955 in reprocessing irradiated nuclear fuels solvent extraction, 6,940 Iron-sulfur cluster compounds, 6,634,1203 dinuclear, 4,235 electrochemistry, 4,236 hexanuclear, 4,241 mononuclear, 4,235 tetranuclear, 4,238 trinuclear? 4,237 Iron-sulfur proteins, 6,626 clusters characterization, 6, 633 . 3-Fe, 6,631

151

Cumulative Subject Index

[2Fe-2$], 6,627 model compounds, 6,629 structure, 6,628 [4Fe-4S], 6,629 Rieske, 6,629 Irradiated fuel reprocessing, 6, 925 Irving-Williams series transition metal extraction, 6,824 Isatin alkylation, 6, 175 Isobacteriochlorins, 2,851 iron, 6,625 Isobutyric acid metal complexes geochemistry, 6,867 Isobutyric acid, hydroxymetal complexes IR spectra, 2,470 NMR, 2,467 Isocitric acid absolute configuration, 2,478 Isocyanates imido metal complexes synthesis from, 2, 167 insertion reactions metal alkoxides, 2,354 metal complexes hydrolysis, 1,429 synthesis, 2,237 synthesis from aromatic nitroso compounds, 6,276 Isocyanides metal complexes electrical conductivity, 6, 151 technetium complexes radiopharmacy, 6,980 Jsodecanol solvent extraction gold, 6, 808 Isokinetic effect ligand exchange solid state, 1, 469 Isoleucine epimerization geochemistry, 6,866 Isomaleonitrile, dithiometal clusters, 2, 585 Isomerases zinc, 5, 1002 Isomerism, 1, 179-208 classification, 1, 180 configurational, 1,180,188 conformational, I , 181 constitutional, 1, 180, 182 coordination, 1, 183 detection, 1, 180 geometrical, 1, 181 tridentate azo compound metal complexes, 6,63,68 history, 1,24 hydrate, 1, 183 ionization, 1, 183 linkage, 1, 184 biological compounds, 1. 186 molecular structure and, I , 182 K-Np tridentate azo compound metal complexes, 6,62,65 optical. 1. 181 separation, I , 180 solvate, 1, 183 stereochemistry and, 1, 179 tridentate azo compound metal complexes, 6,62 ligand non-planarity, 6, 65,72

Itoic acid

Isomerization catalysis platinum hydride complexes, 5,354,371 iridium catalysts, 4, 1158 metal catalysis, 6,477 platinum complexes, 5,497 polymerization, 1. 186 Isoniazid metal cornplexcs, 2,799 Isonicotinohydroxamic acid metal complexes with nicotinohydroxamic acid, 2,506 Isanitriles -.we lsocyanides fi-Isophorone oxidation manganese catalysts, 6,379 Isopolyanions, 3,1023-1055 Anderson structures, 3, 1043 stoichiometry, 3, 1025 Isopolymolybdates, 3, 1029-1032, 1256, 1259 aqueous solutions, 3, 1029 nonaqueous solutions, 3, 1031 Isopolyniobates, 3, 1028 Isopolytantalates, 3, 1029 Isopolytungstates, 3, 1032, 1033 catalysts water cleavage, 6,498 Isopolyvanadates, 3,1025-1028 aqueous solutions, 3, 1025 Isoprene hydrogenation catalysts, platinum complexes, 6,249 Isopropyl alcohol oxidation hy chromium(VI), 1,367 electron transfer, 1,332 Isoqulnoline zinc complexes, 5,952 Isothiocyanato complexes linkage isomerism, 1,184 Isothiouronium salts aminoalkyl photographic stabilizer, 6, 103 Isothiuram disulfide metal complexes, 2,591 Isotope dilution analysis metal complexes biology, 6,550 Isotopic cxchange amino acids metal complexes, 6,467 Isotrithione, dimercaptometal complexes. 2,624 Isovaleric acid metal complexes geochemistry, 6,867 Isoxanthoammines structure, 1 8 Isoxazole metal ccxnplexes, 5.951 Itaconic acid asymmetric hydrogenation catalysts, rhodium complexes, 6,256 Itai-itai, 5, 1000 I toic acid Bacillus subtilis, 6, 676 ~

Jahn-Teller distortions cobalt and copper complexes, 2,91 hydratcs, 2,308 Jahn-Teller effect, 5,535 lahn-Teller theorem, 1,247 Ja rosit es

formation thermodynamics, 6,827 Jouravskitc, 4,104 JGrgensen’s reaction. I , 17 Julienite structure, 6 , 847

152

Kdla-AZar, 3,278 Kaolinite minerals prebiotic systems, 6,872 solubility geochemistry, 6,868 Kappa notation, 1, 115 Kefchydrocyanite structure, 6,847 Keggin anions, 3, 1034 electrochemistry, 3, 1050 Keggin structurcs, 3, 1035 heteropolyanions. 3, 1037 B-Ketoiminates metal complexes gas chromatography, 1,560 Ketones alkynic synthesis by carbonylation, 6; 283 hydrogenation catalysis, rhodium complexes, 6,241, 245 catalysis, ruthenium complexes, 6,232 P-mercapto metal complcxes, 2,654 metal complexes reactions, 6,216 reactions with metal alkyls, 2,331 reduction with formic acid, catalysts, 6,303 Ketones, methyl synthesis by carbonylation. 6,279 Ketones, methyl isobutyl in reprocessing irradiated nuclear fuels, 6,935 solvent extraction gold, 6,808 niobium and tantalum, 6.813 in reprocessing irradiated nuclear luels, 6,937

in uranium ore processing, 6,910 Ketones, methyl vinyl hydrogenation catalysis, ruthenium complexes, 6,234 Ketoxime, 2-pyridylmethylin gravimetry, 1,533 Ketoxime, 2-pyridylphenylin gravimetry, 1,533 Kidneys chronic cadmium poisoning, 5, 1000 diagnostic imaging tcchniques technetium complcxcs, 6, 987 Kinases activation magnesium ions, 6,579 Kinctic compensation effect ligand exchange solid state, 1,469 Kinetic template reactions imine metal complexes, 6,185-192 Kladnoite structure, 6,849 Klebsielia pneumoniae nitrogenases, 3, 1425 Klcinite structure?6,817 Kremersite structure, 6, 846 Krogmann salts, 6,136143 one-dimensional metallic complexes, 6, 135 Kroky hair syndrome, 5,721 Kroll process, 3,325 Krypton compounds difluorides. 3, 313 fluoride, 3,313 platinum complexes, 5,492 Kurnakov, Nikolai Semenovich, 1,17

153

L Laccase, 6,699 copper, 6,654 cytochrome oxidases concerted electron transfer, 6,683 fungal Raman spectra, 6,652 kinetic studies, 6,699 Rhus verniciferu spectra, 6,652 type 2-depleted, 6,699 p-Lactam antibiotics bacterial resistance, 6,462 P-Lactamases zinc, 6, 612 Lactams hydrolysis metal catalysis, 6,442,461. a-methylene synthesis by carbonylation, 6: 285 spthesis by carbonylation, 6,285 Lactic acid metal complexes, 2,465,473 conformational isomers, 2: 470 geochemistry, 6,867 IR spectra, 2,469,470 NMR spectra, 2,467 Lactobacillus bifidus cell division calcium, 6, 596 Lactobacillus bulgaricus cell division cakium, 6,596 Lacio bacillus leichmanii ribonucleotide reductase, 6 , 642 Lactofemn, 4,231; 6,669 amino acid sequence, 6,669 animal infections, 6,679 binding to gallium-67,6,992 human milk, 6,670 Lactones a-me.thy1ene synthesis by carbonylation, 6,2S5,288 synthesis from carbon dioxide, 6,294 by carbonylation, 6,282 Lactonization cobalt hydroxide catalysis, 6,434 intramolecular cobalt(II1) complexes, 1, 440 D-Lactose alkaline earth metal complexes, 3,25 Lacunar complexes preparation metal template reactions, 1.453 Lanthanide complexes, 3,1059 acetylacetone, 3, 1077 acetylhydrazine, 3,1090 amides electronic spectra, 2, 169 structure, 2,171

amine oxides, 3,1081 X-ray crystallography, 3, 1081 amines, 3 , 1072 applications, 6. 1024 arsine oxides, 3.1082 aza-crown ethers, 3, 1095 azides, 3. 1075 bipyridyl, 3, 1069 bis(methy1irnido)triphosphoric acid pentakis(dimethylamide), 3,1085 carboxylates. 3, 1085 circularly polarized emission, 3, 1108 complex halides, 3, 1099 coordination number! 1,24 crown ethers, 3: 1091 cryptates, 3. 1097 cupferron, 2,510 2,6-diacetylpyridine bis(benzoic acid hydrazone), 3, 1090 2,6-diacetylpyridine bis(semicarbazone), 3,1090 dialkylamido, 3, 1071 diethylphosphate, 3, 1084 diisoprop yl N,N-diethylcarbamylmethylenephosphonate, 3,1084 1,3-diketones, 2,373;3, 1077 adducts, 3: 1078 synthesis, 2,377 X-ray structure, 3>1079 dimcthyl sulfoxide, 2,488 dipicolinates, 3, 1090 dipivaloylmethanates: 3, 1077 dipositive oxidation state, 3, 1109 electronic spectra, 3, 1112 nitrogen donors, 3, 1111 oxygen donors, 3,1111 phosphorus donors, 3,1111 solvation, 3,1110 dithia-N-crown-6,3, 1093 dithiocarbamates, 3,1087 dithiophosphates, 3, 1086 dithiophosphinates, 3, 1087 edta, 3, 1087 electronic spectra, 3, 1105 emission spectra, 3, 1106 excitation spectra, 3, 1107 formamide, 2,491 glycolates, 3,1085 6,6,7,718,8,8-heptaRuoro-2,2-dimethyloctane-3,S-dione, 3,1078 heptafluorodimethyloctanediones NMR Schiff reagents, 2,386 hexafluoroace tylacetone synthesis, 2, 377 hexamethylphosphoramidc, 3,1084 hydrated carboxylates, 3, 1076 hydrated iodates, 3,1076 hydrated perrhenates, 3,1076 hydrated pcrtechnetates, 3, 1076 iminodiacctate, 3, 1088 iminodiacetic monomethylenephosphonic acid, 3, 1085 macrocyclic ligands, 3, 1091

154

155

Cumulative Subject h d e x

l&naphthyridine, 3,1069 nitrato, 3, 1086 nitrilotriacetate, 3, 1088 nitrogen and oxygen donors. 3,1087 nitrogen donor ligands, 3,1069 nitrogen donor macrocycles, 3,1094 nitrogen-oxygen macrocycles, 3,1097 NMR, 3,1100-1105 nonamethylimidodiphosphuramide,3, 1084 octakis(dimethy1formamide) solvent exchange, 1,285 oxalates, 3, 1085 o-phenanthroline, 3, 1069 phosphine oxides, 3,1082 phosphines SHAB theory, 1040 photoreactivity, 1,407 photosubstitution, 1,408 phthalocyanines, 2: 864; 3, 1095 picoline oxides, 3,1082 polyamines, 3, 1072 polyethylene glycols, 3, 1093 porphyrins, 2,822 sandwich complexes, 2, 823 4-pyridinecarboxylic acid hydrazide, 3, 1090 pyridine oxides, 3, 1081 selenides, 2,490 sulfato, 3, 1086 sulfur donor ligands, 3,1086 2,2':6',2"-terpyridyl, 3, 1070 tetraphenylimidodiphosphate, 3, 1084 tetrapositive oxidation state, 3, 1113 catechol oxygen donors, 3,1115 hydrated ions inorganic oxyanions, 3, 1114 nitrogen donor ligands, 3,1114 oxygen donor ligands. 3, 1114 tetravalent chlorides, 3,1116 tetravalent fluorides. 3, 1115 thiocyanates, 2,236; 3,1075 thioethers, 3,1087 thiosemicarbazidediacctic acid, 3, 1090 triphenylphosphine oxide, 3 , 1083 2,4,6-tri-a-pyridyl-l ,3,5-triazine1 3, 1071 Lanthanide(II1) complexes dodecacoordination, 2 , 9 2 hydroxy acids circular polarized luminescence, 2,471 pyridine oxide, 2,495 Lanthanides alkoxides physical properties, 2,346 synthesis, sodium salts. 2,338 calcium probes, 6,563,567 coordination numbers, 3, 1068 disposal, 6,895 ionic radii, 3, 1068 leaching, 6,914 macrobicyclic complexes, 2,938 magnetic interaction with coordinated ligands. 3,1101 magnetic properties, I , 263 Purex process, 6,941 reactions with alcohols, 2,336 with 2-propanol, 2,337 separation, 3,1068 source, 6,914 Lanthanide shift reagents applications, 3, 1103 complexation, 3,1105 silver complexes, 5,806

Leaving group effect

Lanthanide sulfates solubility, 6,922 Lanthanite structure. 6. 848 Lanthanum, hexanitratostructure, 1. 101 Lanrhanum, uctakis(hexanedi0ne)structure, 1- 84 Lanthanum, pentaaquatrinitratostructure, 1, YY Lanthanum complexes phthalocyanines, 2,864 porphyrins, 2, R22 salicylhydroxamic acid complexes, 2,507 Lanthanum(II1) complexes minerals, 6 , 8 4 6 Lasalocid A metal cation transport, 6,554 metal complexes, 2,480 Lasolocid alkaline earth metal complexes, 3,67 calcium transport, 3, 66 Lattice energy gravimetry and, 1,525 Law of average cnvironment angular overlap model, 1,230 Lawrencite, 6,855 Leaching, 6,785788 non-oxidatiye, 6,784 oxidative, 6,784 Lead elemental structure, 3, 184 hydrometallurgy, 6,787 Lead, cyclopentadienyl-, 3,218 Lead. perchloratotetrakis(1,lO-phenanthroline). structure, 1 , 9 7 Lead, tns(ethy1dithiocarhonato)stereochemistry: 1,82 structure. 1, 82 Lead bromide, 3,194 Lead bromide hydrate, 3, 195 Lead carboxylatcs, 3,222 Lcad complexes, 3,183-223 +arene, 3,220 bivalent stereochemistry, 3, 188 coordination geometry, 3, 185 dialkyl or diaryl, 3,216 fulvic and humic acids, 6,860 phthalocyanines, 2,864 porphyrins, 2,822 tetravalent, 3,205 transition metal, 2, 15-18 Lead(I1) complexes organic ore formation, 6,869 Lcad fluoride: 3,193 Lead halides, 3, 197 bivalent structure, 3. 193 Lead iodide, 3, 194 Lead oxide structure, 3,202 Lead phosphates. 3,222 Lead selenide structure, 3,202 Lead sulfate, 3,222 Lead sulfide structure, 3,202 Lead telluride structure, 3,202 Leaving group effect platinum complexes

Cumulative Subject Index

Leaving group effect substitution reactions, 5,494 Lectins manganese, 6,587 Leghemoglobin, 6, 688 dioxygen transport, 6,683 Leucine ethyl ester hydrolysis, metal catalysis, 6,421 Leucine aminopeptidase models, 6, 415 zinc, 5, 1005; 6,606 Leucocytes indium-Ill labelled abscess imaging techniques, 6, Y 9 4 labelled, 6,994 Levelling agents electroplating, 6 , 5 Levextrel solvent impregnated mineral processing, 6,826 Lewis acids catalysis coordinated ligand reaction, 6,411-477 Lewisite, 3, 256 Lichens metal complexet;, 2,964 Lidocaine technetium complexes hepatobiliary techniques, 6,989 Liebigite, 6,890 structure, 6,848 Ligand angular encumbrance, 2>1024 Ligand exchange neutral complexes, 1,287 solid state, 1,468 Ligand field theory, 1,213-274 free ions, I, 235-243 photolysis, I , 393 Ligand profiles cone angle concept, 2,1023 Ligands abbreviations, 1, 117, 118 n-accepting redox potential, I , 483 anionic, 1,112 bridging, 1,117,126 cationic, 1, 112 connection modes polyhedra, 1,139 coordinated reactions, 1,415 solid state reactions, 1,470 stoichiometric reactions, 6, 155-221 u-donating redox potential, 1,483 naturally occurring, 2,95+985 neutral, I, 111 organic, 1, 113 polydentate, 1, 114 Ligases zinc, 5,1002 Lignins structure, 6,857 Linkage isomerization reactions. 1 165 Linked redox centres, 1,493 Lipids rhodopsin-sensitized vesicular imaging systems, 6, 126 sodium pump, 6,556 Lipoaxygenases, 6,708 Lipophilicity alkali metal complexes, 3,53 Lipopolysaccharides ~

156

metal complexes, 2,985 Liquid ammonia solvents coordinarion complexes, 2,26 Liquid-liquid extraction, 1,538-549 Liquid Metal Fast Breeder Reactor, 6,885 fertile component uranium-238,6,885 fissile component plutonium-239; 6 ; 885 Lithium in psychiatry. 6,772 Lithium aluminum hydride, 3, 124 amine adducts, 3, 124 Lithium complexes amides, 2. 164 crown ethers, 3,40 phthalocyanines. 2, 863 porphyrins, 2,820 urea, 3 , 6 Lithium ions sodium pump, 6,557 Lithium salts in medicine, 6,756 metal melhiixide synthesis and, 2, 338 Lithographic printing plates planographic, 6, 123 Lithography relief-image-forming systems, 6 , 124 Liver copper, 6,672 diagnostic imaging techniques, 6,994 Liver alcohol dehydrogenase, 2,774 catalytic activity. 5 , 1017 Livingstonite, 3,265 Lossen rearrangement, 5.813 Lowry, ThomasMartin, 1, I6 Lubricating oils synthesis by dimerization-carbonylation,6,288 Lungs chronic cadmium poisoning, 5,1000 Luteocobalt -see Cobalt, hexaammineLuteocobaltic chloride -see Cobalt, hexaammine-, chloride Lutetium, aq~atris(6~6,7,7,8,8,8-heptafluoro-2,2dimethyl-3-5-0ctanedione)stereochemistry, 1: 81 Lutetium, (methylpyridine)tris(2,2,6,6-tetrarnethyl-3,5heptancdione)stereochemistry, 1; 81 Lutetium complexes 1,3-diketoncs NMR: 2,387 Lutetium(liT) complexes ethyl glycinate diacetate hydrolysis, 6,422 2,6-Lutidine N-oxide metal complexes. 2.496 Lyases zinc, 5 , 1002 Lymphocytes labelling, 6,994 Lysine copper(I1) complexes reactions, 1,419 metal complexes, 2, 750 Lysine, threonyf-lysyl-prolyl-lysyl-threonyl-lysyl-prolylmetal complexes, 2, 76.5 Lysocellin, 5,838

M-139603 alkaline earth metal complexes, 3.68 Macrobicycles anionic complexes. 2,450 axial metal ion complexes, 2,936 lateral metal ion complexes, 2,939 metal ion complexes, 2,936 synthesis, 2,926 Macrocycles history, 1,21 metal complexes protonation, I , 423 Macrocyclic cffcct, 3,48 nickel(I1) complexes. 5,240 Macrocyclic ligands alkali metal complexes, 3. 3 5 5 9 alkaline earth metal complexes, 3, 35 aminotroponeiminato nickel(I1) complexes, 2,908 arsenic synthesis, 2,925 bis metal ion complexes, 2,939 classification, 2,917 isomerism, 1, 204 metal complexes binding sites, 2. 922 cavity sizc, 2, 924 chirality, 2,924 conformation, 2,923 dimensionality, 2,924 electronic effects, 2,922 shaping groups, 2,923 structural effects, 2,922 molecular neutral complexes, 2.952 multidentate, 2, 899-913: 915-953 nomenclature, 2.920 phosphorus synthesis, 2,925 pol yarsa metal ion complexes, 2.936 polyaza metal ion complexes, 2.934 polycarbonyls classification, 2,919 polyethers alkali metal complexes. 3- 2 polyphospha metal ion complexes. 2- 935 polythia metal ion complexes. 2,933 synthesis, 2 , 925 a,-Macroglobulin zinc complexes, 2,975 zinc transport, 6,672 Macromonocycles anionic complexes. 2,948 metal cation complexes. 2.927 molecular cation complexes. 2.943 COT 7-F*

synthesis chirality, 2,924 Macropolycyclic ligands, 2,942 classification, 2.917 metal complexes binding sites, 2,922 cavity sue, 2,924 chirality, 2,924 conformation, 2,923 dimensionality, 2,924 electronic effects, 2, 922 shaping groups, 2,923 structural effects, 2,922 molecular cation complexes, 2,947 molecular neutral complexes, 2,952 multidentate, 2,915-953 nomenclature, 2,920 Macrotetrolide actins metal comptexes, 2,973 Macrotricycles anionic complexes, 2,951 cylindrical metal ion complexes, 2,941 molecular cation complexes, 2,948 metal ion complexes, 2,941 spherical ammonium complexcs, 2,947 metal ion complcxcs, 2,942 synthcsis, 2,927 Magnesium biology, 6,546,562-598 enzyme activator, 6,565 gravimetry, 1,528 neutral 2,3-diketones, 2,402 photosynthesis, 6,588 reactions with phenols, 2,336 Magnesium, alkylalkoxysynthesis, 2,340 Magnesium, pcntakis(trimethy1arsine oxide)stereochemistry, 1,40 Magnesium, pen takis(trimethy1phosphineoxide). sterenchernistry, I , 40 Magnesium, tris(l,l, 1,5,5,5-hexafluoroacetylacetone)salts structure. 1.66 structure. 1,65 Magnesium complexes acetylacetone. 2,372 complexes. 2,388 amides. 2,162: 164 properties, 2, 168 amines, 3, 8 ammines, 3 , 8 arsine oxides, 3 , 9 biology. 6, 549 fi-diketonates, 3, 13 dimethylphthalate, 3, 16 hydrates, 3. 7 naturally occurring, 3,58 nucleic acids, 2,979

157

Magnesium complexes

Cumulative Subject Index

octamethylpyrophosphoramide?3.15 phosphines, 3,9 phthalocyanines, 2,863 porphyrins, 2,820 pyridine oxide, 3,9 ribosomes, 6,549 Schiff bases, 3,29 urea hydrates, 3,9 Magnesium(I1) complexes maleic acid conformation, 2,475 Magnesium(lI1) Complexes structure, 1,6h Magnesium dibromide complexes, 3, 8 Magnesium halides complexes, 3, 10 Magnesium ions biology structure stabilizers, 6, 564 coordination compounds biology, 6, 563 enzyme activators, 6,578 probes, 6,563 RNA polymerases activation, 6,585 sodium pump, 6,557 transport microbes, 6,569 Magnesium(I1) ions phosphate ester hydrolysis, 6,443 Magnesium salts electrolyte balance, 6, 771 Magnetic behavior types, 1,256 Magneticexchange, 1,257,267 polymetallic complexes, 1, 138 Magnetic moment, 1,259 Magnetic properties atomic systems, I, 260 cubic field systems, I , 263 free-atom states and terms, 1,260 lower symmetry, 1, 264 zero-field splitting, 1,262 Magnetic susceptibility, 1,256,25Y Magnetism ferro and antiferro, 1,256, 258 Magnetization definition, 1,258 intensity, 1,256 Magnetochemistry bipyrazolyl metal complexes, 2, 90 Magnox reactor, 6,883,924 Magnus's green salt, 5,380,427; 6, 150 see also Platinum, tetraammine-. tetrachloroplatinate Malachite, 2,448 Maleic acid cesium complexes structure, 2,471 conformation, 2,467 dimethyl ester hydrogenation, 6,247,248 hydrogenation catalysis, ruthenium complexes. 6,236 IR spectra, 2,469 metal complexes, 2,475 crystal structurc, 2,475 IR spectra, 2,470 protonation, 2,465 reduction catalysts, rhodium complexes. 6.245 Maleonitrile, diaminoprebiotic systems, 6,871

Maleonitrile, 1,2-dicyanoethyIene-l,2-dithiometal complexes, 6, 147 Malic acid metal complexes geochemistry, 6.867 naturally occurring? 2,962 Malonic acid calcium complexes, 2,444 metal complexes naturaily occurring, 2,962 Malononitrile hydrolysis metal catalysis, 6, 450 Mammals iron transport and storage, 6,667 Mandelic acid in gravimetry, 1,532 metal complexes, 2,474 Manganate, aquapentachlorostereochemistry, 1,50 Manganate, tris(oxa1ato)chemical actinometer, 1,409 Manganates, hexachloro-, 4,58 Manganates, tetraalkyl-, 4, 13 Manganates, tetrahalo-, 4, 59 Manganatcs, tetraoxo-, 4.109 Manganates, trihalo-l 4,59 Manganese biology, 6,562-598 electrowinning, 6, 831 microorganisms, 6,681 photosynthesis, 6,588 protein requirement, 6.586 transport. 6, 672. tyrosine-bound, 6,587 Manganese, bromopentacarbonylexchange reactions. 1,290 Manganese, tricarbonyl(q5-cyclopentadienyl)stereochemistry, 1 , 13'1 Manganese complexes, 4, '1-1 11 acctylacetone, 2, 371 antikrromagnctism, 2, 379 complexes, 2, 388 amidines chelating ligands. 2,204 applications, 6, 1016 biology, 6,549 carbonyl-nitrosyl. 4,7 catalysts oxidation, 6: 375-379 corrins, 2,883 cyancmitrosyl. 4, 8 1,4-diaza-1,3-butadiene, 2,210 electronic spectra, 4 , d imines, 2,280 lability, 4: 6 magnetic moments, 4 , 4 neutral 1,3-diketonesl 2.402 nitrogen uses, 4,30 NMR, 4 , 6 organic mobilization, 6, 869 oxidation states. 4 , 7 oxo

oxidation catalysts, 6,355 phosphines SHAB theory, 2. 1030 phthalocyanines, 2, 866 oxygen production from water, 6,523 polypyrazolylborates, 2, 251 porphynns, 2,826

158

159 catalysts, water cleavage, 6, 498 oxygen production from water, 6,523 proteins, 2,773 pseudohalides, 2,230 triazines chelating ligands, 2,204 Manganese( -I) complexes, 4>7 Manganese(0) complexes, 4 , 7 cyanides, 4 , 7 monocyano nitrosyl-carbonyls, 4 , 8 nitrosyls, 4 , 7 Manganese(1) complexes, 4,&9 cyanides, 4 , 8 cyano-carbonyls, 4 , 8 dinitrosyl, 4, 8 magnetic behavior, I, 273 tetrahydroalane, 4 , 9 ureadiide, 2,287 Manganese(I1) complexes, 4,3,9-82 acetylacetonates, 4,48 acetylides, 4, 14 alcohols, 4, 37 alkoxides, 4,37 alkyl phosphines, 4, 13 alkyls, 4, 12 amidet;, 4, 15, 16 amine oxides, 4, 39 amines, 4, 16 amino acids, 4,43,62 sulfur containing, 4>70 ammines, 4, 15 antimony ligands, 4, 31-34 arsenates, 4,45, 46 arsenic ligands, 4, 31-34 arsenic oxides, 4, 39 aryls, 4, 12, 14 azides, 4,22 binary alkyls, 4, 13 bipyridyl, 4, 24, 25 anions, 4,25 2,2'-bipyridyl dioxide, 4, 51 biquinolyl, 4, 24 bis(2-aminoethylamine), 4 2 6 bismuth ligands. 4,31-34 bis(2-pyridy1methyl)amine. 4,26 bis(salicylidene)ethylenediamine,4, 66 biuret, 4,62 borates, 4,41,42 bromides, 4,58,59 4-butyIlactam, 4,39 carbonates, 4,41,42 carbonyl compounds, 4,38,39 carboxylates, 4, 43 catechol, 4,48 chloridcs, 4 , 5 6 , 5 7 chlorophosphates, 4.45 coordination geometries. 4,10 coordination polyhedra, 4. 10 croconic acid, 2,455 crown ethers, 4,52,80 cyanates, 4,22 cyanides, 4, 11 cyano-nitrosyls, 4, 12 cytosine, 4,61.62 1,2-diaminoethane, 4 , 2 3 dicarboxylates, 4 , 4 9 diethers, 4.47 diethylurea, 4,39 diketnnes, 4,48,49 1,2-dimethoxyethane, 4.47 dimethylacetamide, 4, 39 dimethylurea, 4, 39 diols, 4,47

Cumulative Subject Index

Manganese(I1) complexes

dioxane, 4,38,47 dioxygen, 4,41.73 diphenols, 4.47 dithiocacodylates, 4,54 dithiocarbamates, 4,54 1,2-dithioethane, 4,53 1,l-dithiolates, 4,S3,54 1,2-ditbiolates, 4,53 dithiolenes, 4,54 dithiooxalatcs, 4, 51 dithiophosphinates, 4,54 electronic spectra, 4, 11 ESR. 4 , 6 ethers, 4,38 ethylenediaminetetraacctic acid, 4,6Y ethylxanthate, 4,23 fluorides, 4.56 fluorophosphates, 4,45 formamide, 4,39 fulminates, 4, 14 halides, 4 , 5 5 6 0 fluid phase, 4, ( 5 henioglobin, 4,73 hexaaqua bond distances, 4 , 3 hcxafluurophosphates, 4,60 hexafluorosilicates, 4, 60 hexamethylenetetramine, 4, 'I 6 hydrazine, 4, 17 hydrides, 4,60 hydrogen ligands, 4,60 hydroxides, 4,35,36 hydroxycarboxylates, 4,49,51 hydroxylamine, 4,17,62 hydroxy oximes, 2,273 8-hydrwxyquinoline, 4,64 hydroxyquinones, 4,48 imidazoles, 4, 1Y,20 iodates, 4 ,4 7 iodides. 4-58,59 lability, 4, 10 lac,rams. 4,39 macrocyclic ligands, 4,72-82 magnetic behavior, 1,272 magnetic moments, 4 , 5 maleic acid, 4, 50 crystal structure, 2,475 malonates, 4.50 minerals, 6.846 mixed donors macrocycles, 4,80 molybdates, 4,47 monocarhoxylates, 4,43 1&naphthyridine, 4,25 niobates, 4.47 nitrates, 4.44 nitriles, 4,21 nitrites, 4. 22,44 nitrogen donors macrocycles, 4,76 nitrogen-oxygen ligands bidentate, 4 , 6 1 4 4 octadentate, 4,69 quadridentate, 4,66 quinquedentate, 4,69 scxidcntate, 4,69 terdentate, 4.65 nitrogen-sulfur ligands, 4,70 nitrosyls. 21 oxalates, 4. SO

oxides,4,35,36 oxyanions, 4,41-47 oxygen ligands, 4 , 3 4 5 2

Manganese(I1) complexes macrocycles, 4,813 oxygen-sulfur, 4,71 perchlorates, 4, 46 phenanthroline, 4,24 phenoxides, 4,37 phenylenediamines, 4,23 phosphates, 4,45 phosphinates, 4,45 phosphinites, 4,45 phosphonates, 4,45 phosphoramide, 4,52 phosphorus ligands, 4, 31-34 phosphorus oxides, 4,39 phthalocyanine, 4, 75 porphyrins, 4,72 dioxygen adducts, 2, 326 primary amines, 4, 16 propionamide, 4,39 pyrazoles, 4, 19,20 pyridine oxides, 4,39 pyridines, 4, 18 pyridylquinoline, 4,24 quinolines, 4,18 Schiff bases, 4.61 salicylaldirnines, 4,21, 63 salicylates, 4, 51 seciindary amines, 4, 16 selenates, 4,46 selenites, 4,4h selenium oxides, 4.39 selenocyanates, 4,22 silicates. 4, 41, 42 spectra, 1,253 spin states, 4, 10 squaric acid, 2,455 sulfates, 4, 46 sulfides, 4,53 sulfinates, 4, 46 sulfoacetic acid, 4,52 sulfonates, 4,46 sulfoxidcs, 4, 39 sulfur ligands, 4, 53 sulfur oxides, 4,39 tellurates, 4,46 tellurites, 4,46 terpyridyl trioxide, 4,52 tertiary amines, 4, 16 tertiary arsines, 4, 31 tertiary phosphines, 4, 31 tertiary stibines, 4, 32 tetrafluoroborates, 4, 60 tetrahydrofuran. 4,38 thiazyltrifluorides, 4,22 thiocarbonyls, 4, 54 thiocyanates, 4.22 thiolates, 4,53 thiophenolates, 4,53 triazoles, 4, 19,20 tricyanomethanide, 4, 14 tropolones, 4,48 tungstates, 4,47 urea, 4,39 vanadates, 4,47 water. 4,35 decomposition, 6,493 xanthates. 4,54 Manganese(l1T) complexes, 4,82-102 acetylacetonates, 4,89 alcohols, 4,89 aminotroponiminates, 4,85 arsenates, 4, 87 biguanides, 4 , 85 bipyridyl, 4,84

Cumulative Subject Index bromides, 4,92 carbon ligands, 4.83 carbonyl compounds, 4.90 carboxylates, 4,88 catechol, 4, S9 chlorides, 4 ,9 1 cyanides, 4. 83 synthesis, 2 , 9 cyclam, 4.100 dithiocarbamates, 4,91 1,2-dithioethane. 1 , 9 0 ethers, 4,90 fluorides, 4 - 9 1 halides, 4. 91 hcxafluoridcs. 4,92 hydrides, 4- 93 hydrogen ligands, 4.93 hydroxides, 4.85: 86 hydroxycarhoxylates, 4,89 8-hydroxyquinoline. 4,90 iodates, 4 ,8 8 iodides, 4,92 macrocyclic ligands- 4,97-102 magnetic behavior, 1,272 magnetic moments, 4 ,5 meso-*.*,a,cc-tetrakis(o-nicotinamidophenyl)porphyrin,4,9X mixed nitrogen-oxygcn donors bidcntatc? 4.93 quadridentaw, 4,94 quinquedentate. 4,96 septadentate, 4,96 sexidenrate, 4,96 terdentate, 4.93 mixed nitrogen-oxygen-sulfur donors, 4,96 mixed oxygen-sulfur donors, 4,96 nitrates, 4, 84,87 nitrogen ligands, 4, 84 octahedral compounds, I, 53 oxalates, 4$89 oxide.;, 4,85? 86 oxyanions, 4.87 oxygen ligands, 4: 85-90 phenanthroline, 4,84 phenols, 4,89 phosphates. 4. 87 phosphines SHAB theory, 2,1040 phosphorus ligands, 4,84 phthalocyanines, 4- 99 electrochemistry, 4, 99 ESR,4! 100 oxygenation. 4.99 pcllyhydrrix).carboxylates, 4, 89 porphyrins, 4.97 magnetic susceptibility, 4, 97 redox potentials, 4,97 vesicles, water cleavage, 6,529 visible spectra, 4,97 X-ray structures. 4,97 pyridine, 4,84 pyridine oxides. 4.90 Schiff bases, 4,93 salicylaldehyde, 4$85 salicylates. 4. gY selenites. 4. 88 semiquinone%,4,X9 spectra, 1, 252 sulfates. 4.87 sulfides. 4; 90 sulfur ligands. 4, YO thiols, 4, 90 troponiminates. 4,90

160

~

161

Curnulutive Subject Index

urea, 4,90 water, 4,85 Manganese(1V) complexes, 4, 102-109 alkyls, 4, 103 bipyridyl, 4, 103 bipyridyl oxides, 4, 106 carbon ligands, 4,102 catechol, 4,106 chlorides, 4,108 cyanides, 4,83, 102 dialkyldithiocarhamates~4, IM dithiolates, 4, 106 dithiolenes, 4, 107 fluorides, 4, 107 halides, 4, 107 hydroxidcs, 4, 104 iodates, 4, 105 macrocyclic ligands, 4,108 magnetic behavior, 1,272 magnetic moments, 4 , 5 nitrogen ligands, 4, 103 oxalates, 4, 105 oxides, 4, 104 oxyanions, 4, 105 oxygen ligands, 4,104 periodates, 4, 105 peroxo, 4, 105 phosphates, 4, 105 phosphines, 4, 104 phosphorus ligands. 4.103 phthalocyanines, 4, 109 polyhydroxy ligands, 4,106 porphyrins, 4, 108 salicylaldiminates, 4, 108 selenites, 4, 105 sorbitol, 4, 106 sulfates, 4, 105 sulfur ligands, 4, IO6 tellurates, 4, 105 terpyridyl oxides, 4,106 water, 4, 104 Manganese(V) complexes, 4.109-111 magnetic behavior, 1,272 nitrites, 4, 110 porphodimethines, 4. 111 porphyrins, 4,110 Manganese(V1) complexesl 4: 109-11 I Manganese(VI1) complexes. 4>109-1 11 Manganese dioxide oxidation, 6, 356 Manganese gluconate in electrochcmical production of oxygcn from water, 6, 534 Manganese ions enzyme activators, 6,578 probes, 6,563 RNA polymerases activation, 6, 585 transport microbes, 6,569 plants, 6,572 Manganese oxide colloidal catalysts, oxygen production from water, 6, 520 Manganese protein photosystem II,6,590 Manganese salts catalysts oxygen production from water, 6.517 Manganese superoxide dismutase, 6,586 Manganin, 6,572 Manganobalamin, 2,883 Mannich reaction

Mercury

acetylacetone metal complexes, 6, 205 metal complexes, 1, 422 u-D-Mannofuranme a l k a h e earth metal complexes, 3,25 Marcasite, 4, 1240 Marcus cross-reaction equation electron transfer, 1,355 Marcus-Hush theory electron transfer, 1,340 Marinc bactcria manganese transport, 6,570 Masking in gravimetry, 1,535-538 Masking agents, 1,537 Matrix isolation, I, 28 Mcan-field modcl magnetism. 1,258 Medicine coordination complexes in, 6,755-776 Meewein-Ponndorf-Verley reaction, 2,353 Melanostatin metal complexes naturally occurring, 2,967 Melanothallite, 6,855 Mclilutic acid electroplating, 6, h Mellite structure. 6,849 Melonoidins metal complexes, 6, 858 Melts metal complexes geochemistry, 6,854-856 Menkes' disease copper, 6,648 copper metabolism, 6,766 Mercaptides coordinated alkylation, 1: 417 Mercapo compounds chelating resins mineral processing, 6,826 Mercurate, pentachlorostructure, 1,39 Mercury bridging atoms transition metal clusters, 2 , 1 , 3 in catenated heterometallic polymercury species, 2,4 clusters metal-metal bonding, 1, 169 gravimetry, 1,532 Hgo exchange in Hg2+-Hg; ', 2 , 4 exchange in Hg: '-H$ , 2 , 4 resemblance to Br-, 2 , 4 resemblance to VI-carbon donors, 2 , 4 HgSf instability in solvents, 2 , 4 mercury complexes, instability in water, 2,4 Hd' instability in solvents, 2,4 ligands, 2, 1 palladium complexes organic synthesis, 2 , 2 platinum complexes organic synthesis, 2 , 2 polyatomic cations, 2 , 3 transition meial complexes bunding, 2 , l oxidation state, 2 , 3 skeletal electron contribution, 2 , 3 Mercury, bis(trifluoroacetato)tris(pyridine)structure 1 , 7 8 ~

Mercury Mercury. tris( 1,lO-phenanthro1ine)structure, 1,64 Mercury acetate, 5 , 1066 Mercury azide, 5 , 1062 Mercury bromide, 5 , 1059 Mercury cations

w+ lg9HgNMK,2,4

Mercury chloride, 5 , 1059 Mercury complcxcs, 5,1047 amidines, 2, 205 applications, 6, 1024 1.4-diaza-1,3-butadicnc, 2,211 histidine, 2,747 phthalocyanines, 2,868 physical development photography, 6 , 114 porphyrins, 2,842 pseudohalides, 2,235 pyridine oxide, 2,496 triazines, 2,205 Mercury(1) complexes, 5 , 1049 amides, 5 , 1054 amines, 5,1055 antimony ligands, 5,1058 arscnic ligands, 5 , 1058 cobalt ligands, 5, 1058 I ,4-dioxane, 5 , 1050 dithianes, 5 , 1051 n-donor ligands, 5,1058 nitrogen ligands, 5 , 1053 oxygen ligands, 5,1050 phosphorus ligands, 5,1057 phthalic acid, 5 , 1050 pyridine oxide, 5.1050 selenium ligands, 5 , 1053 sulfur ligands, 5,1051 tin(I1) ligands, 5 , 1058 trithianes, 5, 1051 Mcrcury(I1) complcxcs, 5 , 1054 amides, 5 , 1074 amines, 5,1075 antimony ligands, 5 , 1083 arsenic ligands, 5 , 1083 basic salts, 5, 1068 carboxylates, 5, 1066 carboxylic acids reactions, 2,443 cluster compounds, 5, 1049 1,3-diketones, 2, 392 dithiocarbamates, 5, 1072 guanidine, 2,283 hydrazine, 5 , 1077 masking agent, 1,536 metal ligands, 5 , 1085 mixed halides, 5 , 1060 nitrogen ligands, 5 , 1074 oxygen donor ligands, 5,1069 phosphorus ligands, 5,1081 pseudohalides, 5,1060 selenium ligands, 5 , 1072 sulfides, 5 , 1071 sulfur ligands, 5 , 1069 tellurium ligands, 5 , 1072 thiols, 5, 1070 thiones, 5, 1071 thiourea, 5 , 1072 transition metal ligands, 5 , 1085 ranthates, 5, 1072 Mercury compounds ruthenium complexes, 4, 280 Mercury cyanate, 5 , 1062

Cumulative Subject Index Mercury cyanide, 5. 1062 Mercury electrodes potential range aqueous solution, 1,480 Mercury fluoride, 5 . 1059 Mercury fulminate. 2.7,12; 5 , 1063 Mercury halides. 5 . 1049 Mercury iodate, 5. 1068 Mercury iodide. 5. I059 Mcrcury ions Hg:+ cobalt(1) complexes, 2 , 1 lormation in watcr, 2, 3 mercury complexes, 2.3 Mercury nitrate, 5,1050, 1067 Mercury nitrite. 5. 1066 Mercury oxalate. 5. 1066 Mercury oxides. 5 . 1065 Mercury perchlorate. 5 - 1068 Mercury phosphate. 5. 1067 Mercury pseudohalides, 5 , 1049 Mercury selenate, 5 , 1067 Mercury selenite? 5 , 1067 Mercury selenocyanate, 5 , 1064 Mercury sulfate, 5 , 1067 Mercury sulfidc, 5, 1069 Mcrcury tellurate, 5. 1068 Mercury trifluoroacetate, 5, 1066 Meso haem metal complexes geochemistry. 6,865 Mesoperrhenates, 4, 198 Mesoporphyrin iron complexes, 4.1266 Metacinnabarite. 5, 1069 Metal alkuxidrs. 2,335-359 carbon-hydrogen bond activation, 2.359 homoleptic prototypal structures, 2,348 ligand coordination, 2,351 mixed, 2.344 physical properries, 2,334 reactions, 2, 351 spectroscopy, 2$344 synthesis, 2,336-344 exchange reactions, 2,339 Metal alkyls metal alkoxide, 2.340 Metal aryloxides. 2,335-359 carbon-hydrogen bond activation, 2, 359 ligand coordination, 2, 351 mixed, 2,344 physical properties, 2,344 reactions, 2,351 spectroscopy, 2, 344 Metal buffering, 2*790 Metal carbonyls structure. 1, 16 Metal clusters halogen bridges. 2,685 Metal complexes alkali metal cations, 3.16 alkaline earth metal cations, 3, 16 alkoxy hydrides rcactions. 2,359 ammines, 3 , 2 aryloxy hydrides reactions? 2: 359 biological systems, 2,960 catalysts

162

163

Cumulative Subject Index

water clcavagc, 6 , 4 4 5 4 9 8 oxidation, 6, 317-400 oxygen, 6,319 reduction vanadium(I1) complexes. 3.472 Metal dialkylamides reactions with alcohols, 2,339 with phenols, 2. 339 Metal halides metal alkoxide synthesis from. 2,337 rcactions with organooxysilanes, 2.343 Metal hydrides, 2,689 metal alkoxides, 2: 340 Metal hydroxides gels phosphate ester hydrolysis, 6,448 reactions with alcohols, 2, 338 with phenols, 2,338 Metal ions aqua preparation, 2,305 biology analysis, 6,549 coordinated hydroxides, 6,442 labile metal-promoted reactions, 6.413 protons and, 6,412 water complexes bond distances, 2,307 bond strengths, 2,309 Metalla-l,3-diketones. 2.396 Metallization, 6, 31 Metallized dyes photography diffusion transfer system, 6. 106 Metalloarsenates non-Keggin, 3, 1042 Mctalloazaporphyrins axial coordination chemistry, 2,858 Metallocarbonic anhydrases zinc, 6,601 Metallocarboxypeptidases, 6 >604 Metallocenes dithiolato complexes, 2,604 nomenclature, 1 , 126,127 Metallochlorins coordination chemistry, 2 , 854 spectra, 2,851 X-ray structure, 2,851 Metallochromic indicators, 1, 554 Metallocorrins coordination chemistry, 2,883 spectra, 2,877 Metallocorrolcs coordination chemistry, 2, 874 Metalloenzymes, 2, 769 Metallofluorescent indicators, 1 558 Metallomacrocycles non-integral oxidation states. 6, 144 small ring electrical conduction, 6, 147 Metallophosphates non-Keggin, 3,1042 Metallophthalocyanines photochemical properties, 6,511 in photoproduction of hydrogen from water, 6,51&513 Metalloporphyrins carbene reactions, 2,817 coordination chemistryl 2, 820 electrical properties, 6, 144 ~

Metals

clcctron transfer rates, 2,847 mass spectra. 2: 816 in oxygen production from water, 6,522 photochemical properties, 6,510 photochemistry, 2,846 in photoproduction of hydrogen from water, 6,511. 51&513 redox. 2,846 $pectra, 2, 815 hyper type, 2,816 hypso type. 2 , 8 1 5 regular, 2, 815 d type, 2.816 p typc, 2.815 unusual, 2.816 spin states, 2, 819 stability, 2. 818 structure, 6.615 transition metals spin states, 2, 819 structure. 2, 819 Metalloproteins models, 2, 85 Mctallothio anions binuclear complexes mixed ligands, 2. 565 metal cotnplcxes, 2,559-576 Metallothionein proteins, I , 142 Metallothioneins. 2.774 cadmium, 5,1021 cadmium toxicity. 5, 1000 cobalt, 6, 673 copper. 5 , 1022 copper and zinc storage, 6,672 evolution, 5 : 1022 EXAFS, 6, 673 mammals amino acid sequence, 6,673 metal-binding site. 5 , 1022 metal curnplexes. 2,975 microbial copper storage, 6,681 NMR. 6,673 optical properties, 5, 1022 primary structure, 5, 1022 structure. 5, 1022 zinc, 6.599 Metal-metal bonding, 1, 137, 169 gravimetry, 1,525 history! 1.21. 23 nomcnclaturc. 1,122, 123 Mctal nitrosyls structure, 1, 16 Metdl oxides catalysts oxygen production from watcr, 6, 519, 521 precipitation mineral processing, 6,827 reactions with alcohols, 2,338 with phenols. 2,338 supported catalysts Metal oxoalkoxides, 2, 350 Metal phenoxides synthesis, 2,336344 exchange reactions, 2,340 Metal-phthalein metallochromic indicator, 1,557 Metals biology roles. 6, 548 drug absorption, 6.774 electrochemical behaviour, 6,831

Metals electrodeposition, 6, 1-15 metal complexes, 6,134 in mineral processing precipitation, 6, 828 Metal salts catalysts cleavage, 6,493 Metal-semiconductor transitions. 6. 135 Metal sulfides phenolysis, 2, 342 Metal template reactions, 1,416,433 equili brium kinetic, 1,434 thermodynamic, 1,434 Metal tolerance amino acid complexes, 2,964 plants, 2,963 Metal toxicity metal-protein interactions, 2,975 Metathioarsenites, 3,248 Metatungstates, 3, 1034 fiuoro, 3, 1034 isomers, 3, 1035 Metavanadates, 3, 1027 polymeric, 3, 1027 Metazellerite structurc, 6,848 Metazidohemerythrin structure, 6,690 Methacrylic acid methyl ester hydroformylation, 6,261 Methane ore formation, 6,869 Methane, dibenzoylmetal complcxcs stability, 2, 366 Methane, dichloroelectrochemistry in, 1,493 Methane, dihaloreactions catalysts, 6,305 Methanc, dipivaloylmetal complexes decomposition, 2,385 gas chromatography, 1,560 Methane, iodoreduction by pentacyanocobalt electron transfer, 1,333 Methane, nitrosolvent, 1,26 Methanediamine metal complexes, 2 , 3 0 Methanide, dicyanonitrosometal complexes, 2,263 Methanide, tricyanometal complcxes, 2,263 Methanobacterium formicicum formate dehydrogenases, 6.663 Methanobacterium thermoautotrophicwm hydrogenases nickel, 6,647 Methanococcus vannielli formate dehydrogenases. 6 >663 Methanococcus vollae cation transport, 6,558 Methanogenic bacteria nickel, 6,644 Methanogens energy, 6,643 Methanol carbonylation catalysts, colbalt complexes, 6,269

Cumulative Subject Index

164

catalysts, ruthenium complexes, 6, 267 homologation catalysts, rhodium complexes, 6,273 2, 88 Methanol, ~V-methylimidazol-2-yldi(pyrid-2-yl)-, metal complexes, 2,89 Methanosarcina bryantii nickel, 6,645 Methemerqqhrin, 1,254 Methemocyanin. 6 - 692 copper(I1) compiexrs, 5,724 Mcthioninc metal comptcxcs. 2, 749 4-Methoxy hen~clate-~-demethylase iron-sulfur clusters, 6, 634 Methydroxohrmerythrin structure, 6,690 Methylamine ore formation, 6,869 Methylation metal imine complexes. 1,419 Methyl coenzyme M reductase nickel, 6.634 Methyleneamido complexes transition metal, 2,125, 129 bonding, 2, 127 reactions, 2, 128 spectrtiscopy, 2 , 128 structures, 2 , 127, 128 synthesis, 2 , 126 X-ray photon emission spectra, 2, 128 Methylene groups oxidation copper catalysts. 6.394 Methylmagnesium carbonate ketone reactions. 6,216 Methylthymol blue metallochromic indicator, 1, 557 Mcthylviologcn in photochemical hydrogen production from water. 6 . 500 Methylxylentil blue metallochromic indicator, 1, 557 Mica structure, 6.845 Micelles in water cleavage, 6.526 Michenerite. 5 . 1099 Microbes cation transport, 6 , S S Group ITA cations transport, 6.569 Microemulsions in water cleavage, 6.527 Microorganisms iron Ftorage, 6.679 transport, 6,673 magnetotacticl 6 : 680 transition metals transport and storage, 6,680 Microprotease zinc, 5 , 1006 Mimosine metal complexes. 5 , 938 Mineral processing. 6,780 Minerals, 6, 844-850 deposition, 6,681 donor atoms and ligands, 6,845 Minguzzite structure, 6, X49 Mitochondria calcium transport. 6 , 568 electron transfer reactions, 6, 714

165

Cumulative Subject Index

Mitscherlichite structure, 6,847 Mixed valence compounds electrical properties, 6, 149 halogen bridged electrical conductivity, 6. 150 linear chain halogen bridged electrical conduction, 6 . 149 elcctrical properties, 6 , 149 Mixed-valence compounds. 2, SO Models cone angle concept definitions, 2 , 1015 Mohrite structure, 6,849 Molecular assemblies in water cleavage, 6,525-530 Molecular compounds, 1,5 crystals, 1, 15 Molecularit y substitution reactions. 1,282 Molccular mechanics amine mctal complexes, 2 , 2 5 Molecular structurc isomerism and, 1, 182 Molten salts solvents, 1,27 Molten state cadmium halidcs coordination, 5 , 981 zinc halides coordination, 5,981 Molybdate, aquapentachlorostereochemistry, 1, 50 Molybdate, dicarbonyltris(tripropylpheny1thio)triphenylphosphonium salt structure, 1 , 4 5 Molyhdate, octacyanopotassium salt structure, 1, 84 stereochemistry, 1,32 tetrabutylammonium salt structurc, 1, 84 triethylamine saits structure, 1, 86 Molybdate, tetrakis(di0xygen)stereochemistry, 1,94 Molybdates, 3, 1376 bonding, 3, 1378 charge transfer spectra, 3. 1378 IR spectra, 3, 1379 as ligand, 3, 1376 molccular orbital calculations, 3, L378 occurence, 3, 1229 Kaman spectra- 3. 1379 reactions, 3, 1371) reduction, 3, 1238 salts, 3, 1376 seleno, 3, 1377 spectra, 3, 1378 structure, 3, 1376 thio, 3, 1377 in uranium purification from ore. 6,899 UV spectra, 3, 1378 Molybdates, aquatetraoxodioxidation, 3, 125s Molybdatcs, hcptacyano-, 3, 1235 potassium salt structure, 1,72 Molybdates, hexaaqua-l 3, 1235 oxidation, 3, 1236. 1237 substitution reactions. 3. 1235 Molybdates, hexachloro-. 3.1234

Molybdenum

Molybdates, hexaisocyanato-, 3, 1235 Molybdates, hexaoxoreduction, 3,1242 Molybdates, octachlorodiaqueous solution chemistry, 3, 1232 Molybdates, pentachlorooxoI80-exchange, 3, 1254 stereochemistry. 1 , 5 0 Molybdates, tetraaxoI8O-exchange, 3, 1250 Molybdates, tctrathioiron complexes, 3,1426 Molybdenite. 3. 1229, 1431 Molybdenum, 3,122Y aqueom solution chemistry, 3, 1229 biochemistry. 6,656665 biological relevance, 3. 1229 biology, 6.546 role. 6.664 clusters biology, 6.657 complexes history, 1,21 microorganisms, 6, 681 occurrence, 3, 1229 Purex process, 6 . 944 precipitation mineral processing, 6,828 uscs, 3. 1229 Molybdenum. bis(diethy1dithiocarbamato)bis(pheny1nitrilo)angular parameters, 1,57 Molybdenum, bis(dimethy1dithiocarbamato)bis(benzeneazomethane)angular parameters, 1,57 Mulpbdenum, brumohexakis(pentanrnitri1e)bromide structurcl 1, 73 Molybdenum, dichlorohisonc-electron oxidation, 1,493 Molyhdenum, dicyclopentadienylt~l~~carbonyldi-, 3. 1316 Molybdenum, dioxybis(acety1acetone)bond-length ratios, 1,57 Molybdenum. dioxybis(dibenzoy1methane)bond-length ratios, 1,57 Molybdenum, dioxybis(diethy1dithiocarbarnato)angular parameters, 1,57 bond-length ratios, 1,57 Molybdenum, dioxybis(dipropy1dithiocarbamato)angular parameters. 1,57 bond-length ratios, 1,57 Molybdcnum, dodecachlorohexakisstructure, 1,21 Molybdenum, heptakis(acetonitri1e)bis(tetraRuor0horate)structure, 1, 72 Molybdenum, heptakis(benzonitri1e)bis( hexafluorophosphonate)structure, 1 ,7 2 Molybdenum, heptakis(pentanenitri1e)bis(hexafluorophosphonate)structure. 1,72 Molybdenum, hexacarbonyl-, 3,1230 Molybdenum, jodohexakis(pentanenitri1e)iodide structure, 1, 73 Molybdcnum, octacyanophotoreactivity, 1, 406 structure- 1,84 Molybdenum, pentakis(acetonitrile)[ethylenebis(diphenylphosphine)]structure, 1,77

Molybdenum

Cumulative Subject Index

Molybdenum, pentakis(acetonitri1e) [methylenebis(diphenylphosphine)]structure, 1,77 Molybdenum, pentakis(cyclohexanecarbonitri1e)[methylenebis(diphenylphosphine)]structure, 1,77 Molybdenum, tetracarbonylbis(tributy1phosphine)cisisomerization, I, 53 Molybdenum, tetrachloronitridotetraphenylarsenate stereochemistry, 1,44 Molybdenum, tetrachlorooxytetraphenylarsenate stereochemistry, 1,44 Molybdenum, tetracyanodioxysix-coordinate compounds structure, 1,53 Molybdenum, tetrakis( 1-adarnantoxo)( dimethylamine)stereochemistry, 1,44 Molybdenum, tetrakis(diethy1dithiocarbamato)stereochemistry, 1,94 Molybdenum, tetrakis(dithiobenzoat0)stereochemistry, 1,94 Molybdenum, tetrakis(nonaflu0robutoxy)oxystereochemistry, 1,44 Molybdenum, tricarbonyldiiodo[ethylenebis(diphcnylphosphine) 1structure, 1.78 Molybdenum, tricarbonyldiiodo(propy1enebis(diphenylphosphine)]structure, 1,78 Molybdenum, (trichlorotin)hexakis(pentanenitrile)salts structure, 73 Molybdenum, tris(acety1acetone)structure, 1.65 Molybdenum, tris(diethy1dithiocarbamato)nitrilostereochemistry, 1,82 Molybdenum, tris(2,3-dimercapto-Z-butenedinitrile)structure, 1,63 Molybdenum, tris(dimethy1 dimcrcaptosuccinate)structure, 1,63 Molybdenum, tris(dimethy1dithiocarbamato)bis(azobenzene) angular parameters, 1,59 Molybdenum, tris(dimethyldithiocarbarnato)( phenylazo stereochemistry, 1, 82 Molybdenum, tris(dithioglyoxa1)structure, 1,63 Molybdenum, tris(hexafluorodithiodiacety1)structure, I , 63 Molybdenum, tris(mercaptoani1ino)structure, 1,63 Molybdenum, tris(phenylenedithi0)structure, 1,63 Molybdenum alkoxides physical properties, 2,346 synthesis, 2,339 Molybdenum blue liquid-liquid extraction, 1,548 Molybdenum cofactor, 6,657 Molybdenum complexes acrylonitrile, 2,263 alkoxides, 3,1307 alkoxy carbonyl reactions, 2,355 alkyl, 3,1307 alkyl alkoxy reactions, 2,358 alkyl peroxides oxidation catalysts, 6,342 allyl, 3, 1306

amides molecular complexity, 2, 168 amidines bridging ligands. 2. 198 chelating ligands, 2,203 applications, 6>1015 aqua, 3,1230 aryl, 3,1307 bis(trifluoromethyl)dithietene, 3, 1436 bromide, 3.1306 carbainic acid paddlewheel structure, 2,451 carboxylatcs. 3, 1232 decarboxylations, 3,1304 reactions, 3,1302 stereochemistry, 3, 1304 structure, 3, 1302 synthesis, 3. 1302 carboxylic acids?2,438 reactions, 2,443 synthesis, 2,442 chalcogenides, 3.1331-1436 Chevrel phases. 3,1321 tetrameric clusters 3,132 I chlorides pentameric, 3, 1321 tetrameric clusters, 3, 1319 chromium derivatives, 3, 1307 clusters, 3, 1317-1322 bonding, 3.1318, 1319 hexameric, 3,1321 95MoNMR, 3,1318 structure, 3, 1317, 1319 trimeric, 3. 1317, 1319 corroles. 2,874 cyanide sulfur, 3, 1433 redox reactions, 3, 1433 cyclooctatetraene, 3,1306 cyclopentadienyl dithiolene, 3, 1435 cyclopentaditnyl y-etbane-l,2-dithiolate,3, 1435 cyclopentadienyl sulfur. 3, 1435 L-cysteine, 3, 1360 1,4-diaza-l.3-butadiene,2,209 cis-1,2-dicyanocthane-l,2-dithiolate, 3, 1436 dihydrogen, 3.1438 dimeric, 3,1230, 1355 carboxylates, 3-1362 chloride bridges, 3,1362 cyclic voltammetry, 3,1361 cysteinato, 3, 1361 dioxo, 3,1358 dithiocarbamato, 3,1360,1361 dithiocarbonate, 3, 1356 dithiocarboxylate, 3, 1356 1,l-dithiolate, 3, 1356 dithiopfiosphate, 3 , 1356 electrochemistry, 3, 2361, 1365 electronic absorption spectra, 3, 1357 glycinate, 3, 1361 heterocyclic ligands, 3, 1362 L-histidine, 3, 1361 2-hydroxyethanethiol, 3,1366 8-hydroxyquinoline, 3,1357,1366 IR spectra, 3,1357,1361 isothiocyanate, 3,1357, 1362 nitrogen bridges, 3,1362 NMR, 3,1357 one bridging ligand, 3, 1355 oxalate, 3,1358 persulfide bridges, 3,1362 porphyrins, 3,1357 pyridazine, 3,1362 pyridine, 3,1362 ~

167

Cumulative Subject Index

realgar, 3, 1363 thiolate bridges, 3. 1365 thiol bridges, 3, 1365 thiophenolates, 3, 1361, 1365 thiourea, 3, 1362 three bridging ligands, 3, 1365 4-t0lyl,3, 1357 1,5,9-triazacyclododecane, 3; 1358 1,4,7-triazanonane,3, 1361 trithiocarbonates, 3, 1356 two bridging ligands, 3. 1358 xanthate, 3, 1356 dimeric dioxo CD spectra, 3, 1361 dimeric disulfido CD spectra, 3, 1361 dimeric oxo 95MoNMR, 3,1361 structure, 3, 1355 dimeric sulfido 95MoNMR, 3,1361 dimetallic, 3, 1302-1310 dinitrogen, 6,718 dinitrosyl, 3, 1272 alkene dismutation catalysis, 2, 106 dinuclear catalysts, water cleavage, 6,398 dioxygen reactions, 2,328 dithiocarbamates, 3, 1305 dithiocarboxylates, 3, 1305 dithiolenes, 3,1432,1436 dithiophosphinates, 3,1305 double bonds, 3,1316 extended arrays, 3, 1321 halides, 3, 1306 dimetallic, 3, 1316 tetrameric, 3, 1321 heteronuclear quadruple bonded. 3,1307 hexaaqua dimers substitution reactions, 3. 1236 humic acids, 6, 84U hydrides, 3,1438 hydrido-bridged, 3,1307 hydridotetraoxo reaction rates, 3, 1260 2-hydroxypyridine, 3,1305 imides bridging ligands, 2, 176 imines, 2,279 iodides tetrameric clusters, 3, 1319 isothiocyanates, 3. 1306 metal-metal bonds, 3, 1301-1322 molybdenum-molybdenum bonds, 3, 1301-1322 monomeric, 3, 1230 neutral 1,3-diketones, 2,402 nitriles displacement reactions, 2,265 formation, 2,264 nitrosyl sulfur, 3, 1433 oligomeric, 3, 1355, 1363 hydroxide bridging, 3, 1363 methoxide bridging, 3. 1363 oxalate, 3, 1363 sulfide bridges, 3, 1364 trifluoroacetate, 3,1364 organolead, 2, 16 oxo

oxidation catalysts, 6,354 peroxo binuclear, 2, 323 oxidation, 6, 330

Molybdenum complexes

oxidation catalysts, 6,340 persulfides, 3,1431 perthiocarbonates, 3, 1432 phosphines, 3, I306 phthalocyanines, 2,865 polypyrazolylborates, 2,248 bidentate, 2,246 biological applications, 2,256 polysulfides, 3:1431 porphyrins, 2,825; 3,1305 dioxygen adducts, 2,325 proteins, 2: 773 pseudohalides, 2,229,230 quadruple bonds, 3.1308 cleavage, 3; 1310 ligand substitution, 3,1309 metal-metal, 3, 1302-1310 oxidation, 3, 1309 reactions, 3, 1309 redox reactions, 3,1309 single bonds, 3,1317 sulfur ligands, 3: 1421-1425 N,N.N',,Y.-tetrakis(2-acetic acid), 3, 1362 Ar,N,N'JV-tetrakis(2-acetic acid) 1,2-diarninopropane. 3, 1362 N,N',N'-trimcthyl-l,4,6-triazanonane,3, 1357 thiocarbamates electrochemistry, 2, 587 thiocarboxylates, 3, 1305 thionitrosyl, 2, 119 thioxanthates, 3,1305 1,4,7-triazacyclononane,3,1358 triazines bridging ligands, 2, 198 chelating ligands, 2,203 triple bonds, 3, 1315 cleavage, 3,1315 mulybdenurn-mulybdenum, properties, 3,1314 oxidative addition. 3, 1315 reaction with alkynes, 3, 1315 reaction with CO, 3,1315 reaction with cyanamide, 3, 1315 reaction with diazomethane, 3,1315 tripIe metal-metal bonds, 3, 1310-1315 aikoxy, 3,1310,1311 diethylamino, 3, 1310 dimethylamino, 3,1310,1311 dimethylcarbamoyl, 3,1311 ethylmethylamino, 3, 1310 properties, 3, 1314 reactions, 3,131 1-1314 with alcohols, 3,1311 with bidentare ligands, 3, 1313 with bridging ligands, 3, 1313 with COz, 3, 1313 with p-diketonates, 3, 1313 with isocyanates, 3, 1313 with isocyanides, 3,1313 with N donor ligands, 3,1313 with P donor ligands, 3,1313 with PF3,3, 1314 with phenols, 3, 1313 with phosphines, 3, 1313 silyl, 3. 1310, 1311 thiolato, 3, 1314 tris(thio1ene) electrochemistry, 3, 1436 prcparation, 3, 1437 structure, 3, 1436 tropulone synthesis, 2,376 tungsten derivatives, 3, 1307 vinyl sulfide, 3,1432

Molybdenum complexes

Cumulative Subject Index

xanthates, 3,1305 Molybdenum(0) complexes, 3,1265>1266 carbon dioxide, 3,1277 carbon monoxide, 3,1266 diphenylphosphinoethane, 3.1266 95MoNMR, 3,1266 carbonyl sulfide, 3,1277 dinitrogen, 3,1267,1268 binding, 3,1267 NMR, 3,1271 oxidation, 3,'I271 preparation, 3,1267 reactions, 3,1271 dinitrosyl, 3,1271 dithiolene, 3,1277 isocyanides, 3,1266 oxidation/reduction, 3,1266 magnetic behavior, 1,273 mononitrosyl, 3,1275,1276 nitrogenase, 3,1267 nitrogen donor ligands, 3,1276 nitrogen monoxide, 3,1271 phosphinc ligands, 3,1277 sulfur dioxide, 3,1277 Molybdenum(1) complexes, 3, 1265,1278 carbon monoxide, 3, 1278 dinitrogen, 3,1278 isocyanide, 3,1278 nitrogen donor ligands, 3,1280 nitrogen monoxide, 3,1279 nitrosyl, 3,1279 phosphorus donor ligands, 3,1280 Molybdenum(I1) complexes, 3,1230,1265.1280 arsines, 3,1283 azido. 3,1296 bimetallic reduction, 3,1293 carbonato carbonyl, 3, 1296 carbun monoxide, 3,1280 alkoxy, 3,1282 coordination number, 3; 1281 dithiocarbamato, 3,1282 hydride, 3,1282 loss of carbon monoxide. 3,1282 monocarbonyl, 3,1283 preparation, 3,1281 structure, 3,1282 cyanide, 3,1283 diazenido, 3,1292,1294,1295 dicarhonyl, 3,1295 reactions, 3,1295 synthesis, 3, 1293 dicarbonyl, 3,1281 diethyl dithiocarbamato reactions, 3,1296 disulfido, 3, 12% halides, 3,1321 hydrazide, 3,1292 isocyanide, 3,1283 alkyne, 3,1283 oxidation, 3,1283 protonation, 3,1283 mandelic acid, 2,474 monometallic reduction, 3,1293 q*-nitrosodurene,3,1296 nitrosyl, 3, 1285,1286 nitrosyl dithiocarbamato, 3,1290 nitrosyl pyrazolylborates, 3,1287 pentachloronitrosyl, 3,1290 pentacyanonitrosyl, 3,1290 phosphines, 3, 1283 phosphites, 3,1285

168

sulfido, 3,1296 tertiary pliosphines. 3, 1285 thionitrosyl. 3.1290 trichloronitrosyl, 3,1285 Molybdenum(II1) complexes, 3, 1234,1329-1332 acetylacetone. 3,1331 cyanides, 3. 1332 diamines, 3.1331 diazadienes, 3!1331 dimeric, 3, 1332 oxidation, 3 , I251 preparation. 3. 1239,1241 substirution reactions, 3,1239 dithiocarbamates. 3.1331,1333 dithiophosphates, 3,1331 electronic absorption spectra, 3,1332 electronic properties, 3,1332 ESR, 3,1332 ethylenediamineterraacetate, 3,1333

1,4,7,10,13,16-hexathiacyclooctadecane, 3,1331 magnetic behavior, 1. 272 magnetic properties, 3, 1332 nitrogen ligands. 3.1331 oxo-bridged dimers, 3 , 1333 oxygen ligands, 3,1331 phosphorcscenccl 3-1332 polymeric, 3, 1332 s p e c h , 1,252 sulfide bridges. 3. 1333 sulfur ligands. 3. 1331 thiols, 3, 1330 1,4,7-triazacyclononane,3,1333 trichlorotris(tetrahydrofuran), 3,1331

1,4,7-trimethyl-l.4,7-triazacyclononane, 3,1331 Molybdenum(1V) complexes, 3,1243,1332-1347 alkoxy, 3:1343 azides, 3, 134U

2,6-bis(2.2-diplicny1-2-mercaptoethyl)pyridine.3. 1337 bromidcs, 3: 1334,1342 l-bulylthio, 3, 1344 carbunyldioxu, 3,1339 chloride bridges. 3,1347 chlorides. 3,1334,1342 cyanides, 3,1338,1345 synthesis, 2,9 cyanothio, 3? 1347 cyclopentadienyl, 3,1346 dialkylamides. 3;1344 diazenides, 3: 1340 dichloroseleno. 3,1334 dichlorothio, 3,1334 difluorodithiophosphate, 3, 1337 dimeric, 3,1346 dioxide. 3>1334 dithiocarbamates, 3, 1336,1343 dithiocarboxylatcs, 3, 1343 dithiolenes, 3, 1344 electrochemistry, 3, 1340 electronic properties, 3,1345 eIectronic spectroscopy, 3,1339 fluorides, 3.1334,1342 halides. 3,1333%1342 histidine, 2,737 hydrazides, 3,1340 imides, 3,1340 isocyanides, 3, 1338,1345 isothiocyanato reduction, 3, 1247 magnetic behavior, I , 272 magnetic properties, 3, 1345 molybdenum-nitrogen bonds, 3,1340 nitride, 3,1340 nitrogen ligands, 3,1338

169

Cumulative Subject Index

NMR, 3,1339 oxo, 3, 1336 bonding, 3, 1335 crystal structure, 3, 1336 monomeric, 3, 1335 mononuclear, 3, 1334 oxo-sulfido trimers synthesis, 3,1246 oxychloride, 3, 1334 oxygen ligands, 3, 1337 perthiocarbonates, 3, 1311 1,10-phenanthroline. 3, 1339 phosphines, 3, 1337 photolysis, 3, 1345 phthalocyanate, 3, 1338 polymeric, 3,1346 8-quinolinolate, 3, 1343 redox reactions, 3, 1337 Schiff bases, 3, 1338, 1342 spectra, 1,252 spectroscopy, 3, 1244.1339 sulfur ligands, 3, 1337 tetracyanoethylene, 3, 1336 tetraphenylporphyrin>3, 1338 1,5,Y ,13-tetrathiocyclohexa~e~~ne, 3, 1337 tctratolylporphyrin, 3, 1338 thiocyanatcs, 3, 1344 thio-1,3-diketoncs, 3, 1343 thiolates, 3, 1343 2,4,6-triisopropylbenzenethiolate,3, 1344 trimers oxidation, 3, 1246 UV spectroscopy, 3, 1345 vibrational spectroscopy. 3. 1339. 1315 Molybdenum(V) complexes, 3: 1249, 1347-1366 bidentate ligands. 3- 1349 N,N'-bis(2-mercapto-2-methylpropyl-l,2ethylenediamine, 3- 1351 N,N'-bis(2'-1nercaptophenyl-'I .2-cthylcncdiamine, 3, 1351 carbodithioatcs, 3, 1350 chlorides, 3, 1348 chloro alkoxides, 3, 1354 cyanides, 3,1248,1354 cyclohexane-1,2-dione dioxime. 3. 1351 cyclopentane-1 ,?-diene dioxime, 3, 1351 dichlorotrifluoro, 3. 1348 dimers p-oxo bridged, 3,1253 reduction, 3, 12.56 N,N'-dimcthyl-N.N'-bis(2'-1nercaptoerhq.l-l,2ethylenediaminc, 3, 1351 di-p-sulfido prcparation, 3, 1252 di-p-sulfidocysteinato dimers. 3. 1247 dithiocarbamates. 3. 1354 dithiolenes, 3, 1354 electronic spectra, 3, 1353 ESR, 3,1352 fluorides, 3. 1347 halide oxo crystal structures, 3, 1348 monomeric, 3, 1348 halides, 3, 1347. 1353 imido, 3,1353 magnetic behavior, 1. 271 8-mercaptoquinoline, 3, 1351 monomeric oxo, 3,1250 mononuclear, 3, 1248 nitratc reduction, 3. 1350 nitrido, 3, 1353 nitrite reduction, 3, 1350

Molybdenum(V1) complexes

nitrogen bonds multiple, 3,1353 oxo monomeric, 3, 1348 y-oxo-~-sulfidol3,1252 polydentate ligands, 3, 1349 polypyrazolylborates. 3, 1253 quinolines, 3, 1349 Schiff bases. 3,1349, 1351 selenium ligands, 3, I350 selenocyanates. 3, 1351 spcctra. 1,251 spectroscopy, 3,1250,1352,1355 sullur ligands. 3, 1350,1354 2,3.17,18-tettamethyl-7,8,12, 13-tetraethylcorrole1 3 1351 tetraphenylporphyrin, 3,1351 thiocyanates, 3, 1351 thioxanthates, 3, 1354 tribromooxo, 3,1348 trichlorooxo, 3. 1348 trichlorosclcno, 3, 1348 trichlorothio, 3, 1348 M ( $ h l en u m ( V r )complexes, 3, 1256, 137S-1414 alkyl, 3: 3407 alkylidyne. 3, 1407 alkylimidol 3, 1396 arylimido. 3. 1396 hipyridyldibromodioxo, 3, 1388 bis(acety1acetonate) dioxo, 3, 1388 catecholate dioxo, 3, 1389 citric acid, 2,476 IR spectra, 2; 369 dimethyl. 3. 1406 dinuclear , 3 . 1408 TR spectroscopy, 3,1412 0 or S bridge, 3, 1411 preparation, 3, 1411 Raniail spectroscopy, 3, 1412 single oxo bridge. 3, 1408 Structure, 3, 1408 triple bridge, 3, 1410 dioxo catalysis of air oxidation of benzoin to b e n d , 3. 1392 electrochemistry, 3, 1392 oxo removal, 3, 1390 as reactants toward enzyme substrates, 3,1391 reactions with cyclohexyl isocyanate, 3,1391 reactions with heterocumulenes, 3, 1390 reactions with phosphines, 3,1390 reactivity? 3, 1390 rcdox reactions, 3,1390 dioxo Schiff bases, 3, 1389 1,l-dirhiolate dioxo, 3, 1388 ferriicenecarhodithioate dioxo, 3, 1388 guanidine. 2. 283 hydrazido, 3,1397 hydroxamic acids, 2.506 hydroxylamido, 3,1404 reactions, 3. 1405 structure, 3, 1404 imido. 3. 1396 maleic acid. 2,475 conformation, 2,467 crystal structure, 2,476 monomer-dimer equilibria, 3, 1259 Moo"', 3. 7392 "Mo NMR, 3, 1394 MoOz2".3. 1380 distorted trigonal prismatic, 3, 1384 EXAFS, 3: 1388 IR spectra. 3, 1386 1 7 0 NMR, 3,1386 ~

Molybdenum(V1)complexes

Cumulative Subject Index

9 5 MNMR, ~ 3,1386 octahedral, 3,1381-1386 preparation, 3,1388 Raman spectra, 3, 1386 skew trapezoidal bipyramidal, 3,1385 spectra, 3,1386 cis structure, 3, 1381 tetrahedral, 3, 1383 trigonal bipyramid, 3,1384 nitrido, 3, 1394 preparation, 3,1395 reactions, 3, 1395 structure, 3, 1395 peroxo, 3,1398 coordination numbers, 3,1398 dinuclear, 3, 1402 mononuclear, 3,1398 mononuclear, structure, 3,1399 reactivity toward organic molecules. 3, 1403 spectral indicators, 3,1403 tartaric acid, 2,479 NMR, 2,468 tetrahedral sulfido, 3,1260 tetrahedral thiolate, 3, 1260 tetranuclear, 3, 1411 1.4,7-trimethyl-l,4,7-triazanonanehalodioxo, 3, 1388 tris(dithiolcne), 3, 1413 without oxo ligands, 3, 1412 Molybdenum enzymes ESR, 6,661 spectra, 6,658 structure, 6,659 Molybdenum hexafluoride. 3, 1412 Molybdenum-iron-sulfur complexes. 1,241 Molybdenum oxide amino acid formation prebiotic systems, 6, 872 Molybdenum storage protein microorganisms, 6,681 Molybdenum telluride, 3, 1431 Molybdenum tetraalkoxrdes physical properties, 2,347 Molybdenum tribromide, 3, 1330 Molybdenum trichloride, 3, 1330 Molybdenum trifluoride, 3, 1330 Molybdenum trihalides, 3, 1330 bond lengths, 3,1330 magnetic moments, 3,1330 preparation, 3,1330 properties, 3, 1330 structure, 3,1330 Molybdenum triiodide, 3, 1330 Molybdenum trioxide complexes, 3, 1379 Molybdenum triselenide, 3, 143 I Molybdenum trisulfide, 3, 1431 Molybdoarsenates. 3, 1041 non-Keggin, 3, 1042 Molybdoarsenic acid liquid-liquid extraction, 1,548 Molybdoborates, 3,1042 Molybdocerophosphoric acid determination, 1, 548 Molybdoenzymes, 3, 1352 molybdenum site, 3, 1391 Molybdogermanates, 3,1038 Molybdogermanic acid liquid-liquid extraction, 1,548 Molybdoniobic acid

liquid-liquid extraction, 1,548 Molybdophosphates, 3, 1031 ammonium salt in gravimetry, 1,534 non-Keggin, 3, 1042 reduced, 3, 1050 Molybdoproteins terminal oxidases aerobic carboxydobacteria, 6,698 Molybdopterin, 6,657 Molybdosilicares, 3,1038 Mnlybdnsilicophosphoric acid liquid-liquid extraction, 1,548 Molybdovanadates non-Keggin, 3,1043 Molysite, 6,855 structure, 6.846 Monazite, 6,911 Monensin, 5,838 alkali metal complexes, 2,973 alkaline earth metal complexes, 3,66 metal complexes selective binding, 6,552 sodium transport, 6,554 Monoclonal anribodies radionuclidc transport, 6 , Y95 Mononuclear compounds neutral nomenclatu~e,1,120 Monooxygenases, 6.326,682,6,709 external, 6,326 internal, 6,326 Monsanto process acetic acid synthesis mechanism, 6.272 Montmorillonite electrode modification, 6.23 minerals prebiotic systems, 6,872 weathering. 6, 868 Mosesite structure, 6,848 Miissbauer spectroscopy iron, 4,1181 Mugineic acid, 6. 680 iron complexes naturally occurring. 2,964 Multimetallic systems electrochemistry, 1,485 Murexide metallochromic indicators, 1,554,555 My ambutol copper-64 complexes hepatobiliary system imaging techniques, 6 , 990 Mycobacterium phlei cation transport, 6,559 Mycobactins, 6,675 Myeloperoxidase. 6, 705 Myhemeryrhrin dioxygen binding, 6,689 Myocardial imaging radiopharmaceutical agents, 6,968 Myoglobin, 2,315,772,982; 4,263, 1269; 6,688 dioxygen transport, 6,683 reactions, 2,829 Myoglohin, nitrosyl-, 4, 1194 Myoglobin, oxy-: 6.688 Myosin light chains, 6,576

170

Nafion electrodes, 6. 15 Naphthalene-3,7-disulfonic acid, 1,2-diaminoiron complexes filter dyes, 6, 104 Naphthoic acid, hydroxymetal complexes, 2,480,482 2-Naphthoic acid, 3-hydroxycopper(I1) complexes, 2,483 metal complexes IR spectra, 2,469 2-Naphthoic acid, l-hydroxy-4,7-disulfoiron(II1) complexes, 2,483 3-Naphthoic acid, 2-hydroxy-l-(2-hyiroxy-4-sulfo-1naphthylaz0)metallochromic indicator, 1,556 2-Naphthoic acid, 1-hydroxy-7-sulfoiron(II1) complexes, 2,483 2-Naphthoic acid, 1-hydroxy-4-sulfonatometal complexes structure, 2,482 2-Naphthoic acid, 3-hydroxy-7-sulfonatometal complexes structure, 2,482 2-Naphtho1, ~-(2-carhoxyphenylaztl)chromium complex geometrical isomerism, 6,68 2-Naphthol, 1-(2-hydroxy-4-nitrophenylazo)chromium complexes geometrical isomerism, 6,69 2-Naphthol, 1-(2-hydroxyphenylazo)chromium complex geometrical isomerism, 6.68 copper complexes demethylation, 6,54 1-Naphthol, d-methoxyphotothermography, 6,121 2-Naphthol, 1-(2-methoxyphenylazo)copper complexes demethylation, 6,54 2-Naphthol, 1-(4-nitrophenylazo)copper complexes, 6,42 1-Naphthol, 2-nitrosoliquid-liquid extraction. 1-545 2-Naphtho1, l-nitrosoin analysis, 1, 522 in gravimetry, 1, 531 liquid-liquid extraction, 1,545 2-Naphtho1, l-phenylazometal complexes structure, 6,42 2-Naphtho1, pyridylazometal complexes dyes, 6,74 2-Naphthol, L(2-pyridy1azo)hexaamminecahalt(IIT) complex electron recording system, 6: 'I27 metallochromic indicators, 1,546,556 Naphthols metal complexes color photography, 6 , 107

5.Naphthol-7-sulfonic acid, 2-amino-6-(2-hydroxy-6-nitro4-sulfonaphth-1-y1azo)chromium cornpiexes geometrical isomerism, 6 , 70 stereochemistry, 6,62 2-Naphthol-4-sulfonic acid, 1-(2-hydroxy-3-methyI-lp heny1azo)metallochromic indicator, 1,556 2-Naphthol-4-sulfonic acid, 1-(2-hydroxynaphthylazo)metallochromic indicators, 1,556 I-Naphthylamine, N,N-dimethyl-2-ethylcomplexes chirality, 1 , 199 2-Naphthylamine, 1-(2-hydroxyphenylazo)copper complexes, 6,57 2-Naphthyiamine, l-phcnylazometal complexes structure, 6,44 1,8-Naphthyridine metal complexes, 2, 92,93 Nee1 temperature, 1,258 Neocupferron in gravimetry, 1,532 liquid-liquid extraction, 1,544 metal complexes, 2,509-512 Neodymium, octakis(dimcthy1formamide)solvent exchange, 1; 285 Neodymium, octakis(pyridy1oxy)structure, 1,84 Neodymium complexes trinitrato structure, 1,97 Neodymium hypophosphate hydrated, 3,1076 Neptunium breeder reactor fuels Purex process, 6,955 reprocessing, 6,954 determination, 1,548 electrolytic reduction Purex process, 6,949 cnvironmcntal chcmistry, 6,961 extraction Purex process, 6,951 Purex process, 6,946,950 recovery from nuclear fuel waste, 6,960 Neptunium(1V) oxidation Purex process, 6,951 Neptunium(V) reduction to neptunium(1V) h r e x process, 6,951 Neptunium(V1) rcduction Purex process, 6,951 Neptunium complexes, 3, 1131-1215 cupferron, 2,510 Neptunium dioxide ions disproportionation Purex process, 6,950

171

Nerve growth factor

Cumulative Subject Index

Nerve growth factor snake venoms zinc, 6,613 Neurospora crassa calcium transport, 6,571 cation transport, 6,559 Neurosporin, 6,676 Neurotransmitters secretion calcium, 6,595 Neutral complexes electrical properties, 6, 143 Neutron absorbers reprocessing irradiated nuclear fuel criticality, 6, 926 Yeutron activation analysis metal complexes biology, 6,550 Neutron capture fission product, 6, 883 Neutron diffraction hydrates metal-oxygen bond distances, 2,307 Nickel analysis, I, 522 biochemistry, 6,643448 biology, 6, 546 dimethylglyoxime complex gravimetry, 1,525 electroplating, 6, 10 extraction cation exchange resins, 6, 817 gravimetry, 1,533 hydrometallurgy, 6,786 microorganisms uptake, 6,680 natural isotopes, 5,3 occurrence, 5 . 2 physical propertics, 5 , 3 powder mineral processing, 6, 829 recovery chelating resins, 6,825 solvent extraction o-hydroxyoximes, 6,7Y9 titrimetry, 1, 533 transport, 6.672 uptake plants, 6,648 Nickel, bis(acety1acetone)polymerization isomerism, 1, 187 Nickel, bis(dinitrogen)(oxygcn)synthesis matrix isolation, 1,28 Nickel, btomotetrakis(trimethy1phosphine)te trafluoroboratc stereochemistry, 1 , 4 4 Nickel, carbonyltris(dinitrogen)synthesis matrix isolation, 1, 28 Nickel, (cyclam)chirality, 1, 198 Nickel, diacetylbis(benzoy1hydrazonato)-.5 ?203 Nickel, dibromobis(benzyldipheny1phosphine)allogonism, 1,207 Nickell dibromobis[ tris(3-aminopropfl)ph~sphine]synthesis, 1, 27 Nickel. dibromoethylbis(pyridy1)solid state reactions, 1,470 Nickel, dibroinoisopropylbis(pyridy1)solid state reactions, 1,470 Nickel, dibromotris(trimethy1phosphine)structure, 1,45

Nickel, dichlorn(2,9-dimethyl-.l,10-phenanthro1ine)isomers, 1,187 Nickel, dihalobis(tria1kylphosphine)allogonism, 1,207 Nickel, dihalobis(tris(2-cyanoethyl)phosphine]polymerization solid state, 1,470 Nickel, diiodobis(2-methy1pyridine)structure, 1,207 Nickel, diiodotris(trimethy1 phosphite)structure, 1.45 Nic el hcxaammine-. riactions, 1.27 Nickel, hexaaquareactions, 1,204 Nickel, hexaRuorwl 5,186 Nickel, hexakis(N,N’-dimethy1urea)tetrachloronickelate isomerization. 1,470 Nickel, me thyltetrakis(trimethy1phosphine)tetraphenylborate stereochemistry, 1 , M Nickel, pentacyanoisomerism, 1,206 structure. 1 - 4 0 Nickel, tetracarbonylcxchangc reactions- 1,288 Nickcl, tetracyano-, 5,67 Nickel, tetrahalu-, 5 , 186 Nickel, tetrakis(dinitr0gen)synthesis matrix isolation. 1, 28 Nickel, tetrathiocyanatotetraethylarsenate solid state reactions, 1,470 Nickel, trichlorobis( 1 14-diazabicyclo[2.2.2]octane)perchlorate structure, 1.45 Nickel, trihalo-, 5. 186 Nickcl, tris(2,2’-bipyridyl)racemization, I. 24: 466 structure, 1. 64 Nickel, tris( 1,lO-phenanthro1ine)racemization 1 24.466 solid state, 1,167 structure, 1,64 Nickel complexes, 5: 1-300 acetylacetone alcoholysis, 2, 380 pyridine complexes, 2,386 solvoIysis: 2.379 structure, 2.388 arnidines bridging ligands. 2,201 amino oximes, 2,274 applications, 6, 1019 bcnzencdithiols optical recording systems, 6. 126 biguanide, 2,284 biology, 6.549 q3-bonded, 5,33 arsenic sulfide. 5 , 36 arsines, 5.34 C3Ph3,5,33 cyclopropenyl, 5 ) 33 q3-P3, 5 , 33 phosphines, 5,34 phosphorus sulfide, 5,36 catalysts carbon dioxide reactions, 6,295 carbonylation, 6,27Y hydrogenalion, 6,248 hydrogen cyanide reactions, 6,296

‘r

172

~

173

Cumulutive Subject Index

citric acid crystal structure, 2,477 corrins, 2,885 corroles, 2,875 cyanides synthesis, 2 , 9 1,4-diaza-l,3-butadiene, 2,211 dimethylglyoxime, 2,271 dinitriles, 2, 262 a$-dionedioximates electrical properties, 6, 143 dioximes oxidation, 2,271 dioxygen reactions, 2,329 electrophotography, 6, 123 neutral 1,3-diketones, 2,402 nitrosyl, 2, 107 phthalocyanines, 2, 868 polypyrazolylborates, 2,246,252 electron density distribution, 2, 257 porphyrins, 2,841 crystal structure, 6, 146 electrical conduction, 6,145 electrical properties, 6, 144 Miissbauer spectra, 6 , 144 metal to semiconductor transition, 6 , 146 Raman spectroscopy, 6 , 244 stoichiometry, 6 , 146 superlattice spacing, 6, 145 pseudohalides, 2,232.233 squaric acid, 2,455 tellurides, 2,669 triazines bridging ligands, 2,201 tridentate azo compounds N,-Np isomerism, 6,65 Nickel(0) complexes, 5,s-32, S alkene phosphincs X-ray crystal structure, 5 , Ih alkenes, 5 , 14 NMR, 5, 18 properties, 5, 17 reactions with carbon dioxide. 5, 32 alkynes reactions with carbon dioxide, 5 , 3 2 arsine alkene, 5 , 15 arsine alkyne, 5 , 15 arsines, 5 , 8 , 9 azobenzene, 5,22 2,2’-azopyridine, 5 , 2 3 benzonitrile, 5,20 2-butene, 5, 14 carbon dioxide, 5,24,25 carbon disulfide, 5,24.25 carbonyl, 5,6, 10 1R spectra, 5 , 11 carbonyl arsines, 5 , IO, 11 carbonyl phosphines, 5,10,11 chloro alkenes, 5 , l j cyano, 5 , 6 cyclic nickelacarboxyiates, 5,32 cyclohexene, 5 , 14 diazafluorene X-ray ciystal structure, 5,23 diazenato, 5,22,27 diazene, 5,21,22 diazomethane, 5,21 dinitrogen, 5,26,27 dioxygen, 5,21,28 heteroalkenes, 5,18, 19,20 imino, 5,20 isocyano, 5 , 6

Nickel(I1) complexes

ketenimine, 5,23 nickelacycles, 5,32 nitriles: 5,20 NMR,5,21 oxidative addition reactions, 5 , 32 nitroso, 5 , 18 nitrosyl, 5, 12, 13 structure, 5 , 14 oxidative addition reactions, 5,31 phosphaalkene, 5; 21 phosphine alkene, 5,15,17 phosphine alkyne, 5, 15 phosphines, 5 , 8, 9 oxidative addition reactions, 5,31 structure, 5,10 phosphorus selenide, 5,30 phosphorus sulfide, 5,30 salicylaldiminato, 5,21 stabilization, 5 , 6 stibines, 5 , 8 , 9 sulfur dioxide, 5,29, 30 tetraazadiene, 5,21,23 tetraphosphorus, 5,30 Nickel(1) complexes, 5,5,36-45 4-aminopyridine, 5,39 arsines, 5 , 3 9 synthesis, 5,40 hipyridyl, .S1 37 cyano, $ 3 7 dithiocarbamates, 5: 44 1,3-dithioketonato, 5,45 dithiolenes, 5,44 imidazole, 5 , 3 9 macrocycles ESR, 5,39 electrochemistry, 5,39 magnetic properties, I , 274 maleonitriledithiolato, 5,44 2-methylimidazole, 5,39 phosphincs, 5,39 synthesis. 5,40 properties, 5,36 pyridine, 5,39 spin Hamiltonian parameters, 5,37 tertiary- arsines molecular parameters, 5,42 tertiary phosphines molecular parameters, 5,42 tetraaza macrocycles, 5 3 8 Nickel(I1) complcxes, 1,470; 5,45-287 2-acetamidopyridine, 5,214 acetate tetrahydrate, 5,155 acetophenone, 5,145 acetylacetone, 2,370; 5,142 keto form, 5, 144 2-acetylpyridine N-oxide oxime, 5,214 alanine, 5,219 albumin. 2,975 alcohols, 5, 139 aldehydes, 5 , 141 alkanesulfinamides, 5,165 alkoxides! 5 , 140 alkoxyhahdes, 5,140 alkyl phosphines, 5 , 112 alkyl phosphites, 5 , 114 alkylsulfide, 5,154 allogonisrn, 1,207 amides, 5, I S 1 6 5 amine oxides, 5,159-165 aliphatic, 5, 162 aromatic, 5,162 amines deprotonated, 5,96

Nickel(I1) complexes

Cumulative Subject Index

monodentate, 5,7&107 polydentate, 5,72 tetragonal, 5,61 amino acid esters hydrolysis, 6,425 amino acids, 5,219,221 2-aminobenzenethiol, 5,212 a-aminobutyric acid, 5,219 aminocarboxylic acids, 5,218-221 2-aminoethanethiol, 5 , W8 l-amino-2-ethanol,5,214

N-(2-aminoethyl)-l,2-ethanediaminc,5,72 p-amino imines, 5,96,97; 6 , 162 o-aminophenol, 5,214 aminopolycarboxylic acids, 5,218 l-amino-2-propanol,5,214 aminopyridine, 5 8 6 2-aminopyridine N-oxide, 5,214 ammines, 5,70 anionic organic phosphorus, 5,152 antimony ligands, 5,108-131 aqua, 5,139 arsenic ligands, 5 , 108-131 arsenic oxides, 5,15%165 arsines bidentate tertiary, 5 , 116 halo, 5 , 108 monodentate tertiary, 5.108 organometallic, 5,111 pseudohalo, 5,108 tetradentate tertiary, 5, 125 tridentate tertiary, 5 , 125 arsine sulfides, 5 , 185 arylphosphines, 5,112 aryl phosphites, 5 , 114 aspartic acid, 5,220 au'des magnetic properties, 5,282 azido, 5 , 104 benzamide oxime, 2,274 benzenedicarboxylic acid, 5 , iS7 benzenseleninato, 5 , 154 benzimidazole, 5,82 1,2-benzoquinone, 5,145 1,2-benzoquinonedioximato, 5 , 98 2,2'-bipyridyl, 5,80,162 2,2'-bipyridyl N-oxide, 5,214 bis(acety1acetonato) NMR, 5,57

N,N-bis(2-aminoethyl)-l,2-ethanediamine, 5 , 72 bis(aminotroponiminato), 5 , 97 bis(biguanide), 5 , 101 1,4-bis[bis(2-aminoethyl)amino]benzenc. 5,226 bis(dialkyldithiophosphinato), 5 , 175 bis( 1,l-dialkylethylenediamine) thermochroism, 2,43 1,5-bis(dimethylamino)-3-oxapentane,5,217 1,5-bis(dimethylamino)-3-thiapentane,5,217 1,2-bis(mercapto)-o-carborane.5,182 bis(o-phenylenediiminato), 5 , 9 7 bis(pyrrole-2-aldiminato), 5,97 bis(salicyla1doximato) structure, 6,800 1,4-butanediamine, 5,71 camphorquinone dioxime, 5,214 camphorquinone monooxide, 5,215 carbonyl phosphines, 5,112 carboxylates, 5 , 155-159 magnetic properties, 5,282 carboxylic acids naturally occurring, 2,963 chlorins, 5,275 citric acid, 2,476

174

crystal structure, 2: 477 corrins, 5,275 croconates, 5 , 158 cryptands, 5,270 cupferron, 5 >165 cyano, 5 6 8 2-cyano-8-hydroxyquinoline, 5 , 106 2-cyano-l,l0-phenanthroline,5 , 106 2-cyanopyridine, 5 , 106 cyclam, 5,238 cyclic hydrazones. 5,256 truns-l,2-cyclohexanetctraaceticacid, 5,219 deprotonated macrocycles, 5,256257 2,6-diacetylpyridine hydrazones, 5 , 198 dialkylarnide, 5 , 107 N,N-dialkylethylenediamineN-oxide, 5,214 diamines, 2,31; 5,71 1,2-diaminopropanetetraacetate,5,219 1,5-diazacyclooctane-N,N'-diaceticacid, 5 , 157,221 1,s-diazacyclooctane-N-monoaceticacid, 5,221 dibenzo[b,i]-l,4,8,11-tetraazacyclotetradeca2,4,6,9,11,13-hexaene, 5,250 dicupferron, 5,165 diethylenetriaminepentaaceticacid, 5,219 2,6-diformyl-4-methylphenol, 5,226 (3-diimines,6,166 1,3-diketones, 5 , 142-14.5 TR spectra, 5,143 dimers magnetic properties, 5,276 N,N-dimethylformamide, 5,164 dimethylglyoxime, 6, 184 dimethyl selenooxide, 5 , 164 dimethyl sulfoxide, 5 ! 164 2,21-dimethyl-3,7,11,17tetraazabicyclo[l1.3. Ilheptadeca1[17),2,11,13,15-pentaene,5,249 2,12-dimethyl-3,7,11,17tetraazabicyclo[ 11.3:llheptadeca-l( 17),13,15triene, S, 240 dinuclear binucleating ligands, 5,221-226 a,b-dionedioximato, 5 , 98 dioximes, 2,271 l-diphenylarsino-2-diphenylphosphinoethane, 5, 175 1,2-diphenyl-l,Z-ethanediamine, 5,71 1,3-diphenyltriazene, 5,79 diphosphates, 5, 154 di-2-pyridyl ketones, 5,217 disilylamide, 5. 107 ditertiary arsine oxides, 5 , 161 ditertiary phosphine oxides, 5, 161 dithiocarbamates, 5,172 dithiocarbamic acids, 5,213 dithiocarbuxylates, 5. 173 1,2-dithiolene, 5 , 177 dithiooxalate, 5 ; 181 dithiosquarate, 5 , 282 EPR spectra, 5,55 electronic spectra, 5,45-68,46 energy levels, 5,46 equilibrium constants solvent effect, 1,516 esters, 5,141 1,2-ethanediarnine, 5, 71 ethers, 5 , 141 ethylenediaminetetraacetic acid, 5,218 ethylene-2,2-dithiolates, 5 , 17.5 five-coordinate, 5,3,49,61,65 fluoro-1,3-diketones, 5 , 145 formate, 5, 155 formazans dyes, 6,78

Cumulative Subject Index

175 formazyl, 5,97 four-coordinatt, 5 , 4 gluconic acid, 5, 159 glycine, 5,219 glycine peptides, 5,220 glyoximes, 5,98 ground states magnetic properties, 5,51 spectra, 5,51 halides, 5, 186 heterocyclic amines magnetic properties, 5,283 heterodinuclear magnetic properties, 5,283 hexafluoroacetylacetone, 2,377 hexamethylphosphoramide, 5,159

5,7,7,12,12,14-hexamethyl-l,4,8,11tetraazacyclotetradeca-4,14-dienej 5,249 5,7,7,12,14,14-hexarnethyl-l,4,8Jltetraazacyclotetradeca-4,ll-diene, 5,249 5,7,7,12,14,14-hexarnethyl-114,7,9, 11tetraazacyclotetradecane, 5,239 histidine, 5,220 hybrid polydentate ligands, 5,216 hydrazones, 5 , 198; 6, 180 hydrogenopyridine-2,6-dicarboxylic acid, 5,221 hydrogen sulfide, 5,166 hydrogen sulfite, 5, 154 hydroxamic acid deprotonated, 5,165 hydroxymethylenecamphor, 5,145 hydroxy oximes, 2,273 8-hydroxyquinoline, 5,214 image dyes photography, 6,112 imidates, 2,277 imidazoles, 5,81 imides, 5,165 imines, 5,96 isocyanato, 5, 103 isomerism, 1, 184 isoselenocyanato, 5, 103 isothiocyanato, 5, 103 p-ketoamines, 5,204 ketones, 5,141 liquid-liquid extraction, 1,544 low spin, 5,65 macrobicyclic ligands, 5,270 macrocycles, 5,226-275 addition reactions, 5,268 reactivity, 5,267-270 redox properties, 5,267 substitution reactions, 5,268 template synthesis, 5,226-231 magnetic properties, 1,274 magnetic susceptibility, 5,52 maleic acid, 5, 157 conformation, 2: 475 mandelic acid, 5, 159 mercaptoacetic acid, 5,213 p-mercaptoamine alkylation, 1,417 2-(2-mercaptoethyI)pyridine,5,212 2mercaptopyridine, 5,185 mercaptosuccinic acid, 5,213 methanesulfonate, 5,154 methionine, 5,220 rnethylthiohydroxarnate, 5. 165 methylthiohydroxamic acid, 5,214 2-methyl-8-thiomethylquinoline, 5,213 N-methylthiopyrrolidinone,5 185 mixed donor atoms, 5,187-226 mixed macrocycles, 5,257-266 I

Nickel(I1) complexes

monothio-P-diketones stability, 2, 649 1&naphthyridine, 5,79 nitrato, 5, 147 nitrilotriacetic acid, 5,219 nitrito, 5 - 147 nitroaminoguanidine, 2,283 nitro compounds, 5,141 nitrogen donor ligands, 5,70 a-nitroketones, 5,145 1-nitroso-2-naphthol, 5,214 2-nitroso-l-naphrhol,S, 214 nitrosyl, 5, 106 NMR, 5,56 octahedra1 amines, 2,28 electronic spectra, 5,49 magnetic properties, 5,60 oligonuclear magnetic properties, 5,284-287 organonitriles, 5, 105 organophosphorus, 5,159-165 oxalates, 5 , 158 magnetic properties, 5,282 oximates, 5,214 oximes, 2,26Y, 270,272 magnetic properties, 5,282 physicochemical studies, 2,272 oxygen-nitrogen chelates, 5,214 oxygeerr-sulfurchelates, 5,213 peptides, 2,768; 5,219 perchlorato, 5,152 phenanthraquinone, 5,146 phenanthroline, 5,80,162 N,N'-o-phenylenebis(salicylideniminato),5, 197 l-phenyl-l,2-ethanediamine, 5,71 phusphates, 5,154,161 phosphinates, 5.154 phosphine oxide, 5, 159 phosphines bidentate tertiary, 5,116 halo, 5 , 108 hydrido, 5,111 monodentate tertiary, 5,108 organometallic, 5,111 pseudohalo, 5, 108 tetradentate tertiary, 5, 125 tridentate tertiary, 5,125 phosphine sulfides, 5,185 phosphites: 5, 154 phosphonates, 5, 161 phosphoramide, 5,161 phosphorodithioates, 5, 174 phosphorus ligands, 5,10&131 phosphorus macrrxycles, 5,257-266 photoreactivity, 1,407 phthalocyanine, 5,271-275 phthakonitrile, 5,106 plant roots, 2, 962 polymethyIenebis(phenylthiourea), 5, 185 p o1y n u c1ea r magnetic properties, 5,276-287 polypyrazolylborate. 5, 102 porphyrins, 5,271-275 evolution, 2,961 1,2-propanediamine, 5,71 pseudooctahedral

NMR,5,57 pseudotetrahedral, 5,61 electronic spectra, 5,51 pyrazoles, 5,81 pyridine-2-acetic acid methyl ester, 5,214 pyridine-2,6-carbaldehyde

NickeI(I1) complexes

Cumulative Subject Index

reaction with o-aminobenzenethiols. 5 , 198 pyridine-2-carbaldchyde Schiff bases, 5, 198 pyridine-2-carboxamide, 5 . 106 pyridine-2-carboxylate, 5,106 pyridine-2-carboxylic acid, 5,221 pyridine-2,6-dicarboxylicacid, 5.221 pyridine N-oxide, 5,162 pyridines, 5,76 p-(2-pyridyl)alanine, 5,220 pyrocatechols, 5 , 145 quinones, 5 , 145 quinoxaline-2,3-dithiol, 5 , 182 reduction, 5 , 8 regular octahedral, 5,47 Schiff bases, 5,8Y, 188-204 salicylaldimines, 5 , 188 bidentate, 5 , 188 salicylates, 5 , 159 salicylideniminato ligands, 5,197 saturated polyaza macrocycles structure, 5,231-241 thermodynamics, 5,231-241 saturated tetraaza macrocycles, 5,231 saturated triaza macrocycles, 5,231 selenato, 5 , 152 selenium ligands, 5, 166186 semiquinones, 5,145 six-coordina te spectra, 5,60 stereochemistry, 5,3 spectra, 1,255 spectromagnetic properties, 5 , 4 5 4 8 squarate, 5,158 square planar, 5 6 7 square pyramidal electronic spectra, 5,19 squaric acid magnctic effects, 2,455 stibines bidentate tertiary, 5, 116 halo, 5,108 monodentate tertiary, 5,108 organometallic, 5 , 111 pseudohalo, 5,108 sulfato, 5,152 sulfoxides, 5,159-165,164 sulfur ligands, 5, 166186 sulfur macrocycles, 5,257-266 sulfur-nitrogen chelates, 9: 208-213 tartaric acid, 5 , 159 tellurium ligands, 5 , 166186 terpyridyl, 5,81 2,2,2-tet, 5,76 2,3,2-tet, 5 , 7 6 tetraarnminedinitro electronic and magnetic structure, 5.61 1,4,8,11-tetraazacyclotetradecane,5.238 tetraaza macrocycles, 2,909; 5: 95 tetradentate tripodal ligands, 5 , 131 tetragonal distortion, 5 4 8 tetrahedral, 5,61 electronic energy levels, 5 5 1 NMR, 5,57 6,7,13,14-tetramethyI-l,2,4,5,8,9,11,12octdazacyclotetradeca-~,7,12,1.4-tetraene, 5,256 1,4,8,1l-tetramethyl-l,4,8,9-te traazacyclotetradecane, 5,239 5,8,16,1Y-tetraphenyl-l,12-dithia-S1X,b,l9tetraphosphacyclodmcosane: 5,266 4,7,13,1dtetraphenyl-l, lO-dithia-3,6,13,16tetraphosphacyclooctadecane, 5,266 tetrasulfur tetranitride, 5,212

tetrathia rnacrocycles. 5 , 169 tetrazole. 5 - 86 thiazole, 5 : 82 thioacetamide, 5,185 thioacetic acid, 5 , 157 thiobenzoic acid; 5. 157 thiocarboxylic acids. 5,213 thiocyanides magnetic properties, 5,282 thio-1 .Miketoncs, 5, 1x3 thioethers, 5. 164 thiols, 5 , 166 thiopropionic acid, 5,157 thioscmicarbazides, 5,213 thiosulfate, 5 , 153 thiourea, jl 18.1 thioxanthates. 5 , 172 transition metal complexes hydroxy oximes, 5,215 1,5,7-triazabicyclo[4.4.0]dec-5-ene,5,275 triazines monodentate, 2, 196 1,2,4-triazole, 5,86 trihenzti[h,f: j]-1 .i,9-triazacyolododccanc, 5,241 tridentate Schiff bases, 5,221 tridentate tripodal ligands, 5 , 'I31 trigonal bipyramidal electronic spectra, 5,49 magnetic moment. 5.65 trigonal distortion. 5,47 trimethyl phosphate, 5 , 154 2,4,4-trimethyl-1.5,9-triazacyclododec-l-ene, 5 , 241 trinuclear binucleating ligands, 5,221-226 tropolone, 5,145 unsaturated macrocycles, 5 , 241-250 xanthates, 5. 172 Nickel(II1) complexes. 5,5,287-300 amides, 5,241 amines, 5,291) amino acids, 5: 290 arsines, 5,296 cyano, 5,290 dynamic voltammetry, 5, 288 EPRI 5,288 electronic structure, 5,288 fluorine; 5,296 macrocycles. 5,294 oximes, 5,291 oxygen, 5,296 peptides, 5,291; 6,647 phosphines. 5,296 SHAB theory, 2, 1040 sulfur ligands, 5,298 synthesis, 5,288 Nickel(1V) complexes. 5.5,287-280 amides, 5.291 amines, 5.290 amino acids, 5,290 arsines, 5,296 cyano, 5,290 electronic structure, 5,288 fluorine, 5.296 imine oximes, 2,273 macrocycles, 5: 294 magnetic properties, 1,273 oximes, 5,291 oxygen, 5,296 peptides, 5,291 phosphines, 5,246 sulfur ligands, 5,299 synthesis, 5,288 Nickel sepulchrate., 5,271

176

177

Cumulative Subject Index

Nickel-tin alloys electroplating, 6, 14 Nicotinamide zinc complexes, 5,952 hydride-transfer reactions, 5,954 Nicotinic acid cadmium complexes, 5,954 Nicotinic acid hydroxylase molybdenum, 6,662 Nicotinohydroxamic acid metal complexes with isonicolinohydroxamic acid, 2,506 Nigericin alkali metal complexes, 2, 973 alkaline earth metal complexes, 3,66 calcium uptake, 6,570 sodium transport, 6,554 Nine-coordinate compounds stereochemistry, 1,95-98 Niobate, heptafluorostructure, 1, 72 Niobate, hexafluorooxysodium salt structurc, 1 , 7 3 Niohate, pentafluoropcroxystructurc, 1, 76 Niobates, halo-, 3, 592,640 Niobates, pentabromooxo-, 3,627 Niobates, pentachlorooxo-, 3.627 Niobium, 3,585-686 atomic radius, 3, 588 coordination numbers. 3; 588 heterocycles, 3,639 nuclear fuel reprocessing Purex process, 6,954 oxidation states, 3,587 Purex process, 6,944 zinc compounds, 3. 639 Niobium, icosaethoxydecaoxyoctakis-, 1, 164 Niobium, pentatluorooxystereochcmistry, 1, SO Niobium, pentakis(dimcthplamin0)stereochemistry, 1,40 Niobium, pentakis(dimethy1carbamato)structure, 1,9@ Niobium, pentakis( tetrahydropyridy1)stereochemistry, 1,40 Niobium, tetrakis(2,2,6,6-tetramethyl-3.5-hep1 tanedione)stereochemistry, 1,94 structure, 1 , 9 3 Niobium, tris(diethy1dilhiocarbamato)oxystereochemistry, i . 82 structure, 1,83 Niobium, tris(oxa1ato)oxystereochcmistry, 1. 82 Niobium, tris(phcny1cncdithio)structure, 1,63 Niobium alanate, 3, 685 Niobium complexes alkyl alkoxy reactions, 2, 358 amides, 2, 164 properties, 2, 168 synthesis, 2, 165 applications, 6, 1014 carbamic acid, 2,450 clusters, 3, 672,673,675 hexarnethylhenzene ligands, 3,669 cyanides synthesis, 2 , 9 p-dinitrogen, 3, 418 fluoro transfer reactions, 3- 593

Niobium(1V) complexes

imido synthesis, 2, 168 mixed valence, 3.685 non-integral oxidation states, 3,667-677 octahedral bonding, 3,676 octahedral clusters, 3,670 electronic spectra, 3, 676 hydrates, 3. 671 iodides, 3, 677 ionic halides, 3, 671 magnetism, 3.676 neutral binary halides, 3, 671 oxidized. 3,673 standard potentials, 3,674 oxidation states, 3, 587 pentahalo, 3; 589 phthalocyanines, 2,865 polypyrazolylborates, 2,248 porphyrins, 2,824 pseudohaiides, 2,229 reactions with alkynes thrcc-mcmbcrcd mctallacyclcs, 3,661 telranuclear clusters, 3, 670 triangular clusters, 3,667 solvolysis, 3, 668 Niobium( -111) complexes, 3,684 carbonyl. 3,684 Niobium(-I) complcxcs, 3,684 carbonyl. 3. 684 Niobium(0) complexes. 3,683 Niobium(1) complexes, 3,67%683 alkenes: 3,682 carbonyl, 3,680 carbonylcyclopentadienyl, 3,682 dienes. 3,682 phosphines, 3,679-683 Niobium(1T) complexes, 3,677-679 dihalo. 3, 667 Niobium(II1) complexes, 3,655-667 acetylacetone, 2,376 activation reactions, 3,660 alkoxa, 3,664 carboxylatotrihalo, 3,664 dialkylphosphido, 3,665 p-diketonatotrihalo, 3,664 dithiocarbarnato, 3,664 halo anionic, 3,655 nitrenes, 3; 665 organometallic. 3, 665 oxalato, 3 ; 666 pseudohalo, 3,666 sulfato, 3,666 ihiolato, 3,664 trihalo, 3,655 neutral adducts, 3,656 solvolysis. 3,663 Niobium(1V) complexes, 3,639-655 activation of small molecules, 3,654 alkoxo, 3?649 alkylamido, 3,652,653 carboxylato, 3,650 chalcogeno. 3, 654 clusters. 3,667 dialkyldithiocarbamato, 3,651 dialkylphosphido, 3,652 [Mikctonato, 3,650 ESR,3,645 halovxv, 3, 646 haloseleno, 3,646,647 halotelluro. 3,646 halothio, 3,616.647

Niobium(1V) complexes hydrazido, 3,653 iminoethyl, 3,653 magnetic behavior, 1,271 nitrido, 3,654 phthalocyanines, 3,653 poly( 1-pyrazolyl)borato, 3,653 porphyrins, 3,653 dioxygen adducts, 2,325 pseudohalo, 3,645 silylamido, 3,653 tetrahalo, 3,639 neutral adducts, 3, 640 solvolysis, 3,649 thiolato, 3,651 rhiophosphato, 3,652 trihalo neutral adducts, 3,657 Niobium(V) complexes N-acetamido, 3,622 alkoxo, 3,601 oxygen ligands, 3,604 properties, 3,602 reactions with P-diketones, 3, 603 reactions with nitrogcn ligands, 3,603 reactions with Schiff bases, 3,605 structure, 3,601 alkoxohalo, 3,603,607 adducts, 3,606 alkoxooxo, 3,632 N-alkyl-N-nitrosohydroxylaminato.3,623 amido, 3,608 structure, 3,608 synthesis, 3,608 amidooxo, 3,634 amidopentahalo, 3,595 arsenato, 3,638 azido, 3,619 bromo anionic, 3,593 bromooxo, 3,625 carboxylatohalo, 3,606 carboxylatooxo, 3,633 chloro anionic, 3,593 chlorooxo, 3,625 chloroperoxo, 3,636 cyano, 3,623 N,N'-dialkylacetamidinato, 3, 622 dialkylamido, 3,609 dialkylcarbamato, 3,611 N,N-dialkyldithiocarbamato, 3,606 dialkyldithiophosphato, 3,639 difluorophosphinato, 3,639 b-diketonatooxo, 3,632 dimethyl sulfoxidc, 2,488 dithiocarbamatohalo, 3,647 fluoro anionic, 3,591 fluorooxo, 3,625 anionic, 3,626 halo arsenic donors, 3,600 phosphorus donors, 3,600 halooxo, 3,625-632 neutral adducts, 3,628 nitrogen donor adducts, 3,630 haloperoxo, 3,636,637 halophosphonato, 3,607 halo-8-quinolinol, 3,606 haloseleno, 3,626 halothio, 3,626 halothiolato, 3,607 hexafluoroperoxo, 3,636

Cumulative Subject Index iodo anionic, 3.593 iodooxo, 3,625 isocyano, 3,623 isoselenocyanato, 3,624 isothiocyanato. 3,624 isothiocyanatooxo, 3,634,635 metaphosphato. 3,639 mixed alkoxo. 3,602 mixed halo. 3,594 mixed pentahalo, 3,591 nitrato, 3,638 nitrenes, 3,613 reactivity, 3,616 structure, 3,513 synthesis, 3.613 nitrido, 3,620,621 nitrogen-containing insertion products, 3,623 orthophosphato. 3,639 OXO,3,635-639 oxygen abstraction reactions, 3,631 pentabromo, 3.590 pentachloro, 3,590 pentadialkylarnido cyclometallation, 3, 611 reactivity, 3,610 pentafluuro, 3,589 pentahalo, 3 . 5 S 5 9 1 amines,'3:'596 applications, 3,591 arsenic donors, 3,599 arsine oxides, 3,595 dialkyl esters, 3, 595 ethers, 3,595 imidazoles, 3,596 ketones, 3,595 neutral adducts, 3,594 nitrogen complexes, 3,597 nitrogen donors, 3,596 phosphines, 3,595 phosphorus donors, 3,599 Schiff bases, 3,596 selenium ligands, 3.596 solvolysis, 3,600 sulfur ligands, 3: 596 tellurium ligands, 3,5% pentahalonitrido, 3,596 pentahalothiocyanato, 3,596 pentaiodo, 3: 590 peroxo, 3,635,636 peroxo acids, 3,635 phosphato, 3* 638 phosphinato, 3,639 phosphineiminaro, 3,619 phosphonato, 3,639 porphyrins, 3,620 pyrazolylborato, 3,622 seleno, 3,638 selenocyanato, 3,624 sulfato, 3,638 tetrachloro with phosphorus donors, 3,642 tetrahalo amines, 3,641 oxygen ligands, 3,643 sulfur ligands, 3,643 with arsenic donors, 3, 642 thio, 3,635639,638 N-thioacstamido+3,622 thiocarbamato, 3,634 thiocyanato, 3,624 trihalooxo solvolysis, 3,632

178

179 Niobium fluoride NbJzo structure, 1,28 Niobium isopropoxides synthesis electrochemistry, 2,337 Niobium pentaalkoxides physical properties, 2, 347 Niobium selenide, 3,685 Niobyl phosphoniobate, 3.685 Nitrate reductase, 3, 1334 assimilatory, 6,663 Chlorella vulgaris structure, 3, 1438 dissimilatory, 6,663 ESR, 6,664 Escherichia coli .structure, 3, 1438 Nitrates asymmetric bonding ligands, 2,419 Escherichia coli respiration, 6,715 fertilizers, 6, 717 ligands solvents, 2,414 metal complexes, 2.423 reduction oxomolybdoenzymes, 3,1437; 6.17 Nitration copper(I1) acetylacetonate, 6,203 copper(I1) nitrate in, 1, 421 Nitrenes, 2, 114 Nitric acid metal extraction from. 1,540 Nitric oxide coordinated reactivity, 2, 109-115 IR spectroscopy, 2, 101 insertion reactions transition metal complexes. 2, 115 ionization potcntial, 2, 101 molecular orbital diagram. 2, 101 reduction by carbon monoxide, 6,276 reduction by carbon monoxide catalysts, ruthenium complexes, 6,269 Nitrido species, 2, 118 Nitrification, 6,717.727 Nitriles a-amino prebiotic systems, 6 *871 hydration catalysts, 6,304 hydrogenation catalysts, rhodium complexes, 6,242 imido metal complexes synthesis from, 2,167 metal complexes, 2,261-266 displacement reactions, 2.264 formation, 2,264 IR spectra, 2, 264 LCAO-MO calculations. 2 . 261 nitrido formation, 2,265 nucleophilic addition. 2, 265 reactions, 6,449 structure, 2,262 polynuclear complexes structure, 2,262 a,@-unsaturated metal complexes, 2.263 Nitrite reductases, 6, 698 denitrifying, 6, 727

Cumulative Subject Zndex

Nitrosomonas europaea

dissimilatory, 6,726 reduction to ammonia, 6,725 respiration, 6,717 Nitrites metal complexes, 2,423,431 reduction, 6,725 Nitnto compounds isomerization, 1,465 Nitro complexes, 2,423 Nitro compounds arcncs reduction, 6,292 carbonylation catalysts, palladium complexes, 6,290 catalysts, rhodium complexes, 6,276 hydrogenation catalysis, ruthenium complexes, 6,233 Nitrodehalogenation 1,3-diketonemetal complexes, 6,203 Nitrogenase, 6,718,719 dinitrogen tungsten complexes, 3,1011 dioxygen sensitivity, 6,725 iron-molybdenum cofactor, 3,1425; 6,721 structure, 6,721 iron protein, 6,720 mechanism, 6,722,723 molybdenum, 6,657,681 molybdenum bridging to iron, 3, 1379 molybdenuwiron protein, 6,720 reactivity, 6,722 vanadium(I1) complexes, 3,473 Nitrogen compounds oxidation copper catalysts, 6,394 Nitrogen-containing ligands, 2, 10C-151 Nitrogen cycle, 6,717-728 Nitrogen fixation, 1,29; 6,717,718 genetics, 6,720 Klebsiella pneumoniae, 3, 1425 molybdenum, 6.657 oxomolybdoenzymes, 3, 1437 prebiotic systems, 6, 872 symbiotic molecular biology, 6,720 Nitrogen ligands, 2,23,18%238,261-266,269 classification, 2,24 prochiral, 2,24 Nitrogen tribromide stereochemistry, 1,36 Nitrogen trichloride stereochemistry, 1, 36 Nitrogen trifluoride oxide metal complexes, 2,497 stereochemistry, I , 36 Nitrogen trihalides stereochemistry, 1,36 Nitrogen triiodide stereochemistry, 1,36 Nitro ligands metal complex catalysts oxidation, 6,372 Nitroprussides, 2,106; 4,1189 reactions, 2, 114 reduction, 4, 1206 Nitroso compounds aromatic carhunylation, 6,276,279 o-hydroxy metal complexes, 6,84 C-Nitroso ligands metal complexes, 2,269 Nitrosomonas europaea

Nitrosomonas europaea

Cumulative Subject Index

ammonia oxidation, 6,727 Nitrosyl clusters, 2, 116 bonding, 2, 116 I R spectroscopy, 2,116 15N NMR, 2,116 reactions with electrophiles, 2, 117 reduction with hydrogen, 2,117 substitution reactions, 2, 118 Nitrosyl complexes. 2,100 bent bonds, 2,101 iridium reaction with carbon monoxide; 2. 113 metal hydroxides chemistry, 2,356 transition metals, 2, 101-118 bent, 2,102 bent mononuclear, IR spectroscopy, 2,103 bridging, 2, 107 carbonyl, substitution kinetics. 2 , 106 decomposition, 2, 111 electrophilic addition, 2, I l l linear, 2,102 mononuclear, bonding, 2! 101-108 mononuclear, IR spectroscopy, 2,103 mononuclcar, structure, 2, 101-108 nucleophilic addition, 2, 109 oxidative processes, 2 , 112 preparation, 2,108 reductive processes, 2,114 spectroscopy, 2,121 square pyramidal, 2, 105 Nitrous acid in plutonium extraction Purex process, 6,948 Nitroxides 1,3-diketone metal complexes, 2 >388 Noble gas compounds oxo acids, 3,320 Noble gas(I1) compounds, 3,313,319 Noble gas(1V) compounds, 3,313,320 Noble gas(V1) compounds, 3, 315,320 heptafluoroxenate, 3, 315 Nuble gas(VII1) compounds, 3,316 Noble gases, 3,311-321 carbon ligands, 3,316 coordination compounds, 3,312 coordination geometry. 3,312 halogen ligands, 3, 313-316 nitrogen ligands, 3,319 oxidation states, 3, 312 oxygen ligands, 3,319 selenium ligands, 3,321 sulfur ligands, 3,321 Nocardamine, 6,678 Nomenclature, 1,109-134 additivc, 1, 110 aminc metal complexcs, 2,25 binary, 1, 110 compositional, 1, 110, 111 parent-substitutive, 1, 110 Nonactin alkali metal complexes, 3 , 6 4 potassium complexes, 2,973 3,8-Nonadienoic acid synthesis by carhonylation, 6,288 Nonametallic complexes, 1, 164 confacial bioctahedron, 1, 164 double cubanes, I , 165 monocapped square antiprism. I , 165 plymetallic anions, 1, 165 tricapped trigonal prism, 1, 165 Non-blue copper oxidases, 6,700

Nonradiative transitions photochemistry, 1,396 L-Nopinoquinone dioximes metal complexes, 2,271 Norbornadiene carbonylation catalysts, palladium complexes, 6,288 hydrocyanation catdysrs. palladium complexes, 6,298 hydrogenation catalysts, iridium complexes, 6, 246 N orhornene hydrocyanation catalysts, palladium cornplcxcs, 6,298 oxid ation catalysts. palladium-nitro complexes, 6,373 Norvaline metal complexes prebiotic systems, 6,872 NQR cadmium complexes, 5,926 zinc complexes, 5.926 Nuclear fuel dccanning and dissolution, 6, 927 oxidcs reprocessing, Purex process, 6,954 preparatirm, 6 . 4'19-925 reprocessing, 6, 885 Nuclear fuel cycle: 6.881-996 thermal reactor; 6.883 Nuclear fuel waste immobilization, 6,961 Nuclear magic bullets radiotherapy, 6,996 Nuclear magnetic resonance spectroscopy 1 3 c

amine metal complexes, 2,25 cadmium complexes, 5,926 15N

amine metal complexcs, 2 , 2 5 redox potentials and, I , 499 zinc complexes. 5, 926 Nuclear reactors breeding gain, 6,885 Nuclear relaxation rates lanthanide shift reagents, 3, 1103 applications, 3: 1103 Nucleating agents in photographic development, 6, 99 Nucleation solid state reactions, 1, 464 Nucleic acid bases prebiotic systems, 6, 873 zinc conrplexes, 5.957 Nucleic acids bases, 2,976 metabolism. 6,673 metal complexes. 2,796,976-980 biology. 6,546 geochemistry, 6, 867 nucleotide transfer, 2,976 phosphate transfer, 2,976 reactions osmium tetroxide, 4,591 Nucleophilic attack catalysis transition metal complexes, 6, 231 Nucleosides binding sitcs, 2,971 complexes linkage isomers, 1,186 metal complexes. 2*976

1so

Cumulative Subject Index

181 nomenclaturc, 2,976 reactions osmium tetroxide, 4,591 structure, 2,976 zinc complexes, 5,956 Nucleotide cyclases activation magnesium ions, 6,584 Nucleotides binding sites, 2,977 complexes linkage isomers, I , 186 metal complexes, 2,796,976

coc 7

4

biology, 6,546 nomenclature, 2,976 ordering alkali metal ions, 6,562 polymerization prebiotic systems, 6,873 reactions osmium tetroxide, 4,591 structure; 2,976 Nylon-12 synthesis, 6,232 Nystatin metal complexes, 2, Y73

Nystatin

Octadienes cyclic hydrogenation, 6,248 Octahedral complexes Cis

angular distortion, 1,56 bond-length distortion, 1.57 repulsion energy coefficients, 1,33,34 stability, 1,53 structure, 1,92 distortion, 1,58 Octametatlic complexes, i , 162 cube, 1,162 dicubane, 1,163 [ M a 6 ] core, 1, 162 planar octagon, 1,162 tetracapped tetrahedron, 1, 163 Octamolybdates, 3, 1054 isomerization, 3,1032 I-Octene epoxida tion cobalt-nitro complex cataiysts, 6,373 hydroformylation catalysts, rhodium complexes, 6,263 hydrogenation catalysts, rhodium complexes; 6,243 oxidation rhodium(II1)-nitro complex catalysts, 6,374 Odta -see Acetic acid, octamethylenedianinetetraOil energy resource, 6,488 Oklo phenomcnon, 6,894 01iv in e structure, 6,856 One-dimensional complexes, 6,134 One-dimensional conductors, 6, 134 One-dimensional metals Krogmann salts, 6, 136 Optical isomerism cobalt ammines, 1, 12 history, 1,180 Optical recording systcms, 6, 126 Optical resolution amine metal complexes, 2,25 Oral contraceptives iron deficiency, 6,764 Orbital angular momentum quenching, 1,262 f-Orbital systems crystal field theory, 1,224 Ore formation metal complexes organic ligands, 6, 868 metal sulfides, 2,525 Organic ligands metal complexcs geochemistry, 6, 856-870 Organoantimony compounds bond lengths and angles, 3,258 Organoarsenic compounds, 3,239 geochemistry, 6,868

Organoarsonates mctal complexes, 3, 1053 Organocobalt compounds, 6,638 bond dissociation energy, 6,639 cobalt-carbon bond cleavage, 6,638 heterolytic, 6, 639 Organoiron, 4,1181 Organoiron(1) complexes, 4,1203 Organolead compounds, 3,210 structure, 3,212 Organolithium compounds asymmetric addition to, 6,220 reactions, 1,447 Organornagnesium compunds asymmetric addition to a$-unsaturated carbonyl compounds, 6,220 reactions, 1,447 Organometallic complexes solubility in organic solvents, 2, 1014 Organophosphine ligands, 2,990 Organophosphonates metal complexes, 3, 1053 Organophosphorus acids lanthanide complexes solvent extraction, 6,795 metal complexes solvent extraction, 6,792 solvent extractions base metals, 6,792 beryllium, 6>795 rare earths, 6,794 thorium, 6,798 uranium, 6,796,797,798 Organophosphorus sulfides metal complexes, 2,641 OrganosuIfur compounds reactions metal catalysis, 6,456 Organotin complexes, 3,210 hydroxylamines, 2,507 polyketoncs, 2,400 structure, 3,212 Organotin(1V) compounds platinum(0) complexes. 2, 16 reactions with nickel Schiff base complexes, 5, 196 Ornithine copper(I1) complexes reactions, 1,419 metal complexes, 2,750 Ornithine, N-hydroxyferrichromes, 6,676 Orotic acid metal complexes, 2,797 Orthoperrhenates. 4:198 Orthovanadates, 3,1025 Osmates dioxo, 4, S K I tluorohalo, 4,610 Osmium coordination numbers, 4,523

182

183

Curnulalive Subject Index

history, 4,522 oxidation states, 4,522 reviews, 4,522 Osmium, pentachloronitrilostereochemistry, 1,50 Osmium, pentakis(trifluor0phosphine)NMR, 1,41 Osmium, quinuclidinetetraoximestereochemistry, 1.44 Osmium, tetrachloronitridotetraphenylarsenatc stereochemistry, 1.44 Osmium, tris( 1,lO-phenanthroline). structure, 1,64 Osmium complcxcs, 4.515L619 alkaloids, 4, 569 alkoxo, 4,596 amides synthesis, 2, 166 amidines, 2,276 chelating ligands, 2.204 amido, 4,557 amines, 557 bidentate, 4,530 monodentate, 4 , 3 0 amino acids, 4,602 8-amino-7-hydroxy-4-methqlcoumarin, 4,569 2-aminomethylpyridine, 4,534 ammines, 4,528 aqua, 4,529 binuclear, 4, 530 carbonyl, 4,529 halo, 4, 529 hydroxo, 4,529 phosphines, 4,529 substituted, 4,529 triflato, 4,529 unsubstituted, 4,528 antimony ligands, 4. S69-579 applications, 6, 1018 aqua, 4,579 arginine, 4,602 arsenic ligands. 4, 569-579 arsines bidentate, 4, 578 polydentate, 4, 579 azido, 4,565 benzamido, 4,616 benzotriazole, 4,568 biguanides, 4,567 binuclear dinitrogen-bridged, 4.556 oxo-bridged, 4.593 bipyridyl, 537 cyclic voltammetry, 4. 541 differential pulse polarography, 4,541 dimers, 4,541 electronic spectra, 4,540 polymers, 4,542 redox properties, 4,540 spectroscopy, 4,540 surface-enhanced Raman spectra, 4,540 2,2’-bipyrimidinyl, 4,537 2,2’-biquinolinyl, 4,542 bis(2,6-di(2’-quinolyl)pyridine), 4,544 boranes, 4,616 bromo, 4,613 2,3-butanediimine, 4,533 carbohydrates. 4.602 carbonates, 2,448 carboxylates, 4. 600 catalysts hydrogenation, 6,250

Osmium complexes

catecholates, 4,597 chloro, 4,613 cyanides, 4.525 dialkyl sulfides, 4,603 1,4-diaza-I,3-butadiene,2,210 diazenide, 4,551 diethylselenocarbamato, 4,609 djisopropyldithiophosphate, 4,608 fi-diketonates, 4,596 4-p-dimelhylaminoanilino-3-penten-2-one. 4,569 dimethyl sulfoxide, 4,602 dinitrogen, 4,554 dioxvgen, 4,596 disulfur. 4,603 dithioacctylacetonates, 4,606 dithiocarbamato, 4, 604 dithiocarboxylates, 4,607 dithiolene, 4,606 ethylenediamine, 4,530 deprotonated, 4,531 fluorides, 4,609 fulminates, 4, 526 glycine, 4,602 Group IV donors, 4,524,525 Group V donors, 4,524 Group VI donors, 4, 524 Group VI1 donors, 4,524 halogen ligands, 4,609-615 he teronuclear dinitrogen-bridged, 4,556 histidine, 4,602 homogeneous catalysis, 4,524 hydrazine, 4.556 hydrides, 4,615 hydrogen, 4,615 hydrosulfides, 4,600,603 hydroxo, 4,579 hydroxybenzamido, 4,616 hydroxylamine, 4,557 2-hydruxypylidine, 4,534 imidazolidint-2-selones, 4,609 imidaznlidine-2-thiones,4, 607 imides structure, 2, 175 imido, 4,557 iodo, 4,613 isonicotinamide, 4,534 isonicotinic acid, 4,534 ketones. 4,598 lysine, 4, 602 mercury ligands, 4,525 N heterocycles, 4,533-544 nitrato. 4,598 nitrido, 4,56&565 nitriles, 4, 566 nitro, 4,588 nitrogen ligands, 4,527-56’3 nitrosyl. 4,544-551 ammines, 4,546 arsines, 4,547 azido, 4.546 cyano, 4,546 halides, 4,546 nitro, 4,546 phosphines, 4,547 reaction with carbon monoxide, 2 , 113 stibines, 4,547 X-ray structure, 4, 548 octaethylporphyrin, 4,617 oxo, 4,579-596 alkenes, 4,585, 587 alkynes, 4,587 dienes, 4,586,587

Osmium complexes diols, 4,585 oxidation catalysts, 6,356359 trienes, 4, 586 oxo esters nitrogenous bases, 4,585 oxyamino, 4,551 oxygen-containing ligands, 4,579-603 peroxo, 4,596 l,lO-phenanthrolinc, 4,537 electronic spectra, 4, 540 redox properties, 4, 540 spectroscopy, 4,540 2-(phenylazo)pyridine, 4,535 phosphates, 4,5Y9 phosphineaminato, 4,568 phosphinciminato, 4,568 phosphines bidentate, 4,578 halo, 4,572 polydentate, 4,579 phosphorus ligands, 4,569 phosphorus trihalides, 4, 575 phthalocyanines, 2,866; 4,618 picoline, 4,534 piperidine, 4,535 polymers, 4,524 polypyridyl, 4,537 porphyrins, 2,829; 4,617 proline. 4,602 pseudohalides, 2,230,231; 4,565 pyrazine, 4,535 pyrazine-bridged binuclear, 4,536 pyridazine, 4,535 pyridine, 4,533 2-(2'-pyridyl)quinoline, 4,542 pyrimidine, 4,535 selenido, 4, 609 selenium-containing ligands, 4?(io9 selenoether, 4,6tr!) strychnine, 4, 569 sulfamato, 4,616 sulfates, 4,599 sulfides, 4,599, 603 sulfur-containing ligands, 4,603-608 sulfur dioxide, 4,606 superoxo, 4,596 tellurium-containing ligands, 4,609 terpyridyl, 4,542 tertiary arsines, 4,576 halo, 4,576 hydrido, 4,576 tertiary phosphates, 4,575 tertiary phosphines, 4,57&579 dihydrido, 4,570 hexahydrido, 4,571 hydrides, 4,570 monohydrido, 4,570 pentahydrido, 4,571 polynuclear hydrides, 4,572 tetrahydrido, 4,571 trihydrido, 4,571 tertiary stibines, 4,577 tetrahydroborates, 4,616 thiazolidinethiones, 4, 607 2-thioamidopyridine, 4, 617 thiocarbamateu, 4,604 thiocarboxylates, 4,607 thiocyanato, 4,565 thio-P-diketonates, 4,606 thiaethers, 4,603 thiolates, 4,607 thiones, 4,607

Cumulative Subject Index thionitrosyl. 2 , 119; 4,552 thionitrosyl chloride, 4,552 thiourea, 4,608 tin, 4,526 triazines chelating ligands. 2,204 triflates, 4,600 trithiocarbamato, 4.604 tropolonates, 4,597 d-tuhocuramine, 4,544 Osmium(-11) complexes phosphorus trihalide, 4,575 Osmium(C1) complexes phosphorus trihalide, 4,576 tcrtiary phosphates, 4, 575 OsmiumjI) complexes cyanides. 4?525 Osmium(I1) complexes ammines halo, 4,529 biguanides, 4,567 binuclear oxo-bridged, 4: 594 bipyridyl, 4,538 spectroscopy, 4,538 bis(thionitrosyl), 4,552 cyanides, 4,525 inelastic clectron-tunelling spectroscopy, 4, 525 vibrational spectra, 4 , 525 p-diketonatesl 4,597 dinitrogen amines, 4 +554 ammines, 4,554 arsines, 4,555 phosphines. 4,555 ethylenediamine, 4, 531 deprotonated, 4,532 monothionitrosyl, 4,553 nitriles, 4,567 octacthylporphyrin, 4.617 1,lO-phenanthroline, 4,538 spectroscopy, 4,538 phosphines halo, 4, 572 phosphorus trihalides, 4,576 phthalocyanine, 4: 618 polymerization electrochemistry. 1.488 pseudohalides. 4,566 pyrazines, 4,536 pyridazines, 4,536 pyridines, 4,533 pyrimidines. 4,536 sulfides, 4, SY9 terpyridyl. 4,542 redox properties, 4,543 speotroscupy, 4.542 tertiary phosphates, 4,575 thiourea, 4,608 Osmium(II1) complexes ammines halo, 4,529 benzotriazole, 4,568 biguanides. 4>568 binuclear oxo-bridged, 4.594 hipyridyl, 4,538.541 electronic spectra, 4,541 electron transfer, 4.539 polarography, 4,539 redox properties, 4,539,541 spectroscopy. 4,538 cyanides, 4,526

184

185 a-diimines, 6 , 189 $-diketonates, 4,597 dinitrogen amines, 4,555 ammines, 4,555 dithiocarbamates, 4,604 ethylenediamine, 4, 531 deprotonated, 4,532 halides, 4,613 magnetic hehavior, 1,273 nitriles, 4,567 octaethylporphyrin, 4,618 lJ0-phenanthroline, 4,538,541 electronic spectra, 4,541 electron transfer, 4,539 polarography, 4,539 redox properties, 4,539,541 spectroscopy, 4,538 phosphines halo, 4,573 phosphorus trihalides, 4,576 phthalocyanine, 4, 619 pseudohalides, 4,566 pyrazines, 4,536 pyridazines, 4,536 pyridines, 4,534 pyrimidines, 4,536 sulfides, 4,599 terpyridyl, 4,543 redox properties, 4,543 tertiary phosphates, 4,575 thioethers, 4, 603 thiolates, 4,607 thionitrosyl, 4,553 thiourea, 4,608 Osmium(1V) complexes ammines halo, 4,529 bipyridyl, 4,539,541 cyanides, 4,526 $-diketonates, 4,597 dinitrogen amines, 4,555 ammines, 4,555 dithiocarbamates, 4, 604 ethylenediamine, 4,531 deprotonated, 4,532 fluorides, 4,609,610 halides, 4,613 magnetic behavior, I, 272 nitrido, 4,560 binuclear, 4,563 bonding, 4,564 polynuclear, 4,565 structure, 4,544 trinuclear, 4, 564 octaethylporphyrin, 4,618 oxo, 4,580 p-oxo, 4,594 lJ0-phenanthroline, 4,539.541 phthalocyanine, 4,619 pseudohalides, 4, 566 pyridines, 4,534 sulfides, 4,599 terpyridyl, 4,543 tertiary phosphates, 4, 575 thioethers, 4,604 thiolates, 4,607 triazenido, 4,565 Osmium(V) complexes bipyridyl, 4,541 ethylenediamine deprotonated, 4,533

Curnulutive Subject index fluuru, 4.611 halides, 4,615 imino, 4,558 magnetic behavior, 1,272 nitrido. 4,560 oxo, 4,580,595 I,lO-phenanthroline, 4,541 terpyridyl, 4,543 Osmium(V1) complexes biguanides, 4,568 binuclear oxo-bridged, 4,594 halo: 4,594 bipyridyl, 4,541 cyanides, 4,526 dioxo, 4,581 ethylenediamine, 4,531 deprotonated, 4,533 fluorides, 4.611 hexaoxo, 4,580 imino, 4,558 magnetic behavior, 1,272 nitrido, 4, 560 halo, 4,561 octaethylporphyrin, 4,618 oxo, 4,58U, 595 oxo esters, 4,584 pentaoxo, 4.580 I.l@phenanthroline, 4,541 phthalocyanine, 4: 619 sulfides, 4,599 terpyridyl, 4,543 tetraoxo. 4, 580 thiourea, 4,608 trioxo, 4: 580 Osmium(VI1) complexes hisirnido, 4: 559 fluorides, 4,612 hexaoxo, 4,588 imido, 4,558 monuoxo, 4,588 oxo halo, 4,596 pentaoxo, 4,588 tetrakisimido, 4,560 tetraoxo, 4+588 trisimido. 4,560 Osmium(VII1) complexes dioxo, 4,593 fluorides, 4,612 hexaoxo, 4,588 imido properties, 2, 170 monooxo, 4,593 nitrido, 4,562 oxo, 4,588 aqua, 4,591 halo, 4,592 hydroxo. 4,591,596 pentaoxo, 4,588 tetraoxo, 4,588 trioxo, 4,593 Osmium tetroxide, 4,588 adducts nitrogen donors, 4,592 biological tissue, 4,591 electrochemistry, 4,589 IR spectra, 4, S89 oxidation alkenes, 4 590 polarography, 4,589 preparation, 4,589 properties, 4,589 reactions, 4,590

Osmium tetroxide

Osmium tetroxide

Cumulative Subject Index

solutions, 4,589 spectroscopy, 4,589 Osmyl complexes cyano, 4,583 halo, 4,583 nitrogen donor ligands, 4,583 oxo, 4,584 halides, 4,584 oxy, 4,583 thioether, 4,584 Osteocalch, 6,597 Ovatransferrin iron, 6,634 Overvoltage, 6,3 Ovotransferrin, 6,669 amino acid sequence, 6,669 l-Oxabicyclo[3.3.0]octa-3,6-diene-2,4-dione, 3,6diphenylsynthesis by carbonylation, 6,274 l-Oxa-4,6-dithia-5-bismocane, 5-phenyl-, 3,285 l-Oxa-4,6-dithia-5-stibocane, 5-chloro-, 3,265 Oxalic acid dimethyl ester synthesis, 6,370 metal complexes, 2,443 geochemistry, 6,867 naturally occurring, 2, 962 photolysis, 2,446 minerals weathering, 6,868 Oxalic acid, dimethylmetal complexes, 2,444 Oxaloacetate decarboxylase sodium ions activator, 6,559 Oxaloacetic acid decarboxylation metal catalysis, 6,453 metalcomplexes, 1,427 tautomerism metal catalysis, 6,473 Oxamide, N,N'-dibenzyldithiothermography, 6,122 Oxamides metal complexes, 6,177 Oxamidoxime in gravimetry, 1,533 Oxaporphyrins, 2,850 Oxaziridines metallo synthesis, 2,798 2-Oxazolidinethione photography diffusion transfer process, 6,102 Oxazolines a,p-unsaturated asymmetric addition, 6,220 Oxidases concerted electron transfer, 6,683 Oxidation alcohols chromium-oxo complexes, 6,351 biological, 6,325 catalysts hydrogen peroxide, 6,334 nitro complexes, 6,372 by ferrates, 6,356 heterolytic metal catalyzed, 6,324 homolytic metal catalyzed, 6,324 hydrocarbons

chromium-perouo complexes, 6,334 palladium-oxo compounds, 6,361-371 vanadium-peroxo complexes, 6,333-396 industrial, 6,327-330 iridium catalysts, 4,1158 manganese catalysts, 6,375 by manganese dioxide, 6,356 metal complexes, 6,317-400 metal peroxides, 6,330-350 oxo-metal complex catalysts, 6,35&361 by permanganate, 6,355 surface coppcr(I1) complexes, 5,718 Oxidation-reduction potcn tials non-aqueous solvents. 1,27 Oxidation state nomenclature, I , 120 Oxidative addition reactions, 1,282 catalysis transition metal complexes, 6,230 mercury to transition metals, 2 , 3 platinum hydride complexes synthesis, 5,355 Oxidative cleavage cohalt catalysts, 6,388 Oxidative coppcring o-hydroxydiarylazo compounds, 6,54 Oxidative coupling palladium catalysts, 6,371 Oxidative dehydrogenation coordinated imines, 1,455 Oxides bridging ligands, 2,301 double, 2,302 triple, 2,302 metal complexes, 2,295-310 N-Oxides metal complexes, 2,487-501 F-Oxides metal complexes, 2,487-501 Oxidoreductases zinc, 5, 1002 Oximes amino metal complexes, 2,274 azo metal complexes, 2,274 cyclization reactions, 2: 905 hydroxy chelating rcsins, 6,825 Rotation, 6,782 metal complexes, 2,273 o-hydroxypalladium complexes, solvent extraction, 6, 807 separation of nickel and cobalt, 6,801 solvent extraction. copper and nickel, 6,799 lithium salts reactions, 6,218 metal complexes, 2,269,797; 6,184 ambidentate, 2,270 clathrochelates, 2,272 encapsulating, 2,272 gas chromatography, 1,528 structure;2,269 nickel complexes, 5 , 5 suhstituted metal complexes, 2,272 Oxinates gravimetry, I , 527 P-Oxo acids decarboxylation metal catalysis, 6,453

186

187

Cumulative Subject Index

Oxo cations, 2,296 Oxo complexes catalysts oxidation, 6,35&361 structure, 6,324 Oxomolybdoenzymes. 3.1436, 1437 EPR spectra, 3,1437 Oxovanadium(1V) complexes cupferron ESR spectra, 2,511 Oxovanadium(V) complexes aqueous solution, 3, 1026 Oxyanions coordinated single crystal X-ray 2,419 structure, 2,419 coordination number, 2,414 five-coordinate, 2,429 four-coordinate, 2,429 four-to-twelve-coordinate, 2.429 ligands classification, 2,415 IR spectroscopy, 2,420 Raman spectroscopy, 2,420 metal complexes, 2,413-432 EXAFS spectroscopy, 2,422 IR spectroscopy, 2,421 profile analysis of X-ray powder data using synchrotron radiation, 2,422 Raman spectroscopy, 2,421 1 7 0 NMR. 2.422 nine-coordinate, 2,430 one-coordinate, 2,422 polyatomic ligands, 2,413 thermochemical radii, 2,414 polynuclear ligands, 2,417,431 rigid geometry ligands, 2,414 seven-coordinate, 2.430 six-coordinate, 2,429 size ligands, 2,414 stoichiometry, 2,418 ten-coordinate, 2,430

Oxytyrosinase

thrcc-coordinate, 2,427 twelve-coordinate. 2,430 two-coordinate, 2,425 weak donor properties, 2,414 Oxycarbonyiation palladium catalysts, 6,368-370 Oxychlorination palladium catalysts, 6,370 Oxycyanation palladium catalysts, 6,370 Oxygcn and hydrogen production cyclic water cleavage, 6,523 carriers synthetic, 1, 28 electrocatalytic reduction, 1,488 electrochemical production from water coordination complex catalysts, 6,532 photoelectrochemical production from water, 6,531 photoproduction from water intermolecular electron transfer reactions, 6,515 production from water hettrogeneuus catalysts, 6,519 homogeneous catalysts, 6,517 metal salt catalysts, 6,493 thermodynamics, 6,489 reduction vanadium(I1) complexes, 3,471 Oxygen abstraction reactions niobium and tantalum complexes, 3,631 Oxygenases, 6,318,325,681 copper(I1) complexes, 5,721 electron transfer to dioxygen, 6,682 Oxygenation wpper(Tj complexcs, 5,577 copper@) complexes, 5,716 a-diimine complexes, 1,455 0-diiminc complexes, I, 455 Oxygen ligands. 2,435-456,461-483 Oxyhemerythrin, 4,254 Oxyhemocyanin copper(I1) complexes, 5,724 Oxytyrosinase copper(I1) complexes, 5,718

. ..

PAN -see 2-Naphthol, 1-(2-pyridyiazo)PAR -see Resorcinol, 4-(2-pyridyla~o)Pachnolite structure, 6,846 Palladiotype process photography, 6,124 Palladium, 5,1099-1115 applications, 5, 1100 determination, 1,544,545; 5 , 1144 electroplating, 6, 11 gravimetry, 1,532,533 isotopes, 5,1100 occurrence, 5,1099 physical properties, 5 , 1100 recovery from nuclear fuel waste, 6,960 Palladium, bis[methylenebis(diphenylphosphine)]bis(thiocyanat0)dilinkage isomerism, 1, 185 Palladium, bis(trialkylphosphine)bis(thiocyanato)isomerism, 1.185 Palladium, (diammine)bis(thiocyanato)isomerism, 1,185 Palladium, dichlorobis(amine)substitution reactions stereochemistry, I , 318 Palladium, dichlorobis(pyridine)substitution reactions, 1,314 Palladium, dinitritobis(triisopropylph0sphinc)substitution reactions, 1,314 Palladium, ethylenesynthesis matrix isolation, 1,28 Palladium, ethylenebis(dipheny1phosphine)bis(thiocyanat0)linkage isomers, 1,185 Palladium, methylenebis(diphenyiph0sphine)bis(thiocyanat0)linkage isomers, 1,185 Palladium, octafluorocrystal structure, 1,24 Palladium, polymethylenebis(dipheny1phosphine)bis( thiocyanate) linkage isomers, 1, 185 Palladium, tetraamminete trachloropalladate history, 1 , 2 Palladium, tetrachlorocrystal structure, 1, 16 Palladium, tris(dinitr0gen)synthesis, 1,28 Palladium complexes a,p-dione dioximates electrical properties, 6, 143 acet ylace tone hydrolysis, 2,379 alkylperoxo oxidation catalysts, 6,347 amid in es bridging ligands, 2,201 anticancer drugs, 6,758

. .

.

applications, h, 1022 carboxylic acids organoinerallic ligands. 2,442 catalysts carbon dioxide reactions, 6,295 carbonylation, 6,280 hydrocyanation. 6,298 hydrogenation, 6,248 hydrosilylation. 6,300 water cleavage, 5 ; 497 corrins, 2. 885 corroles, 2, 875 'I ,4-diaza-1,3-butadiene, 2,206,211 1.3-dikctoncs acctylcnes, 2,393 carbon bonded, 2.394 displacement reactions, 2,389 dimethyl sulfoxide, 2,490,641 guanidines, 2: 283 hexafluoroacetylacetone displacement reactions, 2,380 methanolysis, 2,379 NMR, 2: 388 orthometallation, 2,394 phenylazophenyl, 2,394 oxo

hydrocarbon oxidation, 6,361-371 peroxo oxidation catalysts, 6,337 in photochemical nitrogcn production from water, 6. 509 phthalocyanines, 2,868 physical development photography, 6,113 polypyrazoiylborates, 2,252 porphyrins, 2,841 pseudohalides, 2: 232,233 pyridine oxides, 2; 496 triazines bridging ligands: 2,201 monodentate, 2, 196 Palladium(0) complexes, 5,1101-1103 phosphine, 5,1101 oxidativc addition, 5 , 1102 synthesis, 5,1102 31P NMR, 5,1102 phosphite, 5, 1101 photography physical development, 6, 116 Palladium(1) complexes, 5 , 1103-1111 binuclear crystallography, 5, 1108 insertion reactions, 5 , 1105 structure, 5 , 1106 bis(dip heny1phosphino)methane Pd-Pd bond lengths, 5,1106 clusters, 5 , 1103-1111 halocarbonyl: 5,1110 high nuclearity, 5; 1110 high nuclearity iron, 5, 1111 tetranuclear, 5,1108

188

189

Cumulative Subject Index

trinuclear, 5 , 1.108 dimers, 5, 1103 triangulo diphenylphosphido, 5, 1108 diphenylphosphinop yridine NMR,5,1108 heterobinuclear, 5, 1104 heterometallic dimers, 5, 1106 homometallic dimers, 5. 1106 isocyanides, 5,1104 fluxionality, 5, 1104 lH NMR, 5,1104 X-ray crystal structure, 5 , 1104 phosphines, 5 , 'I 104 Palladium(I1) complexes, 5, 1131-1152 acetylidc bis(diphenylphosphino)methane, 5,1164 alkoxides, 5,1113 allyl bis(dipheny1phosphino)methane. 5,1161 amine-carbonyl condensation products, 5, 1118 amines, 5,1115 palladium-nitrogen bond lengths, 5, 1116 amino acid esters hydrolysis, 6,423 a-amino acids, 5 , 1115 N-(2-aminoethyl)-l,2-ethanediamine, 5 , 11 16 areneseleninates. 5, 1135 arenesulhates, 5, 1134 aromatic heterocyclic amines, 5 , 1117 arsine, 5, 1157 azido, 5,1160 cyclometallation, 5, 1167 fulminate, 5, 1160 halo, 5, 1158 cis-trans isomers, 5 . 1158 hydride, 5,1160 isocyanate, 5,1160 multidentatc, 5, 1165 pscudohalidc, 5, 1159 thiocyanate, 5 , 1159 unidentate, 5 , 1157 arylazo oximes, S111 19 azides, 5, 1120 azo oximes, 2,275 bidentate ligands, 5. 1146 one As atom, 5, 1165 one P atom, 5, 1165 one Sb atom, 5. 1165 sulfur-phosphorus ligands, 5,1165 two As atoms, 5, 1162 two As atoms, dihalo, 5, 1162 two P atoms, 5,1162 twci P atoms, dihalo. 5, 1162 two Sb atoms, 5, I. 162 two Sb atoms, dihalo, 5 , 1162 bipyridyl, 5 . 1117 bis(arsine) tetrahalo, 5, 1161 bis(dipheny1phosphino)methane. 5 , 1164

2,1l-bis(diphenylphosphinomethyl)benzo[c]phenanthreneI 5,1163 bis(diphenylstihino)methane, 5, 1165 bis(phosphine) tetrahalo, 5, 1161 bis(sa1icylaldimine) reaction with mineral acids, 5 . I l l 8 bis(stibine) tetrahalo, 5. 1161 camphorquinone dioxime. 5. 1 I18 carboxylates, 5, 1113 crystal structure, 5, 1113 NMR, 5, 1113 substitution reactions, 5. 1113 COC 7 4 .

Palladium(I1) complexes

dialkyl thioethers, 5, 1131 diamines cis, 5,1115 trans, 5 , 1115

N,Nf-di(2-aminoethyl)-1,2-ethanediamine, 5,1116 diaminopropane NMR, 5,1116 polymorphism, 5,1116 113-diaryltriazjnes, 5,1118 dioarbuxylic acids, 5, 1114 antitumor properties, 5,1114 dicyanobk( 2,9-dimcthyl-l, 10-phenanthroline), 5,1117 1,&-dihydro-5,7,12,14-tetramethyldibenzo[b,i][ 1,4,r(,ll]tetraaza[14]annulene, 5, 1120 1.2-dihydroxyhenzene, 5,1115 immunoassay indicators, 5 , 1115 a-diimines, 5,1118 1,3-diketonates, 5, 1114 crystallography, 5 , 1114 IR spectroscopy, 5,1114 substitution reactions, 5, 1114 X-ray crystallography, 5,1114 dioximes, 2,271; 5, 1118 ethanediyl bridged phosphine, 5, i 161 glutaraldehyde bis(dimcthylhydrazone), 5, 1120 halobis(2,9-dimethyl-l ,lo-phenanthroline), 5,1117 humic acids: 6,861 hydrazones. 5.1120 hydroselenides, 5 , 1132 hydrosulfides, 5,1132 hydroxy oximes, 2,273 o-hydrox yoximes solvent extraction, 6 , 801 imidazoles, 5, 1117 imines, 5,1118 isonitroso compounds, 5, 1119 macrocyclic nitrogen ligands, 5 , I120 magnetic properties, 1,274 monamino ahd esters, 6,417 muhidentate, 5 , 1346 multidentate amines, 5 , 1116 crystal structure, 5, 1116 1,8-naphthyridine, 5, 1117 nitrato, 5, 1113 nitriles, 5. 1121 nitro oxidation catalysts, 6,373 nitrogen donor complexes, 5, 1 15-1122 nucleosides, 5.1117 nucleotides, 5,1117 oximes, 2,270,272; 5,1118 oxyanions, 5,1112 oxygen-containing solvents, 5, 112 oxygen donor ligands, 5, 1112- 115 1,lO-phenanthroline. 5 , 1117 o-phenylenediarsine, 5, 1163 . . o-phenylenediphosphine, 5, 1163 o-phenylenedistibine, 5, 1163 phosphine, 5,1157 azido. 5,1160 cyclometallation, 5, 1167 fulminate, 5 , 1160 halo, 5,1158 cis-tram isomers, 5 , 1158 hydride, 5,1160 isocyanate, 5,1160 muhidentate, 5, 1165 pseudohalide, 5. 1159 thiocyanate, 5,1159 unidentate, 5, 1157 phosphinite, 5.1166 phosphinoacctylene, 5, 1168

PaIladium(I1)complexes

Cumulative Subject Index

phosphite, 5,1166 phosphonite, 5,1166 phosphorus donor ligands, 5,1157 purine nucleosides, 5,1117 pyridyl, 5,1117 pyrimidine, 5,1117 reduction, 5,1101 in carbonylation, 6,281 salicylaldimines, 5 , 1118 selenium dichloride, 5,1132 denocyanates, 5,1141 selenoethers, 5, 1144 dimeric, 5,1145 IR spectra, 5,1144 Raman spectra, 5,1144 selenoureas, 5,1143 semicarbazones, 5,1120 spectra, 1,255 square planar cis-trans isomerization, 1,515 solvolysis, 1,505 stibine, 5,1157 azido, 5,1160 fulminate, 5,1160 halo, 5, 1158 cis-trans isomers, 5,1158 hydridc, 5,1160 isocyanate, 5 , 1160 mult~dentate,5,1165 pseudohalide, 5,1159 thiocyanate, 5,1159 unidentate, 5,1157 sulfides, 5,1132 sulfites, 5,1131,1133 sulfoxides, 5,1142 IR spectra, 5,1142 NMR, 5,1142 sulfur dichloride, 5,1132 sulfurdiimine Auxional behavior, 2, 192 reactivity, 2, 194 sulfur ligands trans effect, 5 , 1131 telluroethers, 5,1144 dimeric, 5,1145 IR spectra, 5,1144 Raman spectra, 5,1144 tertiary arsine selenides, 5,1143 tertiary arsine sulfides, 5.1143 tertiary phosphine selenides, 5 , 1143 tertiary phosphine sulfides, 5,1143 tetraammines, 5,1115 photoconductivity, 5,1116 physical spectra, 5,1116 semiconductivity, 5 , 1116 solid state structure, 5. 11 IS tetrabenzo-l,5,9,13-tetraazacyclohexadcca-1,5,9,13tetraene, 5,1120 te trakis(arsine) dihalo dinuclear, 5 , 1162 hydroxo bridged, 5,1162 tetrakis(ph0sphine) dihalo dinuclear, 5,1162 hydroxo bridged, 5,1162 tetrakis(stibine) dihalo dinuclear, 5,1162 hydroxo bridged, 5,1162 tetrasulfide, 5 , 1132 thiocyanates, 5, I138 bidentate As ligands, 5,I162 bidentate P ligands, 5, 1162 bidentate Sb ligands, 5 , 1162 dimeric, 5,1141

five-coordinate, 5, 1141 X-ray diffraction, 5 , 1138 thioethers, 5;1144 dimeric, 5,1145 IR spectra, 5: 1144 Raman spectra, 5,1144 thiolates, 5,1136 thiolato, 5 , 1131 thiosulfates, 5,1131,1136 thioureas, 5,1131,1143 triammincs, 5, 1116 crystal srrucrure, 5,1116 triazines monodentate, 2, '196 triphenylphosphine. 5,1113 tris(arsine) dihalo, 5 : 1160 halo, ionic, 5 , 1160 tris(phosphine) dihalo, 5,1160 halo, ionic, 5,1160 tris(stibine) dihalo, 5,1160 halo, ionic! 5: 1360 unidentate ligands, 5, 1132 Palladium(II1) complexcs. 5, 1100 Palladium(IV) complexes, 5,1122-1124 amines, 5,1123 ammines, 5 , 1123 arsenic donor atoms, 5,1123 cyanides synthesis, 2 , 9 cyano, 5,1124 fluoride neutron diffraction, 5,1122 group VI donor atoms, 5,1124 halides, 5,1122 hexabromo, 5 , 1122 hexachloro. 5.1122 hcxafluoro structure, 5,1122 hexaiodo, 5,1122 ionization potential, 5 , 1122 magnetic properties, 1,273 nitrogen donor atoms, 5,1123 phosphines SHAB theory, 2: 1040 phosphorus donor atoms, 5,1123 spectra, 1,254 Palladium(V) complexes, 5,1100 Palladium compounds photothermography, 6+118 Palladium dichloride solid state oligomerization, 1, 187 Palladium(I1) salts sensitizers silver halide light sensitivity, 6,97 Paludrinc metal complexes, 2,282 Panulirus Interruptus hemocyanin, 5,581 Papain imaging systems, 6,126 Parabactin, 6 , 676 Paramagnetism. 1.257 temperature independent, 1,261 Paramecium

calcium, 6,595 Paramolybdates, 3, 1030 Paraquat --set Methylviologen Paratungstate A: 3: 1033 Paratungstate B, 3, 1033 Paratungstates, 3 , 1033

190

191

Cumulative Subject Index

a-Particles P-Particles in medicine, 6,965 Parvalbumin, 6,576 structure, 6,573 Passivation gold cyanides, 6,784 Patton-Reader's indicator. 1,556 Pectic acids metal complexes, 2,984 Pegmatites, 6, 846 Peierls distortion, 6 , 135 Penicillamine disulfide metal complexes, 2,749 metal complexes, 2,748 photographic emulsion stabilizers, 6.98 D-Penicillamine chelating agents heavy metal poisoning, 6.768 rheumatoid arthritis, 6,769 technetium complex in medicine, 6,979 Penicillin, benzylzinc complexes, 5,997 Penicillins hydrolysis metal catalysis, 6,461 Pentaaza macrocycles synthesis, 2,903 Pentabromotellurates, 3,301 Pentachlorotellurates, 3,301 Pentaethylenehexamine cobalt complexes, 2,58 metal complexes titrimetry, 1,553 Pentafluoroselenates. 3: 301,302 Pentafluorotelluratcs, 3, 301 Pentagonal bipyramids repulsion energy coefficients, 1,34 seven-coordinate compounds, 1,69 stereochemistry, 1,60 Pentaiodopolonates, 3,302 Pentaiodotellurates, 3,302 Pentametallic complexes, 1. 154 centro-fefruhedro,1, 155 edge-bridged tetrahedron, 1, 155 pentagon, 1,155 square pyramid, 1,155 trigonal bipyramid, 1, 155 Pentamines cyclic configurational isomerism, 2,908 metal complexes, 2, 56 Pentamolybdates, 3,1032 Pentarnolybdobis(organophosphwates), 3, 1053 Pentan-2-amine, 4.4'-( ethy1enediimino)biscomplexes structure, 1,25 Pentane-2,4-diamine metal complexes, 2,44 Pentane-2,4-dione, 3-hydroxyiminometal complexes, 2,797 Pentaphyrin, 2,888 synthesis, 2,891 Pentapyrrolic macrocycles, 2,888 2,1.2-Pentathiadiazole-4,7-dicarbonitrile in hydrogen production from water, 6, 508 Pentatungstobis(organophosphonates),3, 1053 4-Penten-1-a1 reaction with ethylene catalysts, rhodium complexes, 6, 300

Permanganate strike

1-Pentene hydroformylation catalysts, rhodium complexes, 6,259 iron complexes, 6,258 platinum complexes, 6,263 2-Pentene. 3-methylhydro formylation catalysts, rhodium complexes, 6,260 3-Pentenoic acid, 4-methylsynthesis by carbonylation, 6,288 Pcptidases acyl transfer, 6,471 zinc, 5. 1004 Peptides bond formation cobalt catalysis. 6,436 metal-catalyzed, 6,426 cyclic metal complexes, 2,764,969 cysteine-containing, 2,764 esters synthesis, metal-catalyzed, 6,427 formation amino acid metal complexes, 2,758 glycine metal complexes, 2,764 hydrolysis carboxypeptidase A , 6,463 catalysis by labile metal ions, 6,414 metai-catalyzed, 6,425,431 metal complexes, 2,757 large linear metal complexes, 2,968 metal complexes, 2,739-774 binding sites, 2,759 bond Eormation, 2,767 a-C-H bond activation, 2, 768 decarboxylation, 2,762 deuterium exchange, 1,426 hydrolysis, 1,428,440; 2,767 ligand transfer reactions, 2,766 naturally occurring, 2,966 prebiotic systems, 6,872 proton transfer reactions, 2,766 reactivity, 2,766 redox reactions, 2,768 stability constants, 2,759 stereochemistry, 2,759 stereoselectivity, 2,766 structure, 2,762 models protein denaturation, 3 , 6 N-rnercnptoacctylglycylmetal complexes, 2,764 N-mercapropropionylglycylmetal complexes, 2, 764 reactions osmium tetroxide, 4, 590 Schiff bases metal complexes, 2,766 synthesis metal catalysis, 6,439 metal complexes, 6,215 transition metal amine complexes in, 2,28 zinc complexes. 5,940 Peptidoglycans. 6,680 Perchlorates ligands solvents, 2,414 Permanganates, 4, 109 oxidation, 6,355 Permanganate strike

Permanganate strike

Purex process, 6,954 Perovskites, 4, 196 mixed copper(II/III) complexes, 5.744 Peroxidases, 2,982; 4,263,264; 6,703 compound I, 6,704 compound II,6,704 imaging systems, 6, 126 Peroxides formation, 6,682 metal oxidation, 6,330-350 photography image amplification, 6, 117 Peroxocarbonic acid metal complexcs, 2,449 Peroxo complexes, 2,315-330 binuclear, 2,323,324 IR spectra, 2,324,325 cobalt catalysts, 2, 90 metal oxidation, 6,330-341 mononuclear, 2,318,319 IR spectra, 2,318,320 Raman spectra, 2,320 reactions, 2,328 oxidation, 6,320 p-Peroxo complexes alkyl structure, 6,322 bimetallic, 6,322 synthesis, characteristics and structure, 6.322 Perrhenates, 4, 127, 197 Perrhenic acid, 4,198 Perthiocarbonic acid metal complexes, 2,590 Petroleum structure, 6,856 Petroporphyrins metal complexes spectrophotometry, 6,863 Peyrone’s reaction, 1, 17 Peyrone’s salt configuration, 1,17 history, 1 , 3 Pfeiffer, Paul, 1, 15 Pfeiffer effect, 1,26 Pfeiffer’s cation, 2, 300 PH

192

Cumulutive Subject Index

water decomposition hydrogen and oxygen production. 6,191 Phallusia mammilata vanadium(II1) complcxes, 3,486 Pharaoh’s serpents, 5, 1063 Pharmacology radionuclides, 6, 963-996 Phase transfer method carbonylation benzylic halides, 6,280 1.10-Phenanthroline in analysis, I , 523 complexes history, 1,21 dehydrogenase inhibitor, 5.1017 electrode modification, 6,25 liquid-liquid extraction, 1.544 metal complexcs, 2,89, YO, 93; 5,958 steric cffects, 2,90 1 ,lo-Phenanthroline, 2-cyanohydrolysis metal catalysis, 6,449,452 metal complexes hydration, 1,428

1,lo-Phenanthroline, 2,4-dichlorozinc complex, 6. 195 1,lo-Phenanthroline, 2,9-dimethylcopper complexes absorptiometry, 1, 549 1,lo-Phenanthroiine 4,7-diphenylelectron recording system, 6, 127 liquid-liquid extraction, I , 544 1,10-Phenanthroline-2-carbaldchyde reduction for metal catalysis, 6,475 1,lO-PhenanthroIine-2-carboxylic acid ethyl ester hydrolysis. metal catalysis. 6,439 9,10-Phenanthroqlunone iron complexes, 2,398 Phenol, trans-2-(2-butenyl)asymmetric intramolecular oxidative cyclization, 6,365 Phenol, 4-cyanohydrolysis metal catalysis, 6,449 Phenol, o-nitroalkali metal complexes, 3,30 Phenol, 2-nitrosometal complexes, 2,797 tautomcrization+ 2, 272 Phenolic acids metal complexes naturally occurring, 2,961 Phcnolphthalcin metallochromic indicator, 1,556 Phenolphthalexene metalfochromic indicator, 1,557 Phenols carbonylation catalysts, palladium complexes, 6,280 metal complexes geochemistry. 6.867 oxidation cobalt catalysts, 6, 387 copper catalysts, 6.391 oxidative carhonylation palladium catalyzed, 6, 369 oxycarbonylation palladium catalysts, 6. 370 reactions with metal halides, 2.337 with metals, 2: 336 Phenol-4-sulfonic acid, 2-(2-hydroxynaphthyl-l-azo)copper complexes, 6 - 5 5 Phenolysis metal sulfides, 2,342 Phenylalanine esters, coppcr(l1) complexes hydrolysis- 6,425 Phenylalanine, dihydroxymetal complexes, 2,750 naturally occurring, 2,966 oxidation, 2.758 Phenylalanine, L-dihydroxyMonsanto synthesis, 6, 251 Phenylalanine hydroxylase iron. 6,636 o-Phenylenediamine metal complexes, 2,59 Phenyl exchange betwcen I-Ig” and PhHg” Iy9HgNMR, 2,4 PhenyI phosphatosulfatc hydrolysis in catalysis. 6,444 Phlorins, 2,855 Phormidium uncinatum ~

193

Cumulative Subject Index

activity calcium, 6,595 Phosphabenzene transition metal complexes, 2,1041 Phosphacymantrenes transition metal complexes, 2, 1043 Phosphaferrocenes transition metal complexes, 2. 1043 Phosphatases activation magnesium ions, 6,580 Phosphate, tributylliquid-liquid extraction from, 1, 541 in solvent extraction, 1.523 Phosphate blues, 5,471 Phosphates P-aminoethyl esters hydrolysis, metal catalysis, 6,448 biosynthesis, 6,582 competition with vanadates physiology, 6,665 dialkyldithio metal complexes, 2,643 diaryldithio metal complexes, 2,643 gravimetry, 1,533,534 hydrolysis metal catalysis, 6.443 P-hydroxyethyl esters hydrolysis, metal catalysis, 6,448 leaching uranium, 6,788 metal complexes hydrolysis, 1,428 isomerism, 1, 202 P-methoxyethyl hydrolysis, metal catalysis. 6.448 1-methoxy-2-propyl ester hydrolysis, metal catalysis, 6, 448 4-nitrophenyl ester hydrolysis cobalt(ll1) complex catalysk 6,446 protonation, 3,1026 2-pyridylmethyl esters hydrolysis, copper(I1) carallsis. 6,445 8-quinolyl esters hydrolysis, copper(I1) catalysis. 6,445 salicyl esters hydrolysis, copper(l1) catalysis. 6,445 transfer biology, 6, 582 trialkyldithio metal complexes, 2,642 trialkylthio metal complexes, 2,641, M2

2-(4(5)-irnidazoyl)phenyl ester hydrolysis, metal catalysis, 6, 444 Phosphinates liquid-liquid extraction, 1,542 Phosphine, alkylidenebis(dimethy1-, 2.993 Phosphine, [(alkylphenyiphosphino)ethyl]diphenyl-,2, 994 Phosphine, aminorhodium complexes catalysts, hydroformylation, 6,261 Phosphine, 3-aminopropyldimethylphotographic fixer, 6,100 Phosphine, bis(2-carboxyethyl)rnethylphotography diffusion transfer process. 6, 102 Phosphine, bis[(dimethylphosphino)ethyl]methyl-,2,995 Phosphine, bis[(dimethylphosphino)ethyl]phenyl-, 2,995 Phosphine, bis[(diphenylphosphino)ethyl]phenyl-, 2,994, 995

Phosphine

Phosphine, (2-bromophenyl)dichloro-, 2,991 Phosphine, (w-chloroalky1)dichloro-,2,991 Phosphine. chlorodimethyl-, 2,991 Phosphine, chloro(dimethy1amino)-, 2,991 Phosphine, chlorodiphenyl-, 2,990 Phosphine, cyclohexyl(o-anisy1)methylrhodium complexes asymmetric hydrogenation, 6,251 Phosphine, I(dialkylphosphino)alkyl]diphenyl-, 2.994 Phosphine, dichloromethyl-, 2,991 Phosphinc, dichlorophenyl-, 2,990 Phosphine, diethylphenyl-, 2,992 Phosphine, dimethyl-, 2,992 Phosphine, dimethylphenyl-, 2,992 Phosphine, diphenyl-, 2,992 Phosphine, ethyldiphenyl-, 2,992 Phosphine, ethylenebis(diethy1-, 2, 993 Phosphine, ethylenebis(dipheny1-, 2,993 Phosphine, ethylenebis(pheny1-, 2,992 Phosphine, ethylidynetris[methylene(diphenyl-, 2,994 Phosphine, [(ethylphenylphosphino)hexyl]dipben yl-, 2, 994 Phosphine, methyl-, 2,992 Phosphine, methyldiphenyl-, 2,992 Phosphine, mcthylenebis(dipheny1-, 2,993 Phosphine, methylphenylpropylcornp1exes inversion, 1, 199 Phosphine, methyl-n-propylphenylrhodium complexes asymmetric hydrogenation, 6,250 Phosphine, neomenthyldiphenylrhodium complexes asymmetric hydrogenation, 6,250 Phosphine, phenyl-, 2,992 Phosphine, o-phenylenebis(dimethy1-,2,993 Phosphine, p-phenylenebis(dipheny1-,2,993 Phosphine, selenometal complexcs, 2,664 bidentatc, 2,664 Phosphine, triarylphotographic stabilizer, 6,103 Phosphine, tributyl-, 2,992 oxide in uranium ore processing, 6,907 Phosphine?trichloro-, 2,990 Phosphine, tricyclohexyl-, 2,992 Phosphine, triethyl-, 2,992 Phosphine, trifluoroJC acidity, 2,1034 metal complexes solvolysis, 1,418 19F NMR, 1,47 Phosphine, triisopropyl-, 2,992 Phosphine, trimethyl-, 2,990,992 oxides metal complexes, 2,498 Phosphine, trimorpholinosulfides metal complexes, 2,642 Phosphine: trioctyloxide in uranium ore processing, 6,909 oxides metal complexes, 2,501 Phosphine, tri-n-octyloxides liquid-liquid extraction, 1,542 Phosphine, triphenyl-, 2,990 oxide geometry, 1,35 oxides metal complexes, 2,498,500

Phosphine

Cumulative Subject Index

rhodium complexcs catalysts, hydroformylation, 6,260 fhosphine, tripiperidinosulfides metal complexes, 2,642 Phosphine, tripropyl-, 2,992 Phosphine, tripyrrolidinosulfides metal complexes, 2,642 Phosphine, tris(cyclohexy1amino)sulfides metal complcxes, 2,642 Phosphine, tris(dimethy1amino)sulfides metal complexes, 2, 642 Phosphine, tris(dimethy1dithiocarbamato)stereochemistry, 1, 81 structure, 1,82 Phosphine, tris(dimethyltriazin0)spectroscopy, 2,196 Phosphine, tris[(diphenylphosphino)ethylj-, 2,995 Phosphine, tris(2-(diphenylphosphino)phenyl)-, 2,995 Phosphine, tris(phydroxypheny1)photography diffusion transfer process, 6, 102 Phosphine, tris(methy1amino)sulfides metal complexes, 2,642 Phosphine, vinylenebis(dimethy1cis-, 2,993 Phosphine, vinylenebis(dipheny1-, 2>993 Phosphines, 2,990,992 n acidity, 2, 1034 aryl bonding, 2,1030 basicity, 2, 1031 complex stability, 2, 1030 u bonding basicity, 2, 1030 chid cone angle concept, 2,1014 complexes calculations, 2, 1036 quantum mechanical, 2,1034 gas phase basicity, 2,1031 gas phase ionization energy, 2, 1032 hexa tertiary, 2,995 ionization potentials, 2, 1031 ligands history, 1,21 liquid phase basicity, 2, 1032 macrocyclic, 2,995 multidentate, 2,994 oxides liquid-liquid extraction, 1,542 metal complexes, 2,497,498.500,501 nephelauxetic series, 2,501 31 P NMR, 2,501 in solvent extraction, 2,501 penta tertiary, 2,995 polydentate cone angle concept, 2,1013 primary, 2,992 secondary, 2,992 solubilization in water, 2,1014 spirocyclic, 2,995 sulfides metal complexes, 2,641,642 tertiary, 2,992 Phosphinic acid solvent extraction

cobalt and nickel. 6,793 in uranium ore proccssing, 6,906 dimerization, 6,905 Phosphinimato complexes transition metals, 2, 122, 125 bonding, 2. 124 IR spectroscopy. 2, 124 reactions, 2: 125 structure, 2.124 synthesis, 2: 123 Phosphinimines imido metal complexes synthesis from, 2, 167 Phosphinodithionates, 4.604 Phosphoenolpyruvate carboxykinase manganese. 6,S88 Phosphoglucomutase activation magnesium ions, 6,582 zinc complexes, 2.965 Phosphoglycerate kinase activation magnesium ions, 6,580 Phosphoglycerate phosphomutase inactivation manganese transport, 6,572 mangancse, 6,588 Phospholamban, 6.566 Phosphole, triAuoro19FNMR, 1,47 Phospholes transition metal complexes, 2, 1041 two-electron donors, 2, 1042 4x ring donors, 2, 1042 Phospholipase A2 activation calcium, 6 : 594 Phospholipase C zinc, 6,613 Phospholipids biological tissue osmium tetroxide, 4, 591 Phospholyl complexes transition metal complexes, 2, 1043 Phosphometallocenes transition metal complexes, 2, 1043 Phosphomolybdates ammonium salts in analysis, 1; 523 Phosphonate esters cyclic, 2,998 Phosphonates liquid-liquid extraction, 1, 542 Phosphonic acid, butyldibutyl ester in thorium ore processing, 6,918 Phosphonic acid, 2-ethylhexyl2-ethylhexyl ester solvent extraction. cobalt, 6,794 Phosphonic acid, methylenedilabelled with technetium-99 bone scanning agent. 6,978 Phosphonic acids alkaline earth metal complexes, 3,32-35 dibutyl ester Purcx process, 6.954 dihexyl-N,N-dicthylcarbarnoylmethyleneester nuclide recovery horn nuclcar fuel wastc. 6.959 metal complexcs, 2,500 solvent extraction cobalt and nickel. 6,793 Phosphonium ions, tetraphenylliquid-liquid extraction, 1,548

194

Cumulative Subject Index

195

Phosphonoacetic acid antiviral activity, 6,771 Phosphoprotein phosphatases activation magnesium ions, 6,581 Phosphoproteins dentine, 6,597 Phosphoramide, hexamethylmetal complexes, 2,499,500 Phosphorane, triaryphotographic stabilizer, 6, 103 Phosphorancs metal complexes isomerism, 1,206 Phosphorescence, 1,395 Phosphoric acid butyl ester in uranium ore processing, 6,909 dibutyl ester in uranium ore processing, 6,906 di(2-ethylhexyl) ester liquid-liquid extraction, 1, 542 metal extraction, 6,792 solvent extraction, 6,795 solvent extraction, base metals, 6,792 solvent extraction, indium and tbalium, 6,798 solvent extraction, uranium: 6,796,797 solvent extraction, vanadium, 6,796 solvent extraction, zinc, 6,794 in thorium ore processing, 6,917 in uranium ore processing, 6,903 dineooctyl ester dimerization, 6,906 dioctyl ester dimerization, 6,906 esters in thorium ore processing, 6,916 2-ethylhexyl ester in uranium ore processing, 6,903 monoalkyl esters solvent extraction, uranium, 6,798 production uranium and, 6,Y 11 trialkyl ester metal complexes, 2; 500 tributyl ester dimerization, 6,904 radiolysis, 6,940 solvent extraction, irradiated nuclear fuels, 6,936, 940 in uranium ore processing; 6*W3,910 2,6,8-trimethylnonyl ester in uranium ore processing, 6,909 Phosphorous acid trialkyl esters technetium complexes, radiopharmacy, 6,980 Phosphorus PZ

ligands, 2,1059 p4

ligands, 2,1056 Phosphorus, pentaphenoxystereochemistry, 1, 40 Phosphorus, pentaphenylstereochemistry, 1,40 Phosphorus acids liquid-liquid extraction, 1,542 Phosphorus complexes amides synthesis, 2, 163 phthalocyanines, 2, R 6 4 porphyrins, 2,822 Phosphorus-containing macrocycles, 2,990,996,998

Photophysical processes

macrocyclic effect, 2, 1002 ring size. 2,1003 stereochemistry, 2, 1003 Phosphorus heterocycles transition metal complexes, 2, 1041 Phosphorus ligands. 2,989-1061 n-acid series. 2,1033 bonding, 2.1030-1041 cone angle concept, 2,1012 trigonal bipyramidal cornplcxes, 2, I036 Phosphorus oxychloride metal complexes, 2, 500 Phosphorus pentachloride structure, 1, 5 Phusphorus pentafluoride 19F NMRI 1,41 Phosphorus tribromide stereochemistry, 1,36 Phosphorus trichloride metal complexes solvolysis, 1,418 stereochemistry, 1,36 Phosphorus trifluoride stereochemistry, 1 , 36 Phosphorus trihalides stereochcmistry, 1,3h Phosphorus triiodide stereochemistry. 1,36 Phosphorus ylides transition metal complexes, 2, 1056 Phosphorylation biological, 2,978 Phosvitin, 2,975; 6,670 Photoaquation solid state, 1,471 Photocalorimetry, 1,410 Photochemical reactions, 1,397 applications, I, 408 mechanisms, 1,385 solid state, 1,470 Photochemistry water decomposition intermolecular electron transfer reactions, 6,498-530 Photochromic systems, 6,125 Photochromism, 1,409 bidentate Schiff base metal complexes, 2,726 Schiff base complexes, 2,718 Photoconductors electrophotography, 6, 122 light-sensitive agents photography, 6, 114 Pho toelectrochemistry water dectmposition, 6,530 Photuelectron spectroscopy cadmium complexes, 5,929 zinc complexes, 5,929 Photographic developers, 6,98 modifiers, 6,98 Photographic emulsions stabilizers, 6, 97 Photography, 6,95-127 fixation, 5,807 iron-based, 6; 124 silver complexes, 5,777 silver halide-based, 6,96112 silver halides, 5,822 silver image stabilization, 6, 102 Photolysis ligand held theory and, 1,393 water hydrogen and oxygen production, 6,490 Photophysical processes, 1,395

Photopolymerizable coatings

Cumulutive Subject Index

Photopolymerizable coatings relief-image-forming systems, 6, 125 Photoreactivity environmental effects, 1,394 Photoredox properties bipyridyl metal complexes, 2 , 9 0 Photoresist systems, 6,125 Photosensitive materials, 6, 113 Photosynthesis anoxygenic, 6,589 magnesium and manganese, 6,588 water decomposition models, 6,498 Photosynthetic(I1) chloroplasts, 2,773 Photosystem I1 dioxygen evolving centre manganese, 6,586 manganese protein, 6,590 Photothermography, 6,118 Phthalarnic acid, N-(2-phenanthrolyl)hydrolysis metal catalysis, 6,442 Phthalamic acid, N-(2-pyridyl)hydrolysis metal catalysis, 6,442 Phthalamic acid, N-(tl-quinoIyI)hydrolysis metal catalysis, 6,441 Phthalein purple metallochromic indicator, 1,557 Phthalic acid metal complexes geochemistry, 6,867 soils, 2,962 2-pyridylmethyl ester hydrolysis, metal catalysis, 6,440 Phthalic anhydride hydrolysis metal catalysis, 6,463 Phthalimide metal complexes minerals, 6,849 Phthalimide, N-thiometal complexes, 2,800 Phthalimide, N-vinylasymmetric hydroformylation catalysts, 6,265 hydroesterification catalysts, palladium complexes, 6,286 Phthalocyanine, chloroferric, 4,1261 Phthalocyanines, 1,29; 2,863-870 alkali metal complexes, 1,22 alkaline earth metal complexes. 3-58 cadmium complexes, 5,993 chelate complexes, 2,374 cobalt(I1) complexes dyes, 6,88 copper complexes color photography, 6,106 dyes, 6,87 filter dyes, 6, 104 demetallation, 2,863 doped polymers, 6, 146 dyes, 6,39 electrocatalgtic reduction of oxygen, I, 488 electrode modification, 6 , 24 history, 1,21 IR spectra, 2,861 kinetic formation kinetic template reactions, 1,451 m a s spectra, 2,861 metal complexes catalysts, oxygen production from water, 6,517

dyes, 6,87 electron transfer processes, 1,495 synthesis and reactions, 6, 192-202 metallation, 2,863 nickel complexes, 5 , 5 dyes, 6,91 NMR, 2: 861 photochemistry. 2,869 reactions, 2,863 at metal, 2,869 redox chcmistry, 2,870 spectra, 2. ShO synthesis, 2,861 two-metal complexes, 2,868 zinc complexes, 5.993 template synthesis. 5,993 Physarum polycephalum mitosis calcium, 6; 596 Physical development photography, 6.113, 115 Phytic acid zinc complexes, 2,985 Phytophthoru cinnamorni sporulation calcium transport, 6, 572 Phytosiderophores, 6,680 2-Picoline metal complexes, 2,79 Picolinic acid ethyl ester, palladium(I1) complexes hydrolysis, 6, 423 iron complexes naturally occurring, 2.964 metal complexes, 2,796 p-nitrophenyl ester hydrolysis, metal catalysis, 6,442 zinc transpart, 6,672 Picolinic acid. 2-(hydroxymethyl)es1et-s hydrolysis, metal catalysis, 6, 440 Picolylamine chelating resins mineral procussing, 6,825 Picrolonic acid in gravimetry, I. 534 Piezoelectric effect ethylenediamine metal complexes, 2,30 Pigments, 6: 35-91 Pigotite structure, 6,849 Pimelic acid, 2,6-diaminometal complexcs, 5,939 Pinacol. perfluororeactions, 2,343 Pinacolone, o-(dipheny1phosphino)benzoylcoordination chemistry, 2,401 Ping-pong reactions copper(I1) complexes. 5 , 717 Piperidine, N-hydroxymetal complexes, 2 , 797 pK, values azole ligands, 2, 77 Plant roots amino acids, 2, 962 carboxylic acids, 2,962 Plants ethylene effect copper, 6,656 Group IIA ions transport, 6,572 infections microbial iron transport, 6,679

196

197

Cumulative Subject Index

nickel uptake, 6,648 Plasmin labelled deep vein thrombosis diagnosis, 6,995 Plastocyanin, deoxystructure, 5,581 Plastocyanins, 6,652 amino acid sequence, 6,650 copper, 2,272;5,721; 6,649 binding sites, 2,557,770 electron transfer reactions, 6,653

NMR, 6,652 oxidized poplar structure, 6,650 spectra, 6,651 structure, 6,693 Platelets labelled, 6,994 Platinacycles, 5,395,412 Platinacyclobutanes skeletal isomerization. 5,396 Platinalactones, 5, 417 Platinblau, 5,434 Platinocyanide discovery, 1,3 Platinum colloidal in photoproduction of hydrogen from water, 6,513 Platinum, amminechlorination, 1,416 structure, 1,5 Platinum, amminebromochloro(l.2-ethanediamine)pyridylisomerism, 1,26 Platinum, amminebromochloroiodonitropyridylisomerism, 1,26 Platinum, amminedichloro(l.2-ethanedian1inc)pyridylisomerism, 1,26 Platinum, bis(g1ycinate)photoreactivity, 1,407 Platinum, bis(oxa1ato)-, 6 , 139 cadmium complexes superstructure, 6,142 cobalt complexes, 6,140 electrical conductivity, 6 , 141 superstructure, 6,141 thermopower, 6,141 divalent cation salts, 6,140 iron complexes structure, 6,142 lead complexes superstructure, 6,142 magnesium complexes, 6,140 electrical conduction, 6 , 142 structure, 6,142 thermopower, 6, 142 modulated superstructure, 6 ; I39 monovalent cation salts, 6; 139 nickel complexes structure, 6,141 partially oxidized, 6,139 Platinum, chlorobis(triethylphosphine)(rn-tolyl)cis-trans isomcrization, 1,510 Platinum, chloronitritobis(pyridine)trans-

ligand exchange, I, 288 Platinum, chlorotris(rrimethy1phosphine)isomerization, 1,318 Platinum, diamminedichloroconfigurational isomerism, 1,180 polymerization isomerism, 1, 187 Platinum, diamminedihalodinitro-

Platinum

chirality, 1, 195 Platinum?dibromobis(thi0phane)isomerization, 1 468 Platinum, dichloro(2,2’-bipyridyl)reactions with thiourea, 1,508 Platinum, dichlorobis(benzonitri1e)IR spectrum, 2,264 Platinum, dichlorobis(dimethy1 sulfide)isomcrization, 1,318 tratfiligand exchange, 1,288 Platinum, dichlorobis(dimethy1 su1foxidc)isomerization, 1.320 Platinum, dichlorobis(pyridine)photoreactivity, 1,407 substitution reactions, 1,312 Platinum, dichlorobis(tributy1phosphine)isomerization, 1,319 Platinum, dichIorobis(triethy1phosphine)photoreactivity. 1,407 Platinum, cis-dichlorodiammineanticancer drugs, 6,756 antitumor activity, 2,34,979 labelled anticancer drugs, 6,969 Platinum. dichloro(4,4’-dicyano-2,2‘-bipyridyl)reactions with thiourea, 1, 508 Platinum, ethylenebis(tripheny1phosphine)reactions with 5,6-dimethyl-2,1,3-benzothiadiazole, 2.

194 Platinum, hexachloroammonium salt structure, 1,16 Platinum, tctraammineamminctrichloroplatinate polymerization isomerism, 1 , 187 dichloride structure, I , 16 polymerization isomerism, 1, 187 te trachloroplatinate history, 1,2 polymerization isomerism, 1, 187 Platinum, tetrachloropolymerization isomerism, 1,187 potassium salt crystal structure, 1,16 triamminechloroplatinate polymerization isomerism, 1, 187 Platinum, tetracyano-, 6,136 anion-deficient salts, 6,136 electrical conduction, 6,138 optical propertics, 6,138 cation-deficient salts, 6,138 discovery, 1,3 oxidation states, 6 , ‘136 partially oxidized, 6,138 semiconductors, 6,134 Platinum, tetrakis(ethy1amine)tetrakis(ethylamine)dichloroplatinate structure, 1, 187 Platinum, triamminechloroammine trichloroplatinate polymerizatiun isomerism, 1,187 Platinum, trichloro(ethy1ene)phororeacrivity, 1,407 potassium salt history, I , 21 potassium salt, monohydrate history, 1,3 Platinum, tris(pentasu1fur)structure, 1,26

Platinum blue Platinum blue formation, 2,265 Platinum complexes, 5,351-500 acetylacetone reactions, 2,380 acetylides reactions, 5,402 alcohols, 5,465 alkene-l,2-dithiolates optical recording systems, 6,126 alkenes, 5,403 bonding, 5,403 hydrogen-deuterium exchange, 5,410 NMR, 5,407 reactions, 5,407 structure, 5,407 vibrational studies, 5,408 alkyl, 5,387 alkyl transfer, 5,391 binuclear elimination, 5,398 cleavage, 5,393 electrophilic cleavage, 5,398 insertion reactions alkenes, 5,401 alkynes, 5,401 carbon monoxide, 5,400 isocyanides, 5,401 sulfur dioxide, 5,401 isomerization, 5,393,399 photochemical cleavage, 5,397 redox cleavage, 5,398 reductive elimination, 5,398 structure, 5,387 synthesis, 5,387 acetylacetonate reactions, 5,390 alkali metal salts, 5,387 Grignard reagents, 5,387 organomercury reagents, 5,388 organosilicon reagents, 5,386: organotin reagents, 5,388 oxidative addition, 5 , 388 rcplacernent reactions, 5. 389 ring-opening rcactions, 5,390 alkylperoxo oxidation catalysts, 6,349 alkynes, 5,414 synthesis, 5,414 allyl, 5,417 reactions, 5,419 structure, 5,419 synthesis, 5,418 amides, 2,491 amid in es bridging ligands, 2,201 amines, 2,28;5,422 anthranilaldehydes, 5,469 anticancer drugs, 6,156 application, 6,1022 aqua, 5,465 aryl, 5,387 cleavage, 5,393 isomerization, 5,393 structure, 5,387 synthesis, 5,387 acetylacetonate reactions, 5,390 alkali metal salts, 5,387 Grignard reagents, 5,387 organomercury reagents, 5,388 organosilicon reagents, 5,388 organotin reagents, 5,388 oxidative addition, 5,388 replacement reactions, 5,389 ring-opening reactions, 5.390

Cumulative Subject Index azides, 5,437 bis(diphenylphosphiny1)methanide reactions, 5,402 boron halides, 5,374 boron hydrides, 5.372 bridged binuclear

NMR,5,462 bridging carbyne, 5,385 bridging hydrides, 5,363 bridging thiocarhyne, 5.385 carhenes, 5,381,382 carbonato, 5.468 carbon di~elenide~ 5 ?466 carbon disulfide, 5,486 carbon sulfide selenide, 5,486 carbonyl, 5,377 monomeric, 5: 377 multimetallic, 5,379 carboranes. 5,373 carboxylato, 5,466 catalysts asymmetric hydroformylation, 6,266 carbon dioxide reactions, 6,295 carhonylation, 6,291 hydroformylation, 6 , 263 hydrogenation. 6,248 water cleavage, 6,497 catecholates, 5,468 chelated aryl synthesis, 5,392 complementary redox reactions, 5,498 corrins, 2,885 cumulenes, 5,410 cyanide chain partially oxidized, 5,376 cyclopentadienyl, 5,419 delocalized ligands, 5,417 dialkyl sulfides, 5,476 2,3-diaminopropioriic acid optical diastereomers, 5,428 1,4-diaza-l,3-butadienc, 2,206,211 diazabutadiencs, 5,438 diazo, 5,438 dihydrides, 5,361 1,3-diketones, 5 , 467 displacement reactions, 2,390 dimethyl sulfoxide, 2,488 diphenylboron, 5,372 dipyrazolyl ketone, 2,256 diselenocarbamates, 5,481 dithiocarbamates. 5,481 dithiolates, lithium complexes magnetic susceptibility, 6,148 optical reflectivity, 6,148 structure, 6, 148 superstructure, 6 , 148 thermopower, 6,148 1,2-dithiolenes, S1 484 dithiophosphates, 5.481 ethers, 5,465 ethylenediamine, 2,30 Group IIIA ligands, 5,372 Group IVA ligands, 5,375,422 Group VI ligands, 5,463 Group VI1 ligands, 5,488 structure, 5,488 synthesis, 5,488 Group VI11 ligands, 5,491 glyoximes, 5,438 guanines, 2,93 halides electronic specrroscopy, 5,490 ESCA, 5,491

198

199 IR spectroscopy, 5,489 Mossbauer spectra, 5,491 NQR, 5,491 Raman spectra, 5,489 spectroscopy, 5,489 hexafluoroacetylacetone, 2, 376 hydrazides, 5,438 hydrides, 5,354 catalysis, 5, 371 germanes, 5,358 insertion reactions, 5,365 NMR, 5,370 phosphido bridged. 5, 357 reactions, 5, 362 with bases, 5,369 with electrophiles, 5,369 silanes, 5,358 spectroscopy, 5, 369 structure, 5,362 synthesis, 5,354 from alcohols, 5,359 from water, 5,359 thiolato, 5,355 hydrogen sulfide, 2,516; 5,473 hydroperoxides, 5,465 hydrosulfides, 5,473 hydroxy, 5,465 hyponitrites, 5, 469 imidates, 2,277,278 imines, 5,438 isocyanides, 5,380 physical properties, 5,380 reactions, 5,381 synthesis, 5,380 mechanisms, 5,492 methionine S-oxides, 5,480 nitrates, 5,468 nitriles, 5 , 436 nitrites, 5, 437 nitrogen, 5,422 nitrogen oxide ligands, 5 , 436 nitrosyl, 5,436 organolead, 2, 16 oxalic acid, 2, 446 oxidation states, 5.353 oximes, 5,438 oxygen bonds, 5,463 partially oxidized, 6, 136 perfluoropinacolate, 5.471 peroxo, 5,465 oxidation catalysts, 6 . 335 reactions, 2,328 phosphazenes, 5,462 phosphines, 5,439 cluster compounds, 5,462 IR spectra, 5,448 reactions, 5,449 phosphinous acids, 5,459 phthalocyanines, 2,868 platinum-germanium bonds, 5,420 platinum-lead bonds, 5,420 platinum-silicon bonds, 5,419 platinum-sulfur bonds, 5, 471 platinum-tin bonds, 5,420 polypyrazolylborates, 2,252 porphyrins, 2,841 pseudohalides, 2,232.233 pyridine oxide, 2,494 quinones, 5,468 secondary phosphites. 5 , 4 j 9 selenides, 5,475,478 sensitizers silver halide light sensitivity, 6,97

Cumulative Subject Index

Platinum(I1) complexes

squaric acid, 2,455 stannyldithioforrnate, 5, 487 stannylene, 2, 17 substitution reactions, 5,492 charge effects, 5,496 steric effects, 5 , 496 sulfato, 5.470 sulfides, 5,471.475 inversion, 5,478 sulfinato, 5,470 sulfites, 5,470 sulfoxides, 5,479 sulfurdiimine monodentate, 2, 191 reactivity, 2, 194 sulfur dioxide, 5,485 sulfur ligands, 5,471 tellurides, 5,475 tertiary arsines, 5,462 tertiary stibines, 5,462 tetrathiafulvalenes, 5,485 tetrathiolenes, 5,485 thiocarboxylates, 5,480 thiocyanates, 5: 487 thio-1,3-diketonates, 5,483 thiolato, 5,473 thionitrites honding, 2,192 thiourea. 5,480 triazenes, 5,438 triazines bridging ligands, 2,201 urea, 2,286 uridine, 5,434 vinyl reactions, 5,402 xanthates, 5,481 ylides, 5,385 Platinum(0) complexes acetylides, 5,387 alkenes, 5,410 synthesis, 5,410 alkynes, 5; 415 electrophilic attack. 5,416 NMRl 5,415 properties, 5, 415 allenes, 5,412 cyclopropene, 5,411 haloalkenes reactions, 5,414 rnethylencbis(diphenyIphosphine), 5,457 merhylene~cyclopropanc,5,410 nitriles structure, 2,262 organotin(1V) compounds, 2,16 phosphines, 5,440 NMR, 5,44U reactions, 5,443 structure, 5,440 synthesis, 5,440 physical properties, 5,413 pnictides, 2, 1052 reactions, 5,414 squaric acid, 5,411 tertiary phosphites, 5,442 Platinum(1) complexes isocyanidcs, 5,380 Platinum(I1) complexes acetylacetone iodine complexes, 2,386 ace tylides synthesis, 5,387 alkenes, 5,403

Platinum(l1) complexes reactions, 5,408 synthesis, 5,403 alkyl diphenylphosphinites, 5,447 amines, 5,422 a-amino acids chlorination, 5, 427 aromatic nitrogen ligands, 5, 429 bibenzimidazolyl, 5,433 biimidazolyl, 5,433 binuclear (p-0,O')-bridged, 5,471 bipyridyl, 5, 430 carbon-metalated phosphines, 5. 453 carbon-metalated phosphites. 5 . 453 cationic alkoxycarbenes, 5, 384 chelated amines ring conformation, 5,424 chelating phosphorus ligands, 5. 450 chemotherapeutic agents, 5,433 cyanides, 5,375 spectroscopy, 5,375 structure, 5,375 cyclic amines, 5,424 dX

configuration, 1 , 17 magnetic properties, I , 274 spectra, 1,255 square planar cis-trans isomerization. 1. 515 substitution rcactions, 1,311 germyl, 5,420 glycine IR spectra, 5.427 reactions, 5,427 guanidine, 2, 283 halides, 5,488 heterobimetallic, 5,433 hexafluoro-2-butyne, 5,415 homornetallic, 5,433 hydrazoncs, 5,438 irnidates, 2,278 imidazole, 5 , 433 isocyanides, 5, 380 2,6-lutidine, 5, 430 l.S-naphthyridine, 5,431 oximes, 2,270,272 I,lO-phenanthroline, 5,430 phosphido-bridged. 5,456 phosphines, 5,445 bond enthalpies, 5,447 NMR, 5,448 structure, 5,447 synthesis, 5 , 445 phosphites, 5,446 phthalazine, 5,432 phthalocyanine, 5,434 planar substitution reactions, 5, 492 polydentate phosphorus ligands, 5.452 porphyrin, 5,434 pyrazolates, 5,432 pyrazolylborates, 5,432 pyridine, 5,429 Schiff bases, 5,426,439 sulfurdiimine fluxional behavior, 2, 192 triazines excited-stated geometry, 1.407 monodentate, 2, 196 Platinum(I11) complexes sromatic nitrogen ligands. 5. 439 binuclear (p-0,O')-bridged, 5,471 Platinum(1V) complexes amines, 5,428

Cumulative Subject Index

200

aromatic nitrogen ligands. 5.435 cyanides, 5,377 isocyanides. 5, 350 macrobicyclic. 5?328 magnetic properties. 1.273 phosphines. 5.462 reduction vanadium(l1) complexes, 3,473 six-coordinate substitution reactions. 5 , 497 spectra, 1.254 I'latinum electrodes potential range aqueous solution. 1, -180 Platinum group metals electroplating? 6. I 1 recovery anion exchange resins, 6,823 refining. 6>830 smelting, 6: 834 solvent extraction, 6. 806 Platinurn oxides colloidal catalysts, oxygen production from watcr, 6. 519 in photciproduciion of hvdrogen from water, 6>513 Platinum salts, his(croconato)partially oxidized, 6, 112 Platinum salts. bis(squarat0)partially oxidized, 6, 142 Platosamminc chloridc -see Rcisct's sccond chloride Platosemidiammine chloride -see Peyrone's salt Plumbacarboranes. 3,219 Plumbate, diphenyltris(acetato)tetramethylammonium salts structure, 1,90 Plumbates. 3,204 Plumbocene lunctionally substituted, 3.218 nomenclaturc, 3,217 Plumbunic acid. 3,206 Plumbylene complexes transition metals, 2, '17 Plutonium envirorimental chemistry. 6, 961 fast reactor fuel, 6.924 Purex process. 6,946 ooisonin. ' chelaticng agents. 6. 769 237PU

determination. 1.548 purification. 6.925 recovery from nuclear fuel waste, 6,960 separation from uranium in reproccssing irradiatcd nuclcor tuck, 6, '138 sequestering agents. 6,962 Plutonium- 147 recovery. 6,959 Plutonium breeder LMFBR fuels, 6,926 Plutonium carbide nuclear fuels. 6.928 Plutonium complexes, 3,1131-1215 cupferron, 2,510 Plutoniurn(II1) complexes autocatalytic reaction with nitric acid, 6,947 Plutonium(1V) complexes reduction by uranium(IV), 6,949 Plutonium dioxidc rcprocessing irradiated nuclear fuels, 6,927 Plutonium dioxide ions disproportionation Purex process. 6,946

20 1

Cumulative Subject ladex

Plutonium ions extraction from nitric acid by tributyl phosphate, 6, 947 Purex process, 6,950 hydrolysis Purex process. 6.946 oxidation state reduction, 6.947 Pnictide ligands double bonds. 2. 1045 triplc bonds, 2, 1046 Podandocoronands classification, 2, 919 Podands alkali metal complexes. 3.3. 17-23 NMK,3,20 classification, 2,919 Polarization, 6, 3 Polarography, 1,481 hydrogen or oxygen production Crom water coordination complex catalysts. 6, 532 Polaroid SX-70 metallized dyes, 6 , 106 Polonium, 3,299-307 bonding, 3,299 coordination compounds. 3. O ;n geometry, 3,2YY toxicity, 3,307 valence, 3,299 Polonium complexes diethyldithiocarbamate. 3.307 thiourea, 3,307 Polonium(1V) complexes solubility in carboxylic acids. 3.304 Polonium hydroxide solubility in acids, 3, 304 Poloniuni perchlorate complexes with tributyl phosphate. 3 . 304 Polonium tetrachloride complexes with tributyl phosphate. 3.303 Polyamines titrimetry, 1, 553 Polyanions complete ligands, 3, 1047 lacunary ligands, 3, 1047 organic, 3,1052 Type I, 3, 1050 Type I I , 3 , 1050 Polyazamacrocyclcs, 2.899913 anionic complcxcs, 2,948 Pol yazapolyoxamacrocycIes anionic complexes, 2 , 948 Polybipyridyl electrode coatings, 6, 19 Polyborates minerals, 6, 844 Polycarboxylic acids alkaline earth metal complexes, 3. 32-35 amino chelating agents, heavy metal poisoning, 6,768 Polychromates, 3,94 1 structures. 3. 943 Pol yethers alkali metal cotnplexcs. 3.48 alkaline carth mcral complexes. 3 . 4 8 Polygalacturonic acids metal complexes. 2. 985 Poly(L-glutamic acid) metal complexes. 2.764

Polypyrazolylgallates

Polyisothiouronium group chelating resins mineral processing, 6,826 Polyketones metal complexes, 2,399 Poly( L-lysine) metal complexes, 2, 764 Polymerization solid state, 1, 470 Polymers boron-nitrogen, 3, 101 corirdination nomenclature! 1. 125 electrode surfaces, 6, 16 linear nomenclature. 1, 126 nomenclature, 1, 125 Poly(2-methyl-8-quinolinol) electrode coatings, 6, 19 Polymolybdate clusters, 2, 149 Polyrnolybdates cyclic voltammetry, 3, 1051 clcctrochcmistry, 3, 1051 electronic slruclure. 3, 1051 in photogalvanic hydrogen production from water, 6. 332 spectroscopy, 3,1051 Poly(N-vinylimidazole) metal complcxes color photography, 6, 109 Polynitriles metal complexes, 2, 263 Polynuclear aqua cations, 2,296 Polynuclear aromatic hydrocarbons hydrogenation catalysis, ruthenium complexes, 6,233 oxidative cleavage ruthenium tctroxide, 6,358 Pol ynuclcar cations hydrates metal-oxygen bond distances, 2, 308 p-hydmxo

hi-idgingligands. 2,299 Polynuclear compounds cyclic nomenclature, 1, 125 nomenclature. 1, 122, 125, 133 Polynucleo tides stability magnesium ions, 6,565 structure. 6 >562 Poly(L-ornithine) metal complexes, 2, 764 Polypeptides mcral complcxcs geochemistry, 6, 866 tx-Polypeptides 0-Polypeptides, 6,556 models. 6,556 Polyphosphate complexes isomerism, I , 202 linkage. 1. 186 Polypodands alkali metal complexes, 3.23 Polypropylene dyes. 6 : 73 Polypyrazolvlhorates metal complcxcs, 2 , 87,245-257 bidctitatc. 2.246 biological applications, 2.255 preparation. 2, 246 tridentate, 2,247 Polypyrazolylgallates

Polypyrazolylgallates metal complexes, 2,257 Polypyridyl ligands metal complexes, 2,90 Poly( 8-quinolinol) electrode coatings, 6, 19 Polysaccharides metal complexes geochemistry, 6,868 Polyselenides metal complexes geochemistry, 6,854 Polysulfide ligands bond distances and angles. 2, S41 metal complexes, 2,54C-547 bonding, 2,546 dinuclear, 2,542 geometry, 2,546 mononuclear (~~ ring4 systems, ) ~ 2,541 polynuclear pn-S atoms, 2,543 reactions, 2,545 b-S, type atoms, 2,545 solid state structures, 2,545 synthesis, 2,545 solutions, 2,541 Polysulfur oxides metal complexes, 2,636 Polytungstates electrochemistry, 3, 1050 Pol yt yramines electrode modification, 6,23 Polyuronic acids metal complexes, 2,985 Polyvanadates, 3, 1028 mixed valence, 3,1028 Polyvinylferrocene electrode coatings, 6, 19 attachment, 6,19 Poly(4-vinylpyridine) electrode coatings, 6, 17 redox centres, 6,17 eicctrodes, 6, 16 Porins cation transport, 6,553 Porphin metal complexes geochemistry, 6,862 synthesis, 2,816; 6,202 Porphinoids metal complexes synthesis and reactions, 6, 192-202 Porphodirnethanes, 2,855 Porp hyrazines metal Complexes dyes, 6,91 Porphyrin, N-alkyldemetallation, 2, 848 metallation, 2,848 synthesis, 2,847 Porphyrin, N-amino-, 2,849 Porphyrin, N,N’-dialkyl-, 2,849 Porphyrin, dihydrometal complexes geochemistry, 6,862 Porphyrin, hydrometal complexes biology, 6,546 Porphyrin, octaethyliron complexes, 4,260, 1266,1267 Porphyrin, tetrahenzozinc complexes template reactions, 5,993

Cumulative Subject Index Porphyrin, tetrahydrometal complexes geochemistry. 6,862 Porphyrin, tetraphenylindium complexes radiopharmacology. 6,971 iron complexes, 4,260,1266 zinc complexes spectra, 6,617 synthetic leaf experiments, S,99S Porphyrinogens, 2 - 855 Porphyrins, 2,814856 acid-base reactions, 2,817 alkaline earth metal complexes, 3 , 5 8 aromaticity, 2. 815 basket handle. 3. 1269 cadmium complexes, 5.993 capped iron complexes, 4,1269 cavity metal complexes. 6,548 chelate complexes, 2,374 coal and oil shales, 6,615 cohalt oxidation catalysts. 6 , 387 cobalt(I1) gable model compounds, 6, 688 complexes solution studies, 6,616 coordination chemistry, 6,615 copper(I1) geochemistry. 6.862 copper complexes, 2.982 cycloaddition reactions, 2>817 demetallation, 2,817 deuteration, 2. 817 diamagnetic NMR. 2,816 dimeric, 6,615 electrocatalytic reduction of oxygen, 1,488 electrophilic attack, 2,877 epoxidation, 2, 845 gallium(I11) geochemistry, 6,865 hydroxylation, 2: 844 inner protons, 2,815 IR spectra, 2,816 iron, 2,981: 4,259; 6,614 dioxygen carriers, 6,684 electronic effects, 6, 617 magnetic properties, 6,618 oxidation catalysts, 6,381 oxidation state, 6>617 redox chemistry, 6.616 iron(l1) cymidc ion binding, 4. 1268 dioxygen adducts, 2,317 iron( JII) geochemistry, 6,862 kinetic formation kinetic template reactions, 1,450 manganese oxidation catalysts, 6.376-379 metal complexes, 2.980 biology, 6,546 catalysts, oxygen production from water, 6,517 dioxygen, 2,325 electron transfer processes, 1,495 evolution. 2.961 gcochemistry. 6. 861-866,873 minerals, 6,850 prebiotic systems, 6, 873 redox potentials, 1,498 metal insertion reactions, 2, 818

202

203

Cumulative Subject h d e x

metallation. 2,817 metal-metal bonding, 2.843 models carbon monoxide binding, 6.698 nickel(I1) geochemistry, 6,862,864 nickel complexes, 5,271 niobium(V) complexes, 3,620 nomenclature, 3,350 nucleophilic attack, 2,817 osmium(lI), 6,615 oxidation, 2,844 N-oxides, 2,849 oxygenated cobalt dioxygen carriers, 6,686 in oxygen production from water, 6,523 photochemistry, 2, 846 photoreduction, 2,846 photosensitizers, 5,994 picket fence iron complexes, 4,1269 reactions at metal, 2,844 at periphery, 2,817 reactions with oxygen. 1: 515 redox chemistry, 2, 846 reduction. 2, 852 resonance energy, 2.8'14 ruthenium(II), 6,615 sitting atop metal ion complexes, 2,818 spectra. 2,815; 6,615,617 N-substituted, 2,847 synthesis, 2, 816; 6, 196 tantalum(V) complexes, 3,620 transition metals, 6,615 transmetallation, 2, 817 zinc complexes, 2,982 vanadyl geochemistry, 6,861.862 zinc complexes, 5,9393 ligand modification, 5,993 Post transition elements amidine complexes, 2,205 triazine complexes, 2,205 Potassium absorption radiopharmaceutical agents, 6,968 biology, 6,546 reactions with alcohols, 2,336 transport microorganisms, 6,559 Potassium autunite carnotite from. 6,891 Potassium complexes o,o'-catecholdiacetic acid. 3, 16 biology, 6,549,551-562 crown ethers, 3 , 3 9 phthalocyanines, 2, 863 porphyrins, 2,820 ribosomes, 6,549 Potassium ferricyanide discovery, 1 , 3 Potassium hexachloromolybdate, 3, 1230 Potassium hexacyanoferrate discovery, I , 3 Potassium ions biology, 6,559 selective binding biology, 6,551 Potassium iron hexacyanoferrate -see Prussian blue Potassium peroxodicarbonate

Propan-2-01

synthesis, 2,449 Potassium salts electrolyte balance, 6,771 gravimetry, 1,525 Povarnin, Georgii Georgievich, 1, 15 Powders metal mineral processing, 6,829 Praseodymium Purex process, 6,941 Praseodymium, tetrakis(dimethy1dithiophosphonium)stereochemistry, 1,94 Praseodymium, tris(2,2,6,6-tetramethyl-3,5heptancdione). photosubstitution, 1,408 Praseodymium complexes edta, 3,1089 tetrapositive oxidation state hydrated ions, 3, 1113 tetravalent fluorides, 3, 1115 Praseodymium(I1) complexes structure, 1. 101 Prebiotic atmosphere, 6, 870 Prebiotic systems, 6,843-873 Precipitation mineral processing, 6.827-830 Preproinsulin, 5.999 Pressurized Water Reactor, 6,883 Procarboxypeptidases, 5,1004 Proinsulin, 5,999 Proline peptides metal complexes, 2,764 synthesis metal catalysis, 6,468 L-ProIine lanthanide complexes NMR, 3, 1103 Promethium Purcx process, 6,941 1.2-bis(diphenylphosphino)Propane (R)rhodium complexes asymmetric hydrogenation, 6,251 1.2-Propanediamine complexes conformation, I , 197 isomers, I , 202 1.3-Propanediamine complexes isomerism, 1,25 metal complexes, 2,43 conformation, 2,45 1,S-Propanediamine, N-[2-(2-aminoethyl)amino]ethylmetal complexes, 2,51 i ,3-Propanediamine, N,N'-bis(2-aminoethyI)metal complexes, 2,52,54 1,3-Propanediamine,N,Nr-bis(3-aminopropyI)metal complexes, 2.56 Propane-1 &diol, 3-mercaptometal complexes, 2,804 Propan-l-ol,2-amino-2-methylcopper(r1) complexes, 2,795 Propan-l-ol,2,3-dimercaptochelating agent heavy metal poisoning, 6,767 Propan-l-ol,3-(methylamino)copper(I1) complexes, 2,795 Propan-2-01 asymmetric carbonylation catalysts, palladium complexes, 6,293 carbonylation catalysts. rhodium complexes, 6,273 Propan-2-01, l-amino-

Propan-2-01

Cumulative Subject Index

metal complexes, 2,795 Propene acetoxylation palladium catalysts, 6,367 allylic oxidation molybdenum-oxo catalysts, 6,354 ammoxidation molybdenum-oxo catalysts, 6,354 epoxidation cobalt-nitro complex catalysts, 6,373 oxidation tellurium-oxo compounds, 6,360 oxidative carbonylation palladium catalyzed, 6,369 Propene, 3,3,3-trifluorohydrocarbonylation/hydroesteri fication catalysts, palladium complexes, 6,286 Prop-2-en-l-ol,3-ethylthiodehydrogenase inhibition, S1 1017 fropionaldehyde hydrogenation catalysis, ruthenium complexes, 6,235 Propionic acid metal complexes geochemistry, 6,867 Propionic acid, 2-(N-acetylhydrazono)methyl ester hydrolysis, metal catalysis, 6,442 Propionic acid, u-[{2-[(a-carboxy-Z-hydroxybenzyl)imino]ethyl}imino]metal complexes, 2,788 Propionic acid, 2,3-diaminometal complexes. 2,750 methyl ester hydrolysis, metal catalysis, 6,421 Propionic acid, ethylenebis[ (carboxymethyl)imino]dimctal complexes, 2, 787 Propionic acid, cthylcncdiiminotetrametal complexes, 2,787 Propionic acid, 3-hydroxymetal complexes NMR, 2,467 Propionic acid, 2-oxalodecarboxylation metal catalysis, 6, 456 Propionic anhydride hydrolysis metal catalysis, 6.464 Propionitrile, aminometal complexes reactions, 6,451 Propicinohydroxainic acid metal complexes, 2,506 Propylene carbonylation catalysts, cobalt complexes, 6 , 271 hydroformylation catalysts, cobalt complexes, 6,259 catalysts, rhodium complexes, 6, 260: 262 reactions catalysts, 6,298 Propylene, 3-phenylhydroformylation catalysts, rhodium complexes, 6,261 Propylenediamine metal complexes, 2.34 Propylene oxide rcaction with carbon dioxidc catalysts. ruthenium cornplexcs. 6,294 Propyne reactions catalysts, 6,298 Prosopite

204

structure, 6.846 Pmsthecochloris aesfuurii photosynthesis. 6.591 Protactinium. 3, 1131-1215 chemistry, 6,955 environmental chemistry, 6,961 Protactinium complexes cupferron, 2.510 Proteases imaging systems, 6 , 126 Protcctive coatings electrophotography. 6, 123 Protein C blood coagulation. 6,593 calcium, 6,591 Proteins calcium binding to, 6,563 y-carboxyglutamate residues, 6, 577 denaturation alkali metal salts, 3 , 6 electron transfer active sites, 2, 525 electron transfer reactions, 6,653 I abeI Ied diagnostic nuclear medicine, 6,994 radiopharmacology, 6,972 labelling with indium radiopharmacology. 6,972 manganese requirements, 6,586 metal complexes, 2.759-774 binding sites, 2.769,771 biology, 6.546 geochemistry. 6. 866 naturally occurring. 2.974 occurrence, 2,962 reactions osmium tetroxide, 4,590 Proteolytic enzymes snake toxins zinc, 6,613 Proleus nz irabih molybdenum cofactor. 6 : 663 Prothrombin blood coagulation. 6,591 calcium binding, 6 - 564 Protocatechuate 3.?-dioxygenase, 4,232; 6,707 iron, 6,634 Protonation catalysis transition metal complexes, 6,231 platinum hydride complexes synthesis, 5,354 Proton electrochemical gradicnt, 6,714 Proton exchange amine ligands. 2 , 24 Proton loss catalysis transition metal complexes, 6,231 Protonolysis metal alkoxides. 2,352 Protons metal ions and, 6.312 Protoporphyrin IX iron, 6,614 iron(I1) complexes. 4. 1266, 1267 Prototype fast reactors fuel reprocessing, 6.955 Prussian blue. 1:2,29; 2, 7 , s ;4,221. 1203, 1206, :208 in cyclic water clcavage hydrogen and oxygen production, 6,525 electrode modification, 6,2'1 history. 1.2.22 Pseudobactin. 6,678

205

Cumulative Subject Index

animal infcctions, 6,679 Pseudocatalase Lactobacillus plantarum manganese, 6,706 manganese, 6,586 Pseudocotunnite structure, 6,847 Pseudocubanes structure hydroxide metal complexes: 2, 300 Pseudohalides metal complexes, 2,225 bonding, 2,225: 227 synthesis, 2,236 transition metal complexcs. 2: 228 Pseudometatungstates. 3,1034 Pseudomonas aeruginosa azurin structure, 6,651 nitrate reductase. 6. 664 Psychiatry lithium in, 6,772 Psychotria douarrei nickel uptake, 6,658 Pulse radiolysis nickel complexes synthesis, 5,290 Purex process, 6,926,939 actinides, 6,945 fission products, 6,940 flowsheets, 6,953 Purine, 6-benzylaminoantistain agent, 6, 104 Purines hydroxylation molybdenum hydroxylases. 6,659 metal complexes, 2,89,92,796, 976 gcochcmistry, 6,867 linkage isomers, 1, 186 zinc complexes, 5 , 956 Purlex process, 6,91 I Purple acid phosphatase iron, 6,634,636 manganese, 6,586 Purple bacteria anoxygenic photosynthesis, 6 : 589 Purple manganese acid phosphatase, 6,587 Purpureocobalt -see Cobalt, chloropentaamminePurpureocobaltic chloride -see Cobalt, ch!oropentaammine-. chloride Putidamonooxin, 6 , 71 1 Putrescine copper(I1j complexcs, 2,44 Pvochelin, 6,678 Pyrazine-2-carboxamide metal complexes, 2,796 Pyrazine-2-carboxylic acid metal complexes, 2,746 Pyrazine-2,3-dicarboxamidemetal complexes, 2,796 fyrazine-2,3-dicarboxylicacid metal complexes, 2,796 Pyrazines metal complexes, 2, 80 Pyrazole, 3,s-dialkylmetal complexes, 2,78 Pyrazole, 3,5-dimethylcadmium complexes, 5 : 951 metal complexes, 2,77 Pyrazole, 3,5-di(2-pyridyl)metal complexes magnetic exchange, 2,77 Pyrazole, l-thiocarbarnyl-

Pyridine

metal complexes, 2,801 Pyrazoles basic pK, metal complexes, 2,74 dehydrogenase inhibitor, 5,1017 metal complexes, 2,76,86; 5,948 steric aspects, 2,74 pK,, 2,77 Pyrazolines metal complexes; 2,79 2-methy1-6j-Pyrazulune, 1-(4-bromophenyl)-3-methyl-4-( carboxypheny1azo)chromium complex geometrical isomerism, 6,69 5-Pyrazolone, o-carboxyarylazometal complexes geometrical isomerism, 6, 68 5-Pyrazolone, l-phenyl-3-methyl-4-(2-carboxyphenylazo)chromium complex geometrical isomerism, 6,68 5-Pyrazolone, l-phenyl-3-methyl-4-(2-hydroxy-4sulfonaphth-1-y1azo)chromium complex geometrical isomerism, 6,69 Pyrazolones mctal. complexes color photography, 6,107 Pyrazon dioxygenase, 6,708 Pyridazines metal complexes, 2.80 Pyridine, tacetylenolization metal catalysis, 6,473 Pyridine, 2-(alkylthio)metal complexes, 2,801 Pyridine, 2-aminomctal complexes, 2,83 Pyridine, cinnamoylreduction for metal catalysis, 6,475 Pyridine, 2-cyanohydrolysis metal catalysis, 6,449 reactions with metal halides in alcohols, 2. 277 Pyridine, 4-cyanometal complexes, 2, 83 Pyridine, 2,6-diacetylcondensation with linear polyamines, 4,258 macrocyclic metal complexes template synthesis, 6, 160 reactions with amines aza macrocycles from, 2,903 reactions with hydrazine iron(I1) Salts, 6, 183 in template synthesis of imine chelates, 6 , 15Y Pyridine, dihydroin electroplating, 6 , 7 Pyridine, 4-(dimcthylaminojligands in carbonylation, 6,274 Pyridine, 313-dimethyl-2-thiabutylmetal complexes, 2,801 Pyridine, 2-hydroxymetal complexes, 2,795 Pyridine, 2-hydroxy-6-methyldodecacobalt complexes, 1, 168 metal complexes, 2,795 Pyridine, Z-mcrcaptooxide metal complexes, 2,805 Pyridine, methyiN-oxide metal complexes, 2,495

Pyridine

Cumulative Subject Index

Pyridine, 2-(methylaminomethyl)I-oxide metal complexes, 2,795 Pyridine, methyL2-(methylthio)metal complexes, 2,801 Pyridine, N-salicylidene-2-aminohydrolysis metal catalysis, 6,461 Pyridine, 2-vinylhydroesterification catalysts, cobalt complexes, 6,271 Pyridinecarbaldehyde hydration metal catalysis, 6, 474 hydrazone metal complexes, 6, 180 imine chelates, 6, 156 oximes metal complexes, 2,272 reduction for metal catalysis, 6,475 2-Pyridinecarboxaldoxime,O-acetylhydro 1y sis copper(I1) catalysis, 6,438 Pyridine-2-carboxamide metal complexes, 2,796

Pyridine-2,6-dicarbaldehyde in template synthesis of iminc chclatcs, 6. 159 Pyridines basic pK, metal complexes, 2,74 metal complexes, 2,76,79,83; 5.952 geochemistry, 6,867 linkage isomers, 1, 186 steric aspects, 2,74 N-oxide metal complexes, 2,495 Pyridine-Zsulfonic acid metal complexes, 2,796 Pyridinium compounds, I-benzyl-3-carhoxy in electroplating, 6 , 6 Pyridinols metal complexes color photography, 6; 107 Pyridoxal amino acid 9chiff bases metal complexes, 2,751 Pyridoxamine metal complexes, 2,795 Pyridoxylideneamine hepatobiliary imaging agent, 6,979 2-Pyridyl phosphonosulfate hydrolysis zinc(I1) catalysis, 6,444 Pyrimidine, 2,4-dihydroxyphotography diffusion transfer process, 6, 101 Pyrimidine, 4,6-dihydroxyphotography diffusion transfer process, 6, 101 Pyrimidine, 2-mercaptometal complexes, 2,802

Pyrimidines bases metal complexes, 2.976 hydroxylation molybdenum hydroxylases, 6,659 metal complexes, 2,80 geochemistry, 6.867 linkage isomers. 1.186 zinc complcxcs, 5,957 Pyrimidine-2-thione, 4$-dimethylmetal complexes, 2,802 Pyrimidine-2-thiune, 1 -methylmetal complexes, 2, 802 Pyrimidine-2-rhione. 1,41h-trimethylmetal complexes, 2,802 Pyrite, 4, 1240 brines, 6, 853 Pyrocatechol dioxygenases. 6,325 Pyrocatechol violet metallochromic indicator, 1,556 Pyrogallol in gravimetry, 1,524,532 Pyrometallurgy; 6,780,832-835 Pyrophosphatase inorganic activation, 6 , 581 Pyrophosphatc complcxcs cobalt( Hi) isomers, 1: 202 isomers: I. 203 Pyrophosphates copper electroplating, 6, 10 hydrolysis metal complexes. 6,447 Pyrophosphoramide, octamethylmetal Complexes. 2,499 Pyrophosphoric acid dialkyl esters uranium, 6,7Y7 Pyrotite, 4, 1240 Pyroxenes structure, 6, 845 2-Pyrrolecarbaldehyde Schiff bases metaI complexes, 2,721 Pyrroledithiocarboxylic acid metal complexes, 2.586 Pyrroles metal complexes. 2.79 geochemistry? 6>867 Pyrutite, 4, 1240 Pyruvate kinase activation magncsium ions, 6,580 activators sodium ions, 6,561 Pyruvic acid amino acid Schiff bases metal complexes, 2,752 asymmetric hydrogenation catalysts, rhodium complexes, 6,257

206

Quartz flotation, 6,783 Quatcrenes alkali metal complexes, 3,57 Quilon chromium complexes, 1: 22 Quin 2 calcium determination, 6,594 Quinaldine zinc complexes, 5,952 Quinaldinic acid in gravimetry, 1,524,530 Quinaldohydroxamic acid as metal precipitant, 2,506 Quincite structure, 6,850 Quinodimethane, tetracyanometal complexes, 2,263 Quinodimethane, 7,7’,8,8’-tetracyanoelectrode polymer modification, 6,24 Quinoline, 8-acetoxyhydrolysis metal catalysis, 6,471 Quinoline, 8-(alkylthio)metal complexes, 2; 801 Quinoline, 8-(2-~arboxyphenyl)aminochromium complexes isomerism, 6, 72 Quinoline, 2-cyano-8-hydroxyhydrolysis metal catalysis, 6,452 Quinoline, 5,7-dichloro-8-hydroxyin gravimetry, 1,528 Quinoline, &hydroxymetal complexes, 2.795 in analysis, 1,523 carboxylic acid esters hydrolysis, metal-catalyzed, 6,438 in gravimetry, 1,527 metal complexes bromination, 1, 418 electrophotography, 6,122 Quinoline, 8-hydroxy-2-methylaluminum complexes liquid-liquid extraction, 1.545 in analysis, 1, 523 cobalt(I1) complexes, 2,795 in gravimetry, 1,529 Quinoline, 8-mercaptometal complexes, 2,800

Quinoline, 8-mercapto-2-methylmetal complexes, 2, 800 Quinoline. 2-methyl-8-(methylthio)metal complexes, 2,801 Quinoline, 8-methylthiometal complexes, 2,801 Quinoline-2-carboxylic-acid, 8-hydroxymethyl ester hydroiysis, metal-catalyzed, 6,439 Quinolines metal complexes, 5,952 geochemistry, 6,867 zinc complexes, 5,952 8-Quinolineseienol metal complexes, 2 , 807 Ouinolinc-5-sulfonic acid, 8-acetoxyhydrolysis metal catalysis, 6,471 Quinoline-5-sulfonic acid, &hydroxyiron complexes gravimetry, 1,524 metal complexes iodination, 1,418 Quinoline-5-sulfonic acid, 8-hydroxy-7-iodometal complexes absorptiometry, 1,549 Quinoliniurn salts in gravimetry, 1.535 Quinolinol metal complexes color photography, 6,107 8-Quinolinol biological activity, 6,771 gallium and indium complexes radiopharmacology, 6,971 radionuclide complexes radiopharmacology, 6,994 8-Quinolyl sulfate hydrolysis metal caralysis. 6,465 Quinones metal complcxes, 2,397 photoreduction zinc complexes, 5,994 o-Quinones oxidative addition reactions to metal complexes, 2,398 Quinoxaline-2,3-dithiol metal complexes liquid-liquid extraction, 1,547

207

Racemization amino acids metal complexes, 6,467 solid state, 1,466 trigonal twist mechanism, 1, 466 Radiative transitions, 1,395 Radioactive waste high level disposal, 6,895 Radiochemical purity technetium-99 in medicine, 6, 976 Radionuclides diagnostic and therapeutic applications, 6: 963 drugs, 6,882 man-made generation, 6,882 metallic nuclear properties, in medicine, 6- 965 nuclear properties medical applications, 6,964 pharmacology, 6,963 positron emitting in medicine, 6, 965 production, 6,963,964 recovery from nuclear power reactor fuels. 6 , 959 Radiopharmaccutical agents chemistry, 6,968-985 classification, 6,983 diagnostic imaging techniques, 6.985 technetium essential, 6,973, , 83 structure, 6,977 in vivo stability, 6,976 . Radiopharmacy, 6,881-996 Radiotherapy, 6,963 Radiotracer techniques, 6,963 Raman spectroscopy metal in watcr complcxcs, 2, 309 Rare earth complexes acetylacetone synthesis, 2,377 guanidinium, 2,282 hydroxamic acids, 2,506 Rare earth metals extraction cation exchange resins, 6 , 817 Rate of reaction solvent effects, 1,503 Reaction mechanisms, 1.24 Red blood cells labelled, 6,994 Redox catalysts in photoproduction of hydrogen from water, 6, 513 Redox centres electrode coatings poly(4-vinylpyridinc), 6 , 17 Redox indicators, 1,558 Redox potentials aqueous solution, 1,4&3 isostructural, isoelectronic species, 1 498 ligands, 1,496

solvent effects. 1 , 5 I R structure coordination compounds, 1, 496 transition metal complexes biology, 6,549 Redox process. 6.936 Redox properties bipyridyl metal complexes, 2,90 excited electronic states, 1,489 Redox proteins multi-centre electron transport, 6, 712 Rcducrion carbonyl compounds for metal catalysis, 6,475 coordinated imines? 1,454 electrolytic in reprocessing irradiated nuclear fuels, 6,940 Reductive coupling nitrile metal complexes. 2,265 Reiset’s second chloride configurationl 1 . 17 history, 1 , 3 Relaxation sclcction rules spcctral band intznsities, 1, 244 Relief-image-forming systcms photography. 6. 124 Repulsion energy coerlicients, 1, 33, 34 Repulsion lawl I: 32 Resin-in-pulp process gold extraction. 6,822 Resolution amino acids metal complexes, 1,425 Resorcinol, 2-4-dinitrometal complexes, 2,273 Resorcinol, 4-(2-pyridylazo)metallochromic indicator, 1,556 vanadium determination, I , 548 Rcspiration Escherichila coli, 6. 715 electron transfer reactions. 6,712 Reverse micelles in water cleavage, 6,527 Rhenates, h e p t q a n o potassium salt structure, 72 Rhenates, hexahalomagnetic properties. 4, 173 polarography. 4. 173 spectra, 4, 172 substitution reactions, 4, 173 Rhenates, octachlorobishistory, 1.23 Rhenates, tetracyanodioxysix-coordinate compounds structure, I , 53 Rhenium liquid-liquid extraction, 1,541 Rhenium, dichlorobis(l.2-ethanediamine)-

208

209

Cumulative Subject Index

cyclic voltammetry, 1,483 Rhenium, dioxytetrakis(pyridyi)six-coordinate compounds structure, 1 , 5 3 Rhenium, octachlorodiphotoreactivity, 1 , 4 M Rhenium, tetrachloronitridotetraphenylarsenate stereochemistry, 1. 44 Rhcnium, tetrachloroouystereochemistry, 1. 44 tetraphenylarsenate stereochemistry, 1.34 Rhenium, tris(ci.7-1,Z-diph'nyle~hyI'ne-l,2.-diihiolaici)structure, 1.24 Rhenium, tris(dithiodibenzoy1)structure, 1, 63 Rhenium bromide Re,Br, structure, 1, 28 Rhenium complexes, 4.125 acetylacetone, 2, 376 synthesis, 2,375,378 amides synthcsis, 2 , 166 amidincs, 2,276 bridging ligands, 2: 199 chelating ligands, 2, 204 applications, 6, 1016 arsines, 4, 162 catalysts alkylation, 6, 298 1,4-diaza-1,3-butadiene. 2.210 1,3-diketones synthesis, 2,377 dinuclear, 4, 128 imidates, 2,277 imines, 2 , 280 mononuclcar oxidation statcs, 4, 127 neutral 1,3-diketones72,402 nitrosyl, 4, 202 2-aminobenzenethiol, 4,207 tris(2,2'-bipyridine), 4,202 tris(1,lO-phenanthroline). 4.207 oxo oxidation catalysts, 6 , 355: 356 phosphines, 4, 162 phthalocyanines, 2.866 polypyrazolylborates, 2.251 porphyrins, 2,826 pseudohalides, 2, 230 thionitrosyl, 2 , 119 triazines bridging ligands, 2, 199 chclating ligands, 2, 204 trinuclcar, 4, 128 Rhenium(0) complexes, 4, 128 Rhenium(1) complexes, 4, 12g135 alkyl isocyanides, 4. 128 aryl isocyanides, 4, 128 cyanides, 4, 128 dinitrogen, 4, 130 dinuclear dinitrogen, transition metals. 4. 133 magnetic behavior, 1,273 mixed dinitrogen-phosphines mononuclear, 4, 129 mixed metal dinuclear, 4, 132 trinuclear, 4, 132 phosphines, 4, 134 phosphites, 4, 135

Rhenium(II1) complexes

ureadiide- 2,287 Rhenium(I1) complexes, 4, 135-143 dinuclear bidentate arsine.s. 4, 139 bidentate phosphines, 4, 139 hydrides. 4$142 monodentate phosphines, 4, 136 Rez*+>4. 136 4. 136 sulfur. 4, 142 magnetic bchavior, I , 273 mononuclear. 4. '135, 137 alkyl isocyanides, 4, 135 arsines, 4, 136 aryl isocyanides, 4, 135 cyanides, 4- 135 phosphines, 4,136 trinuclear. 4, 142 Rhenium(II1) complexes, 4, 143-164 cyanides, 4, 143 alkyl isocyanides, 4. 143 amides, 4, 144 amidinez, 4, 146 amines, 4,144 arsines, 4, 147 aryl isocganides, 4. 143 cyanaks, 4, 145 diazines, 4,144 diethyldicarbamato, 4, 150 fi-diketones, 4, 149 dinitrogen, 4, 144 N heterocycles, 4,144 nitriles, 4, 146 oxygen compounds, 4,149 phosphines, 4,147 phosphites, 4, 147 stihines, 4. 147 sulfur compounds, 4, 149 synthesis, 2! 9 thiocyanates, 4, 145 thiuurea, 4, 150 triazines, 4, 144 dinuclear alkyl carboxylates, 4, 158 amidines, 4, 156 arsines. 4, 157 aryl carboxylates, 4, 158 halides. 4, 154 hydrides. 4,150 mixed donor atom ligands, 4,153.160 Y heterocycles, 4, 156 phosphines. 4, 157 ReZ6+,4.154-160 selenocyanates, 4, 156 sulfates, 4, 158 sulfur ligands, 4, 160 thiocyanates, 4, 156 hexanuclear. 4, 164 sulfides, 4, 164 tellurides, 4, 164 magnetic behavior, 1. 272 mononuclear, 4,143-154 hydrides, 4.150, 151 trinuclear alkyl isucyanides, 4, 161 amines. 4, 161 ainmines, 4, 161 arsines, 4, 162 aryl isocyanidcs, 4, 161 azides, 4. 161 cyanides, 4: 161 dinitrogen, transition metals, 4, 133 halides, 4: 163

Rhenium(II1) complexes nitriles, 4, 161 nitrogen compounds, 4, 161 oxygen compounds, 4,162 phosphines, 4,162 Rea9+,4,160-164 selenium compounds, 4, 163 sulfur compounds, 4,163 thiocyanates, 4,161 Rhcnium(1V) complexes, 4,165177 dinuclear, 4, 176 magnetic behavior, 1,272 mononuclear, 4, 165-376 acetylacetonates, 4, 170 alkoxides, 4, 170 alkyl isocyanides, 4,165 amidatcs, 4, 167 ammonia, 4,166 arsines, 4,168 cyanates, 4,166 cyanides, 4,165 diazines, 4, 166 hydrides, 4, 174 imides, 4, 166 mixed donor atom ligands, 4: 175 mixed oxide-halides, 4, 171 N heterocycles, 4,166 nitriles, 4, 167' nitromethane, 4, 171 oxygen compounds, 4, 170 phosphines, 4,168 pyridines, 4, 166 [ReCISL]-, 4,172 [ReXS(OH)IZ-,4,172 [Rex,]*-, 4,172 spectroscopy, 4,172 stability, 4, 172 structure, 4,172 stibines, 4, 168 sulfites, 4,171 sulfur compounds, 4, 170 thiocyanatcs, 4, 166 water, 4, 150 spectra, 1,252 Rhenium(V) complexes, 4,177 2-aminobenzenethiol, 4: 188, 192 2,2'-bipyridyl, 4, 187 4-chloro-2-aminobenzenethio~, 4,192 cyanides, 4,187 dialkyldithiocarbamates, 4, 188 1,2-ethanedithiol, 4, 192 ethylenediamine, 4,187 halides, 4,192 hexacyanates, 4, 193 hvdrides, 4, 192 imides, 4,188 lanthanidcs, 4, 192 magnetic behavior, 1,272 mononuclear acetonitrile, 4, 179 amines, 4,177,186 arsines, 4,179 aryl isocyanides, 4, 177, 185 1,2-bis(ethyIthio)ethane, 4, 182 cyanides, 4,177,185 dimethyl sulfoxide, 4, 187 dioxane, 4,182 dithiocarbamates, 4, 183 N,N'-ethylenethiourea, 4, 182 halides, 4, 183 macrocycles, 4, 184 mercaptothioacetic acid, 4, 183 mixed donor atom ligands. 4,184 N heterocycles, 4,177, 186

Cumulative S'ubject Index

210

octaethylporphyrin, 4,185 1,4-oxathiane, 4. 182 oxygen compounds, 4,181 phosphines, 4. 179?186 phosphites, 4,179 [Reo,]+, 4,185 [Re0I3+.4,177-185 Schiff bases, 4, 184 stibines, 4, 179 sulfur compounds, 4,181 thiocyanatcsl 4.179,187 thiols, 4, It12 thiourea, 4.182,187 vinyl amides, 4, 185 N heterocycles, 4,187 nitrides, 4: 188 octaethylporphyrin, 4, 188 oxo-bridged mixed Ruoro-hydroxo-oxalato, 4,188 p-oxo-bridged [Re,0,l4', 4, 187 oxygen compounds, 4- 192 polymolybdates, 4: 192 polytungstates, 4, 192 pyridine, 4,187 Schiff bases, 4, 188 sulfides, 4,192 Rhenium(V1) complexes, 4,194 alkoxides, 4, 196 amides, 4, 194 amincs, 4, 199 carboxylates, 4, 199 dimethylformamide, 4, 199 dioxane, 4,198 halides, 4,195,199 2-hydroxypyridjne, 4, 199 imides, 4,194 magnetic behavior, 1,271 mixed sullur-nitrogen compounds, 4,196 N heterocycles, 4,199 nitrides, 4, 194 oxide halides, 4, 195 oxoanions, 4, 'I96 pyridinc, 4, 199 sulfates, 4, 198 sulfur compounds, 4,196 tellurates, 4, 198 Rhenium(VI1) complexes, 4, 196202 amides, 4, 196 deuterides, 4,201 halides, 4,201 hydrides, 4: 201 imides, 4, 196 nitrides, 4, 196 thiols, 4,201 Rheumatoid arthritis gold drugs, 5,875 a-peniciIlamine, 6, 769 Rhodate, aquapentachlorostereochemistry, 1.50 Rhodate, diaquabis(su1fonyldiimino)structure. 1,26 Rhodium cationic catalysts hydrogenation, 2,710 clusters metal-metal bonding, 1, 169 electroplating, 6 , 11 occurrcncc, 4,9U2 Rhodium, benzonitrilcpentoamminehydrolysis, 4, 962 Rhodium, his(2,3-his(diphenylphosphino)-l-propanol)tetrafluoroborate, 4,928 Rhodium, bis(dipheny1phosphinoethane)-, 4,906 chloride, 4,926

211

Cumulative Subject Index

perchlorate structure, 4,928 Rhodium, bis(vinylidenebis(dipheny1phosphine))perchlorate, 4, 928 Rhodium, bromotris(tripheny1phosphine)structure, 4,917 Rhodium, carbonylhydridotris(tripheny1phosphine)catalyst alkene hydroformylation. 6 ; 260 Rhodium, chiorotetrakis(difluoro( dimethylamino) phosphine)-, 4,924 Rhodium, chlorotetrakis( triffuoro(diethy1amino)phosphine)-. 4,924 Rhodium, chlorotris(tripheny1phosphine)-,4,913 catalyst hydrogenation of unsaturated compounds, 6,241 NMR, 4,918 solution chemistry, 4,918 structure, 4,917 thermal decomposition, 4,918 X-ray emision spectrum, 4, 918 Rhodium, dicarbonyl3-trifluoroacetylcamphorare gas chromatography, 1,560 Rhodium, dicyanotris(dipheny1phosphinoethane)di-, 4, 928 Rhodium, hexa.kis(trifluorophosphine)di-, 4, 905 Rhodium, hydridobis(dipheny1phosphinoethane)-,4,924 Rhodium, hydridotetrakis((buty1idynetrimethylene)phosphite)-: 4,921 Rhodium, hydridotetrakis(methyldipheny1phosphine)-, 4, 924 Rhodium, hydridotetrakis(triary1 phosphite)-, 4,922 Rhodium, hydridotetrakis(triethy1 phosphite)-, 4, 921 Rhodium, hydridotetrakis(trifluorophosphine)-, 4,921 Rhodium, hydridotetrakis(trimethy1phosphine)-,4,924 Rhodium, hydridotetrakis( tripheny1phosphine)-, 4,921, 922 Rhodium, hydridotetrakis(tripheny1 phosphite)-, 4,923 Rhodium, hydtido(trifluorophosphine)tris(ttipheny1phosphine)-, 4.921 Rhodium, hydrido(triphenylarsine)rris(tripheny1phosphine)-, 4,921,924 Rhodium, hydridotris(tripheny1phosphine)-,4,916 preparation, 4,916 Xhodium, iodotetrakis(difluoro(diethy1amino)phosphine)->4,924 Rhodium, pentaamminethiocyanatobase hydrolysis, 1,504 Rhodium, pentaammincurealinkage isomerism, 4,461 Rhodium, pentaamrninc(urea)decomposition, 1,186 Rhodium, pentakis(trialky1 phosphite), 4, 929 Rhodium, tetrakis(acetat0)diantitumor properties. 4: 936 ozonization, 4,951 Rhodium, tetrakis(trimethy1phosphine)reactions, 4,926 Rhodium carboxylates, 4,903 chemotherapy, 4,903 Rhodium complexes, 4.901 acetylacetone synthesis, 2,376 alkylperoxo oxidation catalysts, 6, 349 amidines bridging ligands, 2,201 chelating ligands, 2, 205 amine base hydrolysis, 2,28 anticancer drugs, 6,758 applications, 4, 903; 6, 1019

Rhodiurn(1) complexes

asymmetric hydroformylation, 6,265 bimetallic, 4,1074,1076 carboxylic acids reactions, 2,443 catalysts alkyne hydration, 6,299 asymmetric hydrogenation, 6,250,257 carbon dioxide reactions, 6,294 carbonylation, 6,272 hydroformylation, 6,259 hydrogenation, 6,239,245 water cleavage, 6,494,497 cationic, 4, 1072, '1074 chlorunitrosylnitrobis(tripheny1phosphine). 4, 1070 corrins, 2,884 corroles, 2,874 1,4-diaza-1,3-butadiene, 2,210 dichloronitrosylbis( triphenylphosphine), 4, 1068 1,3-diketones carbon bonded, 2,393 mixed metal clusters, 2,394 dimethyl sulfoxide, 2,490 2;6-luridine oxide, 2,496 mercury, 4,1075 mkccllaneous, 4, 1065, 1076 mixcd oxidation state, 4, 1065 molybdenum, 4,1076 nitrosyl, 2,104; 4,1065,1074 reaction with carbon monoxide, 2, 113 nitrosylbis(carboxylato), 4, 1071 nitrosylbis(di-(p-tolyl)triazenido), 4, 1071 nirrosylbis(tertiary phosphine), 4, 1072 nitrosyldinitratobis(triphenylphosphine), 4, 1070 nitrosylsulfatobis(triphenylphosphine), 4,1070 nitrosyLtris(tnphenylphosphine), 4, 1066 peroxo oxidation catalysts, 337 k-peroxo mononuclear, 2,320 phosphine hydrogenation, 6,241 photosensitivity, 4,903 phthalocyanines, 2, 867 polypyrazolylborates, 2,252 porphyrins, 2, 837 dioxygen adducts, 2,326 reactions, 2, 845 pseudohalides, 2,231,232 ruthenium, 4,1076 thionitrites bonding, 2,191 thionitrosyl, 4, 1074 triazines bridging ligands, 2,201 chelating ligands, 2,205 monodentatc, 2,196 trifluoroacet ylacetone irradiation. 2,384 tungsten, 4,1076 Rhodium(-I) complexes, 4,904,905 Rhodium@) complexes, 4,905,906 triphenylphosphine, 4,905 Rhodium(1) complexes, 4,906-929 anionic, 4,906 bidentate anions N-methylsalicylaldiminato, 4,908 pentane-2,4-dionato, 4,908 trifluoroacetato, 4,908 bridged, 4,908-911 cupferron, 2.512 dinitrogen, 4,919 binuclear, 4,920 four-coordinate

Rhdium(1) complexes

Cumulative Subject Index

anions, 4,925 hydrido, 4,921 hydrido dinitrogen, 4,920 magnetic properties, 1,274 pent acoordin ate anions, 4,929 sulfurdiimine fluxional behavior, 2, 192 monodentate, 2, 191 reactivity, 2, 194 three-coordinate, 4,906,907 bis(tricyc1ohexylphosphine). 4,906 bis(trimethylsilyl)amido, 4, 907 bromo, 4,907 dinilrogen, 4,907 fluoro, 4,907 iodo, 4,907 sulfur dioxide, 4,907 Rhodium(I1) complexes, 4,93&952 acetates dimeric, 4,934

4-amino-5-(aminomethyl)-2-methylpyrirnidine, 4,937 bicarbonates dimeric, 4,938 Carbonates, 2,448 dimeric, 4,938 carbon bonded adducts, 4,938 carboxylate bridged dimcric, 4,941 dihydrogen phosphates dimeric, 4,938 dimeric, 4,933-952 asymmetrically bridged, 4,939,9.10 bonding, 4,944 catalytic activity, 4,950 electrochemistry, 4,948 electronic structure, 4,944 isonitriles, 4, 943 mixed bridge, 4,940,942 oxo bridged, 4,934 oxypyridine bridged, 4,939 reactivity, 4,947,951 Schiff bases, 4,943 steric crowding, 4,936 structure, 4,934,939 substitutions, 4, 947 synthesis, 4, 934, 939 without bridging ligands, 4,942,944 dimers redox potential, 1,514 dimethyl sulfoxide dimeric, 4,937 Auorinated carboxylates dimeric, 4,937 guanidine, 2,283 monomeric, 4,93&933 tertiary arsine, 4,933 tertiary phosphine, 4,932 tertiary stibine, 4,933 N donor adducts dimeric, 4, 938 1.8-naphthyridine bridged dimeric, 4,941 nitrosyl dimeric, 4,938 polynuclear, 4,951,952 salicylates dimeric, 4,936 sulfates dimeric, 4,938 Rhodium(li1) complexes, 4,952 acetylacetone, 4, 1050 (+)-3-acetylcamphorate, 4, 1053

212

acyl, 4,953 allylamine, 4,964 amine oximes, 4: 1012 amines, 4,963 excited state, 4, 981 stereochemistry, 4,986 amino acids, 4,971 4-amino-315-mercapto-l,2.4-triazole, 4, 1048 aquacarboxylatobis(ethy1enediamine) trans-, 4, 978 aqua halo: 4,1057 arylazooximes, 4. 1012 azidopen taammine photochemistry, 4,985 bidentatc aliphatic amines, 4, 965 bidentate amines photochemistry, I, 980 biguanide, 4.1014 bipyridyl electrochemical reduction, 4, 1000 photochemistry, 4,998 reduction, 4,999 2,2'-bipyridyl luminescence, 4,999

N,N'-bis(3-aminopropyl)cthyleticdiamiiic stcreochekistry, 4,991 bis(bidentate phosphines), 4, 1035, 1039 disulfur, 4,1038 oxygen, 4: 1036 bisfbidentate stibine:). 4. 1039 bis(3-diphenylphosphnopropy1)phenylphosphine. 4. 1040 bis(eth~lenediamine),4, 966 cis-,4, 967 NMR. 4.971 substitutions, 4, 972 trans- 4>967 X-ray structures, 4,972 his( 1-(phenylphosphine)-3-(diphei~ylphosphine)p~~l., 4, 1042 carboxylato his(ct1i~lcnediaminc) decarboqlation, 4,977 chlorodioxygenbis('1-(phenylarsino)-3(dimcthq-Larsino)propyl-,4, 1042 crystal structure, 4, 1028 IR spectroscopy, 4,1028 NMR, 4.1028 cyano, 4,952 cyclic polysulfides. 4- 1056 cyclohexanehexanonethiosemicarbazide, 4,1048 dichlorobis(bipyridy1). 4, 997 dichloro(N,N'- bis(7-aminoe thy1)- 1,3-propanediamine), 4,990 dichlorotrtrapyridine, 4,995 dichlorotriethylcnediarnine, 4,989 I , l-dicyanri-2.2-diselenoethylcne, 4, 1057 difluorodithio phnsphates, 4, 1055 dihalobis(e1hylenediamine) ammoniation. 4,974 dihydridobis(bidentate phosphines), 4, 1035 dihydrido t etrakis(phosphine), 4, 1032 dihydridotriphosphine. 4,1026,1027 dimethylformamide. 4,953 dimethyl glyoxime. 4, 1014 dimethyl sulfoxide. ZI 490; 4, 1053 dioxygen- 4,1052 1,2-diphenylthioethane9 4, 1055 dipicolinic acid?4+ IW7 I ,2-diselenocyanatoethanc, 4, 1056 2,5dithiahexane, 4.1055 dithioacetylace tnne 4, I056 dithiocarbamates, 4,1054 dithiocarboxylates, 4, 1054 I

213

Cumulative Subject Index

N,N'-ethylenebis(salicylidineimine),4, 1047 ethylenediamine, 2,33:4,965 ethylenediaminedisuccinic acid. 4. 1045 ethylenediamine-N,N'-diacetic-~\~.~~'-di-3-propionic acid, 4, 1045 ethylenediamine-N,A'-di-S-propionate, 4, 1047 ethylenediaminetetraacetic acid. 4, 1045 o-ethylthioacetothioacetic acid, 4: 1056 Group IV ligands, 4,952 Group VI ligands, 4, 1051 guanidine, 2,283 halo, 4, 1057 halonitrilcs, 4, 1005 hexaammine photochemistry, 4,984 hexaaqua, 4, 1049 hexabromo, 4, 1057 hexachloro, 4, 1057 hexafluoro, 4,1058 hexafluoroacetylacetonate. 2.376; 4, 1050 hexanitro, 4, 1012 hydridobis(bidentate phosphinesj, 4, 1036 hydridotriphosphinc, 4. 1026. 1027 (+)-hydroxymethylenecamphorate. 4.1053 iminodiacetic acid, 4,1045 ligand field states reactivity. 1,400 magnetic properties. 1,773 mcsoporphyrin, 4. 1010 N-mcthyliminodiacetic acid, 4, 1045 6-methyl-2-thiouraci1,4, 1048 mixed nitrogen-oxygen ligands, 4,1044 mixed nitrogen-sulfur ligands, 4.1044 monodentate amines, 4,953 photochemistry, 4, 980 myoglobin, 4, 1010 nitrilotriacetic acid, 4. 1045 nitrito pentaammines isomerization, 4, 961 nitro oxidation catalysts, 6 . 373 nitrogen ligands, 4,953, 1015 octahedral, 4,903 oxygen ligands, 4. 1049 pentaamminechloro photochemistry, 4, 982 solvent cage, 4,985 pentaammineiodo photochemistry, 4,982 pentaammine nitriles hydrolysis, 4,962 pentaammines, 4- 953 anation, 4,956 volume ol activation, 4,958 aquation, 4,956 charactcrization, 4,953 luminescence, 4,9KS photochemistry, 4.982 reactions, 4, 956 substitution reactions, 4.959 synthesis, 4, 953 peptides hydrolysis, 6.433 phosphines dinuclear, 4, 1024,1026 phthalocyanines, 4, 1006. 1012 polydentate aliphatic amines, 4,989 polydentate phosphines. 4. 2040, 1044 polypyridine, 4, 997 porphyrins, 4, 1006. 1012 1,3-propanediaminetetraaceticacid, 4, 1045 1-propylidenediaminetetraaceticacid. 4. 1045 pyridine, 4,995 coc 7-n

Rhodoxime

antibacterial activity, 4,995 substitution, catalysis, 4, 1003 reactivity. 1. 298 seienido. 4. 1057 selenocyanates, 4, 1056 spectra. 1.254 stereochemistry, 4, 902 structure. 4, 1028 sulfides, 4. 1054 sulfur ligands, 4, 1054 five-inembered rings, 4, 1055 four-meinbcred rings, 4, 1054, 10.55 tnonodentale, 4, 1054 six-membered rings, 4. 1056 Tertiary arsines. 4, 1027 tetraamminediiodo photochemistry, 4,982 1,4,8.1l-tetraazatetradecane.4,992 tetrakis(phosphinej, 4, 1032 1,4,8111-tetrathiacyclotetradecane, 4, 1056 thiocyanates. 4, 1056 thiolato. 4, 1057 thiosemicarbazidediaceticacid, 4, 1048 1,4,7-triazacyclononane, 4,992 trichlorostannyl, 4,953 trifluoroacet).lacetonate, 4,1050 tripyrarolylboratc, 4, 1012 tris(alanine), 4, 1044 trisjarnino acids). 4, 'LO44 tris(2-aminoethyl)amines, 4,991 tris(bipyridq.1).4.997 tris(methionine). 4,1044 t1.is(S-methylene-2-dithiolato) crystal structure, 4, 1056 tris(oxa1ato). 4, 1049 tris(tertiary arsines), 4, 1031 tris(terliary phosphines), 4, 1028 uis(tertiary stibines), 4, 1031 Rhodium(TV) complexes, 4, 1061, 1063 anionic, 4. 1061. 'I062 hexac.hlnro, 4, 1061 heaafluoro, 4,1061 halo

neutral. 4.1062 magnetic properties, 1,273 tetrafluoro. 4, 1062 Rhodiurn(V) complexes, 4, 1063 anionic, 4. 1063 hexafluoro. 4. 1063 oxyanions, 4, 1063 pentafluoride, 4, 1064 Rhodium(V1) complexes, 4, 1064 hcxafluoro, 4, 1064, 1065 Rhodium effect photography, 4. '106.1 Khildjum oxides, 4, 106.5 hydrated, 4. 1062 Rhodium sesquioxide, 4, 1053 Rhodizonic acid metal complexes, 2,453 Rlrodopseudamonas viridis photosynthesis reaction centres, 6,591 Rhodopsin lipid-sensitized vesicular imaging systems, 6, 126 Rhodotorrulic acid N-hydroxyornithine, 6,676 Rhodoxime, 4, 1015 anionic arsenic ligands. 4, 1015 phosphorus ligands, 4, 1015 six-coordinate, 4, 1022, 1024

Rhodoxime

Cumulative Subject Lndex

bis(phosphine), 4,1017 five-coordinate, 4, 1017, 102l1 1026 hydridogermyl, 4, 1019 hydrosilylation, 4, 1019 silyl, 4,,1019 chlorotris( triphenylphosphine) reaction with dioxygen, 4,1021 1.3-diaryltriazenido, 4, 1023 ethyl (triphenylphosphino)acetate,4. 1023 nitrato, 4,1023 tertiary arsine, 4,1015, I044 tertiary phosphinc, 4, 1015, 1044 triphenylphosphine, 4,1016, 1017 Rhusicyanin Thiobacillus ferrooxidaw function. 6,651 Rhw vernicifera stellacyanin structure, 6,651 Riboflavin S'-phosphate zinc complexes, 5,958 Ribonucleotide reductases cobalt, 6,642 iron, 6,634 manganese, 6,586,587 Ribosomes stabilization magnesium ions, 6,565 potassium ions, 6,562 Ring closure reactions alkynic alcohols, 6,289 Ring-forming reactions chelate, 1,433 non-chelate, 1,416 Ring-modifying reactions metal complexes, I, 454 Ring opening metal catalysis, 6,477 Rinneite structure, 6, 846,847 RNA metal complexes, 2,979 structure, 2 , 979 structure, 2, 976 tRNA metal binding sites, 2,980 RNA polymerases activation magnesium ions, 6,584 zinc, 5, 1007 Roseocobalt -see Cobalt, aquapentaammineRoseopentaamminc -sre Aquapenuaarnmine Roussin's black, 4, 1191 Roussin's red, 4, 1191 Roussin's salts. 4,240, 1243 Rukber vulcanization zinc complexes in, 5 , 998 Ruheanic acid -.we Dilhiooxarnid Rubidium complexes 1.3-diketones, 2, 366 podands, 3,19 porphyrins, 2,820 Rubredoxins. 2,773; 4, 1240; 6. 626 bacterial, 4, 1240 Rut henium anticancer drugs, 6,758 properties, 4, 279 in Purex process, 6,941,945 recovery from nuclear fuel waste, 6 , YMJ spectrophotometric determination, 1 546 Thorex process, 6,957 Ruthenium-97

214

complexes hepatobiliary system imaging techniques, 6, 990 Ruthenium, (411'-bipyridyl)bis(pentaammine)equilibrium constant solvent effect, 1,516 Ruthenium, bis(arene)redox potential, 1,515 Ruthenium diaquabis(2,2'-bipyridyl)polarography, 1,481 Ruthenium, dichlorobis(ethy1encdiamine)phatoreactivity. 1,407 Ruthenium, dichlorotris(tripheny1phosphine)structurc. 1,45 Ruthenium. (ethylenediaminetetraacetic acid)chemical analysis. 1,488 Ruthenium. hexaammineoxidation, 1,370 redox potential. 1,485 Ruthenium, hydroxyoxobis[bis(2,2'-bipyridyl)]chloride oxidation, 1,488 Ruthenium, iodotris(dimethy1dithiocarbamato)stereochemistry, l1 82 Ruthenium, nitrosylcomplcxcs liquid-liquid cxtraction. I , 541 Ruthenium, pentaammineaquachemical analysis, I . 488 electron transfer, I, 346 Ruthenium, pentaamminechloroaquation, I, 377 photorcacti\?ity. 1:407 Ruthenium, pentaammine(dimethy1)linkage isomers, I? 186 Ruthenium, pentaammineformylaquation, 1,377 Ruthenium, pentaammineisonicotinamidoelectron transfer, 1,375 with copper(1). 1.369 with hexaaquachromium, 1,367 Ruthenium, pentakis(trifluorophosphine)NMR, I , 41 Ruthcnium, pyruinebis(pentaammineelectron transfcr- I , 360 Ruthenium, tetraamminedichlorocyclic voltammetry, 1,483 Ruthenium. tetraamminedihalocyclic voltammetry, 1,482 Ruthenium, tetrachloronitridotetraphenylanenate stereochemistry, 1,44 Ruthenium, tris(acety1acetone)structure. 1.65 Ruthenium, tris(2.2'-bipyrazinyl)in photochemical nitrogen production from water, 6. 510 Ruthenium, tris( bipyridy1)in hydrogen production from water, 6, 500,506 in photochemical hydrogen production from water, 6. 499-5101 502-506 in photochemical nitrogen production from water. 6. 508 in photochemical oxygen production from water, 6.515 photochemical properties, 6,499 water cleavage. 6,499 Ruthenium. tris(2.2'-bipyridyl)chemical actinometer, 1.409 cxcited clectronic states rcdox prupcrtics, 1,4YO structure. 1 . 6 4 Ruthenium, tris(2.2'-hipyrimidyI)in photochemical nitrogen production from water, 6. 510 Ruthenium, tris(pyridy1)-

215

Cumulative Subject Index

in photoelectrochemical cleavage of water, 6, 531 Ruthenium complexes, 4, 271 acetamide, 4,466 amidines chelating ligands. 2,204 amines binuclear, 4,325 halides, 4, 324 nitrogen donor ligands, 4.322 . oxygen donor ligands, 4, 323 amino acids, 4,465 ammines, 4,289 alkenes, 4, 29.1 amines, 4,292,311, 321 amino acids, 4,310 amino esters, 4, 310 binuclear, 4, 311 carbonyl, 4,291 carboxylates, 4, 306 cyanates, 4, 301 cyanides, 4,291 dinitrogen, 4,299,317 halide bridged, 4,319 halides, 4,308 heterocycles, 4, 312 metalloflavins, 4, 310 monodentate heterticycles, 4: 292 mononuclear, 4,321 nitriles, 4, 301, 312 nitrogen donor bridged, 4,311.320 nitrosyls, 4,297 nitrous oxide, 4>301 oxygen donor bridged, 4?318,320 polynuclear, 4, 320 sulfoxides, 4, 306 sulfur donor bridged, 4>318 sulfur donor ligands, 4, 307 thiocyanates, 4 , 301 trinuclear, 4, 320 antimony ligands, 4,366-120 applications, 6, 1018 aqua, 4,420 arsenic ligands, 4, 3 W 2 0 carbonates, 2,448 carbonyl tellurides, 2,669,671 carboxylates, 4,425 carboxylic acids reactions, 2,443 trinuclear, 2, 441 catalysts alkyne rcactions. 6,298 carbon dioxide reactions. 6. 293 carbonylation, 6,267 hydroformylation. 6.258 hydrogenation, 2,711; 6.231 cyanides, 4,281 synthesis, 2, Y 1,4-diaza-1,3-butadicne, 2,208,210,212 dicarboxylatcs, 4, 429 diimines, 4,363 dinitrosyl cation five-coordinate. 2. 105 diothiocarboxylates. 4>436 dipicolinic acid, 4,465 dithiocarbamates, 2.586; 4.432 dithio-P-diketonates. 4,436 dithiolenes, 4, 436 dithiophosphato, 4.436 dithiophosphinato, 4,436 ethylenediaminctctraacetic acid, I , 466 fulminates, 4.281 Group IV, 4,281-289 germanium-containing ligands. 4.287

Ruthenium complexes

halogens, 4,44(.!-450 heterocvcles. 4.325 bideitate, 4,'32? binuclear, 4,357 carbon donor ligands, 4,326 carbonyl donor ligands, 4,356 halide-bridged, 4, 361 halides, 4, 327,357 mixed donor ligands, 4,353 mononuclear. 4.325 nitrogen donor bridged, 4,357 nitrogen donor ligands, 4, 326,356 oxygen donor bridgcd, 4,360 oxygen donor ligands, 4,327,357 polynuclear, 4, 357 sulfur donor bridged, 4, 360 sulfur donor ligands, 4,357 tridentate, 4,354 heterocyclic carbon donor ligands, 4,345 carbonyls, 4,345 cyanides, 4,345 nitrogen donor ligands, 4,347 nitrosyls, 4, 348 oxygen donor ligands, 4.350 tertiary amines, 4,347 histidine, 2,747 hydrazines, 4,363 hydrides, 4.450 catalysis, 4, 463 hydrogen, 4,450 hydroxy, 4,421 8-hydroxyquinoIines, 4,465 isonitcoso ketones, 4,464 ketoenolates. 4,423 ketoximes, 4,464 macrocyclic, 4,469 mercury ligands, 4,280 mctallothioanions, 4,432 6-mclhyl-2-pyridinolates, 4,466 monothio-B-diketonates, 4, 430 nitrides, 4, 361 nitriles, 4. 365 nitrogen-carbon ligands, 4,468 nitrogen ligands, 4,289-364 nitrogen-oxygen ligands, 4,463 nitrogen-sulfur ligands, 4,467 nitrosyl, 2. 107 reaction with carbon monoxide, 2, 113 nitrosyls, 4. 361 halides. 4, 362 nitrogen donor ligands, 4,361 oxygen donor ligands, 4,362 sulfur donor ligands, 4, 362 oxalic acid 2,444 oximes, 4, 464 oxo, 4,421 oxidation catalysts, 6,356-359 oxygen ligands. 4,42&429 phosphines acetone, 4.399 acyl. 4.386 alcohols, 4.399 alkenes, 4,390 alkyl, I ,386 aminm, 4,391 ammines. 4- 391 aryl. 4,386 azido, 4,393 bidentatc N heterocycles, 4, 391 carbamates, 4,403 carbamoyl complexes, 4, 391 carbenes, 4,384

Ruthenium complexes carbimides, 4,384 carbonates, 4,401,403 carbon donor ligands, 4,380 carbonyl halides, 4,380 carbonyls, 4,370 carbonyl selenides, 4, 383 carbonyl sulfides, 4,383 carboxylato, 4,402 cyclometalated, 4,388 diazines, 4, 394 diazinido, 4,394 dimethylacetamide, 4, 399 dimcthylformamidc. 4,399 dimethyl sulfoxide, 4,4118 dinitrogen, 4,393 dioxygen, 4,401 dithiocarbarnato, 4,405 dithiocarbonato, 4,405 dithiocarbonimidato, 4>405 dithiocarhoxylato, 4,406 dithiolene, 4,406 dithiophosphato, 4,405 dithiophosphinato, 4,404 formamidinato, 4,395 formamido, 4,395 formazan, 4,3Y5 hydrazines, 4,391 hydroxo, 4,399 isocyanides, 4,370,384 ketoenolates, 4,400 monodentate N heterocycles, 4,391 monothiocarbamato, 4,407 monothiocarbonato, 4,407 monothiocarboxylato, 4, 407 nitrato, 4,401 nitriles, 4, 396 nitrogen donor ligands. 4,391 nitrosyls, 4,367, 393 oximes, 4,397 oxygen donor ligands, 4,399 perchlorato, 4,401 phosphorus-nitrogen ligands, 4: 408 phosphorus-oxygen ligands. 4: 408 phosphorus-sulfur ligands, 4,109 quinones, 4,400 Schiff bases, 4,397 selenocyanates, 4,396 sulfato, 4,401 sulfido, 4,404 sulfur dioxide, 4,408 sulfur donor ligands. 4. 404 tctrahydrofuran, 4.399 thiocyanates, 4, 396 thioformamido, 4, 395 thiolato, 4,404 thionitrosyls, 4.393 triazenido, 4,395 tridentate N heterocycles, 4,391 urylenc, 4,395 water, 4,399 phosphinimato paramagnetism, 2, 124 phosphorus ligands. 4,366-420 photographic developer, 6,99 phthalocyanines, 2,866; 4,474 polypyrazolylborates, 2,251 porphyrins, 2,829; 4,469 pseudohalides, 2,230,231 reactions with nitric oxide, 2, 115 Schiff bascs, 4,463 selenium ligands, 4,439 silicon ligands, 4,284 carbonyl, 4,284

Cumulative Subject Index carbonyl, phosphine, 4,285 tertiary arsines. 4,287 tertiary phosphines, 4,287 sulfido, 4,430 sulfoxides. 4,437-439 sulfur donor Iigands halides. 4,352 oxygen donor ligands. 4, 352 sullur ligands, 4.430 sulfur-oxygen ligands, 4, 468 tellurium ligands. 4.439 tetraaza rnacmcycles, 4,475 tetrathia niacrocycles. 4,477 thiazolcs, 4, 43D thiocyanates, 4,365 thioethers, 4.432 thiolato, 4.430 thionitrosyl, 2, 119 thiourea, 4-437 tin-containing ligands, 4, 287 triaza macrocycles, 4.477 triazine 1-oxide, 4,467 triazines chelating ligands, 2 , 204 urea, 2 , 2 8 6 Ruthenium(0) complexes, 4,279 binuclear phosphinos, 4,372 hydrogen, 4,450 mononuclear phosphines, 4,366 phosphines carbonyl, 4>373 nitrosyl. 4:372 tetranuclear phosphines, 4; 372 trinuclear phosphines, 4. 372 Rutheniumrl) complexes, 4,279 ammilies

dinitrogen. 4,299 binuclear phosphines. 4.374 carbonyl halides. 4.340 cyanides. 4,281 halides, 4,440 hydrides. 4.450 mononuclear phosphines, 4,374 tetranuclear phosphines, 4.374 Ruthenium(l1) complexes, 4, 279 amincs halides: 4:374 mononuclear. 4. 321 ammines, 4. 289 bidentate. heterocycles, 4, 297 carboxylates, 4,306 dinitrogcn, 4.299 halides- 4.308 hydroxy. 4,304 monodentate heterocycles, 4,292 nitriles. 4. 301 nitrosyls, 4. 297 nitrous oxide. 4.301 sulfoxides, 4,306 aqua, 4. 420 aqua halides, 4,442 binuclear hydrido. 4.461 carbonyl bromides, 4,442 carbonyl chlorides. 4,442 carbonyl fluorides, 4,442

216

217

Cumulutive Subject Index

carbonyl halides, 4,442 anionic, 4,443 carbonyl iodides, 4,442 cyanides, 4,281 ammines, 4,282 arsines, 4,282 binuclear, 4, 283 bipyridyl, 4,282 nitrogen donor ligands, 4,282 phosphines, 4,282 pyrazine, 4,282 dimethyl sulfoxide, 2,490 halides; 4,441 heterocyclic oxygen donor ligands, 4,350 hydrogen sulfide, 2,516 lead-containing ligands, 4, 289 magnetic behavior, 1,273 mixed valence, 4,415 mononuclear anionic, 4,460 antimony donors, 4,379 arsines, 4,379 cyclometallated, 4.4% dihydrido, 4,450 hydrides, 4,450 monohydrido, 4,452,458 phosphines, 4, 376 nitriles, 4, 365 phenanthroline in photochemical hydrogen production from water, 6, 506 polydentate arsines, 4,380 phosphines, 4, 380 stibines, 4, 380 polymerization elcctrochemistry, 1,488 polynuclear hydrido, 4,461 reactivity, 1, 300 reduction vanadium(I1) complexes, 3,472 spectra, 1,254 sulfur donor ligands halides, 4,352 tetranuclear hydrido, 4,461 thiocyanates, 4, 365 tin-containing ligands carbonyl, 4,288 carbonyl halide, 4,288 halidcs, 4,288 trinuclear hydrido, 4,461 Ruthenium(II1) complexes, 4.279 amines halides, 4,324 mononuclear, 4,322 ammines, 4,290 amides, 4,302 aqua, 4,304 bidentate heterocycles, 4,297 carboxylates, 4,306 dinitrogen, 4,301 halides, 4,308 hydroxy, 4,304,305 imines, 4,302 monodentate hetcrocycles. 4.296 nitriles, 4, 302 sulfoxides, 4,307 aqua, 4,421 aqua halides, 4,445

Ruthenium(VII1) complexes

hinuclear arsines. 4.417 phosphines, 4,410,417,418 polydentate phosphine bridges, 4,414 bromides, 4,444 carbonyl halides, 4,446 chlorides, 4>444 cyanides. 4,283 rx-diimines. 6 . 189 Ruoi-ides,4, 443 halides, 4.443 anionic. 4.444 he tcrocyclic oxygen donor ligands, 4,351 hydroxyl halides. 4: 445 iodides, 4,444 magnetic behavior, 1,273 mixed valence, 4,415 mononuclear arsines, 4.416 phosphines, 4,416 stibines. 4,416 nitriles, 4,366 phosphines double halide bridged, 4,410 triplc halide bridged, 4,410 polynuclear arsines, 4,417 phosphines, 4,410,417 reactivity, 1, 300 sulfur donor ligands haIides, 4,353 tetranuclear phosphines, 4,410 thiocyanates, 4,366 trinuclear phosphines, 4,410,418 Rulhenium(1V) complexcs, 4,279 arnniines- 4,291 monodentate heterocyclcs, 4,297 aqua halides, 4.448 cyanides. 4: 284 halides, 4.446 anionic, 4,447 neutral. 4. 446 oxo halides. 4,448 heterocyclic oxygen donor ligands, 4,352 hydroxo halides, 4,448 magnetic behavior, 1,272 oxo. 4: 421 phosphines. 4,419 sulfur donor ligands halides, 4,353 Rutheniurn(V) complexes, 4,280 ammines, 4: 291 cyanides. 4.284 halides, 4.448 heterocyclic oxygen donor ligands, 4,352 oxo, 4,427 Ruthenium(V1) complexes, 4,280 halides. 4,449 heterocyclic oxygen donor ligands, 4, 352 oxo. 4, 422 Kuthenium(VI1) complexes, 4,280 cyanides, 4,284 heterocyclic oxygcn donor ligands, 4,352 OXOI4.422 Ruthenium(VII1) complexes, 4,280

Ruthenium(VI11) complexes

Cumulative Subject Index

halides, 4,450 heterocyclic oxygen donor ligands, 4,352 oxo.4.423 Ruthenium dichloride in electrochemical production of oxygen from water, 6 , 534

218

Ruthenium oxide catalyst hydrogen and oxygen production from water, 6,524 colloidal catalysts. oxygen production from water, 6,519 Ruthenium purple. 4,281 Rutherfordine. 6.890

Sl00 proteins, 6,577 structure, 6,573 Saccharic acid aluminum(II1) complexesl 2.480 Saccharomyces cerevisiae cation transport, 6 , 559 manganese transport, 6: 570 Salicylaldehyde alkali metal complexes. 3.30 amino acid Schiff bases metal complexes, 2 , 751 oxime in gravimetry, I , 531 oximes metal complexes, 2,273.798 Schiff bases metal complexes, 2,725,730 IR spectra, 2,730 NMR, 2,730 X-ray analysis, 2, 731 Salicylaldehyde, 5-nonyloxime metal complexes, 2,274 Salicylaldiniine copper(I1) complexes; 6, 156 Salicylaldoxiines adsorption minerals, 6 , 782 metal complcxcs stability, 6 , 800 Salicylhydroxamic acid lanthanon complexes, 2,507 as metal precipitant, 2, 506 Salicylic acid inhibitor binding dehydrogenases, 5 , 1016 metal complexes, 2,465,480.481 IR spectra, 2, 469 soils, 2, 962 structure, 2,471 minerals weathering, 6,868 Salicylic acid, thiophotographic stabilizer. 6, 103 Salmonella typhimuriurn tryptophan biosynthesis, 6 , 582 Salt hydrates, 2,296 Salting out in reprocessing irradiated nuclear fuel, 6,933 Salvosan, 3,255 Samarium, tris( triphenylphosphine oxide)bis(diethyldithiophosphat0)structure, 1 , 7 8 Samarium complexes dipositive oxidation state hydrated ions, 3, 1109 Samarium(lI1) complexes salicylic acid crystal structure, 2,481 Sampsonite, 3,265

Sandwich complexes nickel. 5. 35 Sapphyrins, 2,888 demetaHation, 2.891 metallation. 2,891 reactions, 2, 891 synthesis. 2,889 Sarcoplasmic reticulum calciumimagnesium ATPase, 6,566 skeletal muscle calcium pump, 6 , .56S Sarcosine, glycylmethyl cstcr hydrolysis, copper(1T)-catalyzed, 6 , 422 Scacchite. 6*855 Scandium reactions with 2-propanol,2,337 Scandium! hexakis(su1fur)exchange reactions, 1,286 Scandium. pentakis(nitrat0)structure. 1 , 9 8 Scandium, tetrakis(tropo1one)stereochemistry. 1 94 Scandium, tris(acety1acetone)structure. 1.65 68 Scandium, tris(tropo1onate)structure, I , 68 Scandium ar);loxides spcctroscopy, 2,346 Scandium chloride Sc,Cl, strucrure, 1,27 sc,cllo structure, 1 ,2 7 SC7C~1, structure, 1,27 Scandium complexes, 3, 1059-1116 alkoxides. 3, 1065 amides, 3. 1062, 1066 amine uxides. 3, 1065 amines. 3: l0Ml amino acids, 3,1066 applications. 6 . 1024 aromatic amines, 3,1061 arsenic compounds, 3, 1065 2.2’-bipyridq-l,3, 1061 1,2-bis(pyridine-a-carbaldimino)ethane13>1061 bromides. 3.1067 carboxylates, 3,1063 carboxylato ammines, 3, 1060 chlorides, 3, 1067 cupferron, 2,510 cyclic crown polyethers, 3, 1065 &dikctonatcs, 3, 1062 dimerhylacerarnide. 3, 1066 dirncthyiformamide, 3, ‘1066 ethylenediamine, 3, 1060 fluorides. 3. 1067 formates, 3, 1063 hydrated carboxylates, 3, 1063 ~

219

Scandium complexes

Cumulative Subject Index

hydrated ions, 3,1073 properties, 3, 1074 structures, 3, 1074 thermodynamic parameters. 3,1073 hydrates, 3, 1064 hydrazines, 3,1060 hydroxo, 3, 1064 hydroxyacetates, 3,1063 8-hydroxyquinolinate, 3,1066 malonates, 3, 1063 nitrate hydrates, 3, 1076 nitratu, 3, 1064 nitrogen donor ligands, 3,1060 octaethylporphyrin, 3, 1061 oxalates, 3, 1063 oxalato ammines, 3, 1060 oxyanions, 3,1064 oxygen donor ligands, 3, 1062>1073 lJ0-phenanthroline, 3, 1061 phosphine oxides, 3,1065 phosphines, 3,1073 phosphorus donor ligands, 3,1073 phosphoryl, 3,1065 phthalocyanines, 2,864; 3,1062 porphyrins, 2,822; 3, 1061 pyridine, 3, 1061 salt hydrates, 3, 1073, 1075 sulfate hydrates, 3,1076 sulfato, 3,1064 sulfoxides, 3,1065 2,2’ :6‘,2”-terpyridyl, 3, 1061 tetrahydrofuran, 3,1064 tetraphenylporphyrin, 3, 1061 tripyridyltriazine, 3, 1061 tris(silylamide), 3, 1062 urea?3, 1065 Scandium isopropoxides synthesis, 2,337 Scavenging in gravimetry, 1,535 Scheelite, 3,974 Schiff base reactions metal complexes, 2,84 Schiff bases acyclic polydentate ligands. 2: 715 amino acids metal complexes, 6,467 bidentate bonding to metals, 2,723 metal complexes, 2,720 electronic spectra, 2,724 IR spectra, 2,724

NMR, 2,723 spectroscopy, 2,723 structure, 2,725 cadmium complexes, 5,940 cobalt complcxcs oxidation catalysts. 6. 387 in gravimetry, 1,531 heptadentate metal complexes, 2,735 hexadentate metal complexes, 2,734 NMR,2,717,727 spectroscopy, 2,716 structure, 2,717 thermodynamic metal template efkcts, 1,434 uv Spectra, 2,717 monudentate, 2,718 bonding to metals, 2, 7’18 metal complexes NMR,2,718 spectroscopy, 2,718

structurc, 2.719 multidcntate metal complexes, 2.733 pentadentate metal complexes? 2.733 synthesis. 2.716 tetradentate, 2,727 tridentate, 2 - 726 metal complexes. KMR, 2, 726 zinc complexes. 5 - 930 Schizokinen structure, 6.678 Schroekingcritc structure, 6 , K4K Scintillation counting techne tiurn-99 medical applications, 6, 973 Scotch Guard chromium complexes. 1 22 Scrubbing Purex process. 6.953 in reprocessing irradiated nuclear fuel, 6, 932 Sea squirts vanadium, 6,666 vanadium(1tl) complexes. 3,486 Seawater composition, 6: 851 inorganic complexes genchernistrg, 6 , 851 trace element complexes, 6, 851 Secocorrin nickel complex, 6,201 Secocorrinoid complexes carboxylic acid cadmium, 6,201 photocyclization, 6, 201 Sedimentary rocks structure. 6.856 Segregation uranium from thorium gcochcmistry, 6, 886-895 Selection rules orbital/vibrational, 1 , 245 relaxation spectral band intensities, 1,244 spectral spin. 1,245 spectral bands, 1 243 Selective ion electrodes, 1,559 Selenates cffcctive bond length ratios, 1, 37 Selenates. pcntafluoroelectroncgalivity, 3. 319 Selenides metal complexes, 2,662 Selenites stereochemistry, 1 , 3 7 Sclcnium, 3,299-307 bonding, 3,299 coordination compounds, 3,300 geometry, 3,299 metal clusters. 2.667 metal complexes, 2.661-672 toxicity, 3,307 valence, 3,299 vitatnin E and. 6.774 Selenium, his(diethyldiselenocar1~amato)stereochemistry, 1,hO Selenium. bis{diethy~dithiocarbamato)stereochemistry, 1 , 6 0 Selenium. bis(dithiofurancarhamato)stcrcochcmistry. I , hD Selenium complexes

220

22 1 porphyrins, 2, 822 Selenium(11) complexes bis(dithiochelate), 1,60 cis-dibromobis(thiourea), 3.305 cis-dichlorobis(thiourea), 3,305 four-coordinate, 3.305 triselenocyanate, 3,305 dimeric, 3,305 triselenourea, 3,305 trithiocyanate dimeric, 3,305 Selenium compounds catalysts alkene cpoxidationl 6,332 heterocyclic metal compounds, 2,664 oxidation catalysts, 6,359 Selenium dioxide allylic oxidation, 6,359 Selenium ligands palladium(I1) complexes, 5. 1131-1 152 Selenium monobromide complexes with amines, 3,304 Selenium oxychloride complexes. 3,302 Sclcnium tetrachloride complexes with amines, 3,304 with pyridine, 3, 304 Selenium trioxide complexes, 3,304 a-Selenoacetic acid cobalt(II1) complexes, 2,808 Seleno anions metal complexes, 2, 521 Selcnoarscnous acid, 3, 219 esters, 3,249 Selenocyana ter, linkage isomers, 1 IXh metal complexes, 2,225-238? 662 molecular geometry, 2.226 Selenocysteamine metal complexes, 2,807 Selenocysteine glutathione peroxidase. 6.706 Selenoformaldehyde metal complexes, 2.665 Selenoguanine metal complexes. 2.807 Sclenolates mctal complcxcs, 2.663 Selenometalates synthesis, 2, 559 Selenonium ions, trifluorastereochemistry, 1. 37 Selenophene-2-aldehyde oxime metal complexes, 2, 806 Selenopurine metal complexes, 2,807 Selenosalicylaldimine metal complexes, 2, 807 Selenothiocarbazides metal complexes, 2 , 807 Selenothiocarbazones metal complexes, 2 , 807 Sclenotungstates, 3, 1042 Sclcnourca metal complexes, 2, 663 Selenourea, 3-benzoyl-l .I-disthylmetal complexes, 2, 808 Selenoxide, dimethyl COT 7-H'

Cumulative Subject Index

Siderophores

metal complexes, 2, 490 Sclenoxide, diphenyl metal complexes, 2.490 Selenoxides metal complexes, 2.487 synthesis, 2,490 Self-exchange reactions, 1,333 electron transfer rate constants, 1,347-353,366 rate constants calculation, 1, 348 rateconstants. I , 362 Scmicarbazidel 1,4diphenylthioruthenium determination, 1,546 Semicarhazones, thiophotagraphy diffusion transfer process, 6 , 102 Semiconductors metal complexes, 6, 134 Semi-coordination copper(I1) complexes, 5,604 Semi-glycinecresol red metallochromic indicator, 1,557 Semiquinone, 3,5-di-r-butylchromium complexes, 2,398 Scmiquinones metal complexes, 2, 398 Semi-xylenol orange metallochromic indicator, 1,557 Senility trace elements and, 6,773 Sensitization electrophotography, 6, 123 Separation techniques mineral processing. 6,780 Sepiolite ruthenium oxide support catalysts, hydrogen production from water. 6,523 Scpulchrates classification, 2,920 metal ion complexes, 2, Y40 synthesis, 2, 927 Sequestering agents actinides, 6,962 Serine epimerization geochemistry, 6, 867 metal complexes, 2,750 prebiotic systems, 6, 872 Serine. 2,Cdihydroxybenzoylmicroorganisms: 6.676 1.-Serine. glycylmetal complcxcs, 2, 764 Scrinc. 13-hydroxymethylsynthesis mctal catalysis, 6 , 469 Serum albumin labelling. 6 , 995 Serum proteins labelled radiopharmacology, 6,994 Serum transferrin, 6,669 Sesquisiloxanes, 3.206 Seven-coordinate compounds stereochemistry, 1,69-83 Shales structure. 6. 856 Shell process. 6: 327 Siderophores, 4.230,233; 6,674 catechol iron release, 6, 679 catecholate, 6.675 citrate-hydroxamate, 6,678 hydroxamate, 6,676

Siderophores iron complexes binding to receptors, 6>678 metal complexes, 2,968 peptides for metal complexes, 2,970 reduction vanadium(I1) complexes, 3,473 Sidgwick, Nevi1 Vincent, 1, 16 Silabenzene, 3, 190 Siladiimides, 3, 191 Silacthylcnc, 1,I-dimethylSi=C ~d bond cnergy, 3, 184 Silaethylenes preparation, 3, 188 Silaimines, 3. 191 Silanediol, di-r-butyl-, 3,206 Silanediyl complexes transition metals, 2, 16 Silanes electrode modification, 6,20 organooxy reaction with metal halides, 2.343 Silanones, 3, 191 Silathiones, 3, 191 1-Silatoluene, 3, 190 Silarranes, 3,212 Silica polymerization, 6,832 structure, 3, 192,201 Silicates, 3,202 depression, 6,783 groundwaters geochemistry, 6,852 metal complexes geochemical melts, 6, 855 minerals, 6, 844 structure, 6,845 structure, 3,203 synthetic ion exchange resins, 6, 814 Silicates, hexafluorominerals, 6,847 Silicon elemental structure, 3, 183 Silicon, tris(acety1acetone)configuration, 1, 195 Silicon alkoxides physical properties, 2, 346 Silicon complexes, 3, 183-223 acetylacetone hydrolysis, 2, 379 coordination geometry, 3, 185 hydroxamic acids. 2,507 imines, 2,279 multiple bonding, 3, 188 phthalocyanines, 2,864 porphyrins, 2,822 tetravalent, 3,205 Silicon compounds amides synthesis, 2, 162 Silicones, 3, 188 Silicon ethoxides synthesis electrochemistry, 2,337 Silicon halides, 3, 197 Lewis acidity, 3, I99 Silicon ligands transition metal complexes. 2, 1.i18 Silicon monoxide, 3, 191 Siloxanes redistribution iridium complex catalysts. 4 > 1160

Cumulative Subject Index Silver analysis, 1?522 clusters metal-metal bonding, 1, 169 electroplating, 6 . 11 extraction, 5,777: 6, 822 recovery anion exchange resins, 6,823 Silver bromide grains photography, 6.96 Silver chloride purification, 6,78S Silver complexes, 5,775450 amidines bridging ligands, 2,201 medical applications, 5,777 phthalocyanines. 2.868 polypyrazolylborates. 2.254 porphyrins, 2,841 pseudohalides, 2,233,233 triazines bridging ligands. 2 , 201 Silver(1) complexes acetylacetone. 5,806 alcoholsl 5,805 alkoxides, 5 , 805 alkylamides, 5.793 amides, 5,812 amino acids. 5.826 aminopyridines, 5, 787 ammines, 5.779 aliphatic monodentate, 5 , 781 aromatic, 5, 782 antimony ligands, 5,803 aqua, 5,804 arsenic ligands. 5, 803 arsines, 5,803 ascorbic acid, 5,810 azides, 5 , 794 aziridincs, 5. 782 azomethinc dq’cs?5- 792 azo salts, 5 , 702 benzimidazoles, 5.785 2,2’-bipyridyl, 5,791 bismuth ligands, 5. 803 bithionol, 5, 815 carboxylates, 5 , 808 complexones. 5,828 crown ethers, 5, 834 cryptands. 5, 836 cupferron. 5 . 813 cyanates, 5.794 cyanides. 5 , ‘777 IR spectra, 5,777 Raman spectra, 5.778 cyanines physical development, 6, 114 cyanopyridines. 5.787 dialkylarnides, 5,793 dimethylformamide, 5,811 dimethyl sulfoxide, 5,810 NJ”dimethylthioformamide, 5 , 821 dinitrogen, 5,792 dioxygen, 5: 805 diphosphines, 5.801 dithiocarbamates, 5,817 1,2-dithiolenes, 5.818 ‘1,2-ethanediamine. 5,782 fuorcscein, 5.805 fulminates, 5,779 grisorixin, 5 , 838 guanidine

223 light-sensitive compounds. 6. 115 humic acids, 6,861 hydrazine, 5,792 hydrides, 5, 824 hydroxamates, 5,813 hydroxy acids aliphatic, 5,810 aromatic, 5, 810 hydroxylaminc, 5,792 imidazoles, 5,784 imides, 5,793 1.3-kctoenolates, 5, 8oh metallothio anions, 5,815 1-methylcytosine, 5,789 methylpyridine halides, 5, 824 1-methylthymine, 5,789 monothiocarbamates, 5, 817 morpholine copper halides, 5, 824 nitrides, 5, 793 nitriles, 5 , 797 nitrosyls, 5, 792 N-oxides, 5, 812 oxalates, 5 , 809 oximes, 5,797 peptides, 5,828 peroxides, 5,805 l,lO-phenanthroline, 5,791 phenolphthalein, 5,805 phosphines monodentatc, 5,798 phosphites, 5,801 picolinate, 5,788 piperidine copper halides, 5 824 piperidines, 5,782 po1yamines aliphatic, 5,782 polyaza macrocycles, 5, 833 polyether antibiotics, 5 , 838 polynuclear thio, 2, 566 poly(pyrazolyl)borates, 5 , 796 polyuridine, 5,789 porphyrins, 5,833 proteins, 5, 828 pyrazines, 5,786 pyrazoles, 5, 784 pyridines, 5,786 pyrimidines, 5,786 quinoline halides, 5,824 8-quinolinyl, 5,829 quinuclidines, 5,782 Schiff bases, 5, 825 selenium ligands, 5, 821 selenocyanates, 5, 794 stibines, 5,803 succinimide, 5,812 sulfates, 5, 818 sulfonamides, 5 , 818 sulfur diimines, 5,793 reactivity, 2 , 194 superoxides, 5,805 tartaric acid, 5 , 810 tellurium ligands. 5. 821 tellurocyanates, 5,794 2,2’,2”-terpyridyl, 5 , 791 2,4,5,7-tetrabrornofluorescein. 5,805 thioacetamide, 5, 820 2-thioamidopyridine, 5, 820 thiocarboxylides, 5,819 thiocyanates, 5, 794 thioethers, 5,815 thiolates, 5,813 thiosemicarbazides. 5,830 thiosemicarbazones, 5,830

Cumulative Subject Index

,

Single electron transfer reactions

thiosulfates, 5,807 thiourea, 5 , 819 triazenes, 5,793 Siiver(I1) complexes, 5, 83%850 amino acids, 5,846 aqua, 5,844,850 biguanides, 5.849 Z,Z’-bipyridyI, 5,843 carboxylates, 5, 844 cinchomeronic acid, 5,842 dipicolinic acid, 5, 842 dithiocarbamates, 5, 845 isocinchclrneronic acid, 5,842 isonicotinates, 5,840 lutidinic acid, 5 , 842 magnetic properties, 1,274 N-heterocyclic ligands, 5, 839 nicotinates, 5,840 1.10-phenanthroline, 5,843 phthalocyanines, 5 , 848 picolinates, 5, 840 polyaza macrocyclic ligands, 5,848 porphyrins, S , 846,850 pyrazine, 5: 842 pyrazinccarboxylatc. 5,842 pyridinecarboxylates, 5,840 uxidative effects, 5, 842 pyridinedicarboxylates X-ray photoelectron spectra, 5, 842 pyridines, 5.840 ESR, 5,840 secondary-ion mass spectrometry, 5, 840 quinolinic acid, 5,842 tetraaza macrocyclic ligands, 5,850 thiocarbamates, 5,845 Silver(lI1) compkxes magnetic properties, I , 274 phosphines SHAB thcory, 2,1040 Silver compounds applications, 6,1024 brines geochemistry. 6,853 photography physical development, 6, 116 photothermography, 6,118 Silver cyanate, 2,7 Silver dye-bleach process photography, 6,105 Silver fluoride, 5, 846’ Silver fulminate, 2 , 7 , 1 2 Silver halides cubanes with Lewis bases, 1, 153 light sensitivity chemical sensitization, 6, 97 photograp by diffusion transfer process, 6, 101 grain precipitation, 6,96 physical development, 6, 113 stabilization photography, 6, 102 Silver(1) halides. 5,822 Silylamines imido metal complexes synthesis from, 2, 166 Silylenrs, 3,192 structure, 3, 193 Silyl enol ethers reacticins with carbonyl compounds, 6,217 Single crystal spectra, 1,249 Single electron transfer reactions, 1,493 chemistry following, 1,499

Siroheme

Curnulutive Subject Index

Siroheme, 6,614 iron, 6,625 metal complexes biology, 6, 546 Site symmetry symbols, 1, 128 Six-coordinate compounds stereochemistry, 1 , 4 9 4 9 Six-membered rings metal complexes, 2,79 SkeIetal muscle sarcoplasmic reticulum calcium pump, 6,565 Slags acid/base properties, 6, 832 classification, 6,833 properties. 6, 832 structure, 6,833 transport, 6,833 Smaragdyrin, 2,888 metallation, 2,891 synthesis, 2, 889 Snake toxins zinc, 6,613 Sodium absorption radiopharrnaccutical agcnts. 6,968 biology, 6,546 ion selective electrodes, 6. 26 reactions with alcohols, 2, 336 Sodium, tris(hexafluoroacety1ace tone)rubidium salt structure, 1,65 structure, 1,65 Sodium chloride structure, 1, 15 Sodium complexes biology, 6,549,551-562 crown ethers, 3 , 3 7 lanthanidc alkoxidc synthesis, 2,338 phthalocyanines, 2,863 porphyrins, 2,820 Sodium hexakis(formato)molyhdate. 3, 1235 Sodium hypochlorite alkene epoxidation manganese catalysts, 6,378 Sodium ions biology, 6,559 selective binding biology, 6, 551 Sodium molybdate, 3, 1230 Sodium peroxoborate, 3, 101 Sodiumipotassium ATPase, 6 , 555 vanadatc inhibition, 3, 567 Sodium pump, 6,555 mechanism, 6,556 Sodium pyroantimonate, 3.265 Sodium salts electrolyte balance, 6,771 Sodium tetrahydroborate, 3, 101 Sodium thiosulfate photography diffusion transfer process. 6. 101 Sodium triphosphate masking agent, 1,536 . Soft and hard acids and bases principle. 2. 1040 Soft-tissue calcification, 6. 597 Sogrenite structurc, 6, 849 Soils metal ion binding, 2, 961 Soil solutions, 2.951 amino acid metal complexes. 2- 963

Solar energy. 6,488 surface modified electrodes, 6, 30 Sol-Gel process fast reactor fuel. 6, 924 Solid state reactions. 1.463-471 fraction of reaction. 1,464 geometric, 1,464 growth, 1,464 nucleation. 1.464 ratc laws, 1,464 Solochrome black T metallochrtimic indicators, I , 555 Solubility gravimetry and. 1,521 Solubility effects cone angle concept, 2,1014 Solution equilibria polarography, 1,481 Solutions high temperature inorganic complexes, 6, 854 metal complexes, 6.854 inorganic complexes geochemistry. 6,850-854 Solvation mctal ions, 2,297 solvent extraction hase metals, h , 810 Solvent association reactions in uranium ore processing organophosphates, 6.903 Solvent effects cluster synthesis. 1: 171 equilibrium constant. 1,515 platinum compiexes substitution reactions, 5,494 quantitative, 1,503-518 redox potential. 1,484,510 Solvcnr cxchmgc kinetics. 1,%3 Solvent exlractirm, 6,928 hase metals amine salts. 6, 802 solvating extractants. 6, 810 computer modelling reprocessing irradiated nuclear fuels, 6,935 irradiated nuclear fuels, 6, 936 mineral processing, 6,78&814 classification, 6, 789 nuclear fuel cycle, 6,882 nuclear fuel reprocessing criticality, 6, 926 platinum-group metals. gold, 6, 806 reprocessing irradiated nuclear fuel, 6,925 uranium ore processing, 6,900 coupled transport. 6, 902 solid supported liquid membrane, 6,902 in uranium purification, 6,920 Solvents aprotic electrochemistry. 1,493 non-aqueous. 1.26 non-interfering substitution reactions, 1,285 radiolytic degradation Purex process, 6,952 resin impregnated mineral processing, 6, 826 Solvent trapping electron transfer, 1.339, 354 Solvolysis aquation. 1.290 base catalyzcd: 1,300

224

225

Cumulative Subject index

amido conjugate base, 1 , 303 amido group, 1,305 blind alley deprotonation, 1,304 dissociative, 1,305 double deprotonation, 1, 304 ion association, 1, 304 limiting cases, 1, 302 mechanism, 1,301 E2 mechanism, 1,303 normal limit, 1,302 simple rate law depature, 1.303 coordinated phosphorus atoms, 1,418 niobium and tantalum oxu trihalides, 3.632 niobium pentahalides, 3,600 rate limiting deprotonation. I, 302 tantalum pentahalides, 3,600 Soybean oil hydrogenation catalysts, platinum complexes, 6,249 Sparteine metal complexes, 2,88,90 Spectroelectrochemistry, 1 476 Speleands classification, 2,920 shaping groups. 2,924 Spermatozoa activation calcium, 6,595 Spermidine metal complexes, 2,50 Sphalerite activator mineral processing, 6,782 deactivation mineral processing. 6,782 Sphenocorona repulsion energy coefficients. 31 ten-coordinate compounds. 1,98 Spherands alkali metal complexes, 3, 43 classification, 2,919 metal ion complexes, 2,936 synthesis, 2,925 Spiroarsoranes, 3,245,269 2,2’-Spirobi( 1,3,2)5-dioxastibolan. 2-phenyl-4,4,4!,4!,5,5,5’ 3’-octamethyl- 3>269 Spiropyran thermochromic, 6, 122 Spleen diagnostic imaging techniques- 6>994 Sporulation microbes Group IIA ion transport, 6,569 Spot tests, 1,552 Square antiprisms dodecahedra, cubes and, 1 84 eight-coordinate compounds, 1 83 repulsion energy coefficients, 1 , 3 3 34 Square planar complexes, I?191,204 structure, 1,37 Square pyramids five-coordinate compounds. 1,39 repulsion energy coefficients. 1,34 Squares repulsion energy coefficients, 1 34 Squaric acid metal complexes, 2,435456 four-atom coordination, 2, 455 two-atom coordination, 2,454 solubility, 2,456 Stability cyclic bonding and. 1, 14 gravimetry, 1,526 ~

~

~

Stibines

Stabilization image dyes photography, 6,112 silver halides photography, 6 , 102 Stabilizers photographic emulsions, 6,97 Stannacarborates, 3,219 Stannate, hexachloroammonium salt crystal structure, 1, I6 Stannatc. trichloro-, 3, 195 Stannate tri halogenometal complexes, 2, 18 Stannates, 3, 204 electroplating, 6.4, 12 Stannatranes, 3,212 Stannocene, 3,217 functionally substituted, 3,218 nomenclature, 3,217 Stannocenium salts, pentamethyl-, 3,218 Stannonic acid, 3,206 Stannyienc complexes, 3, 192 structure, 3,193 transition, 2$ 17 Stathcrin, 6.578 Stearic acid nickel(I1) complcxcs weathering. 6,868 Stellacyaninr 6,651 copper(I1) complexes, 5,721 Raman spectra, 6.652 Stepanovite structure, 6,849 Stereochemistry action of drugs and, 6,774 copper(I1) complexes, 5,596 isomerism and, 1, 179 nomenclature, 1,127, 188,191 rigidity. 1, 180 tridentate azo compound metal complexes, 6 , 6 2 Stereoselectivi ty amino acid ester hydrolysis metal-catalyzed, 6,424 Steric effects redox potential, 1,484 Steroids hydrogenation catalysts, iridium complexes, 6,246 Stibine. amino-: 3.260,282 Stibine, aminocMoro-, 3,259 Stibine, (o-bromophenyl)dichloro-,2, 1007 Stibine, chlorodimethyl-, 2, 1007 Stibinc, chlorodiphenyl-, 2,1007 Stibine, dihalo-, 3, 258 Stibine, ethylenehis(dipheny1-, 2, 1008 Stibine, ethylidynebis(dimethy1-, 2 , I008 Stibine, germyl-, 3.259 Stibine, o-phenylenebis(dimethy1-,2, 1008 Stibine, stannyl-, 3,259 Stibine, triethyl-, 2, 1008 Stibine, trimethyl-, 2 , 1008 Stibine, triphenyl-, 2, 1008 sulfide metal complexes, 2,644 Stibine, tris(dimethy1amino)-, 3,259 Stibinc, tris(dipropyldithiophosphonato)structure, 1, 82 Stihine, tris(Jipropyldithiophosphonium)stereochemistry, 1 , 81 Stibine, trisilyl-, 3, 259 Stibine, tris(organoplumby1)-, 3,259 Stibines, 2,1007 ~

Stibine5 alkyl primary, 3,262 halogenation, 3,257 tertiary, 2, 1008 Stibonous acid thioesters, 3,269 Stibotungstates, 3, 1042 Stilbenediamine complexes structure, 1 , 2 5 metal complexes, 2 , 3 4 Stoichiometric reactions coordinated ligands, 6 , '155-221 Storage copper microorganisms, 6,681 dioxygen, 6,683 iron mammals, 6,667 microorganisms, 6,679 plants, 6,680 transition metals, 6,667-681 metallothioneins, 6,672 microorganisms, 6, 680 Stottite structure, 6, 849 Streptococcus faecalis calcium efflux, 6,570 cation transport, 6,558 Streptomyces spp. sporulation calcium transport, 6,572 Streptonigrin zinc complexes, 5,956 Stripping voltammetry metal complexes biology, 6,550 Stromeyerite brines, 6, 853 Strong-acid resins ion exchange, 6,814 Strontium Purex process, 6,940 Strontium-90 recovery, 6,959 Strontium, aquatetrakis(diacetamide)structure, 1 , 9 8 Strontium, heptaaquadodecaiodide structure, 1, 72 Strontium, octaaquastructure, 1, 84 Strontium alkoxides synthesis, 2,336 Strontium complexes porphyrins, 2,820 pyridine oxide, 3 , 9 Structure nomenclature, 1,124 StjTtme asymmetric carbonylation catalysis by palladium complexes. 6, 293 asymmetric hydroformylation catalysts, 6,265 catalysts, platinum complexes. 6.266 hydroesterification . catalysis by palladium complexesl 6, 293 isomerization, 6,286 hydrogenation catalysis by cobalt complexes. 6 , 2 3 8 oxidation cobalt catalysts, 6,387 oxidative coupling palladium catalysts, 6,371

Cumulative Subject Index Styrene, a-ethylasymmetric hydroformylation catalysts, platinum complexes, 6,266 asymmetric hydrogenation catalysts, rhodium complexes, 6 , 250 Styrene, a-methylasymmetric carbonylation catalysis by palladium complexes, 6,293 carbon yla tion catalysts. palladium complexes, 6 , 286 Styrene, pentafhoro-

hydrocarbonylationihydroesterification catatysts, palladium complcxes, 6 , 2 8 6 Substitution reactions, 1,281-329 basecatalyzed. 1, 300 four-coordinate complexes planar d8, 1.311 planar d * . dissociative activation, 1 , 320 solvents non-interfering. 1,285 Substrate activation catalysis transifion metal complexes, 6,230 Succinic acid! 2.3-dimercaptochelating agent heavy metal poisoning, 6 , 768 technetium complcxes, 6,984 Succinic anhydride protein modification with, 6,995 Succinimide, Wvinylasymmetric hydroformylation catalysts, 6,265 Sucrose alkaline earth metal complexes, 3 , 2 5 Sugar phosphates alkaline earth metal complexes. 3, 34 Sugars metal complexes geochemistry, 6, 868 synthesis prebiotic systems. 6,873 Sulfates effective bond length ratios, I , 37 hydrolysis metal catalysis, 6.465 leaching uranium, 6,788 in photochemical nitrogen production from water. 6. 508 Sulfenic acid metal complexes, 2, EO0 Sulfide complexes, 2,519-526 p2-bridging ligands, 2, 520 p3-hridging ligands, 2,522 p,-bridging ligands, 2,522 me.tal classification, 2,525 gcometrics, 2,532 side-on coordinated, 2,533 terminal metal-sulfur bonds, 2, 519 types, 2,519 Sulfide minerals structure, 6,783 Sulfide oxidases, 2,773 Sulfides base metal smelting, 6,833 in matte-slag systems, 6,834 metal complexes geochemistry, 6,853 prcbiotic systems, 6, 871 mineral processing precipitation, 6, 828

226

227 photographic fixer, 6, 100 Sulfinylamines imido metal complexes synthesis from, 2,167 Sulfite oxidases, 3, 1334 molybdenum cofactor. 6.663 structure, 3, 1438 Sulfites metal complexes. 2,424, 637 bidentate, 2,638 bonding, 2, 637 bridged, 2,638 unidentate 0-bonded. 2.638 unidentate S-bonded, 2,638 stereochemistry, 1,37 Sulfonates metal complexes hydrolysis, 1,428 Sulfonium ions, trichlorostereochemistry, 1,37 Sulfonium ions, trifluorooxide geometry, 1,3S stereochemistry, 1; 37 Sulfonphthalein metallochromic indicator, 1 556 Su 1foxide complexes enantiomers, 1, 199 Sulfoxide, benzyl methyl metal complexes, 2,640 Sulfoxide, dibenzyl metal complexes, 2, 640 Sulfoxide, dimethyl hazards, 2,487 metal complexes, 2>487-501.640 bonding, 2,489 bridging, 2,489 TR spectra, 2,489 N M K spectra, 2,489 1')3Rh,2, 490 S coordination, 2,490 metal salt solubility in, 2,487 properties, 2,487 ruthenium(II1) complexes, 2.641 Sulfoxide, diphenyl metal complexes, 2,640 Sulfoxide, isopropyl methyl metal complexes, 2,64@ Sulfoxides hazards, 2,488 metal complexes, 2,487,640 structure, 2,488 synthesis, 2,488 Sulfur, 3,299-307 bonding, 3,299 coordination compounds, 3,300 geometry, 3,299 valence, 3,299 Sulfur complexes, 2, 515-547 synthesis, 2,519

Cumulative Subject Index

Syphilis treatment

Sulfurdiimine metal complexes, 2, 190 bidentate, 2, 191 bonding. 2.191 fluxional behavior, 2, 192 reactivity, 2, 194 platinum complexes monodentate, 2, 191 Sulfurdiimine. NJ"'imethy1electron diffraction, 2, 19G195 NMR,2, 190 Sulfur dioxide metal complexes, 2,634,806 bonding, 2,634 IR spectroscopy, 2,635 structure, 2,634 Sulfur ligands, 2,633-655 coordination ability, 2,516 palladium(I1) complexes, 5,1131-1 152 Sulfur monoxide metal complexes instability, 2, 636 Sulfur tetrafluoridc complexes, 3,301 with pyridine, 3, 304 Sulfur trioxide complexes with pyridine, 3.3U4 Supcroxidc dismutascs, 2,773; 6,682,700 antiarthritis drugs, 6, 760 copper complexes, 2,772; 5,721 copper-zinc, 6,701 iron. 6.703 manganese, 6,703 Superoxides Cormation, 6,682 Superoxo complexes, 2,315-330 binuclear, 2, 323, 325 reactions, 2: 330 bridged X-ray studies. 2,324 mononuclear. 2.32'1,322 IR spectra, 2,323 reactions, 2.329 oxidation, 6.319 Superphthalocyanine, 2,888 synthesis, 6: 192 uranium complexes reactions. 2,892 Surface-enhanced Raman scattering, 5,787 Swartzite structure, 6,848 Symmetry! I, 190 Synergism liquid-liquid extraction, 1,547 Synexin. 6,578 calcium. 6,595 Synroc in nuclear fuel waste immobilization, 6,961 Syphilis treatment organoarsenicals, 6, 756

Talspexk process, 6,959, Y6(:l Tanabe-Sugano diagrams, 1,238 Tannic acid in gravimetry, 1,524 Tanning chromium(II1) complexes, 3, 907 Tantalate, tetrachlorobis[ethylenebis(dimethylphosphine )Iphosphonium salts structure, 1,89 Tantalates, halo-, 3,592,640 Tantalates, pentachlorooxo-, 3, 627 Tantalum, 3,585686 atomic radius, 3,588 coordination numbers, 3,588 oxidation states, 3,587 zinc compounds, 3,639 Tantalum, (bipyridinejdichlorotrimethylstereochemistry, 1,77 Tantalum, octafluorostructure, 1 , 8 4 Tantalum, pentabromo(dimethy1 sulfide). ligand exchange, 1,287 Tantalum, pentafluoroperoxystructure, 1,76 Tantalum, tetrachlor~~bis[ethylenebis(dimethylphosphine)]structure, 1 , 8 9 Tanralum, tetradecachlorohexakisstructure, 1,23 Tantalum, tetrakis(dimethy1dithiocarbamato)stereochemistry, 1,94 Tantalum, tris(diethy1dithiocarbarnato)thiostereochemistry, 1, 82 Tantalum, tris(phenylenedithi0)structure, 1 , 6 3 Tantalum chloride Ta,CI*o structure, 1,28 Ta6Cll5 structure, 1,27 TantJum complexes alkyl alkoxy reactions, 2,358 amidcs synthesis, 2, 165 applications, 6, 1014 clusters, 3,672,673,675 y-dinitrogen, 3,418

fluoro transfer reactions, 3,593 hexamethylbenzene ligands, 3.669 imido synthesis, 2, 168 mixed valence, 3,685 non-integral oxidation states, 3,667477 octahedral oxidized, 3,673 octahedral clusters, 3, 670 bonding, 3,676 electronic spectra, 3,676

hydratcs, 3,671 ionic halides? 3. 671 magnetism, 3,676 neutral binary halides, 3, 671 standard potentials, 3, 674 oxidation states: 3.5S7 phthalocyanines, 2,865 polypyrazolylborates, 2.248 porphyrins, 2.824 pseudohalides, 2,229 tctranuclcar clustcrs, 3?670 triangular dusters, 3,667 solvolysis, 3,668 Tantalum(- 111) complexes carbonyl, 3, 684 Tantalum(-I) complexes, 3,684 carbonyl, 3,684 Tantalum(0) complexes, 3, 683 Tantalum(1) complexes, 3,679-683 alkenes, 3>682 carbonyl, 3 , 6 N carbonylcyclopentadienyl, 3,682 dienes. 3, 682 phosphines, 3,679483 Tantalum(I1) complcxcs, 3,677-679 dihalo, 3.667 Tantalum(T1T) complexes, 3,655-667 activation reactions, 3, 660 alkoxo, 3,664 carboxylatotrihalo, 3,664 dialkylphosphido, 3.665 13-diketonatotrihalo, 3, 664 dithiocarbamato, 3-664 halo anionic, 3,655 nitrenes, 3.665 organometallic, 3,665 oxalato, 3,666 pseudohalo, 3,666 reactions with alkynes three-membered metallacycles, 3,661 sulfato. 3,666 thiolato, 3.664 trihalo, 3, 655 neutral adducts. 3.656 solvolysis. 3, 663 Tantalum(1V) complexes. 3,639-65s activation of small molecules, 3,654 alkoxo. 3,649 alkylamido, 3.652 carboxylato, 3,650 chalcogeno, 3,654 clustersl 3,667 dialkyldithiocarbamato, 3,651 dialkglphosphido. 3,652 P-diketonato, 3,650 ESR,3, Tr35 halooxo- 3,646 haloseleno, 3:646, 647 halotelluro, 3,646 halothio. 3.646,647

228

229

Cumulative Subject index

nitrido, 3,654 phthalocyanines, 3,653 porphyrins, 3,653 pseudohalo, 3,645 tetrahalo, 3,639 neutral adducts, 3, 640 solvolysis, 3,649 thiolato, 3,651 trihalo neutral adducts, 3,657 Tantalum(V) complexes N-acetamido, 3,622 alkoxo, 3, 600, 601 oxygen ligands, 3,604 propcrtics, 3,602 reactions with p-diketones, 3,603 reactions with nitrogen ligands, 3,603 reactions with Schiff bases. 3,605 structure, 3 , 601 alkoxohalo, 3,603,607 adducts, 3,606 alkoxooxo, 3,632 N-alkyl-N-nitrosohydroxvlaminato? 3,623 amides properties, 2, 168 amido, 3, 608 structure, 3,608 synthesis, 3,608 amidooxo, 3,634 amidopentahalo, 3.595 arsenato, 3,638 azametallacycles, 3,611 azido, 3,619 bromo anionic, 3,593 bromooxo, 3,625 carboxylatohalo, 3,606 carboxylatooxo, 3,633 chloro anionic, 3, 593 chlorooxo, 3,625 chloroperoxo, 3,636 cyano, 3,623 N,N'-dialkylacetamidinato: 3+627 dialkylamido, 3,609 dialkylcarbamato, 3,611 N,N-dialkyldithiocarbamato. 3,606 dialkyldithiophosphato, 3,639 difluorophosphinato. 3, 639 P-diketonatooxo, 3.632 dithiocarbamatohalo, 3,607 Auoro anionic, 3, 591 Ruorooxo, 3,625 anions, 3,626 halo arsenic donors, 3,6W phosphorus donors, 3: 600 halooxo, 3,625-632 nitrogen donor adducts, 3,630 haloperoxo, 3,636,637 halophosphonato. 3.607 halo-8-quinolinol. 3.606 haloseleno, 3, 626 halothio, 3, 626 halothiolato, 3,607 hexafluoroperoxo, 3,636 iodo anionic, 3,593 iodooxo, 3,625 isocyano, 3,623 isoselenocyanato, 3,624 isothiocyanato, 3.624

Tartaric acid

isothiocyanatooxo, 3,634,635 metaphasphato, 3,639 mixed alkoxo. 3,602 mixed halo, 3: 594 mixed pentahalo, 3.591 monothiocarbamato, 3,610 nitrato, 3: 638 nitrenes, 3.613 reactivity. 3. 616 structure, 3,613 synthesis, 3,613 nitrido, 3, 620,621 nitrogen-containing insertion products, 3,623 orthophosphato, 3,639 oxo, 3,635639 oxygen abstraction reactions, 3,631 pentabromo, 3.590 pentachioro, 3,590 pentadialkylamido, 3,611 reactivity. 3,610 pentafluoro, 3,589 pentahalo, 3.589-591 amines, 3,596 applications, 3,591 arsenic donors, 3,599 arsine oxides, 3, 595 dia1k.y) esters, 3, 595 ethers, 3,595 ketones, 3,595 neutral adducts, 3,594 nitrogen complexes, 3,597 nitrogen donors, 3,596 phosphine oxides. 3,595 phosphorus donors, 3,599 Schiff bases, 3,596 selenium ligands, 3,596 solvolysis, 3, 600 sulfur ligands, 3,596 tellurium ligands, 3, 596 pentahalonitrido, 3, 596 pentahalnthiocyanat(1, 3, 596 pentaiodo, 3.590 peroxo? 3,635.636 peroxo acids, 3.635 phosphato. 3.638 phosphinato, 3,639 phosphineiminato, 3,619 phosphonato, 3,639 porphyrins, 3,620 pyrazolylborato. 3,622 seienn, 3,638 srlenocyanato, 3, 624 silylamido. 3- 610 sulfaco. 3,638 tetrachluru with phosphorus donors, 3,642 tetrahalo amines, 3,641 oxygen ligands, 3,643 sulfur ligands. 3,643 with arsenic donors, 3,642 thio, 3,635-639 N-thioacetamido, 3,622 thiocarhamato, 3,634 thiocyanato, 3,624 trihalooxo solvolysis, 3,632 Tantalum ethoxides synthesis electrochemistry. 2, 337 Tanialum pentaalkoxides physical properties, 2,347 Tartaric acid

Tartaric acid

Cumulative Subject lndex

cobalt(II1) complexes structure, 2,471 metal complexes, 2,465,478 bidentate chelation, 2,479 bridged binuclear, 2,479 geochemistry, 6,867 IR spectra, 2,470 naturally occurring, 2, 962 NMR spectra, 2,467 protonation, 2,465 Tartronic acid metal complexes, 2,480 NMR, 2,467 Tautomerism anils, 2,717 1,3-diketones, 2,365 Technates blood labelling with, 6, 994 chemical reduction, 6,973 electroreduction, 6,973 labelled biological half life, 6, 973 complexations, 6,974 reduction, 6,974 reactions with thiourca, 6, 975 with trispyrazolylhydroborate, 6. 975 reduction, 6,977 structure, 6,973 Technetium isotopes medical diagnosis, 6,969 medical applications, 6,973 Purex process, 6,944 radiopharmaceuticals, 6,882,972 recovery from nuclear fuel waste, 6,960 Techne tium-99 antibody labelling, 6,995 biodistribution, 6,975 brain scanning agent recent development, 6,996 diagnostic imaging techniques in medicine, 6,965 generation, 6,964 handling precautions, 6,973 heart imaging agents recent developments, 6,996 lower oxidation state complexes radiopharmacy, 6,980 Technetium, tris(mercaptoani1ino)structure, I , 63 Technetium complexes applications, 6, 1016 chemistry, 6,981 cupferron, 2,510 dimethylglyoxime in medicine, 6,974 glucoheptonates labelled, 6,975 in medicine, 6,983 iminodiacetate imaging agents, 6,985 phosphines, 6,981 phthalocyanines, 2,866 polypyrazolylborates, 2, 251 porphyrins, 2,826 pseudohalides, 2,22Y, 230 radiopharmaceuticals diagnostic imaging techniques, bone, 6,985 structure and biodistribution, 6 , 985 structure, 6,973,977 synthesis, 6,977 thiolates, 6,981

Technetium(II1) complexes phosphines electrochemistry, 6,983 high performance liquid chromatography, 6, 976 Technetium(1V) complexes hydrolysis, 6,982 magnetic behavior, 1,272 oligomerization. 6.983 Technetium(V) complexes citrates, 6,982 glucoheplonates. 6,982 mercaptoacetic acid: 6,975 'I'echnetiurn dioxide in pharmacy. 6.971 Teichoic acid, 6.680 Tellurate. hexabromostructure, I . 73 Tellurate, hexachlorostructure, 1 , 7 3 Tellurates effective bond length ratios, 1,37 Tellurates, pentafluoroelectronegativityl 3: 319 Tclluratcs, tartrato-. 3.303 Tellurites stereochemistry. 1 . 3 7 T~llurium,3,299-307 bonding, 3,299 coordination compounds, 3,300 geometry, 3,299 metal complexes. 2- 661-672 six-electron donor, 2, 671 toxicity. 3, 307 valence, 3,299 Tellurium, bis(acetophenonejdich1orophotothermography, 6 . 120 Tellurium, bis(dithiofurancarbamato)stereochemistry, 1, h0 'l'ellurium, bis(ethy1dithiocarbonatojsterecichemistry, I - 60 Tellurium, bis{in~inobis[(diphenylphosphino)thio]}structure. 1.60 'Tellurium, bis(rnethy1dithiocarbonato)stereochemistry, 1,60 Tellurium, dichlorodimethyllone electron pair, I, 44 Tellurium, pentafluorolone electron pair structure, I. 50 Tellurium, tetrakis(diethy1dithiocarbamato)stereochemistry, I, 94 Tellurium. tetrakis(thi0urea)dichloride structure, 1,60 Tellurium. tetraphenylbenzene complex structure, 1,44 Tellurium. tris(diethy1dithiocarbamatojphenylstereochemistry. 1.82 Tellurium complexes acetylacetone. 2, 370 heterocyclic metal complexes, 2,670 metal clusters, 2.671 oxidation catalysts, 6,359 phototherrnography, 6. 120 porphyrins, 2: 822 Tellurium(I1) complexes bis(ditbiochelate), 1 , 60 dithiocarbamate photothermography, 6.121 four-coordinate. 3.305

230

231

Curnulutive Subject Index

bidentatc ligands, 3, 305 six-coordinate compounds structure, 1, 53 thermography, 6, 122 tris(ethylxanthato), 3.305 Tellurium(1V) complexes eight-coordinate, 3,307 liquid-liquid extraction, 1,546 seven-coordinate, 3,307 six-coordinate, 3, 307 truns-tctrachlorobis( tewamethylthiourea), 3, 3U7 tetrakis(4-morpholinccarbodithioato), 3,307 thermography, 6, 122 Tellurium dichlorobromide complexes, 3,302 Tellurium dioxide complexes with thiourea, 3,305 Tellurium dithiocyanate complexes, 3,303 Tellurium hexafluoride complexes, 3,303 with amines, 3,304 Tellurium ligands palladium(I1) complexes, 5, 1'131-'1 152 Tellurium sulfatc complexes, 3, 303 Tellurium tetrabromide complexes, 3,302 Tellurium tetrachloride complexes with acetamide. 3.304 with amines, 3. 304 with pyridine N-oxide, 3,304 Tellurium tetrafluoride complexes with amines, 3,304 with dioxane, 3,304 Tellurocarbonyl compounds metal complexes, 2. 671 Tellurocyanates metal complexes, 2,225-238.668 molecular geometry. 2,226 Tellurol metal complexes, 2, 669 Tellurotungstates, 3, 1042 Tellurourea metal complexes, 2,670 Temperature effects spectral band widths, 1- 218 Temperature-jump studies molybdenum(V1) complexcs. 3. 1259 Template effect catalysis transition metal complexes, 6.230 Ten-coordinate compounds stereochemistry, 1,Y8 Terbium, tris(2,2,6,6-tetramethyI-3.5-heptanedione)photosubstitution, 1,4118 Terbium complexes f3-diketones, 3, 1081 tetrapositive oxidation state hydrated ions, 3, 1113 Terephthalic acid manufacture cobalt catalysts, 6 , 386 Terlinguaite, 5 , 1050 Terminal oxidases aerobic carboxydobacteria. 6,698 2,2',2"-Terpyridyl, 4,26 2,2'-iminobis(ethyleneiminocthylaminc), 4.29 metal complexes, 2,89,91, 94 2,2' ,2"-propylidynetris(methyleneiminoethylamine), 4, 30

Tetranactin

tricthylenetetrarninc, 4,27 tris(2-dimethylaminoethyl)amine,4,29 Teta -see Acetic acid, tetramethylenediaminetetraTetra-L-alanine metal complexes, 2,765 Tetraazaannulenes 163-electron electrical conduction, 6, 147 Tetraaza- 1.3-butadiene metal complexes, 2,217,218 bonding. 2,224 reactivity, 2,222 structure, 2.224 synthcsis. 2.217-224 1,4,7,10-Tetraazacyclododecane metal cumplexes sensitizers, silver halides light sensitivity, 6 . 97 1,4,8.11-Tetraazacyclotetradecane,5,5,7,12,12, I4hexamet hylnickel(I1) complexes, 1,204 1,4,8,1l-Tetraazacyclotetradecane, 1,4& 1I-tetramethylzinc complexes, 5,996 Tetraaza macrocycles nickel complexes, 5 , s synthesis, 2,903 Tetraazaporphyrin, octaphenylmetallation, 2, 858 Tetraazaporphyrins synthesis, 2, 857 1,4,8,1 I-Tetraazaundecane metai complexes sensitizers. silver halides light sensitivity. 6. 97 Tetrabenzoporphyrins metal complexes, 6 , 194 Tetracatecholamide sulfonated sequcstering agents, actinides, 6,962 'retrachromates electroplating, 6 , 8 Tctradecametallic complexes, 1, 1.67 Tetrad effect solvent extraction lanthanides, 6,795 Te traethylenepentamine metal complexes, 2,56 Te traglycine metal complexes, 2,764 Tetragonality copper(I1) complexes, 5,603 Tetrahedra repulsion energy coefficients, I , 33, 34 Tetra hedritc brines. 6,853 'Tetraketones meral complcxes, 2,399 1.3,5.7-Tetraketones metal complexes, 2,400 Tetrametallic complexes, 1, 146 butterfly, 1,149 disphenoid, 1, 149 double three-atom bridges, I , 147 no bridging ligands, 1, 146 single one-atom bridge, 1, 146 single three-atom bridges, 1, 146 tetrahedral. 1 , 150 three-atom bridges, 1, 148 trigonal pyramid, 1, 149 Trtramines cyclic complexes, thermodynamics, 2,912 metal complexes, 2 , 5 0 Tetranactin alkali metal complexes, 3,64

~

Tetrapeptides

Cumulutive Subject Index

Tetrapeptides synthesis cobalt(II1) catalysis, 6, 437 1.3.7 10-Tetraphosphadecane, 1,1-dimet hyl-4,7.10,10tetraphenyl-, 2,995 174.7.10-Te~raphosphadecane, 1, I ,4.7.10,10-hexapheny1 2.995 cyclo-Tetraphosphates hydrolysis metal catalysis, 6,444 Tetraghoyphine ligands, 2,995 Tetrapyridyls metal complexes, 2, 91 geometry. 2.91 Tetrapyrroles metal complexes, 2,79 biology, 6,546 template cyclization, 6,201 Tetraselenoether metal complexes, 2,666 Tetraselenomolybdates IR spectra, 3, 1379 Raman spcctra, 3, 1.379 Terrasulfur tetranitride metal complexes, 2, 799 Tetrathiolane, his(imino)metal complexes, 2, 591 Tetrathiomolybdates, 3, 1377 IR spcctra, 3, 1379 Raman spectra, 3, 1379 Tetrathiooxalic acid metal complexes, 2,585,606 Tetrathiosquaric acid metal complexes, 2,606 Tetrawickmanite structure, 6,849 Tetrazole, 2-methylmetal complexes, 2,77 Tetrdzok, pcntamethyimetal complexcs, 2,77 'I'errazoie, I-phenyl-5-mcrcaptophotographic stabilizer. 6, 103 Tet razoles metal complexes, 2,76 PK,, 2,77 Thallium cubanoid alkoxides, 1, 153 determination, 1,535 ion selective electrodes, 6, 26 'Thailiurn-201 complexes heart imaging techniques, 6, 990 Thallium, aquatetra!&[( tritluoroacetyl I)acetonc]bond lengths, 1, YS structure, 1,97,98 Thallium, tetrakis(acety1acctonc)stereochemistry, 1,94 Thallium, triaquatrinitratostructure, 1,97 Thallium complexes, 3, 153-175 amidines, 2,205 phthalocyanines, 2, 863 porphyrins, 2,821 triazines, 2,205 Thallium(1) complexes, 3, 167 alkoxides, 3, 168 bromides, 3, 170 carboxylatcs, 3, 169 chlorides, 3, 170 crown ethers, 3, 170 cyanides, 3, 167 b-diketonates, 3, 169 dithiocarbamates, 3, 169

fluorides, 3, 170 hexafluoroacetylacelone, 2, 372 hydrides, 3 , 170 hydrogen. 3.170 hydroxides, 3, 168 iodides. 3. 170 macrocyclic ligands: 3, 150 nitrogen ligands. 3. 168 oxides, 3, 168 oxyanions, 3, 169 peroxides, 3. I68 selenides, 3, 'lh9 sulfides, 3 , 169 tellurides. 3: 169 thiourea, 3. 170 Thallium(I1) complexesl 3>171 Thallium(II1) complexes, 3, 171 amines, 3. 172 ammines, 3,172 aqua, 3, 172 bipyridyl, 3, 172 bromates. 3. 173 bromidcs, 3, 174 carboxylates. 3, 173 carboxylic acids reactions, 2 , 44.3 chlorates. 3. 173 chlorides, 3,174 cyanides, 3. 171 dichlorophosphates, 3, 173 1.3-diketones synthesis: 2.377 ethers, 3, I73 fluorides, 3. 174 hydrides, 3,175 hydrogen, 3, 175 hydroxides. 3. 172 iodalrst 3. 173 iodides? 3. 174 macrocyclic ligand\. 3,175 mixed halides. 3, 171 nitrates, 3, 173 orthophosphates. 3,173 oxides, 3, 172 perchlorates, 3. 173 1,lO-phenanthroline. 3. 172 porphyrins, 3: 175 pseudohalides, 3, 172 pyridines, 3, 172 selenates, 3, 173 sulfides, 3, 174 tellurates, 3 , 173 terpyridyl, 3, 172 Thallium cyanatc, 3! 168 Thallium nitride, 3, 168 Thallium selenocpanate, 3, I68 Thallium thiocyanate. 3, 168 Theophylline cadmium complexes. 5.957 Therapeutic agents radionuclides. 6 %964 Thermal neutrons uranium-235.6> 883 Thermal oxide reprocessing plant, 6,885 Thermal reactor fuels, 6,926 dissolution, 6: 927 irradiatcd solvent extraction. 6 . 934 reprocessing solvent extraction, 6. 936 Thermal reactors fuel preparation? 6 , 9 2 3 Thermochromism, 1.470

232

233

Cumulative Sicbjecr Index

anils, 2, 717 bidentate Schiff base metal complexes, 2, 726 Schiff base complexes. 2. 718 Thermodynamic template reactions imine metal complexes. 6 , 156-161 Thermography, 6.121 Thermolysin stability calcium ions, 6,565 zinc, 5 , 1006; 6,606 Thermus aquaticu.7 ribonucleotide reductasc, 6,642

Thia-5-azacyclooctilne-5-methylmctal complcxcs. 2. 802 Thiabendazole metal complexes. 5.951 Thiadiazepines metal complexes. 2.81 3-Thiapentanedioic acid photography diffusion transfer process. 6. 101 3-Thiapentanoic acid photography diffusion transfcr process, 6 : 101 Thiaporphyrins, 2, 8.50 Thiatriazcilethiolates mctal complcxcs, 2.588 Thiazole, N-salicyliclene-2-aminohydrolysis metal catalysis, 6,460 Thiazole, thioacetamidometal complexes, 2, 647 Thiazolines photographic stabilizer. 6. 103 2-Thiazolinium carboxylate, ?-aminophotographic stabilizer, 6. 103 2-Thienylmcthylcnciminc, NI:Wcthylcncbishydrolysis metal catalysis, 6.4W Thioacetals, 6. 457 hydrolysis metal catalysis. 6.463 Thioacetamide metal complexes, 2,647 Thioacetamide, N,N-dimethylmetal complexes, 2,637 Thioacetic acid metal complexes, 2,585. 645 Thioamides N-substitutcd metal complexes, 2 , 804 Thio anions metal complexcs, 2: 521 Thioantimonates. 3 , 265 Thioarsenates, 3. 248 Thioarsenious acid, 3.248 cstcrs, 3,248 Thioarsenites, 3, 248 Thiobacillus ferrooxidans in oxidative leaching of uraniferous ores, 6, 900 Thiobacillus thiooxidans in oxidative leaching of uraniferous ores, 6,900 Thiobenzamide metal complexes. 2-6-17' Thiobenzohydroxatriic acid. N-mevhylmetal complexes. 2, 806 Thiobenzuic acid metal complexes. 2.585.645 Thiocarbamic acid metal complexes. 2?806: 5.978 Thiocarbamic acid, diniethylIR spectra, 2,587 Thiocarbazide

mctal complexes, 5,978 Thiocarbazide, diphenylreaction with fatty acid metal salts thermography, 6, 121 Thiocarboxamides metal complexes, 2,647 Thiocarboxylic acids metal complexes, 2,584,645,806 reactions m e t a l catalysts, 6,458 Thiocyanates hydrometallurgy, 6,785 metal cornplrxcs, 2,225-238 sylthcsis, 2, 237 molecular geometry, 2,226 photographic stabilizer, 6 , 103 Thiocyanato complexes linkage isomerism, 1,184 Thiocyanic acid metal extraction from, 1,540 Thioesrers b-mercapto metal complexes, 2,655 Thioethers complexes chirality, 1, 199 cyclic metal complexes, 2,552 formation alkylation of thiolate complexes, 1,443 macrocyclic metal complexes, 2,552 metal complexes, 2,551-557 biology? 2.557 bonding, 2,555,556 bridging ligands, 2,552 chelating ligands, 2,553 electrochemistry, 2, 556 equilibriuni stndics, 2, 554 formation, 2.553 inversion, 2, 555 kinetics. 2, 554 S alkylation, 2,554 S dealkylation, 2,554 spectroscopy, 2,556 structure. 2, 555 X-ray diffraction, 2, 555 Thioformamide. N,N-dimethylmetd complexes, 2,647 Thioglycolatc chelating resins mineral processing. (1, 826 T h iI) hydratcs metal complexes, 2,516 Thiohvdroxamic acid metal complexes, 2, 806 Thiolates aggregate metal complexes terminal ligands, 2,527 dinuclear complexes p?-bridging ligands, 2, 527 metal complexes, 2, 526 polydentate, 2.529 reactions, 2, 530 synthesis, 2 , 530 metallothioneins, 6,673 monodentate metal complexes sterically hindered, 2, S2h mononuclear complexes. 2,526 poly~uclcarcomplcxcs y,-bridging ligands, 2,527 p,-bridging ligands, 2,529 sulfur-sulfur interactions, 2,530

Thiolates

Thiols Thiuls aminoalkyl photographic stabilizer, 6, 103 esters hydrolysis, metal catalysis. 6.456 heterocyclic metal complexes, 2, 802 metal complexes, 2,516 Thiometalate ligands chain-type complexes doubly bridging, 2, 565 electrochemistry, 2,574 electronic structure, 2,571 Mossbauer spectra, 2,574 physical properties, 2,575 spectroscopy, 2,570,571 vibrational spectra, 2,570 electronic structure, 2,559 heterometallic clusters, 2, 568 heteronuclear metal complexes. 2,563 homonuclear metal complexes. 2- 562 metal complexes bonding, 2,570 metal sulfide aggregates, 2, 569 muhimera1 complexes, 2,565 properties, 2,559 reactivity, 2,559 substituted metal complexes, 2,570 trinuclear bis complexes, 2, 564 trinuclear complexes doubly bridging, 2,565 Thiomolybdate anions, 3, 1421 copper derivatives, 3, 1421 cyclic voltammetry, 3, 1424 gold derivatives, 3, 1422 TR spectoscopy, 3, 1424 nickel derivatives, 3, 1422 NMR, 3, 1424 palladium derivatives, 3, 1422 platinum derivatives, 3, 1422 properties, 3, 1421 Kaman spectroscopy, 3, 1421 ruthenium derivatives, 3, 1422 silver derivatives, 3, 1422 structure, 3, 1421 synthesis, 3, 1421 UV spectroscopy, 3, 1424 Thiomolybdates preparation, 2,562 Thionalide in gravimetry, 1,533 Thiones esters hydrolysis, mctal catalysis, 6,456 heterocyclic metal complexes, 2,802 oxidation tellurium-oxo compounds, 6,361 Thionitrites metal complexes, 2, 190-195 bonding, 2,191 fluxional behavior, 2, 192 Thionitrosyl complexes synthesis, 2, 119 transition metals, 2, 118, 122 bonding. 2,120 NMR, 2,121 photoelectron spectroscopy, 2 , 121 reactions, 2,121 spectroscopy, 2, 120, 121 structures, 2, 120 Thionitrosyls, 2, 100

Cumulative Subject Ifidex Thioperrhenates, 4.100 Thiophene, tetrahydrooxide metal complexes, 2,640 trans-2-Thiophene-rrans-aldoxime in gravimetry, I, 532 2-Thiophenecarbohydroxamic acid as metal precipitant. 2,506 Thiophosphinic acid metal complexes, 2,643 Thiophosphoryl halides metal complexes, 2,642 ’Thiciselenometalares synthesis, 2,560 Thiosemicarbazides metal complexes. 2. SO2 Thiosemicarbazones copper tumor imaging techniques, 6,994 iron complexes tumor imaging techniques, 6,994 metal complexes. 2. SO2 Thiostibinous acid esters, 3,269 Thiosulfates metal complexcs, 2,636 photographic fixer, 6,100?102 Thiotungstates preparation, 2.562 2-Thiouracil metal complexes, 2,802 Thiourea diphenylphosphinot hioyl derivatives metal complexes, 2,640 leaching gold, 6.785 metal complexes, 2,639 photographic fixer, 6, 100 photographic stahilizer, 6 , 103 substituted metal complexes, 2,639 Thiourca, l-amidinomctal complcxcs, 2- 804 Thiourea, 3-benzoyl-l ,l-diethylmetal complexes, 2.804, 806 Thiourea, N,N’-dimethylmetal complexes, 2,640 Thiourea, N,NI-dimethyl--N’-phenylmetal complexes, 2, 804 Thiourea, ethylenemetal complexesl 2.639 Thiourea, N-hydroxy-,V-methylmetal complexes, 2,798 Thiourea, N-rnethylmetal complexes. 2, h40 Thiourea, N,N,1V’,l\i’-tetramethylmetal complexcs, 2: 640 Thioxanthic acid metal complexes. 2,590 Thiuram disulfide metal complexes. 2,598 Thomsenolite structure, 6,846 Thorex process, 6,926,954 breeder reactor fuels, 6,955 flowsheet. 6,957 third phase formation, 6,955 thoriumiuraniurn oxides irradiated. dissolved, 6 , 955 Thorianite, 6,911 Thorides in reprocessing irradiated nuclear fuels, 6,928 Thorite, 6,911

234

235

Cumulative Subject Index

structure, 6,912 Thorium leaching, 6,886, 912,914 minerals, 6,889 processing, 6, 912 in natural waters, 6, 886 occurrence, 6,886 purification, 6,922 recovery from ores, 6,895-919 uranium processing, 6,915 reserves, 6,889 segregation of uranium from geochemistry, 6,886495 solvent extraction, 1,523 Thorium, aquatetrakis(propyltropo1one)structure, 1.98 Thorium, aquatetrakis(tropo1one)structure, 1,98 Thorium, (dimethylformamide)tetrakis(tropolone)structure, 1,98 Thorium, hexanitratostructure, 1,101 Thorium, pentacarhonatostereochcmistry, 1,9Y Thorium, tetrachlorobis(octamethy1pyrophosphoramide)structure, 1,89 Thorium, tetrachlorotetrakis(dipheny1 su1Coxide)salts, 1, 87 Thorium, tetrakis(dimethy1dithiophosphonium)stereochemistry, 1,94 Thorium, tetrakis(4,4 .4-trifluoro-l-thienyl- 1,3butanedione)(trioctylphosphine oxide)structure, 1,98 Thorium, triaquatetranitratostructure, 1,99 Thorium complexes, 3, 1131-1215 groundwaters geochcmistry, 6.852 polypyrazolylborates, 2. 255 Thoriurn(1V) complexes cupferron, 2,512 peptides hydrolysis, 6,425 pyridine oxide, 2,495 solubility in natural waters, 6,887 Thorium dioxide, 6, 927 Thorium ions hydrolysis, 6,914 Thorex process extraction by trialkyl phosphatcs, 6, 958 Thorium pyrophosphate precipitation, 6. 914 Thorium tetraalkoxides physical properties, 2,347 synthesis, 2, 338 Threonine epimerization geochemistry, 6,866$867 metal complexes, 2,750 prebiotic systems, 6,872 synthesis from glycine metal complexes, 2,757 metal catalysis. 6- 468 metal complexes, 6 , 466 Thrombin blood coagulation, 6,591 Thymine bases metal complexes, 2,976 Thymolphthalexone

Tin complexes

metallochromic indicator, 1,557 Thyroid technate uptake, 6,973 Tiglic acid methyl ester hydroformylation, 6,261 Time dependent peturbation theory electron transfer, 1.342 Tin electroplating. 6, 11 elemental structurc, 3, 184 masking, I, 538 Tin, bis(diethy1dithiocarbamato)diphenylangular parameters, 1,57 Tin, bis(diethy1dithiocarbonato)diiodoangular parameters, 1,57 Tin. bis(diethy1 dithioph0sphate)diphenylstereochemistry, 1,59 Tin, bis(diethy1dithiophosphonium)diiodoangular parameters, 1,57 Tin. chlorotris(tropo1one)stereochemistry, 1,82 Tin. cyclopentadienyl-, 3,218 Tin, dibromobis(ethy1dithiocarbonato)angular parameters, I , 57 Tin. dichlorobis(ethyldithiocarbonat0)angular parameters, 1,57 Tin, dimethylbis(acety1acetone)structure, 1,58 Tin, dimethylbis(dimethy1dithiocarbamato)stereochemistry, 1, 59 Tin, dimethylbis(dimethy1dithiophosphorane)Stereochemistry, 1,59 Tin, dimethyldinitratostereochemistry. 1,59 Tin, methoxytrimethyl-, 3,208 Tin, methyltrinitratostereochcmistry, 1. 82 Tin, nitratodiphenyltris(dirnethy1sulfoxide). structure, 1,77 Tin, nitratotris(tripheny1tin)structure, 1,47 Tin, tetrakis(acetat0)stereochemistry, 1,94 Tin, tetrakis(diethy1dithiocarbamato)angular parameters, 1,57 Tin, tetrakis(ethyldithiocarbamat0)angular parameters, 1,57 Tin, tetranitratoStereochemistry, 1,94 Tin, tri-n-butylmethoxy-, 3,208 Tin alkoxides physical properties, 2,346 Tin bromide, 3, 194 Tin bromide hydrate, 3,195 Tin carboxylates, 3,222 mixed valence, 3,222 Tin chloride, 3, 194 hydroformy lation platinum complexes, 6,263 Tin chloride dihydrate, 3, 195 Tin complexes, 3,183-223 ace tylace tone ligand exchange reactions, 2,381 Miissbauer spectra, 2,391 rearrangement, 2,383 synthesis, 2,377 benzoylacetone, 2,372 bivalent stereochemistry, 3, 188 coordination geometry, 3, 185 cupferron, 2.512

Tin complexes

Cumulative Suhject Index

dialkyl or diaryl, 3,216 multiple bonding, 3,188 phthalocyanines, 2,864 porphyrins, 2,822 pyridine oxide, 2,496 skew-trapezoidal bipyramidal structuresI 1.58 tetravalent, 3,205 tropolone, 2,373 q6-arene, 3,220 Tin(I1) complexes bis( B-ketonolates) transition metals, 2, 18 Tin(1V) complexes carbamic acid, 2,451 hydroxamic acids, 2, 508 Tin flnoridc, 3, 193 Tkn halides, 3,197 bivalent structure, 3,193 Lewis acidity, 3,199 Tin iodide, 3,194 Tin ligands transition metal complexes, 2, 15-18 Tin oxides structure, 3,192,202 Tin phosphatcs, 3,222 Tin(I1) salts in photographic development, 6 , 99 Tin selenide structure, 3,202 Tin sulfate, 3,222 Tin sulfide structure, 3,202 Tin telluride structure, 3,202 Titanium, 3,32>358 coordination numbers, 3,327 discovery, 3,324 isotopes, 3,325,326 oxidation states, 3,327 preparation, 3,324 properties, 3,325 Titanium, alkylin metal alkoxide synthesis, 2,341 Titanium, hexaaquaspectra, 1,249 Titanium, tetrakis(diethyldithiocarbamat0)stereochemistry, 1.94 Titanium, tetrakis(trimethysily1)oxy-, 3.334 Titanium, tetranitratostereochemistry, I , 94 'Titanium, triaquabis(oxalat0)structure, 1,78 Titanium. tris(acety1acetone)structurc. 1,65 Titanium alkoxides oligomeric structure, 2,346 synthesis ammonia, 2,338 Titanium chloride photographic developer, 6,99 Titanium complexes ace tylacetone dinuclear, 2,372 alkyl nitric oxide insertion reactions. 2. I15 alkyl alkoxy reactions, 2,358 alkyl peroxides oxidation catalysts, 6,342 alloy hydrides, 3,353 amides

synthesis, 2, 166 amino acids, 3.342 antimony, 3.345 applications, 6 . 1011-1027 arsenic, 3,345 bromides, 3.357 chlorides? 3.355.356 cupferron, 2.509

1,4-diaza-l.B-butadiene,2,209 fluorides. 3,354 Group IV derivatives, 3, 352 halides, 3.354 clcctron spectra, 3,358 hexamethylphosphoramide, 3,335 +hydrazido(i-), 2,150 hydrazido(2-) mononuclear, 2, 148 in hydrogen production irorn water, 6,508 imines, 2.279 iodides- 3.357 macrocyclic ligands, 3,349 mixed donor ligands, 3,340 sulfur. 3.343 nitrogen ligands low valent, 3>327 oxygen-nitrogen ligands, 3,345 N-phcnylbenzohydroxamic acid, 2, 506 phosphorus, 3.315 phthalocyanines. 2.865; 3,352 polypyi-aznlylhorares, 2, 248 porphyrins, 2,823; 3-349 pseudohalides, 2,228 Schiff bases, 3,340 stereochemistry. 3,327 sulfur ligands anionic ligands. 3.338 neutral donors. 3.338 trifluoromerhanesulfonic acid, 3,335 tritium isotope effects, 3,353 Titanium(I1) coinplexes antimony. 3.336 arsenic, 3:346 phosphorus, 3, 346 Titanium(II1) complexes antimony, 3,347 arsenic, 3,347 charge-transfer spectra, 3,357 magnetic behavior. 1.271 nitrogen ligands. 3.328 magnetic properties, 3,328 octae thylporphyrin reaction with dioxygcn, 2,325 oxygen ligands hidentate. 3.330 elcctronic spectra, 3, 330 monodentate. 3.330 phosphorus, 3.347 porphyrins. 3,349 six-coordinate electronic spectra. 3,331 spectra, 1,250 Titanium(1V) complexes a1koxides, 3,333 antimony, 3,347 arsenic, 3,347 charge-transfer spectra, 3,357 1.3-diketones. 2.376;3;336 nitrogen ligands bidentate, 3,329 monodentatel 3.329 polydentate, 3, 329 oxygen ligands bidentate, 3,335

236

237

Cumulative Subject ludex

monodentate. 3,333 peroxo, 3,350 crystallography, 3, 351 phosphorus, 3,347 triazines monodentate, 2, 196 Titanium dihalide porphyrin complexes, 3,352 Titanium dioxide photography physical developmentl 6: 115 Titanium ethoxides synthesis electrochemistry, 2,337 Titanium oxide in cyclic watcr cleavage hydrogen and oxygen production, 6,524 metal oxide support catalysts, hydrogen production from water, 6,521 Titanium salts catalysts, 3,348 Titanium tetrachloride photoreactivity, 1,406 Titanocene dichloridc dithiolato complexes. 2. 6M pentaselenide dithiolene complexes, 2,607 pentasulfide dithiolene complexes, 2,607 Titanyl complexes, 3, 350 Titrimetry, 1, 552 Tmta -see Acetic acid. trimethylenediaminetetraTollen’s reagent, 5,780 Tolman’s cone angle, 2, 1015 Toluene acetoxylation palladium catalyzed, 6 . 368 Toluene dioxygcnases, 6,708 Tolucnc-3,4-dithiol in gravimetry, 1, 534 metal complexes liquid-liquid extractiun, 1,547 Toners electrophotography, 6, 123 Topochemical reactions, 1.463 Topotactic reactions, I , 163 Torbernite structure, 6,892 Toxicology heavy metals sulfides, 2, 526 Trace elements, 2, 959 illnesses and, 6,773 Trace rnctals protein complexes. 2.974 Tramex, 6,959 Tramex process, 6, 960 Transcription DNA polymerases, 5,1007 Trans effect, 1, 16, 26, 315 metal complexes, 2: 705 palladium(I1) amine complexes, 5 , 1115 platinum complexes. 5 3 5 3 , 4 9 3 six-coordinate compounds. I , 49 Transestcrification mctal alkoxide synthesis, 2, 340 Transferases zinc, 5 , 1002 Transfer chemical potentials solvation metal ions, 2.298 Transferrins, 2, 772; 6, 669

Transmetallation

amino acid sequencc, 6,669 anima1 infections, 6,679 binding to gallium. indium and iron ions, 6, 971 human serum carbohydrates. 6,669 iron, 6- 634.671 coordination environment, 6,669 iron centres, 6,670 iron complexes, 2,975 iron removal, 6,670 receptors, 6, 671 Trans influence tnetal hydrides, 2,705 square planar cornplexcs, 1, 38 Transition mctal complexes alkyl nitric oxide insertion reactions, 2, 115 amides, 2, 163,491 structure. 2, 171 synthesis, 2.165 amine oxides. 2,497 amino oximes, 2.274 biguanide? 2,754 biology, 6. 549 d photoreactions, 1,406 diazenido, 2.13cCl4l dinitrogen, 6,718 dioxygen, 2,315 dithiocarbamates, 2,586 electron transfer, 1,353

f

photoreactions, 1,406 fluorinated rnonothio-P-diketones, 2,649 Group I V metaIs synthesis, 2: 15 guanidine, 2,283 hydrazido, 6,719 hydrides coordination, 2, 69’1 photochemistry, 2, 711 hydroxarnates, 2,505 macrocyclic ligands,. 2, 920 mercury bonds, 2 , l metal-oxygen bond distances, 2,308 methyleneamido, 2. 125 nitrosyl, 2. 101-118 nucleotides, 2,977 pentaftuorides bridging, 2,680 peroxo. 6,320 phosphinimato, 2 , 122 polypyrazolylhoratcs, 2,248 pseudohalidcs: 2,228 sulfur dioxide, 2,634 thioarsinyldithioformates, 2,589 thionitrosyl. 2, 118 thiophosphinoyldithioformates, 2,589 tropolones rearrangement, 2,382 Transition metal ions antibiotin, 6,728 Transition metals arscnic compounds coordinated open-chain, 3,244 basicily borane complexes. 3,101 boron complexes, 3.99 microorganisms transport and storage, 6,680 transport and storage, 6,667-681 Transmetallation

Transmetallation amido complexes synthesis. 2,163 Transplutonium complexes, 3,1215-1220 Transplutonium(I1) complexes, 3, 1215 Transplutonium(II1) complexes, 3, 1215 aliphatic hydroxy acids, 3. 1217 aqua, 3,1215 aromatic hydroxy acids, 3, 1217 carbonates, 3, 1217 halogeno, 3,1218 hydrides, 3,1218 hydroxides, 3, 1216 P-ketoenolates, 3, 1216 monocarboxylates, 3, 1216 oxalates, 3,1217 oxides, 3, 1216 phosphates, 3, 1216 phosphorus oxides, 3,1217 phthalocyanine, 3,1218 selenium ligands, 3,1217 sulfates, 3, 1216 sulfur ligands, 3, 1217 tellurium ligands, 3, 1217 trihalides, 3, 1218 Transplutonium(1V) complexes, 3, 1214 halogeno, 3,1219 P-ketoenolates, 3,1219 oxides, 3,1219 tetrahalides, 3, 1219 Transplutonium(V) complexes, 3,1219 aqua, 3, 1219 carbonates, 3,1220 halogens, 3,1220 rnonocarboxylates, 3, 1220 oxalates, 3, 1220 oxides, 3,1219 Transplutonium(V1) complexes aqua, 3, 1220 carbonates, 3, 1220 carboxylates chelating, 3,1220 halogens, 3,1220 rnonocarboxylates, 3, 1220 nitrato, 3, 1220 oxides, 3,1220 oxoanions, 3, 1220 Transport cations biology, 6,552 copper, 6,671 dioxygen, 6,683 Group IIA ions microbes, 6,569 plants, 6, 572 icon, 6,671 mammals, 6,667 microbial, 6,679 microorganisms, 6,673,675 plants, 6,680 transition metals, 6,672,667-681 microorganisms, 6,680 zinc, 6,672 biology, 6,599 Trialkylamine N-oxide metal complexes, 2,494,497 Triamines cyclic complex formation, 2,911 metal complexes, 2,44 Triangular dodecahedra eight-coordinate compounds, 1,83.84 repulsion energy coefficients, 1-34

Curnulutive Subject Index

238

square antiprisms. cubes and, 1, 84 Triazacyclononanes metal complexes, 2, 82 Triazine, 1,3-diarylcarbonylation catalysts, palladium complexes, 6, 290 Triazines heterobinuclear complexes bridging ligands, 2,202 mctal complexes, 2. XI. 195-206 bonds, 2, 196 bridging ligands. 2, 198.200 chelating ligands, 2,203 insertion reactions, 2, 197 monodentate, 2, 196 NMR, 2, 197 spectroscopy, 2. 196 1,2,4-Triazole. 315-bis(2-pyridyl)complexes, 1, 22 1,2,4-Triazole, 1.4-diphenyl-3,5-endanilo-4,5-dihydrogravimetry. 1,534 Triazoles metal complexes, 2. '76 1,2,3-Triazoles p K , , ,2.77 1,2,4-Triazoles pK,, 2-77 1,2.4-Triazolium-3-t~iols photographic stabilizer, 6, 103 s-Triazolo[l ,S-alpgrimidine metal complexes photographic emulsion stabilizers, 6, 98 Triazolopyrimidine. dirnethylmetal complexes, 2 . 93 Triboluminescence. 1. 396 Tributyl phosphate rare earth complexes, 6, 811 solvent extraction iridium and rhodium, 6, 809 iron, 6: 8'13 niobium and tantalum, 6, 813 platinum group metals, 6, 809 rare earths, 6,811 uranium, 6,810 zirconium and hafnium, 6, 811 thorium complex solvent extraction, 6,810 uranyl nitrate complex solvent extraction. 6, 810 zirconium complex, 6,812 Tricapped trigonal prisms nine-coordinate compounds, 1 ,9 5 repulsion energy coefficients, 1,33,34 Tricarboxylic acids metal complcxcs naturally occurring. 2,962 Tridecametallic complexes, I . 167 Tridodecylamine in uranium ore processing sulfur extraction, 6,900 Trienes reactions osmium tetroxide, 4,590 Triethanolamine alkali metal complexes, 3 ,2 3 'I'riet hylamine N-oxide metal complexes. 2,197 Tricthylamine, 2,2',2"-trimethoxyalkali metal complexes, 3,24 Triglycine cobalt(I1) complexes. 2. 759 copper(1I) complexes, 2*759

239

Cumulative Subject Index

hydro 1y sis copper(I1)-catalyzed, 6,426 metal complexes, 2,764 Trigonal bipyramids five-coordinate compounds. I ? 39 repulsion energy coefficients, 1 33.34 Trigonal prisms repulsion energy coefficients, 1.34 Triisooct ylamine coppcr, cobalt and nickcl complexes separation, 6, 803 in uranium ore processing sulfur extraction, 6, 900 1,3,5-Triketones metal complexes, 2, 399 Trilaurylamine in uranium ore processing sulfur extraction, 6,901 Trimetallic complexes, 1, 132 six multi-atom bridges, 1: 143 six single-atom bridges, 1, 142 three single-atom edge bridges. 1, 142 triple bridges, 1, 143 Trimethylamine N-oxidc metal complexes, 2,497 Trimethylamine oxidase molybdenum cofactor, 6, 663 Trimethylenediamine, N-(2-arninoethyl)metal complexes, 2 , 4 9 Trimethylenediamine, N,.hr,h‘-ethyIidynetrimethylenetrismetal complexes, 2, 58 Trimolybdates, 3, 1032 Trioct ylamine cobalt and nickel complexes separation, 6, 804 in uranium ore processing. 6.907 Tripeptides metal complexes blood plasma, Z1 966 Triphenylmethane dyes metallochromic indicator, 1,556 Triphenyl phosphite rhodium compIexes catalysts, hydroformylation, 6,260 1h5,3k5,5k3-Triphosphabenzene, 1,I,3,3tetrakis(dimethylamino)-4-t-butyltransition metal complexes, 2.1043 2,6,10-Triphosphabicyclo[9,4~ IOIpentadeca-11( 1),12,14triene-2,6,10-triphenyl- 2. 1003 Triphosphates hydrolysis metal complexes, 6 , 447 cyclo-Triphosphates hydrolysis metal catalysis, 6.344 Tripodal ligands nickel complexes, 5 , 131 Tripyridyls metal complexes, 2,91 Trirhombohedra repulsion energy coefficients, 1 - 3 3 ten-coordinate compounds, 1.98

1,3,5-Tris(alkylthia)cyclohexane metal complexes, 2.552 Tris(bipyridy1) cornplcxes structure, 1, 63 Tris(diketonate) complexes structure, I , 65 Trisdithiolencs metal complexes synthesis, 2,597 1,3,5-Triselane

Tungsten

metal complexes, 2,665 Tris( 1 ?lO-phenanthroline) complexes structure, 1,63 Trithiane metal complexes, 2,552 Trithioarsenates, 3,249 1,3,6,2-Trithioarsocane, 2-chloro-, 3, 249 Trithiocarbonic acids bridging ligands; 2,590 metal complexes, 2,646 Trithiocthers mctrrl complexes, 2,551 Trithiulane, bis(imino)inctal complexes, 2 , 591 Trithiomolybdates, 3, 1378 Trithiooxalic acid metal complexes, 2,585 Trivanadates. 3. 1027 Trolite, 4, 1240 Tropolone metal complexes electrophilic substitution, 1,422 ’I’ropolone. bisdithiometal complexes, 2, 608 Tropolones mctal complexes, 2: 397 hydrolysis, 2: 379 Troponin C, 6,575 calcium sites, 6. 575 structure, 6.573 Tryptophan biosynthesis Salmonella typhimurium, 6,582 esters, nickel(I1) complexes hydrolysis, 6.424 Tryptophan 2.3-dioxygcnasc, 6,326,708 Tryspin activation calcium, 6. 593 ‘l’umors imaging techniques radionuclides, 6,969 radiopharmaceuticals. 6,992 ’lungstate, pentachlorothiostereochemistry, 1, 50 Tungstates molybdenum uptake inhibition microorganisms, 6,681 in photogalvanic hydrogen production from water, 6, 532 Tungstates. decachlorooxydi-, 3,990 Tungstates. nonahalodi-, 3,999 Tungstates. thio-. 3, 982 Tungstate X, 3, 1034 Tungsten biology, 6,667 separation from molybdenum, 6,828 sulfurdiimine bidentate, 2, 191 Tungsten, hexahalodi-, 3, 1000 Tungsten, hexahydridotris(diisopropylpheny1phosphine)structure, 2,700 Tungsten, octacyanophotoreactivity, 1.406 sfructure. 1, 84 Tungsten, tetrakis(diethy1dithiocarbamato)stereochemistry, 1,94 Tungsten, tetrakis(ethy1trithiocarbonato)stereochemistry. I , 94 Tungsten, tetramethylbis[ (methylhydrazino)dioxy]structure. 1,89 Tungsten, tricarbonyIdiiodo[methylenebis(diphenylphosphine)]-

Tungsten

Cumulative Subject Index

structurc, 1,78 Tungsten, tris(2,3-dimercapto-2-butenedinitrile)structure, 1,63 Tungsten alkoxides physical properties, 2,346 synthesis, 2,339 Tungsten complexes, 3,973-1015 alkoxy carbonyl reactions, 2, 355 alkyl alkoxy reactions, 2,358 amidcs molecular complcxity, 2, 168 properties, 2, 168 amidines, 2,276 bridging ligands, 2, 198 chelating ligands, 2,203 applications, 6, 1015 carbamic acid, 2,450 paddlewheel structure, 2,451 carboxylic acids, 2,438 114-diaza-1,3-butadiene, 2,209 dichlorodiazwmelhane, 2>146 dimethyl sulfoxide, 2,490 dinitrogen, 3, 1011-1014; 6,718 protonation. 6,718 dioxo, 3,978 hydrido, 3,10141015 hydrwgen sulfide, 2,516 imines, 2,280 nitrosyl, 3, 1014 structure, 2,115 organolead, 2, 16 oxo oxidation catalysts, 6,354 peroxo oxidation, 6,330 phthalocyanines, 2,865 pcilypyrazolylborates, 2,248 porphyrins, 2,825 pseudohalides, 2,229,230 quadruple bonds, 3, 1010 triazines chelating ligands, 2,203 triple bonds, 3, 1002 Tungsten(0) complexes magnetic behavior, 1,273 Tungsten(I1) complexes, 3, 1005 carboxylic acid, 2,441 cyanides synthesis, 2 , 9 hexanuclear clusters, 3, 1011 monomcric, 3, 1005 quadruple bonds, 3, 1008 seven-coordinate, 3, 1007 Tungsten(II1) complexes, 3, 99G1005 dinuclear, 3, 998 mononuclear, 3,998 Tungsten(1V) complexes, 3,988-998 carbon multiple bonds, 3, 997 cyanides, 3,997 synthesis, 2,9 eight-coordinatc complexes, 3, 996 magnetic behavior, 1,272 metal-metal bonds, 3,990 metal-metal douhle bonds, 3, 991 nitrogen multiple bonds, 3, 997 sulfur multiplc bonds, 3, 997 trinuclear clusters, 3,993 Tungsten(V) complexes, 3,98.1-988

magnetic behauior. 1.271 metal-metal bonds, 3,986 oxo. 3,985 selenium, 3,986 sulfur. 3* 986 thiocyanato. 3,985 Tungsten(V1) complexes. 3,974-983 alkylidcnc, 3.981 alkylidync, 3, 981 azohenzene. 3.977 carbon multiplc bunds. 3, Y7Y dioxo. 3.977 dithiolene, 3.983 guanidine, 2.283 hydroxamic acids, 2.506 maleic acid. 2, 475 conformation?2.467 nitrido, 3,980 nitrogen multiple bonds, 3.979 oxo. 3,976 peroxy, 3,977 selenium multiple bonds: 3.979 structure, 3. '180 sulfus multiple bonds. 3.979 tartaric acid. 2.479 NMR, 2.468 trioxo. 3,978 Tungsten halides. 3.974.984,988 synthesis, 3,974 Tungsten hexaalkoxides physical propcrties. 2,347 Tungsten oxide ruthenium oxide support catalysts, hpdrogcn production from water. 6, 523 Tungsten oxyhalides, 3,985, 990 synthesis, 3,975 Tungsten steel, 3. 974 Tungsten tetraalkoxides physical properties, 2, 347 Tungstoarsenates. 3. 1040 12-Tungstoborates. 3, 1041 Tungstomolybdntes, 3, 1036 Tungstophosphatcs. 3, 1038 cryptands, 3, 1019 non-Keggin, 3, 1042 reduced, 3, 1050 Tungstosilicates, 3. 1036 Tunicates-see Sea squirts Tunichrome B-1.3.486 Tunneling electron transfer. 1.345 Turnbull's blue, 1,221, 1206 Twelve-coordinate compounds stereochemistry, 1,99 Tyrosinase, 6: 692. 71 1 coppcr(l1) complexes, 5,724 cytochrome oxidases, 6,683 Tyrosinc minerals prebiotic systems. 6.872 'I'yrtisine fLhydruxglasc copper. 6.553 Tyuyamunite. 6.891

240

Ultraviolet spectroscopy metal in water comple?tes, 2.309 redox potcntials and, I , 4Y8 Ultraviolet-visible spcctroscopy. 1 , 243 Umbellicomplexone metallofluorescent indicator, 1. 558 Undecametallic complexes, 1, I67 Unithiol chelating agent heavy metal poisoning. 6.767 Unsaturated compounds hydrogenation catalysts, r h d i u m complexes, 6 , 241 Uracil bases mctal complexes, 2. 97h photography diffusion transfer process. 6. 1 0 1 Uracil, 5-methylantistain agent, 6. 104 Uranate, octathiocyanatocesium salts structure, 1, 86 structure, 1 , 24 Uranate, pentafluorodioxystereochemistry, 1, 74 Uranate, triacctatodiuxostructure, 1,24 Uraninite leaching, 6 , 7x8 Uranium in borosilicate glass. 6 . 961 determination, 1,548 dissolution reprocessing irradiated nuclear fuel, 6.927 environmental chemistry. 6.461 extraction anion exchange resins. 6 . 820 cation exchange resins, 6,817 in groundwater, ti, 888 hydromctallurgy. 6. 788 leaching, 6,886.R91,897. XYX milling, 6 , 896 minerals precipitation, 6,892 in natural waters, 6. 886 occurrence, 6.886 oxidation states. 6.949 Purex process, 6.95 1 purification, 6. 919 fractional crystallization. 6. 920 recovery from nuclear fuc! waste. 6.960 from ares, 6, 895-9 19 from seawater. ti, Yh2-996 rcscrvcs. 6. 8x9 segregation from thorium geochemistry, 6, S8k-895 separation from plutonium in reprocessing irradiated nuclear fuels, 6, 938 Uranium(1V)

as pIutonium(IV) reductant

Purex process, 6,949 photolytic reduction, 6,949 plutonium(1V) reduction Purex process, 6,949 solubility in natural waters, 6, 887 Uranium, chIoroheptakis(dimethylformamido)salts structure, 1,87 Uranium. chIorohcxakis(trimcthylphosphineoxide)salts structure. I,73 Lranium, dioxypei1tathicicy;inatostereochemistry, 1, 74 Uranium, octathiocyanatostructurc. 1- 84 Uranium, pentaaquadioxystereochemistry, 1,74 Uranium, pentakis(dimethy1 su1foxide)dioxystereochemistry, 1,74 Uranium, pentakis(urea)dioxystereochemistry, 1,74 LJranium, tetrakis(bipyridy1)stereochemistry, 1 , 94 structure, 1, 24 Uranium, tctrakis(dibcnzoy1nicth~ne)stereochemistry, 1, 94 Ilranium, tetrakis(oxa1ato)Ftructure, 1,99 Uranium. tetrakis(phenoxy)his[ethylenebis(dimerhylphospliine)]structure, 1, 89 Uranium. teirathiocyanatobis(octamethy1pyrophosphoramide)srructure. 1 , 89 Uranium. tetrathiocyanatotetrakis[tris(dimethy1amino)phosphine oxidelstructure; 1 . 8 7 Uranium carbide nuclear fuels dissctlutionl 6. 925 Uranium cotnplcxcs, 3, 1131-1215 carbamic acid paddlewheel structure, 2, 451 carbonates. 6, 887, 891 chitin geochemistry. 6,868 groundwaters geochemistry. 6, 852 hgdroxocarbonates, 6,888 organic ore formation, 6,869 organic geological units enrichment, 6, 860 pcat, 6,858 polypyrazolylboratcs, 2, 255 thermodynamics, 6,887 Uranium(1V) complexes cupferron ESR spectra, 2,511

24 1

Uranium(IV) complexes

Cumulative Subject Index

neocupferron ESR spectra, 2,511 tetrakis(cupferr0nato) ESR spectra, 2,511 tetrakis(neocupferronat0) ESR spectra, 2,511 Uranium(V1) complexes dioxoneocupferron. 2,512 liquid-liquid extraction of, 1,541 Uranium dioxide dissolution reprocessing irradiated nuclear fucl, 6,927 for fuel, 6,924 in groundwater dissolution, 6,897 hydration, 6,888 leaching, 6,784 oxidation, 6, 897 Uranium hexaalkoxides physical properties, 2,347 Uranium hexafluoride, 6,924 Uranium tetrafluoride, 6,923 Uranophane structure, 6, 892 Uranothorianite, 6,91 I Uranyl carbonate stability constant, 6,888 Uranyl complexes carbonates in natural waters, 6,889 cupferron, 2,512 formamide, 2,491 glycolic acid, 2,472 hexafluoroacetylacetone, 2,373,377 photochemistry, 2,385 rearrangement, 2,384 humic acid, 6,894 maieic acid conformation, 2,467 neutral 1,3-diketones, 2,402 polyketoncs, 2,399 reduction, 6,892 six-coordinate compounds structure, 1,53 stereochemistry, 1.74 Uranyl compounds uranium leaching, 6,788

Uranyl ions photoreactivity, 1,408 precipitation by vanadates, 6, 891 Uranyl nitrate ion exchange and absorption, 6,898 Uranyl oxalate solid state structure, 6, 919 in uranium purification. 6,919 Uranyl peroxide solid state structure, 6.920 in uranium purification. 6, 920 Uranyl phosphate in natural waters, 6,889 Uranyl sulfate formation thermodynamics, 6,898 structure, 6,898 Urea complexes linkage isomers, 1, 186 hydrolysis metal catalysis, 6,470 metal complexes, 2,285 synthesis hy carbonylation, 6,277 Urea, N-(2-pyridylmethyl)hydrolysis catalysis, 6 , 470 Urea, thiometal complexes. 5 978 Urease mechanism, 6: 470 nickel, 6,643 Uric acid metal complexes minerals, 6.849 Uricitc structure, 6,849 Uroporphyrin I, 2,982 Uroporphyrin Ill, 2,982 Urothione oxomolybdoenzymes and, 3, 1438 Urylene metal complexes, 2,285 Uteroferrin, 6, 669 iron, 6,634,636

242

Valence shell electron pair repulsion theory, 1,32-39 effective bond lcnath ratios. 1. 34 halogenium species, 3, 312 noble gas compounds. 3.312 repulsion energy coefficient 1 33 Valency structure and, 1 , 5 Valeric acid metal complexes geochemistry, 6,867 Valine ethyl ester hydrolysis, metal catalysis. 6.421 Valinomycin alkali metal comp1exe.i. 3,3,62 cation transport, 6 , 553 metal complexes, 2,969 selective binding, 6,552 potassium complexes, 3.60 selective ion electrode. 1.559 synthetic analogues, 3, 65 Vanadate, ammineoxybis(dioxygen)ammonium salt structure, 1.61 Vanadate, dioxybis(oxamato)bond-length ratios, 1 , 5 7 Vanadate, heptacyanopotassium salt structure, 1, 72 Vanadate, hexafluorodipotassium salt history, 1.21 potassium salt history, 1,21 tripotassium salt history, 1 , 2 1 Vanadate, pentachlorostereochemistry, 1,40 Vanadatc, pcntafluorooxystereochemistry, 1. 50 Vanadates hiochemistry, 3,456 calciumimagnesium ATPase inhibition, 6. 567 competition with phosphates physiology, 6,665 protonation, 3, 1026 sodium pump, 6,557 in uranium purification from ore, 6,899 Vanadates, hexafluoro-, 3.482.531 Vanadates, oxoperoxo-, 3,501 Vanadates, pentacarbonyl-, 3, 457 Vanadium biology, 6,665 determination, 1.548 extraction in uranium ore processing. 6 , 909 oxidizingireducing properties. 3,453 sea squirts, 6,666 transport, 6,672 Vanadium, hexaaqua-

.

electron transfer, 1, 367,369 Vanadium, hexacarbonylexchange reactions, I , 288 Vanadium, hexacarbonyl[ (tripheny1phosphine)goldlstructure, 1 , 7 3 Vanadium, oxybis(acety1acetone)structure, 1,47 Vanadium. oxybis(diethy1dithiocarbamato)structure. 1,47 Vanadium. oxybis[oxybis(dioxygen)ammonium salt structure 1, 6 I Vanadium. oxytris(diethy1dithiocarbamato)structure, 1,83 Vanadium, tetrakis(dithiobcnzoato)stereochemistry, 1,94 Vanadium, trichlorobis(trimethy1amine)structure, 1,45 Vanadium, tris(diethy1dithiocarbamato)oxystereochemistry, 1, 82 Vanadium, tris(2.3-dimercapto-2-butenedinitrile)structure, 1- 63 Vanadium, tris(dithiodibenzoy1)structure, 1,63 Vanadium, tris( l,l0-phenanthroline) redox indicator, 1,559 Vanadium complexes, 3,45>569 acetylace tone exchange reactions, 2,380 alkyl peroxides oxidation catalysts, 6,341,342 applications, 6, 1013 biochemistry, 3,455 1,2-bis(dimethylphosphino)ethane,3,460 1,4-diaza-l,3-butadiene, 2,209 dioxygen mononuclear, 2,321 humic and fulvic acids, 6,860 hydrazido(2-), 2, 148 hydroxarnic acids, 2.506 low oxidation states, 3,457 hipyridyl, 3,457 cyanides, 3.457 dinitrogen, 3,459 diselenolene, 3,460 dithiolene, 3,460 hydrido, 3,462 nitrosyl, 3,458 o-phenanthroline, 3,457 phosphorus ligands, 3,460 terpyridyl, 3,457 mixed IV/V valence, 3,510 oxidation state. 3,454 peat. 6,858 peroxo oxidation, 6,333 photoreactivity, 1,406 phthalocyanines, 2,865 polypyrazolylborates, 2,248 porphyrins, 2,824 dioxygen adducts, 2,325 ~

243

Vanadium complexes pseudohalides, 2,229 trifluorophosphine, 3,460 Vanadium(0) complexes magnetic behavior, 1,272 Vanadium(1) complexes magnetic behavior, 1,272 Vanadium(I1) complexes, 3,462 acetonitrile, 3,464 alcohols, 3,466 amines, 3,463 ammonia, 3,463 hcnzimidazole, 3,463 bipyridyl, 3,464 bromide, 3,467 carbonates, 3,467 chloride, 3,467 cyanides, 3,462 p-diketones, 3,466 dimethylimidazole, 3,463 ethers, 3,466 fluoride, 3,467 guanidine, 2,283 halides, 3,467 imidazole, 3,463 iodide, 3,467 isocyanides, 3,462 isoquinoline, 3,463 isothiocyanates, 3,464 macrocyclic ligands, 3,469 magnetic behavior, 1,272 I-methylimidazole, 3,463 2-methylimidazole, 3,463 oxalates, 3,467 oxygen ligands, 3,465 phenanthroline, 3,464 phosphines, 3,465 &picoline, 3,464 y-picoline, 3,464 polypyrazolylborate, 3,463 polypyrazolyl ligands, 3.463 poly( 1-pyrazoiyl)methane ligands: 3, 463 porphyrins, 3,469 pyrazole, 3,463 pyridine. 3,463 reducing agents, 3,469 spectra, 1,252 terpyridyl, 3,464 tris( 1-pyrazolylethyl)amines, 3.463 water, 3,465 Vanadium(II1) complexes, 3,473 adenine, 3,475 alcohols, 3,478 amides, 3,474,480 amines, 3,474 amino acids, 3,484 ammonia, 3.474 aqua, 3,477 arsines, 3,476 azide, 3,47S bipyridyl, 3.475 bromides, 3,483 carboxylates, 3,479 catecholates, 3,478 chlorides, 3,482 complexones, 3,485 cyanides, 3,474,476 dimethyl sulfoxide, 3,480 dioxygen, 3,478 dithiocarbamates, 3,481 dithiolates, 3,481 dithiophosphinates. 3,481 ethers, 3,478 ethylenediaminetetraacetic acid, 3.185

Cumulative Subject lndex guanine, 3,475 halides, 3,482 hydroxy acids, 3,48Q isocyanides, 3,474 p-ketoenolates, 3,478 magnetic behavior. 1.271 mixed donor atom ligands, 3,483 nitrilotriacetic acid. 3,485 oxosnions, 3,479 oxygen ligands, 3,477 phenanrhroline. 3,475 phosphates, 3,476 phosphinatcs. 3,479 phosphincs, 3.476 phosphonates, 3,479 purine, 3,475 pyridine, 3, 475 Schiff bases, 3.483 sea squirts. 3.486 seleninates. 3,479 selenocyanates. 3.475 silazanes. 3.476 spectra 1,251 sulfates, 3,479 sulfinatcs, 3,4779 sulfur ligands, 3.481 thiocyanates, 3,475 thioetliersl 3, 481 Vanadium(1V) complexes, 3,487 acetates, 3,513 acetylacetonates. 3,504 electrochemistry. 3.505 ESR spectra, 3.505 adenine, 3,568 adipates. 3,516 alcohols, 3,502 amines, 3,489 amino acids. 3,544 : equilibria. 3,544 ammonia. 3,489 arsenates. 3: 513 arsenic ligands. 3,496 arsines, 3,498 ascorbic acid, 3,502 benzilato. 3.522 biguanide. 3.496 binucleating ligands. 3,561 bipyridyl, 3,492.494 bromides, 3:530 butanedjaminetetraacetate, 3,548 carbazolc, 3,492 carbonato, 3.515 carboxylatcs, 3.513 carnosine, 3,547 catecholates. 3.502 chlorides, 3,530,531 chlorophyll. 3>557 citrates. 3.522 compartmental ligands, 3,561 complexones. 3,547 cyanides, 3,489,496 cysteine, 3,546 deoxophylloerythroetioporphyrin, 3,557

N,N-dialkyf-2-aminoethanethiol, 3,554 dicyclohexylphosphide, 3,498 diethylenetriaminepentaacetic acid, 3,548

4,6-dihydruxycoumaran-3-one, 3,510 p-diketunatcs, 3,504 solvent effects, 3.505 3.7-dimethyl-7-hydroxyoctan- I-al, 3,S IO 2.6-dimethylpyrazine, 3, 492 dithioarsinate. 3,527 dithiocarbamates. 3.524.526

244

245

Cumulative Subject Index

spectra, 3, 524 structure, 3,524 dithiocarboxylates, 3.524 dithiolates, 3,528 dithiophosphates. 3. 527 dithiophosphinates, 3,521 ENDOR, 3,489 ESR spectroscopy, 3,488 ethylenediaminetetraacetic acid, 3,548 fluorides, 3, 529 formates, 3,513 fulvic acid, 3. 568 glutaratcs, 3, 5'1.6 glycine, 3, 546 Group IV ligands, 3.389 guanine, 3,568 halogen ligands, 3,529 halogenoacetates, 3,513 heteropolynuclear. 3.565 histidine, 3,494.547 humic acid, 3,568 hydrazine, 3,494 hydrolysis, 3, 489 hydroxyaldehydato, 3,510 hydroxycarboxvlatcs, 3.517 !-hydroxycyclohexanecarboxylate, 3,522 hydroxyketonatci. 3, 510 2-hydruxy-O-methylpyri~ine,3, 523 (3-hydroxynaphthaldehydc.3, 510 hydroxyoximes, 3,552 3-hydroxyquinazoline-4(3H)-rhiones: 3,554 8-hydroxyquinoline, 3,551 imidazole, 3,494,547 iodides, 3,531 lactates, 3,520 lutidinato, 3, 551 magnetic behavior, 1.271 malates, 3,522 maleates, 3, 516 malonatcs, 3, 516 mandelatcs, 3,522 8-mercaptoquirioline, 3- 553 mcthanol, 3, 502 2-mcthyl-8-quinolinoI, 3,552 mixed donor a tom ligands. 3,53 1 553,555 naturally occurring ligands. 3.567 N heterocycles, 3.492 stoichiometry, 3,492 nitrates, 3, 513 nitrilotriacetic acid. 3. 548 nitrogen ligands, 3,489 N macrocycles, 3,557 nucleotides, 3<561: oxalates, 3, S l h N-oxides, 3,522 f'-oxides, 3. 522 oxo aqueous solutions. 3,498 bonds, 3,488 oxo, porphyrins evolution, 2,961 oxoanions, 3,511 oxygen ligands, 3.498 perchlorates, 3, 513 perfluoropicanolate. 3.523 phenanthroline. 3.494 l-phenyl-l,3-butanediona1u, 3, SO4 phosphates, 3, 512 phosphines, 3.496 [(phosphononomethyl)imino]diacetic acid, 3,55 I phosphorus ligands. 3.496 phosphotungstates, 3,513 phthalocyanines, 3,559 I

COC 7-1

Van VIeck equation

polycarboxylates, 3,515 polynuclear, 3,561 porphyrins, 3,557 structure. 3$557 proteins, 3,567 ENDOR, 3,561 ESR spectra, 3, 567 purine, 3,568 pyrazine? 3.492 pyridinc, 3. 492,494 pyridinecarboxylic acid, 3,551 [ 1-(2-pyridyl)et.hyl]iminodiaceticacid, 3, 548 [ t-('-pyridyl)~nethyl]iminodiacetic acid, 3,548 pyrrole, 3, 992 salicylaldehydato, 3 , 510 salicylates, 3.520 Schiff bases. 3,531 bidentate. 3.536 (3-diketone diamines, 3,535 polydentate, 3,544 salicylaldehyde diamines, 3,531 tridentate, 3,538 selenates. 3,513 selenides, 3,529 selcnitcs, 3,513 selenium ligands, 3.529 selenupurphyrins, 3,559 spectra, 1,251; 3,488 structure, 3, 487 succinates? 3.516 sulfates, 3, 511 sulfides. 3. 529 sulfites. 3, 513 5-sidfosalicylatesl 3,520 sulfoxides. 3,522 sulfur ligands, 3. 523 tartaric acid, 2,479 tartrates, 3.517 tctraaza[14]annulenes, 3,559 iV.NIN'.N'-tetramethylurca, 3, 523 tetrasulfur tetranitrides, 3,554 thio. 3. 523 clcctrochcmistry, 3,524 IR spectra, 3,523 stability, 3, 523 structure. 3, 523 thiocarbohydrazones, 3,553 thiocyanates, 3,495 thio-ft-diketones, 3,554 thiophene, 3,529 triethylenetetraminehexaacetic acid, 3, 547 tropolone. 3,510 xanthates, 3,527 Vanadium(V) complexes cup f t r r on IRspectra, 2, 511 Vanadium tctramcthoxidc spcctroscopy, 2,347 Vanadyl acetylacetonate, 2, 388 hydrolysis, 2,379 Vanadyl complexes cupferron diamagnetism. 2,511 hexafluoroacety lacetone nitroxide complexes, 2,388 Vanadyl ions hydrolysis. 3.499 oxidation. 3,501 rate of exchange, 3,498 rcdox behavior, 3,501 Vanadyl porphyrins, 3,558 Vanadyl uroporphyrin I, 3,558 Van Vleck equation, 1,260

Vaska’s compound

Cumulative Subject Index

Vaska’s compound, 6,247 history, 1,21 reactions with hydrochloric acid, 1,515 Vauquelin’s salt -see Palladium, tetraammine-, tetrachloropalladate Versatic 10 acid metaI extraction, 6, 790 solvent extraction copper, 6,791 indium and gallium, 6, 791 lanthanides, 6, 791 nickel and cobalt, 6,791 Vesicles in water cleavagc, 6,528 Vezes’s red salt, 2,303 Vibrational spectroscopy cadmium complexes, 5,929 metal ion water complexes, 2,309 zinc complexes, 5,929 Vibrational trapping electron transfer intramolecular, 1,337,353 Vicinal elements, 1, 198 Vilsmeier reactions amino acid metal complexes, I, 425 Vinyl acetate manufacture, 6,330 oxidative coupling palladium catalysts, 6,371 synthesis from ethylene, 6,365 Vinyl halides reactions catalysts, 6, 306 Violeo tetraammines geometric isomerism, 1. 12 Viologen chemically modified in photochemical hydrogen production horn water. 6, 502-SO6 polymers in photochemical hydrogen production from watcr, 6, 505 vesicles in water cleavage, 6,529

246

Viologen, tetradecamethylin photochemical hvdrogen production from water. 6* 502

Vismirnovite structure. 6,849 Vitamin A zinc and, 6,774 Vitamin B1 metal complexes, 5,980 Vitamin BIZ.2, 887,983; 6,637 cobalt(II1) complcxcs geochemistry. 6: 86s cobalt deficiency, 6,766 coenzymes, A, 637 formation kinetic template reactions, 1,452 metal cornpiexes geochemistry, 6.868 model compounds, 6,194,637 synthesis, 6,200 Vitamin B,* coenzymes terminal hydrides, 2.692 Vitamin C iron availability and, 6,773 Vitainin D calcium-binding proteins, 6,576 calcium uptake, 6, 596 Vitamin E selenium and. 6,774 Vitamins interactions with elements and drugs, 6,773 metal complexes, 6,773 Volan electrode modification, 6 ,2 3 Volcanoes metal complexes, 6,854 Volon chromium complexes, 1,22 Volume of activatim pentaamrnine rhodium(III), 4,9S8 Volzi te structure, 6,849 Vulcanization diene rubbers metal-accelerated, 2, 802

Wacker process, 5,717; 6.327,364 Walsh diagram iron(I1) porphyrin dioxygen adducts. 2,317 Water bridging ligands, 2, 298 cleavage metal complex catalysts, 6,495 metal salt catalysts. 6.493 molecular assemblies, 6,525530 decomposition coordination complexes, 6,487-534 electrochemical production of hydrogen or oxygen coordination complex catalysts, 6, 532 hydrogen production from thermodynamics, 6,489 metal complexes, 2,295-310 pki,2,310 properties, 2,305 stability, 2,297 photocatalytic decomposition metal phthalocyanine complexes, 5,995 photochemical decomposition intermolecular electron transfer reactions, 6,498-530 photoelectrochemical decomposition, 6,530 reduction vanadium(I1) complexes, 3.471 solvent electrochemistry. I . 47') Water-gas shift reaction, 5,421; 6,269 catalysis iridium complexes, 4, 1164: 6.278 platinum complexes, 6,292

rhodium complexes, 6,275 Water of crystallization, 2,297 Water softening, 6,814 Weak-acid resins ion exchange, 6,815 Weat hering minerals, 6.868 Weathering agents humic and fulvic acids, 6,861 Weberite structure. 6, 846 Weddellite structure. 6,849,849-854 Weiss field, 1.258 Weloganite structure. 6,848 Werner's coordination theory, 1,6 Whewellite structure. 6,849 Wickmanite structure, 6,849 Wilkinson's catalyst, 6,239 Wilson's disease, 5,721 copper, 6 , 6 4 8 removal, 6.169 copper complexes, 2,959 copper metabolism, 6,766 radiopharmaceutical agents, 6,968 Wolfram's red salt, 5,427 Wurzite structure, 6,849 Wyckoff, Ralph W. G., 1, 16

247

X-206,5, 838 X-537A, 5,838 X-573A metal cation transport, 6 , 5 5 4 Xanthates collectors mineral processing, 6. 781 Xanthic acid metal complexes, 2, 588 Xanthine dehydrogenase molybdenum, 6,658 Xanthine oxidase, 3, 1334 mcchanism, 6,662 molybdenum, 6,658 rnolybdcnum complex center. 3.140S structure, 3, 1438; 6,659 Xanthoammines structure, 1, X Xanthocobalt -see Cobalt, nitropentaamrnineXenates. octafluoro-, 3, 315 Xenon platinum complexes, 5,491 Xenon, pentafluorolone electron pair structure, 1, SO Xenon, trifluorostructure, 1 , 4 5 Xenon anions XCFV-, 3,316 XCF,’ , 3 , 3 1 5 , 3 1 6 Xenon cations fluoride, 3,313 XSFS‘, 3,314 XeF,+, 3,315 Xe2FII+,3,315 Xenon complexes FXeN(SO,F),, 3,319 nitrogen ligands, 3,319

oxygen ligands, 3,319 Xenon(1I) complexes difluorides. 3.313 [(FeXO),SOF]-. 3,320 FXeOSO’F. 3,320 nitrogen ligands, 3.312 Xe(OTeF&, 3.320 Xenon(1V) complexes six-coordinate compounds structure, 1 , 5 3 Xe(OTeF,),. 3.320 Xcnon(V1) complexes Xe(OTeF&. 3,320 Xenon hexafluoride, 3,315 geometry, 1.37 monomer, 3,315 stereochemistry, 1,74 Xenon hexafluorobismuthmate, trifluorofluorine bridging. 3,313 Xenon pentatluorotellurate, 3,320 Xenon tetrafluoride, 3,315 X-ray diffraction aqueous solution, 2,307 cadmium complexes, 5,929 cobalt ammines. 1 , 13 cone angles estimation. 2, 1022 configuration. 1,16 crystal structure. I , 15 hydrates

metal-oxygen bond distances, 2,307 water-metal complexes, 2,296 zinc complexes, 5,929 Xylenol orange metallochromic indicator, 1,557 Xylenyl orange metal complexes, 2,789

248

Yeast alcohol dehydrogenase, 5 . 1009 cobalt-containing, 5 , 1013 manganese-containing, 5,1014 Yeast enolase activation magnesium ions, 6,584 Yellowcake in uranium ore processing, 6,898,900 Yohimbane, hexadehydrosynthesis by carbonylation, 6,285 Ytterbium, aquatris(acety1acetone)stereochemistry, 1,&1 Ytterbium, trinitratotris(dimethy1 sulfoxide)structure, 1.97 Ytterbium, trk( acetylacetone)(4-amino-3-penten-2-one)stereochemistry, 1,81 Ytterbium complexes acetylacetone, 2.373 dipositive oxidation state hydrated ions, 3,1109 polypyrazolylborates. 2,255 Ytterbium(II1) complexes ethyl glycinate, diacetate

hydrolysis. 6,422 Yttrium isopropoxtdc synthcsis elcctrochemistry, 2,337 Purex process. 6,941 reactions with 2-propanol, 2,337 Yttrtum-90 serum labelling. 6,996 Yttrium. aquatris(benzoy1acetone)stereochemistry, 1,81 Yttrium. octaaquasalts structure, I, 84 Yttrium. triaquatrinitratostructurc, 1,97 Yttrium complexes, 3, 1059 ace tylacetone ligand exchange reactions, 2,381 applications, 6,1024 phthalocyanines, 2,864 porphyrins. 2,822 Yttrium( 111) complexes pyridine oxide. 2,495

249

~

Zearalenone synthesis catalysts, palladium complexes, 6.282 Zeise's salt. 5,353,403 history, 1,3 Zellerite structure, 6, 848 Zeolites. 3, 113 ruthenium oxide support catalysts, hydrogen production from water, 6,523 Zhemchuznikovite structure, 6,849 Ziegler-Natta catalysis, 3, 358 Zinc, 5,925-1022 absorption radiopharmaceutical agents, 6,968 binding to metallothioneins, 6,673 biochemistry, 6,598-613 deficiency metal complexes, 6,764 detection l-(2-hydroxy-5-sulfophenyl)-3-phenyi-5-( 2carboxyphenyl) formazan, 6.83 electroplating, 6,5, 12 extraction cation exchange resins, 6,817 in gold precipitation, 6, 829 masking, I , 538 rnetalloenzymes, 5, 1001, '1002 biomimetic modelling, 5 , 102'1 X-ray crystallography, 5, 1002 zinc-carbonyl mechanisml 5,1003 zinc-hydroxide mechanism. 5,1003 storage, 6,667-681 metallothioneins, 6,672 tetrameric alkyl alkoxides, 1, 1.53 tolerance Agrostis tenuis, 2,963 transport, 6,667-681 biology, 6,599 vitamin A metabolism and, 6,774 Zinc, alkylalkoxysynthesis, 2,340 Zinc, alkylphenoxysynthesis, 2,340 Zinc, his(thiocarbamato)in electrochemical production of hydrogen or oxygen from water, 6,532 Zinc, chlorohexadecakis(pheny1thio)octakis-, 1 137 Zinc, dialkyloxidation, 2,342 Zinc, dicyanosolid state oligomerization, 1, 187 Zinc, (tetrasulfur)hexadecakis(phenylthio)decakis-, 1 , 137 Zinc blende brines, 6,853 humic acids, 6,861 Zinc complexes acetate, 5,969 acetylacetone, 2,372 alcohols, 5, 964 I

250

~

~~~~~

amides, 5,944 amidines bridging ligands. 2,201 amine oxides, 5.964 amines, 5,933 amino acids, 5. 938 1,4-aminobutyne-2-tetraacetate,5,946

4-[(2-aminoerhyI)amino]-l-butylamine, 5,936 ammonia, 5,931 aniline, 5,933 applications, 6. 1024 azides: 5,931 azo compounds, 5, Y48 biology, 5,1001; 6; 549

1,4-bis~bis(Z-arninoethyl)aminomethyl~benzene hexahydrochloride, 5,936 bis(diethylenetriamine), 5,936 11,1I-bis( dirnethylamino)-3,6,9-trimethyl-3,6,9triazaundecane. 5,938 carboxylates, 5, 968 corrins, 2,885 cyclic amines, 5,990 cyclic ethers. 5.990 cyclic triamines. 5, 936 1,2-~ran.~-cyc~ohexylenedinitrilotetraacetic acid 5, 947 1,4-diaza-113-butadienel 2,211 1 ,5-diazacyclooctane-N,N'-diacetic acid, 5,937 5,12-diethyl-1,4 A, 1l-tetraazacyclotetradeca-4,ll-diene, 5,935 diketones, 5,967 1,3-diketoncs bond lengths, 2,387 neutral, 2, 402 5,12-dimethyl-1,4,8,ll-tetraazacyclotetradeca-4,11diene, 5,935 dithiolene catalysts. water cleavage, 6,495-498 1,Zethanediarnine, 5,933 1,2-ethanediamine-N,N'-diaceticacid, 5,946 ethers, 5, 964 ethylenebis[N,N'-(2,6-dicarboxy)piperidine],5, 936 EXAFS, 5,929 fluorosulfato. 5.964 fulvic and humic acids, 6, X60 glyoxalbis(N-r-but4.lamine),5,938 guanidinium, 2,283 hydrazides, 5. 946 hydrazines, 5,931 hydrazones: 5>940 hydroxides, SI 960 hydroxylamine, 5,931 imides, 5.944 iminodiacetic acid, 5,946 insulin, 5,999 ketones, 5,964 kinetics, 5,996 macrocyclic, 5,690 in medicine? 5 W9 multinuclear, 5. 988 nitrato, 5,962 nitrito, 5,962 ~

25 1

Cumulative Subject Index

NMR, 5,926 NQR, 5,926 organosulfur oxides. 5,964 p-oxalato-bis[di(3-aminopropyl)amine],5,935 oximes, 5, 940 oxygen ligands, 5.960 phosphinates, 5,962 phosphine oxides, 5,964 phosphine selenides, 5,980 phosphine sulfides, 5,980 phosphorus ligands, 5,959 photoelectron spcctroscopy, 5,929 phthalocyanines, 2.868 polynuclear, 5,973 porphyrins, 2,842 catalysts, water cleavage, 6.499 vesicles, water cleavage. 6.529 1,2-propanediamine95,935 1,3-propanediamine, 5,935 proteins, 2,773 pseudohalides, 2,235 pyridine oxide, 2,4% reactivity, 5,996 salicylaldimine, 5,942 salicylic acid crystal structurt', 2+481 selenium heterocyclcs, 5,980 sulfinato, 5,964 sulfur heterocycles, 5,980 sulfur ligands, 5,972 tetramethylcyclam, 5,937 tetramethyltetrazene. 5,948 meso-tetraphenylporphyrins in photoproduction of hydrogen from water, 6,511 thioacids, 5,976 thioamides, 5,976 thioethers, 5,972 thiols, 5,972 1,3,5-~is,ci.~-triaminocyclohexane, 5 , 935 1,4,7-triazacyclnnonane, 5,935 triazines bridging ligands, 2,201 l,l,l-tris(aminomethyI)ethanel 5.936 vibrational spectroscopy, 5 , 929 water, 5,960 X-ray diffraction, 5,929 Zinc(1) complexes, 5,989 Zinc(I1) complexes acetylacetone, 2,371 albumin, 2,975 0-amino imines, 6 , 165 ATP, 2,977 croconic acid, 2,455 glycolic acid, 2.472 lactic acid, 2 , 473 maleic acid, 2,475,476 conformation, 2,467 tetra(N-methy1pyridinium)porphyrinatoin photoproduction of hydrogen from water, 6,511 tetra(4-sulfonatop heny1)porphyrinatoin photoproduction of hydrogen from water, 6,511 Zinc compounds industrial uses. 5,998 Zinc deficiency Euglena gracilis, 6,584 humans, 6,599 Zinc enolates, 6. 217 Zinc halides, 5, 981 molten state coordination, 5,981 solution chemistry. 5.893 Zinc hydrides, 5,931 Zinc naphthalocyanine

Zirconium complexes

preparation, 5,993 Zincon metallochromic indicator, 1,557 Zinc oxinate gravimetry, 1,529 Zinc proteins models, 2, 85 Zinc pseudohalides, 5,981 solid state, 5,985 Zirconate. octafluorosalts structure*1,86 Zirconate, tctrakis(oxa1ato)stereochemistry, 1,94 Zirconates, bromo-, 3.430 Zirconates, chloro-, 3,430 Zirconates, Ruoro-, 3,423 alkali metal salts, 3,425 alkylammoniurn salts, 3, 427 divalent metal salts, 3, 427 guanidinium salts, 3,427 hydrazinium salts, 3,427 vibrational spectra, 3,429 Zirconates. iodo-, 3,430 Zirconate salts tris(tetraphcnyldisi1oxancdiolato) structure, 3,418 Zirconium breeder reactor fuels reprocessing, 6,954 decontamination from fission products Purex process, 6,953 gravimetry, 1.532 nuclear fuel reprocessing Purex process, 6,954 Purex process, 6,943 Thorex process, 6,957 Zirconium, alkylin metal alkoxide synthesis, 2,341 Zirconium, his(bipyridine)tetrathiocyanatostructure, 1,8Y Zirconium, chlorotris(accty1acctonc)stereochemistry, 1, 82 Zirconium, octafluorostructure, 1,84 Zirconium, tetrakis(acety1acetonate)stereochemistry, 1, 32,94 Zirconium, tris(phenylenedithi0)structure, 1, 63 Zirconium alkoxides oligomeric structure, 2,346 Zirconium chloride separation from hafnium chloride, 6, 812 (ZrC1),, structure, 1 27 Zr6ClI2 structure. 1.27 Zirconium complexes, 3,363-440 acetylacetone, 2,372,377 ligand exchange reactions, 2,381 rearrangement, 2.383 alkyl nitric oxide insertion reactions, 2, 115 alkyl alkoxy reactions. 2,358 applications. 6, 1012 binuclear, 2,323 coordination geometries, 3,364 cupferron, 2,512 imides bridging ligands, 2, 176 oxidation states, 3,364 peroxo

Zirconium complexes

Cumulative Subject Index

phthalocyanines, 2,865 polypyrazolylborates, 2, 248 porphyrins, 2, 823 pseudohalides, 2,228 tetrakis chelate stereochemistry, 3,364 Zirconium(0) complexes, 3,364 2,2'-bipyridyl, 3,366 cyanides, 3,364 Group IV ligands, 3,364 nitrogen ligands, 3,366 tris(1 ;IO-phenanthroline), 3. 3 M j Zirconium(II1) complexes, 3,361~370 acetonitrilc, 3,366 ammines, 3,366 aqua, 3,370 arsenic ligands, 3,369 2,2'-bipyridyl, 3,366 1,2-bis(dimethylarsino)-3,3,4,4-tetrafluorocyclobutene, 3,369 halogen ligands, 3,370 2,4-lutidine, 3,369 3,5-lutidine, 3,369 nitrogen ligands, 3,366 oxygen ligands, 3,370 l,l0-phenanthroline, 3, 366 phosphines, 3,369 dissociation, 3,369 structure, 3,369 phosphorus ligands, 3,369 pyridine, 3,366 X-ray structure, 3,364 Zirconium(1V) complexes, 3, 3 7 W M 2-acetylpyridine, 3,373 acylamido, 3,375 4-acyl-3-methyl-l-phenyl-2-pyrazol-5-one3 3,401 aldehydes, 3,403 aldimines, 3,434 alim5n red S, 3,403 alkoxides, 3, 389 bimetallic, 3,392 degree of association, 3.389 reactions, 3,390 reactions with isocyanates, 3.391 S-a1kyldithiocarbazates Schiff bases, 3,434 alkyl thioglycolates, 3,439 amides, 3,414 amines, 3,371 amino acids, 3,410 aminopolycarboxylates, 3,436 ammines, 3,371 aqueous solution NMR, 3,384 polynuclear, 3,384 Raman spectra, 3,384 arsenic ligands, 3.383 arsines, 3, 383 N-arylnaphthylaldirnines, 3,438 aryloxides, 3,389 N-arylsalicylaldimines, 3,437.438 azides, 3,379 azines, 3,434 benzoquinolines, 3,372 2,2'-bipyridyl, 3,372,374 bis(amido)silane, 3, 375 bis(benzenese1eninato)oxo. 3.418 bis(diketonates), 3,400 bis(trimethylsilylaniido), 3, 375 NMR, 3,377 spectroscopy, 3,377 X-ray structure, 3,377 carbamates, 3,410

carbonares, 3,110 carboxylates, 3,409 catecholates, 3. 403 chlorooxo, 3: 386 citric acid, 3: 412 cupferron, 3,417 cyanates, 3,379 cyanides! 3,370 cyanogen iodide. 3,381 cyanogen selenide, 3,381 cyanogcn sulfidc, 3,381 3-cyanopyridine, 3,373 diacyl hydrazines. 3.436 dialkylamido, 3,375 photoelectron spectra, 3, 375 reactions, 3,375 diamines, 3,372 dichlorooxo anhydrous IR spectra. 3.386 dichlorophosphates, 3: 407 diethanolamine. 3,437 diethyldithiophosphate, 3,421 diethylenetriaminepentaacetate,3, 436 N,N-dicthylhydroxylamido,3,438 2,6-dipicolinoyl dihydrazine, 3,440 dithiociirbarnates. 3,419 dithiolenes. 3. 420 esters. 3.403 ethanolamine, 3.437 cthcrs, 3,403 ethyl acetoacetato, 3,402 ethylenediaminetetraacetate. 3, 436 N-ethylsalicylaldiminato, 3,438 fluorosulfates, 3.407 glycolic acids, 3.412 glycoxides, 3,391 Group 1V ligands. 3>370 halogenoids, 3,351 hydrazine, 3. 374 hydrides, 3,432 hydrohoratcs, 3. 132 hydroperoxo. 3,387 hydroxamates, 3.417 hydroxide, 3,384 hydroxy acids aliphatic, 3. 412 aromatic, 3,412 hydroxyalkylaminesl 3.434 imidazoles. 3: 372. 377 indazoles, 3,372 interhalogen-halogenoids, 3. 38 1 interhalogenoids, 3,381 isopropoxides Lewis base adducts. 3, 391 NMR. 3,389 ketamines, 3 - 434 fi-ketoenolates. 3,392 ketones. 3,4U3 lactic acid, 3. 412 2,4-lutidine, 3: 372 2,64utidine, 3?372 3.5-lutidine, 3.372 malic acid, 3.412 mandelic acid. 3.413 mercaptoalkylamines, 3, 434 o-mercaptophenulato, 3, 421 3-methoxysalicylaldehydato, 3,402 N-methylaminoalkoxides. 3. 39 1 methyl isorhioqmatc. 3-43!) molybdates, 3: 108 monti(diketonares), 3.401 monothiocarbamares, 3.419 N heterocycIic ligands. 3- 372

252

253

Cumulative Subject Index

IR spectra, 3,372 oxo, 3,374 nicotinamide, 3, 373 nitrates, 3,406 nitriles, 3,382 IR spectra, 3, 382 Raman spectra, 3,382 nitrilotriacetate, 3,436 nitrogen ligands, 3,371 nitro ligands, 3,374 octaethylporphyrin, 3,439 oxalates, 3,411 oxides, 3,384 N-oxides. 3,414 P-oxides, 3.414 oxoanions, 3,406 oxycyanogcn, 3,381 oxygen ligands, 3,384 perchlorates, 3,408 peroxo, 3,387 IR spectra, 3,388 Raman spectra, 3,388 1,lO-phenanthroline. 3. 372 1,lo-phenanthroline mono-N-oxide, 3,439 phenyl isocyanate, 3,439 phosphine, 3,383 phosphorus ligands. 3, 383 phthalocyanines, 3, 440 phthalonitrile IR spectra, 3,382 poly(pyrazolyl)borates, 3.381 porphyrins, 3,439 primary amines, 3,372 pyrazine, 3,373 pyridine, 3,372 N-(2-pyridyl)salicylaldiminel3 438 pyrrolyl, 3,377 8-quinolinol, 3, 437 quinones, 3,403 Schiff bases, 3,434 salicylaldehydalo, 3, W2 salicylic acid, 3, 413 selenates, 3, 407 selenium ligands? 3.421

COC 7-1.

Zirconium phosphate

selenocyanates, 3,380 selenoxides. 3,414 semicarbazones, 3,434 sulfates, 3, 407 sulfoxides, 3,414 sulfur ligands, 3,418 tartaric acid, 3,412 tertiary amines, 3,371 tetrahalides. 3.422 tctrakis(diketonates), 3,397 bromination, 3,3Y8 intramolecular rearrangement, 3,398 ligand exchange, 3,398 mass spectra, 3,399 NMR. 3,398 volatility? 3, 399 X-ray crystal structures, 3,397 tetrakis(perfluoroalkanesulfonates), 3,418 tetraphenylporphyrin, 3,440 thioacetylacetonato, 3,439 thiocyanates. 3, 380 thioethers. 3,418 thiolates, 3.418 thiosemicarbazones, 3,434 thiourea, 3,421 tin-cuntaining ligands, 3, 370 trialkylsilyi oxides, 3, 389,391 triazenes, 3, 378 triazincs monodentate, 2, 196 triethylamine, 3, 371 trihydroxyglutaric acid, 3,412 tris(diketonates) 3,399 tropolonates, 3,402 urea. 3,382 water, 3,384 Zirconium ethoxides synthesis electrochemistry, 2,337 Zirconium iodide ZTSI12

structure, 1 , 2 7 Zirconium phosphatc ion exchange resins, 5,720

Cumulative Formula Index JOHN CORFIELD Kingsley, Cheshire, UK

This Formula Index consists of over 28 000 cornpounds that occur in the 6562 text pages of Volumes 1-6. Indexed compounds may appear in the text, equations, Schemes, Figures or Tables. Only specific compounds and not general classes of compound have been indexed: the counter ion has been excluded. Limitations of space d e not permit every coordination compound to be indexed each time it is mentioned, therefore compounds are only indexed when considered to be important in the context of the topic under discussion. The element symbols within each formula are arranged according to a modified Hill system in which the order is metal(s), C, H and then any remaining symbols arranged alphabetically. Compounds containing two (or more) different metals appear twice (or more), being listed under each metal. Common ligand abbreviations which appear in the text have also been used in the index. These include acac (acetylacetone), bipy (2,2’-bipyridyl), diars [o-phenylenebis(dimethy1arsine)], dien (diethylenetriamine), etc.

255

AgAsC,HqNO, Ag(N03)(AsMe3). 5,803 A@sz‘&HmNS Ag(SCN)(AsPh,)Z, 5,803 AgAsG7Hz3Br

AgBr{(2-Me2AsC6H4),AsMe}, 5,SO4 AgAS3C56H4802 Ag(OAc)(AsPh,),, 5,803 AgAsKGiHz304 Ag{ (~-M~ZASC,H~),ASM~)CO(CO)~. 5, 804 AgAs,CzoHs [Ag(diars),]+, 5,804 AgBC>H,F,NO Ag(DMF)BF,, 5,811 A~BC~~H~~PZ AgBHd(PPh,)z, 5,825 AgBC3&37NJ‘ Ag{PhzB(~N=CHCH=~H),}{(4-MeC,H4)3P). 2, 254;5,796 AgBCs5H490zP3 AgHBHzCOzH(PPh,),, 5,825 A ~ B G ~ H S ~ ~ Z P ~

AgC3&3N2 Ag(ACH=NCH&H), 5,786 AR(AN=CHCH=CH), 5,784

AgHBHzCOzEt(PPh3)3,5,825

AgBr, [AgBrJ, 5.822 IAgBr312 , 6 , 9 6 Ag3r4

[AgBrJ-, 5,823; 6.97 AgCHN [Ag(HCN)]*, 5,778 AgCH,Br03S Ag(03SCH2Br),5,818 AgCHpW Ag(O,SMe), 5,818 AgCHSCIN3S Ag(H2NCSNHNH2)C1,2, 803; 5,830 AgCNO AgCNO, 2,7, 12, 13 AgOCN, 2,7 AgC1F302 Ag(O,CCF,), 5,808,809 AgCZH2C102 Ag(OzCCHZCI),5,808 AgC2HzNz [Ag(HCN)z]+,5.778 A$ZH3NZ03 Ag(NO,)(MeCN), 5,797 AgCzH4NOz Ag(OzCCHzNH2). 2,744; 5,826 AgCzHsNzO, Ag(HO2CCHZNHZ)NO3, 5,826 AgCzH,NO,S AgN03(SMe,), 5,815 AgCtHhN04S Ag(DMSO)N03, 5,810 AgC,HsCIN,Sz Ag(H?NCSNHZ)2CI, 5,819 AgC2H8CIN4Sez AgCl{SeC(NH,)2}2.2,663 AgGHsNz

Ag(MeiNAc)CIO,, 5,812 AgC4H9INO ARI{ H~~CH,CH,OCH,CH~), - 5,824 AgCiH91NS AgI{Me,NC(S)Me), 5.822 AgC4HgNPS Ag(SCN)(PMe3).5,799 ~~

256

257

AgI(pipcridine), 5,785,824 A&HzE,Nz Ag{NN=CHC(C,F,-i)=cH}, AgC6H4C1S AESCAHaCl. 1.158

Cumulative Formula Index

5,784

AgC:1ZH36N6PZS2

Curnularive Formula Index

258

849

[Ag{Dt-4-(4-H2NC6H4CHMeCHMe)C,H4NH,},] ' ,5. 782

259

,2.941

260

261

Cumulative Formula Index A1CzH6F AIMe,F. 3. 121 AIC2H6Tz [AIMez12]-. 3. 123 AIC2H6N, AIMe,(N3). 3. 110 A1C2H6N6 [A1Me2(N3)21-,3,111 AIC2HsN AlH2(NMel). 3,109 AIC,H,O, AI(O,CH),, 3, 117 A 1C H C1 [AlMe,Cl]-. 3,123 AlC3H&13N AICI,(NMe,), 3,107 A 1C3H 9I [AIMe,I]-, 3. 123 AIC3H9N03 [AIMe3(N03)]-. 3,116 AIC3H9N3 [AIMe,(N,)]-, 3,111 A1C3H903 Al(OMe),. 2,345; 3,114 A G HI o [AIHMe3] , 3 , 123 AIC3111zN AIFI,(NMe,), 3, 107, 123, 124 AGHi3Nz AIH3(H2N(CH2)3NHZ},3, 108 AlC3N3 AI(CN),. 3. 106 AIC3N3S3 Al(NCS)3.3,111 A1C3012

Al(iti4)(133Hs)z, 3. 125 AIRiBr, AIBr3(BiBr3),3.112 AIBrCI, AICI,Br, 3, 123 AIBrzCl AIClBr,, 3, 123 A I Br N AIBrz(N3),3, 110 A1Br3 AIBr,, 3, 121 AIBr,PS AIBr,(Br,PS), 2,642 AICCI,O AICt,(COCI,), 3, 119 AlCHqCI, [AIMeC13] , 3 , 123 AICH~CI~NOZ A1CI3(MeNOz),3, 118 AlCzHNz AIH(CN)2,3,106 AICzH3CI3N AICI,(MeCN), 3,111 AICZH3CI40 AICI,(AcCI), 3, 118 AIC2H6Br3N2O4 AIBr3(MeNOz)z, 3.118 AICZH~CI AlCIMe,, 3, 122 AICzHhCI3O AICI,(OMcZ), 3, 119 AICZH~CI~S A1CI3(SMez),3, 120

[AI(C204),]3-. 3, 118 AIC4H3NS [AIMe,(NCS)]-, 3,111 AlCdH6C13NZ A1CI3.2MeCN, 3, 11 1 AIC,H,N,Sz [AIMez(NCS)z] , 3 , 111 [AIMe2(SCN)2]-,3, 111 AIC4H8C130 A1C13(THF). 3,118 AlC,H,,CI30 AIC13(OEtz).3. 118 AIC4Hj& I 3 0 6 AICl,(ClO,)(DME), 3,117 AIC,H,,I,S AlI,(SEt,), 3, 120 AIC,H,,CIN AICIEt(NMez), 3, 109 AICdII11CltO AIHCI2(0EtZ),3,118 AIC,H, ,O AlH,(THF), 3, 124 AIC4H12Ct302 AIC13(OMez)z,3, 119 A1C4HI2N AIH,(NEt*), 3,109 AGfIizNz AI(NMe&, 3, 120 AIC,H&3 [AIH(OMe)2(OEt)]-. 3, 124 AICIH130 AlH,(OEt,), 3.109, 123, 124 AIC4N4 [A1(CN),]-. 3,106 AIC,N,S, [AI(NCS),]-, 3, 111 AIC5HSC13N AIC13(py),3,108

AICSHSCl3N

Cumulative Formula Index

AlCsHSIN AICSHSIN AII,(py). 3, 108 AIC5H12CIzNj AIC1z{N=C(NMe2)z},2,282 AIC5HizN A1Me3(MeCN),3, 111 AGHizOz [AIMe,(OAc)]-, 3,118 AIC5H13Cl3N3 AICI~{HN=C(NM~Z)~}, 2,282 AICsH15S

AIMe3(SMe2),3, 120 A~C~FQ~; AI(OzCCF,)X, 3, 117 A1C6H3N309 [AI(NHCOCOz),]3-, 3, 126 AICAHaO, Ai(OA;),, 3, 117 AIC,H,,CIO, AICl(Ofr'),, 3, 113 A1C6Hl5CI2NZ AIClZ(NEtCHZCHzNMeZ), 3, 109 AIC~HI~O~ AI(OEt)3, 3, 114 AIGH1604 [AIH2(0CHzCHz0Me)z]-.3. 124 AIChHl7BrZNZ AlHBr,(TMEDA), 3, 108 AIC~H~~C~~PZ AICI,(PMe,),, 3, 111 AlC,Hi,N AIMe3(NMe3),3,107 AIC~HISNZ [AIH,(TMEDA)]+, 3,108 AIC~HI~N~ A1(NMez)3,2, 164; 3, 109 AIC~HIBN~ AItMeNNNMe),, 2,196 AIC6HIBP AIMe>(PMe,), 3, 111 AILHziNz ~'

AIC7Hz~CIN3Siz AICI{ {NMe(SiMez)}ZNMe),3,109 ALCRHIIF~,N~O, Al(OH)(OCH( CF,),} 2(en),3, I 14 A1C,H,,CI,N4 [AICI,(MeCN),]+, 3, 111 AICBH16C1302 AIC13(THF)z, I, 45; 3, 118 AIC8H,,C1304

AI(OCH(CFJ)2)3,3. 114

262

263

Cumulative Formula h d e x AI(CIO,),, 3, I17 A1CI4

[AIC14]-.3. 111.112, 118, 119. 122. 123 AIC1,NO AICI3(NUCI). 3. 119 AICI,04 [AlCl,(ClO,)]-, 3, 117 AIC14012S4

[Al(SO,CI),]-, 3, 117 AlC1,0,, [Al(ClO,),]-. 3, 117 AICISN202

[AI(HMPA),],+, 1.286 AGHisN303 AI(S-quinolinolate),, I, 528,530,545 AIC~,H~~O~ AIIPr‘COCHCOPr’L. ,.. 2. 382 AIC3’oH24N303 A1(2-methyl-8-quinolinolate),. 1.524.530,545 A1(5-methyl-8-quinolinolate),. 1, 530 AIC~OHZ~N~ Al(bipy),, 3, 108 AIC~ZH~~CINS [Al(phthalocyanine)CI]”- ,2,870 A I C ~ Z HI~FNS AIF(phthalocyanine), 3. 126 AGzHidWz Al(phthalocyanine)(OH)(OH,), 2, 864 AIC36HmCI3P& AI(Ph3PS)2C13,2,642 AICxH45N40 Al(OH)(octaethylporphyrin), 2, 821; 3, 126 AIC,6H,& 3, 109 AI(N=CBU‘~)~, AIC36H10sNi806P6 [AI(HMPA)6I3+,3, 119 AIC37Hz1BrN9 Al(phthalocyanine)Br(py), 2.864 AG8H2iNsO Al(phthalocyanine)(OPh), 2.864 AGsH3iN40 AI(OMe)(tetraphenylporphpn). 3, 126 AIC46Hd4 AIEt(tetrapheny1porphyrin) 3,126 A1C50H31NSOSi Al(phthalocyanine)(OSiPh,). 2.864 AIC54H4503Si3 AI(OSiPh3)3, 3, 114 AlCl AICI, 3, 121 AlClS AISCI, 3, 120 AICIZH30, AI(OH)(OZCH),. 3.117 AICI204S [AlClz(S04)]-, 3, 117 AICIZS [AISCIZJ-, 3, 120 AlC13 AIC13.3, 119, 121, 122 AICIaFjP AICln(PF3), 3, 112 AIC1302S AIC13(SOz),3, 119 A1CI3Ol2

AICI,(NOCl),. 3, I19 AIC15030 [AI(CI04),12 3, 117 AIC1,OP A1Cl3(PUCI3),3.119 AICl6Oz4 [A1(C10,)6]3-. 3,117 AIC1,PS AICI,(CI,PS). 2,642 AIC17Se A1CI3.SeCI4,2.678 AIC1, O,P, RIC13(POC13)6,3. 119 AICrC4H,204 Cr(AI(OMe),), 3,860 AICrC6012 ICr(C201)BAIlx.1.27 AICrC2sH,,N05PSi2 Cr(CO),(pPPh2)AI(CH,SIMe3)2(NMe,). 3. 112 AICuC6H6Cl4 CuAlCI,(C,H6), 5,570 A1F3 AIF3. 3, 120, 123 AIF4 [AlF4]-, 3, 121 AIF; [A1FSl2-.3. ‘121 AlF, [AIFJ-, 3.121; 6,846 AIFfiOJ‘a AI(PO,F,),. 3, 116 AIGeC,Hz, AIMe(GeMe,),, 3, 107 A1GeCi8Hi8 [AIH,(GePh,)]-, 3,107 A1Ge3C9H2, A1(GeMe3),. 3. 107 AlHCli AIHCI,, 3- 123.125 AlHC120s A1(OH)(C1O,)z, 3, 117 AIHCI, [AIHCl,]-, 3, 125 AIHF04P AIF(HPOI), 3, 116 AIHOz AlO(0H). 3.112 AIHZCI AIHzCI. 3.125 AIH2CI2 [AIHZCl,]-. 3. 125 AIHzNS AISNH2.3, 120 AIHZO AlH(OH), 3,113 AIH,Ot [KlO(OH),I-. 3.113 AIHZ04P [AI(H,PO,)IZt, 3, 116 A1Hq AiH,. 3,123

AIH3

AIH,Br,N

Curnulutive Formulu Index

AIH3Br3N AIBr,(NH,), 3, 107 AIH3C13N AICk,(NH3), 3, 107 AIH3CI3P AIC13(PH3),3, 111 AIH303 AI(OH)a, 3, 112, 133 AIH304P [A1(H3P04)13', 3,116

AIHI fAIH41-, 3,114, 123-125 AiH,04[AI(OH),]-, 3, 113; 6,787

[AI(PH2),]-, 3, 112 AIH,,N. [A(NHZ)5]2-, 3,109 A[HloOgS [AI(SO4)(OH,),]*,3, 113.117 AIHI,~~ ~Al(OH)(H20),12', 1, 121; 3, 113 AI'H120~ [A1(OH2)6]3+,3,113, 115.116.117.118,133 A~HIBN~ [AI(NH3),I3+, 3, 107 AlH,,P,Si. [ijP(S'iH3)2}4]-,3,112 AI HgC15 HgAlCl;, 5, 1062 A11309

AI(I03)3,3, 117 AH, [AH4]-, 3, 122,123 AKnS, InA1S3,3, 120 AILiCsH2002 LiAIH4(THF)2, 3, 124 AILiH, LiAIH,, 3,124 AILi3H6 Li,AIH,, 3, 124 AlMgFs MgAIF,, 3, 121 A1MnC12H36P4

Mn(AIH4)(Me2PCH2CH2PMe2)2. 4. 9.32 AIMn&iHi&i8 AI{Mn(CO),(MeC0)2)3, 2,396; 3. 115 A1Mn3C42H30018 AI{ Mn(CO),( MeCO)(PhCH,CO)} 3. 2,397 AIMoCyyHy503 MoH(CO),Cp(COAIMe,), 2,697 AlMoClsH21 MoH2Cp2(AIMe3),2,697 AIMoC~~H~~N~P~ Mo(NZA1Me3)(N2)(dppe)~,3, 1270 AIM06021 I A I M o , O ~ ~ ] ~3,117 -, AIN04 AIONOj, 3,116 AIN, AIN,, 3, 109 AIN309

264

A1(N03)3,3. 113. 115, 116 A"*, [AI(N03)4]-.3. 116 A1NsO I 4 Al(N03)3(N205). 3.116 AINSO,, [AI(NO3)s]'-, 3, 116 AIN9 AI(N3)B. 3. 110 AINaCI, NaAIC!,. 3,122 AINaF, NaAIF4.3. 121 AINa,H, Na3AlH6. 3- 123 AlNbCls NbAICIB.3.591 A10 [AIO]', 3. 113 AIOz [A102]-. 3. 112 A104 [A10,]5-. 3,112; 6,845 A10,P AIPO,,3. 1 Ih AlOePz [A1(P0,)2]J-. 3. 116 AIO,S, [AI(SOd)z]-. 3.117 AlOqP3 Al(P03)~.3. 116 AIOSC~~H~,CIJ~P~ Os(NNAlMe3)(PEtzPh)3C12,4 , 5 5 5 A1Pu03 PuAIO~,3,1133 AISbBr, AIBr,(SbBr,), 3, 112 AISI~C~H,~O~ AI(OSiMe,);, 3, 123,114 AIT&8H4S0.$'4 'I a{H2AI(OCI-12ClIZOMe)2) (drnpe)z, 3,679

AITaClnHrbOx TaAl(OPr'),, 2,344 AITIC14H2iCI TiCp2(@l)(y-CHz)A1Mc3, 5,385 AITIH4 T1A1H4,3.170 AIvi.10~0 [A1V14040]9-.3. 1045 AIWKd3409 {W(CO)&p},Al(THF)3.3, 119 A~WZC~~H%CIBN~P~ { WCl(py)(PMe2Ph)3(p3-N2)}2(AlC12)3. 3, 1012 AIW,OB [AL(WO,)J, 3,117 A1Wi2040 [ A I W ~ & I J3,117 ~ AIZnF, [ZnAIF9j4-, 3,121 AlZrC21H4907 AIZr(OPr'),, 3.392 AI2Br2Cl4 Br2AI(pCI)2A1C12,1. 123 AI2Br, AI2Br6,3. 121,122 A12Br, [A12Br,] -.3,123 A1,GHizCIz 3, 122 (AIMc~)~(cI-CI)Z, A12C4H12CW1 {AICI2(NMe,)},, 3.109 AbGHi,O,S (A1Me2)2S04,3. 117 I

Cumulative Formula index

265

{AiHiNMe,),},, 3, 109 ALCIOH~HN~O {(AIMe2),0}(TMEDA), 3. 108 A~~C~ZHWC~~N~SH {A1Cl(S2CNMe2),},, 3.120 A12C12H30Br2N2 {AIBrEt(NHBu')},. 3. I10 AIzCI~H~~N~ {A1(NMe2)3}2,2, 173; 3. 109 AIzCizOiz AIz{C6(C'02)6}, 6, 844 A1&4Hz2C160s Al2Cl,(benzo-l5-~rrlun-5).3. 119 A12Ci6H3iNO {(A1Et2)20)(NMe2Ph). 3. 108 AI2Ci8HzsNz {AIMe,(NMePh)},, 3. 110 AIzC23H47N06 {A1(OPr')31z(py).3. 108 AIzC&s,O6 (AI(OBu')3}2, 2.348 AbC26HaO6 (AIMe,),(dibenzo- 18-crown-6). 3, 126 A~~C~~HS~NZP~ {A1Me2{N(PPhZ)2)}2, 3,112 A12C64H32N16O {Al(phthalocyanintt},0.2. Sh4 A L C ~ ~ H ~ R O (Al(octaethy1porphyrin)J?O,2,821 A12C16 AIzCI6, 3, 121, 122 A12C16N0 (AIC13),(NO). 3, 119 AI2Cl6N2S2 (AlCI3)2S2N2,3, 121 A12C1602S (AlCl3)2(SO2).3, 119 AI2C17 [AI,CI,]-, 2,681; 3. 112.122 123 AlzClsOS (AICI3)2(SOClz),3, 1 I9 ALXIidW', ( A I C 1 ~ ~ 2 ( P O C l3.~ )119 ~, Ai2CrC12H2806

Cr{OAl(OPr')2}2,3,738 AI2CrCls (A1C13)2(CrC13).3. 122.755 A12F6 ~, ~

A13CllO

AM-3C36H84012

Cumulative Formula Index

266

AWIBHJ'J~

{AIMe(NMe)}6{AlMe2(NHMe)}2, 3,110 A18C24H64Ns { AIH(NPr')} 1.164 AI13H47040 [AIi304(OH)zs(OH2),,16+, 3, 113 A113H48040 [A11304(OH)24(OHd1217+, 3, 1036 AmCO, [ArnD,(CO,)J-. 3. 1220 AmC,O, [Ain0,(C20,)] 3.1220 AmCzOs [Am02(C0?)2]3-,3, 1220 AmC3HOIU [Am(OH)(C03),]4-, 6,961 AmC3H306 Am(O,CH),, 3, 1216 Amc3011 [ A I ~ O ~ ( C O ~ 3,1220 )~]~-. AI~C~HSO~ Am(citrate), 3, 1217 AmCtiH908 [ArnO,(A~0)~1-, 3.1220 [Am0,(OAc),]2- ,3. 1220 AmCl,H2,0, Am(acac),, 3.1216 AmC21H1rO10 Am(2-02CC611,0H)3(H20),2,481,3, 1215 AlnC3,H5,06 Am(Bu'COCHCOBu'),, 3, 1216 AmC39H68F18014Pf Am(hfa~ac),((BuO)~PO>,, 3,1217 AmC64H32N16 Am(phthalocyanine),, 3, 1218 AmC&zo7024P6 Am{HOP(0)(OCH,CHEtBu)2}3{ OP(0)(OCH2CHEtBu)Z},, 6,960 AmCI, AinCL, 3, 1215 AmCI, AmCI,, 3, 1133, 1218 AmC1402 [Am02C14]2-,3.1220 [Am02Ct4]3-.3,1220 AmF,O, AmO2F2,3,1220 AmF, AmF1,3, 1218 AmF, [AmF.1-, 3,1218 AmH? AmH,. 3, 1218 AmH303 Am(OH),, 3. 1216 AmH12CI,06 [AmC12(OH2)6]1.3.1215 AmI, AmI,. 3. 1218 AmLiO, LiAmO,, 3, 1216 AmLi304 Li3Am04.3. 1219 AmN,Ol [Am0,(N03)3] , 3 , 1220 Am0 AmO. 3, I215 AmO, AmOZ,3.1219 AmO,P [Am0,(P04)] . 3 . 1220 AmO& [Am(SO,)J, 3,1216 I

267

Cumulative Formula Index

AmO14S3 [Arn0,(S04)3]4-, 3,1220 AmS AmS, 3, 1215 Am&07 Am,0(C03),, 3,1216 Am~C309 Am2(C03),, 3, 1216 Am2ChOI2 Arn2(CZ04)31 3,1217 Arn,O,S A w ~ O ~3, S ,1217 Am203 Amz03, 3, 1216 Am2012S3 Am2(S04)3,3, 1216 Am2OZsS7 [Amz(S04)7]8-,3, 1216 Am& Am2S3,3, 1217 AsAgC3HgNO3 Ag(NO,)(AsMe,), 5, 803 ASA1C16 AICI,(AsCI,). 3, 112 AsAu [AUAS]~-, 5,881 AsAuC,H9CI AuCI(AsMe,), 5,870 AsAuClzHlo (AuASPh,),, 5,881 AsAuC18HlSBr AuBr(AsPh,), 5,882 ASAuCi8H15CI AuCI(AsPh3). 5,870,875 AsAuC18H15C1S Au(Ph,AsS)CI, 2,644 AsAuCl8HlSCl3 AuCI,(AsPh,), 5,870 ASB~~C~~H~~CI,N~ IrCI2{HB(fiN=CMeCH=CMe)3}(AsPhMez),4. 1134 AsB~AIC~HZI AI(BH4)3(AsMe3).3, I1 I AsBiCsH,NO, AsO(OH)(OBiO)( C6H4NHCOCH20H-4),3,256 AsBr3 AsBr,, 1.36; 3,251 ASCH 3F2 AsMeF,, 3,251 AsCH3F7NOS AsFS(SOF,NMe), 3,252 ASCH 5 03 As(Me)03H2. 6,868 AsCH,Si AsH,(SiH,Me), 3,239 AsCZHZCI~ AsCIZ(CH=CHCI), 3.256 ASCZH~CI~N AsC1,(NMeZ), 3,240 AsC3F9Se3 As(SeCF,),, 3,249 AsC~H~ AsMe,, 3,256 AsC3H,Br [AsBrMe3]', 3,251 AsC3H9CI, AsCI,Me3,3, 251 AsC3H9CI3N AsC13+NMe3,3, 252 A~C3H904 AsO(OMe),. 3.245 AsC,N, As(CN)~,3,252 A~C3N303

As(NCO),, 3,252 AsC~N~S~ As(NCS),. 3.252 ASC~H~CIS~ AsCI{(SCH,CH,),S}, 3,249 AsC4H905 As(OH)(OCH,CH,O),, 3,246 AsC4HI2CIN, AsCI(NMe,),, 3,240 AsC4HI2CI2P AsMeCIz(PMe3), 3,244 AsCSW,,CIP AsMe,CI(PMe,), 3,244 AsC6FiaN3 {AsN(CF&},, 3,243 ASCgH703 As(Ph)O,H,, 6.868 ASC~HIB~PZ Asl,(PMe3),, 3.244 ASCgH18NPz [AsMe,(PMe,N=PMe,)]+, 3,244 AsC,H,P.N, As(NMe2),, 3,240,241 AsC,H6C1S2 AsCI(S&H,Me), 2,hOS ASC,H~~T~P, AsMeI,(PMe,),, 3,244 AsCaHIBCl2F6NSi2 As~CFT)2CI,{N(SiMe3)z}, 3,242 AsC8HIBF6NSi2 As(CF3),{N(SiMe3),}, 3,242 AsCgHi3 AsEtMePh, 1, 199 As&H14C12P AsPhC12(PMe3),3,244 ASCdmN306 As(O2CNMe2),. 3,241 ASC~HI~N~S~ As(S2CNMe,),, 3,241 AsC9H,,Si, As(SiMe,),, 3,239 AsC,,H,ClN ASCI(C6H?NHC6Hd),3,256 AsCizHioCl AsCIPh,, 3,256 AsCi2HnO4 AsO(OBu),, 3,245 AGzHz7S3 As(SBu'),, 3,248 AsCI~HION As(CN)Ph,, 3,256 AsCwH2704 AsMe(OCMe2CMe20),, 3,246 ASC15H30N3S6

As(SlCNEtI),, 1,82; 3,249 AsCI~-&ON~S~~ As(Se,CNEt,),. 3,250 AGsHnO, ASPh( 1,2,-OZC6H4),,3,246 A~cmHisF2 AsF,Ph3.3,251 ASCISHI& As(SPh),. 3,248 AsCmHz@4

AsPh(OCMe,CMe,O),, 3,246 A5C 1s&oN, Se6 As{Se,CNTH,),},, 3,250 AsC,,Hs4PSi6 As{C(SiMe,),) {PC(SiMe,),), 3,243 AsC,,H*, [AsFh,]', 1.534 AsCz7H,&Se6 As(Se,CNBu',),, 3,250

Cumulative Formula Index

ASC28H4104

ASCdLiOa AS(OH)(O,C6H,But~)2, 3,246 AG&,O, AsMe(OzC6H2Bu'z)z.3,246 AGnHzs AsPh,, 1,40 AsC,,H,,CIN, As( oct aeth ylporphyrin)CI, 2,822 ASC36Hd40z IAs(o~taethylporphyrin)(OH)~]+~2,822 AsCwHmO AsPh,(tCPh=CPhCPh=CCOMe): 3.239 AsC,4H28C1N4 As(tetraphenylyporphyrin)CI, 2, 822 A~LHd402 [As(retraphenylporphyrin)( OH),]+ 2,822 AG5H4ASe6 A S { S ~ , C N ( C H ~ P ~ )3,250 ,}~, AsClF, AsCIF,, 3,253 AsCl, AsCI,, 3,251,252 ASCI, [ASCI,]+, 3,251,253 AsCl, AsCI,, 3,253 A~COC,~H~~N~O, Co(HDMG),(AsMe,), 4,774 AsCoC,,H,,CIN,O, CoCl{AS(OH)MePh}(HDMG)2,4,774 AsCoC,,H 6N2 CoH(N,)(AsPh,), 4,769 A s C ~ C ~ ~ H ~ ~ N O ~ Co(NO)(CO),(AsPh,), 4,660 AsCOC~~H,,N,O~P Co(HDMG),(PBu,)(AsMePh) 4,775 AsCoCdW [CO{As(C,jH,A~Ph2-2)3}(CO)]' ,4,769 AsCoFeMo WCZH6S CoFeMoWS(AsMe,), 4,832 AsCoHlbN50J [Co( OAsO,H)(NH,),]+, 4. 775 AsCoH,,NSO, [Co(OAsO~H~)(NH,)sI3',4,775 AsCrClsH1506 CrO(Oz)z(OAsPh,), 3,946 AsCrC19H1403 Cr0(2-Ph2AsC6H4COz),3.901 AsCrF, CrF,.AsF,, 3,756 AsCr3H0,, [(C~O,O),ASOM]~~. 3. 1024 AsCuUO, Cu(UO,)(AsO,), 5,653 AsF, AsF3,3,2.51 AsFS A s F ~3,25 . 1,252 IAsF,]*-, 6,854 AsF, [AsFJ. 3,251,253 AsFeC4H6N0, 1. 125 [F~(AsM~,)(CO),(NO)]~, AsFeC22H,9 FcAsPh,. 1, 127 AsFeH ,sN3OZ 6, 1018 F~{AS(O)(OH)M~)(NH,)~. AsGa04 GaAsO,, 3, 135 AsH,Si AsH2(SiH3j,3,239 AsHrSi2 AsH,(SiH,SiH,), 3,239 I

268

AsIlgC,HqCl [HgCI(AsMe,)]', 5,803,1U83 AsHgCi,Hid2 HgClziA~Ph,).5 , 1084 AsHgClsH15CIIS Hg(Ph,AsS)Cl,, 2.644 AsHgC,oH,,N,S, Hg(SCN),(AsPh,). 5,1084 AsHgZC3FgN03 [Hg,{ A s ( C F ~ ) ~ ) ( N O ~ 5) ]. +1058 : AsHg2.86F6 Hgz,,t,AsFfi.5 - 1 0 4 AsI, Ad,, 3,250 AsI, Ad,, 3,251 AsIrC,,H3,C10P,

[I~HCL(ASM~,P~)(CO)(PM~,P~),]~, 4, 1150 ASI~C,~H~~NO,

Ir(OAc),(AsPh3j(CNC6H4Me-4), 4, 1121 AsIrC38H4nN302

Ir(AsPh,){MeCOCHC(Me)=NCHz}z(CNC,H,Me-4), 4,1124 AsIrC,,H,,N,O, Ir(AsPh,)(salen)(CKC,H,Me-4), 4, 1124 AsM&H5,P4 [ Ir(PPh,){ A S ( C J I ~ P P ~ ~ -J'Z ,)4~,}1'I 35 AsIrPdC19H3,C15Pz PdC1(AsMe,)(pCI),IrC12(PMc,Ph),, 5 , 1162 AsLiSiZC14H3402 LiAs(SiMeZ),.2THF, 3.240 AsMnC8H1,Br,N MnBr,(2-H,NC6H4AsMe,), 4,34 AsMnCi,H,,C1O, [Mn(Cl0,)(Ph,MeA~0,)]~,4,40 AsMnCI6H,,N, ~ M n ( 2 - H z N C ~ ~ , H , A s M e z4,34 )z]z+, AsMnC,,H,,N, Mn {2-(Me,As)C,H4N=C'PhC(Ph)=NNHpyridyl-2), 4,34 AsMn,HC), Mn,(OH)Z,sC),, 4$45 AsMoC~~H,~O~ M O C ~ ( C O ) ~ ( A S B2~, 1052 '~), AsMo~C~H~O~~ [MO~O~~(M~,ASO,)(OH)]~~, 3, 1054 ASMO,CH,,O,, [ Mo601B( M ~ A S O ~ ) ( H , O ) ~3,] ~1054 -, AsMo9H6O3, [AsM09031(Hz0)3]~-,3, 1042 AsNbC18H,jC1j NbCI,(AsPh,), 3.600 AsNbC,,H,,CI,N [NbCI5(NAsPh,)]-. 2.122; 3.620 AsNiC27H2,02P,S, Ni { SZP(0)OMe)(arphos),5 , 175 AsNiC27H42N4S [Ni(NCS){N(CH2CH,WEtZ)Z(CH2CH2AsPh2)}] * 5. 135 AsN~C~~H,,N,S~ Ni{ Ph2AsCH2CH2N( CH2CH2NEt2)2} (NCS),, 5,64 AsNiC34H34PS3 [Ni{M e A ~ ( c ~ H ~ s M e -{ 2PPh2(C6H4SMe-2)}]2+, )~) 5, 66.67 A s N ~ ~ C ~ ~ H ~ ~ ~ ~ Ni,(acac),(OAsPh,). 5 , 143 ASOZS~ [AsO,S,]~-, 3.249 hs0,S [AsO3SI3-, 3 ?249 As04 [As0,I3-, 2.413; 3,255 ASPdC6H15CIjj

[PdCI,(AsEt,)] , 5 , I123 ASP~C~~H~~FGO~ [Pd(hfacac)(AsPh3)]+, 5.11 14 AsPdC3,HZ4N,PS2 5 , 1139 Pd(SCN)(NCS){PhzA~(C6H4PPh2-2))~ AsPdC3,HZ4N,PSe, Pd(SeCN),{Ph,As(C6H4PPh2-2)), 5, 1139 AsPdC36H30CI2 PdClz(AsPh3),, 5, 1158 AsPtC,H 15C13 [Pt(AsEt,)CI,]-, I , 314 AsPtCI8HZ8CINLS [PtCI(McNSNMe)(AsMe,Ph),]' ,2, 191 AsPtC201117C~I, PtC1*(2-Ph,ASC6H4CI~=C~2),5.406 ASPtC24H30C12P PtCI,(PEt,)(AsPh,), 5.445 AsPtCz,H3IClP PtHCI(PEt,)(AsPh,). 5.445 AsR~C,~H,~C~~P ReCl,(arphos), 4, 169 AsRhC9Hl,CI,S (RhCI4(2-MeSC,H,AsMe2)l 4, 1015 &RhC7,H,,P3 RhH(PPh,),(AsPh,). 4.921,924 AsRuC7HqOa KU(C'O)~(ASM~~), 2, 1038 ASRUClZtI1504 Ru(CO)d(AsPh3). 2. 1038;4.371 ASRUC?~H,,,CI,P (RuCI2(AsPh3)(PPh3)}., 4,379 AsRuC38H,ICIN, [RuCI(bipy),(AsPh,)]-, 4. 392 ASRUC~~H~~F~O~P, Ru(O,CCF,)(CO) (PPh,) (arphos). 6,235 ASS, [AsS,12-, 3,248 AS& IAsS3l3-, 3,248 A& [AsS41J-,2, 519 AsSC, [AsSe3I3".,3, 249 AslaCl8H,,Cl5 TaCI,(AsPh,), 3, 600 AsTiC18HlsCI, TiCI,(AsPh,), 3,347 AsUHO, UO,HAsO,, 3, 1196 ASWC~HI~CI~OP WOCI3(Me2PCH2CH2As!vfe,) 3.985 ASWC~~H~~O, WCp(CO),(AsBu',), 2, 1052 A~Wg033 [AsW,O,,ly-, 3, 1042 ASWI~M~~W [ A S ( H ~ ) W I ~ O3,~ 10.12 ]~-, Asl.sCrCl,H,,CI,Nl.s CrC13(2-Me,AsC6H,NMez)l.5~ 3.854 ASI.SC~CISH,,CI,PI,S CrC13(2-Me,PCtiH,AsMe2)l.j . 3: 854 AsAgC37H3oNS Ag(SCN)(AsPh& 5. 803 As&&oHi6N,O6 (AgNO,),(diars), 5 . 804 ASZAGRHI~FIS Au(C6Fs),(diars), 5,898 AS,ALIC~~H~~P~ [ A U ( ~ - E ~ ~ P C ~ H ~ A5.884 SE~~)~]+, As,AuC3blH30 [Au(AsPh,),]+, 5. 871 A~,BC~H~II [BH,(AsMe,),]+, 3,98 I

As2BCuC,,H, N Cu(B(N-H),(diars)}, As~Cl~HlsC12F12N2Siz {As(CF,),C~(NSiMe,)},, 3,242 AS~C~~H~~N,O;

2,254: 5,544

AS2(CbH,OH-4-NH,-3}2,6,756 As,C15S [As2SClj]-, 3,251,253 As,CI, FAs2Cl,1-, ~. 3,251 As,CI,S [As,SCI,l2- 3,253 As,CI, [AsZCl,]": 3,253 AsZCmC26HII12 CoI,(Ph,ASCH=CHASPh,), 4,769 As,CoC,,H,,CI, CoCl2(Ph,AsCH,CH,AsPh,), 4,769 AS~COC~~H~~T, COI~(,ASP~,)Z, 4,769 As&GoH,oN, [CO(CN)~(ASP~J,]-, 4,773 AS~CO,C,,H,,N,O,PZ Co{Co(As(O)MePh}(HDMCi)(PBu,)),, 4,775 As2CrC,Hl,C1, ~CrCI,{Me,As(CH,),AsMe,}1-,3,853 As,CrC,,H.,,C1, [CrClJdiars)] ,3,853 As2CrCL4HZON306S2 [C~(P~ASO~H)~(H~NCSN 3,888 H~)~]+, As2CrC24H32N4S4 [Cr(KCS),(diars)]-, 3, 838 ASzCr(kHz~C14 [CrCI,(Ph,AsCH=CHAsPh,)]-, 3,853 ASzCrC36H3&~202 CrCI2(0AsPh3),, 3, 754 AsZCrC38H2905 Cr(2-PhzAsCsH4C02)2(0H), 3,901 A s ~ C ~ C ~ ~ H ~ ~ ~ ~ Cr(Z-Ph,AsC,H,CO,),(OH),, 3,901 AS,CUCI,O,.~ CU(CIO,),(ASO~)Z,5,716 ASZCULOH~~IIN~ C U ~ I ~ ( ~ - M ~ ~ N C2,682; ~ H ~5,553 ASM~~)~, A s ~ C U ~ W ~ ~ H ~ ~ ~ ~ [(AsW903,),C~3(H20)2]1z-, 3, 1049 A~zF802 { A ~ z F 8 0 2 ] ~3,251,255 -, A~Zio0 [As,F~,O]~-, 3,251,254 As2FeC6HIsCI2S2 FeClz(SAsMe3)z,4, 1240 A~2FeC-10H1SC12 FeCl,(diars). 4, 1234 As,FeCIUH,,'I, FeI,(diars), 4, 1234 As2FcC, ,H16Br202 FeBr,(CO),(diars), 4, 1234 As,FeCi&6% Fe(CO),(diars), 1,47 [Fe(CO),(diars)]*, 4, 1198 As2FeC39ff3003 Fe(CO),(AsPh,),, 4, 1199 AszFeNiC15H201z0 NiIz(CO){Fe(q5-Me2AsC5H4)2), 5, 124 As,GaC,,H, 6Br3 GaBr,(diars), 3, 132 As2Ga2CloH1,CI6

Ga,Cl,(diars), 3, 132 As2HgC6Ht8 [ H ~ ( A s M ~ , ) , ] ~5,803,1083 +: As,H&oHi&I, HgCl,(diars), 5, 1084

270 ASZH~C~~HZZFZO {Hg(C6Fs),}z(dPam), 5, 1084 AszH~zC~OHZ~N~S~ { Hg(SCN)2}Z(PhzAsCHzCHzAsPh2),5, 1084 ASZH~ZC~~H~OC~~~Z HgClz(~-OA~Ph3)2HgCl2,2,498 ASZH~ZCS~H~~N~O~Z IHg{(2,4,6-Me3C6H2)3As}(N03)~}~, 5.1084 AszHgzSbCisHi812 Hgz(AsF6)2(SbPh3), 5, 1058 AsiHgZiz Hg,(RsF,)z, 2,4; 5, 1048 As2Hg4F1Z Hg4(AsFg)zr5 , 1048 As2Hg6O~ Hg6(AsO4)2.5, 1050 As214 AsZI,, 3,250 As21rCz7HzzC10 IrC1(CO)(PhzAsCH=CHAsPh2), 4,1108 AS~I~C~~H~~CIN~O~ IrCI(N03)2(CO)(AsPh3)2,4, 1144 AsZIrC37H30C10 IrCl(CO)(AsPh,),, 4, 1159 AsZIrC37H30C103 IrC1(CO)(Oz)(AsPh,),, 2,320 A%I~C,~~WIO~ IrI(CO)(Oz)(AsPh,)z, 2,321) As,IrC3,H3,0 TrH3(AsPh3),(CO), 4,1134 As~I~C~~H~~CI IrC1(2-CHz=CHC6H4AsPh2)z,4, I1 11 As,I~C~~H~,CIN IrHzCI(AsPh3)2(4-MeC6H4NC)r 4.1125. 1134 AszIrC44H40N IrH3(AsPh3),(4-MeC6H,"). 4,1125. 1134, 1156

Ir(acac)(AsPh3),(4-MeC6H4NC). 4, 1126 As2MnCIZH16BrZOZ MnBr,(CO),(diars), 4, 31 Ah2MnCi9Hz2BrO3 [MnBr(C0)3(AsMe2Ph)z]+, 4,31 A s ~ M ~ C ~ ~ H ~ ~ C ~ ~ ~ ~ MnCI3(Ph3AsO),, 4,90 As2MnFZ4N4S4 Mn(AsF6),(NSF3),, 4,22, 60 AS~MOC~~H~~CI~NZO~ MoC1z(NO)z(diars),3, 1274 As2MoCllH16FzN04 Mo(OzPF2)(NO)(CO)( diars), 3. 1276 AsZMoC,,Hl6NO, [Mo(NO)(CO)(diars)] ' ,3,1276 AszMoCizH,,IzOz MoI,(CO),(diars), 3, 1281 AszMoC,,H16C1N03 MoCl(NO)(CO),(diars), 3? 1276 As~MoC~~H~~NO~ [Mo(NO)(CO),(diars)]', 3, 1276 A~zMoCI~HZZNZ~~SZ MO(S~CNM~~)(NO)(CO)~(~~~~~), 3. 1276 AS~MOC~SH~~NO~P [MO(NO)(CO)~{P(OM~),)(~~~~S)]+, 3, 1276 AS~MOCZ~HZ~NO~P [Mo(NO)(CO),(PMe,Ph)(dian)J+. 3, 1276 AszMoCzsHzzC1zN20z MoCl,(NO),(dpam), 3, 1272 ASZMOC~~H~~CIZNZOZ MoCI,(NO)~(ASP~~)~, 3, 1272 AS~MCJC~~H~~CI~NO Mo(NO)C13(AsPh3)Z,3, 1286 AszMoC~ZH~~N~P~ Mo(N,),(arphos),, 3, 1269 ASZMO~CZH~~Z~

[Mo601e(MeAs0,),14-, 3, 1053 AS2M06Ci2Hi2025

[MO~O~~(P~A~O~),(UH~)]~~, 3, 1053 As2Nic6Hl4C1, NiC1,(Me2AsCH=CHAsMe2), 5, 119 As2NiCl,H3,S, [Ni{(Me2AsCH2CHZCH2SCHz)2CH2)1". 5, 130 As2NiCIsH,9N,P Ni(CN),(PhP(CF.~,CFI,CHzAsMez)z}, 5,67, 125 As2NiC32H1SN2 [Ni{(Ph2AsCH2CH2NMeCHz)2}]2',5, 130 AszNiCxHmS, Ni(Z-SC,H,AsPh,),, I , 432 As2NiC36H30C1202 NiC12(OAsPh3)z. 5.62, 159 A s ~ N ~ C ~ ~ H ~ ~ N ~ ~ ~ Ni(2-OC61~,CH=NCHzCI.IzAsPhz)z, 5, 190 As206S (AszOZ)(SOJ),3: 247 AszO& (As,O)(S0,)2.3,247 AszO1S3 AsZ(S04)3.3,247 As,OSC~,H~~CI~ Os(AsMe,Ph)2C14,4,577 AS~OSCIBH~~C~A Os(AsPr,)zC1gl 4,577 As,OsC,,H,,CI, Os(dpam)Ct,: 4,579 As20sC,,H,,Cl3P OS{PP~(CHZCH~ASP~Z)~}CI~, 4,579 A s ~ O S C ~ ~ H ~ ~ B ~ ~ Os(AsPh,),Brul 4,577 AS~OSC~~H~~CINO OS(NO)CI(ASP~~)~. 4. 550 As~OSC~~H~~CI,NS OsC13(NS)(AsPh3)2, 2, 119 As20sCq4H4 ,Ci,NP Os(NPPhMez)C1,(AsPh,)z, 4,568 As2PaC10H16C14 PaCl,(diars), 3, 1144 AS~P~C~HI~C~Z PdCl,(AsMe,),, 5, 11.61 AsZPdC7H,&I4 PdC14{Me2As(CH,)3AsMez}, 5, 1124 AszPdCloH,,CI, PdC14(diars),5. 1123 ASzPdCIZH16N2Sz Pd(NCS)(SCN)(diars), 5, 1163 ASzPdCiZH20S2 Pd(SCH,CH,S)(diars), 5 , 1149 AsZPdCl2H3&I, PdCLj(AsEt?),, 5, 1123 AszPdC1J3& P ~ ( ~ - M c ~ A s C ~5, H1165 ~S)~, As2PdC,6H3,C1, PdCI,(Me,As(CH,),,AsMe,}, 5 , 1163 As2PdC26HIaC12 PdClz(Ph2AsCH2CH2AsPh,),5, 1162 ASzPdCz6%C& PdC14(Ph2ASCHzCHzAsPhz),5,1124 AszP~CZ~HS~NZSZ Pd(SCN),(AsBu,),, 5, 1141 As2PdCz8H~~N2Se2 Pd(SeCN),(Ph2AsCH,CH,AsPh,),5,1139 As,PdC,,H,,Ct,

27 1

Cumulative Formulu lndex

As2PdC36H30C12S2 Pd(Ph3AsS)2Clz, 2, 644 AS~PdC36H46C12

PdC1z{AsBu‘(C6H4Me-2)2}2. 5 . 1167 As~P~C~SH~ONZSZ Pd(NCS)z(AsPh,)Z, 5,1139.1140,1141 Pd(SCN),(AsPhs)z, 5, 1139,1140 AszP~C~SH~JZS~ 5. 1165 Pd12(2-Ph2AsC6H4SMe)z, As~P~C,ZH~,I PdI(Ph)(AsPh,),, 6,283 AsZPdZC6Hl8Br4 Pd2Br4(AsMe3),,5. l l h l As2PdZClzHzoCId Pd2C14(AsEt3)2r 5 , 1161 As~P~CIOH~~O [PtMe{C(0Me)Me) (AsMe&]+, 5,383 Asd’tCizH~NzSz Pt(SCN),(diars), 5 , 1163 AsZPtCizH30CI2 PtCl,(AsEt,)Z, 5,497 As~P~CI~H~~CI~ PtCl,(AsEt,),, 5,463 AszPtCizH3oIz PtIz(AsEt,),, 5,463 As2PtC24H551 PtHI(AsBu‘,),, 5 , 362 As2PtC24H56 PtH2(AsRut3)2,5,362 Asd’tC2sH4oPz Pt(CSZPh),(AsEt,),, 5,388 A~zPtC3sH34 Pt(CzH4)(AsPh3)2,5,410 A~J’tzCi2H3oC1, PtzCI~(~-Cl)z(AsEt3)~,5.490.497 AszP~zC~ZH~OC~~~Z {PtC1(2-PhzAsC6H4CHCH20Me)),,5,406 As2ReC8H14C14F4 ReCI,{ Me,AsCH{C(AsMe,)CF,CHF,}, 4, 170 As2ReC,Hl,C14F6 R e C 1 , ( M e z A s ~ ~ F F 4,, 170 ) , As2ReC10H,,C1,0 ReOCl,(diars), 4, 181 AS2ReC10H16C14 ReC14(diars),4, 170 R~CI,(ASE~,P~ 4.) 147 ~. A s ~ R ~ C ~ ~ H ~ ~ C ~ ~ P ~ ReCl,(arpho~)~, 4,169 As2ReC62H57P2 ReH3(PPh3)2(PhzAsCH2CHIAsPh2), 4, 150 A S ~ R ~ ~ C I 1%~ H ~ S B ~ ~ ~ ~ R~,B~,(AsO,)~(DMSO),, 4, 162 As2RhC2oH32CIZN2 [RhClz(2-MezNC6H4AsMe2)21’.4, 1024 AsZR~CZ~H~~CI~N~ RhC13(2-Me2NC,H4AsMe,)2, 4. 1U23 AszRhC21H2,C13N RhC13(AsMe,Ph),(py), 4, 1031 ASzRhC26H26ClzNO3 RhC1,(N03)(AsMePh2),. 4. 1022 As~R~C~~H~~CI~N RhC13(A~EtPh,),(py),4, 1031 ASzRhC36H30C12NO Rh(NO)C12(AsPh3),,4, 1070. 1072 As~R~C~~H~J~NO Rh(NO)Iz(AsPh,)z, 4, 1072 AS~R~C~~H,IC~~ RhHCI,(AsPh,),. 4. 1018 As2RhC36H32CI RhHZCI(A~Ph3)2,4.1018 As~R~C~~FI~~CI~N~ [RhCIz(AsMePhz)2(bipy))~. 4. 1U34

As2TiC36H30CL

As~R~C~,H&~N~ [RhHCl(A~MePh~)~(hipy)]+, 4, 1033 ASzRhC36Hb6C13 RhCl:{AS(C,Hjl)3)z,4, 1022 AS~R~C~~H&I~NZ [RhC12(AsMePh,)z(phen)]+, 4, 1034 As~R~C~SH~~CIN~ [RhHCI(As MeP hJ2( phen)]+, 4,1033 As~R~C~~H~~CI~NZ [RhC12(AsEtPh,),(bipy)]+, 4, 1034 As2RhC,8H39C1N2 [RhHCl(A~EtPh,)~(bipy)]+, 4.1033 A52RhCwHd& [ Rh(NO)(MeCN)2(AsPh3)z]2+, 4, 1072 As2RhC,0H38C12N, [RhCI2(AsE tPh2),( phen)]+, 4, 1034 As~R~C~~H&~~NZ {RhC12(AsPh2Pr)z(bipy)]+,4, 1034 As2RhC,,Hj,CIN, [RhHCI(AsPh,Pr),(hipy)]+. 4, 1033 AS~R~C~~H~ON~O~ [~h(ooC(CN)z~(CN)z}(AsPh,),l+, 6,339 As~R~C~~H~ZC~ZN~ [RhCI,(AsPh,Pr),(phen)] ’ , 4 , 1034 AszRhCn,H,qC1N2 [RhHCi(A~Ph2&),(phen)]+4, 1033 As2RhC,,H4,Br,N, [RhBr2(AsBuPh2),(bipy)]+,4, 1034 AsZRhC44&Br2NZ [RhBr,(AsBuPh,),(phen)]+, 4,1034 As,RhGeC,,H,,CI RhHCI(GeMe,)(AsPh,),, 4, 1020 AS~R~S~C~~H~~CI~ RhHC1(SiCl3)(AsPh3),,4, 1020 AsZRhSiC42H46C103 RhHC1{Si(OEt)3)(AsPh3)z, 4, 1020 AsZRUC,~HSOCINO R u C I ( N O ) ( A S P ~ 4,368,394 ~)~, AS2RUC36H30CI2 {RuCl,(AsPh,),},, 4, 379 As,RLIC,,H,~CI,NO, R U C I , ( N O ) ( A S P ~ ~ ) ( O A S 4,394 P~~), As2RuC3JI3oC13NPz RuCl3N(PPh3)2,4,419 As~RuC~~H~,B~~ RuHBr2(AsPh,)2, 4,461,462 AS~RUC~~H~~CI-,~ R u C ~ , ( A S P ~ ~ ) ~ ( M4,379,416 ~OH), AsZRUC~~H~~BI~OS RuBr,(AsPh,),(DMSO), 4,439 AS~RUC&~~C~OZP~SZ RuHCI(DMSO)Z(AsPh3),,4,458 AS~RUC~~H~~NZO~SZ [RuH( Nz)(DMSO),( A~Ph3)2]+,4,459 AS~RUC~~H~~F~OP~S~

RuIs,C,(CE,)z}(CO)(AsPh3)2.4,406 AS~RUC~~H~~CIP~ CH~ASP~~), RuHCl( P P ~ ~ ) ~ ( P ~ ~ A s C H ~ 4,453 As2RuC72H74N4

[Ru(octaethylporphyr~n)(AsPh~)~] +,4,471 ASZRUZC~~H~~C~~ [RuC12{AS(C~H~M~-~)~)(~-CI)~RUC~{As(&H,M~-~)~},]~-, 4,415 A s ~ S3,239 ~. As2TaCloH&I4 TaCl,(diars), 3, 642 As2TiCloHl6CI9 TiCl,(diars), 3,349 As2TiC,,H,,CI,0 TiCl,(diars)(H,O). 3, 349 A s ~ T ~ C ~ ~ H ~ ~ C ~ ~ T1Cla(A~Ph3)2,3,347

272

Cumulative Formula lndex As31rC7,Hs7P2

[Ir(PPh3){P(C6H4AsPh2-2)3}]+, 4,1135 As3NaSb6WZ,O,, [NaSb6As3W210s6]18-. 3,1042 A s ~ N ~ C ~ ~ H ~ ~ B ~ ~

NiBr2{MeAs(CH2CH2CH2AsMe2),), 5,67,125 AS~N~C,~H~~CI,N N~CI,{N(CH,CH,ASM~,)~}, 5,59 As3NiCI3H,,N2S2 Ni(NCS),{MeC(CH,AsMr~)~},5 , 133 As,NiC,,H,,CIP

["~C~{P(CH,CH,CH,ASM~~)~}]~ 5.66 ~

As3NiC16H36NP [Ni(CNj(P(CH,CHzCH,AsM~2)3}]+,5,135 As,NiCa,HazBrN [NiBr(N(CH,CHzAsPh2),)1+, 5,66 As,NiC4,H4,IN NiI{N(CH2CH2AsPh2),),5,41,43 As~N~C~~H~~N [Ni{N(CH2CH2AsPhz)3)]+, 5,43 As3NiC4,H4,N0 [Ni(COMe)(N(CH2CH2AsPh2),}]+,5 , 138 As3NiC47H471N Nil{NrCn2CH2AsPh,),}, 5,42 As,NiC,,H,,N [NiPh{N(CHzCH2AsPh2),)1', 5 , 138 As,NiC,,H,,NP [Ni (N(CH2CH2AsPh,),) (PPh,)]+, 5,41

[Ni(N(CHzCH2AsPh2j3}(PPh3)] ' ,5,42,43 AszNiSbC2.,HInC1

[Ni{Sb(C6H4AsMe2-2),}c1]+, 5.66 As3NiSbCZ5H3,,NS

[Ni{Sb(C6H4AsMe2-2)3}(NCS)]+, 5,66

As2ZrC8H12C13F4

ZrCI,{F,~C(AsMe,)=C(AsMc,)~F,), 3.366,370 AS3AgC17H23Br

AgBr{(2-MezAsC6H4),AsMe), 5.804

AS&CZ.JLO~ Ag(OAcj(AsPh,),, 5,803 As~A&oCZIH~~O~ Ag{(2-Me2AsC6H4)2AsMe}Co(C0)4, 5,804 As3AhMn3C26H2701~

{AuMn(CO),},{(Me2AsCH2j3CMe>, 5 , 905 As3CdzI CdzAsJ, 5,989 As~COC~~HZ~CI~

CoClj{MeAs(C6H4AsMe2-2)2), 4,774 AS&OCd3&

[CO(M~C(CH,ASP~~)~)(CO)~~+, 4,769,773

As$oC5.& CoH,(AsPh,),, 4,769 As3C02C24H23F603

A s ~ N ~ ~ C ~ ~ H ~ ~ P ~ [Ni2(triphos)(q3-As3)]+, 5 , 36 [Ni,(triph~s)(q~-As,)]~+, 5 , 36 As3Ni2C4,H4,1N [NizI{N(CH2CH2AsPhz)3)]+, 5,42 As~OSC~~H,~CI~ Os(AsMe,Ph),CI,. 4,577 As,OsC,,H,,Cl, Os(AsPr,),CI,. 4.577 As3OsC42H4, Os(AsEtPh,),H,. 4.576 AS~OSC~~H~~CI~NZ

Os{As(C6H4Me-4)3}3CIz(N2H4), 4,556 As3PaC18H1801 PaH,O,(PhAsO,),, 3,1182 As3PdCllH2,Br

[ P ~ B ~ ( M ~ A S ( C H ~ C H ~ C H ~ A5 ,S1166 M~~)~}]+, As~P~C~~H~~CI

[P~CI{M~AS(C,H~A~M~~-~)~}, 5, 1166 As3ReC42H50 ReH,(AsEtPh,),, 4, 1M AsJXhClhH2,CI

R ~ C I { P ~ A S ( C H ~ C I ~ ~ C H 2,635; ~ A S M4,~ ~ 1041 )~}, As3RhC,6H29C102

CO,{C~(CF~)~}(CO)~{M~AS(C,H,A~M~,-~)~}, 4,769 Rh(02)CI(PhAs(CH2CH2CH2AsMe2)2}, 4,1042 As3CrClo5H27C13 CrC13{Me2As(CHz)3AsMez) 1.5r 3,854 As3CrCl1H2,Cl3 CrCI3{M ~ C ( C H * A S M ~ 3,854 ~)~}, AS,C~C~~H~~CI, CrCI3(diars),,,, 3, 854 As&WG4H&Is RhC13(AsMezPh)3(HgC1,),4,1076 As3HgRhC39H39CIzF RhClz(HgF)(AsMePhz)3,4,1076 A~&RhC39H&13 RhC12(WgC1)(A S M ~ P ~4,~I076 )~, ASS~H~R~GIH~ZC~ZO~ RhC12(HgOAc)(AsMePh2)3,4, 1076

As,RhC1,H&IO,S

RhC1(S0,)(PhAs(CH,CH2CH2AsMe2)2}. 2,635 A s ~ R ~ C ~ ~ H ~ ~ B T ~

RhBr3{MeAs(C6H4AsMe2-2)2}, 4,1043 As~R~CI~H~~CI~ RhC13{MeAs(C,H4AsMe2-2),, 4,1043 As3RhCid%3N309

R~(NO,),{M~AS(C~H~A~M~~-~)~}, 4, 1043

A~3RhClsH45C13 RhCI3(AsEt3)?.4.I031 As3RhC24H33C13 RhCI,(AsMe,Ph),, 4,1031 As,R~C,,,H,~B~, RhBr3(AsMe2(CH2=CHPh)}3 , 4,1031

Cumulative Formula Index

273 AS3RhC36H63CI3 RhClS(AsBu3)3,4, 1031 A s ~ R ~ C ~ ~ H ~ ~ B ~ ~ RhBr,(AsMePh,),, 4, 1027 ASSR~C~~H~~CI~ RhCI3(AsMePh2),,4.1031 A s ~ R ~ C ~ ~ H ~ ~ B ~ RhHBr(AsMePh& 4,1027 AS~R~C~~H~~CIZ RhHCI,(AsMePh,),, 4,1026 A~jRhC45H5iC13 RhC13(AsPh2Pr),,4,1031 As3RhC4,H,,CI, RhHCI,(AsPh,Pr),, 4, 1026 ASqRhC72H6,P RhH(AsPh,),(PPh,), 4,924 As~RuC~~H~~CI~ R U C I ~ ( A S M ~4,379 ~P~)~, As~RuC~~H~~CI~NO RuC12(NO)(AsMePhz),,4,374

RuC12(AsPh3)3(Oz),4.416 As~RuC~~H~~CI~ RuCI,(AsPh3)3,4,379,416 As~RuC~~H~~CI~O RuCI>(A~Ph3)2(0ASPh,). 4,416 A~~R~zCWH~&I,

[RU~CI~{AS(C~H~MC-~)?}J]-. 4,415

-%CUCZOH32

[CoCl,(diars),]+, 4,773 AGGoH3dz [Col,(diar~)~]+. 4, 773 As~COC~~H,~NO [Co(NO)(diars),]+, 4,773 As~COCZOH~?~~ [C~(O~)(diars)~ 4,773,784 ]+, AS~COC,~H,,O&I~ Co(OCI,),(diars),, 4,772 As~COC,,H~~CI [CoHCl(diars)2j+,4,773 As~COC~~H~~

[Col4,(diars),]', 4,773,784 AS.,COC~~H~,O [CoH(A,O)(diar~),]~+, 4,773 A~4C0CzoH3e.02

[C~(H,O),(diars)~]~~, 4,772,784 As~COCZIH~~O~ [Co(C03)(diars),]+, 4,773 As~COCZZH~~NZS~ Co(NCS),(diars),, 4,769 As~COCZZH~@Z [CoMe2(diars)2]+,4,773 As CoC H C1 [CoCl,{ ~MezAs(CH7)3AsPhCWz}z}]+, 4,773.784 AS~COCI~H~~OZ CO(O~){{M~~A~(CH~)~A~P~CH~}~}, 6,321

,

[Co(O,){

{M~,As(CH,)~A~P~CH,},}~+, 4,773,784

ICo(R,R-C,H,,As,)(O,)]+, 2,319 As~COCNH~ZOZ [Co{(Me2As(CH2)3AsPhCH2}z}(Hzo),)3+,4,784 As,COC,&~B~NO [Co(NO)Br(diars),]+, 4,666 As~COC~~H~~CINO [Co(NO)Cl(diars),]+. 4,658 IC~(NO)Cl(diars),]~+, 4,658 As~COC~~H~~NO [Co(NO)(diars)z]2+,4,658,661,664 AS~COC~~H~~N~OS [Co(N0)(NCS)(diar~)~]', 4,661,664

As3TiCI,HZ7CI4 TiCI4(MeC(CH,AsMez),} 3.344 As3TiC4,H3,C14 TiCI4{MeC(CH2AsPhJ3},3,338 As3ZrCllHZ7Br4 ZrBr4{M ~ A S ( C H , C H , C H ~ A S M ~3,383 ~)~}, As~A~CZOH~Z [Ag(d~ars)~]',5 , 804 A%A&C~~HWI, {Agl(AsPr,)},, 5.803 AS~AUC~~H~, As~COC~~H~~CIOB [Au(diars)2]' ,5,884 C0(0AsMePh~)~(C10~), 2,498 As~COCS~H~~NS ASAL~CZ~KOI~ [CuI(AsEt,)],. 2.685 IColNCS)(Ph,AsCH=CHAsPh,),lf, 4,769 AS&.HisN6 ASJCOC~H~OC~~~IZ A s ~ ( N M ~2,) ~17,5 CO(CIO~)~(OASP~~)~,~,~OO AS~COCIZHZS AS~COC~Z&I [Co(MeZAsCH=CHAsMe2),)+, 4.769 [ C O H ( A S P ~ ~ )4,769 ~]-, As~COC~~H~~B~~ As~COZW~OW'JOI~Z [CoBr2(Me2AsCH=CHAsMez)3]+.4,773 [AS~W~~(NH~)~~~O{CO(OHZ)}Z]~~-, 3, 1049 As~COC~~H~~CI As4CrCi5H&l2 [CoC1(Me2AsCH=CHAsMe?)21+.4,769 [CrC1z(As(CH2CH2CHzAsMe2)3}, 3,855 As4CrC,,H3,C1, As4CoCizH3~ [Co(Me,AsCH,CH,AsMe,)J, 4,769 CrCI,{ AS(CH,CH,CH~ASM~,)~}, 3,854 As,CrC,,H,,Br, As4CGzH3dAO 1 2 Co(CI04),(OAsMe3),, 2, 500 CrBr,(diars),, 3, 734 AS~COC,,H~~B~~ AS~C~C,~H,,CINO [CoBr2{1, ~ - ( M ~ , A S C H , C H ~ C H , A ~ ~ ~ ) 4, ~ C ~ ~ , } Cr(NO)Cl(diars),, ]+, 3,830 774 [Cr(NO)Q(diars),]+, 3,830 As4CrCZoH3,Cl2 A~4CGsH340z [Co(O,){ 1,2-(Me,AsCH2CH2CHzAsMe)2C6H4}]+, 4, CrCl,(diars),, 3,734 774 [CrC12(diars)z]+,3,854 AS~COC~~H~~BT As~CGOH~ZIZ 4, CoHBr{1,2-(Me2AsCHzCHzCH2AsMe)2C6H4}]+. Cr12(diars)2,3,734 774 AS~C~C~~H~~CI~ AS4C0C18H36

[CoH,{ 1,2-(MetAsCHfCH2CHZAsMe),C6H,}]',4,

774 As4CoCzdh [Co(diar~),]~',4.772 As4CoC,oH3,BrN0 [C~Br(NO)(diars)~]+, 4,773 AS4COC20H32C12

CrCl~(PhzAsCHzCHzAsPh,)z, 3,854 AS~C~C~~H~~BT~O~ CrBr,(OAsPh,),, 3,754 A s ~ C ~ C ~ ~ H ~ ~ C ~ ~ ~ ~ ~ Cr(C1O4),(OAsPh3),, 3,754 AS4CUClZH36C12012 C~(Cl0,)~(0AsMe~),, 2,500 As,CGOH~Z

As4CuC20H32

Cumulative Formula Index

[Fe(0A~Me,)~(C10,)]+, 4,1183,1237 As4FeCi,H3,S4 [ F ~ ( S A S M ~ ~ )4, ~ ]1240 ,+, A s ~ F ~ C ~ ~ H ~ ~ C ~ ~

[Fe{As(CHzCHzCHZAsMe2)3)C12]+, 4.226

As4MoC52H44Clz0, MoC1,(CO)z(dparn),, 3,1281 As~MoC~~H~~N~ Mo(Nz)z(Ph2AsCH2CH2AsPh2)2,3,1269 As~MoC~~H~~N~P~ Mo(N,)(triphos)(diars), 3,1268 AS~MOZH~OI~ [MO,(HASO,),]~-~ 3,1303,1309 As~Mo~O~S~~ [ M O ~ O ~ S ~ ( A -., ~ 3, , S1363 ~~)]~ AS&h0&14 [(MO~O,S,),~AS,S,),~~-, 3,1363 AS~MOI~CZ~HZSO~~ M o , ~ O ~ ~ ( H ~ N C , H ~ A3,~1053 O~),, As4Mo,,H,0,, [As4Moy205OH4j4-,3,1043 As4NbCzoH3,Br4 NbBr,(diars),: 3:642 As~N bCzoH32C1, NbCl,(diars),. 1,88; 3,644 [NbCl,(diars),]+, 1,88;3,599 As~N~~CZ~H~~CI, Nb,Clh(diars)213.656 As,N~C,~H,,B~, NiBr(Mc,AsCH=CHAsMe,),, 5, 119 As4NiC1ZH36C12012 Ni(CI04),(OAsMe3),. 2,500 AS~N~C,,H,~C~

274

As4FeC20H32C12 [ F e ( d i a r ~ ) ~ C l ~4,1183.1187 ]~+, AS~F~C~ZH~OC~~OIZ Fe(C104)Z(OAsPh,),, 2.500 As4FeZCl~H,~Oh 3,244 {F~(CO),},(ASM~)~, As4HfCZOH3,Cl4 HfCl,(diars),, 3,383 A~,H~CZZH~ZNZSZ Hg(SCN),(diars),, 5,1084 [N~CI{AS(CH~CH,CH,ASM~~)~}]+, 5,66 As4NiCZoH3, A s ~ H ~ C ~ L ~ HgBrz{(2-Ph2AsC6H4),As), 5.1084 Ni(diars),. 5,9 As41nC20H32C12 [Ni(diars),lz+. 5.66,289 [InCl,(diars),]+, 3,160 As4NiC,oH,2C1 [Ni(diars),Cl]+, 5-67 AdnC7zHso [In(AsPh3),I3+,3,160 AS~NIC~~H~~CI~ [NiCl,(diars),]+, 5,5.289,299 A~JrC~~H4402 [Ir(AsPhMe,),(O,)]' ,2,320; 6,341 [NiC12(diars),12+.5.289 AS,~~C,,H~~NOP, As,NiC:,,H,,I, ~ H ~ ) ] + , NiI,(diars),, 5,124,125 [Ir(NO){ 1, ~ - { ( P ~ z A ~ C H , C H , ) Z P C H , } Z ~ 4, 1114 As4NiCZ1Hn2N [Ni(CN)(diars),]', 5 , 118 AS~I~C~&~'Z [Ir{l,4-{(Ph2AsCH2CH2),PCH,),C,H4)~+.4,1113 As4NiC22H3202 As,IrC,,H,,P, Ni(CO),(diars),, 5,11 "_ .... [IrH,{ l,4-{(Ph2AsCH2CHZ)2PCH2)2C6H4}]+, 4,1114 AS~N~C~~H~~BT As41rC6SH640P2 [NiBr(MePhAsCH,CH2AsPhMe),l+, 5,119 [Ir( CO){ 1,4-{ (Ph2AsCH2CH2),PCH2)2C6H4}]+, 4, As4NiC3,H4, 1114 Ni(AsMe,Ph),. 5.9 As4IrC,,HS7P A s ~ N ~ C ~ ~ H ~ ~ C ~ ~ IIr(PPh3){ AS(C6H4ASPh,-2)3}]+. 4,1135 NiC12{2,2'-(MeAs),biphenyl},, 5,124 As4NiC44H40N8 AsJrC7.HhlPd I;H(AsP~,),, 4,1119 [ N ~ ( M ~ P ~ A S C H , C H ~ A ~ P ~ M ~ ) ~ ( T C5.119 NE),I", AS~N~C~~H~~NO, AS~KW~OOI~O [ICAS~W~~O 3, ~1042 ~~]~~-, [Ni(OAsPh~Me),(No,)]', 5 , 65 As4MnC12H36C120i2 Mn(C104)2(0AsMe3)4,2,500 [Ni(0A~Ph~Me)~(C.10~)]" , 5,51,64 A s ~ M ~ C ~ ~ H ~ ~ C ~ ~ ~ As4NiC54H41Br [Mn(CIO4)(Ph3AsO),]+,4,47 INiBr{As(C,H,AsPh,-Z)~~l+, . .. 5, 66,133 A~4NiC5~H4~C1 As~M~C~ZH~OCIZO~~ Mn(C104),(OAsPh,),, 2,500 [N~CI{AS(C~H,ASP~~-~)~)]+, 5,66 AS~MOC~OH~~CINZO~ As,NiC,,Hm [MoCI(NO),(diars),]+, 3,1272 Ni(AsPh,),. 5,9 AS~MOC~~H~~CI~ AS~NIC~ZH~OCIO~ MoCl,(diars),, 3,1284 [Ni(ClO4)(0AsPh3),]+, 5.64,152 AsaMoCZoH32C14 AS~NIC~~H~~C~ZO~~ [MoCl,(diars),]+, 1,88; 3.1354 Ni(C104)2(0AsPh3)4,2,500 As40sC2oH32ClNO As~MoCZOH~ZNZO~ [M~(NO)~(diars)~]~'. 3, 1273 [Os(NO)(diars)2C1]z++, 4,547 AS*MOC~~H>ZCINO~ AS~OSC~~H~~CIN~ MoCI(NO)(CO)(diars),, 3,1276 [Os(N,)(diars),Cl]+, 4,555,565 As4MoC,,H3,CI0, AS~OSC~~H~~CIN~ [MoCI(CO),(diars),] ' , 3 , 1281 Os(N,)(diars),CI. 4.565 AS,M~C~~H~~B~,O~ A~,OSC~~H~~CI~ MoBrz(CO)z(dpam)z,3, 1281 [Os(diars),C12~-.4,579

Cumulative Formula Index

As~TcC~OH~~CI,

A~4RhC~9H5sC102S

[RhC1(4-02SC6H4Me)(Ph2AsCHzCHZAsPhz)2]f 4, 1040

-_

""

[Pd(NCS){ A S ( C ~ H ~ A S M ~ ~ -5.~ 1141 )~}]+, AS4PdC29H36NS [Pd(NCS){1,8-(Me2As)2C10H6}2]A. 5. 1141 As,P~CS~H~,CI, [PdCl2(As(C,jH,A~Phz-2)3}]~+, 5, 1123 As~P~~C~~H&I~O Rh,CI,( pH)(~-CO)(dpam),.4,911 AsJ'~CZOH~Z [Pt(diars),12' ,5,498 As,PtC20H32CI, [PtC12(diars),12I , 5 4 9 8 AsqPtC24H3oCI [Pt{(2-MezAsC6H4)lAs}Cl]i 1,321 A@fC72H60 Pt(AsPh3)4,5,440,463

.

[ReCl,(diars),]+, 4,162 [ReCl,(diars),]+, 4, 193 AS~R~C~~H~,CI, 4,162 Re3C19(d~ars)Z, A S ~ R ~ C ~ ~ H ~ ~ C I ~ ReCl,(diar~)~, 4, 136 4,148 [ReCIZ(d~ars)z]+. As4ReCS2H5I ReH3(Ph2AsCHZCH2AsPh&,4,150 As~~C~ZHV, Re2H8(A~Ph3)4r 4, 174 AS4Re3C68H66CbP2 Re3C19{(PhzAsCHzCH2)2PPh}z. 4,162 As~R~C~OH~~CINO~ [RhCI(NO,)(diars),]', 4, 1040 As~R~CZOH~ZCI~ [RhClz(d~ars)z]", 4, 1039, 1040 A~4RhC20H3204S [Rh(S04)(diars)2]+, 4, 1040 As4RhCZoH33CI [RhHCI(diar~)~] , 4 . 1037 AS~R~C>,H,,CIO~S [RhCI(OzSMe)(diars),]+. 4. 1040 As4RhC26H36C1N04S [RhC1(4-0,SC,HqN02)(diars)z]T. 4. 1040 AS4RhC26H37CIOzS [RhCl(02SPh)(diars)2]+,4,1040 AS~R~C~~H~~CIOZS [RhC1(4-0,SC6H4Me)(diars)z]+. 4, 1040 As4RhC3zH440z [Rh(AsPhMez),(O,)]', 2,319, 320;6,239 Ai4RhC52H44S2 [R~S,(P~~ASCH=CHASP~J~]+~ 2,533; 4,1037 As,RhC,,H,,CI [RhHCl(Ph,AsCH=CHAsPhz)z]+,4.1037 ASqRhC5ZH46 [RhH2(PhzAsCH=CHAsPh,),I+, 4, 1037 As~R~C~~H~~CIO~S [RhCl(02SMe)(Ph,AsCH=CHAsPhz)2]+, 4,1040 ~~

. AS,RUC~'~H,~CI R u H C ~ ( P ~ ~ A S C H ~ C H ~4,453 ASP~~)~,

Ru2CI5(PhlAsCH2CHzAsPhl)2,4,415 As4RuzCszHsaIaNzOz {Ru12(NO)(AsMePhz),},, 4,374 AS4RU2C54H48CL402

{ RuCI*(CO)(Ph,AsCH2CHzAsPhz)}z, 4,413 As~RuzC~ZHC.OC~~~Z [(RuC121AsPh3)z)z(~-OZ)12+, 4,401 As&zC,&oCIs RuZCI,(A~Ph3)4,4,379 AS4S4 A s ~ S3,239 ~.

ITaBr4(diars)2]+, 1, 88; 3,594.599 As4TaCLnH32C14 TaC14(diars),, 3,644 [TaCl,(diars),]++ 1,88; 3,599 As~TcCZ~H~~CI~ [Tc(diars),CI,]', 1.89; 6,978

Cumulative Formula Index A S ~ T ~ C ~ ~ H ~ ~ C I ~ TiCI,(diar~)~, I, 88; 3.348, 356, 357 AS~T~C~,H,~I~ TiI,(diars),, 3,349 A s ~ T ~ C ~ ~ H ~ ~ C ~ ~ TiC14{1,8-(MeZA~)2C10H6)2, 3.349 As~VCZOH~ZC~~ VC14(diars),, 3,498 AS4VC7zH6005 [VO(OAsPh&I2+, 3,522 As4WCznH3212 W(diars),I,, 3, 1006 As~WC~~H,,B~O, [W(CO)2(diars)2Br]+,3, 1005 As~WCS~H~~B~~O~ W(CO)3(dparn)2Brz,3, 1007 As4ZnCizH3604 [Zn(OAsMe,),lZ+, 2,499 As4ZnC20H3204 [Zn(diars dioxide),Iz+, 5. 966 As4ZrC20H3zC14 ZrC4(diars),, 3,383 As5M&i&sCIzOi, Mg(C104)z(Mt&o)s, 3 , 9 AssMgC15H4sOs [Mg(Me3AsO),lZ’,1,40 AssMnC,sb.Os [ M ~ ( M C ~ A S O )4,40 ~]~+, As5MoZC19H1504

{ M O C ~ ( C O ) ~ ) ~ ( A S 3,241 M~), [Ni(OAsMe3),lZ+, 2,499; 5 , 3>64.159

276

As~R~zCio&oCLOz [{RuCL(AsPh), 1Z ( P ~ Z ) ] ~ 4,416 +, AS6SCC78H72CI;Oi8

SC(C~O~)~{P~ZAS(O)CH~CH~AS(O)P~,),. 3.1065 AS~T~,C,~H,~CI~

(TiC14)2(Ph2AsCH2CH2AsPhz)3, 3,347 AS6Zn4CiaH36S13 Zn4S(S2AsMe2)6,2,522 AS~C:O~C~&I~~O~ [ ( C o ( H , O ) ( d ~ a r s ) ~ } ~4,772 ]~+, AS&fOzC&560~ Mo,(CO),(AsPr)s. 3,244 As9Ni2C48Hb90 NiZ(H20){PhAs(CH2CH,CH2AsMc,),) 3 , 5 , 128 A~izCO&did6 Co3{MeC(CH2;\sPh2),},I6, 4,769 AuA13HIZ Au(AIH&. 5 . 891 AuAs [AuAsIZ-. 5,881 AuAsC,H,CI AuCI(AsMe3). 5,870 AuAsClzHlo (AuAsPhz),, 5. 881 AuAsClsHl ,Br AuBr(AsPh,). 5.882 AuAsClsHl,CI AuCI(AsPh,), 5. 8711, 875 AuAsCl8H1,C1S Au(Ph,AsS)Ct. 2,644 AUASzC28Hdis Au(C6F5),(diars), 5. 898 AUASZC~SH~~P~ [ A u ( ~ - E ~ ~ P C ~ H ~ A 5,884 SE~~)~]+, AuAsZC~~H~~ [Au(AsPh,),]’. 5 , 871 AuAs4C20H32 [Au(dian),l-, 5.884

[Ni(diars){MeAs(C6H4AsMez-2)2>I”,5,66,67, 128 AS6COCisH4z [Co(Me2AsCH=CHAsMe,),13f. 4.773 As6CoCmH48 [Co(diars),13+, 4,773 AS~COC~,H,~ [CO{M~AS(C~H,ASM~~-~)~}~]~’ ,4,772 , ., As~COC~ZHS~ Au{Ph,B(~N=CHCH.=~H)Z}Cl,, 2,254 fCo{I ,8-(Me2As)2CloH6}3]2+,4.772 AuRC~~H~~P As6CozCszHsi Au(BPh2)(PPh3), 5,903 { Co{M~C(CH,ASP~,)~)},( pH),, 4,769,773 As6CrCzzH54Iz AuB;Hiz Au(BH,)~,5,891 [Cr12{MeC(CH2AsMez)3}2]+. 3,856 AuB~CZOHZZP As6IrZC8OH72C1202 A U ( ~ C ~ B ~ H ~ ) 5,903 (PP~~). Ir2Cl,(CO),{PhAs(CH2AsPh,),l,. 4, 1164 AS~ITZP~CSOH~~CI~O~ AuBsCISHZJ’ Au(BSH,)(PPh3), 5,903 [Ir2PdC1,(CO)2{PhAs(CHI,AsPh2),},]+ 4, 1164 AuB~C~H~~NS? AsSNiCZ2HS4Cl2 5 , 133 N~C~,{ M~C(CH,ASM~,),]~, A ~ ( S Z C N E ~ ~ ) ( CI~) ,B5,903 ~HI AuB&,H~~NP As,NiC,,H,,O, [N~{(OASP~,),CH,},]~~, 5. 161 Au(C2BqH Irrp~)(PPh3),5 , 903 A s ~ N ~ C ~ ~ H ~ ~ ~ ~ AuBisGHzz [Ni{(OAsPhzCH2)z}312+,5, 161 5 - 903 [An(CzB9Hll)z]-~ [ A ~ ( C z B g H i i ) 2 ]5,889 ~~. AS6Ni2C38H58N4 AuBrCl Ni2(TCNE){PhAs(CH2CHzCH2AsMe2)z},, 2,263; 5 , [AuCIBrl-. 5,871; 6.852 128 AuBr, As6NiZCs4Hs4IN2 [AuBr2]-. 5,864,871 { Ni[N(CH2CHzAsPhz)3]}z(u-I). 2.681 AuBr, AS~N~ZCS~HS~IZN~ [AuBr31p, 5,886 [NizI{N(CHZCHzAsPhz)3}2]~, 5,43 AuBr, AS~OSC~SH~~NZSZ [AuBr,] ,5,877,889, 895; 6,852 Os(SCN),(dpam),, 4,579 AuCClO As6PdC38H46 [ P ~ { M ~ A S ( C ~ H , A S M ~5~. I-I66 ~)~}~]~+, AuCI(CO), S, 869, 885 AuCH6P A~gRhC34H46 [ R ~ { M C A ~ ( C ~ H ~ A S M4, ~1U44 ~ - ~ ) ~ } ~ ] ~ + AuMc(PH,), 5.867 AuCN AS~R~ZC~SH~ZC~~ Rh,Cl,(PhzASCHzCH,ASPh,), 4, 1025 AuCN, 5,885 AuCO AS~RUC~~H~~CIZP~ R u C ~ ~ ( P ~ ~ A S C H ~4,380 ASP~~)~, AuCO, 5 , 864

Cumulative Formula Index

277

AuC,BrClN, [Au(CN),BrCI] , 5 8 9 8 AuCzHz Au(CzH,), 5,864 AuCZH3ClN AuCI(MeNC), 5,885 AuC~H, A u ( C ~ H ~5,864 ), AuC~H~CIS AuCl(SMe2), 5,870 AuC,H,CISe AuCI(SeMe,), 5,874 AUCZH~CI~S AuC13(SMe2),5 , 870; 6. 98 ALIC~HSNZO~SZ [Au(S0,),(~n)]~-,5,892 AuC2H8N4S, [Au(HzNCSNHz),]+. 5,864, 873; 6,785,818 AuC2H8N4Se2 [Au{SeC(NH,),},]+, 5 , 864 AuCz12Nz [AuIz(CN),j-, 5,891 AuCzNz [Au(CN)J, 2 , s . 10. 12: 5.864.868,871,885,898,6, 784,818,822,823, 829,852.869 AuC,N,O, [Au(CNO),]-, 2 . 7 . 13: 5 . 885 [Au(NCO),] , 5.879. 894 AuCzNzSz [Au(SCN)z]-, 5,864, 873,6.97 AuCZOZ Au(CO),, 5,864 AuC~H~NZ Au(CN)(MeCN), 5,899 Au(CN)(MeNC), 5,868. 885 AuC3H,0,S AuSCHZC02Me 6.102 AuC,H,NO,S AuSCHZCH(NHZ)COZH. 5.876 AuC3H,03Sz [AuS(CH~)>SC)~]-. 6 , 97 AuC31160,S [ AuSCH2CH(OH)CH,SO,]-, 5.876 AuC~H~O~S~ [Au(SCH,CH(OH)CH2S0,)]-, 6,759 AuC3H9C103P AuCI(P(OMe),}, 5 , 870,882 AuC3H9CIP AuCI(PMe,), 5,870,872 AuC4Br2N,S2 [AuBr,{S,CZ(CN),}l-, 5.893 AuC,H,O,S IAu{OZCCH(S)CHZCOL)Iz~~, 6,759 [AuSCH(COZ)CH2CO2J2 5 . 876 [AuSCH(C0,)CH,C0,12 AuC4H6CINz Au(k=CMeNtICtI=tf t)CI>5.881 AuC,H,CIN,O,

. ~

COC 7-J

Au(SO,Me)(PMe,), 5,879 AuC~H~~P AuMe(PMe,). 5.868 AGH,zS, [ A U ( S M ~ , ) ~ ]5,871 +. AuC~H 1 &1N, [AuCl(dien)lz+,2,47;5,896 A U C ~1 H3c14o,s, [AuCl,)[~l(DMSO)J, 2,489 A u CH ~ 1dCIN, [AuCl(dicn-H)]+,2,47 [AuCl(dicn-H)]j ,5,896 AuC4Hl4N30 [ A ~ ( d i e n ) ( O H ) ] ~5,896 +, AuC4A16C12N, [AuCl,(en),] * 5.896 AUGHi6N4 [Au(en)zl”’. 2,902.5,896 AuC4N4 [Au(CN),J-, 5,898; 6, 11,784 AuC4NdS2 [Au(CN)>(SCN)Z]-, 5,892 AuC4N4S4 [Au(SCN),]-, 5,892,6.98,852 AuC404S4 [Au(S2C202),1-, 5, 893 AuC,Fl,CI,N AuCldpy) 6,97,98 AuC,H, ,CIN A u C I ( H S ~ H , } 5,869,880 , AuC6H,C13 [AuCl;Ph]-. 5,870 AuC& Au( C,H,), 5,864 AuC H N [Au( &;I=CHP;HCH=CH)~]+,5,881 AuC,H,N,S,P Au(CN)(SCN),(PMe,), 5 , 892 AuC6Hl [Alt(CNEt),]-, 5,868 AuC6HI1O5S Au(thioglucose), 5 , 876; 6,759 ALIC6H1,Cl,NzS2 [AuC1,{SzC,(~\;Mez),}]+,5,893 AuC~H,~N,S, [ALI(S~NHCH~CH& H)J+, 5,874 AuC6H15CI12P AuCIIZ(PEt,), 5,897 AuC6H15C1P AuCI(PEr,). 5 , 876,877 AuC,H, 5N03P Au(NO,)(PEt,), 5,877 AuC, HlhC1ZT\i2 {Au(TMEDA)Cl,]+, 1,314 AuC~H,~P;S AuEt,(SCH,CH2NH,), 1,417 A u C 8 IGN& [Au{SC(NHMe),},]+, 5,874 AuC6H180PSi Au(OSiMe,)(PMe,), 5 , 872 Auce.flis0e.P~ 5,868 [AU{P(OM~),)~]’, AuC6H18P AuMe,(PMe,), 5,897 AuC604S4 [Au( SC(O)C(O)S} 2,645 AuC,F,N [Au(C,F5)(CN)]-’. 5 , 885 AuC,H,ClN AuCl(PhNC), 5,898 AuC7H5C13N AuC13(PhNC), 5 , H98 A~C,HIOF~OZ I

,

AuC 7HIOFdh

Cumulative Formula lndex AuMe,(CF,COCHCOMe), 2,392 AuC~H~~CIN AuCI{C(NMe,)Ph}, 5,869 A~C7Hi30z AuMe,(acac), 2,392

AUCIIHSFSN Au(C,F,)(PhKC), 5,885,898 AUC~~H~~CI~N AuCl3(7-methy1-4-azafluorene), 5, 870 AUCi3Hi&% Au{S,C,(CN),}( SzCNBuz),2,602 AuC14H1zBr3Nz AuBr,(2,9-dimethyl-l ,IO-phenanthroline), 5,896

AikCHzCONHPh, 5,876 AuCsHizN404 [Au(DMG),]+, 5,886 RuCsHlsClzP AuCI(PBu',Cl), 5, 872 AuC~HZ~NS [AuEtz(EtSCHzCHzNHZ)]+,1,417 AuCsN4S4 [AU{S~C,(CN)~},]-, 2,602: 5. 893 [Au{SZCZ(CN)Z}Z]~-, 5,888 A~cgHioN& [Au(S*CNEtz){SzC,(CN),} I-, 5.888 AuCVH2,NPSiz Au{N(SiMe,),)(PMe,), 5,880 AuCIOHBBrZN2 [Au(bipy)Br,]+, 1,312 AuCioH&lZNZ [AuCl,(bipy)]+, 1,314; 5,896 AuCloHgCI,NS Au(8-methylthioquinoline)C12.2.801 AuGoHioNz [Au(py)z]+,5,871,880 A~CIOHIZNZO~ [Au(fiCOCHMeCHz~O),]-,5,879 AuC10H17BrP AuBrMez(PMezPh),5,391 A~CI,HZON,S~~ Au(Se,CNEt,),, 5,888 AuC H N [A:{&eH2}2] I , 5,871 AuC~~F,,CI [AUC~(C~F,)Z]-, 5, 870 AuCIZN8BrZNz [AuBr,(phen)]', 5,896 AuClzH6Br3N, AuBr,(phen), 5,896 AuCl2HSCl2N2 [Au(phen)CI,]+, 1,314 AuCI2HsCI3SZ AuCl,(thianthrene), 5, 870,893 AUCIZHSN4 [Au(CN),(bipy)l -5,885 AuClzH&lzNz 5 , 895 AUCIZ(~-P~N-NC~H~), AuCnHioC13Nz AuC13(PhN=NPh), 5,895 AuCizHioP (AuPPhz),, 5,881 AuCizHizN4Sz [Au{2-pyC(S)NH,)z]+, 5,874 A~CizHdz AuMedPhCOCHCOMe). 2.392 A~C,,H~-~N, AuMe,{HC($lN=CHCH=CH),). 5 . 897 AuC, zH1,ClzS AuCl,Ph(SPr,). 5,870 AUCizH2zoioSz [Au(thioglucose),]~,5,876 AuC,,H,,CIP AuC1(PBut3),5,882 AuC13H5BrZF5N AuBrz(C6F,)(PhNC), 5,898

AuCI,{S(CH,Ph),}, 5.886 AuCJ l14C13Nz AuCIq{4-(4-MeCJ14N=N)C6H4Mc}, 5,870 A~C~JHIJA [Au(PhC(S)NH,),]+, 2,647 AUCijH16PS Au(SPh)(PMe2Ph), 5,875 AUCI~HZZN [Au(~CfIzCHzNCMeCHCMeNCHzCHzNCMeCHcMe)13+,2,902 AuC~~H~~QN~ [AuCl(terpy)l2-, 5,870, 896 AuC15Hz.dPz AuI(Z-Er,PC,H,CHZPE~Z), 5,884 AuC inH~Nz02

278

[Au{2-(2-OC6H4CH=NCH2CH2N=CH)C6H40)jf, 5, 891 AuC16HzzP2 [Au(PMe,Ph),]', 5,871 AuC~~H~~CINP AuC1(2-~yFPh~), 5,881 AuC18H,zC13NZ AuC1,(2,2'-biquinolyl), 5,896 AUCisHi?NzOz [AuQ3-quinolinolate),]+, 5, 891 AuClaH15CI03P AuCI{P(OPb),). 5,869,882 AuC, nEl,,ClF AuCI(PPh,), 5,869.870,871,882,884 AuCIEHISCIPS AuCI(SPPh,), 5,870,874 AuCl8HI5CI3P AuCIs(PPh3). 2, 1026; 5,870,897 AuC,sH1,N03P Au(PPh,)(NO,). 1, 171 AUCi8HisN3P Au(N3)(PPh3),5,879 AuCIEH~~NZS~ [ A U ( S ~ C N B U ~ 2,602 )~]+, AuC 19H1 ,CIN,PS, AuCI{S,C,(CN),)(PPh,), 5,893 AuCI9Hl5NOP Au(NCO)(PPh,). 5,879 AuCI~HI~NP Au(CN)(PPh,), 5.885 AuC,gHj,NPS Au(SCN)(PPh,). 5,873 AuC~~H~~NPSC Au(SeCN)(PPh,), 5,873 AuCivHi& S I Au{-}(PPh,), 5,879 AUC,~H~~P AuMe(PPhd. 5866,872

AUC&NPS

Au(SCN)(P(GHiiM, 5,901 AuC2,,HI5CIP AuCI(PhzPCECPh), 5.882 AuC& F N P Au(N*,CF,)(PPh,), 5,879 AuCmHisFAU' Au(OzCCF3)(PPh3).5,872 AuC~OH~~F~NOP

.

.-

279

Cumulative Formula Index

Au{ON(CF,)Z}(PPh,), 5 . 872 AuCZOHI~N~P Au(fiCH=NN=CH)(PPh,), 5,880 AUCZOHI@ZP Au(OAc)(PPh,), 5,972 A~CzoH3409PS Au(PEt3)(S-2,3,4,5-tetraacet~l-l-~-~-thioglucose), 5, 876 Au(S-2,3,4,6-tetraacetyl-l-~-glucosylthio)(PEt~), 6,759 AUC21H24P

AuMe,(PPh,), 5.866,897 AuCziW36OioPS Au(S-2,3,4,5-tetraacetyl-l-P-0-thing1ucose){PEt,(OPr')}, 5,877 A~CZZHISNZPSZ Au{SzC,(CN),}(PPh3). 5,886 AuCzzHzoNJ' Au(fiCH=CMeN=cH)(fPh,), 5.880

AUCZ3HI7IP AuI(P=CPhCH=CPhCH=~Ph), 5,882 AUC,~H,,N,P Au(fiN=CMeCH=cMe)(PPh3), 5,881 AUC~~H~~NPS~ Au(SzCNEtZ)(PPhj),5, 879 AuC,,H,oO,PS Au(SO,Ph)(PPh,), 5,879 AuCZ~HZOP AuPh(PPh3), 5, 872 AuCZ~HZ~CIN~P~ AuCI{P(Me)N=PPh,NPPh2$iH}, 5,882 AUCzsH46P0z A ~ M ~ , ( ~ C ~ C ) ( P ( C ~2,392 H,,)~).

c

A U z 6n2 6P2

[Au(PMePh,),]+, 2, 1026; 5,871,883,884 A u C ~ H ~ J ~ P Au(bipy)(PPh,), 5,881 AuC3oHi JIFioP AUCl(C6F,)z(PPh,), 5,870 AGOHZ~N~OZPZS~ {Au(sCN),(NCO)},(dppe). 5.892 AUC3zHi6Ns Au(phtha1ocyanine).2,868 AU c36H 30c1P2 AuCI(PPh,),, 5,883,881 AuC,~H,,PS~ Au(SiPh3)(PPh3).5,903 AUC36H3oPz [Au(PPh3),]', 5,871,884 AuC36H30PZS2 [Au(SPPh,)Z]' ,5,871 AUCJ~HJOPJS~ Au{SP(S)Ph2}3,5. 894 AuCd,iCLOzP, [H(OPPh,),] [AuCI4]. 2 348 Au c36H4 4 N4 [Au(octaethylporphyrin)]A-2,842 AUC36H66P2 [Au{P(C6Hii),}z]+, 5,874,883,884 AuC~~H~OCIPZ AuCI{C(PPh3),}, 5, 886 AuC~~H~~NP~S Au(NCS)(PPh3)2.2. 234 Au(SCN)(PPh&. 5.865.873,883,884 AuC,,HzsCI4N, AuCI,(C,Ph,)(phen), 5. SY6 AuC~~H~~CIP~ AuCl(triphos), 5 , 869 AuC,,H,,CIN, AuCl(tetrapheny1porphyrin). 2.842; 5,897

AuHCI30

AUC,,H,,N, [Au(tetraphenylporphyrin)]+,2,842; 5, 897 AuC52HS2P4

[Au(PMePh,),]', 5,883,884 AuC54H45C1P3 AuCI(PPh3)3,5,883,884 AuC~~H+SN~P~ Au(Nd(PPh3)3,5,879 AuCs&4', [Au(PPh,),]', 5,883,884,904 AuC~~H~~NP~S Au(SCN)(PPh,),, 5,874,883,884 AUC~~&UP~ [Au(PPh,),]+, 5,883,884 AuC103Se {Au(Se03)CI),, 5, 870 AuCl, AuCI,. 5865,886 [AuCI,]-, 5,864.868,869,871,890; 6,852 AuCI~ [AuC13]-,5,886 AuC1, [AuC1,]-, 1,311,314,524,548; 2, 13; 5,870,889; 6, 14, 97.98,457,808,852,869, 1024 [AuCl$ ,5,889 AuCllP AuCI(PCI,), 1,418; 5,869,882 AuCI,

[AUC16]3-. 2,801 AuCORU,C,,H,,O~~P C O R U , ( C O ) & ~ - C O ) ~ ( ~ ~ - A U 5,908 PP~~), AUCO~F~C~~H~~O~~P F ~ C O ~ ( C O ) & - C O ) ~ ( ~ ~ - A 5,908 UPP~~), AuCO~RUC~OH~,O~,P CO~RU(CO)~(P~-CO)~(~~-AUPP~~), 5.908 AuCK~~H~~O~P Au( PPh,)( p-H)Cr(CO),, 5,869 AuF~ (AuF,),,, 5, 889 AuF30& Au(SO,F),, 5,891 AuF4 [AuFa] 5,889 A~F.iod4 [Au(SO,F),]-, 5,891 AuF, AuFS, 2,680; 5, 866,899 AuF, [AuFJ, 5,866,898 AUF~C~~H~~NO~P AuFe(CO),(NO)(PPh,), 4, 1189 AuF~C~~H~~O~P AU(PP~~){F~(CO)~}(~~-C,H,), 5, 904 AuF~C~~H~~NO~P~ AUF~(CO)~(NO)(PP~ ),, 4,~1189 AuF~~C~~~H~XO~~P FedCO) r o ( ~ 2 - A ~ ) ( ~ 2 ~ A ~5,906 PPh,)r AuFe3C32Hz,N0,P Fe3(CO)(~3-HC===NBu')(pz-AuPPh3), 5,908 A~F~~CI~HI~OIJ' Fe4H(CO)&(&-AuPEt3), 5,908 AUFe4C31H1601ZP Fe4C(pH)(C0),,(AuPPh3), 5,910 AuGeC21Hz4P Au(PPh3)(GeMe3),2, 16 AUG~C~~H~~P Au(PPh,)(GePh,), 2, 16 '4uGc,C3,H30 [Au(GePh3),] -,5,903 AuHClO [AuCl(OH)]-. 5,871 A u H C1 0 [Au(OfI)Cl,]-. 5.891

,

AuH,Cl,O

Cumulative Formula Index

AuH,CI,O Au(OH2)CI3,5,891 AuH2OioS6 [AU(S,O,),(OHZ)]~-,5,873 AuH~S~ [Au(HS),]-, 6,853 AuH3Br,N AuBr3(NH3),5,895 AuH3C13N AuCI,(NH,), 5,870,880.895 AuH, [AuH,] ,5,8Y1 AuH402 [Au(HzO),]+, 5,864

AuH6Br2NZ [AuBr,(NH,),]+, 5,895 AuH~N~ [Au(NH,),]+, 5,864,880 AuHs04 [ A u ( H , O ) ~ ] ~5,866 +, AuH,BrN, [AuBr(NH3).,I2+,5, 895 AuHloN,O [Au(NH3),(OH)I2 ’ ,5,895 AuH,,N,O [Au(NH3),(OH,)13+, 5.895 AuHiA [Au(NH3),13+?5,895,896 A& [AuIJ, 5,864.871; 6,852 Ad3 [Ad,]-, 5,886 AuIj [A&-, 5,891 AuIrC60H63P4

Au(PEt,)(p-H)IrH,(PPh3)3, 5, 869 AuIrC65H7N3P4

~lr(CNB~‘)~(p-dppm),Au]~+, 4, 1163 AUrTC7&3P3

AU(PP~~)(~-H)I~H~(PP~~)~. 5. 869 AuMnC,,H,,O,P Au{Mn(CO),}(PPh,), 5.903 AUMOC~~H~~O~P Au{Mo(CO),Cp)(PPh,), 5,904 AuN08S2 [ A ~ ( S O ~ ) Z ( N O Z )5,873 ]~-, AUNIOlZ [Au(NO3),]-, 5,891 AUK, [Au(N3),]-, 5,871,879 AuNI~ [ A u ( N ~ ) ~ ]5,894 -+ AuO& [Au(S0,),l3 , 5,873,892 AuOS, [A;(S,O,),]-, 5,864,876. 877 /Au(S,O,),]~-, 2,637; 5,873,877; 6,97,98,?59,852 AuOI2S4 [Au(SO3),I5-, 5,873,892 AuOs~Ci6Hi6OinP Os3H(CO)10(AuPEt3),5,906 ALIOS~C,~H,~NO~~P O S ~ ( C O ) ~ ~ ( N C O ) ( A U5,906 PE~~), AuOS~C~~H~SNO~~P Os3(CO)11(NCO)(AuPEt3), 5,906 AuOsXmHisCIOioP Os,(CO),,CI(AuPPh,), 5,906 AuOS~C~~H~~NO~~PS Os,Au(CO)l,(PPh,)(NCS). 2,227 OS~AU(CO)~~ ( P P ~,) ( S2.23 C N)I,

AuOs,C1,H,,Ol,P OS~H~(CO)~~(AU 5,908 PE~~), AuOs~Ci,Hi6aid’

AuVC2,HIsO6P Au(V(CO),)(PPh,), 1,73; 5,904 Au W C2?H16 0 5 P Au(~l‘h,)(y-H)W( CO), , 5, 869 Au,BaSnS, Au,BaSnS,. 5.873 AuzBr6 [(AuBr2)(AuBr,)lZ-, 5,871 Au,Br,. 5, 889 Au,CCI.,O Au2Cl4(CO),5,886 Au~CZHRCI,N,

(AuCl,),(en). 6.97 A~2C41112Nt, Au2(p-N&MeJ, 5,894 huZC8H8ClF5N2 AuCl(en)AuC,F,, 5,880 Au~C~H,~CI, Au2C14(MeC=CMe)z.5,886 Au2CaHzoI2P2 Au21,{p-(CH2)2PMe2}2,5,865 AuzC~H~OP~S~ (Au(S,PEt,)},. 5,878 A u z C ~ % PZ S~

Au(PMe3)(SCH2CH,S)Au(PMe,), 5,875 Au2C9H,,CI,P2 Au2C12(p-CH2){lr-(CH2)2PMeZ)2. 5.870 AU~CVII~JPZ (AuMc),{C(PMe,),}. 5.886 Au2C1oHz0~2S4 A u ~ ( S ~ C N E2,662 I~)~~ AuZClzHzoN4S4Se,

280

281

Cumulative Formula Index

Au4C18

Citmulative Formula Index

900

5.900

282

BCI,(NMe2). 3, 82 BC H+jCLN,P2 dCI2NMePCl2NPCI,&Me,3.89 BAgC39H3~W' Ag{ (4-MeC6H,),P}(BPh,(fiCH=CHCH=fi)z},2, 254; 5,796 BAgCs&&zP3 AgHBHZCOzH(PPh3)3,5,825 BAgCs7H5302P3 AgHBH,COzEt(PPh,),, 5,825 BAlCzHlo A1Me2(BH4),3,125 BAlH, AlH2(BH4), 3, 125 BAlO AIBO, 3,115 BAlOt AIBO,, 3,115 BAsZBC~HZ~ [BH2(AsMe3)zl+,3,98 BAs~CUC~~H~~NS Cu{B($IN=CHCH=CH),(diars)}, 2,254; 5,544 BAuC~~H~~CI~N~ A~{B($IN=cHcH=CH),}C~~, 2,254 BAuC~~H~~CI~N~ Au{Ph2B(fiN=CACH=CH),) Cl,, 2 , 2 5 4 BAuGoH2sP Au(BPh,)(PPh,), 5,903 BBrCIF, [BF,ClBr]-, 3,93 BBrC1,F [BFCI,Br]-, 3,93 BBr, [BBr41-, 3,92 BCCI,NO [BC13(NCO)]-, 3>93 BCF, [BF,cF,~-, 3,93 BCF,O,S [BF303SCF3]-,3,93 BCH3Br,S BBr,(SMe), 3,82 BCH,F,O [BF,OMe]-, 3 , 8 7 BCH3N [BH3CN]-, 3,90,91 BCH3NS [BH,(SCN)]-, 3,90,91 BCHq07 [BH,(COZ)]~-,3, 91 BCH.NO

BCSH6N2

[BH,(CN)($ICH=CHCH=cH)]-,3,92 BCiH6Na [B(CN),NMe,l-, 3,97 BC~H~~N [BH,(dN=CMeCH=cMe)]-, BCxHd, (B(NMe,)(NHMe,>]', 3,98 BC,H,CI,N

283

3,91

BC6Hd03

Cumulative Formulu Index

[BH,(dppc),]-. 3, 98 BCIFl [BF&I]-. 3. 03 BCIF304 [BF,CIO4]-, 3,Y3 BCI,N,

[B(acac),]+, 3.98 BCioHziN

FBMe{&CMe,(CH,),CMe,}l+.3.98 B C ~ ~ H ~ ~ N ~ B(fiN=CHCH=cH),.HNMe2, 3.88.89 BCiiHdP iBH,(NMe,)(PMe,Ph)]+, 3,98

284

Cumulative Formula index

285

[Cu(en),(FBF3)]+,5.698 [Cu(en),(F,Br,)]+, 5,541 BCuC9H10N6 [Cu{HB(~N=CHCH=CH),}]+. 5.537 BCuCloHION,O Cu(HB(HN=CHCH=cH),}(CO).5,567,583; 6,395 BCuCiiHisFzN40z Cu{FzB(ONCMeCMeUCH,),CH2}, 5,542,583 Bc~CnHisF&"03 Cu{F,B(ONCMcTMcNCH,)~CH~}(~~), 5,549,567, 576,583 BC'uC,JI,,N2 C'u(',,Y-Me,phen)(l 1213H,)35. 544 BCuC,,H,,N,O, Cu{HB(rSN=CMcCH=~h.lc),)(O,), 5,578,717,718 BCuC17H26N6

Cu(HB(fiN=CMeCHdhfe),)(C,H,), 5,569,583 [Cu{HB( &N=CMeCH=C Me),) (C2H4)]+,5,718 BCUCZOHI~F~N~ [Cu(blpy)2(FBF,)]+. 5.601 [Cu(bipy)z(FzBF,)]-, 5,609.641.741 BCUC21H26N702S Cu( HB(fiN=CMeCH=hlej3}(SC6H4N02), 5,544 [Cu(HB(I';TN=CMeCH=chle)3}(SC6H,N0,)1 ,5, 58 1

BMoC,H,,Cl,N,O

BCeII, [BH,GcH,]-, 3,91 BHC13S [BCI,SH]-. 3.93 BHF3 [BHF3J-. 3,91 BHF30 [BF,OH]-. 3.93 BHF,S [BF,SH]-. 3.93 BH,CI, [BH2C1?] . 3 , 9 0 BHzFxN [BF,NHJ, 3 . 0 3 BH,F,NO [RF,OYH,]-, 3,93 BHA [BH2S3]-: 3,91 BH3F

BCUC22H32NS0ZS2

Ch{ HB(&N=CMeCl I=cMe)l(SChJ 14Me-4)}{SCM,C'H(NH,)UO,Et}. 2,255

Cu(PPh,Me),(HBH,), 5.546. 585 BCuCdLsFJ'3 Cu(PPh,),(FBF,), 5,542. 584 BCU,C~~H~~CIN~ Cu( HB(fiN-CHCH=cH),} (C2H4)(CuCI),5,569. 572,583 [BF,NO,]--, 3,93 BFs [BF41 , I , 537; 3,92,03; 5. h8X; 6 , X47 HF,O,S

[BF,(SO,F)]-. 3,94 BFBN~O~S~ [B(NSOF2),]-. 3, 97 BFls03Te3 B(OTeF5),, 3,88.975 BFZo04T2, [B(OTeF,),I-, 3 , 9 6 BFeC,H,NO, Fe(BNMe,)(CO)4, 3,99 BFeC,HloN04 Fe(BNEt,)(CC)),, 3, 90 HFeC~13H13N,C), Fe{ HB(fiN=CHCH&H),}(C0j2(Ac), 2, 25 I BFeC,sHlsN,03

Fe{HB(NN=CHCH=cH),}(CO)2(OCCHCHMe),2 , 25 1 BFeC16H34F4N4 [Fe(hexamethyl-l,4,8,11 -tetraazacyclotetradecane)(BF,)]+, 4, 1251 BFecl8H9FN6O3P [Fe{FB(ON=CC,H,N),P}]2+. 4,1232 BFeCl9H1,O2 Fe(BPh,)(CO),Cp, 3, 1UU BGaC2Hlo GaMc2(BH4),3, 141 BGaCaH,2F3N GaH,(NMc,)(RF,), .3* 130 BGii04 [GaBO4I2 , 3 , 134 BGeCI6 [BCI,GeCI3]-, 3 , 9 3 COC 7-J'

BirAsC23H3,Cl,N6 IrCI2(HB(kN=CMeCH=cMe),)(AsPhMe,), 4. 1 134 BIrC,H,N,02 Ir(CO),{H,B(r;l'?J=CHCH=~H)2}, 4, 1108 BIrCid16kOz Ir(CO)z{H,B(~N=CMeCH=~Me)2}, 4. 1108 BITC~~H~~P~ I T H ~ ( B H ~ ) ( P B U ~ ,4,M1149 ~)~. BIrC14H27F6N605 BIrC1~H27<~N605 Ir(O,CCF,),(HB(AN=CMeC:I I=cMe),}(HLO). 4. 1134 BIrC20H29CIN602 Ir(acac)CI(HB($lN=CMeCH=CMc),}, 4, 1134 B1rC36H3,CIF4N2PZ frHC1(FBF3)(N2)(PPh3),,4, 1105 BIrC38H69NOP2 I~(CO)(NCBH~){P(C,HI~)~}~. 4, 1108 BLIC~~H~~OZ (MeOCH,CH,OMe). 3. 14 LI(2,4.h-Me3C6HP)2BH2} BLIMoC~~HJ~NTO~ Mo{ HB (hN=CMeCH=e Me),} (NO)I,Li(OEt), . 3, 1280 BhlnlH414 Mn>(BH,)I,, 4,h l B.MnlH,Oa Mn,(OHj,(B(OH),}, 4,42 BMoC,H,,CI,N,O

BMoCqH1 oC12N70

Cumulative Formula Index

MOCI,(NO){HB(~~N=CHCH=CH),}, 3, 1287 BMOC~H~OCI~N~ MOCI,{HB(&N=CHCH=~H ) ~ }3,1342 . BMoCll-H10N703 Mo{ HB(fiN=CHCH=CH),} (NO)(CO), ,3,1276 BMoCl1HI5BrN7O2 Mo(N0) { HB(fiN=CHCH=c H),}Br(OEt) ,3,1287 BMOC,~H,~B~N~O~ Mo{HB(&N=CHCH=cH),}(CO),Br, 2,249 BMoC~~H~JN~O~S

M ~ ( H B ( ~ ~ N = c H c H = ~ H ) ~ } ( c o ) ~ ( c2.249 s)I.

286

Mo(NO){HB(fi%=CMeCH=eMe),jI(NHNHMe). 31288 lik7 ~~

~

BMOC~~H,,NSO~

Mo(N2Ph){HB(&N=CHCH=CH)3}(CO)2,3.1294 BMOC,,H,,N,O, Mo{Et,B(flN=CHCH=CH),} BMOCL~HZ~N~O~S

(CO)ZCp, 2,250

Mo(CO),(NS){HB(I\;TN=CMeCH=CMe),}, 2, 121 RMoC17H2,TIN,0,

BMVC;~H~;N~O~

MO{HB(~~N=CHCH=~H),}(CO),H. 2.249 BMoC12H14CIzNs MOCI, H & N = C H C H = ~ H ) { H B ( N ~ = b H ) , } , 3.1331 BMOCizH16INsO

MoI(NO)(NCMe,){HB(fiNdHCH=cH),}, 2,127 BMoCIZH~IP~ M o H ( B H ~ ) ( P M ~ ,3,) ~1284,1438 , BMOCY 3H13N.503 Mo{HB(~N=CHCH=CH),(CO),(rlZ-Ac), BMOC,,H1,N6O,

Mo(NO)(HB(I\;T;IN=CMeCI1=eMe),}CI(OEt), 3, 1287 BMoC~,H~,IN~OS M o ( N 0 ) {HB(rY’Y=CMeCH=cMe),}I(SEt).3.1288 BMOC,~H~~II~;~O~ Mo(N0) {HB(?JN=CMeCH=eMe),}I(OEt), 3,1292 BMoCl7HzsClNBO Mo(K0) { HB(fiN=CMeCH=CMe),}CI(NHE t), 3, 1287 Mo(N0){ HB(QN=CMeCH=cMe),}CI(NMe,), 3,

1287 2 , 249

M~{HB(~N=cHcH=C:I-~),(CO),(~?-A~), 2,249

BMoC~,H~~N,O~ Mo { B(rirN=CHCH=C I I)&} (NO)(CO)z,3,1276 BMoCISH15CINs Mo(NZPh){ HB( &N=CHCH=cH);}CI, 3.1295 BMoC15H15CIN,O Mo(N0) { HB(&N=CHCH=~’H),)CI(K2Ph), 3,1288,

1294

BMoCi71i,,Iugo

Mo{HB(kN=C.MeCH=tMc)7}(NO)I(NHNMc2), 2, 151:3.1288

BMoC inHd,O,

[Mo{HB(fiN=CMeCH=cMe),}(CO),]-, 2.249 BMOC~~H~,CIN,O~ Mo(NO){HB(AK=CMeCH=CMe),}CI(OPr’),3,

1287 BMoC18HjTNsOI Mo(N0) {HB(&N=CMeCH=cMe),} (0Et)NHMe).

3.1287 BMOC~YH,~N~O~ Mo{HB(&N=CHCH=cH),}(C0)~(Tl3-C4H,), 2,256, MO{ B(&N=CHCH=CH),} (CO),Cp, 2,250 257 BMoC,,H,,N,O,

BMOCI,HI~N~O,

BMOC,~H,,N,O Mo{HzB(fiN=CMeCH=~Me),] (C0),(q3-CH2CH= CHZ), 2,246 BMOCISH,~&O~ Mo{EtZB(&N=CHCH=c H),} (5,)(CO),(y3-CH2= CHCHZ), 2,249 BMcJC~~H~~CI~N~O MoOCI,{HB(&N=CMeCH~Me);), 3,1352 BMoC~~H~~CIZN~P MoCl2(NO){HB(fiN=CMeCH=~Me),J. 3, 1287 BMOC~SH~ZCI~N~ BMIOC,~H,,I,N,O

iMo{HB(&N=CMeCH=Chk),}(NO)I2,2,249;3, 1287,1292

Mo { Et,B(fiN=CHCIi=&H),) (CO),(TI”-C,H,), 2. 250 R MoC qH2eNq0 [Mo{H€3@N=CMcCH=cMe),}( NO)(MCCN)~]+~ 3.

1279 BMoC~~H~~CIYTOS Mo(N0) { HB(AN=CMeCH=cMe),)CI(SBu), 3 1288 BMoCI9Hi;N7O3 Mo(K0) { HB(fiN=CMeCH=C Me),} (OEt ), ,3,1287 BM0C19H335;802 Mo(N0) { HB (&N=CMeCH=c Me),} (OEt)(NHEt).

3.1287 12k8 BMoCI~OH~~N lo08 Mo(N2Ph) { B( NN=CHCH=c BMoCZOH~~N~~

I 1)1} (CO), ,3,12Y.t

Mo(NO){HB(fiN=CMeCH=~Me),}(OEt)(OPr’). 3.

B MoCi 5H24N703 Mo(N0) {HB(&N=CMeCFI& Me),} (OH)Z.3,1287 BMOC~SHJN~O Mo{HB(Me2C3NHZ)3}I(NO)1 3.1279

1287 BMOCz1H25N402 MO{ EtzB(flN=CHCH=cH)2} (CO)2(q3CH2CPhCH2),2,250 BMOC,,H~~CIN~OS

Mo(NO){HB(%N=CMeCH=~Me),jCI(SPh),3, 1288 BMoC~~H~,IN~OS

Mo(NO){HB(fiN=CMeCH=cMe),)I(SPh). 3. I288 BMoC~~H~~TN~O:

Mo(NO){HB(lr”=CMeCH=~Me)3}l(OPh).3,1?87 BMoC,,H;&IN,O BM0C16H17N1002

Mo{B(fiN=CHCH=CH),) (NO)(CO)(EtNC),3,1276 BMOC~~H,~C~NHO Mo(N0) { HB( N=CMcCH=CMe),}CI(N HMe), 3,

1287

Mo(NO)(HB(&N=CMeCH=C‘Me)3}Cl(NHPh),3, 1288 BMoCzlHzSINBO Mo(NO){HB(fiN=CMeCH=CMe),} I(NHPh). 3. 1288

Cumulative Formula Index

287 Mo(N0) { HB(&N=CMeCH& 3.1288

BRuC~H~~P~

Me),}I( NHC,H,SH), BPtC9H 7N4

PtCH2B(fiN=CHCH=cH),)Me,, . 2,253 BPtC,,H,jN6

Pt{HB(fiN=CHCH=cH),}(Me), 2,253; 5.415 BPtCl1Hl3N60

12x8, 1293

Pt{HB(fiN==CHCH=~Hj,)(Me)(CO), 2, 253

BMoC~~H~~IN~OS

M~(NO){HB(~~N=CMCCH=~~~),)I(SC,H,,), 3, 1288 BMoC22HZiFN8S Mo(N2C&F-4 SC,H4Me-4){HB(N'r\i= d H ) 3 ) . 2. 136 RMoC,~H,,IN~O

Mo(NO){HB(fiN=CMeCH=CMc),)I(NHNMePh), 3,1288 BMoCzzH3oClN80 Mo(N0) { HB(fiN=CMeCH=cMe),) CI(NHC6H4Me-4), 3, 1288 BMoC22H3oINsOz Mo( NO) { HB( KN=CMeCH=cMe)3} I( NHC6H4OMe-4),3, 1288 BMoCZ~H~ON~G Mo(NO){HB(fiN=CMeCH=cMe), } (OPh)(OMe), 3, 1287 BMOC~~H~~N~OS Mo(NO) { HB(fiN=CMcCH=c Me)3}(NHMe)(SPh), 3, 1288 BMOC~~H~~N~O~S Mo(NO){HB(hN=CMeCHdMe),}(OEt)(SPh), 3, 1288 BMoC~~H~ON~OSZ Mo(N0) { HB(fiN=CMeCH=CMe),} (SBLI)~, 3,1288 BMoCZ~H~~N~SZ Mo(N,Ph)(SPh),{HB(rl"=CHCH=(?H),}, 2, 134 BMOCZ~H~ZNTOS Mo(NO){HB(&N=CMcCH=~Me),}(SPh),, 3, 1288 BMoC~~H~~NQO Mo(N0) { € i R ( KN=CMeCH=(?Me),} (NHPh),, 3, 1288 HMoC,~H,,IN~O Mo(N0) { HB(&N=CMeCFI=C~e),)I( NHC6H,CH2CnH4NH2),3,1292 BMoCZ9Hz-,N~O2 -' Mo{Ph2B(fiN=CHCH=CH)2(CO)z(q3CH7CPhCH2).2,250 BMOC,~H,~N~OP -' Mo(N2C6H4Me){ HB N=CHCH=cH),) (C0)(PPh?),3, 1294

(s

BPIC,~H;~N~' Pt{ HB($JN=CHCH=kH),}Me,, 2,253 BPtCiaH 13F6N6 PtMe {HB(fiN=CHCH=cH),} (CF3C=CCF3),5 , 3 15 BPtC14Hid602

Pt{HB(&N=CHCH=~H),)(Me)(H2C==CHC02Me),

2.253 BP~CISHZZN~

Pt{HB(fiN=CHCH=cH),}(Me)(CNBut),2,253; 5 ,

380,432 BPG~H&JO~ Pt { Et,B(hN=CHCH=kH)z}(Me02CCMe=CCO,Me), 2,253 BPtCIglI3jN P t { E t , B ( h ? H ) , } ( c o d ) ( M c ) . 2,253 BPtC2dH,oClP2 PtCl(BPh>)(PEt3)2,3, 100; 5,372 BPtC25H29N4 Pt { Et,B($TN=CHCH=tH j2)(Me)(P h M P h ) , 2 254 BPtC33H34F6N4P Pt { Et IB(hN=CHCH=cH),) { C(CF3)=C(CF3)Me}(PPh3), . ~. 2,253 BReBr7N IRe(NBBr,lBr,l-, 4.194 BR~c~H,,cCN,O Re{HB(fiN=CHCH-tH),(O)Cl,, 2,25 1 B ReC2,H2,CI,N,P RdHB(fiN=CHCH=CH),}CI2(PPh3).2,251; 4. 154 BRhC9MIlC12N6 IKh4 HB(~N=CHCH=CH~,la,H1-, 4,1012

BRhCI3HlENb Rh{HB( flN=CHCH=cH),) (H2C==CH2)2,2.252 BR~CI~HI~NBOZ Rh { B(hN=CHCH=tH),) (CO)z, 2,252 BRhCi4H2jF2IN402 RhMeI F kON=CEtCMe==N(CH,),N=CEtCMt== 4,1014 BRhCI6H20NB Rh { B( Pd FI=CHCH=cH),} (H2C=C:H2),, 2 252 BRhC1YHzuNs Rh{B( NN=CHCH=c H),}(n bd) ,2,252 BRhC,,H,,N8 Rh {B(fiN=CHCH=cH),} (cod), 2,252 BRhCzlH26P RhH(€3H4){P(C6H4Me-2),},4,932 BR~CZZHZ~N~OZ Rh{ B(&N=CHCH=eH),} (duroquinone), 2,252 BRhC3oH3806Pz [Rh(BPh)(P(OMe),},, 4,930 BRhCt,H,zPz RhH,(BH,) {P(C,Hi 1)3}2.4, 1022 BRhC4zH36C10P RhHCI(2-@BH)(PPh3)2, 4, 1018 BRUCH~~N, [Ru(BH3CN)(NH,),]+, 4,282 [Ru(BH3CN)(NH3),l2', 4,282 BRuC~H~~P~

h),

BRuC~W~~P~

288

Curnulutive Furrnulu i n d c i

RuH(q2-BH4)(PMe3),,4,4S4 BRuCj jHioCIN602 RU{HB(I;~N=CHCH=CH),} (co),ci, 2,25 1

BZrC19H31C12N60

Zr{HB(fiTN=CMeCH=cMe)3}(OBut)Clz, 2,238; 3, 381

RuH(qZ-BH4)(PMePh,),, 4,354

mUc,,H,,rJ,

K ~ l H ( ~ Z - 1I,){3 1 PhP(CH2CHZCHIPT'h2~L},4,454 BRuC,,H,iOP2 Rul-I(BH4)(CO){P(CbH1,)3}2. 4. 457 BRuC;,H.wNOzP, R~H(BH,CN)(CO),(5-Phctibenzophosphole)~,4,457 BRuC~M'~ RuH(BH4)(PPh3)3,4,454 BRuC,,H,oOP, RuH(BH,)(CO)(PPh,),, 4,457 BSi4ZrCl,H40CIN2 ZrCI(BH,){N(SiMe,),},, 3, 377.433 BSnC3H9F4 SnMc3BF,, 5,689 BSnC3H12 ],HH,SnMe,]-, 3,91 RSnC,J I,,N6 _ " SnMe,{HB(NN=-l l j 3 } .3. 185.211 BSnC'I,

BZ~C,~H,,CI,N~O ZrCIL(OBut){ BuB(fiY=CMeCH=cMe),}, H2AtCIiIl AIMe(Rt-l,),, 3 , 125 R,AlIIq A1H(BH4)?,3. 125

3. 38t

BTCC~~H~~CI~N~P Tc{HB(RN=CHCH=cH),} C12(PPh3). 2,251 BTiC,H ,&13N6 Ti{HB($IN=CHCII=cT I),}Cl,, 2.748

C'o(nPh,),(diphos)z, 3, 99 B2Co~Sn2C'9,HzoC'I,Yl~~l~ Ti{ B( &N=CHCI I=c€I)4} Cp,. 2. 248 BTi7C2H6CI,N TizCl6(Me2NBCI),3,356 BTIzC~ZH~ZN S [Ti,{B(&N=CHCH=cH)1)CpJ1 2.248 BTIH4 TIBH,, 3, 170 BUC12H3606 U(BH,),( 18-crown-h), 3, 1136 BUHC,H,,O, U(f311d4(THF),, 3 . I132 BUHi, U(BH,\,. 3. 1132

BwC,,H',,B~,N~

WBr,(N,Ph){HB(fiN=CHCH=CH),}, 2, 13.5 BWC,,H,,BrCIN,P,

BZrC9MlOCl3N4ZrC'1, { I 1H(NN=CI IC'H=C' H)3}.3. 781 BZICI~H,&N~~

Zr(HB(fJN=CHCH=(?H),}(OBut)CI,,2,248

[Sn2Co,CI,(CO)l,][Co(HB(~N=C€ICH=~H)3]2. 2. 19 ..

B2CrCsHZ4O2 Cr(BH,MTHF),. 3,766

[CrO4(BF3),]*-, 3,944 B2CrHR Cr(BH,),. 3.929 B~CU'C~H~~F~N~ Cu(enj,(FBF,),. 5.688,716,741 B,CuCiiH&, Cu(Me,dien)(NCBH,),, 5,609 BZCuC,,HJ'J, Cu(Me,B(&N=CHCH=CH)z}z, 2,254

289

Cumulative FormuLa index

[Cu{lIB(r;[N=CIIC11=~II)3~CI]2, 2.254; 5,621 BZCU~CISHZONIZ

[CU{HB(fiN=CHCH=cH);}]z32.254; 5,553

B2FeC1&I~2NZOj2P~ Fe(BH,CN),{P(OMe),},, 1.1231 B2FeCisH2oNiz Fe{HB(fiN=CHCH=cH)3)2. 2.251,256

B2KiC36H32N8 Ni(Ph,B(hN=CHCH=cH)2}2, 2,252; 5, 102 B2Ni2Cl,H,,Nlo [ {Ni(KCBH,) {N (CH,CH,NH,),} } 2 ] 2 + . 5 74,75 B2Ni,06 Ni,(O,B),, 2.430

RZkh2C18H20C14N1~ Rh,~HB(rSN=CHCH=~H),),CI,, 2,252; 4,I012 -,BzTaC,IH2~l\;a Ta{HzB(fC'Y=CHCH=tH),},Me3, 2,248 B~T~CZ?H~~B~~NI~ ThBr, (pv razol-l-yl)4B)z,3, 1143

B,MnH;,' MTI(BH,)~,4,h i BZMn306 M~,(Bo,),, 4,42 B2Mo&HziN ,,b4 MO,O, { HB(~~N=cHCH&H),},, BzMOZCZZHZ~NIZO~

AI(BH,j,(BMe,). 3, 125 3. 1253

Moz{HB(fiN=CHCH=eH)3}2(OAc),,2.250

BZMO~C~;H~IZOE [Mo204{HB( r;[N=CHCH=eH),} (MeOH)],( OMe),, 3,1253,1363 BZNiCl2HI6N8 Ni(H2B(&N=CHCH=cH)2)2, 2,252; 5 , 102 B2NiCl6HZ4N8 Ni{H,B(r;[N=CHCH=t H)(fiN=CMeCH=CMe)},, 5,102 Ni{Me,B(fiN=CHCH=tH)2}2, 2.252

B2Ni&H2.,N8 Ni(B(hN=CHCH=~H),)2, 5. 1U2 B~N~C~OH~OFSN~~~ Ni(py N-oxide),(BF,),, 5 , 6 1

B3HfC10H40NP2Si2

~

Cumulative Formula Lndex

B3HfC10H40NP2Si2

Hf(BH4)3{N(SiMezCHzPMe,),}, 3, 384.433 B3Hf2C20H71NZP4Si4 {Hf~N(SiMezCHzPMez)z})z(~)3(B114)3, 3,384,433 B3InHl2 In(BH4)3,3, 166 B3MnHlZ Mn(BH&, 4.93 B3NiClRHZ4Nl2 [Ni{ H,B(fiN=CHCH=cH),) 5 . 102 B3S~CgH2802 SC(BH&(THF)~,3, 1064 B3nC27H30C1N18 ThCl{(pyrazol-l-yl)3BH},, 3, 1142 .,. . B3TiHlZ TifBHA,. 3.348 _,_ , B3UklZH44P4 U(BH4)3(MezPCH2CH2PMez)2. 2. 1041 1

B,P~H& PtClz(B6Hl,). 5 . 372 BAHx AI(BH4)(B3Hs)2.3. 125 B7PrC16H43P2

B3YbC2iH, N18 Yh{HB(~N=CHCH=CH),),, 2, 255;3. 1073

Pt(Me,C2B,H7)(PEt3)Z,5, 373 B,COP~C,,I~,~P~ (CoCzPtBaHio)(PEt3)2(C$), 5,373 BBFePtC2oFTSOPZ FeI't( Me,C4B,H,)(PEt3j2, 5 , 374 RsTrCssfT54P3

2,10-IrCBsH8-1-PPh3-2,2,2-H(PPh,),, 4,1165 B81rPtC13H470P1 PtB8HloIrH(CO)(PMe3)4,4, 1165 B8PGzH4oPzS

H"PtH.,P,

.

.

B~MOZC~OH~~NI~

MoZ{EtzB(&N=CHCH=CH),),. 3. 1305 BaNa2H40q

B4z;caH.t8N32 Zr{B(&N=CHCH=CH),},.

3.382

B~AUC,H,,NS~ A u ( S ~ C N E ~ ~ ) ( CI )~, 5,903 B~H~

290

[Ba([2.2.2]cryptand)]+, 3,46 BaC,,H,,N,O,S ._ " ,

__

[Ba([2.2.2]cryptand)(NCS)(H20)]+,3,46 BaC20H35WAo IBa(MeCONHCOMeLlZt. 1.99 Bak20h.,,Br20 Ba(l5-~rown-5)~Br,, 3,39 BaC2,HdzO, [Ba(3,2,2-crvptate)(0H,),1Zi, 2 , 3 0 6 fiaC2zHdbSa Bd(NCS),(hipy),, 3, 13 BdCz21 I,,CIN 0 4 Ra(C:IO,) { d=CMe(2,6-py)C(Me)=NCH2CH,N= CMe(2.6-py)C(Me)=NCH,cH2}. 3. 1096 BaC2&,N40, [ B a ( ~ h e n ) ~ ( H ~ O ) ,3, 1 ~13 ', BaC2&6Ns [ Ba{HN{CH2CH2N=CMe(2,6-py)C(Me)= KCH2CHz}zNH}IZ+,3,44 BaCz4H32C12N6010 Ba { { MeC0(2,6-py)C(Me)=NCH2CH2NHCH2},) (CI0&, 3-30 B~~C~JH~ZCIZO~~ Ba(dibenz0-24-crown-8)(CIO~)~, 3,40 BaC24H?4K,04 IBa{HOCH (CIrzN=CMe(2,6-py)C:(Me)=NC~z~2CHOH)(H20)2lZ', 3 , 4 4 B~C~ZHI~NB Ba(phthalocyanine), 2,863 BaC32fi3zN804 [Ba (k=CHC=CHCH=COCH=NCH2CH2N= CHC==CHCH=COCH=NCH&H2)21"+. 3 , 4 1 BG6H40Y6024 ">

Ba(dibenz0-23-crown-8){2,4,6-(O~N)~~~H~O}~(H,~)~. 3.40

..

(PtBloH11)Z~PMeZPh)2, 5.372 B20SnC14H3604 Sn(aca~)~{9-( 1,2-B,oC2Hll))2.2. 392 BaAuzSnS4 AuzBaSnS4,5,873 BaCzH6Nz03SZ Ba(NCS)z(Hz0)3,3 , 7 BaC10H1zN208 [Ba(edta)lZ-. 2,784 BaCloH13Nz08 [Ba(Hedta)]-, 2,784 BaCIOH1404 Ba(acac),, 3,27 BaCldd208 [Ba(tmta)l2-, 2,764 BaCllH15N208 [Ba(Htmta)]-, 2,784 BaC1ZH16NZ08

[Ba(teta)l2-, 2.784 BaC1zH17N208 [Ba(Hteta)]-, 2,784 BaCizHz406 [Ba([l8]cro~n-6)]~+. 2,931 BaCizHz606 [Ba{MeO(CH2CHz0)sMe}]z+. 2.931 BaClzH48CI,Nlz BaCl,(en),, 3, 11 BaC14H331ZN30~ BaI, { HOCHZCH2N{ CH2CH2N(CH2CH20H)2}2), 3, 23 BaCi6HdzOio

B~(OAC)~{N(CH~CH~OH)~)~.~.~~

BaCisH36Nz06

[Ba([2.2.2]cr~ptand)]~+, 2,937

W#)z}Iz-, 3,44 BLw H x Y i , O I i Ba(2,1,6-(O?N),C,HzO) z(phcn)Z(Mc2CO)r 3.13 B aC48H30N1 oOlo Ba{2,4-(02N),C,H30}z(phen)3, 3, 13 BaCdOlzPa CdBa(P03)4, 5,962 BaCUN6012 [B~CU(NO,),]~-, 5,702 BaH4C1202 BaCI2(H20),, 3,7 BaNiO, BaNiO,. 5.297 Bas4 Bas,. 2.516 BaSb2CBH32NXSeZ Ba(ShSe),(en),. 3 , I I Ha2CIUIII2N2O8 Ba,(cdta). 2,784 Ba2C3~H64N4010 [ Ba2{k{ (CHzCHz0)2CHzCH2}zNCHzCH20CH2CH,N{ (CHzCHzO)ZCHzCH2}zNCH2CHzOm H q 1 1 4 + .2.941

Ba3Ni308 Ba3Ni308 Ba,Ni,O,, 5,297 Ba68Hi06016 Ba(las~locid)~, 3,68 BeB2C18Hd' Be(BH4MPPh3),3,lO BeC,H403 Be(OH)(OAc), 3,31 BeC,H,CI,N2 BeCl,(en), 3, 11

BeC,O, [Be(C,O,)]", 3,33 BeC,H,,CIN BeHCI(NMe,), 3 , 7 BeCaH4CI2Na BeC12(HCN)4,3, 8 BeC,H,Cl,N, BeCI,(MeCN),, 3 , 8 BeC4HsO3 Be(OEt)(OAc), 3,31 BeC4HzoCl2N4 BeCI,(H,NMe),, 3 , 7 BcC,N& [Be(NCS),12-, 3, 10

Be(NCS),(MeCN),, 3, 8 BcC~H~O, Be(2-(O2C)-3-OC6H30H},2,482 BeCsHisFisO2 Be10(CF2)3CF3)Zr 2,349 BeCBH1802 Be(OBu'),, 2,349 BeCsH20Br20Z BeBr,(Et20)2, 3 , 8 BeC8H20ClzOz BeCL2(Et20),, 3 , 8 BeCmHsF,O4 Be(CF,COCHCOMe),, 1,560 B eCl0H14 0 , B e ( a ~ a c )2,378,392; ~, 3,25,26 BeC12HloOz Be(OPh),, 2,345 BeC12H28N40, [Be(DMF),I2+,2,494 BeC12H36NZSi4 Be{N(SiMe,),}, 2,170 B ~ C I J L ~ ~ P , [Be{OP(OMe)2Me},]Z+, 1,286 BeCizH36016P4 IBe{OP(OMe),},12+, - . 1,286 Be'Cl4Hl2N2O4 Be(2-OC6H4CH=NOH)2, 3,29

Cumulutive Formula Index

292

[BeCI,]*-, 3. 10 BeC140,6 [Be(ClO,)]'-. 3. S BeF, [BeF4I2-, 1.537; 3. 10.6.863 BeH4Br2S2 BeBr,(H,S),. 3. 10 BeH412S2 BeI,(H&, 3, 10 BeH6C12N, Be(12(NH,)I, 3, 7 HeH,N,

[Rc(NH,),]'. 2. 171; 3. I O BeH,04 [Be(H,O),]", 2,306: 3. 6.8; 6,413 BeH ,2C12K4 BeC1,(NH3),.3,7 BeHI6Cl2N8 BeCl2(H,NNH-J4. 3. 8 BeH,,CI,N, BeC12(NH3),. 3. 7 B ~ H ~ W I , BcCI,(I\TH,),~.3 . 7

[Re(N03)41z , 3 , 10 BePdC2UH,1CIN204

Be(acac){MeCOCH~COCH,PdCl(bipy)} ,3,26 Be W C O H ~ O , ~ [BeW1,Co(OH-J039]6-, 3, 1037 I B ~ W , , C O ( O H ,.~.O ~ ~ 3,1037 )'-, B~~,c,H~O~ [Be2(2.6-0,C6H3CO2)]+,2,482 Be2C34H3408P2 Be2(acac)2(0,Pl'h2)2, 3,27 ~~

Cumulative Formula Index

293 [BiBrSlZ-.3, 291 BiBr6 [BiBT6I3-, 1 , 7 3 ; 3,291 BiC2H6N3 BiMe,(N,), 3.283 BiC3H9 BiMe,, 3,294 BiC4H90S2 BiMe,(S,COMe), 3,28Y BiC4N4S4 [Bi(NCS),12+, 3,285 [Bi(SCN),]-, 1 , 4 4 BiC5Hl10Sz BiMc,(S,COEt), 3,289 BiCSH13SZ BiMe(SEt),, 3,287 BiC6Hs (BiPh),, 3,284 BiC6H9NZS BiMe,(S&NCH=CHCH=h). BiC6Hl,0S, BiMez(SzCOPri),3.289

Hi(SEtj,, 3,287 BiCbHIHNSi BiMe,{NMe(SiMe,)}, 3.282 BiC6Hdn Bi(NMe,),, 3,282 BiC7H7S, BiMe( 1,2-S,C6H,), 3,287 BiC7HlSNZS4 BiMe(S,CNMe,)*. 3,288 BiC,H,S, B~PII(SCH,CH,S), 3,287 BiC8HllSe BiMe,(SePh), 3.289

[di(S,C,(CN),},]

, 2. A05

HiC9HIIS2

BiMe{ 1,2-(SCH2),C6K1), 3.287 BiC9H2,N2Si, BiMe{NMe(SiMe,)},. 3.282 BiCloH130S, BiPh{(SCH,CH,),O}, 3: 285 BiClJW2 BiPh(SEt),, 3,287 BiCl.lHZ3N2S4 BiMe(S,CNEtZ)2-3.288 BiCI2HloN3 HiPh,(N,), 3,281 BiCIZH1,NZS4 BiPh(S,CNMe,),. 3,288 BiClzHzo04S,

BiCl2H2',S3 BifSBu'L. 3. 287 B~C~;H,~N; Bi(NEt,),, 3, 282 BiC1,Hl& BiMe(SPh),, 3.287 BiCl~IIIJSez BiMc(ScPh),, 3,289 BGHd2S4 BiMe{S,CNTH,),},. 3,288 BiCL4HI30SZ BiPh,(S,COMe), 3,289 BiCISHTlNzS4

3.287

BiF,

BiMe(Sc=NC6H4S-2)2. 3,287 BiCl5HI50S2 BiPh,(S,COEt), 3,289 BiCl6Hl0f6O4 [BiPh2(O,CCF3),]-, 3,280 BiCl6Hl7OS2 BiPh2(SzCOPr'). 3, 288,289 BiCl,H,,K2S4 BiPh(SZCNEt2)2,3,288 BiCI7Hl90S2 BiPh2(S2COBu), 3,289 BiC I BiPh:, 3, 294 BiC18H15C12 BiPh3Cla, 3,280 BiC,sHlsY6 BiPh3(N3j2.3.283 BiCIEHlSS2 BiPh(SPh),, 3,287 BiCI8HlsS3 Bi(SPh),, 3, 287 BiClsHlSN3S3 Bi{2-SCGH,NH2)3,3,283 RiCisH&,S BiPh{S2CN~H2),)2,3,288 BiC,8H30N,Sh R ~ { S , C N ~ I I , ) ~3,288 ],, BiC,18H12N, Bi(NPrz),, 3,282 BiCIEH,,O,P3S, Bi{S2P(OPr)z}311.81,82 BiClEH4& Bi(SiEr,),: 3.280 BiC1&&&, Bi{N(SiMe,),],, 3,282 BiC20H40C13Nlo0

Bi(CIf34)s(S~NHCH2CH2CH2&H)5, 3,290 E X z ,HZIS3 Bi(SCHZPh)3.3,287 BiCZ4Hzo [BiPh4j+,3,28(1 RiC2,t~IIsN,O, Ri(8-quinolinolate),, 1, 528 BiCz7H,IClN0 BiPh,(8-quinolinolate)C1, 3,280 BiC33H36C13N1209S3 BiC13{&=YC(NHS02C6H,NH2)=CHCH=~OMe) 3. 293 BiC3,H44CIN4 Bi(octaethylporphyrin)Cl, 2.822 BiC&J% [Bi(o~taethylporphyrin)]~, 2,822 HiC4,HzsCIN, Hi(tetraphenylporphyrin)~~l, 2 . 822 BiCS4HajSi3 Bi(SiPh,),, 3.281

,.

BiCLO BiOCI, 3>294 BiC1, BiC1,- 3,290,291 BiCI,NO BiCI,(,NOCl), 3,290 BiCl,(NO), 3,290 BiCI,N20, BiCI,(NO,),, 3, 290 BiCI, [BiCi4] ,3,291 BiClj (BiCI,J2-, 3, 201 RiCI, [BiCI6]*->1 . 7 3 [BiCI,l3-. 3.291 BiF3

Cumulative Formula Index BiF,, 3,290,291 BiF4 [BiF4]-, 3,291 BiFS BiFS, 3,291,292 BiF6 [BiFJ, 3,292,314 BiF9Si3 Bi(SiF,),, 3,280 BiGe,C,,H,, BiEt(GeEt,),, 3,281 BiGezC38HSF30 BtEt{Ge(C6F5)3}2r 3,281 BiGe3CL8H45 Bi(GeEt3),, 3,280 BiGe3C54H45 Bi(GePh,),, 3,281 BiH02 BiO(OH), 3,284 BiH3C16N (BiC13)z(NH3),3,282 BiH303 BiIOH),, 3,284 Bi H9CI N, BiC13(NH3),, 3,282,290 BiIl Gi13, 3 , 2 ~ 1 , 2 ~ 2 BiI, [Bi14]-, 3,292 BiI, [BiI6I3-, 1,73; 3,291,292 BiN2O6 Bi(N03)2, 3,284 BiN30 BiO(N3), 3,283 BiN309 Bi(N03)3, 3,294 3i0,P BiPO,, 3,284 Bi09S6 [Bi(W&13 - 2 , 6 3 7 BiSnC9H,, Bi(SnMe,),, 3,281 BiSn3C,8H45 Bi(SnEt,),, 3,281 Bi(SnPh,),, 3,281 Bi2Br,

[Bi2Br,IZ-. 3,291 Bi2Br9 [Bi2Br9]-. 3,291 [Bi2Br9I3-,3,291 BizBrlo [Bi2Br,o]4~. 3, 291 BiZC12H36Si4 Bi2(SiMe3),. 3.2S4

Bi21Ge(C,F,),J3, 3.281 BizIQ [Bi2I9l3 ,3,291 Bi2MoC8HI2O4PI (BiMe)*Mo(CO),(PMe),, 3,283 Biz03 Biz03. 3,284 Bi2012S3 Bi,(SO,),, 3.284 Bi2Si4 [Bi2S34]4-q3,284 BiZW3CI5Ol5 {W(CO),),Bi,. 2.1046 Bi3C7HZ8CI9Nl4S7 (BiC13)3(HZNCSN~IIZ),. 3, 290 Bi4Br,6 [Bi4Br,,l4-, I , 149; 2, 685 Bi6H408 [Bi60,(OH),j6+, 3.284 Bi6HI2Ol2 [Bi6(OH)12]6+,2.300 Bi, [Bigl5+,1,165 BkGsH3F1806 Bk(hfacac),, 3, 1216 B~G~H~oFIzO~ Bk(CF,COCHCOBu')4, 3, 1219 BkCI, BkCl,, 3, 1211r BkCI6 [BkC1,I2-, 3, 1219 BkF, BkF3,3, 1218 Bk203 Bk,03, 3, 1216 BrF, [BrF4]-, 1.122 ,~

294

C CaCHloN4010

Ca(N03)2(H2NCOIZH2)(H20)3.3.Y CaC3H,04 Ca(O,CCH,CO,), 2.414 CaC3H906 Ca{OZCCH(OH)CH20H}(H20)2. 2.480 CaC4H20s Ca(02CCOCH2C02),6,455 CaC4H40s Ca{(02CCH2),0), 3-33 CaC4H,0, Ca{O,CCH(OH)CH(OH)Coz), 2,479 CaC4Hiz09 Ca( (S)-OzCCH,CH(OH)COl)(H,O),, 2,475 CGHl,N,O,, Ca(N03)2(MeOH)4,1,89 C~C~HI&OOIO Ca(N0&(H2NCONH2),,3. 9 CaC6H6NO6 [Ca{N(CH,CO,),}]-. 2.789;3,33 CaC6H15BrzN306 CaBrz(H2NCH2CO2H),.3.9 CaC6HlsBr20s CaBr,(a-o-fucose)(H20),, 3,25 CaC6HZZBr2011 CaBr,(myoinositol)(H,0)5, 3,25 CaC6H&r2N1206 CaBr2(H2NCONH2)6.3. 9 CaC8H4Ns0, Ca(purpurate), 1,535 CaCloHlzNzO, [Ca(edta)l2-, 2,784.790:3.33;6.768 CaC1~HI3N208 [Ca(Hedta)]-, 2,784 CaCloH1404 C a ( a ~ a c )3,26 ~, CaCioHi6Nz010 [Ca(H,0)Z(edta)]2-,2,783 CaCloH1806 Ca(acac)2(H20)2. 2.372 C~CIIH~ZOR [Ca(tmta)lz-, 2,784 CaCiiHisN& [Ca(Htmta)]- ,2,781 CaCi2H14N6018 Ca(pi~rate),(H,O)~,1, 89 CaCizH16N208 [Ca(teta)12-, 2.794 CaCizHi7Nz08 [Ca(Hteta)]-, 2,784 CaCizH26Brz013 CaBrz(~-~actose)(E120)2. 3,2j CaC12H2&LN404 CaCI,(AcNHMe),. 2.492 CaCi~H36Nz01z Ca(NO3)dEtOH),, 3 , s C~CIZH&WI~ CaCI2(en),, 3. 11 CaCi3HlsN2Os [Ca(peta)]’-, 2,784 CaC13H19N208

295

CazClo~lzNzOs

Cumulative Formula Index

%GnHid'JzOs Ca,(edta), 3,33 Ca2C1zHzsOls {Ca(O2CCH20CH,CH20CH2CO2)(H2o),),, 3,33 CaiCibHi408 Ca2{0,CCH(0)Ph}2(OH)2.2. 474 CaG2HloO14 Ca,(citrate),, 6, 849 Ca 10Hz0J'b Ca,,,(PO,),(OH),, 6,597 C~UHIRN,~, Ca(X-quinolinolate),,1,528 CdBaO12P4 CdBa(PO,),, 5,962 CdBr, [CdBr,]-, 5,986 CdBr, [CdBr4]-, 5,985 CdCH,I,NZO CdIZ(HZNCONH2),5,967 CdCNSe ICd(SeCN)]+,5,987 CdC,H,O, Cd(O,CH),, 5,968 CdC2H4C12N3 CdCI,{H,NC(=NH)NHCN), 5,933 CdC*H4NZ04 Cd(C,O,)(N,H,), 5,933 CdC2H5ClzNS CdCI,{MeC(S)NH,}, 2,617 CdCzH6 CdMe,, 5,927 CdC2H6N03 [Cd(H2NCH2CO2)(Hz0)]+, 2,762 CdC2H606S2 Cd(O,SMe),, 5,961 CdCZHxCIZN4Sz Cd{(H,N),CS},CI,, 2.639 CdC2H,N,0, Cd(en)(NO,),, 5, 930, 934 C4CzO,)(N,H,)2,5,933 CdCzHioN,OS, Cd{HZNC(S)NHNH2)2S04,5.980 CdC2N,SZ Cd(NCS)z, 5,987 Cd(SCN),, 5,985,987 CdC& [Cd(CS,),]*-, 5,977 CdC,H,O, Cd(O,CCH,CO,), 2,444; 5.972 CdC3H306 [Cd(O,CH),]-, 5,969 CdC3H,CI,N CdCI,(HN*H), 5, 948 CdC3HiN3S [Cd(en)(NCS)]' ,5.987 CdC8,,8, ICd(f-1,2-pn)I2+,5,935 CdC3HisNi,S3 [Cd { SC(NHNH,),} ,I2+,5,976 CdC3N3 [Cd(CN),]-, 5,986 CdC3N303 [Cd(NC0)3]-, 5,987 CdC,N& ICdlSCNL-, .~ 5,985 CdC4H2O4 Cd(OZCCH=CHCO,), 5,972 CdCaHaOn Cd(OZCCHCHzC02).6.1026 CdC4H404S Cd{(02CCH2),S}, 5,976 CdC4H4Os I

294

[Cd(O,C'lI),]Z- 5 969 CdC4H604 Cd(OAc),. 5.969.998 CdC,HsCI,N2O4 Cd(02CCH2NH2)2C12. 5,939 CdC4HaK602Sz

Cd(NCS),(HzNCONH2)2,5,967 CclC4H8N6S4 ~ ~ { S C ( N H , ) = N C ( N H , I $2,640 )~, Cd{(H2N)zCS)l(NCS)2. 2.639 CdC4Hlo CdEt,, 5, 927 CdC4tiIoCI,N2O, CdCIl,(lICONllMe)~. 2. 492 C'dC41110C1,N;2S2 CdC1,{MeC(S)YHz)2.2,647 CdC4H,,C1,N, CdCl,(dien), 2,4?; 5.937 CdC,H,,BrIN, Cd(en),BrI, 5: 935 C ~ C ~ H I ~ N ~ [ C d ( ~ n ) ~ ]52, +931 ~ CdC4H16N50t [Cd(en),(NO,)]'. 5 - 935 CdC,N, [Cd(CN),j2-, I , 538; 2. IO, 12: 5,928. 930 CdC5H5CI2N Cd(py)CI,, 5,952 CdCSH,12N0 CdIz(py N-oxide). 5.965 CdCSHSO 10 [Cd(02CH)5]3 5, 969 CdC,H,N20S Cd{L-O2CCH2CH,CH(NH2)C02}(H 2 0 ) ,2,744 CdC5Hi5C12N3 CdCI,{H2NCH,CH2NH(CH2)3NHZ}. 2.47 CdC5HI6CIN5S C:d(en)JNCS)CI, 5,935,987 C X , I I,N,O, Cd(O2CCI-IZCN),.5 . 0 W CdC,H,Cl,Y Cd(PhNH,)CI,, 5,933 CdC,HinF,O, Cd(CF,),(h.leOCH2CH2OMe), 5,965 CdC6Hl,CL,N4O4 CdC12(H2NCOCHICONHz)z,5,945 CdC6Hl,N5S2 Cd(NCS),(dien). 2.47 CdGHi4 CdPr,. 5.927 CdC,I~I14N404S, Cd(Ohc),{ H,NC(S)NII1},, 5, 978 CdC6HI6Br2N2 CdBr,(TMEDh). 5.935 CdC6H,,N,0, [Cd(EtCONHNH2)2]2+.5,945 CdC6H16N6SI Cd(en),(NCS),, 2,235; 5 , 987 CdC6HlsBrN4 [CdBr{N(CH2CH2NH2),)]+,5,938 CdC6Hd6 [Cd(en),12+.5.934 CdC7H15NSSZ Cd(NCS), { H2NCH,CH2NH(CH2)3NH2}.2.47 CdCsHiiCI,NO, Cd(pvridoxInelC:l,. 5.965 CdCsH;IC12P {CdCI2(PPhMe2)),.5 . 950 CdCsHI?CIZNFOS CdCl2~D~S0)(4-mcthyladcninc), 5,957 CdC8HljN206 Cd( H,NCH,CONHCH(CH,CO,H)CH~CHzCO~}(H,OI. 2.763 - 1

297

Cumulative Formula Index

CdC44HZRN4

Cd(2-pyNHAc),CIz, 5,945 CdCi,HmN,O,

Cd~O~CH)z(3-pyCONHz)z(Hz0)z, 5,954 CdC,4H20N208 [Cd((02CCH2CHZ)zNCHZCHLN(CH2CH2C02)2}]2-. 2.787 CIIC',,H,,CIN,C),

[Cd~(McO,CCH,),NCH,CH,N(CIl,COzMe),}C1]+, 5. 947

CdCioNsS2 [Cd{C(CN),},( SCN)2]Z-. 5 987 CdCiiH~TZNzO C:d{(2-py)zCO}1215 . 955

Cd(SCN),{P(C,H,Me-3)3}, 2, 1040; 5,959 C d C d 3,,F,O, fCd(CF3COCHCOC4H30),]-, 1,65 [Cd(OCH=CHCH=cCOCHCOCF,),]-. 5 967

298 CdC,+aH,,N40,

Cd03S2

Cd(tetraphenylp~rphyrin)(dCH~CH~OCH~~H~). 5, CdS,O,> 2,637 993

CdCI3 [CdC13] ,5,985,986

CdCL [CdC141Z-,5,985,986 CdF3 [CdF3]-. 5,986 CdH2C14 CdH2CI4,5,984 CdHJO [Cd(H,O)I]+, 5,983 CdH,O,Se Cd(O,Se)(OH,), 2,429 CdH3S3 [Cd(HS)3]-,6,853 CdH,Br,O.

CdO6S4 [Cd(S203)2]2-,5,963 CdPdC4H,N, (Cd(NH,)z}{Pd(CN)a}, 5,934 CdPdC6HsN6 {Cd(en)}{Pd(CN),). 5,934 CdPdC6N6 CdPd(CN)6, 5.989 CdSl2 [Cd(S,),12-. 2,542 CdSh,F,, Cd(SbF&, 2,501 CdWzSp [Cd(WS4)z]2-.2.575 CdZAs3I CdzAsSI, 5,989 CdzC6HaN6 Cd(en)Cd(CN),. 5.934

Cdl(NCS),(butrz),, 2,235 Cd2C24H5608P4S8 [Cd{(Pr'U),PS,} 2]2,2.644 Cd2C3bH48C14N2P2

{ Cd{PPh,(CHzCHzI\iEtl)jClj2(~-Cl)2, 5,959 CdzGaHdWJiz [Cd(0zCCF3)2PPh3]z. 2,437 Cd2CIz Icd,a,l2+, -. s, 984

cd,cl;

[CdzC15] .5,986.987 Cd,FOJ'

[CdI,]-, 5,983,984,985 CdI4 ICdl,]'-, 5,961,983,985 CdKC13 [K(CdCl,)],,, 1. 125 CdMn2CloOI,, Cd(Mn(CO),}2, 5,988 CdN,Os [Cd(ONO),]Z-, 2,418 CdN,

CdNlz [Cd(N,),]'-. 2,235 CdNiC4H6N6 Cd(NH3)2Ni(CN)4, S,932 Cdh7Cl2Hl6N4O2S4 NiCd(SCN),(THF),, 5,988 CdNiC,,HloN, Cd(py),Ni(CN),. 5,932 CdNiCI4Hl8Ns Cd(en)Ni(CN),(pyrrole), . 5 , 9 3 2

[Cd4F4(HfiN=CHCH=tMe)12]4+, 5 9 51

Cfi,, 3, 1218 CfF, CfF,, 3,1219 CfO, [Cf02]+,3,1219 CfZOZS Cf2OzS, 3.1217 _, ,

,

C~C~ZHJONMO~ Ice{H,NCONHN=CMe&=CHCH=CH~C(Me)= NNHCONH7)+13'. 3.1090 -,I, CeC24H1608

[Ce(02C6H4)4]4-,1,94; 3, 1115 CeC36H30C140zPz CeC14(0PPh3)2,3.1115 C~C~~H~ON~O~~PZ Ce(N03)4(OPPh3)2,3,1115 Ce(OzNO)4(OPPh3)z.2,499 CeC36H4sN40 Ce(octaethylporphyrin)(OH). 2, 822 CeC44H76Os 6 . 1027 C~(BU'COCHCO€~U')~, CeC60H4408

Ce(PhCOCHC0PhL. 3. 1114 ~e~68~6008 Ce(PhCM2COCHCOCHzPh)4,2.373 CeCssH56Ns Ce(tetraphenyiporphyrin),, 2,823 CeC1, CeCI,, 3,1113 CeCI, [CeC16I2-,3, 1116 CeCrzOs Ce(Cr04)z, . - 3,943 CeF, [CeFJ, 3,1115 I

.

CeF, . [CeFSJ4-,3, 1115 CeKC28H4406 K{O(CH2CH20Me)2) ,Ce(cot),, 3, 17 CeMo1204z 3, ~1045 [C~MO~~O ~]~-, CeNsOi5 [Ce(N03),]2-, 3,1086 CeN60i8 [ce(No3)6lZ-, 1,.541;3, 1114 [Ce(OzNO),]2-, 2,417 [Ce(0zN0)6]z+,2,418 CeOI6S4 [Ce(S04)4]4--, 3,1114 CeWiO036 [CeWi0036]~ - ,3,1046 C ~ W J ~ O ~ ~ ~ P ~ [ce(Pzw,,o6,),]'6-. 3, 1048 C~ZFM

Cfz03

Cf203,3,1216 cfZ06s CfzO,(SO4), 3,1216 Cf,O,,S, Cf2(S0,),, 3, 1216 CmCI, CrnCl,, 3, 1218 CmF, CmF,, 3.1218 Cm2C0, Cm202(C0,), 3,1217 CmZC2O7 Cm20(C03)z,3,1217 CmK309 Cm,(CO&, 3, 1216 CmzOfS Cm,O,S, 3.1217 CmA CmtO,, 3, 1216 CmlObS Cm2O2(SO4),3,1216 CmA2S3 Cm2(S04)3,3, 1216 CoAg3ClllH9006P6S6

C~(SZCZO~)~{A~(PP~~)Z}~, 5,816 COASCI~HZ~N,~~ CO(HDMG)~(ASM~,), 4,774 COASC,SH,~CIN~O~ CoCl{As(OH)MePW}(HDMG)2,4,774 COASC~~H~SN~ CoH(N,)(AsPh,), 4,769 COASCZOHISNO? Co(NO)(CO),(AsPh,), 4,660 COASC,~H~~N~O~P CO(HDMG)~(PBU,)(ASM~P~), 4,775 CoAsFeMoWCzH6S CoFeMoWS(AsMeZ),4,832 CoAsHI6N5O4 [Co(OAsO3H)(NH3),]+,4,775 COASH,~N,O, [Co(OASO,H,)(NH~)~]~+, 4,775 CoAS2C26H2212

CoIz(PhzAsCH=CHAsPhz), 4,769 COASZCZ~H~~CI~ CoCl,(Ph,AsCHzCHzAsPhz), 4,769 COASzC36Hdz

COII(ASP~>)Q, 4.769 COASZGUH~VN~ [Co(CN),(AsPh,),]-, 4,773 COAS~A~G~HJ.~~~ 5, 804 Ag{(2-MezAsC6H4)zAsMe}Co(~o)4,

COAS~C~~H~~CI~

Cumulative Formula Index

300

[C~~M~C(CH,ASP~,)~}(CO),]+. 4.769,773 COAS~CMH~R CbHq(A~Ph3)3,4,769

COAS~C,,H,~

[ C O ( M ~ , A S C H = C H A ~ M ~ , )4.769 ~]-, CoAs4CI2HZ8Br2 [C~B~,(M~,ASCH=CHA~M~~)~]4.773 CtlA~jCizH32 [Co(MezAsCH2CH2AsMer)rlf.4,769 COAS~C~~~J~~CIZOIZ C O ( C I O ~ ) ~ ( O A S M2,C 500 ~)~, CoAsJCIRHJ4BrZ [CoBr,{ 1 ,2-(Me2AsCHaCH2CHzAsh.le)2C6H4)1+r 4, 174 CohCd34G [Co(O,){l ,2-(Me2AsCH2CH2CH2AsMe),C6H4}]+, 4, 774 CoAs4C18H3,Br [CoHBr { 1,2-(Me,AsCH2CH2CHzAsMe),C6H4}]+,4, 774 C O A S ~ C ~ ~ H ~ ~ [CoH2{1 ,2-(MezAsCH,CH2CH2AsMe)2CaH,)j’. 4, 774 CoAs,C,,H,, [ C o ( d i n r ~ ) ~ ]4,772 ~+, CoAs4C,,H3,BrN0 [CoBr(NO)(diars),] ‘,4,773 CmAs,C,,H,,CI, [CoCl,(diars),]+, 4,773 C0A~qC20H32C1208 Co(OClO,),(diars),, 4,772 COAS~C~~H~~I~ [CoI,(diars),]+, 4,773 COAS~C~~H~~NO [Co(NO)(diars),]+, 4, 773 C~AS~GOH~ZO, [Co(Oz)(diars),]+,4,773, 784 COAS~C~~H~~CI [CoHCl(diars),] ’ ,4,773 COAS~C~~H~~ [CoH,(diars),]+, 4,773, 784 COAS~CI~H~SO [CoH(HzO)(diars),]”, 4.773 COAS4CzoH3602 [ C ~ ( H , O ) ~ ( d i a r s ) ~4,772,781 ]~+, COAS~CZIH~,O~ [Co(CO,)(diars),]+, 4,773 COAS~CZ~H~ZN~SZ Co(NCS)2(diars)z,4,769 C OA S ~ C ~ ~ H ~ ~ O ~ [CoMe,(diars)J‘ , 4 , 773 CoAs,C,,II,,CI, [CoC12{{Me,As(CH,),AsPhCH,~l)l’, 4, 773,784 C~oAs,C,,H,,O, Co(O,){{Me,As(CHz),AsPhCH,},}. 6, 321 [ Cu(0,) { { Me,As( CH,),AsPhCH2JZ}] 4,773,784 [ C O ( R , R - C * ~ H ~ ~ A ~ ,2,319 )(O~)~~, COAS,C,~H,,O, [Co{{Me2As(CH2)3AsPhCH2}z}(HzO)zj3+. 4.784 COAS,C~~H~,B~NO [Co(NO)Br(diars),]+, 4,666 COAS~CJ~H~~C~NO [Co(NO)Cl(diars),l+, 4, 658 CoAs,C,,H,,NO [Co(NO)(diar~),]~+, 4,658, 661,664 CoAs4CJIHB4N20S [Co(NO)(NCS)(diars),] ’ , 4 , 661, A64 COAS~C.~~I-~~~CIO~ Co(OAsMePh,),(CIO,). 2,498 COAS~C~~H~~NS

[ C O ( O S O ~ C F , ) ( ~ H ~ ) 4,638 ,]~+, [ C O ( O ~ S C F ~ ) ( K H 1~, )186 ~]~~. CoCHl,N,U, [Co(CO3)(NH3),j+.2.447; 4,638,816,960 [Co(CO3)(NH3),l2+,4, 814 [ C O ( O C O ~ ) ( N H ~4,790,814 )~]~, CoCHI5N, [CO(CN)(NH,),]~~~. 1. 186; 4, 650, 654 CoCt-I,&O [Co(NCO)(NH,),jZT,4,677,679 COCH,~N~S [ C O ( N C S ) ( N H ~ ) 1,185,376,504; ~]~~, 4,679,681 [CO(SCN)(NH~),]~-, 1,185,376,465,471;4.680.681, 698 CoCHISN6Se [Co(NCSe)(KH,),12’ 4: 680 CoCH16N402 [Co(NH,),(O2CH)IZ+,1. 376 CoCHl6N4O6P2 [Co{IOP(O)(OH))2CHZ}(NH3)4li4,763,766 COCH,~N~O~ [C~o(O,CH)(NH,),]~ 4,791,792,793 COCHIhNsU3 [Co(OCO,H>(N11,),]’, 4,814 [Co(OCO,H)(NH,),lz+. 4,814 COCHiGN7 [CO(NH,)~(NCNH)]*+, 4.677 I

I

’

~

301

Cumulative Formulu Index

C0CHj7N602 [CO(NH3),(HNCO,H)]'-. 4.682 [Co(NH3)5(02CNH2)I2-,4,679 COCH~ 7N7 [CO(NH,),(NCNH~)]~+. 4.675.677 CoCHlsN503S [CO(OSO,M~)(NH,),]~+, 4,817 CoCHisN602 [CO(NH,),(H,NCO,H)]~' -4.679.682 CoCHI9N70 [Co(NH,),(H,NCONH,)]~+, I , 304; 4,677,682; 6,471 CoCH19N9 [Co(N~I3),{NCN(NH2),)I3-, 4,675 CoCICIN03 [COCI(CO),(NO)]-, 2,112 CoC,H,O, Co(O,CH)Z, 4,791 CoC2H,N40y [Co(NO,),(P!CMe)]-, 1.82 COC~H~N~O~ [Co(en)(NO,),]-, 2,418; 4.668,671 CoCZHsO1o [co(co,),(~r,o),]~-,4,811 COC~HION~O~ [Co(NH,),(H,O),(CN),]+. 1.22.26 CoC,H,,N,O, [Co(NHzMc)2(NOd,]-, 2,2X ChCZHllN606 Co(NH,)(en)(NO,),, 2,418 CoC,H,,N,O, [Co(C20,)(NH3),]+, 2.444; 4.800 COC~HIZN~SZ 4,679 [CO(NCS)~(NH~)~]+, CQC~HI~C~A" [Co(en)(NH,),Cl,]+, 1,27. 469 COCZHISF~NSO~ [CO(NH,),(O,CCF,)]~+. 1 301 COC2H1SN504 [Co(OC,O,)(NH,),J- 4,802 CoC2H16N,0, [ C O ( N H ~ ) ~ ( ~ ~ C C ' H6.O188 )]~+. I

CoC2HI

6N504

[CO(OC,O,H)(NH,),]~-. 4.8U0 COCzHi,IN6

[Co(NH3),(NCCH2I)I3-.4.678 CoCzHisNs02 [CO(NH~),(OAC)]~+. 1.371; 6,135,436 [CO(OAC)(NH,),]~+. 4.790.793 CoCzHisNS05P [Co(NH3)5(0P0,AcjJ+,4- 670.6,443 CoCzHi8N6 [Co(NH,),(NCMe)13-, 4.675. 676.678; 6,449,450,453 COC~HI~N~O [Co(Nl I,),(~IZNCtl,COF;H2)]~' .6.430 CoCZHlsN9 [Co(NH,),(S-rn~thyltetrazolate)]~+, 1, 186 [Co(NH,),( &=NN=NCMe)] '-. 4,698 C~CZHI~NBOZ 6,430 [CO(NH,)~(H,NCH,CO~)]+, COGHIYNY

[CO(NH,),(~~HN=NN=CM~)]~+. 4.697,698 [CO(NH,),(&I=NNHN=C.M~)]~+. 4,697 CoC2H20N6

[Co(en)(NH,),I3+, 2,31 CoC,H, ,N,OS ICo(NH,),(DMSO)l", 2-28:4,690.697,7Y0

COC~N~O,

[CO[CN)(CO),(NO)]-, 4,646 CoC2N4O2 [Co(CN)2(NO),]-, 4,646,658 CoCZN404 Co(C,O,)N,, 2,444 CoC2N6 [Co(CN)z(Nz)zlf34,650 COC~HJ~S~ Co(SZCNH,),. 4,864 COC~H,N& [ C O ( S , G N N H ~ ) ~ ]4,864 ~-, CoC3HRNSOZ [Co(OlCCH,NHMe)(NH,),1+, 1, 198 CoC3H9Nh 4.650 CO(CN)~(NH>)~. COC~H~N~S~ 4,864 CO(S~CNHNH,)~, CoC3H9N9S3 Co(HN=NCSNHz),, 4,858 CoC,H,,N20, [Co(C0,)(H20),(en)l'. 4,815 COC~HIZN,O&Z C ~ ( S O ~ ) Z { N ( C H ~ N4,822 H~)~}, COC~HI~N~S~ CO{H,NC(S)NHNH}~,~,~O~ CoCJ€,,CIN,S [Co(cn)(NH,),(NCS)Cl]+, 1,27 CoCBHi4NJOIS [CO(OSO,)(H,O){N(CH,NH,),}] ' ,4,822 CoC,H,,ClN, [CbCii( H,NCH,)3N}(NH,)]Z+, 2,5 1 COC3H15N9S3 [CO(H,NC(S)NHNH,}~]~+, 2,803; 4,857 CoCiH,&,O, [Co(fiki&[0,CC(Me)=NH}]2+, 6, 186 CoC,H,,N, 4,675 [C~(NH3)3(NCCHzCN)]3t, CUC;H P i a 0 2 [Co(8CH=NC( N02)=C H) (NH3)512- ,4,694 CoC,fI,nN,O, [r~(NFI,),(MeNHC11,CO2), 2,754

[CO(NH~),(O,CCHM~NH,}]~+, 6, 186 CoC3HlsN503 [CO(NH,),(O,CCOM~)]~+, 6, 186,459 CoC,H, .N, [Ci(NH3j5(NCCH=CH2)]3+,1,430; 4,675.676: 6. 449,350

CoC3HI8N7 [CO(N H3), (h-CH=NCH=C H)]'+, 6,435 CoC3HIBNs02

[CO(NH,),(H&CH=NCH=CNO,)]~+,4,699

[Co(NH,),(NCNMe,)13', 4,677; 6,449 COC~HZZN~ ICo(~H,),(R,S-pn)]3+,2,34

[CO(NH,),(NH,CH,CHM~NH,}]~+, 6,189 COC~H~~N~O [CO(DMF)(NH,),]~+,4,682,790; 6,433 [CO(NH,)~(NH,CH~COM~)]~+, 6, 189,458 COC3Ha3N70 [Co(NH2CONMeZ)(NH,),)'+, 4,677,698 COC~H~~N~O~P [CO(NH,),{OP(OM~),}]~', 4,752,755; 6,447 CoC,NO, Co(NO)(CO),, 1,290; 2, 106; 4,662,663; 6,270 CoC,N,O, _

.

i

d

[Co(NO)(CN)(CO),]-, 4,658 CoC>NiOz [Co(CN),(CO)(N0)]2-, 4,646,658

Cumulative Formula Index

COC~N~O

COC~N~O [cO(NO)(CN)3]3-, 4,646,658,662 CoGNziN7 [CO(NH,)~(NCNM~,)]~+, 4,675 ac30H24N6 [Co(bipy),l3+, 6,652 CQc303p3 Co(CO),P,, 4,699 coC303s6 [CO(S,CO),]~-,4,864 coc,o, [CO(CO,),]~-,1,22; 4,638,813,816.866 COC& [ C O ( S ~ C S ) ~4,869 ]~-, CoC4H 04 CoH(CO),, 2,689,694,696.703,706,709; 4,704 CoC4HZN404S [CO(CN)~(SO~)(HZO)]'-, 1,310; 4,652,823 [Co(CN),(S0,)(Hz0)14-, 4,653 COC~HZOS Co(02CCOCH,COz), 6,455 COC~H~CI~N~ COCI,(I~=CHCH=NCH=CH), 2 , 80 CoC,H4S, [ C O ( S ~ C ~ H ~4,876 )~]Gc4H604 Co(OAc),, 6,270 CoC4H,N,0~ [Co(HzNCHzCONHCHzCOz)]~, 2,760

[Co(en),(S2O3)C1]+ 1 294 COC~H~~CIN~O~S~ C O { S ( S ) S O , } C ~ ( ~4,817 ~)~, COC~HI~CIN~O [CoCI(NO)(en)z]-,2,103,104; 4,658,661 COC~HI~CINSO~ [Co(en),(NO,)Cl]+, 1,183,294 COC~H~~CINSO~ [Co(NO)(OClO,)(en),]~,4,658,661 COC4fI16CLN1 [Co(en),(N,)Clj 1,294 CoCJl,6Cl,N, [CoCl,(dien)(NH,)]-. 2,47 CoCl,(en),, 1. 127; 2,805 [CoCI,(en),]', 1,183,190,191,294,295,302,303,304, 307,401.402,467,468,469,50S; 2,28,32.768; 4.638; 6.427 CoC4Hi6N302 [Co (dien)(0H)(H2O)IZ+, 6,432 COC~HI~NJ [ G ~ ( e n ) , ] ~2,32,902 +. COCqH16N403S [Co(en),(SO,)]', 2,638; 4,820 COGH,~~O,S, [Co(SzO,)(en),l', 4,817 COC~H~~N~O~P Cu(en),(P04), 1,203; 6 , 446, 447 Co(OJW,)(en)2, 4,752 [Co(O,Po,)(en),]+, 4,750,753 COC~HI~NJO~S [Co(en),S04]-, 1,27 [ C O ( O ~ S O , ) ( ~ ~4,817 )~]+. COC~H~~X~O~SZ [Co(en),(S03),)-, 2,418,638; 4,822,823 COC~HMNJ~~S~ [ C o ( s A M e n ) J , 4,817 COC~H~~NSO [Co(NO)(en),12+.2, 112 COC~~~NSOZ [Co(NO,),(en),]', 4,667,670 COCqH16N604 [Co(en),(NO,),j+, 2,32,418; 4,638,666,668,473,788 [Co(NOz)(ONO)(en),]+,4,668,672,673 [Co(NO,),(dien)(NH,)]+, 2,47; 4,670 [Co(ONO),(en),]+, 4.668,672,673 CoC4Hie.Nio [Co(en),(N,),]'. 1,367; 2,232 CoC.81601oS4 Co(OzSMe),(H,0)2, 4,835 CoC4HI7C1N40 [Co(en),(OH)C!]+. 1,294,304 COcAfIi7N407Pz Co(en),(W,O,), 6,448 C O { O ~ P ~ O ~ ( O H 4,760 )J(~~)~, CoC4H18BrN40 [CoBr(dien)(NH,)(OH,)]+, 2,47 CoC,H,,ClN,O [Co(en)2(H20)C1]2+,1,304,467 CoC4HlaFN40 [CoF(en),(H,O)]+. 1,254 COC~H~~IN~O~ ~ C O ( O I O , ) ( ~ ~ ) ~ ( H4,826 ~O)]~~, CoGHi8N303 [C0(dien)(OH)(H,0)~]~',6,432 C0C&i&02 [Co(en)z(OH),l+, 1,304 COC~H~&,O~S [Co(S03)(OH2)(en)ll+14,823 COC~H~SN~O~S [ C O ( ~ ~ ) ~ ( S O ~ ) H ~1,294; O ) ] ' ,4,823 COC~HI~N~O~S~ [Co(s,o,)(H,o)(en),l', 4,817,857 COC4HISN404S3 *1

3

CoCl,(dien), 2,47; 4,765; 6,216,436 CoCaHiiNi [CO(dien)l3+,6,448 COC~HI~N~~~ Co(dien)(N0J3, 6,436 Co(NO,),(dien), 2,47; 4,668,670 CoC4HiaNiz Co(N,MdienL 2.47 4,658

[Co(SkN){N(CHzNHz)3}(NH3)]2+, 4,680,681 CoC4H16BrCIN4 [C~(en)~BrCl]+, 1,294,469 COC~H,~B~N&'Z [Co(en),(NO,)Br]', 1, 505 CGHMB~ZN~ [Co(en),Br,]+, 1,294,467,468,469; 2,32 CoC,H16CIH403S Co(en),(S03)CI, 2,638 COC~H~~CIN~ [ C ~ ( e n ) ~ C l ]1,505 ~+, COC~H~~CIN~O~S~

302

Cumulative Formula Index

303 [Co{S(S)SO,}(OH,)(en),]-,

4.817

&C4HlSN40SP

Co(en),(OH)(HP04),6,446 COC~H~~N~OSS [Co(en)z(HzO)S041+,L27 [CO(OSO~)(H,O)(~~)~I-, 4,817 CoC4HmNs04 [Co(NH3)s(0zCCH=CHC02H)]~~, 1,374,376 COC~H~~CIN~ [CoCl(dien)(NH1)z]2+,2,47 [CoCl(en),(NH3)j2+,2, 31 [C0(en)~(NH~)Cl12’, I, 12,25,294 COC~H~~CINSO ~CO(~~),(H,NOH)CI]~’, 1,294 CoC4Hi+’J303

[Co(d~en)(OH~)~]~+, 2,47 CoC4Hd40z [CO(OH)(H~O)(~~),]~+, 4.786,800,822,825; 6,432 COC~H~~NSO~S [C~(en)~(NH~)(so~)l’,2,32,638 COC~HI~N~OZ [Co(ONO)(NH,)(en),]+, 4.668 [CO(ONO)(~H~)(~~),]~+. 4.672

COCSN51

COCSHN~O~ [Co(OOH)(CN),]”-,6,324 COC~H~N~O 2,9;4,650,653,784: [Co(CN),(H20)J2-, 1,186,310; 6,435 [CO(CN)~(H~O)]~-. 6,236 COCSH~N~ [Co(CN),(NH3)I2-,4,650 COCSH~CIZN [ctci,(pyj]-. 4,685 CoC5H5Cl2N5 CoCl,(adenine), 4, 694 COC,H,N~S, CoCp(S2Nz),2. 799

CoCSH,N2O2S, Co(MeC(S)CHC(S)Me}(NO)z, 4,660,880 C0CgH702

ICo(acac)l+, 1.538 CdC5H9N203 [Co{H2NCH2CONHCH(Me)COz}]+, 2,760 CoCsHiiNc Co(CN),(NH,)(en), 4,650 CoC,H,,Cl,N, CoC13(H~NCH,CH,NH(CH2),NH,JI 2,47 COC4Hd604 CoC,H,,CIN,O, [Co(NH3).,{02CCMe(CH2NOz)r\lH,)I””,6,186 [Co(en),(CO,)Cl] I , 1,294 COC4H19N7 COCgH16CINg CO(NH~),(I~CHCH=NCH=CH), 1,364 [Co(en),(CN)CI]-, 1,294 [CO(NH~),(~~=CHCH=NCH=CH)]~+, 4,688 CoC5Hl6C1N5S CoC,HzoN4Oz [Co(en),(NCS)Cl]+. 1,183,294,305 [C0(en),(H,0),]~+,1,284,447,469; 4,679,786,800, 825 CoCsHifiN60z [Co(ONO)(CN)(en),]+, 4,672 CoC.&oN406Pz CoC5Hl6N6OZS [Co{{oP(o)(oH)>,CHz}(en)zj-. 4,766 [Co(en),(NCS)(NO,)]+, 2,32;4,670 C O C ~ H ~ ~ N ~ ~ ~ T ~ [Co(en),(NCS)(ONO)]+, 1,465; 2,32;4,668.670.672, [CO(~~),(O,T~(OH)~)]+, 4.817 673 CGHZONB COCSH~SN~OS [CO{(H~NCH~),(M~NHCH,)N){NH,),]~+,~,~~ [Co(OSCH,CH2NHz){N(CHzNH&}]’+,4.845 CoCJI2oN7 CoC.H,.N.OSc [CO(NH,),(~~CCH=NCH&M~)]~’.4,697 [C’b(OSe*CH2CH2NH2){N(CH,NH,)3}]2’, 4,X82 COC4Hzo06 [Co(MeOH),(OH,),1~2-, 2,2518 COCgH18N604 ~,

C;C4Hz,N70;

[Co(NH&( NCCH2CHzCH2N02)]3C, 1,430 COC~HZ~N~ [Co(dien)(NH3),I3 .2,47 CoC4Hd60~ [CO(NH~)S(HZNCH,CO,E~)]~+, 6.214,430 GC4N4 [Co(CN),]’-, 4,648 [Co(CN),I3-,4,647.655 COC~N~O~S [CO(CN)~(SO~)]”-, 4,653,823 [CO(CN)~(SO,)]”,4,650 COC,+N40&2 [CO(CN)~(SO~)~J’ ,4,638,650,653,773 COC~N~S~ [Co(CNS).,IZ-,I , 548 [CO(NCS),]~-, 6.802,847

COCqN6 ICo(CNMNz)l-, 4,650 . ..

CdC4O4 [Co(CO),]-,1,122; 2,210: 696 COc40, C O ( c 0 ) 4 ( 0 , ) , 4,781

CoCsBrNS [Co(CN),BrI3-,2.10 COCSCINS [Co(CN),C1]3-,2 , 9 CoC,HN5 [CO(CN),Hl2’,2,691 [Co(CN),HI3..-, 2, 10,711; 4.647,649,655; 6,496,497

CoCqHNqO [Ci(CN)s(OH)]3-, 4,652,830; 6,435

CdCSH19N403

[CO(CO,H)(H,O)(~~)~]~+, 4,802 [CO(O~CH)(H~O)(~~)~]~+, 4,791 COC5HI9N6S [Co(SCN)(NH3)(en)z]z+’, 4,680,681 CoC5HznBrzNS [Co(en)zBr(HzNCHzBr)]zi, 6,430 CoC5H20N503

[CO(NH~)~(O~CCQ~H~ 6,468 )]~+, CoC5H2&

[Co(p~)(NH3),1~+, 3, 1110 CoCSHmCING [CO(&),(H~NM~)CI]~+, 1,294 COCSH~INIO [ C O ( N H ~ ) ~ ( A C & - C H = N C H ) ~ ~ ‘ , 6,435 CoCsHzzN~o, Co(NH3)5(OZCCH,CO,Et), 1,377 [CO(NH~)~{O~CCO(CH,)~OH}]~’, 6,468 COCSHZZN~OZ [CO(NH~)~(NCCH,CO~E~)]~+, 4,676 COCsHz4N602 [Co(NH,), { HN=CMeC(CHz0H)2NH2}]3+,6,189 CoCSN302 ~ C O ( C N ) ~ ( C O,4,647,655 )~]~COCSN~

2,9,10,582,709,711; 4, [Co(CN),]”-,I , 334,366,376; 647,448,652,681,830; 6,236,237,497 [Co(CN),j4--, 4,647 COC~NSI

COCSNSI

Curnulutivu Farmulu index

[Co(CN)5II3 ,4,638 CoCSN502 [Co(CN)s(02)]'-, 4,777 [Co(CN),(0,)I3 , 2 , 10.322.323.329,U. 650.654.780 CoC5N503S [Co(CN),(S0,)I4-, 4,650 COC~NSO~SZ [ C O ( C N ) ~ ( S , ~ ~ 4,650 )]~-, C0C5N60 [Co(CN)s(N0)l3-, 4,657, 658 CoCSN60, [Co(CN),(N02)3-, 4,652 CoC,N, ICO(CN),(N,)]~-,2, IO, 4.654 COC~HN~O~S~ [Co{S,C==C(CN),}(S,C=CHNO,). 4,869 COC&,NO6 [Co{N(CH,CO,),)I-, 2,789 c0c6H 6N4 {co(WH=NCH=CH),},.~. 69-1 CoC,H,O,S, [Ci(SCHZC02)3]3+, 4,838 COC~H~CI~N~ CoCI,(HfiCH=NCH=?H),. 4. 694 CoC6HsCI,N4S2 Y

"

I

304

CoClZ(Me3N0),.2,49' CoChHlsC12N4 [CoCl2{(H2NCH2CH2NHCH2),)]+, 1 , 194,201,467: 2, 52-54.6.215,m COC~H,~N~O~P~ [CO(NO),{P(OM~),),]~, 4,750 C O ( N O , ) ~ ( M ~ , P O1,57; ) ~ , 2,498,499; 4,768 COC,H~~N,O~S~ 2,800;4,838 CO{S(O)CHICHINH~)~,

[Co(SCH,CO,)(cn)l]', 2. 805; 4,840.846.856 COCgHlsN40& [Co(en),(SeCH,CO,)]+. 2,808 COC6H 1sN4O:S [Co(OSCH,CO,)(en),]', 4,846 COC6HlsN404 ICo(en),(O,CII],1-. 1.377

c~c,H,,N,o,

[Co(OC203)(OH2)(en),)+,4, 800 CoC,H,,N,C), c~cI,{SC(NH,)=NCH=C'H),. 4,694 Co(NH2j(en),(C2C)4).6 , 190 CoC,HHN,Os CoC,H 1XN602 [Co(en)(C,O,)J, 3,472: 4,638.802 [ C ' O ( ~ ~ O , ) , : ( I - ~ , N C H I C H ~ N H C H4.~670 )~)~~~, CoC,H,CIN,O,S CoC,HIsN6O4 [Co(N0,),{HINCH2CH2NHCI I,),}]+. 4, 668 COC6HisN6S3 [Co(C20zN,H)2{MeC(S)NH2)1'.2. M7 [ C O ( H ~ N N H C S M ~ ) 4, ~ ]858 ~+, COC~HIONZ~~S~ C O C ~ H I ~ ~ P ~ S ~ [Co { SCH2CH(NHZ)C02}2]-,4.837 Co{S,P(OMe)2)3. 1,67: 4,871 CoCAHwNqOSa CoC6HI9Cllr;,O2 Co(NO)(S,CNMe,),, 2, 102-104.49 658, 660,664 [Co(en),(OAc)Cl]+, 1,294 COC~H.~&IN~ CGHd30, Co(Gly-O),, 1,426; 2,754; 6,207 [Co(en)(H,NCH2CH=NCHZCH2NH2)Cl]2i ,6,459 CoC6HI4CINs0 CoC6H 1ZN6% Co(HN=NCSMc),, 4, 858 [CoCl(dienj(HaCH2CONH2)1", 6,433 COC~H~~S~ C0c:J I18K403 [Uo(1,4,7-tri t hiacyclononane)] 2+ 4.819 [Co(cn),(O2C(3I I,0H)J2-', 2, 465 CoC,H,,N,O, COC6Hi86 [CO(SCH,CH,S)~]~-, 4,838 [Co (OC,O,H)(H,OI , 4 , 800 CoC6HI9N6O6P CoC6Hi&O6 CO{O,CCH,)~NCH~CH,NH~} (OH)(H,O), 6,432 [Co(NH,),(NH,) (2-02NC,jH,OPO3H)]+, 1,142 [ C O ( N H , ) , ( ~ ~ P O C ~ H ~ N O , -4,755; ~ ) ] + , 6.417 C~C&MN,O~S, [CO{SCHZCH(NH~)CO~}~(H,~)~]-. 4.837 COC6HiSh" [Co(NH,)j(-l-?lC~py)]~+, 1, 186; 3,846 COC6HI 4O6S2 Co(MeSCH2CO2),(H2O),. 2.805 COC~H,~O~P~ COC~H~~CIZNLS~ CiHiP(OP&)3},. 6, 239 [CoCl,{(HZNCH2CH2SCHz),}]' 4.852 CoC,H,,,BrN, COC,HI~F~N,O,S, [CO(C~),B~(II,NC:F~,CN)]~ ', 6,351 [Co(OSO,CF,),(en),]-, 4, 638 COC~H~~CIN~O [CoCl(H~NCH~CH~NHCH~CII~NI-ICI 1,C'H,NH21COC~H~,N,O~ [Co(SOC,O,)(en),]', 4, 846 (C)H2)]2+32, 52 CoC6H2,,ClN5O2 CoC6Hi6N404 [Co(C,O,)(dien)(NH,)]+, 2.47 [Co(en),C1(H,NCH2C0,)]+, 6,430 [Co(C,04)(en),]', 1,453; 4,801. 802.803 CoC,H,,CIN, [Cb(~n),Cl?H,?JCH,CN)] ,+,6,45 1 COC6Hi6Ns06 CoC6H2oC12N4 CO(NO,)(OC,O,)(~~)~, 4,790 CO{H~N(CH~)~NH~)(O~CCH~CH~NH~)(NO~)~, 2,45 [CoC12(pn)2]+,1, 197,467,468; 2,45 COC~H~~NGO~ COC6Hi6N6 [Co(CN),(en),]+, 2,32; 4,650,651 [Co(Gly-O)(en),]2-. 1,426,428,442,Z. 756; 6,207. 213.427.429.430.433,466,469 CoC6Hi6N6Sz [c~(NCS)~(en),l, 1, 183 l C 6. [Co(NI 13)3 { 0,CCMe(NH2)CH,C(Me)=NH}] COC~H~~CIN~O~ 186 [CoCl(dien)(H2NCHzCO2)]+6.433 CoCnH2&O4 [To{H,N(CH,),NH2},(N0,),]', 2,45 [CO{H2N(CHL),NH,},(NO,),l~+, 4,670 COC6H20N605P [CO(OP(OH)OC6H4N02-4)(NH3)5]2+, 4,766 COC~H~~CINS ~

1 ,

-

Cumulative Formula Index

305

COC7H21 3 6 0

[CoCl(dien)(en)12' ,2.47 COC~H~ICINSO

[Co{SC(0)C(O)S);l3-, 1.68; 2,645 COC~O,~ [CO(~~)~(H~NCH~CHO 6,158 )CI]~+. [CO(C,O,)~]~-, 1,68,466,467; 3,472, 1236; 4,692. 802: 6,496. 531,652 CoC6HziN402 [CO((H~NCH~CH~YHCH~)~}(OH)(H~O~]*+, 2,54 CoCjHF,N5 767; 6,214.215.431.432 [CO(CY),(CF~CF~H)]~-, 4,654 [CO(N(CH~CH~NH,),}(OH)(H,O)]~+, 6.432 CoC,H,NO,, COC~HZ~N~S [Co{ i.64 ?,02)2py)],,.4,685 [Co(MeSCH,CH2NH2) { N(CI-I,NFT, j3}I3+,4.85 1 CoC,H;OZ CoCp(CO),, 1,290; 2, 115,218 CoC,H,CI,N,O COIOC(~N=CHCH=~H),)CI,, 2,256 [C:o(en),(H,NC:M,C")(OfT)12' .6, 45: CoC6HZIN60Z (Co(ONO)(cn)(dicn)12-. 4, 672 . ,

, _

CO(NH~)~((O~CCH,),N).1, 369 CoC6H,,N,0 [Co(NH3)5(4-pyCONH,)]z'. 1.369.372 CoCA,N,<

[C;( OSCHZCH2NH2)(cn)2] -. 4,840 [Co(OSCH2CH2NHa)(cn)~]~. 4,845,846 CoC,I I,,N,OSe [Co(OSeCH,CI 1,NI 12)(en)2]2i? 4; 8x1 ~

COC~H~~NSO~S

[Co(02SCH2CH2NH2)(en),]'.4- 840,845 COC~H~ZN~OZS~

[CO(O~S~CH,CH~NH~)(~~)~]~-, 4,881 COC~H~~N~S

[Co(SCHZCHZNH,)(enj,]'f, 2.800; 4,840,846,850, 856 CoC6H,,N5Se

[Co(SeCH,CH,NH2)(en)z]2--.3.807; 4,881 CoC6HZ2N60

[Co(en),(H2NCH2CONH,)1"'. 6,452,452 CoCOHZ3N40Z [Co(Oll)(C)l 12){li,N(CH2j3NH~}~L+, 4,765 CGHd503 [ C O ( H ~ N C H , C O ~ H ) ( ~ ~ ) , ( O1,442 H~)]~~, COC,H~~N~O, [CO(~~)~(OH)(H~NCH~CONH~)]~-, 6,434 [CO(ONO)(NH~)(H,N(CH~)~NH~)~]~+, 4,672 COC6HwN6 [Co(en),]*', 1,336. 514 [Co(en),13+, 1,22,25,27.67. 197.224, 254,336,356, 454.466, 467, 481.514; 2: 32,34,754,902,927; 3, 1110; 4,808,809.827: 6. 99: 191 [CO(NH,),{(~-I~NCII~C:I~~NI-IC~H~),}~". I , 201; 2, 54 COCgH25CIN5 [CoCl{H,N(CH,),NH(CH,),NH,)(cn)]2*, 2 , 47 CoC6H30C12P,S, C O ( M ~ ~ P S ) ~2,642 CI~, COC~N~ [Co(CN),]"-. 1.3, 183,400.410: 2 , 8 , 10, 11. 13; 4,646, 650,652,654: 6.822. 1018 [Co(CN),]", 4.652 CoC6N60 [Co(CN)j(NC0)I3-, 4.650.680 CoC,N,O, [Co(CNO),13-~. 2. 13 COC6N6S [Co(CNj5(NCS)13-,4, 6513.hXT [CO(CN),(SCN)]~-,4. 65111h X 0 . 081 CoC,N,S, [Co(S,C=NCN),13-, 4,869 COC6N6SC [ C O ( C N ) ~ ( N C S ~.4,650, )]~ hXU [ C O ( C N ) ~ ( S ~ C N ) 4. ] ~ -680.681 .

c0c,0,s,

Co(CN),(dienj, 2,47: 4, (150 CoC7H15N,0,

[ro(2-0-5-C)NC',~I3C'02(NH3)4]+, 4, 803 [CO(2-O-j-ONC6H3CO,)(NH3)4]'+, 4, 803 CoC7H,,N505 {CO(2-O-j-O2NC6H3CO2)(NH3)4]+, 4,803 [Co(2-0-5-02NC5H3CO,)(NH3),I2+, 4,803 COC7HISPSL Co(S*CPEt,), 4, 860

COC~HI~N~O~ [C~(COl,(en)~l-,4,813 C0C7H,,ClW,S, ICoCL{ (HINCHzCHZSCHZ)zCH2)]i, 4.852 CoC,H ,,Cl,N, [Co(NI J3j5(4-NCC6H40)]z+, 6,449 CoCjH20CIN6 [C~(en),(imidazole)Cl]~+,1,304; 4,694.696 COC~H~~CI~K~, [CoCI2{(H2NCH2CH2NHCH2),CH2}]+, 1.302; 2.51 COC,H~~K;,O, [CO{H~N(CH,),NH~},CO,]+,2,45 COC,H,~N~O~ ' ,6, 187 [CO(~~),{O,CC(M~)=NH)]~ [CO(NH~)~(O~CP 1,376 ~~]~+,

CoCTHmN, ICo(NH,),(NCPh)13+, 4,678; 6,449.450,453 COC7H2oN603S [Co(enj~(imidazole)(SO3)]~', 2.32 CoC7H,,N604 [Co( NO2)2( H2hCH,CH,NHCHMeCH2NHCH2CH2NH2)]+. 2,53 COC~H~~N~OLS [Co(MeSCH2C02j(en),12+, 4,846 CoC,HiiN403 [Co(en),Co,ccH(oH)Me}]", 2,465 C'nC,ti,, h&S [C~~(SCH~CH(NHZ)COZ}(CI~)~]+, 3, W4,4,839. XS(1 [CO{SCH,CH(NH~)CO,}(~~),]~+, 1,442 COC,H,~N~O~S [Co{OSCHZCH(NH2)COZ)(cn)z]+. 4,845 CoCTH?
COC~H~~N~O

Cumulative Formula Index

[Co(NH3),(HNCOPh)12+,6,449 COCtH21N6OS [CO(NH,),{SC(O)NHP~}]~+, 4,860 C O C ~ HNAO, , [Co(~H3-)5<4-02C-l-Mepy)]3+, 1,374 CoC7HzzBrN6 [CO(~~),(H,NCH,CH~CN)B~]~+. 6,451 C O C ~ H ~ ~ N J ~ [Co(~n)2(O~CCHMeNHz) 12 + , 6,207 CGHzzNsOzS [CO{SCH~CH(CO~H)NH~}(~~)~]*-, 1.433,442; 4,840; 6,212,213 CoC,H,,N.O,S , ** " [Co{OSCH~CH(NH,)CO,H) (cnj2lZ+,4,845 CoCJLNsO4 1

306

Co(NO)(HDMG),, 2,112,113; 4,658,662,666 COC,HMN,O, Co(N01)(HDMG),,4,662 708

[C&NO&(en)2]1., 4,666 CoC.H.,CIN, [Cki{(H,kCH,),N}(py)12', 2,51 CoCe.H17Ns04 [CO(NH,)~{O~CC=NCM~(OH)CM~(OH)~H~}]~+, 6, Co(HDMG),(NH,)(N,), 3,472 186 CoCaHis.CIN,S, CiCl(HzNCSNHN=CMe2)2, 4,857 aC7HzzN60 6: 449 [CO(NH,),(H,NCOP~)]~+', CoC,H,,CI,N,O, CQC~HZ~CIN~ CoCI,(AcNMe,),, 2,492 [CoCl(dien)(HzNCHMeCHzNH,)J2+, 2,47 CoCaHi d z 0 2 [ C O C ~ ( ~ ~ ~ ~ ) { H ~ N ( C 2.47 H ~ ) ~ N H ~ } ~ ~ + , CoCl,(AcNMe,),, 2.492 COC~H~~C~NSO~ CoCaHisN2P, Co(en)z(HzNCHzCOzMe)C1,2,768 Co(CN)2(fMe3)2,4, 725 ~Co(en)2(H,NCH2C0,M~)C112', 6,427 COC8HI8NZP2S2 Co(NCSj2(PMe3),,4,725 CG+L~N502 [CO(~~),(H,NCH,CO,M~)]~-, 6,436 CoCsN i n N s [ C O ( ~ ~ ) ~ ( H ~ N C H ~ C6,427,436 O~M~)]~~. [C~(CN),(H,NCE~~CH,NHCH~CoC,H,,N, CHZNHCHZC~~ZNHZ)]', 2,54 , " [Co(enjz(HZNCH2CH2N=CH2)I3--. 2,927 CoCaHiJ'Ws Co(NH3)z(Gly4),4.684 CoGHz4N60 [Co(en)2(HZNCHzCHzCN)(HzO)]3-. 6,451 CoCsHi4'b [Co(en)z(HzNCH2CHzCONH2)]3'. 6,451 [Co(NH,)S{ 1.2-(NC)zC6H4}]3+,4,676 [CO(~~)~(H~NCH,CONHM~)]~+, 6,432 CoC8H2DBrzN4 CoC,H,,N,O, [Co(1,4,7,10-tetraazacyclododecane)Br2]+,I, 303 I* _. [ Co{H2N(6H2)4NH(CH2)3NH2}(H20)3]3+, 6,498 COC,H&I~N~S~ [COC~~{(H~N(CH~)~SCH~}~}]+, 1,199; 4,852 CGHzsNsOS [CO(OSM~CH~CH,NH,~(~~)~]~~, 4.846 CoC,HZoCl,N,S CoCI,{S(CH,CH,NMe,),}, 4,849 COC7H25NSSZ [CO(M~SSCH,CH,NH,)(C~~~]~+, 4,856 CoC8H20C1Z04S2 COC~HZ~N~ COCI,{S(CH,CH,OH),}~, 2,805; 4,849 2.35 [Co{H2N(C~-12)3NHz}(en),]3C, CoCgH2&l,O,S4 Co(CIO&(MeSCI I,CH,SMej,,.~ 4,849 COC7H27N7 [CO(~~),(H~NCH,CH~NHCH~NH,)]~-, 2,927 CoC,H

__

I

~

~

[CO(AHCH~CH~NHCH~CH~NHCH~CH~-

NHCH,CH2)lZf,2,912 COCSHZON~OZ [Co(H&CH,CH VHCHz0CH2NHCH2CHzNHCH20CH2)13+,2,902 [Co(CN),Cp]-, 4,650 COC~H~~N~O~P C0CgHgN30zS4 Co(l,4,7,10-tetraazacyclododecane)P04, 6,447 [CO{S~C=C(CN)~} {SZC=C(CN)C02Et}, 4,869 COC&LN~~~ CoC8HsClZN4 [Co(dien)H2NCHzCONHCH2C02)] ' ,6,467 CoCI,(fi=CHCH=NCH=cH),. 4,686 [cO(NH~)~(4-O~CC~H~CMo)1zC, 1,377 CKsHioNzOh COCSHZCINSS~ [Co{O,CCH( CHzO)NCH2CH2NCH( CH,O)CO,}]-, [Co(N,) { (H2WCH2CH~SCH2CHJ2S}]'+,4,852 4,809 C~CSHZON~O~ CoC*HmN,On [Co(NH,),(HDMG),]+, I, 186; 3,472 C~{(CH&[NH(C2H,0z)]z}(C,0,), 1,129 COC~H~ON~OS [Co(dien)(H2NCHzCONHCHzC02)(NOz)]+, 6,433 CGHiiN403 CO{~ = C H N H C H = CH~CH(NHCOCH~NH~)CO~}, ~ COC~HZ~N~S~ 2,768 [CO(NCS)Z{H~N(CHZ)~NHZ}Z]+, 2,45; 4,679 [CO{N=CHNHCH=CCH,CH(NH,)CONHCoCgH2002PZSe2 CHzCO2}]+,2,760 Co{Se(0)PEt2}z.4,871 COGHizOiz CoCsHmOJ'zS4 CO{(S)-OZCCH~CH(OH)CO~)(H,Q)~. 2.47h Co{S2P(OEt),),. 4,870 GCBH14N404 CoC8HzoPA Co(HDMGj2,4,774;6,23&,257,51U CO(SIPEtl)2,4,870 [Co(HDMG),]'. 2,271 CoCaHzoS4 [Co(SEt,)12-. 4, 834 CoGHdaO, CO(H2NCH,CONHCH2CO,}2,2.760 COC~H~~CIN~O [ C O ( H ~ N C H ~ C O N H C H ~ C O2,759,768; ~)~] 4,684, [CoCl{H~NCH~CH~NHCHZCH~N(COCHZNH~)CHZ685 CHzNH,}IZ-, 6,189 ~~

~

Cumulative Formula Index

307

COCSHZ~N~OSP 6, [Co(1,4,7,10-tetraazacyclododecane)(OH)(OP03)]~, 447 COCsHziN6 [(NH3)5Co(NCCHPh)]2+, 2,265 COCRHZ~ N,Oz [Co{02CC(Me)(CN)NH2}(en),12f~ 1,442 [Co{O2CC(Me)(NH2)C(NH2)=NCH2CH2NHZ)(en}lz+,1,442 COC&21N66iS I _

[Co(en)2( H2NCH2CH=CHCH,NH,)] COC~HI~N~O

'+2 , 4 4 ~

[CO{N(CH,CH,NH,)~}(NH~)(DMSO)]~+, I , 304 CoCSHzsN60

[Co(en),(H,NMe)(H2NCH2C0Me)l3f,6,458 COC~HZ~CI~N~OZ

[CO(M~NHCH,CH~NHM~)~CI~](H~O~)C~~, 1,468 CoC8N4 S 4 CoC8HZ1N70 [Cn{S,C,(CN),),]-, 2,611,613;4,876, 879 [CO(NH~)~(~-NCC~H~CONH,)]~+. 2,266; 6,451 [ C O ( S ~ C ~ ( C N ) Z )2,610,613; ~]~-, 4,638,879 COC~H~~CI~N~ [CQ{S,C~(CN)~}~]'-, 2,611,613,617; 4.879 COCSN~OS~ [COCI~{H~N(CH~)~NHCHZCH~NH(CH,),NH~}]+, 2, 55 [COISZCZ(CN)Z}Z(NO)~'-, 4,879 COC~H~F~SZ CoCsH22N402S [ C O ( S C M ~ ~ C O ~*,) 4,856 (~~)~] COCP{SZCZ(CF~)Z}, 2,604 COGHSNZSZ COCSHZZNS~Z [CO(G~~-O){(H~NCH~CH~NHCH~)~}]~+, 1,202; 6, CoCp{SzCz(CN),}, 2,604 C0CgHgN302 215,429,431 Co(NC0),(2,4-lutidine), 2,227 [CO(GI~-O){N(CH~CH~NH~)~}]~+, 1,426; 6,211 CoCgHI2ClzN4 CoCsHzzN, Co{Me,C(fiN=CHCH=~H)z}Clz, 2,256 [c~(en),(NCMe),]~+, 4,675 COGH~ZOIZS~ aCsH22N604 [ C O ( S , C O C ~ H ~ S O ~4,866 )~]~-, [Co(NO2),(HZNCH2CH2NHCHMeCo&H13N,0, CHZCH~NHCW~CH,NHZ)~+, 2,53 [Ni{ N(CH,CO,),} (W2NCH2C02Me)]-,6,418 -,6,451 CoC9HI3N4O2 CO{PS=CHNHCH=C CH=CHNHCO-,2,266 CHzNHCOCH2NH2},2,768 CoCgHi3N403 [CO{N=CHNHCH=CCH,CH(NHCOCH2CH2NH2)C02}]+, 2,760 [CoCi{H2N(CH2CH2NH)3CH2CH2NH2}]2+, 2,56,57 [CO{(H2NCH2CH,),NCH2CH,NHCH:CH,NH2} CGHI~NSO~ Co(NC)(DMGH),, 1, 186 CI]", 1,306 C O C ~ 14N507S H CoC,H2,C1N50 [Co(CN)(HDMG)2(S0,)]2-, 4,650 [CO{(H2NCH2CHINWCHz)z}(~~NC~zC~O)Cl12+, 6, 458 ~C,HI,N@~S, [CO{SCH~CH(NH~)CO~}~]~-, 4,837,838 COC~H~,NSO~S [Co(OS02){ HN(CH2CF12NHCH2CHZNH2)2}]+, 4: 822 COCsHt3N603 [CO(~~),(H,NCH,CONHCH~CO~)]~+. 6,432 C0CsH24ClN402 [CoC1(MeNHCH2CH2NHMe)~(O~)]+, 4,778 .- - . CO(S,COEt),, 1,67;4,638,867 CoCSH,,NOP2 CoMe2(NO)(PMe3),,4,716 COC~ISS~ Co(SCH=CHSMe),, 4,838 COCSHZ~N~OZ 6, 447 [Co(1,4,7,10-tetraazacyclod0decane)(H~O)~~~*, CGHi.& Co(S,CSEt),, 4,866,867 cOC,H,~N~S, 4.852 [Co{S(CH2CH2NH2)2)2J3+, COC&I~N&~ Co(CN)(HDMG),(H,O), 4,654 CoCsH24NsOzS Co(NC)(HDMG),(H,O), 4,653 [Co{MeSC~2CH(NH2)C0,}(en)~]z'1 4,850 [Co{SCHzCH(NH2)C02Me)(en),]*+, 4,850 COCgHt7N604S Co(HDMG)I(NH,)(NCS), 3,472 CoC&24NsO, Co{O,CCH[CH(OH)Me]NH,) (en)Jz+, 1,426 CoGHi,N,O, Co{H,NCH,CH,CO,}3,2,744 CoCsH,.aN,O CO{L-M~CH(NH,)CO~},, 2,744 [C~(fJH3~S(NH2CH2COPh)]3+. 6. 189 COCSH~~CIN~ COC9HisN306S3 C O ( S C H ~ C H ( N H ~ ) C O ~4,837 H}~, [CoCl(dien){MeNH(CH2)3NH2}]2+, 2.47 [ C O C ~ ( ~ ~ ) { H ~ N ( C H ~ ) ~ N H ( C H ~2.24 ) ~ N H ~ } ] ~ ' CoCgHisN3S6 , C O ( S ~ C N M 4,865 ~~)~, CoCSH25ClN502 CoC,H,,BrN, [ C O ( ~ ~ ) ~ C I ( H ~ N C H ~ 6.428 C~~E~)]~+, COCRHMN~O, [C~{en)~(py)Brl~+, 1,469 [Co{(H2NCH2CH2NMeC~*)~}(H20)2]z+, 4,786 COC~HZIN~S~ Co(SzCNHNMez)3,4,864 COCsHz6Ns04 Coc9H,,N4 [CO(NH~)~{O~CCH(NH~)CH,CP,BU~}]~+, 6,477 [CO(NH~)~(O~CCH=CHCO,B~')]'+ 6.477 [CofiH CH )2NH(CH2)2NH(CHZ)2NHCH2& 6 H 2 ] 2 ' , 2,912 COCsHxN6 CoCsHmNaO7S [Co(dien),I3+, 2,46; 4,852; 6 5 3 [Cb{ k M e i C H ( NH2)C02}(dien)]+, 4,847 [Co(en)(HzNCH2CH2NHCH2CHINHCH2CH2NH,)]3f. 2,53 COC9H22N405

[ Co(en),{ O,CCH(O)CH,CO,Me)]

+

6,476

C0GHZ2N503

[ CO{OZCCH(CH0)NHz) (N(CH2CHZNHJ3 )I2' , 1, 426

C O ( H , ~ ) ~ ~ A = C H C H = N C H ~ ~ C O4.686 ~)~, CoCloH,,c1N2os

[COCI{(O~CCH~)~~CH~CH~N(CH~CO~)~}]-, 4.809

[CoCI((02CCH~)2NCH2CHtN(CHZC02)2)]2-,4,811 CoCioHizNzO, [Co(edta)]-, 1.336;2,783,4,638,808-811; 6,652 [Co(edta)12-. 1.336,376; 2,783,784 476 [CO{HZN(CH,)~NH~)~(O,CCH=CHCI)(OH)]+, 6,476 CoCioH,zK,Oio

COC~H~~CIN~O~ [CO{ H&" CHz)3NH2)z { O,CC(Ck)=CHz} (OH)]+, 6,

[CO(NO~){(~~CCH~)~P;CH~CH~N(CH~CO~)~}]'[CO{H~N(CH~)~NH~)~(O~CCHCICH~O)]~~, 6,476 8fl9 ~Co{H2N(CH2)3NH2}2{02CCH(0)CH2Cl}]zT, 6,476 CoC&LN40, Co(en),(acac), 1,447;4,7W

_I

CoCI0Hl3RrN2O8 [CoBr{ (02CCH2)?NCHLC'HZN(CH,C02)CHIcc),H}]-4,808

- -

[Co(N3){(H2NCH,CH,SCH2CHZ),NMe}]2+. 4,852 COC~H~~CI~N~

[COCI~{H~N(CH~)~NH(CH~)~NH(CH~)~NH~}]+, 2.56 COC,,HI3N3O,, [Co(NOZ){(OZCCHZ)~NCH~CH~N(CH~COZ)CH,CO,H)l-. CoC9Hz,N@6 - , _ 4,809 [CO(NH~)~{O,CCH(NH~)CH(CO~E~)~]~+. 6,188,468 CoCloH13N4b6 CO{D-O,CCH,CH(?IH~)CO,}{ L&=CHNHCH&[CO(NH~)~{O~CCH=C(CO~E~),)]~+, 6,468 CH,CH(NH2)C0,}, 2,753 COC~H~~N~O CU{L-O,CCH,CH(NH,)CO,} { L-I~=CHNHCH=U[Co{(H,NCH2CH2NHCH2)2}(H2NCH2CUNHMc)]"'~, ~H,CH(NH,)CO,], 2,753 6,432 C~oC1OH,,NOS, CoCgHZ6N6O3 Co(MeC(S)olC(S)Me),(NO), 4,XXO [Co(en),(H2NCHZCONHCH2C~0,Mc]"l. 2,768 COC~H~~BKP~ C O C ~ ; H ~ ~ N ~ ~ ~ [Co(HZO){ (02CCHJ,NCH,CH,N(CH,C0,)2Jj-. 4, CoBr(PMe,),, 4,722 809,810 CoCgHZ7Br2P3 CoBr,(PMe,),, 4,725 CoC9HZ7ClN5O2 [ C O ( ~ ~ ) ~ C I ( H ~ N C H ~ C 6.428 O~P~~)]~+. C0CgH27C10gP3 CoCI{P(OMe),},, 4,747 CoGHZ7C1P3 CoCl(PMe,),, 4,723 CoCVH271P3 CoI(PMe,),, 4,726 CoC9HZ712P3 CoI,(PMe,),, 4,726 CoC&z+"P, Co(Nd(PMe,),, 4,711 [Co(NZ)(PMe3),l-. 4,710,711 COC~HZ~NSOZ [ C O ( ~ ~ ) ~ ( H ~ N C H ~ C6O>428.432.436 ~P~')~~-, CoCloH16N606S COC~HZ~N~ COC9H26N5O2S

[CO{HSCM~~CH(NH~)CO~}(~II)~]~~. 4-840

CO{N(CH~NHCH~CH~NH~)~}]~* 2.927

COC~H~~OYP~ Co{P(OMe),},, 4,749 COGHZ~P~ Co(PMe?)?,4,718 CoC9H,,N, [Co(dien) { H2NCH,CH,NH(CH,)3?1Hz)3 + . 2,49 [CO(~I~~){(H~NCH~CH~),NM~)]~ ' .2,46 CQCQH~UN, [Co(pn),]", 1.25,129;2.34,35:4. 809; 6 , 125 CoCioHzFizS4 Co{F,CC(S)CHC(S)CF,),, 4.880 COCIOH~N~O [Co(2-cyano-8-quinolinolate)]+,6,453 COCIOH~CI~N~S~ cocl2(pysspy), 4,686 CoCi,W,N404 ICo(NO~)~(bipy)l+, 4,674 CorI~HRNR [Co(purine),#+, 4,685 C G n Hi o COCP,, 2,217.218 CoCjoHI"CIZN2 CoClz(py)2,4,h83, hX6 COCioHioN,O6

CO(NO,),{M~~C(SM~)=NCH=~H)~, 4,694

CoC,,,HlSBrN,O4S Co(DMG),Br(Me,S), 4,638 COCioHisN204Sz [Co({MeSCIi,C~I(CO,)NHCH,},}] ' ,4,837 [CO(D-SCMC~CI t(Nt Iz)CO,}{ I -SCMe2CH(NH2)C O J - . 2.744

CoCinHisN~On Co{H,NCH2COISHCH(Me)C0,), 2,760 [CO{H~NCH,CONHCH(M~)CO,}~] - ,2,768 CoCioHisN ioo, ICo[H,O),(adenine),l", 4,685,694 CoGoHisO, Co(acac)z(HzO)2.2,372 CoC, ,H,,B rN404S CoBr(Me,S)(HDMG),. 4,849 C0CioH20ClzS4

4,852 ICc~Cl,(l,4,8.l-terra~hiacyclolelradecanc)~+, 1

coc, 0 ~ 2 0 ~ 5 ' NHCHZOCHZNHCH2CH2NHCH201,453

[Co(C2&H,).

Cumulative Formula ladex

309

[CO(OP(O)~OC,H,NO~-~}(~~)~]+, 4,753 CoCioH2oP CoMe,(PMe,)Cp. 4, 727 C0CioH~iNz09 CO(H2O) { (02CCH2)2NCH(CH2)*CHN(CH2CO2)CH2C02HJ,4,810 CoCioH2iN404P [Co(PhOPO,)(en),l+. 1.203 COC10H2103P2 Co(CO),(COMc)(PMe3),. 4.727 CoC IOH22CINhS2

[Co(l,3.8.1 l-tetraazacyclotetradecane)(H20)2]z+. 4. 788 CoCloHzsN,

[CO(H~N(CH~CH,NH)~CH,CH~NH~}]~+. 2.58

Co(en),CI(H,NPh), 6.900 [Co(en),Cl(H,NPh)12'. 1.304; 2,59

[Co(d~~en)(H2NCH2CONHCH2CONHCHzC02)(NO,)]+, 6,433 CoCioH23N@iiP~ Co(ADP)(NH3),(I120). 4,766 COC,,~H,~CI,N, [Co(1,4,8,11-te traazacyclotetradecanelCI,1+ , 1,296, 302,303

[CO{ (HzNCH~CH~),NCH~CH~N( CH2CH2NHZ)2}l3+, 3,58 CoC, nH29C1N502 [CoCl{(H,NCH2CH2NHCH2)2{H2NCH,CH(OMe),}12+, 6, 189 COC~~H~~N,OS [<:o(ll,NCt12C112SCH,CH2COMc)(cn)~],-, 4. 85 1 CoCIOHII0N6 [Co(dien) { H,N(CH,),NH(CH,),NH, } j3+, 2.49 [Co{(H2NCH2CH,),NMe},]3+, 2,46 [CO((H,NCH,),CM~},]~'.2, 50; 6, 193 [CO(M~NHCH~CH,NHCH~CH,NH~)~~~ ' ,2,49 COCioH3oN602 [CO(~~)~(H~NCH~CO 6, M 190~ ) ~ ] ~ + , CoCloHi1CIK6 [CoCI{(H2NCH2),CMe)( (H2NCH2),(H3NCH2)CMe}]3+. 2,50

Co(ADP)(NH&. 4.76.1 COCIOH~~N~O~~'~ [Co(NH,),(ATP)]-, 2- 978 COC~~H~~CIN~O [Co(1,4,8,11-~etraazacyclotztradecane)(OH)CI]+,1, 296 SCMe2CH(NH2)CO2},2,744 COC,3H1qN402 CoC1oH25C1NsO3 ~CoCl(clirti)(lI,NC112CONHCH,COzEt)]~ ' , 6, 433 [ Co{ON=CMeC(Me)-N(CH2),N=CMeC(Me)= CoC.,,,H,,N,O,S, N O t l } ] + ,6,257 en),] ,+, 4, XS6 [Co(02CCH2SSCMc2C0,~-~)( CoC,..I L N A - 07 COC,~H~~N~O, [Co(2-C)C,H;CO,)(cn),1', 4,803 [Cor(H,NCH,CH,NHCH,),)[Co(C03){ $J=CHCH2CH,NHCH2CH2N= (H2NCH2CONHCH2COZj]'+.6,432 CHCHzCH2NHCH2(?H2}]+,4,814 CoC, ,H,,CINT,O, COCioH2&"05 [ C O ( ~ ~ ~ ~ ) ( H ~ N C H ~ C O N H C H ~ C ~ ,6,433 E ~ ) ( N O [Co(e&(02CPh)Cl]+, ~)]~+, 1.294 CoC, 1H21N403 COC~OH~~NSO~~P~ Co(NH,),ATP, 6, 447 [Co(en)2(2-02C6H,0H)]2+, 2,465 CoCioH25N9013P3 CoCiiH&~03 Co(ATP)(NH&, 4.763, 764. 765 [Co(N(CH,CH,NH,),} { 02CCH(h'H2)CHO}IZ-, 6. [Co(ATP)(NH3)*]-, 4. 765 21 1 CoC10H26N403 CoCiiHd', [Co([14]aneN4)(H20)(02)]2't, 2,329; 4,780 CoCp(PMc,),, 4,728 CoC,,,I I,,N4S, COC~~H~~CIN~OZ [Co(SCH2CF12NMeCII CH,NMeCH CX2S)(e n)] ' 4. [Co(en),(lheriphylline)CI]+, 2, 32 847 CoC, H24N505 COCIOH~~N~O [CO{N(CH~CH~NH ~)~) { OzCCH(NHZ)CHZOH)J2', 6, [C0([15]aneN~)(OH)]~+. 6.436 211 CoCloH27CIN502 CoC,,H2,CIN60 [CO{(H2NCHZCHzNHCH2)2JCI(HzNCH,Co,Et)]2+, [Co(CICOC(NH,)=CHNMe,) { N( CH2CH2NH2)3J]3+. 6,429 1.426; 6,211 CoCioH2,N402 COGiH27N402 [Co(OH)(OH,)( 1,3.8,1 i-tetraazacycl~tetradecane]~+, [CO(H~N(CH,),NH,},(~C~C)]~+, 2,45 4,763 CoCllH28N,03 CoC,,,H,,N,O,S, [CO{(H~NCH,CH~NHCH,),)[CO(O,CCH,SSB~I')(C~),~~-, 4,856 (H,NCHzCONHCH,C0,Me)]3+, 6,432 COC~~H~~N~O, CoCi >H3oN402 [ C O { ( ~ ~ C C H ~ ) ~ N C H ~ C H ~ N ( C R ~ C O ,,)4~, } ( N H ~ )~] [Co(I,4,8.12-telraa~acyclopentade~an~)(H,0),]~~ ,4, XI1 788 CoCioH2&"02 COCiiH3oN6 [Co(ONO)(NH;)( 1,4.8,11ICO{~M~C(CH,NHCH~CH,NH,)~}]~ ', 6, 191, 192 tetraa~acyclotetradecane)]~+, 4, 672 CoCIIH3,BrP, CaBr(C2H4)(PMe3),,4,722 COCIOH~SN~O~

,

COC 7-K

.

Cumulative Formula Index

COCllH31P3

310

[CoCI, N=CMeCOC(Me&NCH2CHzNH(CH2)3h H , ) l + . 6. 168 {H2N(CH2CH2NH)zCH2CHzNH2},2,471,477

COC~ZHZ~CIIN~ [CoCI- fl=CMeCH2C(Me)=NCH2CHZNH(CH2),'&H,)]+, 1,457; 6, 168 COCizHuN@& C O { S C H , C H ( N H ~ ) C O ~ M4,838 ~)~, COCI~HJ'JSOJ' [Co(O2PO(OChHJ402-4)}{ HzN(CHz),NH2)2] ' -4. 753 COC1,H~4S6 [Co( 1,4,7.10,13316-hexath1acyclooctadecane)]~+,4, 849 COCIZHZ~P~ Co(C,H4Me)(PMe3)z. 4.728 CoC,zH,oCM'z Co(PEt3)zC13,1, 45 COCI?H~ON~O~PZ [C<J(NO),{P(OEt), } 21,. 4,717 CoC,,H,,N603 [CO{(H2NCH2CH~NHCHz)2}(H2NCHzCONHCH~CO,Et)], ' ,6,436 CoC,,H,,,N6O, [Co(HC0NHMe)J2' .2,401,492 CoC,zH,,Na [Co(sep)]*+,1,336; 2,940 [Co(sep)13+'.1.336,454; 2.927,940; 6, 191,507 CoCizH3zN, [Co{MeC(CHzNHCH2CHzNH2)z(CHzNHCHzCH2NHIvie)}13*,6, 192 [CO{ O ~ C C H ~ C H ~ N ( C H ~ C O ~ ) C H CHzCO2)~CH~N( CHzCHzCOz)l-. 4,809 COCIZH~~W~ 2, C O ( P ( O M ~ ) ~ } ~ ( ~ ~4,708; - C ~ H6,238 ~), [Co{ (02CCHz)2NCH~CH2N(CH2CH2C02)z}]z-, 787 COCIZHMN~ [CCI{H,K(CH~)~NH(CH~)~NHZ}~]~*, 2,47.49 ,2,784; 4. [Co{ (OzCCH2)ZN(CHz)4N(CHzCO~)2}] 808 COCI~H~~C~P~ CoCI(PMe,),. 4.723 COC, zHi 6N4S2 [CoC:I(PMe,),J ' , 4, 774 I C o ( 2 - S ~ v ~ ~ ( c 4.840 n~l+, CoC,,t I,,CIzN,P,Sz C0C12H16N604 CO{L-&=CHNHCH=WH,CH(NH~)CO~} {D-N= C'O{(M~,N),PS)~CI,,2 , A42 C H N H C H = ~ C H ~ C H ( N H ~ ) C O2,744,747 ~}, COCIZH~~C~~I& [CO{L-~~=CHNHCH=CCH~CI~(NH~)CO~} { D-NZ CO(CIO4)z(DMSO)6, 2,488 CHNHCH=cCH2CH(NHz)COz)z]+.2,744 COCIZH,~NOI$, CO{ L-~~=CHNHCH=~CH,CH(NH,)CO~L 2,744, , -, 747,758,768 [CO{L-~~=CHNHCH=~CHZCH~NHZ)CO~)~]+, 2, . . I -

II

-

[C&{H;N(CH2)4NHZ),]3+,1,67; 2.44 C0C1ZH36N603 [ C O ( H ~ N C H ~ C H ~ N H C H ~ C H ~ OIH , 419 ),]~+, CoC I,H,,N,O,P, C O ( N O ~ ) ~ ( H M P A1,57 )~, c0c1ZH36u3pZ

[Co(NCMe)6]2+,4,638 CoC12HisN606 [Co(DMG)3I3-, 2,272 COCIZHZON,~~ Co{(MeCOCHC(Me)=NHCH,),)(NO). 2 , 103 CoCi2HzoNbOs Co{H2N(CH,CONH)zCH2C02}z, 2.761 CoCi 2HziN304 Co { {MeCOCHC( Me)=NCH,},) (NH,)(O,) 4.780 COCI~H~~CI~N~O

CuMe,(PMe,),{P(OMe),}, 4,726 CoC?zH36O6S6 [CO(DMSO)~]~-, 2,488 COCizH3601zP4 [CO{P(OM~),)~]-. 4,704,718,747 Co{P(OMe),},. 4.747 [Co{P(OMe),),]+. 4,749 COCizHd') CoMe,(PMe,),, 4,726 COCIZH~'~ Co(PMe,),, 4,711,718 [Co(PMe,),]-, 4,718,773 CoC1ZH37012P4 CoH(P(OMe),},, 4,702,704,747 CoC ,JLJ'a CoH(PMe,),. 4.702 [ C O H ( P M ~ ~ ) ,4,702,725 ]'~

31 1

c0 c1 5 H 3

Cumulative Formula Index

4

6

[Co{$J=CMeC(Me)=N(CH,),N=CMeC(Me)= .4. 869. 876 I

~ H , ) ~ ) ( H , O ) ~ 1,337 ]~+, [Co{k=CMeC(Me)=N(CH,),N=CMeC(Me)= N(CH2),)(H,0)zI3’, 1,336 CoCi4HmNd’,S2 .~ Co(PEt3)2(NCS)2.1.24; 4,725 COCiaH3oNio04 [Co{02NC(CH2NHCH2C1T2NF~CFII),CN02}]3+, 1. 454 tPN4 COC,~F ~

coc13Hl,ciN50, Co(HDMG),Cl(py). 4,638; 6 . 387 COCI~HIP@S [Co(Hpeta)]-, 2,784 COC,,H,oN,O, [~&ibM~j~(py)l .4,774 CoCi,H,sNzS, Co(S2CNEt2)2(S2CSEt). 4.866 COC~~H~~N~O I C O ( [ ~ S ] ~ ~ ~ N ~ ) ( D6.134 MF)]~+. C0C13H32N603 [CO{H~NCH~CH~NHC - H~)~} (H2NCH2CONHCH2C02Pr’)]3+, 6,432 COCI~H~N“ [CO(M~CN)(C,H,)(PM~,)~]+? 4.722 C O G ~ H ~ ~ P ~ CoMe,(Me2PCHPMe,)(PMe3)z, 4,727 C&3HvPs [CO(PM~~)(M~~PCH~PM~~)~]+. 4.736 C°C13H39012P4 CoMe{P(OMe),),, 4,749 C O C ~ ~ H ~ P ~ CoMe(PMe,),. 4,724

COCI~HZONZPS~ Co{Et,P(S)S}py,, 2,643 COC~~H~~CIN~ [CoC1(dien)(bipy)l2+.2, -17 COCI~H~ZN~O~ CoMe(HDMG)2(py),4,771 COC~~H~~N,O~S Co(HDMC;),(nv)(SMel. 4. 835 C~C,,H~~CIN~O , _ _ . . I _

I

[Co{h=CMeC(Me)=N(CH,),N=CMeC(Me)= ~ W H ~ ) ~ ) ( H ~ O ~I . C 337 I]~-,

~

~

[Co(Pi(Me)CH2CH2N(Me)CH2CH2CH2N(Me)CH,CH,N( M~)CH,CH,CH,}p+,2,912

co(2-spy)3,4.838.839 CoCisHi,N,S, C O ( S ~ C ~ ~ C H = C H C H = ~4,865 H)~. CoC15H,jBr2N3 CoBrz(py),, 4,685

c o c i 5H34N60 [Co{MeC(CH2NHCHzCR,NHCHz)3COH)] I + , 6,191 CoCl,H36P, . COCI~H~~N~ CoPh(C,H,)(PMe,),, 4,724 I C O ( C I S H ~ ~ N ~2,941 )]~+, CoCi 7H4n0J', COCi5Hd7 [Co{MeC(CH2NHCH2CH2NHCH2)3CNH3}]6+, 6,191 Co{P(OMe),},{~3-CaH13},4,708; 6,239 CoCi ~H&303 CoCisH&i5P5 Co(N0)(8-q~inolinolate)~. 4,658,666 [CO{P(OM~)~},]+, 4,747 CoCisHi,N,O, COC~&WW~ [Co{OP(OMe),},]*+, 2. SO0 CO(Z-OC~HINO)~. 2,273 CoCIBH,,BrN,OIP CoClbH,N, Co(N0)2Br(PPh,), 4.717 Co(tetraazaporphyrin), 2,858 C0C16HiON304 COC18Hi5BrIF6P3 CoBr2(PF2Ph)3.1,45 [CO{H~N(CM,CONH)~CH>CO~}]+ 2.761 CoCl6HlZFN2O2 COGeI (i,IN,02P Co(N0)21(PPh3),4.660 Co(3-Fsalen), 4,775 CoCiaHi5N304P COCi6H12N304 Co(NO),(NO,)(PPh,), 2, 108;4,662 Co(CO,)(OH)(terpy), 4,686 COC~~H~~CI~N~P CoC12(PPhpyZ), 4,686 COCI~HI~NZ~~ Co(salen), 4,775; 6,387,388 COC16H14N303 Co(NO)(salen), 4,658,660, 664; 6,372 COG~H~~C~N~O~ Cn(CO3)Cl(py),, 4,688 COCI~H~~N~OI& [CO~~-O-~-(~-O-~ -O, S-S-~ , NC~ U, N=N)-~,~-(O,S),-H H2NC,oH3}(NH3)3l2--.6.51 QCI~HI~W' Co(CO),(PPh,Me), 6,270 cOC16HiaN7 [Co(N3)(tren)]', 2, 227 COCI~H~~CIN~ [Co(2-Me2NC6H4N=NC6H4NMe2)Cl]+. 6.60

Cumulative Formula lradex

313

CoC24H40C12N2P2

C O C ~ ~ H ~ ~. .P S I Co(SCH=CHS),(PPh,), 4,838

COCz0H22N406 Co{ON=C(COMe)2)zpy2, 2,797 CoCznHd,Oz Co{HN(CHzC11zC112N=CHC6H40-2)z},4,775 COCZOHZ~N~O~ CO{HN(CH~CHZCH~N=CHC~I 140-2)2}(02), 2,329; 4.780

CoC20H24F1zNsSiz {Co(SiF6)z{ HzC=CHfiCH=NCH=e H)4}, I ,4,694 CoCzoH24N204 Co(acac),(py)p, 2.388 CoCzOHZ4N4O2 [Co(HzO)z(~y)41~+, 4,688 COCZOHZ~B~N~SZ CoBr(PhNHCSNHN=CMez)2, 4,857 COCZOHZSN~O~ [CO(HDMG)~(P~NH~ 3.472 )~~+. COCZOH30N404 Co(D-camphorquinonedioximc monomion),, 2,271 COC21H13N6 Co(octadehydrocorrin)(CN),. 2.879 COCZIH15% C O ( S ~ C P 2,646: ~ ) ~ , 4. E64 C0CZ1H16N403

[Co(CO,)(hipy),]+, 4, M h , 688. 689 C0CziHi9N304 Co(salen)(py)(O,). 4.780 COCziHi9N6 Co(l7,18-didehydrocorrin)(CN),, 2,882 C0C2iHzoN403 [Co(CO,)(py),]+, 4.686.688.814 CoCziHziNz04 Co(salen)(acac), 2.733 C°C2iH21N6 Co(corrin)(CN),, 2,882

Co{MeN(CH2CHzCHzN=CHC6H40-2)2}( Oz), 4,778, 780 COCziHzsN6

653

[C~Cl~(phen)~ 4,686,688 ]+, COCZ4H16NS Co(corrole)(py), 2,876 COCZ~H~~N~ Co(H-corrole)(py). 2,875

{Co(SOPPh,)i},, 4. X71 COC*4~,0C)8S4 [Cu(OZSPh),j2 ,4,835 C0C24HZOPZ~1

CD(S2PPhz)2,4,87(1 CoC,,H20P2Se, Co(Se,PPh2)2,4,871

Co(S2CCk2Ph)3,2,646 CoC?aH,XINaO _ . -_ [CoCl(H2Oj{2-(CHNPh)py},]+, 4,686 COCZ~H~SS~ CdNCSI .(PhfiN=CMeCH=e MeL. 4.694

Cumulutive Formula Index

Co{0zC(CHz)6Me}3,6,386 COCZ~H~OC~~IZP~ [CoCI{P(OEt),},l+, 4,749 CoCz4H60N404 [CO(E~,NO),]~+, 2,497 CoCz4HmOizP4 [Co{P(OEt),},]-, 4,747,749 Co{P(OEt)3)4,4,749 [Co{P(OEt)>},li14,749 CG~HBOP~ Co(PEt3)4,4,722 C~C24~61012P4

CoH(P(OEt)3}4,4,702 COCZ~H~ZC~ZNIZOIZP~ Co(Cl04)z(HMPA)4,2,500 COCZ~H~ZNIZO~'~ [Co{ {OP(NMez)z}zO}3]Z+. 4.768 COCZ~H~ZNIZP~S~ [ C O ( ( M ~ ~ N ) ~ P S2,642 }~]~+, COCZ~H,A"O~ [Co(CO,)(phen),] ', 2,468; 4.638,686.688,693 COCZSH19N404

CO{1,2-(2-OC,&CH=N )&,hH4} (py) (NO,), 6 , 372 COC25H2ON2P Co(CN),(PPh,)Cp, 4,650 C G ~ H ~ I N ~ Co(CN fiCH=CPhCH=NCH=CHCH=NCH= &H,), 6 , 168 CoCz5H2e.P CoMe,(PPh,)Cp, 4,708,727,728 COCZ~H~~OZP~ C O ( O ~ C H ) ( P M ~ ~4,791 P~)~, C o C z d I 6N404 [Co(OzCzO,)(phen),]+, 4.802 COCZ~H~ONZOZP CO(CO)~(N,P~)(PP~,), 2,134 C O C ~ ~~oHN S I,), 2,874 C0(corrole)(4-MeC,~~~Nl COG~H~~N~O~P~ Co(NO)z(PhzPCH=CHPPh,), 4.737 CoC&zzOzPz [ Cd(PhZPCH=CHPPh,)(Oz)1+. 4.784 COC~~H~~CI~NOP~ Co(NO)Cl,(dppe), 4,712 CoCz~Hz4CI,0zPz CoC1z{PhzP(0)CHzCHzP(O)Phz), 4,768

314

C(>(OZ)({PhCOCHzC(Mtt)=NCH,},)(py), 4,320 CnC,,Hl,N,OaP CiMe('HDMG)(DMG)(PPh,), 4,72X coc',7H4,,Kb 2- NHCl I ~ C € I ~ITNI C I I)C'6t11}2C'O{Z-NHC~H~ &H2), 1,44h COC,~H,~O~P~ [Co(CO),(PBu,),]+, 6,259 COC~~HS~YO~OP~ Co(NO) { P(OPr'),} 3. 4.7 12 C°C27H6609P3 Co(H)3{P(OPr')3},.4.702,707 COC~~H&,OS [Co{02CCH(0)CHzC02H}(phen)2]+, 4,803 CoCzsHmN4O6 [Co{0,CCH(0)CH(OH)C02H)(phcn)?]+.4.803 [Co(R,H-0,CCH~OH)CH(OH)C02}(phen),l' .2.465 COC,,I I,,,S, [Co(S2C2Ph2jZ]-. 4; 876 CoCz&2zN4'& [Co{R,R-H02CCH(OH)CH(OH)C0,H)(phen)z]+,2, 468 ~

Co(dppe){S,PIOMe),}{S,P(O)(OMcj},4,871 COC,,H,'~P CoMcz(PPh3)(CsH4Me),4,728 COCz6HdzP3 Co(CN)Z(PMezPh)3,4,725.785 COCZ~H~,C~~NOPZ Co(NO)CIz(PPhzMe)z,4,660 COCz6H3604Pz [Co(a~ac)~(PMe,Ph),]+, 4.728 COCz6Hd%Pz C O H ( C O ) ~ ( P B U6,238 ~)~, CoCz,HiJisO&

CU{SCH=CHCH=W(S)=CHCOC?F,J

C0C27H18N303

Co(ll-quinolinolate),, 1,528 COCZ~HI~N~ Co(corrole)(4-MeC6H,NC) 2,874

?,

2,653

CoC30H12F2103S6 CO{SCH=CHCH=cC(S)=CHCOC,F7) 3,2,653 C O C ~ ~ H ~ ~ B ~ ~ F ~ ~ ~ S ~ Co(3-BrC6H4C(S)=CHCOCF3)3.2,652 CO(~-B~C,H~C(S)=CHCOCF~}~, 2,651,652 COC~OH~~CW~O~S~ CO(~-CIC~H~C(S)=CHCOCF~}~, 2,652 CO{4-C1C,HdC(S]=CHCOCF3}3,2,652 COC~,H~,F~ZO~S, CO(~-FC~H~C(S)=CT.~COCF~J~. 2,652 C~C~H~IN,OI~S~ [CO(l-C)N-Z-O-h-OnSC~~~Hls)3]~-, 6,85 CoCanHi &0& CO{PhC(S)=CHCOCF3}3,2,65 1-653 cOC30H18N306 Co(l-nitroso-2-naphthalenolate),, 1, 531

Cumulative 1Sbrmula Index

315

CoC30HzoNs Co(N-phenylcorrole), 2.876 COC3aHzzN6 [Co(terpy),lz+, 1,273:4,686.688,691.692 [Co(terpy),13~', 4,689 COC~OHZZS~ Co{PhC(S)CHC(S)Ph),, 4,880 COC~~H~J'J, Co(bipy),, 4,638 [Co(bipy),] ' , 1,64; 4,686,688,691 [ C ~ ( h j p y ) ~ ]1,64, ~ + , 348; 4,686.688.6Y 1,6Y2 [Co(bipy),13++,1,64,348; 4.6RX. 691,6Y2 COC3oHz4N606 [Co(bipyridyl bis-hr-~xide),]~'.2,496 COC~OHZ~OA Co{MeC(S)=CHCOPh) 3 , 2.651 COC~OHZ~O~ Co(PhCOCHCOMe),. 2,380 COC3oH3oN606 [Co(pyridine N - o ~ i d e ) ~ ]2,496 ~+. C0GoH3sN504 2, 495 [Co(Z-picoline N-~xide)~]'+. COC~OH~~NSOS [ C O ( M ~ C ~ H ~ N O1, ) ~40] ~ + , COC~OH~,N& Co(S,CNHCHEtPh),, 4,865 COC3oH3604P& [Co(dppe){S~P(OMe),}~l 4. 871 COGoH4zFzNiz ''I

[{Co(~N=CMcCH&Me)3),(~F)z]2+,4,694

COC~ZH~~NZP~ Co(CN),(PEt2Ph),, 4,649 COC~ZH~AJ'~

Co{OP(0)(OCHzCHEtBu)z}z, 6,792 CoCdisFi,O3S3 Co{PhC(S)=CHCOC,F5}3, 2,653 CoC33Hz,FizO& Co{ 3-F.4-MeOC6H,C(S)=CHCOCF,},. 2.652 COC~~H~~F~O~SB 3, h52 Co {3-MeC6H4C(S)=CHCOCF3}3, Co(4-~eC,H,C(S)=CI~COCF,),, 2,65 I, OS2 C0C3,1 t,,Fr0,,S3 CO{~-MCOC~H,C(S)=CHC~CF~}~, 2,652 Co{4-MeOC,H4C(S)=CHCOCF,),, 2,652 COC~~H~ON~O~S~ Co(0,SC,H4Me-4),(brpy),,4,835

Co(sapphyin), 2,889 COC34H36P3 Co(H),{PhP(CH,CH,PPhZ),}, 4,707 CoC36Hl8Fz103S3 Co{PhC(S)=CHC~C)C3F7}3,2,653 coc:,1 IldN6Ol8S6 [C0{4.7-(03S)~phc11}3]' ,6.653 CoC&i&OiiS { 1- ( 2 - 0 -1[CO( 1-(2-0-5-02NC6H3N=N)-2-0CI~IH~) CloH6N=N)-2-0-4-03S-6-O~NC,,H,>)2-, 6,Sl C O C ~ L N ~ [Co(phen),]', 4,688 [ C ~ ( p h e n ) ~ ]1,336,356,4,686,688, ~-, 692,6,23 [Co(phen),13-, 1,64,336,466; 3,712; 4,686.688. 692, 6, 652 COC~~H~~BTZP~ COB~~(PP 4,725 ~~)~. COC~~H~OC~~NOF'~ CoCI,(NO)(PPh,),, 4,724 CoC3,TT3,CI,NO6P,S Co(NS)CI,{P(OPh),},, 4,858 COC~~H~~C~~NO~PZS Co(NSO)Cl,{P(OPh),},, 4,858

COC~OH~~NO~P~ Co(N0) { P(OEt),Ph} 3 , 4,712 C O C ~ ~ H ~ ~ N ~ P S ~ ~ Co{N(SiMe,),),( PPh,), 2,171 COC30H75N505 [CO(E~,NO),]~ 2,~497 , COC32H16N8 Co(phthalocyanine), 1,274; 2. 863; 867-870; 6,88, 1019 [Co(phthalocyaninr)l-, 2. 868 [Co(phthalocyaninc)]2-, 1,8611 [Co(phthalocyaninc)]"- 2,870 COC3ZH16N8012S4 [C~{(O~S)~(phthaIocyanine) )]SA, 2,869 CoCI,(OPPh,),, 4,768 [Co { (03S),( phthalocyani ne) }I". 2, 869 CoC36H30C12P2 COC~ZHI~NS~I~S~ CoC12(PPh3),, 2,205; 4,722 [Co{(03S)4(phthalocyanine)}(Oz)]s-, 2, 869 [C~{(O,S)~(phthalocyanine)}(O~)]~-, 2, 869 COC~&OF~O~S~ Co{?-EtC6H4C(S)=CHCOCF3}3,2,652 COC~ZHISN~~S [CO{I - ( ~ - O - ~ - O ~ N C ~ H J ' L N ) - ~ - O C ~6, O 51 H ~ } ~ ] - , Co { 3.4-Me,C6H3C(S)=CHCOCF3) 3. 2. 652 C~C~ZHISNS~I~S~ C0C36H30F906S3 CO{4-Et OC&C(S)=CHCOCF3} 3,2.649. 652 [Co((O,S),(phthalo~yanint.))0,1~~,2, 869 COC3ZH19N8011S - { 1[Co{2-0-5-OzNC,H3N=N~=C(0)NPhN=CMe) (2-0-3-01S-S-02[*iCGH*N~~)-2-OCloH,)I" ,6, 52 Col,(PPh3)z,6, 270 CoC32H21N608S2 [CO{1-(2-0-5-03SC6H3N=N)-2-OCloH6}{ 1-(2-HzN-5C'oC361130N03P2S Co(NO)(S02)(PPh3),, 4,660 ~

'

COC36H44N4

"_

-.

Co{l-(PhN=N)-2-HNCloH6},, 6,44 COC,;H;,N, [CO( 1-(2-H,NC,H,~=N)-2-HNC,,,H~}Zl+, 6,59 CoC32H32N6

Co{2-flCC,H4N=ChIeCH=CMc-2-NC6H,N=Cm M e ) ( p y ) 2 . 1,451 [cor T ; T = c M ~ c H = c M ~ c ~ ~ ~ ? N = c M ~ c : H = w , H , } ( p y ) , ] - , 6,173

[Co(NO),(PPh,),]+, 2, 113, 114; 4,660,712. 717 COC~~H~ON~ Co(PhNNNPh),, 2,205 CoC36H31Br2P3 CoBr2(Ph2PH)3, 1 , 4 5 COC~~H~~NO~P~S Co(NO)(SO,)(PPh,),, 4. 716 COCd3~N404 Co(protop0rphyrin IX di-Mc-cster), 6,616 CoC,,H,,P, Co(H)z(PPh3)2, 4,704 COC&d% Co(octaethylporphyrin), 2, 837 {Co(octaethylporphyrin)] -,2,837

Curnulutive Formula Index

COC36H44W4

COC&~~OZP~ [CO{O(C~12CH2PPhCH,CHzPPhCH,CH,)20)J”’, 4, 746 CoC36Hs4012P4 Co(P(OPr’),),, 4,747 COC~~HZIN~ Co(phthalocyanine)(py), 2, 867 Gc37H21N902

Co(phthalocyanine)(py)(0,),2,867 COC~~HZ~N~P Co(corrole)(PPh,), 2, 874,876 Co(dchydrocorrin)(PPh3), 6, I99 COC37H30NOZP2 Co( NO) (CO)(PPh3)2,4,660 COC~~H~IN~O~

Co{{PhCOCHC(Ph)=NCHz}2)(py)(02), 2.322,323; 4,779,784 CoC37H33P2 CoMe(PPh,),, 4,723 CGsHz3N9 Co(phthalocyanine)(3-Mepy), 2,867 CoC38H29N802

CO{~-OC,H~N=NC(P~)=NYP~} { Z-HOC,HaN=NC(Ph)=NNPh), 6,81 CoCmHdw Co(NPhN=CPhN=NPh),, 6 , 7 8 CoC38H,,C~ZN, Co(NHPhN=CPhN=NPh)2Clz~ 6 . 7 8

.

.

Co(S2CNPhz)3,4,865 COC39H33N6S6 Co(SzCNHNPh2)3,4,864 C0C39H36F903S3 Co{4-Yr’CsH4C(S)=CHCOCF,J,, 2,652

316

CoC4,H,,OP3S* Co(SzCO)(triphos). 4, (146.868 COC42H3902P3 [Co(triphos)(CO),]’, I , 744 COC~ZH~~P~SZ Co(CS,)(triphos). 4,646,744 CoC4zHd& Co(S,CS)(triphos). 4.868 C~C42H400P3 CoH(CO)(triphus), 4,744 CoC,ZH42BrP4 [CoRr{P(CH2CHzPPh2f3}l+, 4,745 CoC,,H4,UINP, [COCI{N(CH~CH~PP~~ 4,745 )~)]+, CoC,,H4,CI2O,P2 CoCI*{OP(CHzPh),J,.2,498 COC~ZH~ZF~O& CO{~-BU‘C~H~C(S)=CHCOCF~}~, 2,652 COC~~H~~INP~ [CoI{ N(CH2CH,PPh2)3}]+,4,745 COC~~H~~NP; [ C O { N ( C H ~ C H ~ P P ~ ~4,744 )~}]+,, COC~ZH~~NP~ Co(P3){N(CH2CH,PPh2)3),4,700,738 CoC4ZH?2N20P3 Co(No)(N(C.1-r,C~r,PPh,)~},4, 600. 711 [ C O ( N O ) ( N ( C H ~ C H ~ F P ~ 4,658.663,712,71h ~)~)]+. CoC42H43NP3

CoH{N(CH2CHzPPh2)3},4,702 COC~ZH~J’~ CoH(P(CH,CH,PPh,),}, 4,702,706 COC~~H~~P,S [CO(SH){P(CH~CH~PP~~)~)]+, 4,829 CoC42H54N606 [Co(2,dlutidine N-oxide),]*+, 2,496 COC~~NP~S [CO(SH){N(CH,CH~PP~,)~)]+, 4,829 COC~~H~ZNO~’~ [Co(C0){ N( Cf 12CH2PPhz),)] ,4,738,744 COC~~H~ZO~P~ [Co(OAc)(triphos)]-’, 4. 745 COC41H4I42P3S3 ICo(S2CSMe)(triphos)1’,4, 869 [Co(S2CSMe)(triphos)12’,4,867 COC~~H~~NP~S [CO(SM~){N(CH,CH,PP~,)~}]~~. 4,834 COC~~H~~CIN~ Co(tetraphenylporphyrin)Cl, 2, 838 CoCwHmNd Co(tetraphenylporphyrin), 2,837; 4,781; 6,375,388, 389.615 [Co(tetraphenylporphyrin)I --, 2,837 Coc44H@& Co(NO)(tetraphenylporphyrin), 2, 838; 4,660 C O C ~ ~ Z N ~ O ~ [Cottetraphenylporphyrin)(O~~z)~l+, 2, H38 . . . . CoC4aHs4N,oO~ Co{(Me,CCONll),porphyrin)(Mc&CI I=KCI I=CH)+

..

..

. .

Co(triphos)(O,SO,), 2,425 CoCa,H,oPeS [Co(P,S)(triphos)] ’, 4, 738 cOc41fI39p6 Co(P3)(triphos), 2, 1059; 4.699.738 CoCaiH,2P2 [Co(H),(iriphos)] -, 4,702

__

I,

~

C0C42H24F903S1

Co{2-CloH7C(S)=CHCOCF,),.2.652,653 C~C*ZHZbN10 Cn(phthalocyanine)(py)2, 2,867 C0C42H30N13

Co(dehydrophthalocyanine)(en)( 1.3diirninoisoindoleno),6,90

Co(tetraphenylporphyrin)(CO),2, 838 CoCasHz&03 Co(tetraphenylporphyrin)(CO)(O,), 2,838 COC~SH~ON~ Co(l\.‘-mclhyltetraphsnylporphyrin),2,849 COC45H3303S3 Co{PhC(S)=CHCOPh),, 2,651

Cumulative Formula Index

317 COC~~H~~N~P

Co(diethvlhexamethvlcorrole)(PPh.I).2, 873

CoCrC10H16FN10

CoH(PPh3)3,4,726 COC~&~P~

Co(H),(€'Ph3)3,4,702,706 COC~~H~~NZP~ Co(CN),(dppe),, 4,648,649,736,737 [Co(CN)2(d~pe)zl+, 4,649 COCS~HJ'~ Co(H),(FPh3)3,4,638,702,706,707,726 [Co(S2CPEt3)(triphos)12f,4,867 CoHZ(PPh3)3,6,238 CoCanH;;P& [C;( SzCHPEt>)(triphos)]+ 4.868 COCWH~ON~ Co(tetraphenylporphyrin)(piperidine)2, 2,838 [Co(S,CHPEt,)(tripho~)]~' .4.868 coc55114501)3 COC48Hl10C1021P4 cO(CO)(PPh,),, 4,791 [CO(OCIO~)(OH~){OP(C)RU)~),] ', 2, 500 COCSSH~~OP, CdC49H33N602 CoH(PPh,)j(CO). 4,711 Co(tetraphenylporphyrin)(py)(NO,), 4,674; 6,372 COCSSHGOJ'~ COC~~H~~OP~ Co(02CH)(PPh3)3,4,791 CO(P~P(CH,CH~CH~PP~~)~)(CO)(PP~,H)]+, 4,744 COCd%601oP3 CoH(P(OPh)3}3(CO), 4,702 CoCjjH4sP3 CoMe(PPh,),, 4,723 [Co(tetraphenylporphyrin)(N0)(3,5-lutidine), 2, 838 COC55tI49NP3 C G 1H37N602 CoH(BH:CN)(PPh3)3,4,704 [Co(tetraphenylporphynn)(NO2)(3,5-lutidine),2, 838 CGdLNOJ', CoH{P(OPh),},(MeCN), 4,708 Cr;CS2H;;O,P4 CRC64H13S016P4 CO{OP(O)(OCH,CHEtBu),} 2{HOP(0)[ C O ( O ~ ) ( P ~ ~ P C H = C H P P ~4,737; Z ) ~ ~6,321,329 +, (OCH2CHCtBu)2}2,6,793 CoC,,H,,Pn .CoC&,,BrP3 [Co(Ph,PCH=CHPPh,),]+, 4,735,736,737 c~Br(Pbc=cPh)(PPh,)~, 4,722 COC~,H~~B~P~ CoBr(dppe),, 4.736 CoC6SHS5p3 [Co(PhC=CPh)(PPh,),]+, 4,7?2 [CoBr(dppe),]', 4,736 COC~~H~~CIP~ C°C68H70N1006 Co(O,)( Me&CH=NCH=cH){ (2[CoCl(dppe),]+, 4,736 Bu'CONHC,H,),porphyrin}, 2,323 CoC52H48C12P4 CoCl,(dppe),, 4,736 CoC7&s8izP, Co{C6H40P(OPh)2}{ P( OPh)3}3,6,238 [C~Cl,(dppe)~]', 4,737 CoCS,HA,NOP4 COCX&OC~@~ZP~ Co(C104)Z(OPPh3)4,2, SO0 [ C o ( N O ) ( d ~ p e ) ~ l4,712 ~-, COC7ZhOO12P4 C0{P(OPh)3}4,4,747 Co(dppe),, 4,728 [Co(dppe),]+, 4, 735,737 COC~ZH~IN,P~ CoH(N,)(PPh,),, 4,702 [Co(dppe),l*+, 4,736 COC~~H~~CIP~ [C~HCl(dppe)~]+. 4.703,706 CoC52H49P4 Co(CN)(dppe),, 4,648 CoH(dppe),, 4,702,706,728; 6,294 COCWHS~NZP~S C0CszHsoP4 [CO[N(CH~CHZPP~,)~}}Z(~L-S), 4,828 [Co(H),(dppe),I+, 4,703 CoCl, CoCszHsd'4 [CoClJ, 6,789,804 Co(PPh,Me),, 4,718 [CoCI,l"-. 1,236,517 COCS~H~~NP~ C0COjNj Co(CN)(Ph2FJCH=CHPPh&. 4.736, 737 [Co(CN)513 ,6,496 COC~~H~~OP~ CaCrC,H,,N,O, [CO{P~P(CH~CH~PP~,),}(CO)(PP~,)~', 4,744 [(NH3)5C~(C204)Cr(H,0)s14+1 2,444 CoCrCJi,,N,Os [CO(NH,)~(NCCH~)C~(H~O)~]~+, 4,678 CoCrC6HloN,05 Cr(H,O)S(p-NC)Co(CN)s, 2, 10; 3,777 CoCrC6H,,N,,0 CoH{P(C6H4PPh2-2)3}.4,715 CI(NH~)~(H,O)(~-NC)CO(CN)~, 3,779 COC~~H~~NJ'~ COCKC6HljN11 Co(CN)z(Ph2PCH=CHPPhz)Z, 4,736 Co(NH,),(p-NC)Cr(CN),, 3,779 C O C ~ ~ H ~ ~ B ~ P ~ &CrC,H1SN,1$6 C O B ~ ( P P ~ 6.238 ,)~, CO(NH~)~(~-SCN)C~(NCS)~, 3,842 COCS~H~~CIP~ CoCrC,N6 CoCI(PPh,),, 4,721,737; 6,294 Cr(CN),Co, 3,779 COC~~H~~NOP~ Cr(NC),Co, 3,779 Co(NO)(PPh3)3,2, 108,114; 4.662,712,716,717, 1067 CQCTC~H~~N~O~ COC541&6N2I'3 [Cr(en),(y-OH),C~(en)~]~+, 2,299 CoH(N,)(PPh3)3,1,120; 2,691; 4,638, 657,707,708, 709,710, 711; 6,238 CoCrCloH16FNlo [CrF( en)z(p-NC)Co(CN) -, 3,778 COC54H483 I

COC 7-K*

COC~C~~H~~FN~~ [CrF(pn)2(p-NC)Co(CN),] .3,778 CoCrC14H1405PSZ (Me,P)CpCo(CS,)Cr(CO),. 2 582 COC~C~~H~~O~P~S~ Co(triphos)(p-CS2)Cr(CO),, 2. 582;4.646,734 COCTC~,H~~O,P~S~ Co(triphos)(p-CS,)Cr(CO),. 4.869 CoCrH1,N,O4 [Co(NH3),0Cr03]+,4,825 CoCrH,,CIN505 [Cr(HZ0)5CICo(NH3)5]4t, 1,332 CoCr2C51 H 3 ~ 0 ~ ~ P h Co(triphos)( y-P,) { Cr(CO),} 2 , 4.738 CoCr,S, CoCr,S4, 3,883 COCUC,~H~,N,S

[CO(~~)~(SCH~CH~NH~)CU(NCM~)~]~~, 5, 553 COCUCizHlliNio [CO(NH3), (p-fiCH=NCH=c H)Cu (M e dien)] ,4,

694.697

,

+

COCUzC,,H,,N,S [ {CO(~~)~(H~NCH~CH~S)}{CU(NCM~~)~}~]~+, 4,848 CoCuzSnC10H1404 CoCu2Sn(p-AuO),CpMe, 1, 122 COF~P~S~ Co(SzYFZ)z, 4,870 [Co10P63)2(NHl)4].4,762 CoF, CoH I,N,O,,,P, IC0F,13--, 1,224,253,273 [Co(OP,0,)(PiH,),j2-, 4,763 C~F,Nis, [Co(02P30,)(~H3)4]Z-, 4,763 (Co(NSF)#+, 4,858 CoHi,h',O, CoFsNOPl [Co(NO2)(NH3)ql2+.4.670 [Co(N0,),(NH3),]'. 1.9:4,668 [Co(ONO)( N02)(NH3),] ,4,672 [Co(0NO),(NH3),]+, 4,668,672 CoH, .N, +

[Co(NH,),(flCH=NCH=~H)Fe(CN)jl-.4.699 CoFeC,H 19N

~CO(NH,).~(~~=CHCH=NCH=~H)F~(CY jsl-, 4,690 CoFcC9HlqNIZ Fe(CN),(N=CHCH=NCHzH)Co( NH3)5,I , 364 CoFeCl,Nll [ C O ( C N ) , ( ~ - C N ) F ~ ( C N,4,h50 )~]~ [(NC),Co(NC)Fe(CN),J6-, 2 , 9 CoFeCZoH3,NsOPZ [Fe(CN),(p-CN)CO(CN)z(PEt;):(OH,)13-. 4.647 CoFeMoC13HS08S CoFeMoS(CO),Cp, 4,832 CoFeMoC,,H,,O,S CoFeMoS(CO),Cp(PMePrPh). 1. 832 CoFrWI,HZ040 [COW,,Fe( OH2)O3,I7-,3, 1048 CoGeCZ1HI5O4 Co(CO),(GeMePhNp-I), 2. I9 COH

CoH, 2,693 CoHF,,P, CoH(PF,),, 4,702,704,706,718 CoHN,SS Co(SNSNH)(SSSN),4,858 CoH0,P2 C0(02P205H), 4,762 CoH2P3,S4 Co(SNSNH),, 4,858 COH~NO~S [Co(SO>)(NH,)l+,4,820 CoH,N3Q2 [CO(NO),(NH,)]~',4,666 CoH4C12010 Co(H,O),(OCIO,),, 2,421

5,682; 6,801,1018 [Co(H20),]*',t,284,336,2,307; [Co(H20j6I3' . I , 336;2,12;6,50,517,801 COHT3N407P2 C'o{O,P,O,(OH)~(NH,),, 1,202; 4,760,6,447

CoFl,,N.O.

CO(O~P,O&~~(XH~),. 1.203;4,763,764; 6,447 CoH,,N, [C;~NH3)4(NH,)]2-, 1,305 CaH14N503

[Co(OH,)(OKO)(NH,)4]z',4, 668,672 c o t I,,N,O,P [Co(NH3),(Hl\iP0,H)]-, I , 442 CoH,,N.O,P [Ch~O,P(O)NHP(O)(0H)O) (NH3).,]+,4,766 COHiJWU" Co(O,P( O)VHP(O)(OH)O}(NH3)4,4,763 CoHi4N70 [Co(NH,),(H,0)(N,)J2t. 3,472 CoHiSBrN, [CoBr(NH3),]*+,1,302, 393 CoH15C1N, [CoC1(NH,),)2-, 1,3,7,8, 14,24,304,305.309.332,

365,372.317.303,469,510; 2,9,28; 3,472;5, hM; 6,99,517,520,523,531 CoHI5ClN5O2

[CI~(OCIO)(NH,),]", 4, 826 C'oHISCIN,O, [CO(OCIO,)(NH,),]~+,4, 826 CoH,,FN,O,P [CO(OP(O),F)(NH,)~]+,4,760

Cumulutive Formula Index

319

CoHisN30, [CO(NH,),(H,O),]~+, 4.638 CoHiSN40 [CO(NH~)~(OH)(HZO)]”‘.6,432 CoHi&”Oz [CO(NH,)~(OH)(H,O)]’-. 1.27 C0H15N404S [CO(SO3)(OH,)(NH,),I 4. 823 CoHisNs [Co(NH,),12+, 1,465 COH,~N~O~S [Co(NHq),(SO,)]’, 1,293: 2.418. 423,638; 4,820,822, 823,857 CoHiJ’Js08, [CO(S,O,)(NH,),]~, 1,186; 2,637; 4,817 CoH,,N,O,S [CO(OS0,)(NH3),]+. 1,308; 4,817 CoHi5Ns08Pz [CO(OP207)(NH3)5]-. 4.763 C0HisN@ioP3 [Co(0P,O,)(NH,)5IZ-, 4.763 CoH1sN6O [Co(NO)(NH,),]”, 2,103; 4,657,658,661,664 COHisN60z 1,471 [CO(NH~)SNO~]+, [CO(NHI),(NO,)]~ , 1,3,9,184: 2. 418, 423; 4,666, 668.671.673. 822 [Co(NH3);(ONO)]”, 1. 184.465; 2,423; 4,666,668, 67&673.698 COH1sN603 [CO(NO,)(NH,),]~+, I. 185 CoH,sN, [Co(N~)(NH3),]”, 2, 115; 4. 826.963 COH,6FNGO-P [CojOP( 0,H)F) (NH3)5]2+.4.760 COHi6N40z [ C O ( N H ~ ) ~ ( H ~ O ) , ]4.800; ~ + , 6.801 COHIAN.;~ I ! 185. 305, 372; 2, 638; 4, 760, [CO(NH,),(OH)]2’ 790,822,825,8W; 6,433,435,436,443,464,471 CoH1.5N507P2 Co(NH,),(I~IP,O,), 4,760; 6,447 CoH17N50 [CO(NH,),(H,O)]~+. I - 3,292,299,308,309;371,372, 469,471; 2,297; 3,1259; 4,679.690,775,790, 791,800,825,826. 958; 6.99, 188,434,468,801 COH~,NSO~P [Co(NH,PO,H)(H,O)(NH,)?j2+, 4,766 COH17N603S [CO(NH~SO,)(NH~)~]**. 4. 698. 858 [ C O ( O S O ~ N H ~ ) ( N H ~ )4. ~ ]858 *+. CoH,,NsOJ‘ [CO{OP(OH),}(NH,)~]~+. 4.752 CoHlsN6 [CO(NH3)6]2’., 1,26,336,348, 349,350, 353; 2 , 2 6 , 2 8 ; 5,689; 6,52,801 [Co(NH,),]’+, 1 , 2 , 3,5,7,9, 14,26. 183,273,302,333, 336,348.349, 350,353,400; 2,13,26,28; 3, 1110; 4,866; 6,113.117. 118, 119,621,801 CoH19N702S [ C O ( H ~ N S O ~ N H ~ ) ( N H4.858 ~)~]~+. CoH20N602 ICo(NH,),(ONO)lz-, 2.418

-.

’

I

COO&

{C~(Nb),I),, 4: 660,663 CoInC,,,H,,N,O, In(octaethylporphyrin)Co(CO),, 2, 843 CoKCl6HI1N2O2 Co(salen)K, 4,637 COKC,,H,~N,O~ Co( Pr-salen)K( CO,)(THF), 3, 16 {Co(Pr,salen)(CO,)K(THF)},,, 4, 638 CoLiCI6Hi4N,O, Co(salen)Li, 3, 16 COMnC16H16N20~

MnCo(CO),{C,H,N=C(Me)C(Me)=NC,H,)

2,211

C O M ~ C ~ ~ H ~ ~ O ~ P S ~ (Me,P)CpCo(CS,)Mn(CO),Cp, 2,582 COMnC16H,oNzO, MnCo(CO),(Bu‘N=CHCH=NBu‘), 2,210,211 CoMnC4,H,,0,P,S2 Co(tripos)(I*-CS2)Mn(C0)aCp, 2, 582; 4, 646

CnMoCioI IZN1004 ICo(CN),OOMoO( OH,)( CN);IS”, 4,780 CoMoH,,N,O, [Co(NH,),MoO,]+, 3,1377,1379 CoMoH,,N,O, [CO(NH~)~MOO,]+,3,1377,1379 [Co(NH,),(UMoO,)]+, 1,291; 3, 1379: 4.825 CoMo2OZS6 [Co(MoOS&]*-, 2,575 COMO~O~S~ [Co(MoO,S,),]~-, 2,574,575 [Cu(MoO,S,),]’-, 2,575 COh.IO,S, ~CO(h.IOS,),]”, 2,573,575 [Co(MoSd)213-,2,566,575; 3,1422, 1424 CdhIo6H602,-’ [Co(M06018(OH),j}]~ ,3, 1044; 4,827 CON& CO(SSSN),. 4,858 CON,O,S, Co(NO),(S3W), 4,658,660,858 CoN30, Co(NO)(ONNO), 4,658 C0N104 {CO(NO),(ONO)I,~, 4,660 COY,O9 Co(E1O3),, 1. 67; 2,414 Co(O,KO),, 2,415,418 I

-

I

CoN40 12 [CO(O~NO).]~-.2,423 CON& Co(N,S,), 4,858 COx6H18 [CO(NH3)6j3+,1, 121 CON60iz [Co(NOZ),l3-, 1,9; 2,273; 4,638,667 [Co(NO,j$, 1,273 CoNaCz0HzzN2O3 Co(salen)Na(THF), 3,16 CoNb,CH,NO,, [Cu(Nb,0,,)(C0,)(NH,)17-, 4,826 CoNiCIoH29N709

[Co(NH3)j{(02CCH2)2NCH2CH2N(CH2C02)2}Ni(H20)]+, 5,219 C0OJS~ [CO(SO,),]~-, 2,635 C0OBSZ

Cumulative Formula index

CoPtB

9H45P2

(COC~P~B~H~O)(PE~~)Z(CP). 5,373 COP~C~~H~,CI~N~P,

C0Cl,(2~pyd-Cpy-2)Pt(PPh,)~, 5,316 COReC16H~oN206

R~CO(CO)~(BU‘N=CHCH=BU’). 2.21 1 CoRe II15N504 [Co(ORc03)(NH,),j2+, 4, 198, 826 COR~&IH~SN~O~ Co(1etraphenylporphyrin){ Re(CO),IZ, 2,844 CORUC~H;~N~~O$ [Co(NH3),(p-HhCH=NCH&H)Ru(NH,),(SO,)I2+, 4,696 CORUC~H~~N~OO~ [CO(NH~)~(OCCH~PY-~)RU(NH~)~(H~O)]~+, 1,333 CoRGoHi9Nii [Co(en),(NH,)(p-NC)Ru(CN),I-. 4,283 CORUC~~H~INI~O [cO(NH3)4(H20) {NCC(CHzCH2)3CCN}Ru( NHs)s] ’+, 4,679 CoRuC16HliC104P RuConCI(~.-PPh,)(CO),,4,373 CoRuC, @H1 6 N 1 2 0 4 - ’ CO{L-O,CCH(NH,)CI~~C=CHNHCI f=A }z( NC)Ru(CNhl?-, 4.283 CoRuCl,Hio07P R u C C I ( ~ - P P ~ ~ ) ( C4,373 O)~, CORUC&2506P2 RLICO(U-PP~,)(CO)~(PP~~), 4, 373 CORUC~~H~~O~P~ CORU(U-PP~~)(C~)~(PP~~)~, 1.373 cos4 [CoS4I6-, 2,525 CoSiC,H904 Co(SiMe,)(CO),, 4,657 CoSiC,,,I 16203P3 C O H Z { S I ( O E ~ ) ~ } ( P P4,655 ~~)~, ~7

I - 1

CoWC55H4405P8

[CO(P~~PCH~PP~~PPPPP~,CH~PP~~)W(C~)~]+, 2, 1058 cow,02s6 [Co(W0S3),l2-, 2,572,575 [c0(w0s3),]”, 2,575

cow ,04s,

[CO(WO,S,),]~-, 2,572,574,575 [co(wozs2)2]3-,2,575 COW& [Co(WS4),12-, 2,564,566,572.575; 3,982 [CO(WS,),]~-,2,564,566,575; 3. 982 [CO(WS4)2]” , 2,524 COW,1H4040 [Wll~H2)Co(OII2)037]’-, 3, 1048 cow12040 [COO,W~,O,,]~~, 1,336; 3,1037: 4, 827 [ C O O ~ W ~ ~ O1,336; ~ ~ ] 3, ~ -1042.1052 , COZG~H~&”~S~ Co{Zn(NCS),}(en),, 5,988 COZA~CI~H~~N~~& I{ C O ( ~ ~ ) ~ ( O ~ C C H ~ S4.848 )}~A~]~+, COZAg2C8H34N14017 Co,(o,)(NH,)(en),(No,),(AgNO,),, 2,324 ‘&AG&i { Co { MeC(CH2AsPh2),)},(p-H), ,4,773 Co,As,C,,H2,F603 Co2{C,(CF3),}(CO),{MeAs(C,fl,AsMe2-2)2}. 4,769 QIAS~W~OH~NOI~~ [A~aw&H4)0 140{Co(OH2)11123-13. 1049 Co&&zH.e1 {CO(McC(CH,ASP~~)~)}&L-H)~, 4. 769 C02ASsC40H6802

320

321

Cumulutive Formula Index

C02C54H48C12N2P4

4.654

C0ZC12H42N100Z [ C ~ ~ O ~ ( d i e n ) ~ ( ,2,47 en)~]~' Co,C,,H,,O,P,S Co2Cp(PMe2)2(S0z),2,638 C O Z C M HPz ~Z CozCp2(PMez)z,2,636 COZC14H30N2012P4 C O ~ ( C O )MeN{ ~ { P(OMe)2}2},.4,735

COZC54H48C12N2P4

Cumulutive Formula Index

Co7C,H,4N,S4 [CU,(H,NCH,CH,S),I’+,

32 2

2,799

323

Cumulative Formula lndex

CrAlzCla

Co8C36H3 O s 12 [co,(lr4-s)6(Sph)6l5-, 4,833 CosC4,H,,S1, [(COSP~),(U,-S)~]~-, 1,139,162; 2,527; 4,832 Cu9ss CogSs, 1 162,4,833 CO,,C2,025S1 [ C ~ O ( C O ) ~ ~ ~ ~ C ,O2 ~ , 19 (CO)~~}]~~ C O I ~ L H ~ ~ M I N ~ ~ ~ ~ C0~~(OH),(OAc)~(b-Me-2-pyrid1nolatc) 2,746 COlZC84H96N12030 Co,,(OH),( OA~)~(6-Me-2-pyridinone),~ ,2,300 Co,,(p3-OH)6(OAc)6(6-methyl-2-pyridinolate)12~ 1.168 C024H4506 C O { O ~ C ( C H ~ ) ~ 6,386 M~}~, CrAgCH,,&,S [Cr( NH3)5(p-NCS)Ag13+,3,841 CrApC6H16N6 [Ag(CN)2Cr(en)2]Z', 3,776 1

CrRgO,

[ C O ~ ( S P ~ ) ~1, ~ ,139, ] ~ - 151,162; , 2,528',530; 4,832.,834 CO~C~UH&~NL~ [ {CoF(EtfiCH=NCII=cH)3}4j4*2,685 16 COJC~JHWF~NXO {Co2(02)(3-F-salen),(H,0),),, 2,325 C04C96H80P8 C04(PPh)4(PPh3)4, 1. 154 I C O ~ ( P P ~ ) , ( P P ~ , 1.154 )~~+,

AgCrO,, 3,933 CrA&

AgCrS,, 3, 882 CrAgSe, AgCrSe,. 3.889 CrAgz04 AgzCr04.3,943 CrAg3CII J H ~ O ~ S P ~ S ~ Cr(OzC2S2)31Ap(PPh3)2}3r 5,816 Cr(S2CzOJ3{Ag(PPh3)zl3 5,816 CrAIC4Hlz04 Cr{Al(OMe),}. 3.860 CrAIC,O,, [Cr(C,~4),AIl,, 1,27 CrAlSi,C,,H,, NO,P 3

Cr(CO)S(p-PPh,)Ai(UH2S~Me3)2(N Me,), 3, 1 12 CrAIzC1zH2,06 Cr{OAl(OFr1)2}z,3,738 CrAI2Cl8 (AlC13)2(CrC12).3, 122 CrAI,Cl,, 3.755

CTAl~Cd%4012 Cr{Al(OPr')4}3,3, 860 CTASC1&1506 CrO(Oz)2(OAsPh3),3,946 CrAsC19H1403 Cr0(2-Ph2AsC6H4COz),3,901 CrAs, 5C15H~4C13N~ 5 CrC1,(2-Me,AsC,H4NMe2), <, 3.854 CrAs, SC15H24C13P1 CrC13(2-Me2PC6H4AsMe2)1 5 . 3. 854 CrAszC7HlsCl4 [CrCI,( Me,As(CH,),AsMe,}]-, 3.853 CrA5&oH,6Cl, [CrC14(diars)]-,3, 853 C~AS~CI~H~ON~O~S~

[C~(P~ASO,H),(H~NCSNH~)~] ' .3,888

C ~ A S ~ C ~ ~ H ~ ~ N ~ S ~ ICr(NCS)4(diars)l-, . _ 3,838 C~AS~C,,H,~CI~ [CrCL(Ph,AsCH=CHAsPh,)1-, 3,853 CTAS~C~~H&~~~Z CrCI,(OAsPh,),, 3,754 GAS~C~JLK)~ Cr(2-Ph2AsCsH4C02)2(OH),3,901 CrAS&sHw06 Cr(2-Ph2AsC,H,C02)2(0H)2,3, 901 CrAS3C10

5H27C13

CrC13{MezAs(CH2)3AsMe2}1 5, 3,854 CrAs3CllH27C13 CrCI,(AsMe(CH2CH,CH2AsMe,),), 3,854 CrC13{MeC(CH2AsMe,),},3,854 C~AS~C~~H,,CI, CrCl,(diars), ,, 3,854 CrAsJHO13 [(C~O,O),ASOH]~-, 3,1024 CCAS&jH&12

CrC12{As(CH2CHZCH2AsMe2)3}, 3.855 CrAS.&,,H&13 CrC13{As(CH2CHZCH2AsMe,),). 3, 854 CrAb4C2,,HBZBr2 CrBr,(diars),, 3,734 CTAS~C,,,H,,CINO Cr(NO)Cl(diars),, 3, 830 [Cr(NO)Cl(diar~)~]+, 3, 830 CTAS~C~~H~~CI~ CrCl,(diars),, 3,743 [CrC12(diars)z]+,3, 854 C~AS&~H~ZIZ CrI,(diars),, 3,734 C~AS~C,,H,~CI, CrC1,(Ph,AsCH2CH,AsPh,),, 3, 854 C ~ A S ~ C ~ ~ H ~ ~ B ~ ~ ~ ~ CrBr,(OAsPh,),, 3,754 C~AS~C~~H~~C~ZO Cr(CIO,),(OAsPh,),, 3,751 C~AS,C~~H,,I~

[CrI,{MeC(CH2AsMe2),},j'. 3, 856 CrAuC23H1605P Au(PPh,)(p-H)Cr(CO),, 5 , 869 CrBCl3HI2N~O3 [Cr(CO,) { B(&N=CHCH=CH).,}]-. 3.846 CrBC17H17NR02 Cr(CO),{B(fiN=CHCH=~HH),} (a-CsH5),3,846 CrB,C,H,~O, Cr(BH,),(THF),, 3,766 C~BZCI~HI~N Cr{H2B(N-H)2}2, 3,772 CrB2ClsHZgN2

Cr{HB(NN=CHCH=cH),},,3,732 CrB2C20H32N C * { E t , B ( N ~ H ) , ) , ,3.732,772

CrB2C2,H N C r { B ( N w H ) 4 } 2 ,3,732 [Cr{B (NN==CHCH=cH)4}2]'1 3,845 CrB2F604 [Cr04(BF3)2]2-,3,944 CrB2H8 Cr(BH4)2.3.929 CrB4C20H3U0~2 Cr{B,O(OAc),),. 3.752 CrR1&H3,J3rN4 Cr(Blu~Ilo)Br(MeNH1),,3,7X7 CrBrO, [CrO,Br]-, 3.944 CrBr20, Cr02Br2,3,940 CrBr, [CrBr3]-. 3.764.765 CrBr, [CrBr412-,3,753,763 CrBr, [CrBr,13-, 3.766 CrBr,O [CrOBr,12-, 3,935 CrBr, [CrBr614-,3.763 CrCH,CI,O {Cr(OMe)Cl?),,.3. 860 CrCHsN205 [Cr(NO)(CY)(H,O),]'. 3, 823,825 CrCH9N0,S, [Cr(NCS)(SH)(H,O),]', 3,877 CrCHl0NO4S2 [Cr(NCS)(H,0)4(H,S)]2+.3,877 CrCHI,,N05 [Cr(CN)(H20),]Zi . 2 , 10: 3, 774 [Cr(NC)(H2O),I2+.3,774, 842 CrCHl,-,NO,S [CT(NCS)(H,O)~]*+. 3. 842 [Cr(SCN)(H20),IZ-,3.841 842 CrCH,,N,O, [Cr(NH,),CU,I+. 2,28 CrCH,.N.O ICr(CN)(NH,),(HZO)~*+,3,776 CrCHI5N6 [Cr(CN)(NH,),JZ+.1.393, 396; 3,776 CrCHISN60 [Cr(NCO)(NH3)5]Z+, 3.783,844 CrCH15N6S [Cr(NCS)(NH,),]2-, 1,387,398,402,504; 3,844 CrCH,.N,Se [Cr(NCSe)(NH,),]2'. 3.844 CrCH2*N70 [Cr(NH3),(Nk1CONH2)]z~',3, 852

[Cr(NH,)s{OC(NH)NII,}]2+, 3,852 CrCH,,N,O [Cr(NH,) j(H2NCONH2)]3+,3,852 CrC,ClNO, CF(NO)CI(CO),, 3.826,827 CrC2CI2I2N2O2 Cr02C12(ICN)2,3,941 CrC,F,NO, Cr02(N03)(02CCF3),3,940 CrC,F,O,S, CrO,(O,SCF,),. 3,440,941 CrC,H~Cl~O, [CrCI,(AcOH)]* ,3,848,936 CrCzHr NO2 [Cr(Gly-O)]'+, 3,769 CrC,H,CI,N [CrCI,(MeCN)]'-, 3,848 CrC2H6N3O4

325

Cumulutive Formula index

Cr(NO)(CN),(H,O),, 3, 825 CrC2H,02 Ci(OMe),, 3,737 CrC2H8C1,N402 CrCIz(HzNCONHz)z,3,739 CrC,H,CI,N,S, CrCI2(H2NCSNH2)2,3, 754 CrCzH,F,N, ~, ~

CrC4H,,N,0,

[Cr(H20)j(SkNHCHZCH,NH)]3+,3,888 CrC,HjJ%,OS [Cr(CN)(DMS0)(NH3),l2+,3,776,782 CrC3Hz2N60 [Cr(NH3),(DMF)l3+, 3,853 CrC3N304 [Cr(CN),(0,),13-, 1,78; 2,319; 3, 947 CrC3S9 [Cr(CS3),)3-, 3, 885 CTCqF606 C102(02CCF3)2,3,939-941 CrCnHOi Cr(C,O,)(OH), 3, 873 CrC,H2N,Oz ICr(N0)(CN),(H,O)l2--, 3,825 CrC,H,OI -~., [Cr(O,CCH=CHCO,H)]Z+, 1,336 CrC4H,06 Cr(O,CCHOHCHOHCO,), 3,753 CrC,H,O,, fCr(C20&H,0)2]-, 3,870-872; 6,477 CrC&azN, CrCI,(MeCN),, 3,717,732,899 CrC,H,CI,N, [CrC14(MeCN),]-, 3,848 UrCJ 16N& [Cr(NCS),(NH,),]-, 1,398,409; 2,28 [Cr(NSC),(NH,)J, 1,3Y4 CrC,H,O, CriOAc),, 1,272; 2.440 CrC4H6O6 Cr(C2H3O3jZ,3,753 CrO,(OAc),. 6,351 CrC4HsBr40, [CrBr,(AcOH),]*-, 3,758,762 CrC4HaC120 CrCI,(THF), 3,739 CrC4H,C1,0, [CrCI,(AcOH),]-, 3,848,936 CrCIHsNzO4 Cr(Gly-O),, 3,7hX, 769 CrC,H,O, Cr(OAc)l(H,O), 3,740 CrC4H8S4 Cr(SCH2CH&, 3, 772 [Cr(SCH2CH2S)2]2-,3,755 [CCr(S~CzH4)zl,I"-,3,886 CrC,HIoC12N,0, CrCl,(H,NCONHCONH,),, 3,739 CrC4H,,O2 Cr(OEt),, 3.737 CrC4HI0O6 CrO(0,)1(OEt2), 3,945 CrC4H11C:IZN2 CrCI,(H,NCH,CMe,NH,),, 3,721 CrC4H,,C1,0,S2 CrC12(DMS0)2,2,488; 3,754 CrC4HI2Cl2P2 {CrC12(MePPMe,)},, 3,733 CrC4Hi3C1,N3 CrCI,(&en). 3.722 CrC4Hi3CI3N3 CrCl,(dien), 2,47; 3,807 CrC4Hi3N3 [Cr(dien)12+.3,721 CrC4HI3N3O4 Cr(dien)(02)t.3,807,946 CrC4HI3O8S (CC(H~O),(O,CCH,SCH,CO,H)]~', 6,27 ~

[Cr(CN),(NH,),]+, 3.776.777,782.919 CrC,H,,NO, [Cr(MeCN)(H,0),j3+, 3,816 CrC,H,,O, [dr(OAd)(H,0),]2+. 6,49 CrC,H,,NO,S [Cr(SCHzCH2NH3)(H20)j]3T. 3.879 CrC,H, ,CIN,OS [CrCi(DMSO)(NH,),]z-, 3,782 CrC,H,,N,O

[6r(NH3'),(MeNHCONH.Mc)l3-,3,852 CrC,O, Cr(C,O,), 3,752 CrC,F,O,S, Cr(03SCF3),, 3,941 CrC3H2N402 [Cr(NO)(CN),(H,O)]-, 3.825 CrC3H6N303 Cr(CN),(H,O),, 3.775 CrC3H6N3O3S3 Cr(NCS)9(H20),, 3,838 CrC3H9FI2N3P6 Cr{(PF2)2NMe}3,3,714 CrC,H,N,S, Cr(S,CNHNH&, 3, 885 CrC,H,O, Cr(OMe),, 2,349; 3. 860 CrC3H9O6Se3 Cr(02SeMe)3.3.869 CrC3H909S3 Cr(O,SMe),, 3, 815 CrC3H9S3 Cr(SMe),, 3,881 CrC3HioCI2N2 CrC12{H2N(CHz)3NH2}. 3.731 CrC3Hi008 [Cr(02CCH2C02) (H20)4]+I6,477 3.888 CrC13(HZNCSNH2)3. CrC3Hd205 Cr(pn)(H,O)(O,),, 3.946 CrC3HI3O9 [Cr(H20)5(02CCH2C0zH)]2+. 3,873 CrC3Hi6N,0,S

CGH1309

[Cr(H20)5(02CCH=CHC02H)]z+,1,374 C~C~HNN,OS ICI(~ = C H C H = N C H = c H) (H,O) ,] * ,3.822

Cumulative Formula Index

CrC4H&l2N30

CrC4Hl5CI2N3O [CrCl,(dien)(H,O)] ,3.807 CrC4Hi6BrFN4 [CrBrF(en),]+, 3,795 CrC4H16BrN502 (CrBr(NO,)(en),]+, 3,795 [CrBr(ONO)(en),]+, 3,789 CGHdrzN4 CrBr,(en),, 3,721 [CrBrZ(en)2]+r 1,471; 3,795 CrC4HL6C1FN4 [CrCIF(en)z]+,1,297; 3,796,798 CrC,H,,CIN,O, IC~(C~)~(ONO)CI]+, 1,2Y7 CrC4H14C12N4 CrCl,(en),, 1,399 [CrC12(en)Z]+r 1,27,297,298,398,467.371,505; 2, 677; 3,795,796,798,809, 816 CrC4H16C12Ns04 CrC12(H2NCONH2)4, 3,739 CrC4Hl6ClZO4 [Cr(MeOH),Cl,]+, 3,860 CrC4HlhF&" [CrFz(en),]+, 1,393,398: 2,677; 3,796,798

324

CrC4N4 [Cr(CNj4J3-?3,774 CrC,N,Sd [Cr(NCS),I2-. 3.730 CrC4NS0 [Cr(NO)(CN),I2-. 3. 825 CrC,HNFO [Cr(CN),(OH)I3-, 3,774,775 CrC,HO,Se [Cr(CO),ScH]-. 2.662 CrC5H06 [Cr(OH)(CO),]-, 2,297 CrC5HzOs C ~ ( T ~ ~ - H ~ ) {2,690 CO),~ CrC5H,ClN,0, CrCI(x-Cp)(NO),, 2,112, 114;3,833 CrC,H,CI,NO, CrO,Cl,(py). 3.935 CrC,H,NO, CrOlpy, 3.941 CrC,H;NO, CrO(O,),(py). 1,24.61; 2,319,320; 3,945; 6,321.329, 334

+

~

__

I

CrC4H16N303

Cr(OH),(dien), 3,807 CrC4H,,N40,S Cr(S04)(en),, 3,721 CrC4H16N709 Cr(en)z(N03)3,3,867 CrC4Hi6Nio [Cr(N3)z(en)zl+, 3,844 CrC4H1,C1N302 [CrCI(dien)(Hz0)2]2+,3,807 CrC4H17CIN40 [Cr(en),(OH)Cl]+, 1,297 CrC,H,,BrN,O [CrBr(H,0)(~n),]~+, 3.794,796 CtC4H18CIN40 [CrCl(H,0)(en)z]2',1,297;3,795 CrC4H18FN40 [CI-F(H,O)(~~)~]+, 3,796 [CrF(H,O)(en),lZ' ,3,79&798 CrC4HlSN4O4 Cr(OAc)2(NH3)4,3,746 CrC4H18N70 [Cr(N,)(en)z(HzO)lz~, 3,844 CrC4HitPioOz

[Cr{H,NC(=NH)NHC(=NH)NH,}z(Hz0),]3+ ,3,851

CrC4H19C1N5 [CrCI(NH3)(en),lz+, 3,795 CrCdH,,FNS [CrF(NH3)(en),l2+,3,795-797 CrCdHi~N303 [Cr(dien)(H,O),J", 2,48; 3,807 CK4H19N402 [Cr(OH)(H20)(en),]z+,3.799 CrC4Hd602 3.795 [Cr(NO,) (NH3)( CrC4HZOF2N4

[CrF2(MeNH2)4]+, 3,787 CGHz&"Oz [Cr(en)2(OHz)z]3+'. 1, 397; 2. 32 CrC4H21NSO [Cr(NH3)(H20)(en)z13+,3, 795 CrC4H22N304

[Cr(dienH)(H20)4]4+, 2,48;3,807 CrCdHd6 [Cr(NH&(en)~l", 3,795 CrCd%J'L0& [Cr(DMS0)2(NH3)4]3+,3,782 CrC4H25N305

[Cr(dien-HZ)(OH2)5]s*', 2,48; 3.807

[C%(~~),(NCS)CI]+,I , 297 CrC5HI6FN5S [CrF(NCS)(en),]+, 1,400; 3,796 [CrF(SCN)(en),l+, 3,796 CrC5HI6N50 [Cr(CN)(H,O)(en),]'+. 3,795 CrC,H20N06 [Cr(NO)(MeOH),IZ-, 3,824 CrC5HZ5BrN5 [CrBr(MeNH,),]*". 3,787 CrC,H,,CIN, [C~CI(MCNH,)~]~+, 3,787,788 CrC5H27NS0 [Cr(MeNH2)j(H20)]3', 3,787,788 CrC,H,,N, [Cr(MeNH,),QW,)]3f, 3,787 CrC5N5S [Cr(CN),S]*-. 3,773 CrC5N5S5 [Cr(NCS)513-.3.730 CrC5N60 [Cr(CN),(N0)I3-, 2. 103;3,774,823,831 [Cr(CN),(NO)J4-, 3.823 CrC5N60S5 [Cr(NO)(NCS)j]3-. 3,824 CrCSNsS, [Cr(NCS),(N,)If-, 3, 843 CrC,CI,N,Oj& (CrO,CI,(SCN),},, 3,941 CrC6F906 Cr(02CCF3)3.3.941 CTC6F908 [Cr02(02CCF3)3]-,3, 944 Crc6H408 [Cr{(0,C)2CH2}212-,3,752 CrC6H5N202S [CrCp(CO)(NO)(NS)]+,3,833 CrC6HsN,0, CrCp(NO),(NCO), 2,103,230 CrC4H6 [Cr(CN),I3-, 3,773 CrC,W,N,O, [Cr(N,),CN(CH,CO,l?}lz-, 3,845 CrC6H606S3 [Cr(SCH,C0,),]3 .3,901 CrC4H8ClN30, CrCl{O2CCH(NHZ)CH&=CHNHCH=r;J }, 3,768

327

Cumulutive Formula Index

CrC6HZ3FN5

CrCI,(AcNHNH,),. 3,834 CrC6Hl8CI3N& CrC1,(HzPr’CSNHMe),, 3,888 CrC6H,,C130,S3 [Cr(en)(C204),]-. 1. 183 CrC13(DMS0j3,2,488 CrC6HsN208 CrC6H,,CI3S3 [Cr(en)(C204)2]-,3. 871 C I C ~ , ( S M ~ 3, ~ )881 ~, CTC6H8N407 CrC6H,sF2N4 [Cr(N,) { N(CHzCOz),) (HzO)1-?3. 845 [CrF2{(H2NCH2CHz),N)]+,3,811 CrC,H,N,S3 CrC61i,,N, [Cr(CN)(NCS),(en)]-, 3,838 Cr(NMc,),, 3. 835 C~6H8010 CrC,H l e N , 0 3 [Cr(02CCHZC02)z(Hz0)zj-, 6,377 Cr(OCH,CH2KIl&. 3,8‘17 C~C~HVB~~N~ CrBr3(MeCN),, 3,846 CrC6H l E N l [Cr{(H,NCH2CH2NHCHz)2}]2+. 3,722; 6.496 CrC6HgCI3N3 CrC,H, ,N,O,S CrCl,(MeCN),, 3.846 [Cr(O,CCH,S)(en)z]+, 1,457 CTC6H912N3 [Cr(SCH,C02)(en)Z]’, 3,796,879 [Cr12(MeCN),]+, 3,846 C r C 6 H d 10 C~C~HION~O~SZ [Cr(N3)z{(H,I\ICHzCHzNHCHz)z}]+, 3.81 1. 844 [Cr{SCH2CH(NHz)COZ)2]-,2,744; 3.904 CrC6Hl2ci2N4S2 [Cr(rc‘3)2((H,NCHZCHz)3N}l+, 3,811 CrC6H18Nls CrC12(HfiCSNHCH2~H2)z, 3,754 Cr{H,NC(=NH)NC(=NH)NH,),, 2,284,3, 850 CrC&zN2S4 Cr{lI,NC(=NH)NHC(NH,)-N},, 6,49 Cr(S,CNMe,),, 3.754 C‘rC6H1R04SiZ CrC6HizN306 Cr0,(OSiMe,)2, 3,941 Cr(Gly-O)>, 2,744; 3,902 CrC,H,&O, CrC,H,,N40,S4 [Cr(2-pyC02)(NH3j5]2 ’ ,3,899 Cr(N0)z(SZCNMe2)2, 3, 826 CrCAH,&FN, CrC~H12N404 [&F5r{HzN(CHz)3NHz}z]+.3,797 Cr(hexamine)(O,),, 3,947 CrC6HzoC1FN4 CrC~Hi4N20s [CrCIF{HzN(CH2)3NH2}z]t, 3,798 [Cr(H20)5(4-NCpy)]3+.3.818 CrC6H,nC1N,0 CrC6H14Nz06 [CrC~{(H2NCHzCHzNHCHz)2}(H20)]2+, 3,808 [Cr(0zCCH2NHCH,CHzNHCH,COz~(H,0)z]+, 3,910 [CrC1{(H2NCH2CHz)3N}(HzO)]Z+, 3,811 CrC6Hi4N1004 CrC6H2&12N4 [Cr{H2NC(=NH)NHC(=NHWH2} 2(Cz04)]+,3,851 CrC1z{HZN(CHz)3NHz}z, 3,721 C~CSHI~NIZS~ [CrC12{HzN(CH2)3NH2}2]+, 3,798 [Cr{H2NC(=NH)NHC(=NH,NH,),(NCS)2J+, 3,851 CrCJT,r,FN,O CrC6H&12P 3,811 {CrC12(F’Et3j},t, 3,733 C~C~HI&I,P {CrCI,(PEt,)),, 3,853 CrC6HisS3 900 Cr(SEt),, 3, 881 C~C6H16N~06 [Cr(H20)5(4-pyCONH2)]3+3 1.374 CrC,H,,N403S [CrCl(dien)(en)12+.2,47 CrC,H,,CI,N2 CrCli(€tNfiz)3,3,788 CrC,H,,FN,O crC6H16N$ [Cr(CN),(en),]+, 3,776.777.795,797 CrC,H,,N,S [Cr(CNfiNCS)(en),] ’. 3,838 CrC6Hi6N6S2 [Cr(O-II){ (HzNCE12CM2NHCH2)2} (H20)]2’. 3,809, [Cr(NCS)z(en)z]+,1,398; 3. X38 810 CTCgH17N05S [Cr(4-SC6H4NH3)(H20)5]3+. 3.877 C~C~HZIN,~~ Cr(OHj,{(HzNCH2CH2NHCHz)2},3,810 CrC6H18BrCIN4 [CrCIBr{(H2NCH2CH2j3N}]-.3.811 CrC6H21N15 [Cr{H2NC(=NH)NHC(=NH)NH,),l3+, 3,850 CrC6H18Br203S3 CrC6H22FN,0 CrBr,(DMSO)l. ,- 3.754 C~C~HI&~N~ ICrF(0H2)(~n),l2+, 3,798 {Cr{H21*;(CH2)3NH2}2(OH2)F]2+, 2,45;3,797 [CrC12{(H2NCH2CH,NHCRz)2}]+.1.298; 2,53; 3, CrC6HzzN,0 808,809,810 [CrClZ{(H2NCH2CH2)3N}] ‘ 1.298: 3.81 I [Cu{H,N(CH,),NHz},(OH,)l2+, 2,45 CrC,H,,N,S CrC6HlaCI,OsS3 CrO,Cl,(DMSO),, 2.488 [Cr(S~~zCH,NHZ)(en)z]2+, 3,879,880 CrC,H,,CIN,O, CrC6HlsCl3NZ [CrCI(H2O),(trenW)]3+,3,811 CrCI,(Me,N),, 3,788 CrC6H2,ClNF CrC6H&1& CrCl3{(H2NCH2CH2),N}.3.788,812 CrC6H&I,N603

CrC6H&N5

Cumulative Formula Index

[CrF(NH3){H2N(CH2),NH,},]2-, 2,15.3,797,798 CrC6H2,N05S

[Cr(4-SC6H4NMe3)(H20)5]3*. 3,877 CTC6H23N50 [Cr(en) (dien)(H,0)I3+, 3,807 CrC6HdbOz [Cr(N,)(tr~enH)(H,o)~]~+. 3. 811. 814 CrC6H24N6 [Cr(en),]+, 3,838 [Cr(en)3]2+,3,721 [Cr(en),13', I , 27, 183,207, 397,398,470.471; 2 , 3 2 ; 3, 797; 6,621 CrC6H24N1206 [Cr(H2NCONH2),]'+,1,395; 3.867: 6.49 CrC6H,,N403 [Cr(trienH)(H,O),]", 3,810 CrC6H25N5F303S [ Cr( OS02CF3)(MeNH2)5]2+. 3.788 CrC6H26N6 (Cr(MeNH2),(en),I3+, 3,787 CK6H26N703 [Cr(N,)(H,O),(tr~eiiH~)]~+, 3, 81 1 CrC6H2,N60 [Cr(en),(enH)(OH,)'+, 1,397 CrChHZ8N4O4 [Cr(trienI1,)(H,C)),15' ,3, xt0. 81 1 CK~Hd704 ICr(N,)(H,O),(tr~cii€~~)]~+, 3.81 I Crc6H,,Y6 [Cr(MeNH,)6]3+,3,787 CrC6H31N405 [Cr(tr~enH~)(H,O),]~+, 3, 810 CK6N206

[Cr(C0)4(CN0)2]2-,2 , 13 CrC6N6 [Cr(CN),l3-, 1,183,398,410: 2 . 11: 3,703.708,774, 775,197,823,838 [Cr(CN),I4 ,3,703, 708,774. 775 Icr(CN),)6 ,3,704,774 Crk,N,O, ~fCr(NCO),]'-, 3 , 843 CrC,N,S [Cr(CN),(NCS)I3-, 3, 841 CTCtjN& [Cr(CN)4(NCS),]3-, 3, 841 CrC6N6S3 [Cr(CN),(NCS),I3-, 3. 841 CrC6N6S4 [Cr(CN),(NCS),I3-, 3,841 CrC,N,S, [Cr(CN)(NCS),I3-, 3,841 CrC6N6S6 [cr(NcS)6l3-, 2,230,283; 3,837.838. 842, 843 [Cr(NCS)614 , 3, 730 crC~N&e, [Cr(YCSe),13-, 3,842 CrC,O, Cr(CO),, 1,288,496; 2, 13,237,709 Cr(C404)3iz,3, 873 CrC,O& [&(C2S20z)3]3-,3,885 CrC609s3 [Cr(C2SO3),I3-,3,901 CrC& [CT(C~O.,)~]~-, 1, 183,377,366: 2.46,962; 3,799-871; 6 9 CrC7H3N05 Cr(CO),(McCN). 1,496

CrC,H,O, Cr(CO),(OAc), 2,438 CrC7H403 C I ' ( ~ - O C ~ H ~ C3,~753 Z), CrC7H5N02S

328

CrCp(CO),(NS). 2,119, 120, 121; 3,832 CrC,H606S Cr(CO),(DMSO), 2,488 CrC,H,K,O, Cr(NO){2,6-py(C0,),}(H20),,3,826, 835 CrC7H,C1,N, CrCl,{H,C[&N=CHCH=CH),}, 3,728 CrC,H,N,O, Cr(NO){2,6-py(C02)2}(NH20H),,3, 826,835 CrC,I Il,,C12N2 C'rCI2(2-py~H2CH3NH2), 3.727 CrC,H1 ,BrOz Cr(MeCOCBrCOMe),(OEt) 2 , 377 CrC7H,,YU,OCr(CO),(dien). 2.47; 6,70 CrC7HlsC1N5S [CrCI(NCS){(H2UCH2CH,),N}]+. 3,8 11 CrC7HlsClY,Se [CrCI(NCSe)((H2XH2CH2),N}]+,3,s 11 CrC7H2,C12N, [CrCl2((HINCHICH2NHCH2),CH,}]+, I,298,398:2. 54 CrC7H2oF2N4 [CrF,{(~IINCHtCH2NHCHZCHL)LCH~}J+ 3,812 CrC,H,,>N,O,S - [dr(SCH2CH2CC)2)(e~),]+. 3, 871) CrC,H,,CI,N,OS

[CrCl2{(H,NCH,),CMe}(DMS0)]',3,808 CrC,H,,ClN, [CrCi$3,$(CH2),NH,}(dien)]2+, 3,807 [CrCI(pn)(dien)l2-.3,807 CTC~H~~N~O [Cr{H,N(CH,)3NH,;(dien)(H,0)]3+, 3,807 [Cr(pn)(dien)(H,O)l3+.3, 807 CrC7H2,Ni,S [Cr(MeSCH1CH2NH2)(en),I3+, 3, 880 CrC7HP6N, IC:r{II,N(CH,),NH,}(en),J3' , 2 , 4 5 CrC,F,,O,,, [Cr0,(02CUF,),]2-, 3,944 CrCSH,N,0, [Cr{MeNC(H)NhfeCO}(CO)]-, 2,203 CrCsH,N,03 [Cr(NO)(CO),[MeCN),]+, 3,827 CrC,H12ClN50 [Cr(NO)CI(MeCN),]', 3,827 CrC8Hl2CI2N4 CrCl,[Me&CH=NCH=cH)2, 3,727 CrC,H;,N, [Cr(McCN),1*-, 3, 732 CrCSH14N204S2 Cr{ { OzCCH(NH2)CH2CH2S}2}, 3,768 C'rC8HI3NGS3 Cr{H2NC112Ct~2h'H(C'H,)3NH,}(NCS)3, 2 , 50 CrCRH,&1202 CICI,(THF)~, 3.717.739 CrC8Hi6v204S2 Cr(O,CCH(NH,)CH,SMe},, 3,768 CrC8HlSCl3S3 Cr { CMe(CH2SMe),}C13, 3,886 CrC8H18C13S4 Cr{(MeSCH,CH,SCH,),}CI,, 3,886 CrC,H,,N,O, [ C r ( C 2 O a ) { ( H 2 N C H Z C H , N t ~ ~ H ,' ),2,53; ~ } J 3, 809 [Cr(CzO4){(H,NCH2C'H,),". 3,811

CrC8H1804 Cr02(ORu')2, 3,928; 6,351 CrCsH20CIZN4 [CrCI,{ 1,4,7,10-tetraazacyclododecane)]+.3.922 CrCsH20N2 Cr(NEt,),, 3. 931

CrC9H22N,0S [Cr(NCS)(1,4,7,10-tctraazacyclododccane)(H,O)]Z’+.3. [Cr(NCS)2{H2N(CHZ)3NH2}2]+. 2.45; 3,798,838 922 CrCRH2,N405 CGH23NeS [Cr(c,O,)(H,O)(trienH)]z-, 3,809.811 [Cr(NCS) {HN(CH2CH,NHCH2CH,NH2),)l’f, 3,814 CrC9HZ4F2K4 CrC8HZ2Cl2N4 [CrCIZ{H,N(CH2)3NHCH2CH,”(CH2)3NHz}]+, 2, [CrF2{H2N(CH2)3NH(CH2)3NH(CH2)3NH2}]+3>812 55; 3,812 CrC9Hz7Cl2P3 CI-C~~~(PM 3,713,733 ~,)~~ CrC8HzzN402 CrC9H2,CI3P3 [Cr(OH),( 1,4,7110-tetraazacgclododecane)]*, 3,922 CrCI3(PMe3),, 3, 713 3,895 [Cr{(H,NCH,CH2N=CMe)2}(H20)z]+, CrC8HZ2N402S CrCq€i27F&sPh Cr(PF2NMc&{ (PFZ),NMc),3,715 [C1-(tjC:Mc2C02)(en)2] . 3 , 879 CrC9H?J6 CrC8iiZ3CIN5 [ C r ( ~ n ) ~ ) 3,721 ”, [CrCI{HN(CI.12C:Il,NHCt12CHINH2)2}]2+,3, 814 [Cr{H,N(CFr,)3N~J,}3]3+,2 , 4 5 CrC,H,,N4O2 CrC,oH6C1412N2 [Cr(OH)(1,4,7,10-tetraazac!;clododecane)(H20)]z~, 3, CrI,(3,j-CIZpvI,, 3,724 922 CrC8HZ4BrZN4 CrCloH8Br212N;’Cr12(3-Brpy),. 3,724 CrBrZ(H2NCH2CH2NMe,j2. 3. 721 CrCsH24C12N4 CrCloH8ClzNz CrCl,(bipy). 3,710 CrC12(H2NCH2CMe2NH2)2, 3.721 CrC1,(MeNHCH2CH2NHMej2. 3,721 CrCl0HsC1,N2 {CrCI3(bipy)},!.3, 848 CrC,Hz4C1A”04 CrC,,,I18CI,;V20 CrCI2(McNHCONH,),. 3,739 CrC8HZ4CI3N4 CrOCl,(bipy). 3,848,935 CrCI,{H2N(rH2)4NHd)2.3, 798 CrCloH8N2 [Cr(bIpy)12+.3, 712 CrC8H2412C)4S4 CrI,(DMS0)4, 3, 754 CrC,,H8N203 CrO,(bipy), 6, 351 CrCsHz4N4O2 [Cr(1,4,7, lO-tetraazacy~ladodecane)(H,O),]~+,3,922 CrCloH8N,05 CrO(02)2(bipy),2. 319; 3,945 CrC8HZ5N5O [Cr{HN(CHZCH2NHCH2CH2NH2)2}(H20)]3+, 3,814 CrCl,HsN,O Cr(NO)(N,),(bipy), 3,824 CrC8HZ6N6 [Cr(dien),I2+, 2,47; 3.721 CrCIOHIOBr2NL [Cr(dien),13+, 3, 806 CrBr2(py)213. 724 CrC,H2&” CrC,,,H10CIzN2 [Cr(H,N(CH1),NH,),(en)]3+. 2.45 CrCl,(py),, 3, 724,725 CrCBN6 CrUlo€l,,,CI,N,O, Cr{C(CN)3}2,3, 709 Cr02C12(py),,3, 935 CrC’91.1,F6C)4 CrC.,,H ,oCI,N I o CrCl,(adenine),, 3,728 CrCp(C),CCF,),, 3.816 CrCloH.l,CI,N, CrC9H5N50 [CrO(CN)4(,py)lZ-,3,977 CrC9H603 .- .- 1. 131 Cr03(py)2, 3,941; 6,351,352 Cr(C0)3(q6-CfiHfi), CrCloHI2N2O8 CrC9H6012 [Cr(OZCCH,C02)3]3- 3. 872; 6.377 [Cr{(02CCH2),NCH,CH2N(CH,CO,),)]-. 1.336 [Cr{(02CCH2)2NCH2CH2N( CH,C0,)2}]2~~. 1.336 CrC9H8C1,N2 CrCI2(8-am~noquinoline), 3, 727 CrC, ,H,,N50s 3,844 [Cr(N,) {( 02CCHZ)2NCH2CH2N(CH2C02)2}] CrCJ [Cr(N,){ (OzCCf 12)2NCHzCH2N(C:tI,cn,),}]2-, 3, K45 Cr(HCOCHCK10)3, 3.861 Cr(OHCCHCHO)J.6.’206 CrCloH12Y6S2 CrC,H.,,,O,Se Cr(NCS),(HfiC(Mc)=NCH=~H}l, 3.727.773 Cr(CO)S(ScEt,). 2,662 CrC,,,Hl,Br2N2O, CrC9HI5F3P CrBr2(HzO)z(py)2,3,725 CrC10H14K208 Cr(PF,)(C3H5h3 3,714 [Cr{(02CCH2)2NMe}2]’,3,911 CrC9HI5O3S6 Cr(S,COEt),, 3,884, 885 CrClOHl4N2O9 [Ci(edta)(H,O)]-, 1,554; 3,1259 CrC9HiaN303S6 Cr(NCS),(DMSO),, 2.641 CrCloH1404 Cr(acac),, 2,371; 3,717,738,772,912 CrC9H18N306 Cr{02CCH(NH2)Me)31 3,902 CrCloHljC1204 CrCl,(acac)(acacH), 2,402; 3,861 CrC9H18N3S6 Cr(S2CNMe2)3,3, 8R5 CrCl0HI5N2O9 Cr(H,O)(FIedtil), 2,783; 3, 908 CrC9H20NJ04 [Cr(C20,){(H2NCHzC~€,YHTH2),CFT2} I+, 2 , 5 4 CrCIOHjSN6C) [Cr(NO)(hleCN)5]2-‘,3,826,829, 848 CrCyH2,Cl,N,O2 CrCIJ(DMF),, 3,920 [Cr(NO)(MeNC),]+, 3,826 CrCqH2,NO4 [Cr(NO)(MeNC)J2+, 3,826 Cr(OPr’),(NO), 2. 178 CrC10H1BN6S [Cr(NS)(MeCN),I2+,2, 119,121; 3,832: 848 CrC,H2,N6S3 Cr(NCS)3(EtNH,)3,3,788 CrC,0H,6C14P2 ~

-.

CrC LOHlhC14P2

Cumidutive Formula Index

CrCloH1607 [CrO(O,COCMeEt),]- ,3,937 CrCIoH18C12N402 Cr(NO),CI,(CNBu'),, 3, 827 CrCloHl,N4P2S4 ICr(NCS)4(Me3P)2]-, 3,838 CrC, .H,,O, [c;(acac);(lf,o),] ' ,3,86l CrClOHl8O7 C,rO{O,CC(OH)MeEt},. 2,480 CrCloH20N204S2 Cr(O,CCH(NH,)CH,CH,SMe),. 3,768 CrCl0H2,A"S4 Cr(S2CNEt,),, 3,754,884 CrCl0HZON5OI7P3 [Cr(H,O),(ATP)]-, 2,978 CrCloH~oN& 3,922 [Cr(NCS),( 1,4,7,10-tetraazacy~lododecane)]+~ CrC10H22N404 I,}]', [Cr(C,O,){ I 12N(CH2)3NHCH2CH2NH(CH2)3NI 3,812 CrC10H24CI,N4 [CrCI,( I ,4,7,1 I-tetraazacyclotc1radccane)l'. 3, 922 [CrCI,( 1,4,8,1I-tctraazacyclotetradecane)J' , 1,298. 398; 3,919 CrCioH2d6O4 [Cr(N02),(1 ,4,8,11-tetraazacyclotetradecane)]+, 3, 919 CrClnH,aNlo [Cr(N3),(l,4,8,11-tetraazacyclotetradeca~e)]+, 3,919 CrCloH26C1N40 3; [CrCl( 1,4,7,11-tetraazacyclotetrade~ane)(H~O)]~+, 922 [CrCI(l ,4,8,1l-tctraa~acyclotetradecane)(H~O)]~ ' ,3, 919

330

[CrCI(1.4,8,1?-tetraazacycIopentadecane)( H20)I2+.3. 923 CrC11H30N402 [Cr(1,4,8,12-tetraazacyclopentadecane)(H20)z]z~.3. 770 97-1 [Cr(l,4,8~12-tetraazacyclopentadecane)(Hzo),l'-, 3, 924 CrC11H36N8013

[CrC02($3-edta)(pOH)2(NH,),(H,0)]3+,1, 125 CrCIZF8S4 [Cr(S,CbF4),]' ,3,886 CrC JLXSb Cr{.S2C2(CF3)&, 3,886 [Cr{S2C2(CF3M31-,3,886 [Cr{S2C2(CF3),),I2-. 3.886 CrC12FZ405 [CrO{(CF3),C(0)C(O)(CF3)2}21-, 2,344; 3,938 CrCl2H8Cl3N2 CrCl,(phen). 3%821 CrCI2H8IN2O6 Cr(IO,)(phen),, 3,936 CrCI2HRNZOs CrO(phen)(O,),l Z1319 CrCllHSNSOSl Cr(NO)(NCS),(bipy)l 3.824 CrC12H8N90 Cr(NO)(N,),(phcn), 3,824 CrCl2HYNyS4 [Cr(NCS)4(2-guanidinobenzirnidazole)]~, 3,838 C r G 2H90I [Cr{R,R-0,CCH(OH)CH(0)C0,}3]6-, 2,479 CrC12H1002 Cr(OPh),, 3.737 CrCl,H, 1C13N3 CrCl,(bipy)(MeCN). 3.848 CrCI2Hl2 Cr(C,H&, 1,336.351 [Cr(C6H,)>]', 1 , 336, 35 I CrC 12H12C11N402 CrC:1U€i26N402 [Cr(2-pyCH=NOH),CI,]', 3,849 [Cr{( H , N C H , C H 2 C H 2 N ~ C M c ) ~ ~ ( ~ ~ 23,895 (~~),l', C:rCIZHI2NZS2 CG,,HdsO4 Cr(SC6HJH2-2),, 3,770 [Cr(1,4,8,11-tetraazacy~lotetradecane)(NO~)(H~O)~~+, CrC,,H,,K9S3 3,919 Cr(NCS),(HhCH=NCH=cH),, 3,837 CrCloH2,N03Si, CrO( NBu') (OSiMe;),, 3,945 CrC10H27N402 [Cr(OH)(1,4,8,1 l-tetraa~acyclotetradecane)(H,O)]~+, 3,919 CrCl0H28N402 Cr(CO),(C(OEt)NEt,}, 2,182 [Cr( 1, 4 , 7 , 1 l - t e t r a a ~ a c y c l o l e l r ~ ~ ~ c a ~ ~ ) 3, ~ H ~ O ) ,CrClzl~,,O, ]~+, 922 Cr(MeCOCHCHO),, 6,206 [Cr( 1,4,8,1l-tetraazacyclotetrddecane)(H,0),13+, 3, CrC12HI6Br2N4 919 ',3, 804 [CrBr2(2-pyCHLN~12)2] CrC1,,II3,CIN, CrC, ,H,,CI,N, [CrCI(EtNH2)5]2', 3,788 ICrC~,(2-pvCH,NH,),l', 3,803-805 C~C~IH~~NO~P Ck~l,H~,Ci2hi, Cr(CO),{P(O)NPr',}. 2, 1052 CrCIZ(FI~CCH=NCH=~H),,3, 727 CrCllH15N03P CrCI,(H%N&HCH=~HH),, 3,727 [Cr(COCH=PMe,)(cpd)(CO)(NO)]-, 1 , 122 C~C~~HI~~F~NI CrCIIHI7N4O4S [CrF2(2-pyCH,NHz)2]+,3,804 Cr{ L-N=CHNHCH=~CH,CH(NH,)CO,}{ DCrC12H16N,08 SCMe2CH(NH2)C02},2.744; 3,904 Cr(3-pyCO2),(HzO),. 3,725 CrC, 1H~iN704 CrCl,H16N40, [ Cr{2,6-py{C(Me)=NHNI.ICON [ I , } ,} ( t-1,0),l3+, 3, [Cr(2-pyCH=NOH)2(H20),]3', 3,849 896,899 CrCI2Hl6N6O4 CrC,,H,,N,O, [Cr{0,CCH(NH,)CH,~=CHNHCH=fi}2]+. 3.904 [Cr'(C;b4){(H,NCH,CH,NHCH,CH,),CH,)] 3,812 CrC2,1 I 1RHrZN6 CrCi 1H24N6S2 CrBr,(Merj~=CHCH=~H),, 3,727 1 ,}I+, 3,H12 CrCI2HlBC1N3O3 [Cr(NCS), ((H2NCHZCH2NHC~~2CH2)2C:I CrCl,H26C12N4 Cr(NO)CI(CO),( CNBu'),, 3, 827 CrCl,H18C12&Sz [CrC12(1,4,8,12,-tetraazacyclopentadecane)j+,3,921 CrCllH,8CIN40 [ C I ~ ~ ~ ( P Y ) , ( H ~ N C S N3,888 H~)~]+, +,

Cumulative Formula index

33 1

CrClzH18C13N3 CrCl,(bipy)(NCMe), 3,936 CrClZHI8NzO2 Cr{ {MeCOCHC(Me)=NCH,),}. 3, 772 CG~H18NzOlo [Cr{(02CCH2)2NCH2CH20H}2]-, 3,911 CrC12H18N50 Cr(N0 &CHCH=CMeNCH,CH,NC(Me)= ~ H Z 3.832 ] , CrC1ZH18N6

[Cr(MeCN)6]2",3,718, 732 CrC12H18P3S6

Cr(S,PMe(C=CMc)},, 3, 885 CrC12Hi9N402

[CrMe(1.4.8.12- tetraazacyclopentadecane)( H20)]Zt, 3, 923 CG2HfZCl2P4 CrClz(Me2PCHzCH2PMe2)z, 3,713,733 CrC12H32W" Cr(N,),(Me,PCH,CH2PMe2)2,3,713 CrCizHd603 3,924 [Crl(p-0H),( I ,4,7-triazacy~lononane)~]~~, CrC1zHdzN4 [Cr(H2NPr)4F2]f. 2,677 CKizH36F601zPb Cr(PF(OMe),)6, 3,716 CrCllH36Fi2N6P6

Cr(PF2NMe&, 3,715

[Cr(HzO)(OH)(2-pyCHzN~z)z]2+. 3,804,805

CrCl._ ,H,KI,NR __ - CrCl,(pentamethylenetetrazole),,

CrC14H32Br2"I

CrC12H36N4P4

Cr(N,),(PMe,),. 3,713 3,726

Crf(MeCOCHCHMeNCH,),}.3,767 CrCl2HZ0N4O2 [Cr(H20)z(2-pyCH2NHz)2],-, 3, 804 CGH2007 [CrO(0,COCEt,)2]-, 3,937 C~CIZHZI~~S~S% Cr(SSeCOCH,CHzOMe)3. 3.886 CGzHzzNz02 Cr(MeCOCHCHMeNMe),. 3.767 CrC1;HZZNZO4 [Cr{{ MeCOCHC(Me)=NCH,) ,}(H,O),]+, 3,894 CrC,,H,.,CIKL CreI,(THF);, 3,855,867, 892 c~c,,H,~cI,S~ CrC13{mH2)4}3> 3. 881 CrClZHZ4F3O3 CrF3(THF),, 3, 855 CrCl2HZ4I3O3 CrI,(THF),, 3, 856 CrC12H24N6 [Cr(CN),(1,4,8,1 I-tetraazacjclotetradecane)]' ,3,777, 919 CrCl2H2aN6S2 [Cr(NCS),( 1,4,8,1l-tetraazacyclotetradecane)]+,3,919 CrCizHz4S6 [Cr(MeSCH=CHSMe),13+, 3,886 CrCl2HZ7Cl3P {CrCI,(PBu,)},, 3,853 CrCIzH~7N04 Cr(NO)(OBu'),, 2, 178,356,3. 831 CrC1ZHZ703

Cr(OBu'),, 3,928 CrClZHZ709P Cr0(0,)2{0P(OBu)3}, 3.946 CrClZHZ8C1ZN4 CrC12(Me,[14]aneN,), 3, 771 CrCIZH28N604 [Cr(OCONH,),( 1.4,8,1I-tetraazacyclotetradecane)]+ , 3,919 CrC12H30BrN4 [CrBr{N(CHzCH2NMe2),}]+,3.735 CrC1~H30C13S3 CrCI,(SEt,),, 3.881 CrC1~H30C14P~ [CrCI4(PEtl),]-, 3, 853 CrC1ZH30N3

Cr(NEt&, 3, 835. 928,930 CrC,,H3,06P& Cr{S2P(OEt)2}3,3,885.886 CrCizH30083Se6 Cr{Se,P(OEt),},, 3,885 CrC12H3,N40

Cr(NCS),(Et~=NCH=CHr~),(H,O). 3,837 CrCl,H,,C1,N2S

Cumulative Formula Index

CrC14H32Br2N4 CrBr,(l,4,8,11-tctramcthyl-l.4,8,2 1-

tetraazacyclotetradccane) 3.770 CrCflH3,CIN4 [CrCI(1,4,8,11-tetramethyl-l 1418,11tetraazacyclotetradecanej]~,3>770? 773 CGaH3zNz03. Cr(NO)(NPr'z)(OBu')2, 3, 831 CrC14H34N0zSiz Cr{N(SiMe3)z}(THF)2,3,730,772 CrC,,H,,N,O,Si, Cr(NBu')z(OSiMe,)z, 2, 167; 3,945 CTC14H38P4 CrMe2(Me2PCH2CHZPMc2)2. 3, 714.733 CTC~SH~F~~C)~ Cr(hfacac),, 3,863 [Cr(hfacac),13', 1,28 CrC15HllC13N3 CrCl,(terpy), 3,821 CrCi~HizFd& Cr(CF,COCHCOMe),, 1,28; 2, 382,384; 3,863,864 CGSHIK~A" CrC13(bipy)(py), 3,848 CrC1sH,,C13N,O CrCl,(bipy)(py N-oxide), 3,848 CrC15H15C13NZ0 CrCl,(phen)(DMF), 3,820 CrC15H,sCI,N, CrCl,(py)3, 3,788,815 C~CI~HISC~~N~O~ CrCI,(OCH=CHCH=cCH=NOH), ,3: 850 CrC15Hi~N605 Cr(NO)(ONO)z(~~)3, 3,823 C GsHisNiz Cr(N,),(py)3,3,843 C~C~SHI@~P Cr(CO),{C(OMe)PhPMeZH), 2,1056 Cr(CO),{PMe,CH(OMe)Ph), 2 , 1056 CrCISH,,BrCI,O, Cr(McCOCCICOMc),(MeCOCBrCOMe),6,204 CrC1SHlXBrR06 Cr(MeCOCBrCOMe),, 6,203,204 CrCl5HI8Cl3O6S Cr(MeCOCCICOMe)z (MeCOC( SCI)COMe}, 6,205 CrC~sHd306 Cr(MeCOCICOMe),, 6,204 CrClSH18N301z Cr { MeCOC(N0,)COMe) 6 204 CrC&i&1206 Cr(acac)(MeCOCC1COMe),. 6.204, 205 CrC1sH20C1zN4 [CrCI2(2-pyCH2NHCHMeCH2NHCH2py-2)]+, 3,813 CrClSH20F06 C,r(acac)z{MeCOCFCOMe},6.2U.I CrC1sHzoN0s Cr(acac),{MeCOC(N02)COMe} 6,204 CrC15H20N20h [Cr(acac)Z(MeCOC(N,)COh.lc)]'~.6,204 CTC~;H~~BTN~ [CrBr{N(CHzCH2fiN=CHCH=CII), j]+: 3,728 CrCISHz1F9O6 Cr(F,CCOCHCOMe),, 3,864 CrCisHziO6 Cr(acac),, 1,65,422; 2.380, 384,386; 3.738, 861-864, 892; 6,203,204,205*1014 CrC1SH2107 Cr(acac)2{MeCOC(OH)COMe}. 6 %204

332

CrC12(EtfiCH=NC€1=~H),, 3,727 CrClstf,,C1,N,. jPl.s CrC13(2-Me,PC6H4NMez)l5, 3,854

[Cr(NO),(CNBu'),]2 ,3,827 CrC I FHIDNIOSh Cr(S2CNEt2)2(0S2CNEt2), 3, 884, 88s C~C15H30NfS6 Cr(S,CNEt,);, 2,181; 3, X84,885,931 Cr(S2NCEtz),, 3.885 CrC1sH30N40S6 Cr(NO)(S2CNEtz)3.3,826,896 CrClSH32NsS [Cr(NCS)(k,4.8.1 I-tetramethyl-1,4,8,11tetraazacyclotetradecane)]+, 3,771 CrClsH33N20Si2 CrCN(Si~~e3),}(Et,0)(py), 3,730 CrC1SH3bC13N6S3

CrUl,rEtn;l-ICSNHEt),, 3 , 8XX CrCIS13,,Dl5P5 CrH2(P(OMc)3)j. 3.714,734,896 CrC,,H,N,O, [Cr(C;O&jphen)J-. 3.799,819 CrC16HioN304 [Cr(PhNNNPh)(CO),]-, 2,203 CrCi6HioNioS4 [Cr(NCS),(benzimidaz~le)~]-, 3,822,837 CrC16Hl,CtNz02 Cr(salen)Cl. 3.893 CrCl6HI4NzO, [CrO(salen)] ' .3.918; 6,351,352 [CrO(salen)]Z' .3.894

,.

I

CrClSH21S6

Cr(MeCSCHCSMe),, 3,884. 885 CrCIsH,,N06 Cr(acac),{MeCOC(NH,)COhk}. 6 : 204 CrCl,H,4Br2N6 CrBrz(HflN=CMeCH='2Me),. 3.727 C~CI~HZ,C~ZN~

Cr(N,)(salen)(H,O), 3 , 845 CrC16H18C12?j06S

Cr(MeCOCCICOMe)z(MeCOC(SCN)COMej, 6,205 CrC16Hl,CI,0P {CrClz(dppe)o.S(Me,CO)}~, 3,733 CrCi6HisNz04 [Cr(salen)(H,O),]-, 3,892-894; 6,352 [ C r ( ~ a l e n ) ( H ~ O ) ~3,] ~894,918 -, CrC16Hd402 [Cr(salen)(NH,),]+, 3, 893 CrClbHZ2CW4 [CrC12{(2-pyCH2NHCHMe)2}]I , 3,814 CrC16HZ2C12P2 CrC12(PMezPh)2,3.733 CrC1,H,,N,, [Cr(HzNC(=NH)NHC(=NH)NH,),(phen)]3+.

3.851

Cumulative Formula Index

333 CrC1SH24CINs [CrCl(N=CMeNHCH&H)4]+.

CrC 1RHS4C13NY03P3

3.773

CrCi6H24FzNa [CrF2(HNN=CHCH=CMe),If. 3.822 CTC16H27CIN402 Cr(N0)CI(CO)(CNBut),, 3. 827 CrC inH3zNb03 [Cr(NO)(N02){fi=CMeCHICMe2NHC'H2CH2N= CMe CH2CMeZNHCH2CH2)], 3 , 8 3 2 [Cr{1-(2-0-S-03SC,H3N=N)-2-OC'l,,t 1,) { H2NC(= CrCI6H3& NH)NHC(NH,)=N)(HzO)l-, 6,19 [Cr(MeCN)( 1,4,8,1I-tetrarnethyl-l.4,8,Il. .C r C l 8 ~ , ~ C~ , i L' , tetraazacy~lotetradecane)]~'3.771 CrCl,(X-aminoquinoline),, 3,727 CrC16H36C12N4 [CrCI, HfiCHZCH2NHCHMeCH2CMe2NHCH2CH2CrCl8HlSF6N204 Cr(02CCF3),(2.6-Me2py),, 3,724,772 b M e , ) ] ' . 3,771.920 CrCl8HlaN3O6 CrC16H36N606 [Cr(NO,),( HfiCH2CH2NHCHMeCHzCMe2NHCH2- Cr{MeCOC(CN)COMe},, 2,375 CHzNHCIIMeCH&Mc2)]'. 3, Y21 CrC18H,SN603 [ C ~ ( ~ - P ~ C H = N O H' ),3,849 ,]~ CrC16H36Nio [Cr(N,)2(HNCH2CH2NHCHMeCH2CMc2NHC'H2- CrC,,H,,N,O,S, Cr(NO),(CKBu'),{ S,C,(CN),),, 3,827 CH2NHTHMeCH2CMe2)]'. 3.921 CrClsHz,C13N3 CrCi6H360, Cr(OBu').,, 2,339,346, 319; 3.928. 929 CrCk3(4-Mepy),, 3,815 CrC13(PhI'iHZ)3, I , 419; 2,59; 3,788 [Cr(OBu'),l-, 3,928 CrCl,H2zN,0, crcl6H36s6 ,3, 893 [Cr(~alen)(MeOH)~]'' [Cr{S(CHZCH2CHZSMe)2)21'-. 3.886 CrC16H38C1N40 CrClaH2rN402 [Cr(2-OC6H4CH=NCH2CHzNH2)2]+, 3.893.895 [CrC1(HfiCH2CH2NHCHMeCH2CMe,NHCH2CrC1,HZ4Cl2N4 CH,NHCHh,IeCH,C Me2)(H20)]+,3,921 [CrC12{2-pyCH,NH~H(CH,)4~HNHCH,pv-2)1+. 3, 814 . ,

,

~

c~c,~H~~N&

[Cr(OH)(H$4CH,CH,NHCHMeCH2CMe2NHCHz-

CI X2NHCHMcCmMe,) (H,O)]*+, 3,921 C~CI~H~ONJ Cr(NEt2)4r2, 169. 180, 181.3,884.928,930,931 CrC,,H,,N,O, [Cr(HfiCH2CH2NHCHMrCH,CMe2NIJCJ 12CH,NHCHMeCH2CMe2)(H20)2]3+, 3,921 CrC16H44Si4 Cr[CH,SiMeq)a, 3. 930 CrCI;H2,kIN202 Cr{ {MeCOCHC(Me)=NCH2)z)(py)Cl, 3,894 CrCl7H2,CIZO7S Cr(MeCOCC1COMe)2{hIeCOC(S0Et)COMe) ,6,205 CrCi7€i,,N0, Crfacacl~~MeCOC(NHAc)COnle). 6,204

[Cr (NO)(C6),( CNBu') -.3.81-7 CrC17H,,N50 [Cr(DMF)(1,4,8,1l-tetramethyl-l.J.8,11tetraazacyclotetradecane)]z~,3,770 CrClsCl1206 Cr( 1,2-02C6C14)3r3.865 CrCl8CIlZS6 3. 886 [Cr(l,2-S2C6C14)3]Z~. CrCI8HllCl2F7N3 Cr(C3F7)C12(terpy),3.899 CTCiaH12C13N6 CrCI3(CNpy),, 3, 815 CrCiaHI20, [Cr( 1 ,2-02CbH4)313, 3 . 865.866

Cr{MeC(O)=CHC(Mc)=NBu)z, 3,772 CrClnHqaNzOz Cr(MkOCk2HMeNBu)2, 3,767 CrCiaH36"304

[Cr(C,0,)(H~CH2CH,NHCHMeCH,CMe2NHCH2CH2NHCHMeCH2eMe2)]+. 3.921

CIC18HJ2N3 Cr(NFr12)3.2.28, 171, 178; 3.835,836,930.931 CrCIHHazh',Oz CrO(NPr'2j2(0NPr'Z).3.931 CrO2(NPr'J3, 3,836,931 CrC,,H,,\I,O, Ci-03(KPr'2)3.3, 836 CrCiabN40 Cr(NO)(NPr',),. 2. 178; 3,830,836 CrC1&2N606 [Cr(DMF),I3', 3,875 CrCiaH+3Fiz06P6 CrlPF,OPr),, 3,716 CrCIBH48N1ZSh ICr(MeNHCSNHMe),13*, 3,888 ck18'H4$6

Cr(MezPCH2CHzPMe,)3, 3,714 [Cr(MelPCHzCHzPMe~),]3+, 3,856 CrC18H51N9

Cr(C3F7)ClZ(pyj3, 3. 899

2.47 [Cr{Hz~(CH~)3NH(CH2)3NH2}313+1 CrCIBH54C13N903P3 Cr{OP(NMe2)3}3C13,3,876

Cumulative Formula Index

CrC18H54N3Si6

CrC1&54N3Si6 C T { N ( S ~ M ~ 2, ~ )178; ~ } ~3,836 . CrC18H54N40Si6 Cr(NO){N(SiMe3)2}3,2, 178; 3.701.729.830 CrCi~H540isP6 Cr{P(OMe)2}6,3,714

C;(CO),(PhN=CHCH=NPh), 2.208 CrC,,HlSNsPS~ [Cr(NCS),(EtPh2Pj]2--.,3, 838 CrC19H31C1203 Cr(C6H4Me-4)CI2(THFj3,3, 821 CrC19H33N3F7S4 Cr(C~F7)(S2CNEt2)2(H2NC6H,l). 3. 883 CKi9H3d'L04 [Cr{ (02C),CH,} (HfiCH2CH2NHCHMeCH2CMe2NHCH2CH2NHCHMeCH2cMe2jl-, 3,921

[Ckl;(bipy),]+, 3,713,818.819 Ci=Cz0Hl6I2N4 CrI2(bipy),, 3,710 C~CZOHI~N~O~~S~ [Cr{ 1-(I-0-8-O3S-2-CioH5N=N)-2-O-4O$CIOH~}(HIO)~I 6 3 7 CrCZOHl7ClN40 [ CrCl( OH)(bipy),]+, 3,819 CrC20H18C1N40 [CrCl(bipy)2(H20)1Z+. 3,818, 819 I

[CrCIZ(quinoline)2(H2NCSNH2),]' , 3 , 888 CrC,,H 4N6 [Cr(&CH=CHCH=NCH2CH,NCH=CHCH= NCH,CHz)(py)2]+, 3. !E4 CrC20H24N70

Cr(&CH=CHCH=NCH,CH,NCH=CHCH= NCH,CH,MNOL3.92-1

[CrC12{2-(Me2P)2C6H4}21+. 3.854 CrCzoH16C1Nq0

334

CrC13{~1N=C(N~e,)2)1,3. 851 CrC20H,2N202Si, Cr{N(SiMe3)2}z(THF)z. 2, 171; 3,729,737 CrCzoH56N20zSi4 Cr{N(SiMe3)2)2(EtzO)2, 3,729 CrC2,H1,C1N302 Cr(salen)(py)CI. 3, 893 C~CZIHI~F~N~O~ Cr(02CCF3)4py),, 3. 815 C~CZlH1503S3 Cr(PhCOS),. 2.645 CrCZ1HI0, Cr{O~=CH(CH=CH),cO},, 1,422; 3,865 Cr(2-OC6H,CH0),, 3.892,895 CrC21Hl,% Cr(SzCPh)3. 2.646 CrC21HZiN204 Cr(salen)(acac),3,893 CrC21H21S3 CrlSCH,PhL. 3.881 CrC2;H2,cI3GiO3 CrCIq(PhCONHI\IH2)3,3, 834 CrC, lH24N30, Cr{MeCOC(CH,CN)COMe},, 1,422; 6,205 CrCZiH24"6S3

CrCI,(H2NCSNHPh)3,3,888 CrC21H33BrN7

[CrBr{N(CH,CH,fiN=CMeCH=cMe),)j', 3,728 CrC2lH36N50, [Cr(NO)(CO){CNBU')~]+, 3,827 CrCziH3,N5 [Cr(Me,[14]4.1 I-dieneN,)(py)]+, 3,772 CrCZiH42N40 Cr(flCHMe(CH,)3cHMe)3(NO), 2, 178 CrC21H43X02 [Cr(acac H~CH2CHzTiHCHMeCH,CMe2NHCH2-Me2)lz ,3,921

Cr(NCS);(hipy),, 3, 710,712 CG~HI~NJO~ [Cr(OH)(bipy)(phen)(H2O)IZ+,3,818 CrC22H24N20~ Cr{(PhCOCHCHMeNCH,),}, 3,767 CrCZ2HZ4NjS [Cr(NCS) { (2-pyCH,CH2),N)]+, 3,823 CrC22H24N8S2 [Cr(bipy),(H2NCSNH2),J3+, 3,888 CrCz2Hz6N201 Cr(PhCOCHCHMeNMe)2,3,767 CrC22H26N40~ [Cr{ { MeCOCHC(Mt)=NCH,} ,} (bipy)]' , 3 . 8 4 4 CrCZZH32C1N8 [CrCl{H,C(hN=CMeCH=c Me),) 2 ] + , 3.728 CrC22H3804

Cr(BuTCOCHCOBu')Z,3,739 CrCz3H16CIF,N, [Cr(C,F,)Cl( bipy),j-, 3,899 CrC23H&12F7& Cr(C3F7)CI2(bipy),. 3.899 CrC2,H18N307S Cr{ 1-{2-(2-02CC6H4NS02)C6H,")-2-ocloH6)(HZ0)z16.76 CrC23HddW, Cr(02SMe)3(bipy),, 3, 815 CrC& F903S6 Cr{S&=CHCH=CC(Sj=CHCOCF3}.3q2,652 CrC2,H laCI,N, [CrC12(phen)2]+.3,818,810 CrC24H16N404 [Cr(C,O,)(bipy)(phen)]+, 3,820 C T C ~ ~&1N4O H

335

Cumulative Formula Iadex

[CrCl(phen)2(Hz0)]2+. 3,819 CrC24HlsN40z [Cr(OH),(phen),]+, 3.819 CrCZ4Hl8N9 Cr{&C(py-2)=NCH=CH], .3.822 CG4HZON402 [Cr(phen),(H,O)z]Zt, 3.936 [Cr(phen)z(H,0),]3'. 3.819 C~CZ~HZ~N~O~ [Cr(2-OC6H4N=NC6H40-2)lj-,6,711 C~CZ~HZ~O~P~ Cr(OzPPh2)2, 3,740 crcZd~2Is6

Cr(S2CCHzPh)3, 2,646

C~CZ,HZZN~O& Cr{ I-{2-(2-HzNC6H4SOZNCH2CHzNSOZ)C6H4N= N}-~-OC~OH~}(H,O), 6,77 CrCz4Hz306Pz { Cr(H,O)(OH)(0,PP hz),},. 3.868 CrCZ4H~8CIZN4 CrCl,(Mepy),, 3,724 ICrCl,(PhNH,),l*, 3,788 CrCz4H3;N4P2S4 [Cr(NCS),(PhEt2P)J, 3, 838 CrC24H4ZN30h ~

Cr{MeCOC(Cl-12NMe,)CO!vle}3, 1. 422;6,205

CrCz4Hd%

CrC32Hl&

C G H 5J306 [Cr{MeCOC(CHZNMe3)COMe}3]3+, I , 422:6.205 CrC27H57O3 Cr(OCHBu',),, 3,930 CrC,,H6&13N6S3 CrCI,(BuNHCSkHBu),, 3,888 CGsHi4N10 Cr(TCNQ),(MeCN),, 3,848 CrC2BH170SP Cr(COj5(PC5H2Ph3). 2, 1044 CrC,,H,,N20G Cr(phcnanthruquinot1emonoximate),(nH)(H,0). 3. 850 CrC28HZOBrZN4 CrBrz(CNPh)4,3,707 CrC2sHzoC1zN4 CrC1z(CNPh)413.707 CrC2sH23CI,Y20P CrCl,(bipy)(OPPh3),3,848 CrC28H24N404 [Cr(?-O-5-MeC,H3N=NC6H3Me-5-O-2),] - ,6.65 CrCZ9H2,N04P2 [Cr(No)(Co),~dppe)l+, 3,829 C:rC30H,8F903S3 Cr{PhC(S)=CHCOCF3}3, 2,652 CrC30H22Nln

Cr(terpy),. 3.713 [Cr(tcrpy),j3+. 3,817 CrC30€124N6 Crrbipy),, 1,336;3,710,712,713.817 C~CZ~H,,~~ fCr(bipy),l3-. 3,817 Cr(OCHMeBu')4, 3,929 [Cr(bipy),j2-. 3,817 CrC24H,4C14Pz [Cr(bipy),]-, 3,817 [CrCI,(PBu,),]-, 3,853 [Cr(bipy),]-, 1,336; 3,710.712 CrCz5Hz0N4O7S 3,71&712,817,818:5.5W [Cr{1-(2-0-5-03SC6H3N=N)-2-(2-02CC6H4NH- [Cr(bipy)3]2-, 1,396; [Cr(bipy)J3+, 1,396,398-400; 3,710,712.816.817, CHZCH?N)CIOH6}(H30)]~. 6.77 818 CrCZ5H2,N802 CrC3VHt404PZ [Cr{ 1-( OcNPhN=CMc~=I\IN)-2-0-4-NCCl,H,}Cr(CO),(dppc), 3,829 (dien)]', 6 , 7 1 [Cr(CO),(dppc)]+,3.829 CrC25H45N60 CrC311H27Nb0 [Cr(NO)(CNBu'),j+, 3,827 [Cr(bipy),{4.4'-bipyH(H20)}]3+, 3,712 3,827 [C~(NO)(CNBU'),]~~, CGOH&'&J C~CZ~H~~N~S Cr(PhCOCHCOMe),(py),, 3,738 [Cr(NS)(Bu'NC),]+. 2,121; 3,833 CGoH3oN6 [C~(NS)(BU'NC),]~+.3.833 [C~(PY)~]~+, 3,724 C~CZ~HI~C~~N~OSS, CrC30H,zN,07S [Cr(3-(2-0-3,5-Cl2C6H2CH=N)-4-OCr{l-(oChPhN=CMec=NN)-2-0-4-{ ( m N)C,H,SO,NH,}2]-. 6.84 SO*}C~OH~)(~~~C)(H,O), 670 CrCmH16N404 CrC3oH400)6 [Cr(C,O,)(phen)J, 3, 799.819.820 Cr(2-0-3.S-Bur2CGH2C02)z, 6,124 CrCz6H,ASz CrC,oH45C103 Cr(NCS),(phen),, 3.710-712 [Cr(l-adamaiityloxy),Cl~+, 3,930 CrC26HzzCi4P2 CrC10H4SNOJ [CrC14(Ph,PCH=CHPPh2)] ,3,853 Cr(1-adamantyloxy),( NO),3,930 C~CZ~HZ~CI~P, CrC,,H,,O, {CrCl,(dppe)},, 3,733 Cr(1-adamantyloxy),, 3,930 CrC2hHZ4C130P2 CrC30H54N6 CrCl3(HZO)(Ph2PCH=CHPPh2),3,854 Cr(CNBu'),. 3.706 C~CZ~HZ~C~~PZ [C~(CNBU')~]+, 3,707 [CrCl,(dppe)]-. 3,853 IC~(CNBU')~]~+, 3,707,709 CTCZ~HZ~C~~~PZ CrC30H7sC13N,s CrCI,(H,O)(dppe), 3,851 CrC13{HN=C(NMe2)2}6.3,851 C~CZ~HWNZ~Z C'K311135N4 Cr(PhCOCHCHMeNPr'),. ,- 3,767 CrO(tctraethyltetrariicthylcorrolej, 3.917 CrCz&42BrN3P CrC3211f2N80 ,,S4 [CrBr{PhZPCH2CHzN(C1~2CH2NEt2)2}] ' ,3.735 [Cr{(O,S),phthalocyanine}j3-, 3,927 CrC,,H,,CI,F,N, [Cr((O,S),phthal~cyanine)]~~~, 3.927 C~(C3F7)Clz(phen),.3,899 c,rC32H16C1ZN8 CrC,,H,,N,O, Cr(8-quinolinolate),,3,899 Cr(phthalocyanine)CI,, 3,926 [Cr(phthalucyanine)C12]-, 3,926 Cr{(5-C1-2-OC6H3CH~NCH~CH,)3N}, 3,895 CrC32H16Ng Cr(Pr'N=CHCH=NPr'),, 2. 209 cr c2 4 4806 [Cr(THF),J3+, 3,855,867

Cumulative Forrnulu Index

CrC32E116N8

Cr(phthalocyanine), 1,272; 2, 865. 87(1; 3. 925, 926; 6 , 192 [Cr(phthalocyanine)12, 3, 926 [Cr(phthaIocyanine)ln--, 2, 870 CrC&16N90 Cr(,phthalocyanine)(NO),2,866; 3.831.925 CrC32H17NHO Cr(phthalocyanine)(OH),1,865 CrCa17Ns02 ICr(phthalocyaninc)(OH)012-'.2 , 866

CrC32H33N40PZ [Cr(NO)(MeCN),(dppe)]', 3.829 [Cr(NO)(MeNC),(dppe)] ' , 3,829 CrC32H46N802 [{Cr(OH)((2 pyCH,NIICI TMe),] 1.,I**, 3, 814

336

CrC3,H,,0,Si, CrO,(OSiPh,),. 3.941 CrC36HmP& Cr(S2PPh,j3. 3. 886 CrC,,H,,N4O4 Cr(mesoporphyin IX dimethyl ester). 3, 91 1 CrCdL4% Cr(octaethylporphyrinj, 3,912 CrC3JL4N4O CrO(octaethq.lporptiyriii), 3, 9 16 CrC:36H44NS CrN(octaethylporphyrin), 2, 826

[C;(OCHBuT;),]-.3.930 CrC36H83016P3 Cr0,H,{(BuO),PO)3. 1,541 CrC37H21N,00 Cr(phthaloc)raninej(NO)(py),2,866; 3,831,926 CGJI3,& Cr(PhNNNPh),: 3.845 CrC38H40N501 CI{ I -{ s.le~-NNPhC(O)=CN=N}-2-C)-~((I 1OCtl~CH~)~h'SOZ C,,H,) (2,5-(t l(.))zC,H3CWLCHLCC) .=C(O)( .H2)3}(H20), 6. I07 CrC39H26N,03P Cr(phthalocyanine)(H,O)(MePhPO,), 3, 926 CrC39H31N40 CrO(diethy1hexamethyIcorrole). 2 , 874 CrC39H3,Ni,S6 Cr(S,CNHNPh,),, 3.885 C~C~OH~ONSO~OSI [Cr ( 1-(1-0-3-0,S-6-H,N-2-C1,,H,N=N)-L-O-.I-O,S-6OZNCloI[j}2]'-. 6, 71 CrC40H30Ni, C:~-(C:Nl,'h),(py)~3: 707 CIC4"H,,NSO, L'r(Ol)(tetraphenq.lporphyrin)(py), 3, 9 13 CrC,,,H,, Cr(CPh=CMezj4. 3, 92s CrC40H,o04 Cr(1-adamantyloxv),. 3, 929. 930 CrC41H3yC13P3 CrCl,(triphos). 3. 851 CrC42Hz4F903S3 Cr{2-CloH,C( S)=CHCOCF, I,, 2.652

&

,...

CrC34€lIbN [Cr(phthalo~yanine)(CN)~] . 2 , 865 CrC34H19N802 Cr(ph thalocyanine)(OAc) . 3 ; 926 CrC34H21N803 Cr(p hthalocyanine)( OAc)(H,O). 3, 97-6 Cr(phthalocvanine)(OAc)(OH,).2, 865

[CrCI(CNPh),]+, 3,706,707 CrCI5Hh7N7 [C~(CNBU'),]~+, 1,72; 3.708.896 C~C&&HO~ Cr(phthalocyanine)(OAc)(HOAc). 2. 865 C ~ C ~ ~ H N N ~ Cr(phen),, 3,713 [Cr(phen),lz', 3,710-712.818 [Cr(phen),]-' ' , 1, 398: 3. 817 CrCJ 1,,N, [C'rPhz(bipy),J+,3, S21 CrC,,H,,C1202P2 CrCI2(0PPh3),, 3,754 CrC36H30N18 Cr(PhNNNPh),, 2,203

CrFCNPh),, 3,704.706, 708 [Cr(CNPh),]'. 3.70h.707.708 [Cr(CNPh)6]". 3.706,708,709 [C'r(CNPh)6]3 ' . 3. 706, 708 CrC4,1 13,,S6 Cr&C2Ph2j3. 3.886 [Cr(S2C2Ph2)J. 3,886 CrC42H39N606

Cr(5-ON-2-OC6H3CH=NCHMePh)3, 3, 895 CrC4,H,,CINP3 [CrCI{N(CH3CH,PPh2),}]+, 3,735 CrC42H42C1P, [CrCI(P(CH2CH,PPh2)3)]+,3,735

337 Cr(3,5-di-t-hutylquinone 2. 397 Cr(3,5-di-t-butylsemiquinone),, 2 , 397, 398 CrC,,H,,CINP, _[CrCI{N{ CH;CH?P(C,H, I ) 2 } 3 > ] - . 3,735 CrC4,HZ8C1N4 CrCl(tetrapheny1porphyrin). 2.825; 3, 912,913,916, )31

917; 6,353

[CrCl(tetrapheny1porphprin)If ,3, 9 17 C;rC,,H,,CIN,O C:rC)(tetraphenylporphyrin)CI! 2,826; 3,912,916; 6, 353 CrC,,H28C1N4C)4 Cr(ClO,)(tetraphenyll)cii-phyrin):3. 9 Ih CrCd4H2,N4 Cr(tetrapheny1porphyrin)r 2. H25; 3, 772,912, 916, 917 CTC~~H,~N,O C r O ( t e t r a p h e n y 1 p o r p h ~ r2.87-5; ~ ~ ) ~ 3,912,913.916 CrC44H28N4014S4

[Cr{(4-03SC6H,)4porphyrin}(H20)2]3-, 3,913 CrC44H28N50

Cr(tetraphenylporphyrin)(NO). 3.831.912,913,916 CrC44H28N7 Cr(tctraphcnylporphyrin)(T\j;). 3.845 .. . . CrC4,HZ9N40 Cr(tetraphenylporphvrin)(OH), 2. 826 CrC4,Hhx Cr( l-adatnantylmethyl)4 3.928 CrC,,H,,N,O Cr(OMc)(tctraphcnylporphyrin), 3, K31, 916 CrC45H31N502

Cr(OMe)(tetraphenylporph>rm)(NO). 3, 916 CrC45H3303S3 Cr(PhCSCHCOPh)l. 3. 901 CrC4,H,&1N3P2 [CrCl(CNPh),(dppe)]+. 3.706 CG8H3.&"

CrN{(4-MeC,H,)41'"rph!r~n} 3 917

CrC,4H42CIP4 [CrCI{P(C6H4PPhZ-2),}]'.,3,735 CrC5,H5,Pi20P4 [Cr(NO)(MeCN)(dppe),1'+, 3. 828 C~C~~HSJN~ [Cr(CNC,H,~~1e2-2,h),],+, 3,708 CrC56H53Y40 CrO(tetramesitylporphyrin), 3,916 CrC&4:Nd'2 [Cr(CNPhj,(dppm)l2+. 3, 706, 896 CrC,,H,,N Cr( IM~,iCH2),NH02S)4phthalocyanii~~}((3t-1). 3. 927 CrC6A6C131'6 CrCI,(PhP(CH,CH,PPh,)L) L , 3,856 CrC?8H,U2N6 Cr(CNC,H,Pr',-2.6),, 3,706 [Cr(CNChH,Prl,-2,6),]' , 3 , 707 CrCIF02 CrOICIF, 3,938 CrClK,02 CrO,CIK,. 3. 940 CrCIO, [CrO,Cl] - ,3,927,936,944, 946: 6 , 3.51, 352 (XI('), [CrC)(02),CI]-, 3,946 CrCI,N302 Cr(NO)2C12,3, 826 CrC120? Lr02C12.3.935.936,038,940,941,943 [CrO,Cl,] 3,935 CrCI,O5S2 Cr(SO,CI),. 3, 740 CrC1208S2 CrOz(SO3CI),. 3,940 CrC1,0,, CrO2(C1O4j2,3.940

-.

CrCI3

[CrCI,]-. 3. 7(>4,765 CrC4d&6N7 CrN,{ (4-McC,H4),purphvrrrr$. 3.017 CrCI,O . . CrC48H37N10 CrOCI,,, 3, (432.933 Cr(OH){(4-MeChHJ)~porphyrin). 3. Y I 7 CrC1, C ' I C ~I,,N, ~~I [ci(CNChl 14Me-4),l ' .3. 706, 707 CrC48HaN606 Cr(5-ON-2-OC6H,CH=YCHEtPh);. 3, 895 [CrOCl,] . 1.44; 3,935,936 CrCl, CrC4sHlo8C1201ZP4 [Cr(OPBu,),(ClO,),~'. 3.876 [CrClj] .3.766 [CrC1,I2-. 2.297 CrC49H33Ns Cr(tetraphenylporphyrinj(py), 2,325. 825 [CrC1,J3-. 3. 762 ct c1,o CrC49H33Ns02 Cr(tetraphenylporphyrin) (py')(02)2: 323 [CrOCI,l2-, 3,848.932,935,936,938 CrCl, -.-I CrC,,H,,N,O, I C r { r h C ( = N O H ) ~ ~ ~ ~ C [ O ) ~ P h N = t ' M c' j,3,850 ,l" [CrC1,I4 , 3 . 760,761 Crrl,,HjF905 CrC5.,Hh9N5P2 [Cr(CNB~'),(dppc)]~+. 3: 89h [(Wp((I2(,X 'F,),] 3, XI(> C~rC,,H,,CI,N,O, C'rCoC21125N50g { Cr(2-C)-3,5-CI,C,H2CONHCH,CH2NCOC,H2Cl2-3 ,5[(NH,),C~(C,C),)CI(H,C-))~]~+. 2. 444 CrCoCIHL7hi0O5 O - ~ ) ( P Y )3.~ 853 L ~

[CO(PIH~~,(NCCH~)C~(H,O)~]~+, 4,678 C;(CO)2(dppm)2, 1,499 [Cr(CO)2(dppmj2]+.l I 499 CrC52H48CINOP4 Cr(NO)Cl(dppej,, 3,828 [ C r ( N O ) C l ( d p p ~ )' ~ ,3.828 ] C:rC5ZH48C:13P4 CrCl,(dppe),. 3.853 CrCS2H48FNC)P,1 Cr(NO)F(dppej2,3,828 [Cr(NO)F(dppe),]'. 3.826.828,829 CGJL8N6 Cr(tetraphenylporphyrin)(py)Zq 2 . 825; 3,912,913

CrCoC6Hl,N,0, Cr(H,O),( y-NC)Co(CN), .3,777 CrCoC6HI2Y,,O

Cr(NH3),(H20j(p-NC)Co(CN),, 3, 779 CrCoC,H,,Pi, Co(NH,),(u-NC)Cr(CN),, 3,779 CrCoC,H,,N, ,S6 Co(NH,),(u-SCN)Cr(NCS),, 3, 842 CrCoC,N, Cr(NC),Co. 3, 779 C'rC'oC'J 131N80Z [Cr(en),(u-OH),Cu(et1)214+, 2,299 CrCoCloH,6FN [CrF(~n),(p-NC)co(cN)~],3, 778

Cumulative Formula h d e x

CrCoClzHzoFN

CrCoC 12HZOFNI0 [CrF(pn),(p-NC)Co(CN)5]-, 3,778 CrCoCI4Hl4O5PSZ (Me,P)CpCo(CS,)Cr(CO)j, 2,582 CTCOC~~H~~O~P~S~ Co(triphos)(p-CS,)Cr(CO),. 2.582: 4. 646,744 C~COC,,H~~O~P~S, Co(triphos)(p-CS,)Cr(CO),. 4, 869 C~COC~IH&IOP~ Co(triphos)(pL-P3) { Cr(CO),} 4.738 CrCoI.il5NSO, [ C O ( N H , ) ~ O C ~ O4, ~ ]825 +, CrCoH,,CIN,O, l,Cr(H,O),CIC,o(NH,),I,+, 1. 332 CrCs,H8Cl50, Cs,CrCI,, 2,297 CrCuS, CuCrS,, 3,882 CrCuSe, CuCrSe,, 3,889 CrCu2C4OI8P4S2 3,901 Cr((C2S03)Cu(P03)2}z, C~CU~C,I~H~~O~P& 3. 901 Cr{(C2S03)Cu(PPh3)3}2, 1

[CrO,FI3-, 3,945 CrF,N,O, C;O;Fi(N02)2, 3.939 C rF2N2O8 [Cr0zFz(N03)2]2-, 3,939 CrF,O C;OF2, 3,927,938 CrFz02 Cr0,F2, 2,681; 3,938-940, CrF,0,S2 Cr02(S03F),, 3,939.940 CrF, [CrF3)-,3,756,757,762 [CrF,]”, 3,757 CrF,O C;OF3, 3,932,933 CrF302 [Cr02F3]-,3,939,945 CrF30,S3 Cr(SO,F),, 3,933 CrF, [CrF,]-, 3,889 [CrF,]*-, 3,756,757 CrF& CtOF4, 3,938 [CrOF4] ,3,932 CrF401 [Cr0,F,12-, 3,939, 945 Crk,O,P, Cr01(0ZPF2)2r 3,940.941 CrF, CiF,, 2,680 [CrFS]-, 3,927 [CrFJ-, 3,889 CrF,O [CrOFJ, 3,938 [CrOF5I2-,3,935 CrF, [CrF,]-, 3,933 [CrF,]*-, 3,927 [CrF613 ,3,756,79X, 8X9,,Y90 [CrF6J4 ,3,757 CrF60,P3 Cr[O,PF,),, ~. 3,941 CrF,P3S6 Cr!S,PF,),, 3,884,886 ’

~

CrF, [CrF,I3-, 3,927 CrF8010P4 [CrOZ(02PF,),]2-. 3.941 CrFlo04Se2 CrO,(OSeF,),. 3,941 CrF,,,O4Te2 CrOz(OTeF&. 3.940 CrF186 Cr(PF& 3.714 CrFeC,H,,N, ,,O

Cr(NH,),(H,O)(p-NC)Fc(CN),, 3, 778 CrFeC,H ,,N l l Cr(NH,),(u-NC)Fe(C~)~, 3,778 CrFeC,N, [CrFe(CK),] .4.1204 CrFeCssHj6N80 Cr(tetraphenylporphyrin)(uO)Fe(tetraphenylporphyrin), 3,917 CrFeH,O, [Fe(OH)(OH)2Cr]3i.6,852 CrFeH404 [Fe(OH)(OH),Cr(OH)12’, 6,852

[ C r ( H , 0 j ~ ~ - S 2 H ) F e ( H z @ )3.877,882 ~14~, CrGe,Cl ,H,,OiTe Cr(CO)5{Tc(GcMc,),)I 2,670 CrGe&dhOa CrO,(OGeI’h,),, 3,942 CrGe,CI,, [Cr(GeCI3),l6-. 3. 709 CrH CrH, 3.766 CrHO, [Cr04H]-.3. 941.946, 1259 CrHO, (CrO(C),),(OH)] - 3 . 9 4 6 CIH2 CrH,,3 7hh CrH,02 [ W O H ) J + . 6.851 CrH204 CrH,O,. 3.941.6.351 CrH206 CrO(O,),(OH,). 3,945.946 CrH2OlOS2 Cr02(HS04),, 3,940 CrH,O,S

CrBr2iHiO),. 3.772 CrH4Br40Z [C‘rBr,(l120)lj?~.3.759 Cl H4CI3O2 [CrCI,(H,O)J. 3.758.765 CrH4Cl,02 [CrCI,(H20),]z-, 3- 758 CrH6Cl2N, CrC!,(NH:),. 3.719 CrH,F, [Cr(FH),]*’. 3.756 CrH6NL0,S Cr(NII&(SO,). 3.719 CrH,Br,O, [CrBr,(HzO),]’, 3,812 CrH8C12N, C I C ~ ~ ( Y 3.729 ~H~)~~ CrHRCI2O4 [CrCI,(OH,),]-, 1, 183.3666; 3,892

33 x

339

Cumulative Formula Index

,

CrH8CI3N4Ol2 3,834 Cr(N2H4)2(C104)3r CrH8F2N, CrF2(N2HA2, 3,729 ,

1,373

., 3,844

781

CrBr,k1(NH,)3, 3, 781 CrH,CI,N, CrCI,(NH,)?, . . 3,781 CrH,NjO, C T ( O ~ ) , ( N H ~1-78; ) ~ . 2,319,320: 3, 946; 6,320 CrHONhOh Cr(NH3j,(N0,),, 3. 867 CrHd C T ( N ~ ) ~ ( N H3, , ) ~843 . CrHioBr2N,02 [CrBr2(NH3)Z(H20)2]+. 3,781 CrHloCIOs [CrCl(H20)5)2+, 1. 183,365; 3,842 CrH,oC12N202 [CrC12(NH3)2(H,0)2]f.3. 781 CrH,,)N06 [Cr(NO)(H20)5]2+3 3. K2CX26. 842 CrH10N305 [Cr(N,)(H20)5]2+,3,842, 841 CrHioN408Sz 3,736 CrHlo06P [Cr(H20),(H2P0,)]2-, 3. 868 CrH,,OOS [CGH;O),(SO,)]', 3,867: 6,832 CrHi ,C12N,0 [Cr(NH3)3(H,0)C1z]+.2.28: 3.917 CrH,,O,S 2,518: 3. 876. 877 [Cr(SH)(H20)5]2L, CrHi106 [Cr(H,O),(OH)]", 1,370. 378.6,335,436,832 CrH12CIFN4 [CrCIF(NH,),]+. 3.782 CrHi2CIN408S CrCI(S04)(NH20H),,3,835 CrHI2Cl2N, [CrCI,(NH,),]+, 1,298, 398: 3.782,798 CrHi2F2N4 [CrF,(NH,),]+, 2,677; 3.782 CrH12N604 (Co(NH,),(N02)21f, 2.28

[Cr(H,0),(H,S)]3+. 3,877 CrHi206 [Cr(H20),JZ', 1,253,284.332.333,336,366,367, 369-374.376.377: 3.735.736; 6.8 [CT(H,O)~]~+, 1, 183,284,309.336.365,370; 2, 10; 3, 774,856,857,867,876; 6, 8,48, 49.73,435 CrHI3C1N3O5 [CrC1(NH20H)z(H20)2]', 3.835 CrH,?NO, [c;~H,O),(NH,)]~+.3,842 CrHlJW6 [Cr(OH)2(N112011),(1l,O)]'. 3,835 CrH,,BrN,O [CrBr(H,0)(NH,),]2'. 1. 27: 3.782 CrH,,CIN,O (Cr(NH3)4(H20)C1]2-,1,372 CrHi4FN,0 [CrF(H,0)(NH3),]Z ' ,3,782 CrHi4N40

CrNiCsH1&INs

[Cr(NH,),(H,0)I2+. 3,719,773 CrHISBrN, [CrBr(NH3)S]z+.1, 398 CrHl5C1NS [CrCI(NH,),]2+, 1,393,398,399,505; 2,28 CrH15N303 [Cr(NH3)3(H20)3]3+,3,781 CrH,,N,O, [Cr(NH,),(H,0)(OH)]2+, 3,782 CrH,sN5 [Cr(NH,),]". 3.719,773 CrH1,N5O,Se [Cr(NH,),SeO,]+, 1,292 CrH, ,N,O [Cr(NO)(NH&]2+, 3,824,835,845 CrHisN8 [Cr(h',)(NH3),]2-, 3,843, 844, 845 CrHqLNSO? [Ci(NH3),(H20),]3+, 3,776,782 CrH 6 N 5 0 [Cr(NH3),(OH)I2+,3,783; 6,435,436 CrH16Nj06 [Cr(OH)(NH20H)5]2', 3,835 CtH1,N,O [Cr(NH3),(H,0)]3'. 1,292,397,469; 3,783.857; 4.958 [Cr(NH>),(OH,)12+,2 , 2 8 CrHdJ' Cr(NH;),(PH,), . . . 2, 1034 CrHlSN6 [Cr(NH,),I2', 3,719 [Cr(NH3),I3-, 1,27, 111, 183,230,365,397,399, 410: 2.26.28;3,783,787 CrHgO, HeCrO,, 5 - 1068 CrI& [CrOJ-. 3.944 CrIOh ICrO,OIOJ-, 3, 1024 CrIJ [Crl,] .3.761,765 Cr16 [CrIs]"-. 3.764,765,766 CrLiSz LiCrS2.3,882 CrMoC8H,,08 CrMo(OAc),, 3,745,747,1231,1307 CrMoC,,H ?N2O12 [Cr(edta)Mo0413-,3,1377 [Cr(edta)OMo0,J3-, 3,1379 CrMOC&+&O8 CrMo(OPr'),(NO),, 3,830, 1315 CrMoC,,H2,N,0, C r M n ( ~ = C M e C n = C H C H = ~ O ) ~3,747, , 1307 C~MO,H~U,, [C~MO~H,O,,]~--, 3, 1024,1044 CrMo,H,O,, [Cr(u,-~Ofi)6Mo,024]6-,1,161 CrMo,,HO,,Si [Mo,,S~C~(OH)O,,]~-, 3,1048 C~MO,~H~O,~S~ [Mol ,SiCr (OH,) 039]5-,3, 1048 CrNzOs Cr0z(N03)2,3,939,940; 6,351,352 CrN,O, Cr(NO),, 3.832 CTN160 [Cr(NO)(N3),I3-, 3, 824 CrN '8 ICr(N3),l3 .3. 844 CrNiCBFf,BrN8 CrBr(en),(u-NC)Ni(CN),, 3,778 CrNiC,H,,ClN, CrCc(en),(pNC)Ni(CN),, 3, 778

CrNiCl0HzoFNs

Cumulutive Formula Index

CrNiClol-f20FNs CrF(pn),( V.-NC)N~(CN)~, 3,778 CrF{ H,N(C€-I,)3N~~,)2(p-NC)Ni~C~)3. 3, 778 Cr43 [Cr03]*-, 3,928 CrO, [CrO4I2-, 2,413; 3,936,938,941-943,947,1259; 6, 851,1014 [CTO,]~-,3,936 [Cr0,I4-, 3,928 CrO, [CrO5I6’,3,928

CrO, [CrOhlR-,3,928 Cr0,S [Cr030S03]21, 3,1024 [Cr03S04]2-, 3,944 CrOs [Cr(0,)4]3-, 1,94; 3,936, 1261 ICrOs13-, 2,320; 3,936; 6.329 CrPS, CrPS4, 3,883 CIP~C~~H~~O, Cr02(0PbPh&, 3,942 CrPb,C11H,80,Te Cr(C0),{Tc(PbMc3),), 2,670 CrPdCsHI6BrNs CrBr(en),(ln-NC:)Pd(C:N),. 3, 778 CrPdCRH16C1N8 CrCl(en),(V-NC)Pd(CN),, 3, 778 CrPdCloHzoFNs CrF(pn),(p-NC)Pd(CK:),. 3,778 CrF{ H,N(CH,),NH,),( p.-NC)Pd(CN),, 3,778 CrPtC,H5 PtCr(u-CPh), 5,385

340

CrSn2C11H,s05?’e Cr(C0){Tc(SnMe3),) 2. 670 CrSn3Cs8H4s04 [Cr(CO),(SnPh,)&. 2, 16, 19 CrSrF4 CrSrF,. 3.762 CrTe CrTe, 3, 889 CrThH,O, Th(OH),(CrO,)(H,O). 3, 1146 CrUC,H ION20R UOL(Cr04)(AcNHJ2. 3, 1204 CrUS, crus,, 3,883 CrWCt3tlaNZ07 WCp(CO),(YNMe)Cr(CO),, 2, 136 CrZrF, CrZrF6, 3, 757 Cr2Ag08 [Ag(Cr0,),13-. 3,943 Cr,Br, [Cr,Br,l3-, 2,684: 3.891 C~,CH~~?JIOO

ICr(NHR)S(~-OH)Ct(h’H,),(NH2Me)15+, 1, 123 CrzC4H406 Cr2(02CH)4,3,749 Cr,C4 H 4 014 [Cr,(CO,),(I i2C))z]4-. I, 742, 746 Cr,C,H,N,O, Cr,(HCOh’H),, 3.749 Cr2C4HIoOll 3, 741 Cr2(02CH)4(H20)3: Cr2C6C14N,O& {Cr02C12(NCS)3)2.3,941 Cr2C6H5N,0 Cr(NH3)(H2O)(~~-NC),Cr(CN),, 3, 779 Cr2C6H15NllS6

CrF(pn),( y-NC)Pt(CN), ,3,778 CrF{HIN(CH2),NH2}2(V-NC)PI(C”3. 3,778 CrReC40HbnC14N201P4 CrCIS(THF)2{(N2)ReCI(T’h.lt.2Ph)4) 4. 133 CrRe3C24H1801S

Cr{(OCMe),Re(CO),},, 3,86 I CrRuHzlNOlo R u ( O H ~ ) ~ ( ~ - N H ) C ~ ( O H , )4., ]362 ~+, CrRuH25N506 [Ru(NH,)~(OH~)(~-NH)C~(OH,),IS+. 4.299 CrS CrS, 3,882 CrS2 [CrS,] ,3,882 CrShC,H904 CrO,(SbMe,), 3,942 CrSbC‘loII,,U14P [CrC1,(2-Me,PC,H,SbMe2)l-. 3.853 CrSb, ,C,5H,,C13P, CrCl3(2-Me2PC6H4SbMeZ)? s. 3. 854 CrSblF15 CrF4Sb2FlI,3,933 [CrF,Sb,F,,]-, 3,933 CrSb2O2FI5 (CrF4Sb2FI,)02,3,933 CrSe CrSc, 3,889 CrSc, [Crse,]-, 3,889 CrSnCI8Hz,N0, Cr(CO)5(SnRu‘,py), 2, 17. 19

Cr(CO),[Sn{CH(SiMe3)2)2]. 2. 17, I9 CrSnC3hH3004 CrOz(OSnPh3),, 3.942

Cr(NH,),(II-SCh’)Cr(NCS),, 3,842 Cr2C6H24NhFh * [Cr(cn),F,I[Cr(cn)F,], 3, 796 CrZCdH24?18016 Crz(Cz04),.4N,H,,4H,0, 3, 834 Cr2C6H30N1?C)1J 3, 834 Cr,(C204)3.7~2H4.H20, CrZC6H33N9012S3 Cr,(OH)3(en),(S03NH,)3, 3,800 Cr2C6N6 Cr(CN),Cr, 3.779 Cr,C,H,CI,O, (Cr02C12),(PhMe). 6.353 Cr2C8H20,, [{Cr(C,0,),}2(11-OH)212 , 3 , 8 7 3

Cr2CHH,,0, Crz(C)Ac),. 2,276; 3, 717. 741, 750. 752, XI6 Cr2c&16C)1U Cr,(OAc),(H,O),. 2,437; 3, 717. 741, 746, 749, 751. 892.1231

Cumulative Formula index

34 1

[{Cr(en)z}z(p-O)(p-S04)]z+.3.800 Cr,CsH?3C12N80 [{Cr(en),Cl},(p-OH)]3-. 3.795 Cr2C8H33N~0~ [{Cr(en),},(~-O)(~-OH)]3+. 3.800 CrzC~H3&"0~S [ {Cr(en),},(lr-OH)(lr-SO~)13+.3?800 CrZC8H34N802 [Cr,(OH)2(en),]4 ' , 1,272; 3,800 Cr,C,H3,N,0, [{C~(C~),(OH)}~(~~.-O 3.H 800 )]~-', C~ZCRHMNRO~ [Cr(H20)(en),(p+OH)Cr(Pn),(orI)]4+, 3,800 CrZC9H.,6FNloQ [CrF(en),(p-NC)Cr(CN)4(NO)]-q 3. 778 C~ZC~HZ~C~~N~ CrZC16(NMe3)3.3, 788 CrZC9H3SNs03 [{cr(en),},(y-OH)(p-A~O)]~-. 3.800 CrzCloHOlo [Cr,H(CO),o]-, 2,692,701 Cr,CloHOloS [Cr2(CO)Io(pSH)]-, 2.518 Cr2CloHOIoTe [{,Cr(C:O),)?(lr-l'eH)l- 2- 670 Cr2CloHloN404 C r z C ~ 2 ( N 0 ) 42,, I17 Cr2CI J I l o S s Cr2Cp,(S2),S, 2,532.535 C ~ ~ C ~ O H I Z N ~ W ~ [C~,(OAC),(NCS),]~-. 3.751 Cr2C10H12N403 Cr2Cp,(N0)3(NH,j, 2, 114. 117 CrZC10H14C14N204 {Cr(OH)zClz(py)}z. 3.927 CTZCIOHI~FNIO [CrF(en),(p-NC)Cr(CN)J. 3.778 Cr2CioH34N604 [ { Cr(OH){(H,NCH,),CMc})2(p-OH)2]2*, 3,808 Cr2CloH35N604 [Cr(H20){(H2NCH,),CMe}(p-UH),Cr(OH){(H,NCH,)~CMC}]'+,3,808 Cr2Cl HzoFN [CrF(pn),(p-NC)Cr(NO~(CN)41- 3,775 [CrF{H,N(CH,),NH2},( k-NC)CrNO(CN),]-, 3,778 C~2CIZH18N6SIZ Cr2(SZCNHCN2CH,NHCS2)3.3.885 Cr,C12H20FNlo [CrF(pn),(p-NC)Cr(CN),1-, 3,778 Cr2C12H36N6 Crz(NMe&, 3, 835 Cr2C12H36N604 [{Cr(p-OH)(1,4,7-triazac\;clont,nane)(H,0))2]4 ' , 3, 924 I

Cr2CZOHl,Cl4N4OJ Cr,lfi=CCICH=CHCH=CO)a,

Cr2C28H60N6U8

3,743

~ { C r ( O H ) ( o ) ( p h e n ) } , ~3,819 ~+, Cr2C24H18K40,0 Cr2(4-pyC02)4(0H)2, 3,899 Cr2C24H20F4N40s

Cr,(h=CFCH=CHCH=eO),(THF), 3,743 Cr2CZ4H2J4O4 Crz(&;I=CMeCH=CHCH=CO)4, 3,743,747,749-751 Cr,C24H2sNs Cr,(~=C~eCH=CIlCI~=C:N~-l),, 3,734. 742 CrZC2QH16N801 Cr2(fi=CMeN=CMrCH=CO)4, 3,743,747 Cr2C24H320, CI~~(OAC),(~-BU'OC,H~),, 3, 745 Cr2C24H34?JB02 [{Cr(2-pyCH2NH2)2}2(p-OHj2]4' ,3,805 Cr2C24H42N6S,2 Cr2{S2CrU'H(CH2)6NI-ICS2}3, 3,885 Cr3C24H60C16P4 {CrC13(P€t3)d2,3,853 Cr&.&oN6 Cr~(NEt2)6,3,835, 931 Cr2C2JL804 Cr2(2-MeOCGH4),,3,747 Cr2C28H38NS02

[{Cr( OH){ (2-pyCH2NHCH2),}}*I4+,3: 812 Cr2C28H4ONs02 { Cr(2-pyC€IMeNH,),},( ~ - 0 ) , ]3,806 ~+, Cr2C28H41N802 [ {Cr(2-pyCHMeNH2)2}2(pO)(pOH)]31 ,3,805 Cr,C,,H,,N,O, [ (Cr(2-p\:CHMeNH2),(OH)}2]4+, 3. 805 Cr2C28H60N608 COC 7-L

CrZCzsH6oN608

Cumulative Formula Index

Cr,(NEtz),(OzCNEt,),. 2, 1x1; 3, 931 C~,C~SH~ZN~OS 3,742.931 Cr2(0,CNEtz14(NEtzH)2, Cr2C30H4zNs02 [{Cr(OH)(2-pyCH2NHCHMeCH,NHCH2py-2)}z]4+, 3,814 [{Cr(OH){(2-pyCH,NHCH2)2CH,}},]4+. 3. 814 Cr2C3zHzRN405 {Cr(salen)},O, 3,894 C r 2C31H2XN2S8 [(Cr(NCS),(PhNH,)L}z]2 ,3.789 CrZC3z1132N404

Cr,(PhNCOMeL. 3. 743

342

Cr(OH){ (03S)4phthalocyanine}(p-OH)Cr{ (03S)4phthalocyanine}(H20),3,926 C ~ Z C ~ ~ H ~ I ~ O Z {Cr(phthalocyanine)(y-O)),, 3, 925, 926 CrzC6?Hd1603 { Cr( phthalocyanine)(HZO)}2( p-O), 3,926 C~ZC~~H~~NI:O~

Cr(YH3)(phthalocyanine)(p-OH)Cr(phthalocyanine)(OH)?3. Y2h Cr2C68Hdh?. Cr,(,9-anthracen~carboxylrltc)~(DME)~, 3,741,718 CrZCHBHS6N80 {Cr(tetraphenylporphq;rin)}20, 3,913,917 Cr2C:1,14H96v2P8 (Cr(dppe)2)3N2.3.713 CrzCcOs Ce(CrO&. 3. 943 CrzCI9 [CrzC19]3-.2.584; 3,890 Cr2CoS4 CoCr,S413,883 CrzCuH,Oq CU(OH&(C)~CT~O,). 2, 431 Cr,CuS, CuCr,S4, 3.883 Cr2F3N Cr2NF3,3,755 Cr, F4O6S (~:l-o,F,),-so2~ 3,939 Cr,F, Cr2F5,3,757.762 CrzFeClSHsOloPz Fe(PCH=CHCH=CH),{ Cr(CO),},, 2,1044 Cr2FeH2O9 [Fe(02Cr02)2(OH2)]~~, 2.426

343

Cumulative Formula Index

[Cr(NH3)5(p-OH)Cr(NH3)4Cl]4+3 3, 784 Cr2H2,N803 [Cr(NH3)4(HzO)(~-OH)Cr(NH3)4(OH)]~+, 3, 784, 786 Cr2H29N803 [{Cr(NH3)4(H20)}2(p-OH)]5-. 3. 784 Cr,H,,N,O,

936; 6 , 1014 859

[cr2o7]2-, I. 553; 2,3c)1?413: 3.85~,937,941-943, 1024; 6,36,351, 1014 C~ZOS [(CrO,),j3-, 3, 936 CrzO [Cr2OloIi4 ,3,859 C~~OIOP [(Cr04)ZP02]2-.3. 942 Cr2OI2 [ ~ ~ z 0 2 ( 0 2 ) 53,946 12~, CrzPdC3oHzaN20~ Pd{CrCp(C0)3}z(1\'CPh)2, 5. 1108 CrS2 [Cr2(S2)I4+, 2,539 Cr2S3 Cr&, 3,882 Cr2Se3 CrZSe3,3,889 CrZSi4C22H4hN4 { Cr(=NSiMe,)Cp},(FL-NSiMe,)2.3,945 Cr,Te, CrzTc3,3,889 746*762

[Cr;(OAc),(H,O),]-. 3,869 Cr3CILHZ40 16 [Cr30(OA~)G(OH2)3]t. 1. 145; 2, 441 Cr3C18H50N905

[Cr3(p-OH)4(0f3)(I ,3.7-triazacydrinonane)3]4+.3, 924 Cr3Cz2HloF18012 Cr3Cpz(02CCF3)6.3.752. 761

Cr,%

Cr,Se,

Cumulative Formula Index

Cr&, Cr,Se,, 3, 889 Cr;Te6 Cr,Te6, 3,889 Cr,Te, Cr,Te,, 3, 889 Cr6C12H24030 FCr,(0,CH)4(H20),13, 3,744 Cr7Sc8 Cr7Se,, 3,889 Cr,Te, Cr7Te8, 3,88Y Cr12H20N402 ~Cr(HzO)Z(2-pyCH,NHZ)Zls I 3,805

CSCCIS, Cs(S,CCl), 2,591 CsC4H90 CsOBu', 2,348 CSCizH2406 [Cs([l8]crown-6)]+,2,931; 3. 39 CsCi,HmO7 [Cs([2l]crown-7)]+,2,931 CsClsH12N05S Cs(SCN PhCOCH,OkCHOC)(CH,OH)= &O), 3, 15 C~CmH2406 [Cs(dibcnzo[ 18]crown-6)]'. 2: Y3'l CsC2,H,,012 [Cs(lS-crown-6),]+, 3, 39 CSC~~H~ZNO~S Cs(tetramethyldibenzo-l8-crown-6)(NCS),3,38 CsC36HnOi~ ~Cs2(18-crown-6),]*+, 3, 39 CSC~~H~ZN~O~ [Cs(spherand)]+,3,43 CsC,oHj,O 1 2 tCs(nonactin)]-",3,65 CSC44Hb401Z

[Cs(tetranactin)] ' , 3 , 6 5 CsEuF, CsEuF,, 3, 11 12 CsMgCI, CsMgCI,, 3,891 CsScC1, CsScCI,, 3, 1067 CsYbF, CsYbF,, 3, 1112 CsiC,.A,N,Oi& {Cs(l8-crown-6)(SCN))2.3,38 CSYClhXH336084 [Cs,(18-crown-6),,]Yt, 3.39 Cun.z&fnn.mP& Mn,,,7Cu,.,6PS3, 5,690 CuAgC,H6NsS3 Cu(NH,),Ag(NCS),, S1 656 CU(NH,)~A~(SCN),, 5.607, 663, 700 CUAKIZHIONIOZ [AgCu{2-pyCH=NO},]+, 5,798 CuAIC6H6C14 5,570 CUAICI~(C~H ~), CuAsU06 Cu(UO,)(AsO,), 5,653 CUAS~BCZ~HZ~N~ Cu{B(NN=CHCH=CH),(diars)}, 2.254; 5,544 CUASZCI2OlZ C U ( C I O ~ ) Z ( A S O5, ~ )716 ~, CUAS~C~~H~~CI~C)~~ C U ( C I O ~ ) ~ ( O A S 2, M 500 ~~)~, CuAsaCmH32 [Cu(diars),]+, 5,542,583 C~hC52Hs2 [Cu(AsMcPh,),]", 5. 537 CUAS,C~~H~OCI,O~~

344

Cu(ClO,),(OAsPh,),. 2,500 CuAs4C7,H,,04 [CU(OASP~,)~]'.5.588.589 CuBC4Hl6F4N4 [Cu(en),(F,BF,)]-. 5.641,698 CUBCjoHloN6O

CU{HB(~;~N=CHCH=CH),}(CO), 5,567,583; 6.395 CuBCi iH18FzN402 Cu{F,R(ONCMeCMeNCH,),CH,}, 5,542,583 CllBCl 2H1gFIN403 Cu{F,B(ONCMkC:MeNCH,)2CH2}(CO), 5,549,567 576.583 CUBClaHlhN2 Cu(2,9-Meiphcn)(H,BH2), 5, 544 CuBCI5HZZN6O2 Cu{HB(fiN=CMeCH=cMe),}(O,), 5,578,717.718 CUBCI~H~~N~ Cu{ HB(NN=CMeCH=C Me),}( C,H,) ,5,569,583 718 [Cu(bipy),(F2BF2)]+,5,601,609,641,741 C~BC21H26Ni02S Cu{HB(P;"=CMeCH=CMe)3}(SC6H4N02), 5. 544 [Cu{HB(IbkCMeCH=~Me),}(SC,H,NOl)]-, 5 . 581

Cu(PPh,),(H2BHI), 5,546.585 CUBC39H43P3 Cu(PPh,Me),(HBH,), 5,546,585 CUBC&LSFJ'~ Cu(PPh3),(FBF3). 5.542,584 CUB~C~H~~FBN~ CU(~~)~(FBF 5688,716,741 ,)~. CuB,C, ,H2.,N, Cu(Mc,dienl(NCBH,I,, 5,609

CuBaN6012 [BaCu(NO,)J-, 5,702 CuBrCl [CuBrClj-; 5.550 CuBr, [ChRrJ, 5,537. 550.575,585 CuBr, ICuBr,l-, 5,643 C;CF,O$ Cu(O,SCF,), 5?568 CuCH,O, c~(O,CH)(OH), 5,642 CuCH,CIO CuCl(0Me). 6.395 CUCH~N~ Cu(CN)(NH,). 5.565 CUCH~N~O, Cu(ON02)2(02NMe).5,649 CuCH4Nq C'u(CN)(N,H,). 5.565 CuC:E1,O3 5 , 566 [cu(co)(o112)2]+~ CuCH,Ci*N30 C U ( H ~ N C O N H N H ~ ) C5.644 I~. CUCH~N,O, C U ( N H ~ ) ~ ( O ~ C5,643 O), cuco

345

Cumulative Formulu index

[Cu(CO)l', 5,566 CuC,H,CI CuCI(HC-CH), 5,570 CuC,H,Cl, [CuCl,(HC=CH)]-., 5,570 CuC2H204 Cu(O,CH),, 2,437; 5,617,650.716 CUC~H~O~ Cu(C204)(H20),5,690 CuC2H3RrN CuBr(NCMe), 5 , 585 CUCZH~CIIN, CuCI2(1,2,4-triazole), 5: 646 CuC2H31N CuI(CNMe), 5,563,585 CuC2H302 CuOAc, 2,437,690,710; 5- S a , 608,662 [Cu(OAc)]', 5,683 CuC2H4C1N2S2 CuCI(C,N,S,H,), 5,563 CuC2H5CINS CuCI{MeC(S)NH,}. 2: 647 CuC2HSClN3S2 Cu(H2NCSNHCSNH2)ClI 5 , 5 4 5 CuC2H6 [CuMeJ, 5.550 CuC,H,CIN, CuCI(McNNMc), 5,563 CuC,H,Cl,OS CuCI,(DMSO), 5,646 CUCZH~IN, CuI(MeNNMe), 5.585 CUCZH~N~O~ CU(C,O~)(NH~),, 2,445; 5,640,643 CUC~H~N~S~ CU(NH~)Z(NCS)~, 5,733: 741 CUC,H,O, Cu(OMe),, 2,354 CuCzH606 Cu(O,CH)z(OHZ),, 5,642.738 CuCZHSCIZNZ Cu(en)CI,, 5 , 642 CuCZH802 [Cu(CzH4)(OH,),]', 5.569 CUC,H,~N,O~~S C~(en~(OH~),(O,SO,). 5.641 CuCzHizN& Cu(NH3)4(SCN),, 5 , 6201716.734 CuCZN2 [Cu(CN),]-, 2, 10; 5.536.537,563.582; 6 , 9 CUC2O4 CU(CzO,), 2,445 CUC20k

[CU(CO,),]~--, 2.447,448; 5,648: 6. 849,851 CUCSF~O, Cu(O,CCF,)(CO), 5,566 CUC~H~O~ (Cu(O2CH),I-, 5,650 CuC3H5N0,S Cu{SCHZCH(NHZ)CO2}. 2.749 CuC?HsO,S Ci(CO)(O,SEt), 5,566 CUC~H~CIN~S, CuCl(C,N,SZH4), ,, 5.563 CuCTHsNzO Cu(cn)(CO), 5,583 [Cu(en)(CO)] ' , 5 , 5 M j . 567 CUC~H~O~P [Cu{P(OMe),]+, 6 , 113 CuC,H9PS [Cu(SPMe,)] ' ,5,548 CUC~H~~CIPS Cu(Me3PS)C1,2,642

C U C ~ H8N30 ,

CUC~H~~CI~N~S~ CU{SC(NHNH~),}~CI~, 2,803 CUC3N3 5, 545,582; 6,9, 13 [Cu(CN)$ [Cu(CN),]3-, 5.574 CuC,H205 Cu(OzCCOCHZC02), 6,455,456 CuC4H4N406 CuC4H401o [Cu(C,O,), 2H,0J2-,2,444 CuC,HjNO, [Cu{(O,CCH&NH)] , 5 , 6 8 3 CUC~H~CI CuCI(MeC=CMe), 5,557 CuC4H6Cl2N, CuCI2(MeCN),, 5,643 CuC4H6N406 CU(O~NO)~(M~CN),, 2,418; 5,649 CuC4H604 CU(OAC),,I, 271; 2.440; 6,847 CuC4H606 Cu(OzCCHzOH), 2,472 CUC4H7N203 ~Cu(FIzEiCHLCONHCH2C0,)l I ,2,7hO C;C,H,BrOS C ~ B ~ ( S C H ~ C H ~ ~ C H , I :5,563 I.I,), CuC4H,CIzOS C U C I ~ { ~ ~ H5,646 ~ ) ~ } , CuC,H,N,O, Cu(Gly-0),, 1, 13,426,468,524; 5,686 CU(H~NCH~CO 2,753; ~ ) ~ ,6,207,466,463.469 CUC~HSN~S~ ~UCSC(NH,)=NC(NH,)$),,2,640 ~

CuC, H,N, CU(NH&CN)~, 5,588 CUC~H~O CuOBu'.2,349 Cu C ~ H 1oC1Sz CuCl(S2Etz). 5.563 CuC4HIoC12N202 CuCI2(HCONHMe),, 2.492 CUC~HI~ISZ CuI(S,Et,), 5,563 CuC,H,,O, Cu(OAc),(OH,),, 5 , Mt CuCJ I,,CI,N,S Cu{S(CH,CH,NH,),)CI,, 2,553 CUC~H~~CI~OZS~ CuCI,(DMSO),, 2,489; 5 , (140,660 CuC4H,,Nlo

CU{H,NC(=NH)NC(=NH)NH~}~, 2,284 C ~ C ~ H I ~ N ~ [Cu(dien)]'+. 5.683 C ~ C ~ H I ~ N ~ O ~ [Cu(dien)(O,NO)]+, 5,642 CuC4Ht5N30 (Cu(dien)(H,0)l2', 6,213

C:UC~H~~N~S~ [Cu(CH,N,S),]'. 5,543 CuC,H,,ClN,O Cu(en),(OH,)Cl, 5,601.738 [Cu(en),(OH,)CI] ', 2,33 CUCqH18N40 [C~(en)~(0H,)]*+, 5,734,738

Cumulative Formula Index CGH15" [Cu(en),(NH3)J2+,5,609 CUC~N~ [Cu(CN),]-, 5,542 [Cu(CNj4I2-, 5,729 [Cu(CN),I3-, 2.10; 5,574,582; 6. 822 cuc404s4 [Cu(S2C20,)2]-, 5,748 CUC408 [C~(C204),]*- ,2,445; 5,642.619 CuCjH5CIN CuCl(py), 5,563,583 CuC5H,0S C ~ ( O H Z ) ~ ( C @5S, )640 , CuC.H,NC). C~{0,Cd(Me)=NCH2C02}(HzO).2,752; 6,210,466 CuCSHgN203 [Cu{H2NCH2CONHCH(hk)C0,}]+,2,760 [CU{H~NCH~CONHCH~CH~CO~)]*, 2,760 CGHiiNz Cu(CN)(HNEt,), 5,563, 583 CuC5H,,BrN0 CuBr(OCH2CH,CH,NMe,), 5,644 CuC5HI3N30 [Cu(dien)(CO)j ' , 5,566,567; 6,395 CuC,H I,N,O, [Cu(dien)(O,CH)]', 5,642.700,734 cucsos CU(CSOS),2,455 CuC6Br204 Cu(C604Br2),5,690 CUC6H3C1N204 C~(O,CC=NCH=CHN=CCO,)HC~,5,643 C~CgH4N204 CU(OZCCH~CN)~, 5,670,673 CuC,H,N,O Cu(OH)( benzotriazole) , 5 . 646 CuC6H5S (CuSPh).,, 1, 171 CuC6H,C1N30 Cu(4-pyCONHNH)CI,2,799

[CU{N(CH2CO2),}]-,2,789 CUC&~IZ [CLl(0,CH)6]4-, 5,663, 700 CuC6H7N7 Cu(3-Mepy)(N3),, 5,643 CuC6H8Br2N2 Cu(2-pyCH2NH2)Br2,5,642 CUC&,CINO {CuCl(py)(OMe)},,,6,393 CuCbHgCIZN4 CU(HI~CH=NCH=?H),CI,, 5.631 CUC~H~N~ I C U ( H I ~ H = N C H = C H ) ~5,550 ~+,

[Cu{H,N(CH2CONH)~CH2C02}]+. 2,761 CUC&JW~ Cu{MeCH(NHZ)CO2},,2,746 Cu{L-MeCH(NH,)CO,},. 2.753.757 CUCsHi2N206 C U { L - H O C H ~ C H ( N H ~ ) C2.744.750 O~}~, C U { O ~ C C H ( C H ~ O H ) N H1.426, ~ } ~ . 6.207 CUC6H1207 Cu(O,CCH,OMe),(OHZ), 5,705 Cu{S-O,CCH(OH)Mc} { R-02CCH(OH)Me}(H20), 2, 473 CUC6Hi3N304 Cu(C,O,)(dien), 2,47

346

CuC6Hl,NjS2 Cu(NCSj,(dien), 2,47 CUC6H~4Cl2S2 CuCI2(EtSCH2CH2SEt).5,643 CuCf.Hi,O, 5,610,617,698.701 Cu(02CCH20Me)2(0H2)2, CUC6HisN304 Cu(HCO,)Z(dien). 2,47 CUC~HI~N~O~ Cu(TMEDA)(O?NO),, 2,423 CUC~HI~N~S~ C : ~ ( ~ I ~ ) ~ ( S5,716.731, C N ) ~ . 741 CuC',H,,N, Cu(TMET)A)(N,)z,5.629 CuC,H18N205S Cu(TMEDA)(OSO,)(OH,), 2, 424 CUC6HisN2S2 [CU(H~NCH,CH~SM~),]~+, 2,553 CUC~HI~O, [ C U ( H O C H ~ C H ~ ~ H1), ~ 6 6] ~ + , CuC6HzoN4 [ C U { H ~ N ( C H ~ ) ~ 2,45 ~H~)~]~~, CuC,HzJ'J,Od Cu(pn),(OSO,)I 2,425 CuC,H,,N, [CU{N(CH,CH~NH~)~)(NH,)]~', 5,607.668,678 CuC,Ii,,N, [Cu(en),12-, I . 66; 2, 33; 5. ~~00,h17,656,663,669.69U. 691: 698.70&702,704,734 CuC,H,Cl304 Cu(acac)(O,CCCI,), 2, 380 CuC7H8Cl2N20 CuC12{HN=C(OMe)py-2}, 1,439; 2,279 CuC,H91N2 CuI(2,6-Me2py),5.585 CuC7H9N0, [C~{2,6-py(COMe),)]~ ,5,613 I,,jQ,N, CUC~E C~(2-pyCbI ~ C I ~ ~ N I I 2 )5.C643 I~, CuC,HION402 Cu(DMG) (HfiC.H-NCH&H), 5,609

CU(M~SCH~CH,CH(NHCOCH~NH~)CO~}, 2,763 CuC7H14NOS Cu(OSCIVPr,). 2.587 CuC7HlSS2 Cu(CN)(KEt,). 5.563 CuC7H16N30,

[ C U ( H ~ N C H ~ C H ~ N ~ I C H ~ C ~ ~ ) ( H' .~6N, C H ~ C O ~ M

418.419 CuC,H18N5S [Cu(H2NCH2CH2NHCH2CH2NHCHZNH2)(NCSII+.2.54 [Cu(H2kCH~CHlNHCH2CH2NHCHLCHZNHZ) (SCIi)].' .2.54.234 [Cu{(H2NCH;CHJHCH2)2}(NCS)] ' ,5.609 [Cu{(H2NCH2CH2NHCH2)2)(SCN)]+.5,735.741 [CU{N(CH~CH~NH~)~}(NCS)]+, 5,609.734.735 CuCiHI9BrZN3 Cu{H,N(CH2)sNH(CH2)4NH2}Br,,2,47,50 CGHzoN4 [CU{(H~NCH~CH~NHCH~)ZCH~}]+, 2.54 CUC~F~~,N,O~ [C~(dien)(H~NCH~C0&le)]~+, 6 , 4 19 CUC~H~ON~S [Cu(pn),(NCS)]'. 2.233 C'uC8H,CIN,S, 5,563 CuC1(C8H6N4S2), CuCoHLNcO,: Cu(2,2'-hipyrimidinyl)(~-ON02)(0,NO),5,735 CuCsHBCl 1

"

1

"

347

Cumulative Formula lndex

CuCl(cot), 5,570 CuC8H8ClN4OZSz CuCI(2-thioura~il)~. 5,548 CUC~H~N~ [ C U ( N C C H ~ C H ~ C N ) 5~.]565 +. CUCsHsN606

CU(I~=CHCH=NCH=CH),(O,KO),, 5,604 CuGHioOio Cu{S-0ZCCH2C~I(OH)CO,H),,2,475 CUC8H10012 Cu(tartrate),, 5, 668 CUCgHiiIN CuI(2,4,6-Me3py), 5, 563.585 CUCVH,~NO, CulEtOzCCHzN[CH2CO2)*} 6.422 . CuCsHiiN~03 ICuf $J=CHNHCH&CHXH(NHCOCH,NH,-~ - ~

~~,

~

L

I

CH2CH(NH,)CONHCHzC0,)l'. 2.760 CuC8HlZClZ~z' CU(~-PYCH,CH,NHMC)CI~. 5.641,hbO CuC8Hi,CI,N403 Cu(caffcineMO112)C12, -. - 5.614 CuC8H,,N~Ob C L I ( O ~ C ~ H N H C H , O ~6,207 H~)~, CUC8HiZNlS [CU{S~CN*H~)~),]', 5.748 CuC8Hi2N4 [Cu(NCMe),]+, 4, 174,193: 5.536,537,542,574,576. 583,587 [ C U ( N C M ~ ) ~ 5,537 ]~+, c~C~HizN404 Cu(DMG)z, 5,628 CuC8HlZN804 [Cu{hNHCHMeNHNCOCONNHCT-IMeNHNCOcO)l-. . . 6.181 CuC8Hi208 [Cu(OAc),]' ., 5,613,656.6.57. 663,h68,676,700,716 C U G H,,NaO, Cu(DMG),, 1,525 CU(HDMG)~,~,~~X

CuClo~13N2O8

CuC,N,S4 [Cu{S,C,(CN),},]-. 2,617; 5,748 [ C U { S ~ C ~ ( C N ) ~2,608 }~]~-, CUC808S4 [ C U { S ~ C C ( C O ~ ) ~5,748 }~J-, CUC~H~NO~ CU(~-UC~H~CH=NCHZCO~)(H~O), 2,752: 6.21 1 CuC9H9K302 Cu(NC0),(2,4-lutidine), 2,234 CUC~H,~N~CI~ [Cu{N(CH,CO,),}(H,NCH,CO,Me)l-, 6,418; 4'19 CuCgHI3N4O3 [cu{ %=CH?I FICH=~CH,CH(NHCOCH2CH2NH2)C02)l', 2,760 -~~ ~. CuC9H16k406 CU(L-~~=CHNHCH=CCH,CH(NH,)CO,} { LHOCHzCH(NH2)COz} (HzO), 2,744 CuC9H18BrzNSz

[Cu(H,NCH,CH,NHCH,CO,) { L-aMeC:I-1(N11,)C02Et}]' ,6,418 CuCPII2,BrX, [Cu(N(CH,CH,SMc),}nr]', 2,553 CuCddL [ C U ( ~ H C HC H ~ N H C H ~ C H ~ N H C H ~ C H , -H,)IZ+, 2, 912 C~CgH23N302 [CU(TMEDA)(H,NCH,CO,M~)]~+, 6,419 C U C ~ H ~ ~ N ~ [CU{H~N(CH,)~NH(CH~)~NH(CH~)~NH,}]~+~ 2.56 CuC9HZ7CI3P3S3 {Cu(SPMe,)Cl},, 5 . 556 CUC~H~ON~ [Cu(pn),l2+. 5,678 C U C , ~ H>04 ~F~ Cu(hfdcac),, 2. 387, 388 CUCIOH~FI~OS Cu(hfacac),(HZO), 2,387 CuCleH*F,OI Cu(acac)(hfacac), 2,377 CuC8H,6NZ07 Cu{HOCH,CH(CO2)NIICH~CH,NHCH(COz)CuC,oHBNZ CH,OH}(H,O). 2.752 [C~i(bipy)]-~ 5,548 CuC10H8N404 CuCsH,,N& Cu(bipy)(ONO),, 5,604,733 CU(NCS)~{H~N(CH~)~NH(CH~)~NH~), 2.47 CUCaHi806Sz CuC10H8N604 Cu(EtSCH2C02)Z(H20)2.2.805 [CU{I12-(HNCONHCON),C,H4}]-, 5,747 CuC8Hz0BrN2 CUC10bN3 CuBr(Pr'NHCH,CH2NHPr'). 5.547 [CU{(2-py)zNfI) j2+, 5,699 C~CloHloC12N2 CuC8H,,,BrP, Cu(pp),Cl,, 5,577 CuBr(Et,PPEt,). 5.563.583.585 { C U ( P Y W ~ }5,660 ,,, CuCloHloClzN20z CuCl,(pq-ridinc Y-oxidc)z. 2,496 CGoH,o~zNz cu,T,(py)z. 5 : 537 CUCsH20N4 [CU(~~HCH,CH,NHCH,CH,NHCH,CH,CUC~OH~~?J,O~S, m H 2 ) I Z + 2,912 , C~(~-PYSO,)Z(OHZ), 5,705 CUC~H~ON~S~ CuCioHioN, CU(WH=CHCH=CCH=NH),, 2,721 [Cu{MeC(S)NH,},]+. 2,647: 5 , 542,584 CUC~HZ~O~PZ CuCloH,oN408 Cu(py N-oxide),(O,NO),, 5,739 Cu(OzPEtz)Z, 5,607,651 CuC.,0H12ClN4SI CuC8H20S4 CuCI( MeC(S)NHC=NCH=CHS},, 2,647 [Cu(MeSCH,CH,SMe),]+, 5 . 5 4 3 . 591 [Cu(MeSCH2CH2SMc)2]2+. 5,591 CuGoH12N 2 0 6 5 [Cu(MeSCH,CHZSMe),l4'3'. 5.591 5 , 641 Cu(bipy)(OH2)2(02S02), CuC&12404Se4 CuC,,H,lN,O, Cu(cdta). 2: 783 [ C U ( O S ~ M ~ ~ ) , 2.490 ]~'. ICu(edta)l2-, 2.784 CUCgHz6N6 [CU{(O~CCH~)~NCH~CH~N(CH~C 5,996 ~,),>~'-, [Cu(dien),12+, 5.601.610,617.663.675,698,700,701, 707,734 CUC10Hi3N20* ,

I

Cumulative Formula Index

CGOH13NZOII [Cu(Hedta)] -,2,784 CuCioH14NzOa Cu(H,edta), 5,663 CuCioHi4N306 [C~(ON0,)(0H,)~(bipy)]+,2,423 CuCioHi4N504 [cu { & = C H N H C H = ~CH,CH-

2.761

(NHCOCH2NE12)CC)NMC~I,C0,}]+,2.761 CuCioHi,O, Cu(acac),, 1, 120, 157,230,422; 2. 379.383; 5,596,675; 6,107,203,206, 1023 CuCioHiSBrNS CuBr(2-pyCH,SBut), 5,544 CGoHiSNzOB [Cu{N(CH2C0,)3}(H,NCH2C02Et)] 6.418 CUCIOHISNSO~ c U {L-~;~=CHNHCH=~CH,CH(NH~)CO,} ( LH,NCOCH,CH(NHz)CO2). 2,744,748

-.

CU(HiO)(IT,edta), 2,783; 5,601 CuC&iJ%O,

C U ( L - T ; J = C ‘ H N I - I C I I = ~ C ~ ~ ~ ~ ~{L-~ ( ~ ~ ~ ~ ) ~ ~ ~ }

MeCH(OH)CH(YH,)CO,), 2,744,747,750 CuC10H16N506 [CU{H~N(CH,CONH)~CH,CO,}]~~, 2,763.767 CUC10H20C1208S4 Cu(l,4,8,l2-tetrathiacyclotetradecane)(OC1O3),,5 , 601 CUCIOHZONZO~SZ Cu{L-MeSCH2CHZCH(NH2)C0,}z. 2,744 CuC1oHzoNzS4 Cu(SZCNEt,),, 5,605,628,712,6, 1023 CuCinHmS4 Cu(l,4,8,1 1-tetrathiacyclo~etradccane)5.543 [Cu(l,4,8,11-tetralh1acycl~~~tradccantl)l2 ’ , 5 , 682 CuCioHzoS~ Cu(1,4,7,10,13-pentathiacyclopentadecane),5 , 542 CuCloHzzNaOSz Cu( C)CH2CFI,SC~I,CII,NITCITzC H , N H C H , C H , S ~ H ~ ) ,2.553 CuCioH2zN20~ Cu{ (OCH2CHEtNHCH2)2}.6.990 CuC1~HZ2N4O4 CU{02CCH(NHZ)(CH2)3NH1) 2.1.419 C~CioHz3N203 [Cu{(S)-O,CCH(OH)Me} {Pr’NHCHzC(NHz)Mez}2]+, 2.474 I

348

349

Cumulative Formula Index

CuC14H22NI.

C u ( H N ~ c H ) , ( O N O , ) , ,5,714,727

[Ci(Hteta)f, 2,784

CUCi2His06 Cu(MeCOCHCO,Et),. 6.469 CuCizHzoNzO, Cu(02C~HNHCHMeO~HIvIe)z. 6.207 c C~CizHzoN606 CU{L-&=CHNHCH=~CHZCH(VH~)C~,) { D-N= CHNHCH=C CH,CH(NH,)CO~}(H,o),, 2, 744,748 C G z H nNS, [Cu{(&=CHNHCI I=t:CHaNHCHZCHzS)Z}]Z+, 2, 95 CUC~~HZONSO~ [Cu(lI~CH=NCH=C'H),(OI12)z]2+, 5,601,734,738 CUCizH2iN506 c U {&=CHNHCH=~ C H ~ C H ( N H ~ ) C O ~ } {WzN(CHz)4CH(NH2)C02}, 2,753 C~Ci2HziN704 c U {P;T=CHNHCH=CCH~CH(NHJCO~}{HzNC(h'H)NH(CH~)3CH(NHz)CO2},2,753

CuCIzH,,CI,O4 Cu(HO~H(CH2)4~HC)tl}~ 5,628 C1~, CuC12H24N606 Cu{ 02CCH(NH2)(CH2)3NHCONH2} z, 1,419 CUC~LHZ~O~S~ [Cu($CH,CH,OCH,~H,),]*. 5 . 542 CuC1zH26BrN402 CuBr{(HON=CMeCMezNHCH2)2), 2,274 CUC,,H&~O~ Cu((s)-OiCCH(OH)Me),(TMEDA),2,473

902

Cu{S,P(OPr'),},. 6.1023 CuCizH2sS4 [Cu(EtSCH,CH,SEt),]-. 5,542.584 CuClzHZ,BrN6 CuBr(N3)(Et4dien). 2,231; 5,734 CUCizH30N6 [Cu(HzN~HC'I~2C:HNHzCH2CHNHz~Hz)2]z~, 5,610 CUCIZHWN~ [Cu(EtNHCH2CH2NHEt)z]-, 5,572,583 [Cu(EtNHCH,CH,NHEt),]' ' , 1,470 [Cu(EtzNCH2CH,NH,)zl+, 5,542 [ C U ( E ~ ~ N C H ~ C H ~ X H5,605,734 ~),]~+, CUC121132N40 [Cu{N(C11zC€~zNMez)3~ (OH2)j2+.5,681

c;c,,H;,N,O, [Cu{(MeO,CCHz)zNCHzCHzN(Cf T2COzMe1ICH,CO,)l+, - _ 6,423

Cu(hfacac),(A=CHCH=NCH=CH), 5,6W CuCI4H8N4 Cu(phcn)(CN),, 5,729 CUC,~H,N,O,

CU{~-{~-HOC~H~N=NC(CN)=N~X}C~H~O}. 6.82 CuC,,H,oO, C U ( ~ - O C ~ H ~ C H6,157,213,426 O)~, CUCI~HIOO~ CU(~-HOC~H~CO 6,760 ~)Z, CuCIaHiiN02 ~u{OCHPhC(Ph)=fiO}, 1,530 CuC,4H,,N,Oz Cu(2-OC6H,CH=NH),, 1,431; 5,668 CUC14H12NL04 Cu(2-Or,H4CH=NOH),, I , 531,6,800

Cumulative Formula Index

CuC14HZZN6

[Cu(dien){ (2-~y)~NH}1+, 5,707 [C~(dien){(2-py)~NH}]~~, 5,607. 707 CG4HA4 Cu(MeCOCEtCOMe),, 5,675 CUCI~HZ~NZO~ [Cu{(Me02CCHz)2NCHzCH2K( CHzCOzhIe)z}]2+, 6, 423 CUG~H~~NZSZ [ C U ( ~ - ~ ~ C H ~ N ( C H ~ C H5 ,~542 SE~)~}]~, CuCi4HdzOz Cu(H,NCH(CHz).$O),. I , 420 CUCI~H~NZS~ [Cu&CNPr',),]-, 5,687

c ~ c ~ ~ H ~ ~ N ~ [Cu{&[Me)CH2CH2N(Me)CH2CHZCH2Y@fe)CH2CH2N(Me)CH2CH2kH2}]z ' ,2,912

350

Cu{fi=CHNHCH=~CHZCH(NIi2)CONHCH2CO,} z, 2.760 CUCi6Hz4N206 Cu(H2NMe)2(02CPh)2(OHz)z, 5.613 CUCi6Hz4N8 [Cu(MefiCH=NCH=&I),]+, 5,543 CUCi6HmNz02 Cu{1,3-(Et0CH,CHzNHCHz)ZC6H4}, 5,577 CuCi,HwN,

[Cu{fi=CMeCH,CMe,NHCH,CH,N=CMeCH2CMe2NHCH2cH2)]2+, 6 , I64

[Cu{H2NCHICHzNHCMe2CH2C(Me)=NCH2CH,NHCMe2CH2COMe}]2+,6,164 CUC16H3604P3 Cu(OzPBu2),. 5.607, 642 CuC16H40BrN4 CuBr(Pr'NHCH,CH,NHPr'),, 5,585 CUC~~H~~IN~ CuI(PriNHCH,CHzNHPr')2,5,585 ~~

,~

CuCi;H,,N;O5 Cu{4-HOC,HaCH,CH (NHCOCH' (NH;COCH;NH,)CH,CHMe,} ~

'

CO,}, 2.763

.

Cu(5,7-dibromo-8-quinulinolate),, I , 419 CuCixI I12NZ03 Cu(8-quinolinolate)~.1,419; 5,668,683; 6, 1023 CUCi8HizN?Oi*Sd Cu{5,7-(HO,S),-8-quin0linolate}~, 6, 760 CUCiBHi5C13N60 Cu{ 1 14-bis(2-pyidylamino)phthalazine}(OH)C13. 5, 727 C~Ci8Hid3N60io Cu( 1,4-bis(2-pyridyIamin0)phthalazine}(OH)(IO~)~. 5, 727 CUC~~H~SS~ [Cu(SPh),]-, 5 : 547: 584 [Cu(SPh),]l-. 1: 171 CUC.!BH~SN,O, [Cu(terpy)(H,NC1-12C02Me)]*+,6 , 4 19 ChCi~H2oN204

C:u(n,r~-PhCH,CH(NH,)CO,},, 2, 753 CG6Hi4NzOz Cu(salen), 5,668, 673; 6.85 C ~ C I ~ ~ ~ I ~ N Z ~ Z Cu(2-OC6H4CH=NMe),, 5,606,632,665.744 C~Ci,Hi,Nz04 [Cu(2-pyCOzEt)lZ', 6,469 CuC16H18N402

C~(2,4-Me,py)~(NC0),.5,733 CUC,,I-~~~N,S, [ C U { ~ - ~ ~ C H ~ C H ~ S' C5,541 H~)~}] CuCI6HZON5S (Cu{(Z-pyCH,NHCI1,)zC:I IZ}(NTS)]*C.5.609 CUCi.#2zNa06 cu { &=CHNHCH=~ CH~CH(?IHCOCH,NH~)C02}2,2,760

.

CuC1~HZ1N3 [Cu(2-pyMe)Jf, 5,538 CUCi8HnN602 Cu(ON=CMeCH,KNPh)(HON=MeCH,"Ph), 543 CUC18HZ1N10

~CU{(~=CHCH=CH~CH,),NCH,J,~ 2 ,~8+6 .

. .

[Cu(Httha)],-, 2,788

5,

Cumulative Formula Index

35 1 CuC18HZ6N806 Cu(tkCHNHCH=C CH2-

CG4H18N401

[Cu(py .Voxid~),]~*.2,495; 5,688,739 CuC2,,HZ6S2

CuCisHi &,O C U ( ~ - O C , H ~ N ~ N C ( P ~ ) = N N6,79 P~), CUC~N ~5H ~ [CU(~&HCH=NCH=CH)(~C~~~)]~+, 2,95 CuCI9H~~F1zNC)~ Cu(hfaca~)~(tetramethylpiperidinoxyI),2, 388 CUCI~HZOFIZNO~ Cu(hfacac),(4-hydroxy-2,2,6.6tetramethylpiperidinoxyl) 2. 388 CGnHsOz [Cu(bipy),(ONO)]+, 5.612 CuCzoHloBrzF60zSz CU{~-B~C~H~C(S)=CHCOCF,)~. 2,651,652 CuC2oHIoC~ZF60ZS2 CU{~-C~C~H~C(S)=CHCOCF~)~, 2,652

.-.

_ _

C;(PhC(S)=CHCOCF3)21 2,651,652 CUCZOHIZFIZN~O~ Cu(hfacac),(py),, 2,387 CuCzoHizNz04 Cu(quinaldinate),, 1,524, 530 CuCzoHi,N40z C~(~-OZCC~H,N=NC(P~)=NNP~}. 6.79 CGoHi4N403 CU{2-{2-HOC6H4N=NC (Ph)=NN} C,H,COZ}, 6,82 CUC~~H~~CIN, [C~(bipy)~Cl]+, 5,588.607, 676,707,711 CuC'zoHi,CIN4Oz C U { ~ - H ~ ~ C : C ~ I . I ~ N = N C ( P ~ ) = " H P6~, 7}9C I , C~C20HibCIN404 [Cu(bipy),(O,ClO,)]-. 2,426: 5. 641 C~C~IIHI,CI,N,O, Cu(bipy),(O,CIO,),, 5. 711 CUC2oHidN4 Cu(bipy),I, 5 , 714 [Cu(bipy),I]+, 5,741 CuC2oHie.N4 [Cu(bipy),]+, 5,537,574,580 [Cu(bipy),J2+,5, 607,682.686,707.711,734; 6, 113 CUCZOH,~N~OZ 5 >SKO,617,656,663,668,669, [C~(bipy)~(ONO)l+. 698,699,700,7U3.706.708,711

CuCzoH16Ns03 [Cu(bipy),(O2NOj1+,5,612, 711 CUC~OH~~N~O [ C ~ ( b i p y ) ~ ( O H , ) ]5.~ 609,711,739 ". CuC20HlSN6 5,606*607.668,734 [CU((~-P~)ZNH}Z]~', C~CznHisN702 5: 612 [CU{(~-PY)ZNH}~(ONO)]+, CuCzoHisOzSz Cu{MeC(S)=CHCOPh}2, 2.651 CGnHi@4 Cu(MeCOCHCOPh),, 2 , 370; 5.676 CuCzoH19Ns, [Cu(hipy)2(NH3)]+,5. ho9 [ C ~ ( h i p y ) ~ ( N H , ) ]5$676 ~' CGoHznN4 [Cu(py),l+, 5,537,543 [Cu(py)412+,5 , 6 8 6 CGnH,oN404 [Cu(py N-oxide),l3+, 5,746 ~

C u C d k 1 Ne [CU@CH=CPhCH-NCH=CHCH=NCH=CPhCH=NCH,cHJl' , 6 , 168

CuC30H3~o~606 [CU{HfiCOCH=CHCH=~H}6]2+, 1,53 [cu{o~~=cHcH=cHcH=CH)~~+, ~ 5 35,600, ; . 617.704.739

[Cu(phen),(O,CH)]+, 5,612- 704 C~C2sHi7N403 [Cu(phen),(O,CH)]+, 5,580 CUC~~HZ,CIP~S~ Cu{H2C(SPPh,),}CI, 5,547 CUC~~H~~N~SZ Cu(phen),(NCS),, 5,601,611,698 CG,Hi,N,Oz [Cu(phcn),(OAc)]+. 5,5Y4,612. 669. 698,699,704 C U ( ~ - O C ~ H ~ C H = N P6~, 4)3, , 157 Cu(2-C)C6H4N=CHPh),, 6,43 CUCZ~HZ~N,~~ Cu(3-Mepy),(02CPh),(OH,), , 5 , 6 13 CG7HiaN303 Cu(8-quinolinolate),, 1, 528 CUC27H26P2 1.407 [Cu { (Ph2P(CH2)3PPh2}]+. C U C ~ H ~ ~ N ~ [Cu(octamethylcorrole)]~~ 2: 873 CuC2e.HI 4 0 6 Cu(ai1thraquinon-1-olatc),: 6 , M c:uc281~118c1409

[CU(2-C1C6~14Co,),(OH,)]'-. 5. hi3 CUC~HZONSO~ [Cu( tetrabenzo[b.j,f,v][ 1.5 -9,131tetraazacyclohexadecane)(02NO)]".5,609 CUC~~H~~CINZP Cu(bipy)(PPh3)CI, 5,542,585 CuC&&4 [Cu(2,9-Me2phen),]+, 1.407; 5.542,580,583 [Cu(2,9-Mezphen),]*+, 5.682, 686 CUCz8H24Ns03 [C~(2,9-Me~phen)~(O,NO)]+, 5- 580.612 C~C29H31N4 [Cu(diethylhexatnethylcorrole)l"-, 2 , 876 C U C ~ ~ H ~ ~ N ~ Cu(H-diethylhexamcthyicorrole), 2. 875 876

Cumulative Formula Index

353 CUC~~H~~NP~S Cu(NCS)(PPh3)2,2,588 CUC37H300PZS3 Cu(PPh,),(S,CSO), 5.544 CUC~SH~OF~OZPZ Cu(PPh3)z(OzCCF,), 5: 544 CUC38H30N6 Cu(NPhN=CPhN=NPh)s, 6.78

CuG&,oP, [Cu(PPh,),]", 5,542,583 CuCBlH,,BrP3

C~Br{P(C,H,h4e~-2,4,6),}~, 2, 1039

C U C ~ ~ I I ~ ~ N ~

Cu(NPhN=CPhN=NPh)(NHPhNLCPhN-NPh),

6,

78

CuC3sH3,O,P, Cu(PPh,),(OAc), 5,542, 584 C-UC40H44P4 {Cu(C=CPh)(PMezj}+ 5.561 C U C ~ ~ I ~ ~ ~ N ~ ~ ~ ~ S ~ CU{4,8-(HO,S)2-5-0-6-{2-O-3,6-( t 1C),S),-8HOCl0H3N=N)C,oH3-2-NH)ZCO, 6, 105 CUC~IH~SNIIO Cu(dehydrophthalocyanine)(1.3-diiminoisoindo1eno)(OMe), 6,90 CUC~IH~IF~~~P~ Cu(PPh,),(hfacac), 5.544 CUC~ZH~~NOJ'Z Cu(PPh3),(3-pyC0,j, 5,544

CuC44HZsN4 Cu(tetraphenylporphyrio), 2, 841 CUC~~H~~F~OJ'ZS

Cu(PPh3)2($CH=CHCH=cCOCHCOCF,), 5,544 C~C&MO,PZ Cu(2-Ph2PC6H4COCHCOMe),,2,401 CUC~,H~OCIN~ [CU(C~~H~~N,)C 5, I588 ]+, CUC44H60N4 [Cu(C,&oN4)]+, 5,572 CUC,, ti4,O2P3SZ Cu(SPh)(PPh,Mc),(SO,). 2.635; 5 : 545,584 CUC45H44PJS Cu(SPh)(PPh,Me),, 2,635 CUC46H34N208 Cu,(0,CPh)4(quinoline)2, 5: 284 CUC48H4zN6 [Cu{tris(4-methyrbenzo)[bf,j][1,5,9]triazacyclododecanel 5. 600 CuC52H4sP4 [C~(dppe),]+~ S 1 542.543,572.583 C U C ~ ~ H ~ ~ B ~ P ~ CuBr(PPh,),, 6, 250 CUC~~H~Q'~ CuCi(PPh3),,2, 1026 CuC,,H,,CIP,S, CuC1(SPPh3)3,5: 545 CuCsJLsFP, CuF(PPh,),, 5,542.584 CUC~~H~SNOJ'~ Cu(Ph,P),(O,NO), 2.418 CUC54H45P3 [Cu(PPh,),]+, 2,1026 CUC~OHSO~ZP~SZ Cu(SO,)(SPh)(PPh3),. 5.580 CUC~OHSOP~S Cu(SPh)(PPh,),, 5,580

CUH~N~OS

CuCssH9604P4 {Cu(OBu')(PPh,)},, 5,580 CuCaN601z [C~CU(NO,),]~-. 5, 702 CUC1, [CuClJ, 6,497,851

cuc1,

[CuCl,]-, 5 : 600,633,643,652 ICuCI,]*-. 5,563; 6,496,497,853 CUCI, CUCI4,5,709 [ C U C I ~ ] ~I-, ,53,255; 5,542, 5Y5, 601,6U5- 6M. '38, 656,663,668,699,700,707,7091 713,716; 6 , 847,854

CUCI,O [CuOC&I4-,5,639 CUCI, CuC1,; 5,709 ICUC~,]~? 5.607,656,709,712 CUCI, [CUCI,]~-,5: 712 CuCoC,,,H,,N,S [Co(cn),(SCH,CHZNHz)Cu(NCMe)21G' ,5,553 CUCOC~~H~~N~~ [Co(NH3),( p 9 C I i=NCH=~~I)Cu(Mc,dicn)~,'- 4, 694, 697 Cuco,o, co,cuo,l I. 111 CuCrS2 CuCrS,, 3, 882 CuCrSe, CuCrSe?. 3, 889

CuF, [CuF,] ,5,746 [CuF,12-, 5,610, 648,664,741

CUFG [CUF,]'-, 5,750 [CuF6j3-, 1,21; 5,746,749 [CuF6l4-, 5,601,610,664,712,741 CuFeS, CuFeS,. 6,783,786,853 CuFe,PbH,O 14Sz PbCuFe,(SO,),(OH),, 6,827 CuGaInO, CuGaInO,, 5 , 607,650 CuCra2C2,H4,N8 ~u~u(Me,Cia(~N=CMeCTI=~Me),},, 2.254 CuH CuH. 2,693 CuHIO, Cu(OH)(IO,), 5,648 CUH2C1209 Cu(CI04),(H,0), 2,414 CuH*I,O,, [ C ~ ( O ~ ~ O ~ ) ~ ( O2,431 HZ)]~-, CUH~S~ [Cu(HS),]-, 6.853 CUH,S, [CuS(HS)3j3-, 6,853 CLiHJC1,02 CuClZ(OH,),, 5,601,690,738 CUlJ,CI,O? [CuCI,(6HJJ, 5, 643 CuH,N,O, C~(OHz)z(OzN0)2,5,613,642,738

Cumulutive Formula Index

C~Hq04 CuH404 [Cu(OH),]-, 5,745 [Cu(OH),]", 5,739 CUH406S C~(OH2)2(02S02),5,641 CuH40& Cu(OH,),(OSO,), 5,689 CuH4S4 [Cu(HS),IZ-, 6,853 CuII,NZOe.s C~(ON02)2(0I12)2.~, 2,427 CuH6Br2N2 Cu(NH,),Br,, 5,610,642,652,7U6 537,547

354

Cu{ 0,CCHMeNCOCH MeN=CHC,H,{Mn(CO),}CH2NMe2}, 6,209 CuMoCNS, [CuClri(.MoS,)]'-, 2,565-567,570,571,575 CuMoC6H5S5 [CuSPh(MoS4)J2-.2.566; 3, 1421; 5,572 CuMoCz8H5J3rN4Sz Mo(CNBu')4(p-SBu')2CuBr, 3, 1283, 1424 CuMoS, [CuMoS,]; , 3 . 1421 [Cu(MoS,)] ,2,565.566 CuN,O, Cu(NO,),. 1,28.2.414 C ~ ( O ~ r i 02,415.426,428 )~. CuN&

,601,735 [CU(NO,),]'-. 2.423; 5,614,733 CUN, Cu(N,),, 5. 642 CuN,O [Cu(N0,),14 1.53; 5.596,601,610,617,633.652, 656 706 ruNaC,H,CINO, CU{O('HZC(NH,)(UH,OH)[~I~~O}N~~(CI~,), 3, 17 C U N ~ C ~ ~ H ~ ~ N ~ ~ ~ S Cu{ 1-(3-O-5-Na0,SC,H3N=N)-2-OCloH6}(H20), 6, 56 CuNiC4HsO12 NlCu(Cz04)2(H20)4. 5,690 c-~u o .P [CGO,P)]-, 2.429 CUOJS Cu(O,S), 2,429 CUO,S, [CU(SO,),]~+.2. 635 CuOSSe2 Cu(04Se20),2.431 ru0,Sn [ C U ( S ~ O J .2.637 )~~~ CuO& [CU(SO,),]'-, 2.308 CUOllP4 [ C U ( P ~ O ~ ) 6~ .]10 ~-. CUPbN6012 [PbCu(NO2),I2-. 5.656.663,669,690,691,698.700, 701,702.704.707 CUP~C~~H~BCI,O,P~ CuPtC12(2-Ph?PCOCHCOBuf)2, 2,402 [CuPtC12(2-Ph2PCOCHCOBu')zj2+,2,402 CuPtHiZCIdNq Cu(N€I3),PtCI,. 5.652 PI(NH,),CUCI,. 5,653 C U R C C ~1P2 ~H~ [ReH,(PPh&Ie),Cu]+, 5,585 12 CuRe&&O {Re(CO), } (0Ac) 2Cu, 5,652 CURe~Ci6Hi2012 Cu{Re(CO),(MeCOj2}2,2, 397 C U R ~ ~ C ~ ~ H ~ ~ P ~ [{ReH5(PMePh2))2Cu]f,5,572 CuRhC39H36ClKi,OP2

;i

[Cu(NH3),I2+, 1 , 2 ; 2,27.28; 5,588.589? 595,605,656, 667,668,678,686,689,716.725 CuHi2Ne.04 Cu(NH,),(NO2)2, 5,595,601,656.663.675,698,716 CUHd606 Cu(NH3)4(N03)2,5,730 CuHizO6 [Cu(OH&]+, 5,565 [CU(OH2)6I2+,1,53,255.284; 2,308.5.587, 594.601, 603,h17,h67,668,672,h78, h80.681,682,h99, 700,701,71X,719,775 CUH~~N~U [Cu(NH3),(OH2)IZt, 5,607,656- 738 CuHisN, [CU(NH~),]~+, 2,27; 5,607.690. 700. 711 CUHisN6 [ C U ( N H ~ ) ~ 1,53; ] ~ + , 2,26,27: 5,689.730 CUHgCsHi6NsS4 [CU(~~),(NSC)H~(SCN),]~, 1. 126 CuHg&.N2Oio CUH~(OH)~(ONO~)~(OH~)~,~, 652 CUI2012 [Cu(I06)2]'-, 2,418: 5,745,716 CUI, (CUI3]-, 5,548 CuIn2Se3Br CuIn2Se3Br, I , 111 C U T ~ C ~ ~ H ~ ~ P ~ [IrE13(PMe2Ph)2Cu]i, 4 , 1164 CUI~C,~H~~CIN~OP~ IrCuCI(MeNNNMe)(CO)(PhMe,P),, 2.200.202 CuIrC32H25C12N,0P

[IrCI(PPh3){fi=NC(py-2)=CHCH=c(py2)}-(pNO)CUCI]~+, 5,653 CuLiC32H16Ns CuLi(phthalocyanine), 2, 868 CuMgC18H12N206 CUM~{~-O~C-~-OC~H~CH= 3,28 NCH~}~, 16Fl ZNZ06

Cu(salen)Mg(hfacac),, 2,387: 3, I6 CuMnC, b H 1 6 N 3 0 6 CU(02CCH2NCOCHZN=CHC5H3{Mn(C0)3)CH2NMe2},6,209 C U M ~ C ~ ~ H ~ ~ N ~ ~ ~

RhCuC1(MeNNNMe)(CO)(PPh3)2,2,200, 202 cus, [CUS4] ,2.545 CUS406 [CU(S2W213 ,57589 CuSb,C,J 1&2 Cu(Ph3SbS)?I,2,634 CuSb3C5,H4,C1 CuCi(SbPh,),. 5.584

CUS~ZC~H~~N~ Cu(en),(SeCN),, 5,734.741 CuSi2C7Hls [Cu{C(SiMe,),}]-, 5,550 CuSiZC7Hl9Br [CuBr{CH(SiMe& I]-. 5. 550 CuSi2Ol0 [ C U S ~ ~ O , ~5,716 ]~-,

[Cu(Te0,),l9-, 5,745 CllT1206S2 T1z[Cu(S03)z132,638 CuVCioHi,NzO, Cu(MezNCH2CH2NMe2)(Cz04)VO(C204), 3,565 CUVC~~HI~CIZNZO~ (VO)CuClZ{2-0C6H4CH=Y(CHZ),N=CH= C6H40-2}, 3,565 CUVC~~H~~CI~N~OZ VO(salen)CI,CuCl, 5,572 CuVC,,H,,N,O, Cu(VO){(McCOCHCUCHCMeNTCI,)Z)), 3,562 CUVC17H16NzOs Cu(VO){ (2-O-3-O,CC,H3CH=NCH2)2} (McOH), 3, 565 CUVC~HHIZNZO~ CuV0{(2-O-3-02CC,H~CH=?JCH2)L>,5,662 CUVZC~ZHZSC~ZN~~I~ { (V0)(2-OC6H,CH=NCH2CHzN= CHC~H~O-~},CU(CIO~),, 3. 565 CUWCMH~~O~PZ CuW(C0)3(PPh,)2Cp, 5 , 572

CuzC2HsOt{ CU(OH),)~(OOH)(OAc), 5 , 7 17 CU~C?H,N,S, CU;(NCS)~(IU’H~),, 5, 589 CUzC3N3 [Cu,(CP;),]-. 5,565 CU2C3N:S3 2,235 [CU~(NCS)~]-, [CU~(SCN)~]-, 5,565 Cu2CJHloC12N6S2 (CuCI(H,FiCSNHCSNHZ))2, 5, 553

[CU,(H~NM~),(OH)~(OH~)~], 5, 623 Cu2C6H2N6

Cu2Hz(CN),(C,Nz), 6, 872 Cu2C6H4N2SZ [ (Cu(2.2‘-bi-2-thia~olinyl)),]~+, 5,555 CU,C~HJO, Cu2(02CCH2C(0)(C0,)CH,C0,), 2,477 CU2GH10N20bS3 C U ~ { S ~ C ~ ( N C H ~ C H(~0 2OS0 H 2) ~) ,5,642 } c:u2C6II,,N,OI0S, ~ U ~ ( S ~ C ~ ( N C H ~ C H ~ O H ) ~5 }. 662 (OSO~)~, CU&H,,N~~ [ C U ~ ( K ~ ) ~ ( H M T A2,234 )]~-, cu2c606 (CU(CO),),, 5,535 Cu2CsHloBr2NZ {Cu(NCCH=CHMe)Br},, 5,553

cuws,

[Cu(wS,)]-, 2,565,566 CuW& [CU(WS,)~]’-, 2,566,568 C~WI,O,,l [ C U W ~ ~ O 3. ~ ~I042 ,~~-, [cuw,2040]7-, 3, 1050 CuZrF6 CUZrF6,3,427 cui 8 . 5 [Cul 5F6]2-,5,744 C~ZA~C~ZHZSC~N~~S {Cu(salen)}zAg(C104). 5. 826 CUASZCZOHJZIZN~

572.583 578 C U ~ B ~ C ~ ~ H ~ ~ N ~ ~ {cu{HB(~SN=CHCH=CH),})~. 2,254; 5,553 CuzBzCisHzoNizOz CuZ{HB(fiN=CHCH=~H)3)202, 5,578,717 Cu7Brl [CuZ”Br3]-, 5 , 563, 585 Cu2Br, [Cu,Br,]-, 5,585 [CU,B~,]~-, 5, 553 CuZCHO4 Cu2(OH)(C0,),2,448

- . .-

Cuz(OAc),, 1,268,274; 5,634,716 [CU~(OAC)~]’ , 5,634 CU2CBM1 2 0 1 3

CU~(O,CCH=CHCO~)~(OH~)~,~,~~~ Cu,CRH,,CI,N,O4 {Cu(BDMG)C12},, 5,662 Cu&Hi,Cl,N404 CU~CI~(HZDMG)Z, 5,624 CU~CSH~~OIO C U ~ ( O A C ) ~ ( H 2,441; ~ O ) ~ 5,282,552,564.634: , 635, 657; 670; 6, 1022 CUzCpH,,N6 [Cu2{h’(CH2CHzNIIz)~}(CN)zI2+, 5,729 CU&H~~CI~N~ C U , C I , ( M ~ N H C H ~ C H ~ N H 5,624 M~)~, CuzGH,,N,Oz [Cu2(en)2(CO)Z(cn)lZ+,5,583 [Cu,(en),(CO),] ’ .5,567 Cu2C8HJsC13N4P2 Cu{(NPMe2),H}CuC13, 5,606 CUZCSH26C12N6

[Cu2(dien),Clz]*+,5,624 Cu2CsHxN6 [ { C ~ ( d i e n ) ) ~ 5,609 ]~+, CuzC,HioF6O,

Cu,(HOMe),(CF3COCHC0CHCOCF3), 2,399

CUZC~H~~N~ ICu,(N,),( Me5dien)J+, 2, 227 Cu,G,,H,,,Br4N202 Cu,Dr,(py N-oxide),, 5 , 623 CULC~O oC12Nz H~ Cu&(py)*. 5,644 Cu2CloHloN4O8 Cuz(ppN-oxide),(O,NO),, 5,628

CuzCioH1zNz0sSz

356

',Cl},, 5 , 553

[Cu2(TMEDA),(N3)(OH)]2*.5. 675 CU,CnHnNsO6

ICu(dien)(C204)Cu(OH,)2(TMEDA)]2 ', 5,660

Cu2?l,(4-Me-l ,8-naphthyridine),, 5,587 Cu&&i6Nz0a C U ~ { ( ~ - ~ - ~ - ~ ~ C C ~ H ~ C H = N C H5,659 ~)~)(OHZ)~,

C U , { N ( C H , C H ~ N H ~ ) ~ }5.631 ~C~~, Cu2Ci3HiiCINzO5

GU~{~,~-(O~CCH~N=CH)~-~ 6 ,-158 OC~H~M~}C~,

[ (Cu(TMEDA)(CO)},CI]'. 5,567 CU~Ci4H3zN406 { CU(M~~NCH,CH,NM~,)(I-I,O)),(C,~~). 3.565

[Cu2~{(Me,NCH,CH2),NMe}z(N3)2]Z+, 5,629 [ C ~ ~ ( M e ~ d i e n ) 2 ( N ~5,673 ),]~+, CUZC~~HZ~N~O~

[C~~{4,5-(2-pyCH~CH~N=CH)~in~Idazole)(H~O)~]~+,

[CU~(TMEDA)~(C,O~)(OH~)~]~ ' 5,626,640-662 CU~Ci4H36Ndh [CU~{ N(CH2CH2NH2)3}2(NC0)2]2+,5.62Y ~ C ~ , ( t r e n ) ~ ( N C 0 ) , ]2,231 ~+,

6, 1% CuzCzoHisNiOz [{Cu(bipy)(OH)),]2' .5,624,660, 662 CuzCaoHz iN 5 Cu2(CN),(4-Mepy),, 5.563 CuzCzoHzzCW20s

Cumulative Formula Index

357 Cuz(OzCCHzC1)4(3-Mepy)2, 5,635

C~,(OAc)~(2-Mepy)~. 5.635 C U Z C ~ ~ H ~ ~ B ~ ~ N ~ S ~ CuZ(2-pyCHzSBu'),Br,, 5 . 628 CU~C~~H~;B~~N~S~ { Cu{2-pyHCHzSBut)Br2)*.5.553 CuzCzoHwN403

[CU,(TMEDA)~(~-P~CO~)(~-CO)] , 5,567; 6,395

_ Cu2C24H48N

IO

[ C ~ ~ { N ( C I ~ ~ C l l , ~ H ~ ) , } ~ ( b ~ 5,622 nzid~ne)~~+, C~ZC24H4804 Cuz{0(CH2)3NHCMe2CH2C(Mc)=N(CH2)30}2, 6, 164 CuZCZ4H50N10

[Cul{(MezNCH2CH2)2NMe),(biimidazolate)]z+, 5,629 CuZC24H5ZN803 [CUZ{N(CH~CH~NHCH~CH,OCH,CHzNHCHZCHz)3N}]"-, 2,938 CUZC24H52N804 ICu2{(HON=CMeCMe2NHCH2)2) 12', 2,274

Cu,~,,H,,N,O,

.

.

CuzCl2 CU,CI,, 5,746 CuzCln [CU&-, 5,563,585 CU,CI, [CU2CL12-, 5,623,643 -_ CU,Cl, [CU~CI,]~-, 5,696 CUlClR [ C U ~ C I ~2,679; ] ~ - , 5,627 CUZCOC~~H~~N~S

[(~(en)2(H2NCHzCHzS)}{C~(NCMe~)2}~16-, 4,848 Cu2CoSnCloH1404 CoC~~Sn(y-Ac0)~CpMe, I , 122 CuzFb [cu2F6]-, 5,744 CUzH3NO6 Cuz(OH3)(ON02),2,428 CU2H3N306

(CuC1{(PhO)3P)}3, 1,542 CU3C75H63P6 {Cu(Ph2PHCPPh2)),, 5,572 CU3C75H66C12P6 [C~,Cl,(dppm)~]’, 1,145,2.685; 5.556 Cu3(dppm),Cl2,5,583,585 CU3C75H6613P6

Cu3(dppmj2I3,5,585 CU3C75H670P6 [C~,(dpprn)~(OH)]”~ 5,556.584 CU3C80H75P4S3 Cu,(SPh),(PPh,),, 2,528 CU~C~OH~SP~S~ (CuPPh3)2Cu(PPh3)2(p-SPh)3.1,142 C~3C93H78 {Cu(Ph,PHCPh,)),, 5.556 . . CU3Cl5 [Cu,CI,]-, 5,589 cuScl6 [Cu,c1,12-, 5,587 Cu~CrCl14HyoOyP& Cr{(C,SO,)Cu(PPh,),} z , 3,901 Cu3H21207

Cu3(0210)2(OHZ),2.426 C~3H3C103 Cu,(OH),Cl, 6,855 CU3H3NO6 Cu3(0H)3(0N02),5, 619 Cu3HJ208 C ~ ~ ( O Z I O ) ~ 2,246 (OH~~~~ CU~I~ZCWHRIN~’~

[I~,CU,H~(M~CN),(PM~~P~)~]~-, 4, I164 Cu,MoBr,S, [(CUB~),(MOS,)]~ , 2 , 566 CU~MOC~~H,,B~OP~S~ ( C U ~ M O S , B ~ ) ( P P ~2,566 ~)~O, Cu3MoC54H45C10P3S3 (CuPPh3)3(MoOS3)Cl,2.568 (Cu3MoS3C1)(PPh3)30.2.566; 3,1422 CU~MOCS,H,~CIP~S~ ( C U ~ M O S ~ C ~ ) ( P P2,566,567; ~ ~ ) , S , 3, 1422 CU~MOC~~OS~ [ ( C U C ~ ) ~ ( M O O S ~2,566,568; )]~-, 3.1422 Cu3MoC13S, [(CUCI)~(MOS~)]*~. 2, 566.569; 3, 1421; 5, 572 cU306s2

cu2(so3)cu(so3),2.429,5,588 Cu,06Te Cu,(O,Te), 2,431 cu30Sp2

CuRSIs [cu.&]3- 2.541; 5,556 Cu3Te0, Cu3(Te06).5 , 651 cu3wc5,H45cIoP3s3 { Cu(PPh3)13C1S3(WO), 5,572 ( C U ~ W S ~ C ~ ) ( P P 2,566 ~~),O, CU~WC~~H~SCIP~S~ ( C U ~ W S ~ C I ) ( P P2,566 ~~)~S, cu 3WCI 3sa [(CuCl),(WS4)J2-,2, 566; 5, 572 Cu,WO, (3U,W06. 5,651 Cu3ZrZFi4 Cu3(ZrF,j,. 3:428 CU~AS~C?~~H& {CuI(AsEt,)},, 5,559,583,585 Cu4As4Ci2H6J4 Cu,l,(A~Phg),~5, 583 Cu4Br, [Cu,Br,]’-. 5- 557

cu4czcIIo6

Cu,Cl,(C03),, 5,718 CU4C6H9C14E;30L Cu,Cl,O,(MeCN),. 6,392 Cu,C,H,& [CU4(SMe)6]2 , 1, 150 CU4CSHZ1N12S6

[CU,(H~NC:SNIl Z ) 6 l 4 + , 1, 150; 5, 559 Cu4C6N6 [ C U ~ ( C N ) ~5,] 729 ~--~ CU~C~FI~O, CU,(O~CCF~),, 5,557,584 CU4CBH24Ni2 Cu4(MeNNNMe)4,2,200,201; 5,557 CU4C9H36N18S9 [CU.,(H~NCSNH~)~]~+, 1,151; 5,557,559, 584 CU4C10H40NZOS10 [CU,(H,NCSNH,),,,]~+,1,151; 5,556,572 cu,c,,l~&lss, CU,{S(CHJJ)~CI~, 5,589 CU4C12H3014S3 Cu,I,(SEt2),, 2,555; 5,559,584,585 CuXi.X,,O, { CU(OBU~)}~. 2.348

DyC$l12N30,jS-, Dy(NCS),(H,O),, 3, 1076 DYC~HZ~N~O~ [Dy(H2NNHAc)3(H20)3]3 ' , 3 , 1090 DYC&~, D~(Bu'COCHCOBU')~, 2 , 3 7 3 : 3. 1078 DYC~,H&, Dy(13u'COCHCOBu')3(H20), 1.51 DYC~~H~SN~O Dy(octaethylporphyrin)(OH), 2, 822

362

E ErCAH70, [Er(NCS)# , 3 , 1073 ErCsHz6N80s [Er(HzNNHAc)4(HzO)j3+,3.1090 ErCioHi6NzO1o [Er(H,O),(edta)]-, 2,783 . ErCisHz70 ErCp,(Bu')(THF), 1, 144 EG8HsoNiz07 [Er{OC(NHMe),}6(H20)]3+,1,73

EuClz(terpy), 3. 1111 EUCI,H~IO+ EulacacL, 3.1077

Ec20H4F2408

[Er(hfa~ac)~] , 3 , 1081 E~CZ~H~~N~OIQP~

Er(N03)3{0PPr'2(CH2CONEt2)}2(HzO), 3, 1084 ErC24H56N808 [Er(DMF)8]3*,1,286 ErC3,H16C1N8 Er(phtha1ocyanine)Cl.3. 1095 ErC3,Hs706 E~(BU'COCHCOBU')~, 1,65.66: 2,373,385; 3,1078 E~C~~H~SN~O Er(octaethylporphyrin)(OH), 2. 822 ErH8CI2O4 [ErCI,(H,O),]+, 3. 1074 ETH,I,O, [Er12(HzO)41' ,3, 1074 ErH1ZCi3018 Er(C104)3(HZO),,3. 1074 ErMn2H4 I

_

[Eu(CiO,)($2;2-~ryptate)]~+,3, 1098 EUC18Hd206 [Eu( 2 ,2,2-cryptate)lz+,3, 1113 [Eu(2,2,2-cryptate)13+,3, 1097 EuCI~H~~N~S~~ Eu{N(SiMe,),},. 3,1072 EuCzoHJw 0 s [Eu(hfacac),] . 1,94 EUCZOH40N4S8 [Eu(S,CNEtz),]-, 3, 1087 EuCzoH,,N,O,Si, Eu{N(SiMe,),},(THF),, 3,1111 EuCZOHs6NZO4Si4

Eu(N(SiMe,),},(MeOCH,CH,OMe),, 3, 1111 EuC2,HgN30,, [Eu(2,6-(0zC)zpy},13--,3,1090 EG~HIZF~W, Eu(thenoylCHCOCF,),, 2,373 EUC,4H16CI2N, EuCl,(phen),, 3, 1111 EUC24HibN109 Eu(NO,)dphen),, 3, 1109 EUCZ~HZVN~Q Eu(acac),(phen), 3,1079 EuC30H7.706

Eu(PhCOCHCOMe),, 3, 1079 EUC30H3oFz106

Eu(CF~CF~CF~COCHCOBU')~, 3, 1078, 1079, 1104 EUC32H48N204 Eu(Bu'COCHCOBuf),(py),, 3, 1079 E u C ~ ~ H ~ ~ N ~ S ~ ~ Eu{N(SiMe,),} 2(bipy),, 3,1111 EUCmHsd& Eu(Bu~COCHCOBU')~, 1,408; 3, 1078, 1081 Eu'&6HzuF$JiO& Eu(SCH=CHCH=~COCHCOCF,),(phen),3,1081 EuC&,,;"I,O Eu(octacthylporphyrin)(OH), 2,822 EGJLsWO, E ~ ( N 0 ~ ) ~ ( 4 , ~ ' - B u ' ~ b3, i p1070 y)~, EuC36H90N202Si4 E U { N ( S ~ M ~ , ) ~ } ~ ( P3,111 B U ~1) ~ ,

363

EUC36H108N1806Ph

Cumulative Formula Index

E;C38&,707S' -'

Eu(Bu'COCHCOBu'),(O~CH,C~Me2~Hz). 3, 1080 EUC40H3608

IEufPhCOCHCOMeL-. 3. 1081

Euitetraphenylporphyri")(acac), 2.823; 3, 1095 E~C54H45C1303P3 EuC13(OPPh3),.3, 1082

364

FCIZ [FCI,]', 3,314 F5N20,S4Xez [F{Xe{N(SO,F),},]]'. 3.319 F~A~,CII~H~OO~'& Fe(02C2S2)3{Ag(PPh,)l}3. 5.816 FeAsC4H6N03 [Fe(AsMe,)(CO),(NO)], , 1, 125 FeAsClsHl5Cl3 Fe(AsPh,)CI,, 4,226 FeAsCZ2H19 FcAsPh,, 1, 127 FcAsCoMoWC,H,S CoFeMoWS(AsMe,). 4,832 FeAsHI3N3O2 Fe{As(O)(OH)Me](NH,);. 6 . 1018 FcAszC,H,,ClzSz FcCI,(SAsMc,),. 4, 12-10 FeAs2CloH16CI, FeCl,(diars), 4, 1234 [FeCl,(diar~)]~+, 4, 1234 FeAsZCloHl6I2 FeI,(diars), 4, 1234 FeA~2C121T16Rr203 FeBr,(CO),(diarz) 4. 1234 F~ASZCI~HI~O~ [Fe(CO),(diars)] * , 4, I198 Fc(diars)(CO),, 1.17 FeAb2C39H3003 Fe(CO),(AsPh.,)?, 4, 1199 FeAs2C14H25N,S? F ~ ~ A S M ~ ( C H , C H , C H , A (NCS),, S ~ ~ ~ )4,226 ~} FeAs4Cl,H,6CIOs [Fe(ClO,)(OAsMe,),j-. 4, 1153, 1337 F~AS~CI~H~~S~ [ F ~ ( S A S M ~ , ) , ] ~4,* ,1240 FeAs4ClSH&I2 [ F e { A s ( C H , C H 2 C H 2 . 4 s h e * )',~4,226 ~~~~~ FeAs4C20H32C12 [Fe(diars)2CIZ]+. 4: 266 [Fe(diar~)~Cl,]*'. 4,266, 1183.1137 F~AS~C~~H~~CIZO,Z 2, SO0 Fe(C104)2((3AsPh~)4, FcAuCZ1HlSNO4P AuFc(CO),(NO)(PPh,). 4. I 'I 8'1 FeAuC,4H,oO,P Au(PPh,) { Fe(CO),) (q-C,H,). 5.904 F~AUC,~H~~NO~P~ AuFe(CO)z(NO)(PPh3)2.4. 1189

FeCo,(C0)9(p2-C0)3(I"j-;\UPPh3), 5,908 F ~ A u ~ C ~ ~ H ~ ~ ~ ~ P ~ Au~(~,~'-C~H~PP~~)~FC(CO),, 5.905 FeAu2C4,1H3,,04P2 {Au(PPhl)}ZFe(C0)4.5.905 FeAu,C,,H,,P, [ { ( A U ( P P ~ ~ ) ) ~ C ~ H , ) F5: ~C 899 :~~C: FeBC,H6N0, Fe(BNMe,)(CO),, 3.99 FeBC8Hl0NO, Fe(BNEt,)(CO),, 3.99

FcBC,;H,,N,O; Fe{HB(*N=CHCH=C'H),} (CO),(Ac), 2 , 2 5 1 FeBC,,H,,N 0 F e { H B ( N ' ~ H ) , } ( C O ) , ( O C C H C H h l e ) . 2. 75 I FeBC16H34F4N4 [Fe(hesamethyl- 1.4,5,11-tetrdazacyclotetradecane)(BF4)jt, 4, 1251 FeBC,sH9FN603P [Fe{FB(ON=CC,H,N),P}]*+ , 4, 1232 FeBCI9HIsO2 Fe(BPh2)(CO),C,p, 3, 100 FeB2r4IIIOI [Fe(BZH5)ICO)41~, 3,101 FeB2C',H4F,N, Fe(ChH),(CNBF,),, 4, 1205 FeB?C7Hlo02 Fe(B2Hj)(C0)2Cp, 3, 101 FeB2C14H42.U,0,2P4 Fe(BH,CN)2{P(OMe),}4, 4,1234 FeB2Cl8HloNl2 Fe{HB(kY=CHCH=cH),),, 2,251,256 feBZC30H43N12 FC{ H B (I\;=CMCCH& ~ MC),}*, 2.25 1 FCB~C~FISN~ [Fe(CNBF,),]* . 4 , 1205 Fe BrC1; [FeClJ3r] , 4 2 4 8 keBi tCI, [FeCI,BrJ. 4.248 FeBr,CI [FeCIBr,]-. 4.248 FeBr, [FeBr,]-. 4.218,248 FsCH,,NO,S [Fe(H,O),(NCS)]*+, 1,332 [Fe(H20)5(SCN)]2+,4,1180 FeCNS [Fe(NCS)]'+. 3, 842 FeCO, [FeC0,I2-, 3,46 FeC,H,CIN& FcCI(S2CNH2),, 4, 1183 FeC2HjCtN302S FeCI { Mer(S)N H2} (NO),,2, (147 FeC2H6Cl2N,(l2 FeCI,(HCONH2)2,2,491,492 FeC2H61,01P2 Fe(C0)2(PH3)z12,4, 1197 FeC2H10C1,N2 Fe(NH2Me)2C12,4, 1210 FeC,H10hr6S2 4, 1248 [Fe[NH2NHCSNHZ)2)2+, FeC210t Fe(CO),I, 4, 1198 FeC',NIO, Fe(CO),(NO),, I , 290; 2, 100, 108; 4, 1188 FcC2N,S2 [Fe(SCN),]+, 6 , 823 FeC,O4 Fe(C,O,), 4, 1237

365

FeC3H606

Cumulative Formula tndex

FcC3H606 Fe( C2O4)(MeOH)( H,O). 4 1238 FeC3H903 Fe(OMe),, 2,346 FeCsN04 Fe(CO),(NO)l-, 2, 109, 118; 4, 1188. 1189 FeC4CI2N4 [Fe(CN),CI2l5-, 4,1201 FeC,F,04P 2, 1036 Fe.(CO),(PF,), FeC,H04 FeH(C0)4, 4,1198 [FeH(CO),]-, 2,215 FeC4H204 FeH,(CO),, 2,689 FeC4H~Olo [Fe(C20,)z(HzO)z]-, 6, 125 FeC,H6CI2N2 Fe.CI;(NCMe)2, 4, 1210 FeC4H8C130 FeCI,(THF), 4,227 FeC4HloBrzN2Sz FeBr2{MeC(S)NHz}2,2,647 FeC4HqoCI,N*S2 FeC12{MeC(S)NH2},, 2,647 FeC4Hl3Cl2 Fe(dien)CI,, 4, 1211 ’

FeC,N,O, [Fe(NCO),]-, 4,222 FeC,N,O [Fe(CN),(NO)IZ-, . . - 4, 1189, 1190 FeC404 [Fe(C0),l2-, 2,270,700; 4, 1183,1184 Fe(C.,O,), 2,455

366

FeC6H3K6 H,Fe(CN),, 4.221 FeC6H4N6 Fe(CN),(CNH),. 4. 1205 FeC6HSCl30Si FeCp(CO)(SiCI3). 2. 19 FeC6H503 Fc(T~-C,H,)(CO),. 4,1201 FCCgH503S FeCp(C0)(SO2). 2.035 FeC6H6F2O6P Fe(CO),{F,P(UOH3)2}. 2,1036 FeC6H6NOn Fe{(OZCCH2)3N}.1 , 122 beC,H6N6 [Fe(CNH)6]2’ .4.1204 FeC6H6N8S2 Fe(NCS)2(HfiN=CHN=cH)2, 4,1213 FeC6H60,S Fe(COj,(DMSO). 2.490 FeC.&N6 [Fe(CN),(cn)l2-, 4, 1206, 1225 FeC6H,06 Fd(OAC),, 6, 1017 FeC,H100$4 Fe(S2COEt),. 4, 1246 FcC,H ,,,S, [Fc(SEt)(S&SEt)(CS,)]’-, 4, 1246 FeC6H10S7

[Fe(CS,)(SEt)(S,CSEt)]+, 2, 590 FeC6H121N30S, Fe(NO)(S2CNMe&3r, 4, 1192 FeC6H12rY’202& Fe(SOCNMe,),. 4. 1245 FeC6Hi2N30S4 Fe(S,CNMe,),(NO), 2,103, 107; 4, 1192 I

. FeC,H,N;O [Fe(CN),(H2O)l2-, 2,Y [Fe(CN),(HZO)13-, 1,364,366; 2,9,297; 4.1190. 1204, 1205,1206; 6, 18 [Fe(CN),(H,O)l4-, 4,1201 FeC,HqF70,P Fe(COj,(F,POMe),2,1036 FeC5H3N6 [Fe(CN),(NH3)I2-, 2, 10 [Fe(CN),(NH,)I3-, 2,13,28; 4.1190. 1191. 1205, 1206 FeC,H,N,O [Fe(CN),(NH20H)]-, 4,1190 FeC,H,NO, Fe(z-C,H,)( CO),( NO), 2,106 FeCSH6N403 Fe(CO),(MeN=NN=NMe), 2. 218.220.222,224 FeC,N, Fe(CN),I4-, 4, 1201 FeC5N503S [Fe(CN),(SO,)]”, 4, 1205 FeCSN60 [Fe(CN),(NO)IZ-, 1, 122; 2, 103, 106, 109, 110. 114; 4, 1181,1182, 1189,1190,1191. 1206 [Fe(CN),(N0)I3-, 2, 111 FeC,N,OS [Fe(CN),(N0S)l4-, 4, 11%) FeC,NdO, [Fc(CN~,(NO~)]~ ,4, 1190 FeC,O, Fe(CO),, 1,41,288; 2,210; 4, 1198 IFe(CO),l+, 4, 1198

I .

Fe(ONHCOMc);,2.506 FeCJII2N,O3S4 Fe(NO)(S2CNMe2)2(NOZ), 4, 1192 FeC6H13C13N2 FeC1, (N(CH2CH2)3NH},4,1210 FeC6H1312N, Fe12{N(CH2CH2)3NH},4, 1210 FeC6HaN6 [Fe(e11)~1~+. 4.1211 [Fe(en),13*. 4.222.223 FeC6N,0 IFe(CN),(C0)13-, 4.1206 . - ~ Fe‘c$6 [Fe(CN),]’-, 4, 1182; 6,494,873,1017 IFe(CN)J-. 1.2,3,272,336,352,376,504,512. 553; 2 , i ,5 . 9 , I I , 12,84h; 4,220, 1182, 1185, 1186. 1201,12W. 1206; 6, 16, 17,22, 200, 124,494. 529, 530,621,652.822,830, 1017 1.253.273,333,336,349,352,361.509, [Fe(CN),]‘-. 512.539; 2.8.9, 11-13;4,220,526, 1180. 1181. 1187,1189,1201, 1204, 1205, 1206,1209, 1222;6, 17,22,24.30,124,496,652,822,847 FeC6N6O [Fe(CN),(CN0)I4-. 2, 13 FeC,N,O, [Fe(CN0),14-. 2.13 FeC6N,S [Fe(CN),(NCS)]3--, 4, 1190 FeC,N,S, [Fc(NCS),]?-, 4,222 FeC&,Se [Fe(CN),(NCSe)13-. 4. 1190 FeCgOeS6 [Fe(S,C,0,)3]3-. 4.246 . 1

367

Cumulative Formula index

FeC& 12 [Fe(C204)3]3, I , 309,471; 2.446; 4.229; 6 , 114, 117, 125,849, 1017 [Fe(S2C2SzCS),]~~. 2.621 FeC7H404S Fe(CO),(OSCH=CHCH=CH). 1.121 FeC7H51z02 Fe12Cp(C0),, 2,204 FeC7H7CIN302S FeCl{PhC(S)NH, } (NO),. 2.617 FeC,H7CI,O4 Fe(acac)(02CCC1,j, 2.381) FeC7HsN, [Fe(CN)s(en)]3-, 4, 1206 FeC,Hi,CI,N,O FeClJ{N(CH2CH2)3NMe}(H,O). 4. 1210 FeC,H,,CI,N, FeCl;'iN~CH2CHz)3NMe}(NH;j,4. 1210 FeC8FsNO5P Fe(C0)4{F2POC(CF3)2CV)r 2. 1036 FeCRF12S4 F~{sSC,(CF,),),, 2,615 FeC8HjNOzS FeCp(CO),(NCS), 2,231.238 FeC8H502S FeCp(CO),(CS). 2,238 FeCsH8OIz [Fe{2H,3R-o,CCH(OH)CHoCO,) {2S,3SO,CCH(OH)CH(OH)CO,)]-. 2,479 FeCsHl2CI2N4 FeCI,(CNMej,, 4. 1209 FeC8H12N202S4 Fe(CO),( S2CNMe2j ,, 4, 1245 FeC8H14N404 Fe(HDMG),, 4, 1231 FeCsH1601Si2 FeH(CO)3(SiMe,)(SiMez).2. 17 FeCsHZoC12NZ0 FeC'I2{0(CH2CH,NMc2)~}4, 1238 FcC,H,,,O,S, [Fc4S4(SCH2CH201 1)4]2 ,4,239 FeC8HZoS4 [Fe(SEt),lZ-, 4,237 FeCsHzZCl2P2 FeCI2(PEt,H),, 4, 1233 FeC8H22N804 Fe(HDMG),(N,H,),. 4. 1231 FeCsH2,CI,04S4 [FeCI,(DMSO),]+, 2,488.489: 4.227 F~CJL~NZP~S~ Fe{(SMe,P),N},, 4.1240, 1216 FeCBH26CIN6 [FeCl(dienj,]', 1 . 121 FeC,N,S, Fe{S,C,(CN)z}z, 2, hU3 FeC8N,0S, Fe(NO){S,C,(CN),},, 1,1193 [Fe{SzC,(CN)z~,(NO)l-,2.603 FeC9H,N60, [Fe(CN),(NCOCHCOMe)I4-, 4. 1190 FeC H P FeCp(PCH=CHCH=cH). 2,1044 FeC&i&iS6 Fe(S,COEt),, 4,241 [Fe(S,COEt),] ,4, 1246 FeC9H15SY [Fe(SzCSEt),] ,4, 1246 FCC~HI~~~PZ ' Fe(CO)3(MeZPCHZCH2PMt.2). 4, 1196 FeC4HisN,0,S3 Fe{SC(O)NMe,},, 4.247 FeC9Hd;S6

FeC I OH,,01 ips

Fe(S2CNMe2),.1.336; 4,244; 6 , 1017 [Fe(S2CNMe&]+. 1.336 FeC4H2,0, Fe(OPr'),. 2,353 FeC9H,,N,Q

[Fe{HN(CH2CH~NHCH,CH2NH2)2}CO]z+, 4 , 1211 FeC9H2,CI2O9P3 FeC1z{P(OMe)3]3,4, 1197, 1234 FeC9H2,ClZP3 FeC1z(PMe,)3, 4, 1197 FeC,H,,O,P, Fel12{P(OMe)3)3. 4, 1234 FeC9H3,,N, [Fc(H21\r(CH2),NH,},12+,4, 1211 FeClIIH6F I Fc(hfacac)2(H20)2, 4, 1237 FeCloH6N6 [Fe(CN),(2-pyCH=NH)I2-, 4, 1226 FeCloH8CI2N2 FeCl,(bipy). 4. 1221 FeCioHSN,O, Fe(2-Me-quinol1nolate)(NO)~,4, 1195 FeCloHlo FeCp,. 1.3,127. 131,332,336,351; 6,21,30.119 IFeCp,]'. 1.332,316,351

FC'~~~F~,~N~O~

[Fe(edta)] 2, 700; 6 , 25, 100, 652 [Fe(edta)jZ-. 2.784,7Y1; 6,24,652 [~e{(02C'CI~2)2NCH2CH2N(CHzCOz)z}]~, 1,336 [Fe{(OzCCH2)2NCH,CH,N(CH,C0,)2}]2~, 1,336,4. 692 FeCloH12N6 Fe(CN),(CNMe),, 4, 1209 FeCloHlgNzOs Fe(Hedta), 2,790 [Fe(Hedta)]-, 2, 784 FeC ,oH,4C104 Fe(acac),CI. 4. 230

[Fe{ ( O ~ C C H ~ ) ~ N C H ~ C H ~ N ( C(H,0)] H Z C O,~I ). ~ } 554,2,7S3,7XX, 4.253, 11x3, 1185 FeC1oH14O4 Fe(acac),, 2,371; 4, 1236, 1237 FeGoH,,S4 FerMeCSCHCSMe),, 4, 1246 FeCIoH,5N202 Fe(q-CSH,)(CO),(~NMeCH2CH2~ Me, 4, 1201 FeCloHYsN2O, Fe ( (O~CCH2)2NCH2CHZ( CH2C02H)(CH2C02)}(H,O). 2.783: 4.253

F~C~~H,QCI,N;'

FeCl,(~=CMeNMeCH=kHj,, 4, 1213, 1214 FeCIuFllbN2O2P, Fe(NO),(diphos), 4. 1 I94 FeCIoH,,N6 Fe{C(YH,)NHhle} (CNMe),, 4, 1209 FeC,oH20CIN2S4 Fe(S,CYEt,),CI. 1.273 FeC,0H20TN30S4 Fe(NO)(S,CNEt,),I, 4,1192 FeCI0Hz0N2S4 Fe(S2CNEt2)2,4, 1245 FcCI~HL,,N,OS~ Fe(NO)(S,CNEt,),. 4, I1Y2 FcC~(~H~~IO~P~ Fc(Ac)(CO),I(PMe,),, I , 120 FeC10H2JBr2N4 [Fe{Hfl(CH,),NI I(CH,),NH(CH,),NH(~H~)~}Br,l+. 4.2.56 FeCloH2,0 Fe(CO), (P( OMe),},, 4, 1197

&!I

Cumulative Fornliilu Index

1F14N06P

FeC,,F,,NO,P Fe(C0),{F2POC=NC( CF,),OC(CF&), FeC,,F2,02P3 Fe(CO)2{P(CF3)3)3,2, 1038 FeC, ,H202P Fe(q-C3H,)(CO),PEt,. 4. 1201 FeCIIHSN60 [Fe(CN),(ONPh)]?-, 4,1205 FeC, ,H,N,O [Fc(CN),{N(0)NPh)14 . 4 , 1191 FeC,,H,N,

2, 1036

FeClZHBF2N2 FeF,(phen), 4, 1221 FeClzHsN4C13 Fe(NC,H4CN)2CI,, 1,45 FeCI2H8S4 [Fe(l,2-S2C6H,),]* , 2 . 6 0 6 FeCI2Hl2 FeC:p(H2C=CHC5H4),6 , 16, 19 FeCJ I,,N2S2 Fc(SV6114NH2-2)2r4, 1248 Ft.Cl,H1,C'lzC)zt'2 FeCl,(diplins)(CO)?, 4, 1237 FcCI?Hl+,N,O, [F~(phen)(H,O),]~', 4, 1221 FeCllH16N20s [Fe(teta)12 , 2 , 784 F~CIZHI~P~ Fe(PCH=CMeCMc=cH)2, 2. 1043 FeC12H17N208 [Fe(Hteta)]-, 2, 784 ~~C~ZITI~BI'~N~ Fe(MeN=CRi C(Br)-LNMeJ,. 1.414 FeC1zH18N203

368

[FeC13{N(CH2CH2)3NH)2], ' , 4. 1210 FeC,,H3,,f3rK4 [FeBr{N(CH2CH,NMe3),}]', 4. 1183. 121 1 FeC,2H,,C1zP2 FeC12(PEt,j2.4, 1233 F~CIZH~ON~ [Fe(1,4,7-triazac~~lononane),]~+, 4, 1252 FeCI2H&l2P4 Fe(~le?PCH2CH2PMe,)zClz. 4,1197. 1234 FeCIzH32P4 Fe(~lrzPCHzCH,PMe?),, 4, 1197 FcC I2J-i.Jh(:I201:P? FcCI,{P(C)Mej,),, 4. 1233 FCC12Hj6C13018S6 Fc(CIO,),(DMSOj,. 2, 488 FeC,2H36NsOzP1 Fe{P(NMe,),},(NO),, 4, I189 FeC12H3606S6 [Fe(DMSO),j'+. 4, 1238 FeCdd'4 Fe(Phte3)4.4> 1197 FeC12N01z [Fe4N(C0),2]-.2, 118 FeC12NfA [Fe{S,C~,(CN),),J'.'. I, 63 [Fe(S,CI(CN)2)3]3, 4 . 245 FCC~~N,C),~ [Fe(violurate),)-; 4. 12% FeC13H6N601 [Fe(CN)s{NIO)CHCOPh}]4~~, 4,1190 FeC13H9V3S [Fe{2-pq'k=NC(py-2)CH$}]'+. 4,1229 FeCI3Hl2CI3N4 Fe(bip!)(H&N=CHmH)CI,, 2.94

[Fe(Hpeta)] 2.781 FeC13H2J403 I F e ( C 0 ) 3 ( ~ S M e C H 2 C H 2 ~ M e ), ?4 l, ' 3201 FeC13Ha3N7 Fe(CNMe),(IVleNHCNMeCNHMe), 4,1209 FeC13H24N503P [Fe(NChle),(P(Oh~lc),)j21~ 4, 1209 I+CI&,,F~O,P& Fe{S,C.,(CF,),) { P(OMc),) 3 , 2, h IS FcCIII I,N,C)S> F~(s,C,(UN1~)(bipy)(No), 2, 603 FeCI,H,?J, [Fe(CN),(bipy)] , 4 , 1186 [Fe(CN),(bipy)I2-.4, 1217, 1221 FeCI4H8N6O2 Fe(KCO),(J.-pyCN),, 4,1213 FeC,,H,O,S, [Fe(l.2-SzC6H4)2(C0)2]2-, 2,606 FeC14H,oN402 Fe(NO),(CNPh),. 2,110 FeC14Hlo06 F C ( ~ - O ~ C C ~ ~ 2.469 -I~(~II~,, FCCijHi 6C12N2Sl Fe{(2-pyCHZSCHl)l)C11,4,1247 F~CIJTT IS N ~ G < I [Fe(dtpa)13 ',2,788

__-_

Fc(CO),{Me,~N(Ms)C(MelC'(h.le)NMe}, 2 , 20X F~CIZHIHN, FC(CNMC)~. 4, 1208 [Fe(CNMc)#+, 4, 1208-1110 [Fe(NCMej6]2', 1,451: 4. 1204. 1210 FeCJ lz2N8 Fe(CNMe),(MeNHCNHNHCNHhle). 3. 1204 FeC1~Hd6 Fe(MeN=CHCH=NMe),. 1.424 IFe(MeN=CHCH=Nhle),l2+. 1. 456,4, 1223, 1224

F;(1:4,8,1 lltetraazacyclutctradecane)(NCS)z, 4, 1251 FeC12HL4SR [Fe(SCH,CH,SCH,CH,SCH2cH2j2]2+. 4. 1239 FeC1ZHZSCljN4 FeCI,{N(CH,CH,),N} { N (CH2CH2)3NH}. 4,1210 FcC12H26C12PZ FeC12{P112(C6tIl,)},,4, 1233

F~C,~H~,F,N~S~ Fe(SzCNEtzj2{S2C2(CF3)2}, 4,1246 ~

Cumulative Formula Index

369

FeC,4H,oN202S4 Fe(S,CfiCH,CH,CH,CHICH2)202. 1 , 5 7 FeCl4H2,N6 Fe(CNMCNEt),. 4. 1208 FeC14H,,IC'804 Fe(HDMG),( HfiCH=hCH=cH)2, 4. 1231 FeC14H2&12N2 FeCIz{N(CH2CH,),CHJ2,4. 1710

(CO)]"%4. 1252 FeC:,,H3,C1,02P2 FeCI,(PEt,),(CO),, 4*1233 F~CI~H&',O~P, [Fe(NCMe),{P(OMe),),]2+. 4.1210 FeC14H,oN6 4, [Fe(1,4,8,1l-tetraa~acyclotetradecane)(MeCN),]~+. 1251,1152 FeC,,H3,04P2S Fe(CO)2(PEt,)2(S02),4. 1197 FeCIJHJ2CN ~Fe(l,4,8,11-tc~raniethyl-l.4.8,1 Ir e t r a a z a c y c l o ~ c ~ r a d ~ c ~' ~,4, i e j1251 ~l] FcC14H36N5(3 Fc(NO)( 1. ,4 ,S , I I - t r h a m e t hq'l-1,4& 1I tetraazacyclotctradecanc), 4. 1194 FeC14H,,N703P, [Fe{P(NMe2),),(C0),(hO)]' . 4 . 1189 FeC14H42C13019S7 Fe(CIO,),(DMSO),. 2.488 FeC15H3F1806 Fe(hfacac),, 1,65 FeC 15Hl,F90,S3 Fe { MeC(S)=CHCOCF,}3$ 2: 651 FeC, 5H,,F,O, Fe(CF,COCHCC)hle),. 2.380 FeC~,,H,,CI,N, Fe(py),C:l,, 4,122 FeClSII 1 8 N 3 0 3 [Fe{ON-C(COMe)z},l-. 2.797 FeCI5H2,O3S:J Fe{MeC(S)CHC(O)Me),.4,746 FeCi,H,iO6 Fe(acac),, 1,65; 3,375.380.926; 4,229, 1185, 1186; 6, 127. 1017 FeCI5H2,S6 Fe{MeC(S)CHCrS)Me)j.4.246. 1216 FeCl,Hz2O6 Fe(acac),, 4, 1203 FcC,,FI,,NO Fc(COj( N-Cl
FeCMH26"l

FeC,,H,,C1,P4 FeC12{P(CH2CH2CH2PMe2)3}, 2, 1014; 4. 1235 FeCIFH?lOliPJ Fe-(CO){P(OMe),},, 4, 1197 FeC, 5H35015P5 [Fe((hIeO),P(O)Me},]*+, 4, 1237 Fe{P(OMe),},, 4, 1197, 1234 [Fc(P(OMe)j},]2+,4, 1234 F C C I J L O14's [FeH{P(OMc),},]-, 4, 1234 Ft.Cl,H,7O,.lP, [Fc((McO),PO},(H,Ojl"'. 4, 1237 FeC,6F27Y*1;07P Fe(COjt(P(OC(CF,)3CN)3}, 2. 1036 FeC 16 HgN6 [Fe(CNl,(phen)]-, 1,539 [Fe(CN),[phen)]'-, I , 539; 4, 1219, 1221 FeC16H,N6S, Fe(NCS)2(HN=CHCH=NH)2, 4. 1223 FeCI,H,,04Te Fe(CO),(TePh,). 2.669 FeT,,H,,TIN,O, Fe(S-CI-salen)(NC)),4,1194 FeC,,Hl,C1N,02 Fc(salcn)CI, 4.250 FcClhH,,IN?O, Fe(salcn)I, 4 , 251 FeCl6H,,Y2O2 k(:e(salen).4. 251 [Fe(~alen)]-~ 4.251, 1202 FeCi,H,,N,O, Fe(salen)Ol. 4.251 F~c,,H,,Y~s, Fe{(7-SC6H,CH=NCH2),). 4. 1248 FeC,,H1,h~O, Fe(S& j(NO), 4, 1194, 1238 FeCl6HI5NO6 Fe (CO), { PhCH ( Me)N=CHCOIE I } 2 755 P2(:,,1 I,,c:lK,02 Fc(sfilcn.I-l)C:I, 4, 252 FcC16HraSd [Fe{1.2-rSC,H2)2C6H,/2]-, 4,235, '12411 [Ftt(l.2-(SCHZ)2C,H4)21'~ , 4 , 1240; 6, 627 FeC16H16S6 [Fe2S2{1.2-(SCH2)zC6H4}2]2-,4,236 FeC,,HI8N2O2S4 Fe(S1COEt),(bipy), 4, 1246 FeCl6Hlsli40& Fe(4-Acpy),(H2O),(NCS),, 2,23 1 FeC lhH22N40L [Fe{fi=CMeCOCH=N(C~,),"CHCOC( Me)= WH1),}(MeCN),]*', 4,257

FeCI6H2,Cl2N6 Fe(Hr;lN=C~~eCH=~H),C1,, 4, 1213

[Fe{2,h-py(CHMeNHCH2CH2CH2),YH}CI]+, 4, 1258 F~CI,H~~NIO

Fe{2,6-py(CHMcNHCH2CH2CH2),NH) (N,),, 4, 1258 FeC15H30N303S3 Fr{SC(O)NEt2j3,4 , 2 4 7 FeC1511,0N,S, Fe(S2(:NEt,),, 4.144 [Fe(SzC:NEtl)31'.:4,266. 1187 FeC,,H,,N, [Fe { fi=ChieCH2CH=N(CH2),N=CHCH2C(Me)= -H2)2)(MeCN)z]2+. 4,257

Cumulutive Formula Index

FG6H26N6

FeC& N6 [Fe(NcCMeCH,CH=NCH,CR,h'-r HCH,CMe= =H2)(MeCN),I2*. 4.1256 FeC16H2704P Fe(C0)4(PBut3),4, 1196 FeC16H~704P3 Fe(CO),(PBu',), 2, 1036 FeC16H28C1N4 [Fe(fi=CHCH,N=CMeCH,CMe,N=CHCH,N= CMcCH,CMc,)CI]'. 4, 1251 FeC16HzsN4

[Fe(64=CHCH=NCHMeC:HJCMe,N=CHCH= NCHMeCH,cMe,)]', 4. 17132 [Fe($=CHCH=NCMe,CH,Cn?VleV=CHCH= NCMe,CH,CHMe)l2+. 6. 165 [Fe{&=CHCH=NCMe2CH,CH.VeN=CHCH= NCMe,CH2~HMe)lz+. 2. 905 FeC1,H29CIN30S2 [Fe{2,6-py(CMe=NCHzCH2CH2SCH2)2}(MeOH)Cl]'-, 4, 1260 F~CI~H~ONZ~~PZSZ Fe(NCS),(PEt3),(C0),, 4, 1233 I

_

FeCdhN4 IFe(~=CMeCH2CMe2NHCHZCH2N=CMeCH2CMe2NHCH,~Hz)]2'.6. 165

[Fe{&=CMeCH2CMe2NH(CHz)2N= CMeCH,CMe,~Hr~H,)2:.13-~ -~ _ . 4.257 FeC16H34C12N4 Fe(hexamethy1-1,4,8,11-tetraazacyclotetradecane)Clz, 4, 1251 FCCI~H~SNZ

370

Fe(cod)(PMe,),, 4: 1197 FeC17H4sNOlsPs [Fe(NCMe){P(OMe),},12-, 4, 1209 FeC18H10~30S4 Fe(NO){S,C,(CY),} {SzC2PhZ}, 4,1193 FeClsHllN8 [Fe(terpy)(CN),] -. 4 1222 FeCIRHl& [Fe(1,2-0,C,H,)3]3-. 4.230 FcC,~H~~CI,NI FeCl,(quinolinc),l 4, 1213, 1214 FeC,,HISCl3P Fe(PPh$)CI,I 4.22h FeCl8Hl5NeS3 Fe(py),(NCS)??4+222 FeC,,H,&03 Fe{ 1,2-(MeCOCAcC=N),C6H4}(NO), 4, 1195 FeCl8Hl8N2O2S4 Fe(S,CO€t),(phen). 4, 1246

,

..

FeC&2.,I\'&. Fe(NCS),($(CH,),N=~&=N(CH,),S}, 4. 1228 FeCI8HZ4Nl2 [Fe(H&CH=NCH=~H),]Zi, 4, 1213,1214 [Fe(HdN=CHCH=tH),I2+, 4, 1213,1214 FeClsH2SN7S2

Fe{2,6-py(CMe=YCH,CH,NHCH,),CH2)(KCS),,4. 1260

[Fe(1,4,8,1l-tetrainethyl-1.1,8.11t e t r a a z a e y c l o t e t r a d e ~ ~ n e ~ ( N*,~4,~ ~1251 e~1~ FeCi6H3606 [Fe(THF)4(H20)2]q ' ,4,227 FeC16H4~015P~ [FeMe{P(0Me)J 4, 1234 FeCl7H,N,O7 Fe,(CO),(bipy). 4, 1196 FeCI7H1A" Fe(bipy)(q6-toluene),4, 1196 FeC17H20N6S2 Fe(NCS)2{(2-pyCH2NHCH,)zCH,}.4. 1227

F~c,,H,,N,o,S,~

3-Me0-4-HOC6HSCH.-NNHCSNH2)Z(H,0),] *+ . 4.1248 FeC18H30N6 [Fe{&=C51eCMe=N(CH2),N=CMeCMe= mH2)3}(MeCN)z]2+, 4, 1254, 1255 FeC18H3~N& [Fe(2.2'-bi-2-thia~olinVl),\~+, 4,224

Fe{2,6-py(CMe=NCH2CH2C)CH2,2)(NCS)2, 4, 1260 FeCI7H2,N5S4 Fe {2.h-py(CMe=NCI l,CH2SCH2),) ( NCS)274, I247

NCI FeC18H3203PSil F e Q (CO),{ P(Si Me,),} (COBu') , 2 , 1050 FeC18H34N6 2,231,4. 1260 Fe(C15H23Ns)(NCS)2, Fe(hexamethyl-l.J,X,ll-tetraazacyclotetradecane)(CNL. 4. 1251 FeC17H2sCIN3SZ [Fe{ 2,6-py(CMe=NCH2CH2CIH2SCH2),) Cl]' , 4 , 1247 FeC,,H&
I

371

Cumulative Formula index

FeCl9Hl1N3S2 [Fe{2,6-py(c=NC6H4$)2}]2+.4, 1229 FeCl9HI5FO2Si FeCp(CO),(SiFPh,), 2, 19 FeC1&,N,Sa .___ Fe{2,6-py(CMe=NCH,CHzC~l~SC~,)~}(NCS),, 4, 1260 FeC19H4009P3 Fe(+CgHI)) { P( OMc),}, , 2 . 1036

F ~ C l , ( b i ~ ) ,4, ; 1220 FeCzoH&l& FeC13(bipy),, 4, 1221 FeCzoHd, Fe(bipy),, 4, 1196 FcCZOHlN,O,

Fe(Od=CCONPhN=~Me),(H,O).4, 1237 FeC20H18N6S2 Fe(NCS),{(2-pyCH2),N}, 4, 1227 FeCZOH2&12N4 FeCl,(py),, 4, 1212, 1214 FeC20HzoF2N4 FeFdpy),, 4,1221 FeC20H201ZN4

FeCzoI13,, Fe(C,Me,),, 1,351 [Fe(C,Mc,),]', 1, 351 [Fe(y5-C,MeS),]z+,1, 127 FeCzoHwN,

FeCZ4Hl6N4&

Fe(2-OC6H4CH=NOH),, 6,800 Fe(ONHCOPh)3, 2,505; 4,234 FeC21HT9N30Z Fe(salen)(pv), 4,251 FeC,, H,,N3Oz' 4, 1238 Fe{(2-OC6H4CH=NCH2CH2CH2),NMe}, FeCzlH3sF6N402 Fe(hexamethyl-l,~,8,1l-tetraazacyclotetradecane)(hfacac), 4, 1251 FCC22H1j 0 q P Fe(CO),(PPh,), 2 , 1037;4, 1196 FeCx,HiJ% Fe(bipy),(CN),, 1,506; 4, 1186,1217,122U. 1222 [Fe(hipy),(CN),]+, 4,223 FeGA6N602 (bipy),Fe(CNO)z, 2, 13 FeCz2Hl6N6S2 Fe(bipy),(NCS)2, 2,90; 4,1221 FeC22H,9N30S2 Fe{(2-SC6H4CH=NCH2),}(co)(py), 4, 1248 FeC22HZoC12N4 FeClZ{(2-py),CH,},, 4, 1226 FeC&zUN60Z Fe(NCO),(py),, 4 1212 FeCT2H2d6S2 Fc(NCS),(py)4,4. 1212, 1213 FeCZZHzON,Se2 Fe(NCSe),(py),, 4. 1213 FeC2zH22CIN, ~

~~

~

Fe(&C,H4NCMeCHCMeNC6H4NCMeCHcMe)CI. 4. 1256 FeCZ2H2& Fe(fiC6H4NCMeCHCMeNC,H,NCMeCHcMe) 4. 1256

FeC22H2,N,0s

F~{ON=C(COMC)~}~(~-M~~~),, 2, 797 FeClzHzsNs

Fe(fl==CMe-2:6-pyCHMeNHN=CMe-2,6-pV-

CHMcNH)(MeCN)2,4, 1257 FeCnH;ONh04 NCHMeCH2tMe2)(MeCN)z]z+, 4,1251, 1254 },]+, [Fc ~ j - o , ~ C 6 ~ , C ~ = N ( C ~ I , ) z N M e z 4.252 FeCZ2Hd4 FeC2oH34N6 [Fe(&=CHCH=NCHMeCH2CMezN= {Fe{ PhCH=N(CH,),NMe2} ,I+, 4,253 CHCHZNHCHMeCHz~Me2)(MeCN),IZ+,4.FeC22H32N10Sz 1254 Fe( NCS),( fi=CMeNMeCH=cH), ,4,1213 Fe{&=CMeCHzCMe2N=CHCH2K= F~CZ~H~, CMeCHzCMezh'=CHcH,) (McCN),, 4,256 Fe(q5-C5Me5)(q6-C6Me6), 4,1203 FeC23H2002P FeCZoH3&N6 [FC(& = C M C C H ~ C M C ~ N H C H , C H ~ ~ = Fe(q-C,H,)(CO),(PPh3), 4, 1201 CMeCH,CMezNHCHz~H,)(MeCN)Z12.,4, F e C d z iNzOi 1751 Fe(CH,Ph)(salen), 4,251, 1202 FCC~~H~~N~O Fe(VC,H,NCMeCtlCMe"CMe)(CO) 4, t 2% FeC20H40N404 Fe(hexamethyl-l,4.8, I 1-tetraazdcyc1otctradecane)FeC23H22N702 ( O A C ~ 4, ) ~1251 , Fe (2 ,6-py(CMe=NNMe)zphen-2,9} (H,O),, 4.1260 FeCzoH4oN6 FeC23H2& [Fe(hexamethyl-l,43,ll-tetraazacyc1otetradecane)[Fe{(2-ppCH=NCHz)3CMe}]Z+,6, 158 FeC23H26N60 (MeCN)JZt. 4. 1251. 1253 FeC20H49C1P4 C0)Fe( f;JC6H4NCMeCHCMeNC6H4NCMeCHCMe)( FeHCl(depe),. 4, 1234 JNH,NH,). 4, 1256 FeCzoH49NzP4 Ft.CZ4HSCll204 [FeM(N,)(depe),]+. 4. 1131 [Fe(OC6H2C1,-2,4.6),]-. 4. 230 FeC21~~12N906 F e C d1 ~ F ~ 0 3 S h [Fe(7-nitroso-6-indazololate),l-. 6.85 F~{SCH=CHCH=CC(S)=CHCOCF,}~,2,651,652 F~CZ~HI~CI~N~ FeCzlHl,C12N404 Fe(5-Cl-8-quinolinolatc),[NO)(DMF), 4. I 195 [Fc(phen),CI,] + - 4,223 F~CziHid303S3 F ~ C Z ~ H I J , ~ Fe{ONHC(S)Ph),, 4.234 FeF:(phen),, 4, 1220 FeC21H18N306 FeC241-I16NKh

[Fe(fi=CHCH=NCHMeCH2CMe2N=CHCH=

Curnularive Formulu Index

FG4H16N303

Fer 1.2-(PhCOCIIC'=N),C,H4](NO), 4.1195 FG4HI8Nl2 [Fe(2,2-bipyra~ine),]~+, 4,1228 FeCZ&LS4 [Fe(SPh),]-, 6,627 iFelSPhLIZ-,2,526,546; 4.1240, 1242:6,627 F~'C,~H,~N,O, Fe{2-flC H4CH-N 2 C H N-CH-7~ H ; } c " o i c 456 ~ L FeCJ%& (Fe(Z-pyt:=NCH=CIlrS H),j*+. 4. 1228

372

Fc(NCSc),(phen),, 4. 1220 FeCx,Hi&'JioO, Fe(NC0)2(4-pyCN)4.4,1213 FeC&isN6 Fe(CN),(phen),. 4,1220 FeC26H18N8S2 Fe(NCS)z(2-pv~=NC6H4~H),, 4,1228 FeC26H20N802 [Fe{2-phenC(NH,)=NOH}212+, 4,1229

FeCZ7H18N303 Fe(8-quinoiinolatej,, 1, 528 FeC2;Hi4N4S2 [Fe{(2-pyCH=NC,H4SCH2),CHz)l"', 4,1247 FeCZ7H2&O4 [Fe( 1,2-dirneth~l-7-nitros0-6-indazololate),]~+. 6.85

-

-,

.

FCC~~H~,,O,~S~ [Fc(S,C==C(CO,Et),),]-, 4.266 FeC2&6N402 1 [Fe(5-MeOC6H,CH=N(CH2)2Nh.le2)21-, 4,252

F&I,(Pk i(C6ki,1 ) 2 } ,, 4. 1233 FeCdb2C12N12012P4 Fe(C104)2(HMPA)4,2.500 FeC24H72N1204P4 [Fe(HMPA)4]2+, 4,1184, 1237 FeCz5HZ0N,O,P Fe(CO)(NO)(N,Ph)(PPh,), 2,134

FeC25i 145N5 Fc(CNBu'),. 1 . 4 1 . 4 , 1209 FcCZ;HWN~ [F~H(CNBLI')~]*, 4,1209 F~CZ~HI~C~,N& Fe(NCS),(Clphen),, 4,1221 FeC26H14N804SZ Fe(NCS),(O,Nphen),, 4,1221 FeC26H16N404 Fe(C,O,)(phen),, 4,224, 1185.1220 FeC~bHi6Nb Fe(CN),(phen),, 4, 1185,1218, 1219.122U [Fr(CN),(phen),]+,4,223 FeC26H7N 6 0 & FC { I-(~CH=CHN=C.N=N)-~-OC,~H,: *, 4,123~ Fd&H,6N& Fe(NCS),(phen),, 4, 1220.1221 Fe(SCN),(phen),, 4,1187 FeC&l&SeZ

FeC2,H44 Fe(1-norbornql),. 4.267,1183 FeC29Hz40ZZ Fe(COj,(dppe). 4- I199 FeC29H29N4S Ft.{&=CHC Ph)=CHN(CH,),N=CHC(Ph)= &H2),)(SPh). 4,256 FeC30CIJdAS3 Fe(uhr(S)cHC(O)C~,),,4.247 FeC,,,H ,,Br,F,O.& FcC3-BrChF14C(S)=C~TCOCF~]~, 2,652 Fe{4-BrC6H,C(S)=CHCOCF3},, 2,hSl,hS2 FeC30H15C13F903S3

Fe{3-CIC6H4C(S)=CHCOCF3},, 2,652 Fe{4-CIC6H4C(S)=CHCoCF,J,, 2,652 FeC30H~5F1203S3 Fe{4-FC6H4C(S)=CHCOCF~},,2.652 FeC30H15Ni301SS3 [Fe(l-ON-2-0-6-0,SCl,H,)3\4-, 6.85

Cumulative Formula Index

373

[Fe(terpy),la'. 4, 225, 1222 fFe(terpy)ij3+,4, 223,225 FeC30H22N802 IFe{2-phenc=NOC(Me)=N H}JZ+.4,1229 FeC30H2~C12N6 [Fe(bipy),]Cl,, 4, 1220 FeCmHz4N6 Fe(bipy),, 4, 1184, 1195, 1196 [Fe(bipy)J, 4,1196 [Fe(bipy),]z', I , 336,466,506,549; 4, 1195, 1215-1219, 1222; 6,23.494,520 [Fe(hrpy),13', 1 , 330; 4,223; 6.494,516,519,528 Fe(CN),(4,7-Me,phen),, 4. 1220 FcC~OH~~N~S~ Fe(NCS),(Me,phen),, 4.1221 FGoHz4Ns [Fe(2-phenc=NCH2CH2N H),lZ+, 4,1229 FeC30H26N804 Fe(Ofi=CCONPhls=~Me)2(py)2, 4, 1237 .. FeC30Hz7O3S3 Fe { MeC(S)=CHCOPh} 3 . 2 651 FeC3oH3oF2106 Fe{CF,(CF2)zCOCHCOBu'}3, 2. 375 FcC,oH,oN, [Fc(2,7-dimcthyl-l ,8-naphthqridinc),12 ' , 4 , 1212 IFe(py),12', 2,75.4. 1111, 1212 F
.

CHN(hH2),}(SCH2Ph),4, 256 FeC3,F16N8 Fe(perfluorophtha1ocyanine) 4. 1261 FeC32H12N8012S4 Fe{3,10,17,24-(O,S),pht halocyanine ) . 4 , 1202 [Fc{(O,S),phthal~cyaninc}]~-. 4,1265 [Fe(3,10.17,24-(O,Sj,phthalo~yanine}]~-, 4, 1202 [Fe{ 3,10,17,24-(O,S),phlhalocyanine)l6~, 4, 12112 FeC3,11,,C.IN8 Fe(phthalocyanine)C'I,4. 1265 F~C~ZH~~C~ZN~ Fe(phthalocyanine)Ci2. 4.1261 FeC?2H.161Ns Fc(phthalocyaninc)f,4, 1266 FeC32H16N8 Fe(phtha1ocyanine). 1.273- 910; 2,863,866,869,870; 4, 1184, 1201,1260-1265; 6,39, 192 [Fe(phthalocyanine)]. 2,867.868; 4, 1264 [Fe(phthalocyanine)I"-. 2. 870 [Fe(phthalocyanine)]"-, 2,868; 4,1261 [Fe(phthaIocyanine)l3- 4.1204 [Fe(phthal~cyariinr)]~-. 4. 1264 FeGzH,,NsO {Fc(phthalocyaninc)}20, 4, 1265 F~C3~HitiNsOi4S4 [Fe{(03S)4phthalocyanine)(H20)2]4 - ,4, 1205 FeC32H1&0t5S4 [Fe{(O,S),phthalocyanine}( I I2O)(O2)I4-,4, 1265 F e O ~

I

COC 7-M

FeC36H30N202P2

Fe(phthalocyanine)(NO), 2,867; 4, 1262 FeC32H23N403 Fe(8-quinoIinolate),py, 1,552 FeC3zHz$s [Fe(l .8-naphthyridine),lz', 4, 1183.1185, 1211 FeC32H2sC1zN404 {Fe(salen)Ci},, 4,257 FeC32H28N40S4

Fe(2-SC6H~CH=NCH~CHzN=CHC6H~S-Z)~O. 4.253 FeC3A&05 Fe(salen),O, 4,253 FeC,,H,,N, Fc(phthalocyanine)Me, 2, 869 F~C,~HJSO&

Ft.{3-MeC,H,C(S)cCHCOCF3}3,2,652

Fe{4-MeC6H,C(S)=CHCOCF,),, 2,651.652 FeC33H27C12NP2 FeC12{2,6-py(CHzCH2PPh2)2}, 4,1235 FeC33H30N12 [Fe(2-pyC&NNHpy-2),]Z+,4,1225 FeC33H34Pa FeCp(dppe)Et, 2,698 FeC3,H,,K80z Fe(phthalocjanine)(CO),, 4, 1262 FeCd,,N [Fe(phthal~cyaninc)(CN)~]-, 4 , 1266 FeC34H3004P3 Fe(CO)a{PPh(PPh2),), 2, 1037 FeC3,Hj004Si2 Fe(CO),{SiPh,C(Et)=CEtSiPh,), 2,19 FeC34H,2N6 [Fe(2~phenC==NB~')~]~+, 4, 1229 FeC34H33N404 Fe(protoporphyTin IX), 6,614 F~CMHMNS Fe(sapphyrin)?2, 889 FCCMH~S Fe(diethylhexamethylcorrole)(py), 2,876 FeC3,H,,'V,O2S Fe(phthalocyaninc)(DMSO)(CO), 4, 1262 FeC35H250zP Fe Cp(CO) (PCfh=CPhCPh=c Ph) ,2.1043 FeC3,H,,O7Pz 2,1036 Fe(CO){ P( OMe),) 2(q4-C4Ph4), FeG6HI6N8 Fe(phtha1ocyanine).6,25 FeC36H?iN&k [Fe(5-OzNphen)3]Z+. 4, 1216,1217 FeC36H23Y\1,02 Fe(phthalocvanine)(DMF)(CO), 4, 1262 FeC36Hd6 [Fc(phcn)3]2+,1,64,336,353,466,467,.506,538,549; 4. 1183, 1187, 1215-1219; h , 2 6 [Fe(phcn),13+, 1,154,336,353,524,538,544; 4.223. 1185; 6.516 FCC3tiH~N603 [Fe(phen ~V-oxide)~]~+, 4,1238 FeC36H24h'I 2 [Fe{2,4,6-py),-~-tria~ine},]~+, 4, 1230 FeC3tiH2,% [Fe(H,P; hen z+, 4,1217 [ F e ( 2 - p y ~ H ) 3 ] z ' .4,1228 FeC36H28CbN4 FeCl,(isoquinoline),, 4, 1214 F~C~BHZBNB~~Z Fe(phthalocyanine)(DMSO),, 4, 1262 FeCxHdrzP, FeBr,(PPh,),, 4. 1183,1233 FeC36HJOC1202PZ Fc(OPPh3)2C12,4, 1237 ~~

FeC36H3012P2

FeTz(PPh3)z.2,204 F~C~~H~ONZOZPZ

Cumulative Formula Index

FeC36H3&0d'2

374

Fe(octaethylporphyrin)(NCS)(py),

Fe(NO),(PFh,),, 2,114 FeC&3zNs

2,834

FcC,,H,,O, _- "" Fe(3.5-di-t-butyIsemiq~inone)~, 2,398 FeC4,H8CIFzoNT, FeCl{tetrakis(pentafluoropheny1)porphyrinJ,6382 FeC4,H2,N4 Fe(tetraphenylporphyrin), 2,8.52 FeC44Hz8C1N4 Fe(tetraphenylporphyrin)Cl, 2,820,834,844,845; 4,

[Fe(2-methyI-l,8-naphthyridine)4]2c.4,1211 FeC36H44C1N404

[Fe(octaethylporphyrin)(C104)]. 4,261 FeC36H44N4 Fe(octaethylporphyrin), 2,817,829 FeC3&46N4 Fe(octaethylchlorin), 2.852;6.625 FeC&46N603

Fe(NO)(meso-2,3,7,8,12,13,17,1X-ucracthyl-5nitroporphyrinato), 4,I194 FeCdLJ', [Fe{P(C6W,,)2}3]~~1 4,1233 FeC37H3804P2 Fe(acac),(dppe), 2,375 FeC37H46CIN4

Fe(N-methyloctaethylporphyrin)CI+2.849

261,1267,1268; 6,375,381,382,383 [Fc(te~raphenylporphyrin)CI]+,4,265; 6,618 FCC,~H~~CIN~O~ Fe(tetraphenylporphyrinj(ClO4), 2,424,820; 4,261 FeC,,H,,F,N, [Fe(tetraphenylporphyrin)F,]-, 4,260 FeC44HZBN4 Fe(tetraphenylporphyrin), 2,328,820,828;4-

12661268;6,614 [Fe(tetraphenylporphyrin)]-, 2, 836;4,1202 FeC44H28N40z Fe(O,)(tetraphenylporphyrin), 4, 1268;6,383 [Fe(tetraphenylporphyrin)( 0 2 ) ]4,261 -, FeC44H,,N,O Fe(tetraphenylporphyrin)(NO), 2,834; 4,1194,1267 FeC'44HZRNS03 Fe(tetraphenylpnrphvrin)( 02NO), 2,423 FeC441.130N10 Fc(phthaIocyaninc)(3-Mcpy),, . . - 2,867

FeC38H21N90 Fe(phthalocyanine)(py)(CO). 4.1262 FeC38H22N6S4 [Fe{ 2,6-py(c=NC6H4S),} 4.1229 F~C~SHZA Fe(phthalocyanine)(4-pyMe), 4.1262 FcCIXHZ1NZ04 Fc(9,10-phenanthroquinone),(bIpy). 2,398

F~c,,~,,N,o;

[Fe(~hen)~l(NCS),, 4,1221 FeC38H24N12 Fe(phthalocyanine)(HflCH=NCH&H)2, FeC38H301208PZ Fe(CO)2{P(OPh)3},I,, 4.1197 FeC38H3ZN40~ Fe(salen),(quinone), 4, 1238 FeC38H320ZPZ FeH,(CO),(PPh,),, 6,231 FeCsHH38N6

[Fe(tetraphenglporphyrin)(H,O)z]+,

4,1264

[Fe{$4=CPhCPh=N(Cll,),N=(3PhCPh=N(~ (MeCN),],', 4,1255 FeC3,H30C103Pz FeC1(CO)3(PPh3)z,4, 1199 IFeCI(CO),(PPh,),l+, . _ 4,1199 FeC39H3003P2 Fe(C0),(PPh3),, 4,1196.1195.1245;6.258 [Fe(CO),(PPh,)2]+,4,1183,1159 FeC39H3009Pz Fe(CO),{P(OPh),},, 4.1199 FeC,,H,&", Fe(phtha1ocyanine)(BUN El2),. 4.1262 FeC4,H5204 IFc(OChHMea-2,3,5,6)51~, 4. 230 Fec40H54N40 Fefoctaethvlchlorinl(THF1. 2.854 F~C~~H~~N,O Fe(octaethylisobacterlochlorin)(THF), 2.854 FeC4oH56N402 [Fe(octaethylporphyrin)(EtOH),j+. 4,261 FeC~oH6~08, FeH,{P(OEt),Ph},. 4,1234 FeC41H49C1Ns04 Fe(octaethylporphyrin)(ClO,)(py). 2. 834 FeG2HZ4F9O3S3 Fe{2-CloH7C(S)=CHCOCF3)3, 2. 652 FeC42H26Nl~ Fe(phthalocyanine)(py),, 2,869: 1.1262,1264 FeC4J%&" [Fe(4,7-Me2phen)3]2+, 4, 1217 [Fe(5.6-Me2phen)3]2',4,1216 FeC4zH4ZCIP4 [FeCl{(Ph2PCH2CH2PPhCH2)2}]+. 4. 1235 FeC,2H49N6S ,>

I

I

4,261; 6,618

FeC4,H,,N,U2PZ [Fe(CO)z-(X~Ph)(PPh3),]+, 2,134,136,141 FeC44H42N2P4Sz

Fe(NCS)2{(Ph2PCH2CH2PPhCH2)2}, 4,1235 ,

H&}

FeC45H28N40 Fe(tetraphenylporphyrin)(CO), 2,820; 4,1202,1268 FeC4sH,oCL%0 Fc( tetraphcnylporphyrin)(CCI,)(H,O), 4,1270 FCGSHJON~OK [Fe(4-0-3-ONC~HH3C02CoH4~~=CH~-4)~]. ,4, 1238 FeC45H3303S3

Fe(PhC(S)CHC(o)Ph),, 2,651;4,247 F~C~SH~~OG Fe(PhCOCHCOPh),, 1,65; 4,1203 FeC46H28N402 Fe( tetraphenylporphyrin)(CO),, 4,1268 FeC4,Hd6

[Fe(tetraphenylporphyrin)(CN)J, 4,260; 6,618 [Fe(tetraphenyIporphyrin)(CN)J-, 4,1268 FeC4hH42N2P4S2

Fe(NCS),{P(CH2CH2PPh2),},4,1235 FeC,,H,,CI, . . -N [Fe(octaeth~ypflr~hyrin)(3-Clpy),]+,2, 834 FeC'47H34N70 Fc(N0 tctra henylporphyrin)(MeNm= &HI, 4,1194 FeC4,H,,N7 {Fe(tetraphenylporphyrin)C(CN),J,, 2,834;6,618 FeC48Hd80 [{Fe(phen),}0l4-, 1,273 FeC48H34N6 ~

Fe(tetraphenylporphyrin)(&=CMeNHCH&H). 829: 4. 1267

2.

FeC48H34NGO

FeO(tetraphenylporphyrin)(Me&CH=NCH=kH), 6. 383 FeC48H34K70 Fe(tetraphenylporphyrin)(NO)( I-rnethylimidazolc),2.

834 FeC48Hd40 Fe(tetraphenylporphyrin)(THF), 4.1268 FeC4eH4&O~ [Fe(tetraphenylporphyrin)(EtOH),]+, 4,260

Cumulative Formula Index

375 FeC48H40N402S2

[Fe(tetraphenylporphyrin)(DMSO),]+, 2,820; 6, 618 FeC48H54N8 Fe( &=C(C,H,,)NN=(C, 6H10)=NN=C( C8Hl,)NN= (C~~HIO)=N}. 4.1258 FeC49H41N60 Fe(NO)(tetra henvl or hvrin){HN-H&}, 4,1194 FeC,,H,,N,S _" . IFe(tetraphenylporphyrin)(SPh)l .2,820 .. . . FeC,,,H,,NiS Fe(tetraphcnylporphyrin)(NCS)(pv). 2, 834 FeC&L4NR .. . . [Fe(2-phenC=NNPh2),]'C,4.1229 FeC50H36N8 [Fe(tetraphenylporphyrin)(imidx~ole)~]+,4,260 FeC50H41N60 Fe(tetraphenylporphyrin)(NO)(rl-methylpiperidine),2, 834 FeCszH4oN6 Fe(tetraphenylporphyrin)( I-methylimidazole),, 2, 820 FeCs2H40N60 Fe(tetrapheny1porphyrin)(py)(ONCHMe,), 4, 1268 FeC52H44N402 Fe(tetraphenylporphyin)(THF),, 2,820, 829; 4, 1268; 6,618 FeC52H44N4S, [Fe(tetraphenylporpbyrin) W H , } , ] +4,260 , Fe(tetraphenylporphyrinj{ ( H2)4}2.4,1268 FeCs2H48C1P4 FeCl(dppe),, 4, 1184.1198.1199

__

&

Fe(N,)(dppe),. 4, 1197 FeC5,H4,N8 Fc( tctraphcnylporp hyrin)-( 133CHICH2NHCH2CH&, 4. 1267 FGZH48P4 Fe(dppe),, 4, 1197 [Fe(dppe),]', 4, 1198. 1199 FeC52H49C1P4 FeHCl(dppe),, 4. 1198 FeC52H49N2P4 [FeH(N,)(dppe),]', 4, 1198, 1231 FeC52H49P4 FeH(dppe),, 4, 1183, 1198, 1199 [FeH(dppe),]+, 4. 1199 FCCSZHSOP~ [FeH,(dppe),]+, 4. 1198 FeC52H51P4 [ F e ( ~ z - , r 2 ) ( ~ ~ ) ( d p p e )4,, 11234 +. FeC53H480P4 [Fe(CO)(dppe)21'1 4. 1199 FeCSJ-1490P4 [FeH(CO)(dppc),]-, 4,1199 FeC54H34N10 [Fe{2-phenc=NN=CPhC(Ph)=A},]2+, 4, 1230 FeC54H38N6

Fe(tetraphenylporphyrin)(py),. 2.836: 4, 1268 [Fe(tetraphenyIporphyrin)(pj),]+, 2, 820; 4, 260 FeC54H42CIP4 [FeCI{ P(C6H4PPh2-2)3}] 4. 1235 FeC54H4~CM'4 2 , 1013 FeC12{P(C6H4PPh~-2)3}, FeCGIHIAN, _ . ._ " Fe(tetraphenylporphyrin)(Bu'NCj2, 4, 1268 FeCs4HsoN6 Fc(tctraphcnyIporphyrin)(piperidinc),, 2,829 FeCsAH,,NP4 [Fe(MeCN)(dppe),]+, 4. 1199

-.

FeCoW 1H2040

FeC,,H,P4 [Fe(C2H4)(d~pe)zl+, 4,1199 FeCS5HS7O3PS [FeHCP(oMe),}(dppe),]+, 4,1199 FeC56H3,N4S2 Fe( SPh)(HSPh)(tetraphenylporphyrin), 2,517 FeC56H42N2P4 Fe(CN),{ P(C6H4PPh,-2),}, 4, 1235 FeCshH,2N40,2 Fe~meso-tetrakis(2,4,6-trimethoxyphenyl)porph~rin} 2: 327 FeCssH36C12N4 [Fe (tetraphenylporphyrin)(C=C(C,f 14C1-4),)] 4. 205 FeC6,H,,N,05 Fe,(&&HC,H,NCH(OMe C6H4N= CHC6H4NCH(OMe) 6H4)0,4,258 FeC64H&804 Fe{(2-Bu'CONHC6H4),porphyrin}, 2,327 FeC68H66ClzP6 FeC1, (PhP(CH2CH2PPh2)Z}2, 4,1234 I

+

~

FeC68H70N1006

Fe{(2-Bu'CONHC,H4),porphyrin} (l-methylimidazole)(O,), 2,322,323,830: 6,320.665 Fe{(2-B~'CONHC,H,)~porphyrin)(2-methylimidazole)(O,), 2,322,830 FeC6BH71NB06S Fe(O,){~,H,),} {2-Ru'CONHC,H4),porphyrin). 2. 322 FeC7ZH42Nb018S6 [Fe{(03SC6H,), phen},lJ-, 4, 1217 FeC72H60C120 12P4 Fe(C104)2(0PPh3)4, 2,500 FeCnH6004P4 [Fe(OPPhs),l2+, 4, 1184 FeC76H96N408 Fe{ {Me(CH,)9C0,}4phthalocyanine}, 4,1266 FcCtN303 Fe(NO),CI; 4. 1193 FeCI,H,04 FeC12(H20)4r 4, 1250 FeCl2Y20, [Fe(NO),Cl,l+, 4,1194 FeC1,NO [FeCI,(NO)]+. 4,1194 FeCI, [FeCIJ, 1: 122,272,539,548;4,218.227.247,248. 1183; 6,802,803,808,814 [FeCl,]', 4,1182 [FeCl4I2-, 1,273; 4,1182,1184,1246,1249 FeC1, [FeC16]-. 1,111 [FeCI6l3-, 2 , l l ; 4,247,248 [ F C C I ~ ] ~2,- ,11; 4,1250 FeCI,OP FeCI,(OPCI,), 2, 500 FeC1,404P4 [FeCI2(0PCl3j4]+, 2,500 FeCIl8O6P6 [Fe(OPC1,)6]3+,2, 500 FeCoC8H,8N,2 [Co(KH,),(hCH=NCH=cH)Fe( CN)J, 4.699 F~COC~H~~N,~ [Co(NH, j (fi=CHCH=NCH=e H)Fe (CN),]-. 4.690 FeCoCllNll [Co(CN),(p-CN)Fe(CN),l"-, 4,650 FeCoC,,H,,N,OP, [Fc~CN),(~-CN)CO(CN)~(PE~,),(OH,)~~-, 4, 647 FcCUMOC~~H~O~S CoFeMoS(CO),Cp, 4,832 FeCoMoC&12,,0,S CoFeMoS(CO),Cp(PMePrPh), 4,832 FeCoWllH2040 3, 1048 [CoU', 1Fe(OH2)039]7-,

,

FeCo2C909Te

Cumulative Formula Index

FeCo2C909Te FeCo,(CO),Te, 2,671 FeCrC6Hl4NlOO CrlNH,),(H,O)(p-NC)Fe(CN)j. 3,778 FeCrC6HISNlI Cr(NH,),(p-NC)Fe(CN),, 3, 778 FeCrC,N, [CrFe(CN),]-, 4,1204 FeCrl-I,O, IFe(C)lI)(OH),Cr]3+, 6,852 FcCrH,O, IFe(OH)(OH),Cr(oH)]2 ' , 6 , 8 5 2 Fc CrH 0 [Fc(OH),(Oll),Cr(Ol~j]+,6,852 FeCY 121C),oS2 [Cr(H,0),(p-S,H)Fc(H,0),14-. 3. 877,882 FeCr,ClsHsOloP2 Fe(PCH=CHCH=cH)2{Cr(CO)3}2, 2. 1044 FeCr,H,O, ~ F ~ ( 0 2 C ~ 0 , ) , ( O H , )2,426 ]-, FeCr,S, FeCr,S4, 3,883 EeCuS, CdFES,, 6,784,787,853 FcCu,S, C'05FeS4,6,857 FcF4PZS, Fe(S2YFJ2,4, 1246 FeF, iFeF6l3-, 4,218,247 FeF,Si FeSiF,, 4, 1236 FeF,,P5 Fe(PF&, 1,41,4,1197 FeGeC3,H30N06P Fe(GePh,)(CO),(NO)(P{OPh),) .4.1189 FeG2H606 FeCie(OH),, 6, 849 Ft.Gt.1C IOHin04 Ee(CO)4(GeMe3)Z,2, 16 FcH05S Fc(OH)(SO,), 4, 1238 FcH2C150 [Fe(H,0)C15]2-, 1, SO; 4,248 FeH2F50 [FeF5(H,0)12-, 4,247 FeH4N208 Fe(N03)2(0H2)2. 2,414 FeH,O, [F&OH),]-', 2,305; 6,413 FeH, [FcH,]"-, 2,691.6Y3 FeH,C)S [Fe(OH),], ~,2,305 FeH6Cl20, FeCIZ(OHZ),,2,297 [Fe(H2O),CI,]', 4,227,247 FeHsOs [Fe(OH)J-, 2,305 FeHloCIOs [Fe(H2O),CI]*+,4,227 FeH ,,YO, Fe(H20)5(NO),4, 1184 ~Fe(tIzO),(NO)]Z+, 4, 1188. 1203 FeH ,,On [Fe(H20),(0H)]2'. 1,37U FeHlzOb (FC(H20)6]'+, 1,253,273,284,332.33s. 336, 337,344, 348,349,352,355,369.372. 379; 2, 9,11: 4, 1184, 1185,1204,1236; 5.682; 6,494

376

[Fe(IT20)6]3+7 1.272,284,309,335,336,337,344,348. 349.352.367.370,372,379; 2 , l l ; 3,1236: 4. 218.226,1180, 1185; 6,494,808 FeHISN,O [Fe(NH,),(NO)12'. 4,222 FeHlaN6 [Fe(NH,),]2+. 4,1210: 5,689 FeIN,O, Fe(NO),I, 4, 1193 Fel,N,O, Fe(IV0),i2, 4. 1194 Fe1,NO FcI,(NO). 4,1194 FeIn,C,,H,,Y,O, {In(octaethvlporphvrin)),Fe(CO)~,2,843 FeLiC45H9605 FeLi(OCHBu'z)l(HOCHBu',), 4,227 FeMnC,,Hz,N2 Feh;ln(Bu'NCHCHNHHBu'l. , . 2.215 FeMnC,;H,07PS2 (Me3P)(0C),Fe(CS,)Mn(C0),, 2, 582 FeMnCi,HiuNOA (ON)CpMn(CS,)Fc(CO),Cp, 2,583 FeMnC,4H1408PSZ {(MeO),P}(OC),Fe(CS,)Mn(CO),C:p, 2,582 FeMnC:2+tl18U51'S2 ( P h,,MeP)( OC),Pe( CS,)M n( CO),C:p, 2.582 FeMoClzH,,0zS4 [Fe(OPh),S2M~S2]2-, 3,1426 FeMoC12Ht& [F~(SP~),(MOS,)]'~, 2,565; 6,722 FeMoC2sH54C12N,S2 Mo(CNBu'),(p-SBuf)2FeC1,, 3,1425 FeMoC54H59NZP4 [Mo(q6-C6H5Me)(PPh3),(N,)FeCp(dmpe)]~, 3.1270 FcMoCI~OS, [ F ~ C ~ , ( M O O S , )2,565 ]~~, F~MoCI~OS, [FeC1,(MoOS4)]2~. 2, 566 [FeC1,S,MuO(S,)]2 . 2 , 5 7 0 FeMoClz02S2 [FeC12(MoOzS,)]z- , 2.565 FeMoCI,S, [FeC12(MoS4)]'-,2, 565,570,575 FeMoN202S, [Fe(N0)z(MoS,)J2-, 2,566 FeMoS, [Fe(MoS4)].-+ 2,565 FeMoS, [Fe(S5)(MoS,)]2-.2,542, 565 FeMo,C,H,S,, [FeS,{ MOS(SCH,CH,S)}~]~-, 3, 1430 FcMo,C,~~HBO~OP~ F~(PcH=cHcH=CH),{ MO(CO),} 2,1044 FCM~~C~,H&~S~ 3, 1430 Mo2(C5Mes)2S4Fc(CO)2. FeMo2C2,H,o0,S4 Mo2(C5Me5),S2(S,CO)Fe( CO),, 3, 1430 FeMo2S, [F~(MoS,)~]*-. 2.574,575 [Fe(MoS4),J3-.2,564, 565,566,573-576; 3. 1426 [ M O , F ~ S ~4] ~242; - ~ 6,722 FeMo3H&,0S4 [Mo3FeS,(NH3),(H,0)]4C, 3, 1248 FeMo,O,, Fe,(hluO,),, 3, 1376 FeN4012 [Fe(N(3,),]-. 2. 417:4,22Y, 1183, 1185 FcNi.5 [Fe(K3),l2-. 1-40:2.231; 4,222,1183 FeNaC3,H,,N0,P Na{CpFe C O ) AL Ph2PCH22,933 ~ H Z ) ) , ,

377

Cumulative Formula Index

FeNiAsZCSHZOIZO

Ni12(CO){Fe(q5-Me2AsCjH4)z}, 5. 121 FeO, [FeO3I3-,6,356 Fe0,S Fe(O,S), 2,429 FeO, [ F c O ~ ] ~2,296; -, 4,267, 1183,1187;6,351,356,493 [Fe0413-, 4,267, 1183 1 ~ ~ 0 , 1 46,356 -, FcO& [Fe(SOz)a]z' ,2,635 FeO8S2 [Fe(SO,),]-, 6,825 FeO18S6 [Fc(OS0,),J9-, 2,418,421. 638 FeOsC,H,,N,O, [Fe(H,O),OOsO(en),]*+. 4.583 FePbC1,,Hl,OZ FeCp(CO),(PbMe,), 2. 16 FePbN6012 [PhFe(N0,),]2-. 5.691 FePb,Re06 FePb,ReO,, 1, 111 FePdPtC,,H,,O,P, PtPdFc(dppm)2(CO)d.5,457 FePtB8C20H50P2 FePt(Me4C'4H,Ii,)(PEt3)2. 5.374 FePtC4,H3,0,P2S2 (Ph3P),Pt(CSZ)Fe(CO),Cp. 2.583 FePt2C5,H4,0,P, Pt;Fe(dppm),(CO),, 5.357 FePuC,N, PulFe(CN),J, 3, 1133 F~R&H,,N;FeAelPr'NCHCHNHPr'). 2.215 FeReC,;H,O& (OC),Re(CS,)Fe(C0)2Cp, 2,583 FrReC,,11,,N20, RcFcH(CO)e(PriN=C:I IC1I=KPr'). 2, 215

Fe (SnC1,)Cl {P(OMe),},, 4, 1233 FeSnC14Hlo04 Fe(CO),(SnCp,), 2,17 FeSnC1,H,,O, Fe(CO),{Sn(acac),), 2, 18 FeSnCl5H4,Cl,Ol5P5 Fe(SnCl,){ P(OMe),}, , 4 , 1233 FeSnC,oH,,CI,NO,P Fc(SnCl,)(CO),(NO)(PPh3), 4, 1189 FeSnC26H200,Sz I'h?Sii(CS*)Fe(CO),Cp, 2,583 I-eSnC 47tJ,,N4 Fe(tetiaphenylpoiphyrin)SnMe,, 2,843 FeSr,O, Sr2Fc0+,4,266 FcTiH, FeTiH,, 2,693 FeWBr20S, [FeBr2SlWO(S,)]2-, 2,570 [ F ~ B I - ~ ( W O S ~2,566 )]~-, FeWC, 2HtoS6 [Fe(SPh),(WS,)I2-, 2,565 FeWC,,H,,O,P W(CO)S(PhPCHCHPh)FcCpz,2, 1055 FeWC,,H,,WZ ~~'Cp(C0)2(2,4,h-Me~C,t~2PC~-I=PC',H,Me,2,4,6)Fe(CO),, 2, 1055 Fe WClN,S4 [FeCI(N,)(WS,)]z-, 2,565 FeWCI2S4 [FeCI,(WS,)J*-, 2,563,565,574,575 FeWS, [Fe(WS,)]-, 2,564 FeW2C6H,,N,02Ss [Fe(DMF)2(WS,)2]2-,2,566,575 FeW&&W1oP2 Fe(PCH=CHCH=CH)Z{ W (CO),; 2 . 1044 FeW,&O,S, [ F T ( H ~ O ) ~ ( W S ~ )2,564, , ] ~ - , 566 FcW3NOS.

RuCi(FeC14)(C0)2(Ph.Ie3)2. 4.382 FeRuC9H,9N,2

[F~(CN),(~-~~=CHCH=NCH=~H)RU(NH,)~] ,4. 317 FeRuC1,H,,N6 [Ru(NH,),(FeCN)12+, 4.317 FeRuCllN [(NC),Ru(CN)Fe(CN),J"-, 2 , 9 FeRuCI3HL6N6

IRu(NH~),(FcC:I-I=CHCN)]~'. 4,317 Feku2C,,H,,NIz

[{RU(NH~),}~{FC(CI\;)~}]~~', 4.320 FeRu2C,,H,,CIz08P2

{Ru(CO),(PPh,)),(~t-CI),{p-Fe(CO),}, 4,413 FeRu2C44H3209PZ

{Ru(CO),(PPh3)},(u-H)(~~-OH){ y-Fe(CO),), 4,413

FeRu2C44H,201~Pz

FeRu,(p-OH)2(PPh3)2(CO)8. 2,297,299 FeS, FeS,, 6,782 [FeSJ, 6,629 FeS,O, 6 . 849 [FC(SO,),]~~, FcSbC7H90, Fe(COla(SbMe,), _. 2, 1038 FeSbk,,fl,,F6N, Fe(tetraphenylporphyrinate)(FSbF,), 3,271,275 FeSi,CI8H,,N, Fe{N(SiMe,),},. 4.222. 1183 FeSnCi2H36C14012P4 +

Fe2CRH3,&

,.

Fe2CsH20S6

Cumulative Formula Index

[Fe2S2(SEt),j2 .4,238 FezCBOioS {Fe(C0)4)zS02,2,635 Fe2C9H6NO7 Fe,(CO),{pOC(NMe),}. 2.286 FezC9H6N20 Fe,(CO)6{p-MeNC(0)NMe}, 2,285 Fe2C&.Nz07

Fe2(CO),(MeNCONMe),2.220 Fe2C;O9 Fe2(C0)9,I , 122; 2, 194,210,212.218.220,285 Fe2C1&LN [Fe,(CN),0(NH,)14-, 4,221 (NC),Fe(NC)Fe(CN),(NH,), 2, I0 Fe2C10H10S4

(FeSKp),, 2,605 FezCdlo [Fez(CN)10]4-,4,1205 [Fez(CN),O]S-,4, 1205 [Fez(CN)10]6-,4, 1204, 1205 FezCllHloOS4 Fe2Cp,(Sz)z(CO), 2,533 FezC1lN1l [FeZ(CN),,l7-,4,1205 FeG2HloN404Sz {Fe(N0)2(SPh)}Z.4, 1191 Fe,Cl,H1AO6 Fe,(CO),(NCMe,),, 2, 127

378

FeX,,H,,N,SZ

[Fe2Cp,(NCMe)2(SEt)2]z+, 4, 1243 Fe2C18H40N2S4 { Fe { (SCHzCHzNMeCH,)2CH2}} 2 , 4,1247 Fe2C19HioINOs Fe,(COj,(~-I)(lr-N=CPh,), 2,281 Fe2C19Hl~Nz0 Fe,(CO),{y-PhNC(O)NPh}, 2,285,286 Fe2CZOH8Nl2 {Fe(CN),),(4,4'-bipy), 1.362 Fe2CZnHls [(FcC~)~(C,H,-C,H,)]'.1,351,362 ( F ~ C P ) ~ ( C & IC5H4), 1,359 Fe2C20H22C12Y204 {Fe(2-OC'6H,I'H=N(C~12)~~))C1)2, 4,249 Fe2CZ0 HZ4N401 - , 4. [Fez{( 02CCH2)2NCH2CHzN(CH2COzH)2}20]4 253

Fe&-~s-CjH4CH2-q5-CsH4)2r1, 127 Fe,Cz*H,z FeZ(~-r15-C~H~CH,CH2-1i5-C5H4)Cpz, 1, 127 Fe2CzzH3sOsP2Si'b { Fe(CO),},{ (Me,Si)ZCt.lP=PCH( SiMe&), 2, 1045 FcZC24H.,bC12N40 Fe,O(phen),Cl1, 4,223 Fe2C24Hi804P2

{ Fe(C0)2( PhPCH=CHCH=(?'H)} Fe2C24HzoN404P2

[Fez{(02CCH2)2NCH2CH2N(OH)CHzC02) 20]2-, 4, 253

Fe&,H;O,P Fe(C0)4(PhPCH=CHCH=~H)Fe(CO),, 2 , 1042 Fe2C,,HlPl2S, [FeCp{Sz~z(CF3)z}]z, 2,605

2,

2,1042

4, 11 1 1 [Fe,{(2-pyCHz)2NCH2CH2NrCHlpy-2)z)2(H~0)~O]'+, [Ir(CO)3{FePPh2(CO)2Cp}zj+, Fe2MoC,zHlo08~ 4,226 IFe2(0Ph)z(MoS4)]2-, 2,565 Fe,MoC1zH,oSs [FeSz(SPh)2FeS2MoS2]z-, 3, 1426 FezMoC,4H14S8 [Fe(SC6H4Me-4),(p-S,)Fe( MoS4)I3-,2,566 FezMoC22H,802S4 \floO2(S2CCsH4FeCp),, {Fe(phthalocyanine))20.2.301.4,262, 1265 .~ 3,1388 Fe2M~C24&60& Fe,C,d,zN , 6 0 2 3, 1424 MOF~~(SHU')~(C:O)~, rFc(phthalocyaninc)}~O~.2,867 FezMoC,,l I,,N40,PS2 Fe,(CO),S,h.io(NNMePh)z(PPh,), 2, 148 Fc2MoCl,S4 IMoSaFe,ClT12-, -. 3,1426 F&MuC~,S~ Fe2C72H88N80 [(FeCl,),(MoS,)j2-, 2,562,565,574; 3, 1426; 3,242 {Fe(octaethylporphyrin)}20, 2.829 .. . . Fe;C7,H,,Nl9 [ { Fe(phthalo~yanine)(py)}~N]', 4, 1265 FezCszHsiP6 [Fe,(y-H),(triph~s),]~2.702: 4. 1233 Fe2C8sH56N~0 {Fe(tetraphenylporphyrin)),O, 2, 829; 4, 261 1268 [Fe,(tetraphenylporphprm),O] .4,266 [ Fez(tetraphenylporphyr~n)20]2-,4, 266 FG~cwHs6Ns {Fc(tetraphenylporphyrin))lN. 4,761 F~zC.wHdm {Fe(tetraphenylporphyrin)),O. 6,618 FezCs9Hs6Ns {Fe(tetraphenylporphyrin)}zC. 4. 1270 FezClzSz IFe2S2C1212-, 4,1243 - - -_ Fe2CI4S2 [Fe2S2C1412-, 4,236 Fe,Cl, Fez&, 4,248 Fe,C160 [(FeCIJ)z0]2-,2, 301;4.248. 1185 Fe20Q,, 4,225 Fe2C19 [FezCl9I3-,1,273 Fe,CuPbH,O L4S2 P ~ C U F ~ ~ ( S O ~ ) ~6,827 (OH)~, [Fe&1212-,2.546; 4,1240 FeP, FezSb2C13H3007 FezFs, 4,247, 1187, 1249 Fe(CO),(p-SbPhz)Fe(CO)3Ph(SbPh3),2, 1038 Fe2Fz2Ca Fe2SiCZoH,~Clz {Fe(PF3)3}2(~-PFz)2, 4, 1197 {FeCp(C5H4)}zSiClz,6, 19 FeZHz02 Fe2SnC,,C1,0, [FeZ(OH)z]4t,6,413 (FeCp(Cfi)2}2SnC12,2 , I q FezH,F,O, Fe&nC,,H6O4 Fe,F,.2H20, 4,1249 {FeCp(CO)2}2SnMcz,2,19 FezSn2C ,H 0, {Fe(CO)4(SnMcZ)),,2. 19 ,4,228 Fe2Sn2C28H200B {Fc(CO),(SnCpz)}z, 2, 19; 3,219 Fe2VCI,Ss [(FeC12)z(VS,)]3-,2,565 Fe,WC1,S4 189 [(FeC1,),(WS4)12-. 2, 565 . 4 , 1189 FezW2CzzH34NJh Fe2I;N4O4 W2{C~Fe(C0)2},(NMez)4r 3,1002 Fe2iV,Si0 Fe212(NO),,2, 682 [Fe2Sa(WS,)zI4-. 2,566,569 Fe21rC38H30104P2 IrI{FePPh2(C0)2C:p}2.4. 11 11 F~,A~C~OHI&IJ' Fe3(CO)lo(@z-Ac)( p,-AuPPh,), 5,906 FeZIrC381-13004PZ Fe3AuC32H25NOYP [Ir{FePPh2(CO)2Cp}z]' , 4 , 1111 Feq(CO)(v3-HC=NBu')( p2-AuPPh3),5 , 908 FezIrC39H30Br05Pz Fe3Au2C1FH30109P2S [IrBr(CO){FePPh,(CO),Cp),l+. 4. 11 1I Fc3(CO),(~~~-S)(AuPPh,)z, 5,910 FeZIrC39H30C105P2 IIr(CO)(FePPhz(CO)zCp)zC1]. 4.111 1 Fe3CsHzo% [Fe3S4(SEt),j7-, 1.157; 4,237; 6,633 FezIrC41H3007P2 ~

Fe3C909Se6

Cumulative Forrnulu Index

380

[Fe4S,(1~3-NBu')2(rO)~]-. 4,240 Fe4CsHzo04Ss [Fe,S4(SCfT2CH20H),]*~~~, 1, 154; 6, 630 Fc4CsH2oSs [Fe,S4(SEt)4]2-,2,527; 4,238 Fe4C10HlsN604S2 Fe,S2(YUCBu')2(NOj,. 1. 154 [Fe,S,(;uCHu',),(No),] ., 1, 154 FLICIOHZOCLN~SB [Fe,S,CIZ~S,CNEt,),lZ-, 4, 1244 FC4CizHI&L%. [Fe4S4(SPh)zC12]2-, 4, 1244 Fe4CnHi60sSs [Fe4S,(SCH2CH,C0,),]6-, 1,154; 4,239, 1241 Fe4C22H24N40sS8 [Fe,S, (SCH2CH(NHZ)CO2H}J, 6,629 [Fe,S, { SCHzCH(NH,)COzH},]2-, 6,629 [Fe&{ S~l12Cl-I(~H2)COzH},]3-, 6.629 FGCi&O,, Fe,H(CO),,, 2! 705 Fe4C,5H30Cllr;3S,o [ F C , S ~ ( S ~ C N E ~ ~,)4~, C1244 IJ Fe4C16F24SL2

[Fe,S{2-C6H,(CH2S)2},J2-, 1,144; 4,236; 6,633 Fe3CZ5H13011P { Fk (C0)3Fe(C0)4P(C6H40hle-4)CHCPh}Fe(C0)3,2, 1045

[Fe,S4(S2C2(CF,),),I2".,1, 'I54 Fe4Cl6Jlj6S8 [F~,S,(SBU~),]~-, 4,239; 6,630 Fe4C20H20S4 Fe4S,Cp,l 1,154; 4,240, 1243 [Fe,S,Cp,]+, 1.154 [Fe,S,Cp4]2+. 1,154 Fe4C20H20S6 Fe4Cp4(S2)& 2.534 Fe4C20H40N4S12

[Fe,S,(SZCNEt2),]. 4,1244 Fe4C,0&,,Sto [Fe4(SEt)l,,]2-,I , 251 Fe4C22H30N2S10 I

Fe3(CO),{ PhP=CPh(OEr)} (v3-PPh) 2, 1050

[Fe4S4(SPh)z(SzCNEt2j2]2-, 4, 1244 Fe4C2,H2004S, [Fe,S,(OPh),]z-l 1.154; 4,1242 Fe4Cz4H20S4SeI [Fe4Se,(SPh)4]z-,1, 154 Fe4C24H20S8 [Fe,S,(SPh),]-, 1,493 [Fe,S,(SPh),lZ-, I? 154,494; 2,527,531; 4,239, 1242, 1244; 6.630 [Fe,S4(SPh),]3 , 1, 154,494; 4,239 [Fe,S,(SPh),14+. 1,494 F~.&HZ~NQSS [FerS4(2-HzN~,H,S),12-, 4,239 FcqC2.4 L 4 N 8 01 3 s Fe,S4{ SCHzCH(NHAc)C0,NHMe}4]2~, 6: 630 F ~ J C ~ H Z ~ B [Fe4S4(SCH2Ph)4]2-r 1.154; 4,239; 6,508

381

Cumulative Formula Index

[Fe4S4(SCH2Ph)4]3-, 4.239 [Fe4S4(4-SC6H4Me)4]2-, 1.336 1, 336 [Fe4S4(4-SC6H4Me),I3, [Fe4S4(SCHZPh).,]"-,6,630 Fe4C36H3oC14S6 [Fe4(p-SPh)6C14]Z-, 1,151; 4. 1243 F~~C~OHSOSIO [Fe4(SPh),,,l2-,1, 151: 2.528; 4.1242.5,973 Fe,CI,S, Fe4C14S4,6,232 [Fe&C14]Z , 1, 154; 4,230,240, 1212-1244 F C ~ C U ~ 1C5 ~6 ~J 4 {Cu(l-Me,NC'H,Fc)},. 5.557 Fd4S4 [Fe,S4141"-, 2,523 F~&'~OCZ~H~~O~S, [F~,MOS,(SE~)~(~.~-O~C~H~)~]~.3, 1427; 4,241 Fe4N404S4 Fe4S,(NO),, 1, 139, 152. 154: 4,240, 1192, 1243 [FeaSa(NOL-. 1. i51 Fe4N707S3 . [Fe,S,(NO),] , 1. 150; 2,116,523; 4,240, 1192, 1243 L

.

Fe,lRu(CN),], 4,281

FC~C,,H,,,S,, [ F c ~ S ~ ( S P ~ )1.~157 ]~-. Fe6C36H90P6S8

1. 139.160;4,241.1244 [Fe6S8(PEt3)6]2f,

COC 7-M*

Fe,,H,,O,,

GaAsO, GaAsO,, 3,135 taAs2C10~16Br3 GaBr,(diars), 3, 132 GaBrCII, [GaCIBrI,]-, 3,140 GaBrC1, GaCI,Br, 3,140 GaBrC1,I [GaCl,BrI]-, 3,140 GaBrCl, [GaCI3Br] ,3, 140 GaBr,CI GaCIBr,, 3, 140 GaBr,ClI [GaCIBr,I]-, 3,140 GaBr, GaBr,, 3, 139 GaBr,CI [GaCIBr,]-, 3,140 GaBr, [GaBr,]-, 3,139 GaCH205 [Ga(OH)dCO,)I-, 3,133 GaCH,O IGa(OMc)12+,3,134 G~CH~N {GaMe(NH)},,,3,131 GaCNS [Ga(NCS)12' , 3 , 131 GaC&CIO GaClMe(0Me). 3, 134 GaC2H6N6 [GaMe,(N,),I-, 3,131 GaC2H602 [Ga(OMe),]+, 3, 134 GaC2HloN GaH,(NHMe,), 3, 130 GaGHI2N2 [GaMe,(NH,),]+, 3, 129 CraC204 [Ga(C,04)]'. 3,136 GaC3HtiN303S3 Ga(NCS),(H20),, 3, 131 GaC3HbN& Ga(S,CNH,),, 3,138 GaC3H,Br3N GaBr,(NMe3), 3,130 GaC3H9Cl3N GaCl,(NMe,), 3, 130 GaC3H9Cl3P GaCI,(PMe,), 3, 132 GaC,I-I,N, [GaMe,(N,)]-, 3, 131 GaC3Hg0 GaMe2(OMe),3, 134 GaC,H,O, Ca(OMe),, 2,345; 3, 133 GaC3HI2N GaH,(NMc,), 3,129-132,140 GaMe,(NH,), 3, 129

__

GaC3HI2P GdH,(t'Me,), 3, 132 GaMe,(PH,), 3, I32 GaC3N,S3 Ga(NCS),, 3, 138 GaC4H6CI2N2 [GaCI,(MeCN),]+, 3, 132 GaC4H6N2 [GaMe,(CN),]-, 3,129 GaC4H8Cl,0, GaCI,(dCH2CH,0CH,c H,), 3,137 GaC4H,,CI,0 GaCI,(OEt,), 3. 136 GaC4HI2CIN2 CiaCY(NMe,),, 3, 131 GaC4Hl6N2 {GaMe2(NH2)),, 3, 131 . .. GaC4N4S4 [Ga(NCS),]-, 3, 131 GaC,N,Se, [Ga(NCSe),]-, 3,131 GaC40s [Ga(C,O&-. 3,136 GaC5H5CI3NO GaCl,(py iVoxide), 3, 136 GnC,F1,0,

GaMe(OAc),. 3.135 GaC5HI3C1P {GaCIMe(PEt,)),,, 3, 132 GaC,H,,O GaMe3(OMe2),3, 136 GaC6F906 Ga(O,CCF&. 3. 136 GaC6H3N5S, [Ga(NCS),(MeCN)]-, 3.131 GaC6H306 Ga(02CH)3,3. 135 GaC6H,O6 Ga(OAc),, 3, 135 GaC&2N& Ga(S,CNHMc)?, , - 3, 138 GaC6hi4Nh G~H,{NTH,),),, 3, 131 GaCfiH1503 Ga(OEt),. 3. 133 GaC6HltlCI3N2 GaCI3(NMe3),.3. 130 GaC6HI8N GaMe,(NMe3). 3. 130 GaC6HlsN; Ga(NMe,),. 3. I 3 1 Gac6H18P GaMe,(PMe,). 3,132 GaC6H21N2 GaH3(NMe3),,3, 129 GaChH2*06 [Ga(MeOH),]3'. I , 285 GaC6N6OR [Ga(NC0)6]T-.3, 131 GaC6012 [Ga(C,O,),],-. 3.136

382

Cumulative Formula Index

383 GaC7H1302 GaMez(acac), 3, 134 GaC7Hz807 [Ga(MeOH)7]3+,1,285 GaCsFl2O8 [Ga(OZCCF,),]-, 3,136 GaCSHl2N4 [GaMeZ(hN=CHCH=~H),)-, 2.256 GaC,H,,CI,O, GaZCII(~CH2CH20CH2tH*)~, 3 , 128 GaC,H,,Si, GaCI(CH,SiMe,),, 3, 139 GaC8Hz4N4 [Ga(NMeZ)J, 3.131 GaC H 0 {GaMe,(OH)),, 3, 133 GaCsN4S4 [Ga{SzCz(CN)z)zl-,2,605 GaC9H1102 GaMe,(tropolonate), 3. 134 G~C~HIRN~S~ Ga(SZCNMez),,3, 131 GaC9HZlO3 Ga(OPr'),, 3, 133 Cia(OPr),, 3, I33 GaC9HZ4N9S3 Ga(en),(NCS)3, 3, 131 GaC,H,,O,Si, Ga(OSiMe,),, 3, 134 GaC9H2,Si, Ga(SiMei),, 3, 129 GaCloH1~N6

[GaMe(fiN=CHCHdH),l--,2,256

GaCioHi3NzOs Ga{(0zCCHZ)zNCH2CH2N(CH2C02H)CH,Co,)1 3. 142

GaCloHl5N2O9 Ga(H,O)(Hedta), 2,783 GaCmHzJ2Pz [GaI,(depe)]+, 3, 132 GGJ-L2 [Ga(C6&)z] ' - 3 , 127 GaC12HlsN6 [Ga(MeCN)6]3+.3, 132 GaClzHz703 Ga(OBu'),, 2,346; 3, 133 Ga(OBu),, 3, 133 GaC1zH3604Si4 [Ga(OSiMe,),]-, 3,134 GaCizH3606S6 [Ga(DMS0)6]3+,1,286; 2,488;3. 137 G~C~~NGS~ [Ga{S,Cz(CN),},]3 3, 138 G~CIJHBN~O~ Ga(NCO),(bipy), 3, I31 GaCl,H,,CINz GaCIMe,(phen), 3,130 I

GaC14H14NZ

[GaMe,(phen)]+. 3,130 GaCl5H8N5O3 Ga(NCO),(phen), 3, 131 GaCI5HllCI3N3 GaCl,(terpy), 3, 130 GaCi~Hz106 Ga(acac),, 1,65; 3, 134 GaC1SH30N3S6 Ga(SZCNEtz),,3, 138 GaC,,H,,CIN,O, GaCl(salcn), 3, 142 GaC16H2SNZ06

[Ga(acac),( DMF)J, 3. 134 GaC17H35N406 [Ga(acac)(DMF),]*+, 3, 134

GaClsHI5Cl30P GaCI,(OPPh,), 3,136 GaCIBH,,CI,P GaC13(PPh3).3, 132 GaClRH1503 Ga(OPh),, 2.345; 3,134 GaCi8H4zN606 [Ga(DMF)b]3+,1,286; 3,137 GaCdLN,Si, Ga(N(SiMe,),),, 3, 131 GaC,,H,,O,,P, [Ga{OP(OMe),},13 *, 1,286 GaC,,H,,CIN,OZ GaCl(2-Me-8-quinolinolate),, 6,971 GaCzoH,,C1,N, [GaClz(bipy)2]f,3,130 GaCzoHzoC1zN4 [GaCldp~),l+,3,130 GaCZ4H,,CIzP GaC1,Ph(PPh3), 3, 132 GaG7H18N303 Ga(&quinolinolate),. 1,528,530 GaG0H=N3O3 Ga(2-rnethyl-8-quinolinolate),, 1,530 Ga(S-rnethyl-8-quinolinolate),, 1, 530 C;aC,0H24N6 [Ga(bipy),13+,3. 130 G~CXHMFNB GaF(phtha1ocyanine).3. 142 GaCdd' GaPh3(PPh3),3,132 GaC49H43N4015S Ga(xyleno1orange)(8-quinolinolate),, 1,552 GaCl GaCI, 3. 127 GaClO GaOCl, 3,133 GaClTe Ga'l'eCI, 3. 137 GaC1,S [GaSCIII-. 3, 138 GaCI3 GaC13,3,133,136, 13Y GaCI3O9S3 Ga(SO,CI),. 3, 135 GaC130,z Ga(CIO&, 3,135 GaC1, IGaCl,]-, 3, 123,127,130,132,139,140 [GaC14]2-. 6 , 854 GaClnO,,Sn [Ga(S03CI)4]-,3,135 GaCI4Ol6 [Ga(ClO,),]-, 3, 135 GaC16 [GaC161n-,I , 524 GaCuInO, CuGalnO,, 5,607,650 GaF GaF. 3. 127 [GaFIZ+,3.138 GaFO GaOF, 3, 133. 138 GaF, [GaFz]+.3,138 GaF, G ~ F , 3,138 , CaF,O,S3 Ga(S03F)3,3, 135 GaF, [GaFJ, 3,138 GaF, [GaFJ-. 3,138

GaF,

GaF, GaF, [GaF6I3 ,3,138 GaGeC,H, GaMe,GeH,, 3,129 GaGeC,H,Cl [GaMe,C1(GeH3)]-, 3, 129 GaGeC1, GeGaCl,, 3, 139 GatlHr, GaHBi,, 3, 141 GaHC1, GaHCI,, 3,141

GaHF,O GaFZOH, 3,138 GaHOz GaO(OH), 3, 133 GaH0,P [Ga(HPO,)]+, 3,135 GaH2F,02 [GaF,(OH),IZ-, 3,138 GaH2N2 [Ga(NH),]-, 3,131 GaH204P iGa(H2F’04)]Z+, 3, 135 Cim, [GaH,]-, 3, 141 [GaII,1’, 3, 141 tiall,Br,N GaBr,(NH,), 3, 129 GaH3CI3N GaC13(NH3),3, 129 GaH3CI,P GaC13(PH3),3, 132 GaI1303 G A ( O H ) ~3., 133 GaH,O,S {Ga(OH)3S]-, 3, 137 GaHqO4P [Ga(H,PO,)]? , 3 , 135 GaH3S3 Ga(SH),, 3, 13X CiaH, [GaH,]-, 3, 125,140 GaH4F402 [GaF,(OH,),I-, 3, 138 GaH,N {GaH2(NH2)),,3,131 GaH,O, [Ga(OH),]-, 3,133,136 [GaO,(OH,),]-, 3, 133 GdH, [GaH,,I3 , 3 , 140 GaH,N, Oa(NFI,),, 3, 131 C;aHsN4 [Ga(NH2),I-, 3,130 GaH,F,N, GaF3(NH3)3,3, 129, 138 GaHloN5 [Ga(NH2),IZ-,3, 131 GaH1204 [Ga(OH,)4]2+,3,136 [Ga(OH,),I3+, 1,284; 3, 133. 139 GaH1407 [Ga(H,0)7]3+,3, 133 GaI, GaI,, 3, 139 GaI,O, Ga(lO3)3, 3, 135 GaI, [Gar,]-, 3, 123 GaInC1, [IIIG~CI,]~-, 3, 128

Cumulative Formula Index

384

GaInO GaInO, 3. 127 GaMnCIlH,3N503 Mn (3,5- di met h y lpyr azo 1e) -

(NO),(hle,NCH2CH,0GaMe,),4, 9 GaMaC14H,,N403 CiaMnC,, H l l N 6 0 2 Ma{MeGa(dN=CHCl

l=cI I)3}(CC))2(rll-C112C‘II=

CTIJ. 2.26

GaN, [Ga(N.3))2+, 3, 131 GaN309 Ga(N03j3.3. 135 GaN,OI2 [Ga(NO,),]-, 3.135 GaNbCI8 NbGaCI,, 3.593 GaO, [GaOJ, 3. 133 GaO, [ ~ a 0 ~ 1 53.133 -, GaO,P C a p o 4 ,3.135 CaO,Si [GaSiO,l-, 3,135 GaPS, Gaps4. 3, 138 GaS

Gas, 3.127* 128 Gas, [Gas2]-. 3,137 Gas3 [Gas3],-. 3,137 GaSe GaSe, 3, 127. 128 GaSnC,H,, [Gahk,SnWe,] , 3, 12‘1 GaTe Cial’e. 3, 128 DazAsZClulI,,Clb Ga,Cl,(diars). 3, 137 GaZBrC1, [Ga2C16Br]-,3, 140 Ga,BrzCl4 Ga,Cl,Br,, 3>140 Ga,Br, [Ga2Br6J?-.3.128 Ga,Br7 [Ga,3r,]-13, 139,140 Ga,C,H,oBrsO [Ga2Br5(OEtz)]-:3: 128 Ga J4H., ?Nh {GaMc,(N,))2, 3, 131 Ga,C,H,,N, {GaH2(NMe2)},,3, 130, 131, 141 GazC6Hlz04 (GaMe2)2(Cz04), 3. 136 Ga2C6Hd3 [(GaMe3)2(Y3)]-2 3,.131 Ga2C601, Ga,(C,O,),. 3.136 Ga2C’7H18N

[(GaMe3)2CN] 3, 129 Ga,C8HI6Cl2O4 GalCl,(~CH,ClI,OCH,cH,),,

Ga,C,H,,,Rr,O, Ga2Br4(OEt2)2.3. 128 Ga,C,H,,N, (GaMez(NMez)}Z,3, 131 Ga2C8H26C1N2Si2 {GaCIMe(NHSiAMe,)),,3, 131

3, 127

385 Ga2CI0Hl0Br4N2 Ga2Br4py,,3,128 G~zCIOH~~C~~PZ GazC16(depe), 3,132 Ga2C12H3A02

{GaMe,(OCHZCH2NMe2)}z, 3.142 GazCz4H60Pz {GaEt,(PEt2)}2. 3,132 Ga2CZ8H3,,S2 {GaPh,(SEt)},, 3. 138 Ga2C52H52N2P4 {GaMeZN(PPhZ)2)2r3. 132 Ga2CI, Ga2CI., 3, ,127 Ga,CI, Ga,CI,,2,682;3,139 [Ga2C16]2-, 3,127.128 Ga2CI7 [GazC17]-, 3,127,140 GaZC~C24H40N8 Cu{Me,Ga(fiN=CMeCH=~Me),)2.2,254 Ga2F6 (GaF,),, 3,138 Ga2FI2

[Ga2F1217-, 3,138 Ga,H,CI, (GaHCI,),, 3,139 GazHSNOs G~z(OH)S(NO~), 3, 135 GaJ3 Gaz13,3, 127 Ga2L Gaz14,3,127 GaZ16

GaZ16,3,139

GazT7 [Gaz17]-, 3,140 Ga2N4013 GazO(N03)4,3,135 Ga,NiC,,H,,N, Ni{MeC;a(&N=CI lCll=(?H)?}2q 5 . 102 Ga,O

Ga,O,3,127 Cia,O, Ga203, 3,127,133.134 Ga207 [Ga,07]8-, 3,133 Ga,O,Si, [Ga,Si209]4-, 3,135 Ga2OI2S3 GaZ(S04),,3,135 Ga2Pb2S4 Pb,Ga,S,, 3,137 Ga,S Ga,S,3, 127 Ga,Sire Ga,S,Te, 3,137 Ga2S3 Ga2S3, 3,137 GaS4

[Ga2S4I2-, 3,137 Ga,Se Ga,Se,3,127 Ga,Se, Ga,Se,, 3,137 [GazSe312-, 3,128 Ga2Seh [Ga2Se61h-. 3, 137 Ga,Si,O,

[Ga,Si,0,12-,3,135 Ga,SnCI, Sn(GaCI,),, 3, 139 Ga,Te,

Gdi( pIel) {N(CMe,),},(THF), ,3,1087 GdC~,,H,,N,S,Si, Gd,( p-SBu)?{N(SiMe,),},, 3, 1087 GdC,,H,,N,O Gd(octaethylporphyriii)(OH), 2, 822 GdH6N30

12

3,1086 Gd€112C1206 [GdC12(H,0)6]’,3,1076 Gd(NO,),(H,O),,

GdH1608

[G~(HzO),]~+. 1,84 GdN,O9 Gd(N03),, 3,1076 Gd04Si [Gd(O,Si)]-, 2,429 GdReHBOzo [Gd(OReO,),(OH,),]-,2,418,424

Gd,CI, Gd2CI3. 1, 167 Gd,O,S, Gd2(SO,)3,3, 1076 GdzOiS,

Gd2(S04)3,lq261;3,1076

GdioC,Cli,

GdioC4C118 GdioCIi8(C2)2, I , 167 GeAICfHtl AIMe(GeMe,),, 3, 107 GeA1CI8Hl8 [AIH,(GePh,)]-, 3,107 G~AS,R~C,~H~~CI RhHcl(GeMe,)(A~ph~)~, 4, 1020 G~AUC~~H~~P Au(PPh3)(GeMe3),2, 16 G ~ A u C ~ ~ H ~ ~ P Au(PPh,)(GePh,), 2,16 GeBCI, [BCISGeC13]-,3,93 GeBH, [BHSGe€I,]-, 3,91 GeCF, [Ge(CF,)F,]2-, 3,201 GeC2F10 [Ge(CF,)2F4]z-, 3,200,201 GeC3F11 [Ge(CF,),F21-, 3,201 GeC5H, [GeCp]+, 3,217 GeC5H5CI GrCpCI, 3,217 G~CgH7102 GeI(acac), 3,221 GeC5HI1NO2 ~e(OCH,CH,),fiMe, 3,221 GeC8H1802 Ge(OBu'j2, 3,220 GeC8H,,02 GeBu',(OH),, 3,206 GeC8H2004 Ge(OEt),, 2,340 GeCloHlo GeCp2,3,218 GeCloHls [Ge(C,Me,)] " ,3,218 GeCloHlsCl Ge(C,Me,)CI, 3,217,215 GcC1zHsF04 Ge(OC,H4d-2),F, 3,214 GeCl2HSFS4 6e(SC6H,$-2),F, 3,214 GeC12H14 Ge(q-C,H,Me),, 3,218 GeCl2HZ8PZ GeEt,(PBu')z, 3,216 GeC12H3,NZSi4 Ge(N(SiMe,),},, 3,220 GeC,,H,,O, [Ge(acac),J', 1,65 GeCI6HlsO8 Ge{0,CCH(OH)Ph)2(H20)2?2,474 G G O b Ge(C,Me)*, 3,218 GeC,,H38C1204 Ge(Bu'COCHCOBu')zCIZ,2, 382 GeC,,Hz0O4 Ge(OPh),, 2,340 GeC24H37P3 GePh,(PBu'),, 3,216 GeC28H46P4 GePh,(PBu'),, 3,216 GeC30H460z Ge(OC6H2Me-4-But2-2,6)2, 3, 220 G~C~~HI~C~ZNM Ge(phthalocyanine)Cl2,2,864 G~C,ZHI~NE Ge(phthalocyanine), 2,864 GeC,,Hl6N8O {Ge(phthalocyanine)O),, 6. 151

Cumulative Farmiilu tndex

386

GeC,,H,,C12N4 Gc(octaethylporphyrin)CI2, 2,822 GeC38H50N402 Ge(octaethylporphyri.n)(OMe),, 2, 822 GeC44H2MC12N4 Ge(tetraphenylporphyrin)CI,, 2, 822, 853 GeC44H3~C12N4 Ge(tetraphenylchlorin)C12, 2, 853 GeC4JH32CI,N, Gc(te t raphenylisobacteriochlorin)CI~,2, 853 CJtC&dL02 Cre(tt[raphenylp~rphyin)(OMe)~, 2,822 GeCI, [GeCI,]. , 3 , I95 GeCoC2,J Co(CO),(tieMePhNp-I), 2, 19 GeCosHgC1701, 2,1 tGe{co2(co)7S~C~z(CO),[HsCo(CO)41)1~1 GeFs [GeF,]-, 3,200 GeF6 [GeF612-,3,200 GeFeC,,H,,NO,P Fe(GePh,)(CO)2(NOj{P(OPh)3},4,1189 GeFeHaOb FeCre(OH),, 6,849 GcGaCZH, GaMc2GeH,. 3, 129 GeCiaC,H,CI [GaMe,CI(GeH,)]-. 3,129 GeGaCI, GeGaCI,, 3, 139 GeHZF2NP Ge(NH,)(PF2), 3.215 GeH6O6 [Ge(0H),l2-. 2,305 GeHg204 Hg,(O,Ge), 2,330 GeIrC,,H,,ClOP Irlf CI( GePh,) (CO)(PYh,) ,4, I 'I 26 GelrC,,,H,,OP, IrH,(GcMe,)(CO)(PPh,),, 4, 1126 GcIrC,,H4,0,P2 IrH2(CO),(GeMe,)(PPh3)z, 2, 19 GeMnC,,H2,0, (S)-(-)-Mn(CO),{CMe(,OEt)}(GeMePhNp-1), 2. 19 Gehfn3C,,Hl,06 {Mn(CO),Cp},Ge, 2,19 GeMo12O40 [GeMo,,040]4-~ 3, 1037 [ G ~ M O , ~ O # , 3, 1052 GeNiC2,H20C13P NiCp(GeCI,)(PPh,), 2. 19 GCO, [Ge0,I2 .2.295; 3,203 GePtC,,H3,C1P, PtCI(GeMe,)(PEt,),l 5,420 GePtC18H49FP3 [PtHz(GeH2F)(PEt3),]-, 5,358 GePtC3,HJ60P2 Pt(OH)(GePh3)(PEr3),, 5,465 GeRhC,6H31C14Pz RhHCI(GeCl3)(PPh3),,4,1020 GeRhC39H40C1P2 RhHCI(GeMe3)(PPh3),,4,1020 GeRuC7H,04 [Ku(GeMe,)(CO),] -,4.287 CieS, [GeS$-, 3, 205 GeS, [GeSJ-, 3,205 GeSi4C14H38 Ge{CH(SiMe3)2}2,3.216 '

387

Cumulative Formula Iptdex

GeBRhCIls

GeWC13H8Br4N203 W(CO),(bipy)(GeBr,)Br. 3. IOU7 GeW12040 [GeWlz040]4-,3,1038 GezAUc36H30 [Au(GePh,),]-, 5, 903 Ge2BiC14H35 BiEt(GeEt,),, 3,281 Ge2BiCI8H4, Bi(GeEt,),, 3, 280 GeZBiC18H5F30 BiEt{Ge(C,F,),),, 3,281 Ge2C32H38P2

(GePh2)2(PBuL)2. 3, 216 Ge2C36H300 (GePh,),O, 3,206 Ge2C36H3oS (GePh3)zS,3,213 GezC4oH56P4 (GePhZ)z(PBu')4.3,216 GezCrCllH1805Te Cr(C0)5{Te(GeMe3)2}.2.670 Ge&rC&?o04 Cr02(OGePh&, 3,942 Ge2FeCloH180J Fe(CO),(GeMc&, 2, Ih GeZGab013 Ga6GezO13,3, 135 GezHSPtCnH6oPz

Pt(GePh,)(HgGePh,)(PPh&. 5,121 G~zP~C~OH~ZFZOPZ PtH{Ge(C6F5)zHGe(C,F~)~}(~Ph3)2, 5,358 GezPtCllo 5.421 [PtC14(GeC13)Z]Z-, Ge,RuC4C1,0, Ru(GeCl,),(CO),, 4. 287 GezRuCl,,H1804 Ru(GeMe,),(C0)4, 4,287 GezRuClZH,,Oh Ru2(p-GcMez)?(C:O),,4. 2x7 Ge,RuC,4H,p02PZ Ru(GeMe,)Z(CO)z(PPh,)~.4,287

Sb(GeEt,),. 3,259 Ge4 [ G e J - , 3,46 Ge,PbO, PbGe,Og. 3.203 G Q R U ~IC GHB0 0 6 { R ~ ( c L - G ~ M ~ ? ) ( G ~ ~ . I c ~ )4,287 (C~),),,

[Ge4%lo]8-.3,205 Ge5F12 Ge5F12,3, 195 Ge5PtClI5 [Pt(GeC13)5]3-,5.421 Ge5PtHCl15 [PlH(GeC13)5]2-,5,421 Ge6C24H&9 (GeBu'),O,. 3,206 Ge,CrCl18 [Cr(GeC13)6]6-,3,709 Ge,RhCI,, [Rh(GcCI,),]-, 4,1019

HfAq4C2oH32C14 HfC14(diars)2,3,383 HfBCIZH40CINzSi4 HfC1(BH4){ N(SiMe& 2 , 3.433 HfB3CloH40NP2Siz Hf(BH4)3(N(SiMezCHzPMe2)2),3.433 HfBrd HfEir,, 3,422 HfBr, [Hfl3~,]~-, 3,430,431 HfCHSC14N30 HfC14(HzNNHCONH2), 3,438 HICH5CLNqS HfCL4(H2NNHCSNH2),3,438 HfC2C14N202 [HfC&(NC:T))2]’ , 3, 379 H f C C1 N HfCI,(NCCI),, 3,381 HfCzH,Cl4Oz [HfC14(0Me)2]Z-,3,392 HfC3HlN302S3 [HfO(NCS),(H,O)]-, 3,287.380 HfCaH,CI4N, HfCI,(MeCN),, 3,382 HfC4HSC1402 HfCl,(dCH2CHZOCH2~H2): 3,434 HfC4H,Cl,04 HfCI4(HCOzMe),, 3,404 HfC4HIZCl4O2 t-IfCl,(Me,O),, 3,404 ITfC4H1204 Hf(OMe),, 3,389 HfC4N404 Hf(OCN)4,3,379 HfC4012 IHf(C03)4]4-,3,410 HfC,Hi,C1402 HfC14(Me2CO)Z, 3,404 HfC6HizO6 HfO(O,CEt),(H,O), 3,410 HfC6H14N6010 Hf(NOJ,(DMF),, 3,374 HfC,Hl8CI4N2 HfCI,(NMe&, 3,371 HfCsNsOb [Hf(NCO),]’-, 3,379 HfC6N& [Hf(NCs),]’-, 3,380 HfC&,Se6 [Hf(NCSe)6]’-, 3,380 HfCsHi4F4N202 HfC14(8-quinolinol)z,3,438 HfCSH16C1402 HfCI4(THF)2,3,403,404 HfCsH16C14S2 HfCl4{wH~)4)2.3,418 HfCBH&I,Oz HfC14(Et,O)Z, 3,404 HfCsHt4CI2N2Si3 HfClz{(NSiMe3)2SiMe2}, 3,378 HfC&zd%

HQNMe,),, 2 . 179 HfCsOi6 [Hf(C2O4),J4 , 3 , 4 1 1 HfC?H&14N303 IIfCI,(MeCOCN),, 3,405 HfCloH8CI4N2 HfCl,(bipy), 3, 374 H~CIOHIOCW~ HfCh(~y)z, 3,372 HfCioH16NzOio ’

Hf{(02CCH2)aNCH2CH2N(CH2COz)*}(HzO),, 3,436

HfCi,HBCl4N, HfCl,(phen), 3, 374 HfC12H2B04

I If(OPr’),, 2,347; 3,389,390 HfC.1ZH3,,C14N4 HfC14{N(CHZCH2NMe2)3), 3,372 HfCl2H,,ClZN,Si4 HfC12{N(SiMe3)2)z. 3.377 HfC14HisCLNz03 HfC14(2,6-Me2pyX-oxide),, 3,414 HfCi4Hd& HfCp(S2CNMe2)3.3,419 HfCi5Hi&W3 HfCl,(py),, 3>372 HfCl5H2,CIOh Hf(acac),Cl, 3,399 14fCC15H45CINZOSiS HfCI(OSiMe3){ N (SiMe,),} ,, 3,377 HfC16I I,,N,O,S, Hf(NCS),(DMF),. 3,380 HfG6Hd4 Hf(OBu‘),, 3, 340,346; 3,389 HfCi&& Hf(NEtz)4, 3, 375 HfC16H48N4Si6 Hf{(NSiMe3),SiMe2),. 3. 378 HfCmHi20, [Hf(l,2-02C6H4)3]”, 3,403 HfC1fiH54ClN3SLj HfCi{N(SiMe3)2}3,3,377 HfCl9Hs4T4TBSi6 HC(CN)(N(SiMe,),),. 3,370 HfC,oH,,F,,O, Hf(MeCOCHCOCFJ,, 3.398,399 HfC2UHZoC13N4 HfC13(py)4,3.366.369 HfCmH2s08 Hf(acac)4,3,397.398 HfCzoH,40, Hf(OCMe,Et),, 3.389 HfC2iH56C12k2P4Si4 HfC12(N(SiMezCH,PMeZ)z} z, 3,383 IlfC,,H,,N,Se,

388

389

Cumulative Formula Index

HgAsJZhC3gH3&lzF

HfC26H22C14NzOz

HfC14(2-HOC,jH4CH=NPh)2.3,438 HfCxHz4C14Pz HfCl,(dppe), 3,383 HfCzsHzoOs Hf(tropolonate),, 3, 402 Hf(OzCPh)d, 1,94 HfC3oHz4N6 Hf(bipy),, 3,366 HfC32Hi5C13N8 Hf(chlorophthalocyaninz)C1,. 3.440 HfC32H28012 Hf{(k)-PhCH(OH)CO,),, 3,113 HfG‘H24N4O4 3,437 H@-qu~nolinolate)~, HfC36Hz4N6 Hf(phen)j, 3,366 HfC3iH40Ni04S4 Hf{4-MeC6H,C(S)N(0)Me),. 3.439 HfCdU4@4 Hf(NPhCONMez)4,3,439 HfC4oH3608

Hf(acac)z(PhCOCHCOPh)2.3.398 .-

HfC4;H50N404 Hf(octaethylporphyrin)(OAc),, 2,824; 3,439 HfCazHh3CIO? HCC1(OC6H3Bu‘z-2,6)3, 3,392 Hrc44H32N100Se4

3,380 ~If(NCSe)4(phen)3(THF), HfC46Hd404 Hf(octaethy1porphyrin)(acac),. 3 . 4 0 HfC5zH4oN408 Hf(ONPhCOPh)4, 3,417 HfC54H42N404 Hf(tetraphenylporphrin)(acac)z. 2.824 HfC&LoN403 Hf(tetraphenylporphyrin)(acac) (OPh), 2, 824 HfC64H32N16

I,lf(~hthalocyanine)L.3.140 HfCl4’ HfCI,. 3.422 HfC1401’b HC(CIO4),, 3,408 HfCI, lHfClhlZ ,3,430,431 HfCl6O~Pz HfOCl(O2PC1,)(P0CI3),3,407 HfCIRH, RClaNGS, HfC14(PhCH=NNHCSNH2)2.3,437 HfC1,002PZ HfC1,(POC13)z, 3,414 HfFZO HfOFz, 3,287 HfF4 €IfF4,3,422 HfF5 [HE,]-, 3.423 HfF, [HfF61Z-,3,423,426,329 HfF7 [HfF7j3-,3,423,426 H&IF,O, [HfF5(OOH)]2-. 3,388 HfHFhOz

HfRezC,8Hl~0,, Hf { (OC),Re( MeC0)3}2,3,402 HfSn2ClJ L Hf(PhMe)(SnMe,),, 2, 16 HfTiC,H,,Cl,N, HfCI,{Ti(NMe,),), 3,372 HfZB2C10HS7N2P4Si4 { Hf{N(SiMe2CH2PMe,),)(BH4)},( P - H ) ~2, , 1014 T If*R3C,0€I,1x2P4Si4 { Hf{N(Si~e2CH2PMez)2}}Z(H)3(BH4)3r 3,384,433 Hf2CJLOm [Hfz(OH),(C03),I6-, 3,411 Hf*C7N,O& [(HfO),(NCS),I3-, 3,287,380 HfiCloHz8C1,NPzSiz {HfC13{N(SiMezCHzPMez)Z}HfC14},,, 3,384 HfZCL2H30N4 {Hf(NBu‘)(NMe,)},, 3,375

HfiF140.3,287

HgAs3KhC39H39C12F

Cumulative Formula Index [(HgMe)z(CN)]-, 5,1062 HgC3HBCl2S HgCI,(EtSMe). 5. 1071 HgC3HgCIzP HgCIz(PMe3).5.1082 HgC3Hi,CIzN& Hg(HzNCSNH,)3C12,5, 1072 H~C~HIZIZN~S~ Hg(H2NCSNH&IZ.5 . 1072 HGN, 062

THiBr,]-, 5,1061 HgBr, [HgBr4I2-,5, 1061 HeBrh THgBr6l4-,5 , 1061 HgCClNS Hg(SCN)CI, 5, 1063 HgCCltN [HgCl,(CN)]-, 5 , 1062 HeCCLNS lHg(kN)CIzl-, 5,1063 HECFBNB a-CF,Hg(NS), 2,235 HaCHNO Hg(CN)(OH), 5,1062 HgCHO3 [HgHCO,]+, 5,1066 HgCHO, [HgOHC03]-, 5,1066 HKH, THgMe]+,2,967,979 HgCH3CIS HgMeSCI, 5,1070 HgCHsN3 MeHg(N,), 2,235 HgCH,N [HgMe(NH,)]+, 5 , 1079 HgCNzO3 Hg(CN)(NO,), 5,1062,1067 HgCZF3NO CF3HgNC0,2,235 HgCzH3NO (HgNAc),, 5,1074 HgCJLNzS4 Hg(S&NHZ)z, 5, 1072 HgCzHSS [Hg(SEt)]+,6,456 HgC2H 6S z Hg(SMc)z, 5, 1071 HgCzH&IzNz Hg(en)CI,, 5,1080 HSzHsClzOz HgCI,(MeOH),, 5, 1070 HgCzINz [Hg(CN),I]-, 5, 1062 I

W W z

Hg(CN)2,5,1062 HgCJ'JzOZ Hg(CNO),, 6,1026 HgCzN50, [Hg(CNO)z(N3)]-, 5, 1062 HgCaH6CI S HgCI,(-H,), 5,1071 HgC3H6N

390

391 Hg(Et,PS),CI,, 2,641 HgC L z H ~ ~ C I ? N ~ F ~ S Z Hg{(MezN)3PS)zC12, 2,642 HgCiJW8204 Hg(bipy)(OzCCF3)2,5, 1078 H ~ C I ~ H S ~ Z ~ ~ S ~ Hg(saccharinate),, 5, 1075 HgCi&ioO, Hg(tropolonate),, 5. 1066

H~C,~H~~N,O,

He(NHC0PhL. 5.1075 H&;H,NO' ~PhHgCNO., 2.13 . HgC86F606 Hg(OCHzCHz0CHz~H2)( OZCCF3),,5,1066

HgC14H N 4 [Hg{NyMe)CHzCH2N(Me)CHCH2CH2N(Me)CH2CHzN(Me)CH2CH2kH2)]2i. 2.912

HgC1z(SBu'2),2,553 HgCsH1sSz Hg(SBut),, 5,1071 HgGHzoN4

[Hg(&HCHZCHzNHCH2CHzNHCHzCHz-H2)l2+,

2,912 HgC&HzoBr02 HgBr(~HPhCH(Ph)OORu'),6,347 H&,H,,CI,YP

Hge'H ClN H , ' ~ 3 - ~ y ~ M e ) C5 -I1078, , . 1081 -'

Cumidative Formula index Pt(GePh3)(Hg GePh,) (PPh,),, 5, 421 HgHBrO, Hg(OH)BrO,, 5,1069 HgHClO, Hg(OH)C103. 5.1069 HgHFO Hg(OH)F, 5.1059. 1069 HgHN04 Hg(OH)(NO,). 5.1069 HEHO [Hg(OHj]+. 2,299; 5, 1066 HgH0,P '

HgCl [HgCII+,2,4 HgCLOs Hg(CIO,),, 5 , 1068 HgCh [HgCI,l-, 5,1061; 6,851 HgC& [HgC1,]2-, 5, 1061; 6,851 HgC15 [HgCl$ , I , 39; 5, 10h2 IlgCoCt I,,N,S [c~(NH,),(~-Nc:s)I1gl4+ 4,681 HgCoC6N6S6 [ C O H ~ ( S C N ) ~ 5, ] ~ 1064 -, HgCoSe2C6N6S4

kgNH,Br, 5.1077 HgHzFN HgNH2F. 5.1076 HgHA [HgS(HS),]'-. 6.853 HgH3N03S Hg(NH,)(SO,). 5 . 1079 HgH3S3 Hg(HS)3, 6,853 HgH& HgS(II,S),, 6 . 851 HgI lbBr2NZ Hg(NH,),Br2, 5.1U77 1 IgH6Cl2N2 Hg(NH3)aC12,2.28; 5 , 1076 HgHizO6 [Hg(Hz0)6]2+,5.1068 HgI [HgIl+, 2, -1 HgIN03 HgI(N03). 5 , 1062. 1067 HELO, -Hg(103)z,5. 1068 HgI3 [HglJ. 5.1061 JId4

[IIg1412-. 5 , 1061: 6.8.53

w6

[HgI6I4-. 5. 1061 HgIrC7Hl8Br3OP2 {IrCOBr,(PMe3)2}HgBr, 1, 123 HgIrC37H30Br2C10P, IrBrCI(HgBr)(COj(PPh,),, 4, 1124 HgIrC37H3aCIN20P2 {IrC1(CO)(PPh,)2}Hg(NO~)z, 4, 1125 HgIrC37H30C1301'2 IrCl(~igClz)(CO)(PPh,),, 4, I125 IrCI,(HgCI)~CO)(PPh,),, 4, 1124, 1127 HgIrC3rH30CINIOP2 IrCI(CN)(HgCN)(CO)(Pph,),, 4, 1125 HgIrC3,H,,CI,F,NPz IrC12(HgCI)(I\ICFzCHFCF3)(PPh3)Z, 4, 1124 HgIrC53H30CIOP2 IrCI(HgC=CPh)(CO)(PPh,),(C=CPh), 4, 1121 HgIr3C1iiH9aC1303P6 [{IrCl(CO)(PPh,),}3Hg]z+, 4, 1125 H~I~,CI~SH~ZOC~~O?PR [{IrCl(CO)(PPb,)2}JHg]z-, 4, 1125 HgMnC,N,S, HgMn(SCN),, 4.22

392

Cumulutive Formulu index

393

Sn(tetraphenylporphyrin)Mn(CO),HgMn(CO),, 2,843 HgMoCRH,Cl

HgPS3 HpPS,. 5.1070

HgS4 [HgS,I6-, 2,525; 5 , 1070 HgSs [Hg(S,),j2-, 2,542,546

HgSb4Ss. 3.265 HgSeCH,ClZN2 HgCI,(W2NCSeNH,), 5, 1074 HgSeCl8HlSCI2P HgCI,(SePPh,), 5 , 1074 HgSeO, HgSeO,. 5.1067 HgSeO, I IgSeO,, 5, 1067, 1069 HgSc2C2HsC12N4 HgCI2(H,UCSeNH2),, 5 , 1074 HgSe,C',H,CI, HgC1,($eCHICHzSeCH,~H,), 5,1074 HgSeZC,H,,Clz HgC12(MeSeCHzCH,SeMe), 5 , 1074 HgSezCz4H,,CI,P, HgClz(SePBu3)z,5 , 1073 HgSe3C3N3 [Hg(SeCN),]-, 5, 1064 %Sea [HgSe,I6-. 5, 1071 1 IgSe,C,N, [EIg(ScCN),j2-, 5, 1064 HgSlaCizHJJ2 Hg{N(SiMe,),}2, 5 , 1074 HgSnCAHT8 Hg(SnMe,),. 5 . 1085 HgSrC4H,N40& SrHg(SCN)4. 2,297 HgSrSe,C,N, SrHg(SeCN),, 5 , 1064 HgTeC4H, ,C1, HgCl,(TeEt,). 5 . 1074 HgTeC12H1& HgIz(TcPh,), 5 , 1074 HgTeO, Hglen3,5,1O6X HgTe,C,d 115 [Hg(TePh)3] , 5 , 1074 HgWzSs [Hg(WS,),]2-, 2,566,575 HgZnCI6H8N6S4 Zn(phcn)Hg(SCN),, 5,1064 HgZnC2sH16NsS4 z n ( ~ h e n ) ~ H g ( S C N5,) ~1064 , Hg2AgOJ Hg,AgPO,. 5.1051 Hg2AsC3FgN03 Irrg,{As(CF,~,}(NO,)]+, 5, 1058 H ~ z A s ~ C ~ H ~ ~ N ~ S ~ {Hg(SCN)2)2(PhzAsCHzCHLAsPhz), 5 , IO84 HbbC,,H&LO,

HgC12(~-OAsPh3)2HgC1~,2,498 v

-

[HgS2I2-, 2,525; 5, 1070: 6,853 HgS,O, [Hg(SO,),l2-, 5>1070

Hg2AS2C51H66N4012 (Hg{(2,J,h-Me3C6t1,),As}(N03)2)2, 5, 1084 I ~g,AszSbCl,H,,Fl, Hgl(ASF,)z(SbPh3), 5, 1058 Hg,BrN

Bg,ErN

Cumulative Formula Index

394

IHg(DMSO),( pDhlSO),Hg(DMSO),]4+, 2,489 H~&EHI~Nz [Hg2(quinoline),jz+,5, 1056

1069

_____

395

Cumulative Formula index

-.

Hg,(OH);(SO,),, 5 , 1069

Hg3PS4,5,1070

!),

5, 1064

Cumulative Formula Index

396

kfoC33H570, HO(BU*COCHCOBU~)~, 1,408; 2,373; 3, 1078, 1106 HoC~~H~SK~O Ho(octaethylporphyrin)(OH), 2,822 HoC4sH3306 Ho(PhCOCHCOPh),, 3,1077 HoC4sH&, Ho(PhCOCHCOPh)3(H20). 1,81

HOGSH~NA H ~ ( B U ' C O C ~ C O B U ' ) ~ ( ~2,-386; M ~3,~ ~1079 )~, HoHfiNxOu Ho(NO,);(H,O),. 3. 1086 IiON501j

[Ho(NO,),IZ-. 1.99 HozOi~S3 Ho2(S04),, 1,261

IC1, [ICl4]-, I, 50 IF< iF5, 1,50 IF,O IOF5, 1,49 IF7 IF,, 1,71 InAlS, AlInS,, 3, 120 InAb&sH8401z In{Al(OPr'),},, 3, 161 It1AsjCzoH3ZClz [lnCl,(diars),] ' , 3, 160 InAs,C,,H,,, [In(AsPh,),]'+, 3, Ihll In BrCI [InCI,Rr]-, 3, 166 InBr3C1 [InBr,Cl]-, 3, 166 InBr, [InBrJ, 3, 155, 166 InBr, [InBr,13-, 3, 166 InCH,O InMeO, 3,161 InCH,P {InMe(PH)),, 3, 164 InCzf1, [GMe,]+, 3, 165 InC,N,O, [In(NCO),]-, 3, 155 InCzNzSz [In(NCS),]-, 3,155 InC3H306 In(O,CH),, 3, 163 InC H 0 InMe,(OMe), 3,161 InC3HI2P InMe,(PH,), 3, 160 InC,NJ In(CN),, 3, 157 InC3N3S3 In(NCS),, 3, 159 (Tn(NCS),lz-, 3, 155 InC4H4010 [In(C,04)z(OHz)~1-,3,163 InC4H604 In(OAc),, 3,156 InC4H8S4 [In(SCH2CH2S)2]-.3. 161 InC,H,O, InMe,(OAc), 3, 163 1nC4Hl2 InHzEtz,3, 166 InC,H,,CI,N, [In(en)zClz]+,3, 158 InC,N,O, [In(NCO),]-, 3. 159 InC4OU [In(C204),]--,3. 163

,

InC,HS InCp, 3, 155 I~C,H,,OSI InMe2(OSiMe3),3, 161 InC5N5S, [In(NCS)5]Z-,3.160 InC6F906 In(O,CCF,),, 3.163 TnC6H9C130,8 [ I ~ ( O A C ) ~ ( C I O ~3,) ~163 ]~-, InC6M9F60 InMe,{OC(CF,),Me}, 3,161 InC,H,O, In(OAc),, 3. 356, 163 II1C6Hl3O2 InEt,(OAc). 3, 163 I"CdlT;dN6 ' [In(e11)~1~-, 3,158,159,163 IflChNhSfr [In(I*U'CS)6)3-,3,160 InC6N6Se6 [In(NCSe),13-. 3, 160 InC6OI2 [In(Cz0,)313-, 3,163 InC7H130z InMe,(acac), 3, 162 InC,ClN,S, IIn{S,C,(CN),}U-, 3,164 InCUH4F3O2S

InlSCH=CHCH=cCOCHCOCF,I. 3. I55 I,

InC8ji16N202 [Tn(l;JCH,~~,OCH,tH,),]+, 3,155 InC8Hz1Br2N2 InBr,Et(TMEDA), 3.158 ' InC,Hz~I,O,S, [InI,(DMSO),j+, 3, 164 InC8HZ4o2SiZ [InMe,(OSiMe,)J, 3, 161 InC,N,S, [InJS2C2(CN)Z)2]-r 2,605; 3, 164 In&H,NO ln(8-quinolinolate), 3, 155 9

1nC,HlsN3OhS3 In(NCO),(DMSO),, 3, 159 IfiC9H2103 In(OP& 3, 161 InC9H2,Si3 In(SiMe&, 3. 158 InCIoH8Cl4N2 [InCl,(bipy)]-, 3,159 InCIoHI2N2OllS [In(edta)(S0,)l3-, 6,971 InCl0H2,N,

[ln(lq4.8.11-tetraazacyclotetradecane)lf , 3 . 155

397

Cumulative Formula Index

In(NC0)3(phen),3, 159 InClSHllC12N3 InCl,(terpv), 3, 159 InCl5H;,F90, In(MeCOCHCOCF,L.- 3.162.163 InCI;HISC12N202 InCl,(acac)(bipy), 3, 162 hCl5HlSS4 InMe(3,4-SzC6H,Me),, 3, 165 InC&2106 In(acac)3, 3,156, 161, 162 InC17H15C12N202 -I

.

In(S-rnerhyl-8-quinolinolate),, 1, 530 InC3oHxN6 [In(bipy),13-. 3.158 InC36Hz4N6 [In(phen),j3*, 3.158 InC36H3oC13P2 InC13(PPh3)z,3, 160 InC36H44C1N4 In(octaethylporphyrin)Cl, 2,843 lnC3&~4N903 In(NCO),(phen),, 3-159 InC3,H,,WM" In(NC0)3(0PPh3)2,3, 15Y InC4,HZ,CIN4 In(tetraphenylporphyrin)CI, 2,843 InC45H31N403S In(tetraphenylporphyrin)(OSO,Me), 2,821 InCs2H48P4 [ I n ( d i p h o ~ ) ~ l3,~ + , 160 InCnH6004P4 [In(OPPh3)4]3+'.3. 163 InC72H6nP4 [In(PPh3),I3-, 3, 160 TnC96H204024Pb

In{OP(O)(OCH,CHEtBu),}, { HOP(0)(OCH2CHEtBu)z)3, 6,798 InU1, [InClJ, 3,157,166 InCI, [InClslZ-, I , 40; 3, 166 InCi, [InCI6l3-,3. 166 InCoC40H44Y404 In(octaethylporphyrin)Co(CO),, 2,843 InduGaO, CuGaInO,. 5,607,650 InF30& In(O,SF),, 3, 162 InF, IInF,]-, 3,165 InF5 [InF# , 3, 165 InF6 [InF6I3. 3. 165 InGaC1, [InGaC16]2-,3,128 InGaO GaInO, 3, 127 InGe3C18H4s In(GcEt3),, 3, 158 InHClO [In(OH)C1]',3,lhl InHFzO In(OH)Fz, 3, 161 InIi02 InO(OH), 3, 161 InH0,S In(OH)(SO,), 3. 162 InHzCIsO [InC1,(H20)]-: 3,166 InHzFsO [InFs(Hz0)]2-.3.165 InH203 [In03H2]-.3+161 InH, (InHA, 3,166 [IIIH,]+~ 3,141 InH3F3N InF2(NH3),3,I65 InH303 In(OH),, 3.16'1 InH, [1r1H,]-~3.166 ~

I~(S-quinoIinolate),, 1,528,530; 3. 156, 166; 6,971 InC2SHZO08 2, 397; 3, 162 [In(tr~polonate)~]-, InC3oHzzN6 [In(terpy),13+,3, 158 InC30H24N303 In(2-methyl-8-quinolinolate),. 1,530

398

399

Cumulative Formdu Index

lnH4CI4O2 [InC14(H,0)2]-, 3. 166 InH4F402 [InF,(H,O),]-, 3, 165 InH404 [In(OH),]-, 3, 161 InH4010S, [In(H20)2(S04)21-,3, 162

I

~

H

~

~

~

[I~I(OH),]~-, 3,161 InH9F3N3 InF,(NH?),, 3, 129 InHI2CI3N6 InCI3(N2H4)?,3, 158 lnHI2O6 [In(H,0),]3+, 3,160. 166 InHl,BrN, [In(NH3)5Br]Z+, 3, 158 InHiSN6 [III(NH,)~]~+, 3,158 In14 [InI,] , 3 , 166 InMnC41H44N405 In(octaethylporphyrin)Mn(CO),. 2.843 InMoC44H49N403 In(octaethylporphyrin)MuCp(CO), ,2,843 InNaO19 [IA(NO,)J, 3,162 In0,P2 [In(P04),]3-, 3,162 InO& [In(SO,),]-, 3, 162 InOSe, [Ii(Se04),]-, 3, 163 1nOl2S3 [In(02S02)3]3-,2,418,426 [In(S04),13-, 3,162

Ins, Ins,, 3, 164 Ins, [Ins,] , 3 , 164 InSiC6HisN3 InMe3(N3SiMe3).3, 159 InSnC12H30 [InMe3(SnMe3)]-,3, 158 InSnClsH,,CI, InCl,(SnPh,), 3,158 InSnClsHl5CI3 [InCI,(SnPh,)]-, 3,158 InSnC36H39N2 In(C6H4CH2NMe2-2),(SnPh,),3, 1% lnWC44H49N403 In(octaethylporphyrin)WCp(C0),, 2,843 In,Br,I In,Br,I, 3. 156 InzC4Hlz0 (InMe,),O, 3, 161 hC6H80i6 h ( C ~ 0 4 ) 3 ( H ~ O3,163 )~, In2C8H2d6 {InEtz(N3)),, 3, 159 1n2C8H24N2 {InMez(N=CMe2)),,3, 159 InKloOloSlo [In2(C20zS2)5]4-. 3, 167 In2C12H30Br4P2 In2Br4(PEt3),,3, 156 In2C12H3002 {TnMe,(OBu')},, 3, 161 I ~ z C I ~ H ~ ~ I ~ N ~ In214(H2NEt)6, 3, 156 InzCisHaJ'42 {InMe,(NMePh)),, 3,159

lrAsPdCIVH3 ,CI,P,

hC20H20Br4N4 In&(pyh, 3, 156 InzC24Hzo0 (InPh,)20. 3,161 rnzCz8H4414N8 In2I4(blpy),(H,NEt)4.3, 156 In2C28HShLN I n z 1 4 ( E t 4 b i ~ ~ ) ( b l ~ y ) ( N H3,3 )156 S, In2C13 Tn2CI,. 3. 157 Tn,C16 [In2CI,]'-, 3, 157 In,CuSe,Br CuIn,Sc,Br, 1, 111 h2F, [In,F,]-, 3. I65 h,FeC&mNsOi

(In(octaethylporphyrin)},Fe(CO),,

2, 843

InJ,. 3. 165 InJ4 In214.3, 157 In,O In,O, 3. 127 h016P4 [Inz(P04),jb 3, 162 InzSs [InzS612-,3, 164 Iti3CbH,8Ki6 {InMe2(N2)13, 3,159 In,CI, In,C14. 3. 157 In3FlI [In,F,,]Z-. 3, 165 In,Mol,Se19 In3Mol5Sel9.1,164 hCizHd, {InMc,(CN)},, 3, 158 - 1

InJW,

[In4(OH)J6' , 2 , 3 0 0 In,Slo [ i n , s , , y . 3, 164 In,Se, In,Se,. 3. 157 In4Te3 InlTe3, 3. 157 In,Clg InjC19.3. 157 hF14 [In5Fl.,j5-. 3, 165 InjS,. 3.157

In6S7 I@,, 3, 157 In,Se, In,,Se,, 3.157 IrAgC5eH53C1NOP4 Ir(CNBu')(CO) (p-dppm),AgCI, 4, 1163 I~ASBC~~H,CI~N, IrC12{HB(fiN=CMeCH=cMe),} (A,PhMe,), 4. 1134 IrAsC25H34C10P2 [IrHCI(AsMe,Ph) (CO)(PMe,Ph),]+, 4, 1150 IrAsC30H2sN04 Ir(OAc),(AsPh,)(CNC6H4Me-4), 4, 1121 ITASC~,H~~N~O~ Ir(AsPh3){.MeCOCHC(Me)=NCH,},(CNC6H4Me-4). 4,1124 ITASC~~H~~N~O~ Tr(AsPh3~(salen)(CNC6H~Me-4), 4, 1124 IrAsC72H5,P, [lr(PPh,) { As( C,H4PPh,-2) 3 } ] + , 4, 1135 IrAsPdC19H31CljPl PdCl(AsMe,) (p-CI)21rCI,(PMe2Ph),, 5 , 1 162

IrAs2C27H22CI0

Cumulutive Formula Index

400

IrRr, IrXs2C27H22C10 [IrBr,lZ-, 4, 1157 IrCl( CO) (Ph,AsCH=CHAsP h2). 4 1108 [IrBr6J3-,4: 1149.1157 IrAsZC17H30CIN207 IrCH, 5N,0 IrC1(N03)2(CO)(AsPh3)Z, 4, 1 1 4 4,960 [Ir(NH3)5(C03j]7. I~AS~C~~H~~CIO [Ir(OC0,)(NH3)5J+,4.1141 IrCI(CO)(AsPh,),, 4, 1159 IrC2CI2NO6 I~AS~C~~H~~CIO~ IrClz(N02)(C204)]3-, 4, 1142 IrCl(CO)(O,)(AsPh,),, 2, 320 IrCzClzOz IrAs2C37H,010, [Ir(CO),Cl,l-l 6: 136, 142 Irl(CQ)(O,)(AsPh,),, 2,320 IrC,CI,NO, I rAs2C37H330 ~IrCl,(NO,)(C,O,)]"~~: 4,1142 4,1134 11H~(A\Ph~)z(CQ), ll-c,cI4o4 1rAs2C4,,1f3,CI [IrCI,(C20,)]3-. 4, 1142 IrC1(2-CH,=CHC6H,AsPh2)z. 4, 1111 Ir.C2H,8N6 IrAs,C,H,,CIN [Ir(NH,),(NChle)]3*, 6 , 449 IrH,CI(AsPh,),(4 . _MeC,H,NC). 4. 1175, 1134 IrC21,0, IrAszC44H40N [IrI,(CO)&, 6,278 IrH3(AsPh3)2(4-MeC6H4NC), 4, 1125.1134. 1156 IrC,BrO, trAs?CasHaaN02 Ir(CO),Br. 6. 151 Ir(acac)(AsPh~),(4-MeC6H,NC). 4.1126 IrC3C103 I ~ A s ~ C ~ ~ H ~ ~ P ~ Ir(CO),CII 2,201; 6 , 151 [Ir(P~h,){P(C6H4AsPh,~2j3}]~~. 4, 1135 IrC3H,Nj IrAsqC3,H4,02 Ir(Ch)3(VI.13)I,4, 1125 [Ir(AsPhMe,),(O,)]+. 2, 320; 6 . 341 IrC,H,,N,O IrAs4C64H64NOP2 [Ir(NHJs(DMF)]3-, 6,433 [Ir(NO){I,4-{(Ph,AsCH,CH2),PCH2).2C',I 14)] , 4 , TrC,IO, 1114 Ir(CO),I? 6 * 151 I ~ A s ~ C ~ ~ H ~ ~ P ~ IrC31303 [Ir( l.4-{(19h2AsCH2CH2)IPCH2)LC6H,)]', 4. 1 I13 IrI,(C0)3. 6.278 IrAs4C64H66P2 ',4,1114 IrC3N3 [IrH,{ 1,4-{(Ph2AsCH,CH,),PCH2}2C,H4)] 1r(CNj3: 4: 1125 IrAs4C65H640P2 [ I ~ ( C O ) { ~ , ~ - { ( P ~ , A S C H , C H ~ ) ~ P C ~ T,4, ~ ) ~ C G HIrC4CI2O8 ,)I~ 1114 [IrC12(Cz04)2]3-4. 1142 1rC4Hl2Cl3S2 I~As,C~~H~~P IrCI,(SMc2),, 4, 1145 [Ir(PPh3){As(C6H4AsPh2-2),}]-. 4. 1135 IrC,HI2C1,O2S2 I~AS~C~~H,,P, IrH(AsPh,),, 4, 11 19 1rAuChOH6,P4 Au(PEt,)(~~-H)lrH,(Prli,),.5 g69 IrAuC6,H7.,N,P, [Ir(CNB~')~(pdpprn),Au]~+. 4. 1163 IrAuC,,H,,P, Au(PPh,)(K-H)IrH,(PPh,),, 5 , 869 IrC,H16C12N4 IrAu4Cl0&9d'6 [IrC12(en),]+. 4 . 1 1 3 , 1161 [IrAu,H,(PPh,),]+, 4.1166 IrBC8HsN402 IrC4H16h' [Ir(Ni)2(en)2]-.4. 1133 Ir(CO),{H,B(&N=CHCH=cH)2}. 4. 1108 IrC4H18CIN40 [IrCI(en),[IIzO)]z+, 4 , 1 I29 IrC,HI,N,O, [Ir(OH)2(en)2]+.4. 1129 IrH;(BH,)(PBu',Mr),, 4,1149 TrC,H,,N,O, 1rBCl9Hz7F6N6Q4 [Ir(OH)(en),(H,O)I+, 4,1161 Ir(D,CCF,),{HB(N'N=Ch.leCH=C' Me);)( I L 2 0 ) - 4, IrC4H2zN6 1134 [Ir(en),(iTH,),] 4 , 1129 IrC5CIN5 [Ir(CN),Cll3-, 4?1125 IrC5HN5 [Ir(CN),(H)l3-. 4: 1166 IrC5H2N50 [Ir(CN),(H,0)]2-, 4, 1125 IrC5H5C15N [IrCl,(py)lz-, 4;1130 IrC6HIsCLN& IrC1,{MeC(S)NH2),, 2,647 1rCJ-L 7CI,0,S3 IrHC12(DSM0)3,4, 1160 IrBSPtCl,H,,OP, IrC6H&lF6N3P3 PrB,H,,IrH(CO)(PMc,),, 4: 1165 IrC:I(PF,NMe,),, 4, 1163 IrBrzC14 IrC,H,,Cl,N, [IrCl4BrZJ2-,4, 1157 [IrC12~~H2NCH2CH2NHCHz)z}]+r 4, 1130 IrBr4C12 IrC6H,,Cl,0,S3 [IrBr4C12]2-,4, 1157 ~

401

Cumulative Formula Index

IrCI,(DMSO),. 4, 1160 IrCgH18C14P2 IrCI4(PMe3),, 4, 1134, 1155 IrC,H,9C1,0,S3 IrHCl?(DMSO)>.4, 1159 1rC6Hz3P2 IrHS(PMe3),, 2, 1039; 4 , 1158. 1160 ,.

IrC7H70, Ir(acac)(CO),, 2.376: 1.11 16 IrC7Hl,ClOP, IrCI(CO)(PMe,),, 4, 1109 IrCRHIZCl Ir(cod)CI, 2,698 IrC8HI2NJ [Ir(CNMc),]'. 4, 1107 lrCRHIJCIZ IrHCl2(CsHl2), 6 , 350 IrC,H,,Cl,S, IrCI,(SEt,),, 4, 1145 [IrC1,(SEt2),]-, 4, 1145 IrC9H13CIN IrHCl(CN)(cod), 4 , 1149 IrC9H150z Ir(acac)(C,H,),, 4, 1140 IrC9H2,C13P3 IrCI,(PMe3)3, 4, 1124 IrClllHl,lC14N, [IrCl,(py),l-, 4, 1130 IrCl,H ,,Cl,N,O IrC13(H20)(py),,4, 113l1 Ti-C ,H ,8 [IrH3(C5Me5)1-.4, 1166 IsioHi9 IrH4(C5Me5),4, 1166 IrCIZHloC1,S [IrCI,(SPh,)] ~,4. 1157 IrCl2HlOCI,S [IrC15(SPh,)]2 , 4 , 1157 IrClzHIHNz [1r(~od)(McCN),]~-, 4, 1159 I~CIZH19C14N3 Ir(4-Me,NC6H,CH=?.JCH2C,H~CH2~H~)Cl,, 4, 1162 IrCIzI [Ir(CNEt),] ' , 4, 1101 IrC,,H,,ClS, IrCl(cod)(MeSCH,CH,SMe). 4, 1117 IrC12H30C13S3 IrCl,(SEt,)7, 2, 552; 4 , 1145 ~

IrH5(PEt3),. 2, 1039; 4,1151 IrClZH36C12P4 IrCI2(PMe3),, 4, 1134 IrC13H1902 Ir(acac)(cod), 4. 11 15 IrC,,H,,P IIrH(C,Me,)(PMe,)]', 1.1166 IrCI3HZbP 2.699: 4 . 1166 IrHL(C5MeS)(PMe3). IrC,7H7,CIOP7 IrHCI(CO)(€'Et,),( PH,) 4. 1 163

IG0H1RN4

[rCl3H3,OPJ [IrH(CO)(PEt;)2(PH,)(PH,)lt , 4 , 1163 [rC1JH1003PSL Ir(CO),{SSP(OPh),}, 4, 1119 IIC~~H~~N~SZ Ir{ SZC2(CY)2)(q-C5Me5)r 4, 1147 IrC, 4H2,0?PSZ Ir(C0)2{SSP(C6Hll)z},4. 1119 1rClSH1SC13N3 lrC13(p!)3. 4, 1 !30 IrCl5lI,,F,C)? Ir(hfacac)(y5-C5Mes). 4, 1115 IrC, jH,,O, Ir(acac),. I , 65 IrC15H220L Ir(acac)(qS-C5hle5),4, 1115 IrCljH24N7S6 Ir(S2CNC4H8)3,4, 1145 IrC16H22CW2 IrC14(Ph.le2Ph),,4, 1156 {lrC14(PMezPh),]-, 4, 1156 IrC,6H,,Ki,SJ Ir(S2CNR.lel),(r~-CSMe,),4, 1147 IrC laH2,CI, TrCI(C,H,4)Z.6 , 246

IrC,,H,,ClSi

[Ii?1,(S
Cumulative Formula Index

IrC20H18N4

[IrMz(bipy)z]+,4, 1162 IrC2~H~oCLN4 [ I r C l , ( ~ y ) ~4, l ~11, 30 IrCdLJN2 lrI(phen)(cod), 4,1139 IrCzoHzoN2 [Ir(phen)(cod)]+,4,1139 IrC?OH20NZ02 [Ir(O,(phen)(cod)]+, 4, 1139 IrC20H2q04 Ir(acac),(q5-C5Me,).4, 1 1 15

IrCI(CNC,H,),(CO), 4, 1102 IrC,,H,,N,OP Ir(C0) {H,B(Ih=CHCH=kH),}(PPh,), IrC2SH27N20PSz [Ir(CO) (PPh3)(qz-SCNMe2)2]+, 4,1154 IrCZ5H2,N20PS3

4.1108

[Ir(CO)(q2-CSNMe2)(PPh3)(S,CNMe,)]f, 4. 11 18

IrC20H3sPZ

IrHS(PEt2Ph),,4, 1 1 % IrC20H~6N4 I I ~ ( C N B U ' ) ~4, ] +11 >02 IrC21Hls03P [Ir(CO),(PPh,)]-, 4, 1100,1103 IrC21HisS6 Ir(S2CPh),, 2,646 IrC21H20CINOP IrCI(C0)(2-Ph2PC6H,NMe2),4, 1124 IrC21H30Br03P2 IrBr(CO)(OZj(PPhEtz)2, 2, 320 IrC,,H,,,CIOP, IrCI(CO)(PEt,Ph),, 4,1108 TrC21H30C130P2 IrCl3(CO)(PEt2Ph),, 4, 1 I09 IrC2,1 I,,CIP, IrC1{,C(CH2CH,PBu',),), 2, 698 IrC2,H4&1P2 IrHC1(CH(CH2CH2PBut2)2),2,698 IrC2iH4,1'Z Ir(PPr13)z(C3Hs),2, 1026 I~CZZHI~F~N~~~SZ [Ir(bipy),(OS02CF3),]+, 4, 1162 I~zzHBINP [Ir(cod)(py)(PPr',)] I , 6,246 II-C2,H46CIP2 1rHCI(CkI=CI KH,P Bu',)(Bu',PCH,CI 1=CH), 4, 1137 IrC&49PT 1rH(PPri3),(C4H6),2, 1026 IrC2,H,,C1NP2S2 IrHCl(PPh,)z(S,CNEt,). 4. 1106 IrC24H15Br4N03P Ir(NO)(1,2-02C6Br4)(PPh,). 4, I116 IK?~HI~C~ZN~ [IrCl,(phen),]+, 4,1162 IrC24H19N03P ~~

402

~~

Ir(NO)(1,2-02C6H,)(PPh3), 4. 1116 IrC24H21S6

IrC25H2,N302 Ir(acac)(cod)(phen). 4, 1165 IrCZ5H,,C10P, [IrHCi(CO)(P~le,Ph),]C,4, 1150 IrC2,H20CL2N4 [IrCl,(phcn)(5.6-Mc,phen)]+, 4, 1 130 IrC,,H,,O,P, [Ir(Od(dppe)l+, 6,329 IrC,,H,,BrCIP IrC1( '-2-BrC6H4PPh2)(cod), 4, 1163 IrC26H2,BrP [h(q2-2-BrC6H4PPh2) (cod)]+, 4,1163 IrC*,H,,BrP

[ZrH,(q2-2-BrCgHqPPhz)(cod)Jt, 4,1163 1 r C 2 J L0, Ir(acac)(nbd),, 4, 2115 IrC,,H,,ClP IrCl(codl~PICH,,)~1,4, 1109 -, IrC26H46CloPZ IrCI(CO){(Bu~2PC~CCl-12CH2)2CH2), 4, 1 1 12 IrC2,H2,F6NZOP 1r { NHC (CF, )=C (CMe=CH, )C(CF3)=R H } (C0 1(PPh,). 4. 1108 IrC27HZ4C10P2 IrCI(CO)(dppe). 2.695 IrCZ7Hz6BrOP, IrBrH,(CO)(dppe), 4, 1163 IrC2,H26C10Pz IrH,CI(CO)(dppe), 2.695 IrCZ7H2&12P2 IrC:I,(PR.lePh,),~Me), 4, 1108 IrC,J I,,CI,N, [IrC1,(4,7-Mc,phen),]', 4, 1162 IrC,,H,,BrOP2 IrBr(CO){(PhzPCH2)CH2), 4,1162 IrC2RH29C10P2 IrC1(CO)(PMePh2)2(hfe),4,1109 IrC28H29CI,03P2S IrCl,(MeSO,)(CO) (PPh,Me),, 4,1146 IrCZsH3,,02P Ir(OAc)(cod)(PPh,), 4,1159 IrC28H44N4 [Ir(CNC,H,,),]+, 4. I101 TTC*8H4&0Z

Ir(S2CCH2Ph)3,2, 646 IrC24HZ8N2 IIr(3,4,7,8-Me4phen)(cod)]+ 4. 1160 TGJ3oS3 ~

Ir{S(CHzCH2SPh),)(cod)]".4.Ill7

IrC24H32ChP3 kC1,(CHZPMePh)(PMe,Ph),. 4,1137 IrC24H32C14P3 IrC13(PMezPh),(PMePhCH,Cl). 4.1137 IrC24H33C12N03P3 IrCIz(NO3)(PMezPh),,4,1144 IrC24H33CI3P3 IrC13(PMe2Ph)3, 4,1137 1rC24H36P3

lrFIB(PMe2Ph)3r 164 ,~ 4,I

IrC24Hj7P3

~

[IrH4(PMe2Ph),]+,4,I164 IrC,,H56C1P, 1rH,ul(PB~',),, 4,1134 IG4H59P2 IrH,(PBu',),, 2, 1039 rrC2,H,,CIN30

IrH2C1(PBu'2Ph)z,4,1150 IrCz&LP, IrH,(PBu',Ph)l, 2, 1039 I~c,~H,,cINP, krHCI(cH=CHCH2PBut2)(But2PCH2CH=CH2)(4Mepy) 4,1137 IrC29H30CI03P2 IrCI(CO)(O,#PPh,Et),, 2,319; 4,1138;6,321 IrC29H30NOP2S ~

[Ir(dppe)(MeCN)(r~~-SOMe)]~+, 4,1165 IrC?,H,,P2P

Ir(cud)(PPh,)(AN=CHCH=C'H), 4,1167 IrC29H300P2Sz IrH(CO)(SCH2CH2PPh,)(HSCH,CH,PPh,). 4,1163 IrC,,H3,Cl,OP2 IrC1,(COEt)(PMePh2)2,4,1109

403

Cumulative Formula Index I~CWH~~OJ', Ir(C0) (BU'~PCH=C(O)P~)(B~'~PCH,COP~), 4. I136 IrH(CO){Bu',PCH=C(O)PhL, . , , - 4,1136 T~c~~H~~CIO~P~IrHCI(CO){ BU'~PCH=C(O)P~}(BU'~PCH~COP~). 4. 1136

irC30H24N6 [Ir(bipy),I3+, 4, 1130,1162 I ~ C ~ O H Z ~ N ~ ~ [Ir(bipy)3(OH)]2', 4, 1111 IrCwHmN,O [Ir(bipy),(H,0)]3+, 4,1131 IIC~~H~~CI~OP~ IrC12(C3HS)(CO)(PMePhz)2. 4. 1164 IGOH~SCW~ IrC13(PEt2Ph)3,6,303 I~C~OH~~C~ZP~ IrHCI,(PEt,Ph),. 4, 1159 IrC30H470PZ Ir(CsPh)(CO)(PPri3),. 4, 1162 IrC30H4703PZ h(CO) { PButZ(C6H4O-2)}{PBu',( C,H40Me-2)}, 4, 1110 Irc30H4704p2 kr{CH,c MezPButC6H,(OMc-B)~){OC6H3(OMe-3)(PBu'z-2)). 4. I138 1rC30H4804P2

~rrOC,H,(0Mc-3)(PBut,-2)),, 4,1121, 1138

IrC31H25N40P

IIr(CO)(PPh,)(PhN=NN=NPh)l+, 2.218 IrC31'Hz7NP [Ir(+H,)H(PPh3)(7.8-benzoquinolinato)]', 2, 690 IrC,,H,,,NP [Ir(c;d){P(CdH,,),}(py)]', 2,709. 71U; 4, 1166; 6,246 1rC3ZH15C1ZN8

Ir(chlorophthalocyanine)CI,2. 868 IrC3,H16CIN8 Ir(phthalucyanine)CI, 2, 868.870 IrCwHi6Ns Ir(phtha1ocyanine). 2. 863 IrC3ZH29N505PS~

Ir(NO)(PPh3)(4-MeC6H4S02N=NN=NS02-

[ 1I(d ppe) (cod)] , 4, 1160 1rC14Hd'~ [Ir(cod)(PMePh,),]+, 6,246 ItCy,H5003P2 h ( C 0 ) {PBu',(CH=CoPh)} { PBu*,(CH=COMePh)) 4. i l l 0 +

IrC36H30BrN20zP2 IrBr(N0)2(PPh3)2,2, 113; 4,1159 IrC36H30Br3NOPZ IrBr,(NO)(PPh,),, 4, 1120 TrC36H30ClNOP2 [IrCl(NO)(PPh3)2]', 4, 1104 I rC3,1-1&lN,O,P2 Ir(NO),CI(PPh,),, 4, 1099 IrC36H30C1N203P2 IrCl(NO)(NO,)(PPh,),, 2, 113 IrC36H30CIN,P2 IrCI(N2)(PPh3),, 4, 1105, 1106, 1159, 1160 IrC,,H,,CI,NOP IrC12(NO)(PPh3),4, 1106 IrC36H30C12NOPz IrC12(NO)(PPh3),, 2,103,105; 4,1104 IrC36H30C12N03P2 IrC1,(N03)(PPh3),, 4, 1144 IrC36H3,C13NOP2 [IrC13(NO)(PPh3),]' , 4 , 1104 1rC3bH3~N~O~P~ [Ir(NO),(PPh,),]+, 2, 103, 113; 4, 1105, 1159 1rC36HmNz06Pz Ir(N03)3(PPh3)z,4, 1143 I~C~~H~ON&P~ Ir(N03)z(NO)(PPh3)Z,4, 1144 IrC36H3,C1NOP2 IrH(NO)CI(PPh3),, 4,1100

C6H4Me-4). 2,218.222; 4. 1106 IrC32H4402P4 [Ir(Oz)(PMe,Ph)4]+, 2,319; 4, 1139; 6,329 IrC H P [ m 6 H 4 ) ( P M e 2 P h ) , l ' . 4. 1136

[Ir(C8H1z)4]+, 6,350 IrC3zH49C1z0P~

IrC12(Bu'2PCHzCOPh){Bu',PCH=C(0)Ph}, 4, 1136

[I;(2-Phpy)3]3+, 4, 1162 IrC33H2VN506PS~

Ir(NO)(PPh,)(CO)(4-MeC6H4S02N=NN= NSO,C,H,Me-1). 2,218 TrC33H46CIOPZ IrCI(CO){PBu',(C=CPh))2.4, 1110 IrC33H470ZP2 'lr(CO){ PBut2(CH=CdPh)} {PBu',(C=CPh)}, 4,1110

.. ..

..

IrC13(PBu3j3. 6,303

.

IrC37H290P2

Cumulative Formula Index

IrC3,HZ9OP2 Ir(CO)(C,H,PPh,)(PPh,), 4, 1114 IrC37H30Br03P2 IrBr(CO)(Oz)(PPh3)2r2,320 IrC37H30C1N02P2 [IrCI(CO)(NO)(PPh,),]+, 2.102, 103.109; 4, 1104 IG~H~OC~N~O,P~

IrCI(NO~)(NO~)(CO)(PPh~)~,4.1143.1144 IrC37H3oCINzO7Pz IrCI(N03)2(CO)(PPh3)2,4. 1143 IrC37H,oC10P2 IrCI(CO)(PPh3)2,2,218,220,318: 4. 1105, 1108, 1109, 1138, 1158-1160, 1163; 6, 247.263. 3113, 1019 IrC37H,oC10,P2Se IrCI(CSe)(O,)(PPh,),, 4,1148 ~G&OCIO~PZ IrCI(CO)(O,)(PPh,),, 2,31&-320; 4. 1139, 1140, 1159; 6,1019 IrC37H30C103P2S IrCl(C0)(PPh3),(SO,), 2,635; 4, I118 IrC37H3,,CI05P2S IrCI(CO)(02SOz)(PPh3)2.4, 1140 I K C ~ ~ H ~ ~ C ~ P ~ S ~ IrC1(CSe)(PPh3),, 4,1148, 1165 IrC37H30C1P2S~2 IrCI(CSe2)(PPh3),,4, 1148 IrCt,H30C12NOP2S IrC12(CO)(NS)(PPh3)z,2, 121 IrCJ7H3(,CI3OPZ IrCI3(CO)(PPh3),,4, 1117 IrC37H30C13P2Se IrCI3(CSe)(PPh3),, 4, 1148 IrC37H301N02P2 [IrI(CO)(NO)(PPh3),]t. 2. 103 IrC37H3010ZPZ [IrI(NO)(CO)(PPh,),]+, 4, 1104 IIC~~H~~IO~P IrI(C0)(02)(PPh3)2,2,319 IrC3,H~oIO~P~ IrI(CO)(O,)(PPh,),, 2.320,328,6,329 IrC37H30130P2 Ir13(CO)(PPh3)2,4, 1141 1e37H30N02P2

Ir(NO)(CO)(PPh,),, 4, 1100. 1104 [Ir(NO)(CO)(PPh,),]+, 4, 1100 1rC37H30N06P2 Ir(N03)(CO)(Oz)(PPh3)2, 2,320 IG~H~oN~OPZ Ir(N,)(CO)(PPh,),, 4, 1161 IrC37H30N303P~ ~ ~ ( N ~ ) ( C O ) ( O Z ) ( P P2,320 ~,)Z, 1rC37H30N309P2

Ir(N0,)(N03),(CO)(PPh,),, 4, 1143. 1144 IrC3,H3oN409P2 Ir(NO,),(NO),(CO)(PPh,),. I I00 IrC3,H,,CIIOP, IrHCII(CO)(PPh,),, 4, 1119 IrC37H31C120P2 IrHC12(CO)(PPh3)2,4, 1149 IrC37H31CM'~S~ IrCI,(S,CH)(PPh,),, 4. 1146 IG7H31N~06P2 IrH(N02)(N03)(CO)(PPh3)2~ 4. 11-43,1144 IrC37H31N207PZ IrH(N03)2(CO)(PPh3)2,4, 1144 IrC3,H&2Pz Ir(OH)(CO)(PPh,),, 4, 1116 IrC,,H,,O,PZS IrH(CO)(PPh,),(SO,). 4. 1118 IrC37H3,CIOP2 IrH,CI(CO)(PPh,),, 4, 1150. 1159 IrC3,H3,CIOP2S IrHCl(SH)(CO)(PPh,),, 4.1145,1165

404

XrC371133Ci2P2 IrCI,(PPh,),(Me), 4, 1137 TrC37H331NOP2 IrI(Me)(NO)(PPh,),, 2, 103; 4, 1100 IrC37H330P2 IrH3(CO)(PPh3),. 4, 1150 IrC37H33P2S~ IrH2(S2CH)(PPh3),,4, 1146 IrC,,H,,ClN40 IrCI(CO)(octaethylporphyrin), 2, 840;4, 112U. 1155 I~C.J~H&IZNJ IrCI,(CL-mclhvloctaeIhylpclrphryin), 2, 840; 4, 1155 IrC37H17N4

IrC1(CO){P(C,H,,),}2, 4,1110; 6,247 IrC38H2902PZ Ir(CO)2(C6H4PPh2)(PPh3), 4, 1114 IrC38H3nC10P2Se2 IrCI(CO)(CSe,)(PPh,),, 2,664,4, 1148 lrC38H30CI02Pz IrCI(C0)2(PPh3)2. 4, 1159 IrC38fITollF2Se2 IrCl(q2-CSc2)(CSc)(PPh,), 4, 1148. I165 IrC,JLoFPV2 Ir(O2CCF,)(N0)(PPh,),, 4, 1100, 1116 IrC38H3010P2 IrI(SCS)(CO)(PPh,),. 4. 1146 IrC38H,oNOP2 Ir(CN)(CO)(PPh,),. 4. 1101 ITC~~H~~NOP~S Ir(NCS)(CO)(PPh,),, 4, 1107 Ir(SCY)(CO)(PPh,),, 4, 1139 IrC38H3002P2 [Ir(CO),(PPh&]', 4 , 1111,1167 IrC38€730P3S3 [xl(cs)(PPll,),(;l-cs,)]*. 4, 1118 IrC38X131CIEI;OP2 IrHCI(CN)(CO)(PPh,),, 4, 1125, I150 IrC,J& ,OPzSz Ir(CS,H)(CO)(PPh,),. 4. 1146 Ir(S,CH)(CO)(PPh,),. 4. 1146 IrC38H3102P, IrH(CO)Z(PPh3),,4,1120; 6,303 IrC38H3,04Pz Ir(OCO,H)(CO)(PPh,),, 4, 1116 I~C~SH~~O~PZ 1r(0C0,H)(C0)(0,)(PPh3),,4, 1116 IrC,,H,,N,P ,_ _- . [IrH(bipy),(PPh,)12+,4. 1162 IrC,,H,,C.I,O,P,S IrCI,(McSO)~CO)(PPh,),,4, 1146 IrC,,H,,CI,O,P,S I;CI,(,reS~~)~CO)(PPh3),, 4, 1146, I147 11C38t134CIOzP2 IrC1(02)(C,I14)(PPh3)2, 2, 320; 6 , 341 IrC39H30C1F,N02P2 IrCl(CO)(PPh3)2{ON(CF3)z}, 4,1143 IrC39H3nCf NzOPIS IrCl(CN)(h-CS)(CO)(PPh3)2, 2,232; 4, 1125 TrC39H30F6N02PZ [Ir{OK(CF3),}(CO)(PPh3),]+, 4, 1117 TrC39H30F6N01P2 IrION(CF3)2}(CO)(0,)(PPh,),,4, 11 17 IrCwHw03P2 [Ir(CO),(PPh,),l-, 2,113; 4, 1105, 1159 TrC39H30PZS3 [Ir(PPh,),(CS)(n-CS,)(n-CS,)J+, 4, 1118 IrC3911,,CIF6NP, Ikl(NCF,CHFCF,)(PPh,),, 4, 1107 IrC,,H,,OP,S,

Cumulative Formula index

405 Ir(CSSH)(CO)(PPh,),(rc-CS,).4, 1146 Ir(SSCH)(CO)(PPh,),(n-CS2), 4, 1146 IrC39H32CIOPz

IrC1(2-Ph2PC6H4CH2CH2C6H4PPh2-2)(CO), 4, 1114 IrC,.H,,NOP, ”” [Ir(CO)(PPh,),(MeCN)]-. IrC3,H33NP2Se I ,

4. 1109

[1r(CSe)(PPh3),(MeCN)1+. 4. I118 IrC&2?OJ‘7 _ _ __ - Ir(OAc)(CO)(PPh,),. 4. 1 j I6 ~ ~ C W H ~ ~ ~ S P Z Ir(OC03)(CO)(PPh3),(Me)l 4. 1141 IrC.3,H34CINOP,S KrHCI(CO)(lll-SCN~~c)( PPh,),, 4: 1154 IrC9PH?5NOI’2 4, 1104 [Tr(NO)(PPh3)2(q3-C,Hjl--, IrC39H36C1N20P2S IrCI(CO)(MeNSNMe)(PPh3)z7 2.194 IrC39H36C12NSPZ IrCl,(q2-SCNMez)(PPh3)2.4. 1154 IrC39H36N20PZS [Ir(CO)(PPh,),(MeYSNMe)]+, 2, 191 IrC,,H3,CIP3 IrCl(PMePh,),, 4, 1109 I~C~YHMC~OZPZ IrCl(diopj(cod), 4 , 1113 IrC411H30FhNC)5P2 I r ( N 0 j ( O,CCF,),( PPh3)?,4, I ‘I 61 IrC40H31CIF6NOP2 IrC:I(COj(NCF,CHFCF,)(PPh,),. 4, 1107 lrC40H33F61N02PZ IrI(Mej{ON(CF3),)(CO)(PPh,),, 4, 11 17 IrC40H34C1P2 IrC1(2-CH2=CHC6H4PPh,),. 4. 1111.1114 IrC40H,,CINOP,S [IrCI(COj(~Z-CSNMe2~(PPh3),]+. 4. 1118, 1154 IrC4,,H3,12P2Se3 IrI,(MeSeCSeCSeMe)(PPh,)z. 4. 1118 IrC40H37NOPZS [Irt1(C‘C))(112-SCNMe,)(PPh,),j ’ , 4 , 1154 IrCa,,H3xN2Pz [IrH,(Mk?N)2(FPh3),]+ 4. I I M IrC40H3&”07P3 [Ir(N0,),(CO)(PMePh,)3). 4. 1144 IrC40H3903P3 [Ir(CO)(PPh,Me),( O,)] -. 2.320 IrC41H30C1F10NZOjPZ h{ON(CF,)CF,CF,V(CF,)~ JC1(CO)(PPh3)2,4. 1143 .

.

,

IG4H4ZPZ

’.

[IrHz(HN=NC6H4F)(PPh3)2] 4. 1132 IrC12H39CIOP3 IrCI(CO){triphosj, 4, 1135 IrC42H39C1203Pz IrC12(0,CBu‘)(CO)(PPh3)2, 4, 1142 IrC42H&03P2 4, 1142 k~2(0,C3ur)(CO)(PPh3),, IrC42H390P3 fIr(triphos)(CO)].4.1113

IrC,3H3,ClFh~OP2

rC1(HN=NC6H3F-4)(CO)(PPh3),, 4, 1153 [IrC1(c O ) ( N=NC6H,F)(PPh3),]+, 4. 1132 IrC4JL4C12N303P2 IrCl2~CO)(N=NC6H4NO2-2)(PPh3jZ, 2, 136.4. 1132 IrCJ I?+N30P2 lr(CO)(PPhl)z(ben70triazolatc),2,78 TrC43H35C1N10P2 [IrCI(CO)(HN=NC6H4)(PPh3),]+, 4, 1132 IrC,qHq,C1,N,0P7 Ir&(CO)(N,Ph)(PPh,),, 2, 134, 140 I G ~ H ~ ~ O J P ~ Ir(CO)(0,)[PPh3),(Ph), 4, 1140 IrC43H37C12N20PZ ’IrCl2(HN=N~,H3OMe-4)(PPh3),, 4, 1153 IrC43H3702P2Se IrH2(PhSe02)(PPhlj2,4, 1148

IxH1(HN=NCbH3hle-4)(PPh,)2, 4, I132 IrC43H390ZP3 [Ir(CO),(triphos)l+, ,. 4, 1135

IrC,,H,,CioP,

IrCI( CO) { P(C6H4Me-2),),,2, 1025 IrCJ7H,,N,0P,S4 [I;(S~CNMe,),(CO)(PPh3)2]+, 4, 1145 IrC,,H,=O,P,

.

IrC4,H3,C1,N;P2’

IrHCI,{N,~C(Cl)=CC~C(Cl)=~CI}(PPh,),, 4, 1107 IrC41H31 F605P2

IrH(02CCF3)2(CO)(PPh3)ll 4, 1 1 17 IrC4,H,5CIN02P; I r c l ( ( ~ , ) ( i ~ y j ( P I ’ h ~2,320 )2, ITC~~F~~~NO~PZS~ Ir(CO)(NCSe)(Me2CO)(PPh5),,4, 1107 IrC41H3hP2 [IrHCp(PPh,),]+, 2,699 IrC,1H3,CI0,P, IrHCl(acac)(PPh&, 4. 11-111 IrC41H3902P2 IrH,(acac)(PPh,),, 2. 375; 4. 1140 IrC41H41CIN02P2 IrHCI(PPh3)2(02CCHPrNH2). 4, 1106 IrC421-135CIN2P, 2 , 134, 136. 139, 131: 4, 1106 [lrCI(N2Ph)(PFh3)2]+. IG2H3JN2P2 [IrH(HN=NC,H,F)(PPh,),] 4. 1132 lrC42H3nC1P2S IrHCI(SPh)(PPh,),, 4. I150 ITC~~H~,FN,P~ I .

COC 7-N

[Ir(tetraphenylporphyrinj]--,2,840 IrC44H30NlE1 Ir(phthalocyanine)(H,”h),, 2,868 1rCJ4HJIN4O2 Ir(tetraphenylporphyrin)(O~)(Ol~~), 2,840 Irc74,H,,CI0,P, Ir(0,CC,H4Cl-3)(CO)(PPh3),, 4, 1116 IrCJi3,C120P2S IrCI,(SC,H,Me-4)(CO)(PPh,),, 4, 1146 IrC44H,,03P2S Ir(O2SC,H4Me-4)(CO)(PPh3),, 4, 11 18 IrC,,H,,0,P2S Ir(O~SC,H~Me-4)(CO)(Oz)(PPh3jz, 2,320 IrC44H38C10f2Se IrHCl(CO)(PPh3)2(SeC6H,Me-4),4, 1148 IrC4,1 I&INOP, [IrCl(NO)(dppe)(PPh,)]+, 4, 1104 IrC4,HllC1N204P2 IrCl(N,)~PPh,)2(Et0,CCHCHC0,Et), 4, 1I06 IrC14H42NZ02P2Sz (Ir(C0 )( p-SCNMe2)(PPh3)}2 . 4, I 154 1rCdL2P2

Cumulutive Formuiu index

IG4H42P2

[Ir(cod)(PPh,),]+, 4, I110 IrC44Hs& Ir(cod)(octaethylporphyrin), 4. 1155 IrC45H28C1N40 Ir(tetraphenylporphyrm)(CO)Cl, 2.811 IrC45H2sCIN404

Ir(tetraphenylporphyrin)(CO)(OCIO,). 2.840 I~C~SHZSN~O [Ir(tetraphenylporphyrin)(CO)]+.2. 840 IrC4SH&Pz Ir(COl(C,Ph)(PPh,),. 4. 1109

IrC12iCO)(PPh3)2(COCH2Ph),4.11 17 TrC4SH4,CINP, IrHCI(MeN=CHC,H4Me-J)(PPh,),,4, 1152 IrC45H44C1N2P3 [lrC1(N,Ph)(PMePh,)3]+. 2,136.139 IrCnsHnRCIO?P, IrCl(O0B;?~(CO)(PPh3),, 6,330 IrC4,-HSOCIO5P2 IrC1(CO)(PPh3)Z(Bu'OOH)2.4. I109 ITC~~H~~NSOP ~~

Ir(NO)(NC6H4Me-4),(PPh3), 4. 1100 1rC47N30C150P2S4 IrC1(CO)(PPh,)(tetrachlorotetrathionaphtl~alene), 4, 1165 IrC48H3606P3 IrWH(CO),(lr-PPh,),(PPh,)(OAc). 4 1 I63 IrC4sH38N30P~ [Ir(NO)(phen)(PPh3),]Z+.4. 110.1 IrCdW'4 [lr(HPPh2)4]+,4,1111 IrC48HsOC12NP2 'rrHCl(PhC-CClCH=~Pr){P(C,H,,),}2. 4, 1 153 ~~

1rC49H38F2N40P2 [ I r ( C C ) ) ( F C 6 H , N N = N N C ~ t . 1 4 ~ ) ~ P P ,h4, ~ ~1132 ~l~ Ir(CO)(PPh,),(4-FC,H4N=NN=~:C,H,F-4), 2,220, 224 IrC4,H,,0P3S IrH(CO)(PPh,),(SPPh,), 4:11 19 IrC50H4402P4 [Ir(dppm),(O,)]+, 2, 319; 4, 1139 IrC51H~&WP~ Ir(C0)(4-MeC6H4NN=NC6H&Ie-4)(PPh,)2, 4,1107 IrCSlH40C102Pz -,H,)Ph,) (PhCOCHCOPh)(PPh,). 2,394 iiGiH44N30P~ Ir(CC))(4-MeCGH,NNNC:6t 14Me-4)(PI'h3),, 2 , I96 IrCszI Il4P4 ~lr(Ph,PCH=CHPPh,),]+ 4. 11 I 1 11 12 IrC52H4sC1P4S2 Ir(dppe)Z(S,)CI, 2,538 IrC52Hd204P4 4,1143 [1r(NO,)~(dppe)~]+, IrCszH4sOP4Sz [Ir(dppe)2(+SzO)]',4, 1117, 1121. 1165 IrC5LH480P4SeZ [Ir(dppe)2(q2-Se20)]+, 4,1165 IrC51H40W4 [Ir(dppe)&O)]+, 2,636 IrC52H4802P4 [Ir(dpp~)~(OJ]',2.319.330;4. 1112. 1139 IrCs2H4AP4S2 [Ir(dppe),(l12-S,0,)l+, 4, 1117. 1165 IrCdWMJ'4 [Ir(dppc),(OSSO)] ' ,2,636 llr(dppe)~(SO)~]' ,2.636

406

IrC5,Hd', [Ir(dppe),]+,4,1111,1112, 1160 IrC5,H48P4SSe [Ir(dppe)2~T'-SSe)j+, 4, 1165 IrCszH4sP4S2 [Ir(dppe),(S2)]+. 2,532. 533; 4, 1112, 1117, 1147 IrC52H4sPISe2 [Ir(dppe),SeJ+. 2,667; 4, 1038 IrC5,H4&P4 [Ir(dppe)z(SJI+. 2,636 IrC,,H,,CIP, [IrHCl(dppcj,l+. 4, 1150 lrC5,H5,,P4 [IrH,(dppc),]'. 4.li.50 IrCj2Hs1T5P4 {IrI(PMcPh2i,)2(~-I),,4, 1035 IrCS2HJ'4 [Ir(PMePh,),]+. 2, 1026 IrC53H440P4 [Ir(CO)(Ph,PCH=CHPPh,)2]+, 4, 1113 IrCs3H4506Pz Ir(OzCPh),(PPh&. 4. 1141 I~CS~H~EOP~ [Ir(CO)(dppe),]+, 4, 1112, 1113 IrCs3Hs,0P4Sz [Ir(dppe),(r12-S,0Me)j2', 4, 1165 IrC,$IS 1P4Sz [Ir(dppe),(rc"-S,Me]', 4, I I17 [Ir(dppe)z('lZ-S2Me)lz-,4, 1121; 6,350 IrC,4H42C1P4 IrC1{P(C6H,PPh2-2)3},4, 1135 IrCS4H4,Cl2P4 [IrC1,{P(C6H,PPh,-2)3}]+, 4, 1136 IrC,,H,,CIP, [i;HCj{ P(C,H4PPh,-2),}]+, 4, 1136 IG4H44P3 Ir(C,H4PPh2)(PPh;),, 4, 1114 IrC,,H,,CINOP, [IrCI(NO)(PPh,),]+, 4, 1104 IrC54HJ5C102P3 IrCl(O&PPh3)362. 320 IrC,,H,,ClO,P TrCI{P(OPh),),, 4 , 1136 IrC H, CIP -6rHCI(Ph,P H4 )(PPh3)Z,4, 1137 IrC1(PPh3)3,4,1114,1159; 6,246 IrC5,H45NOP3 Ir(hO)(PPh3I3. 2, 103. 111,218, 1026; 4, 1099-1101. 1104. 1105 IrC54H45NJ'3 Ir(N,)(PPh&- 4. 1161 IrC,,H4507P2 Ir(O,CPh),(CO)(PPh,),, 4,1141 IrCs,H46CIl'; IrHCl(I'I'h3)33 4, I106 Ircs4~-IJ6c12ogP3 IrHCIZ{P(OPh)3)3.4, 1136 IrCi,H4,CI,P, IrHC12(PPh3)3.4. I150 IrCS4H4,NOP, IrH(NO)(PPh3J3.2. 105,4, 1100 [IrH(NO)(PPh,),]+, 2, 103 I~CS?H,~P; IrH2(C6H,PPhz)(PPh,),, 4, 1114 IrC54H47CIP3 Irl 12C'I(PPh3)7. 4,1150; 6,303 I~c~~H~~No~P;Ir(NO)(PPh,l),(H,O), 4, 1100 IrC,,Hn7N,P, IrH2(N&PPh3)3,4. 1161 IrC54H48P3 1rH3(PPh3)?.4. 1114. 1150, 115% 5, 869; 6.245. 291 IrC,4H5,NP,

407

Cumulative Formula Lndex

IrHgC3,H3,CIN,0P2

IrFe2C,9H&O,P, [Ir(dppe),(SCN)( SMe)]'. 4 1122 IrC5~H440P3 Ir(COj(C6H4PPh2j(PPh,),. 4, 1114 IrC55H45P3S2 [Ir(PPh,),(n-CS,)]+, 4, 1118 IrCssH460P3 IrH(CO)(PPh,),, 4, 1119, 1159,6,247 IrC5sH46P3S IrH(CS)(PPh,),, 4, 1120 lrC,,H,,P,Se IrH,(PPh,),(ScMe), 4, 1138. 1165 1rC5,HS4NPQS [Ir(dppe),(CNMe)(SMe)j"-. 1. 1122 IrC56H502P3 IrH,(OAc)(PPh,),, 4. 1150 IrCS6H4,NOP3 Ir(CN)(CO)(PPh,j,, 4, 1109 I~CS~H~S~P~SZ [Ir(C0)(S,CPPh3)(PPh3)J+4, 11I 7 I~CS~H~SP~S~ [Ir(PPh3),(o-CS2)(n-CS2)]+. 4.1118 IrCS7H5,NOP3 I r ( N O ) ( P P h l ) , ( ~ H 2 ) 4.. 1099 I~C~OHTZN~~~P~ [IrH2(HN=NC6H4~0,)(PPh,),) ' . 4 , 1132 IrC H N OP, [ ~ , H , O M e ) ( P P h & j + ,4, 1153 IrC&b404P4 [ I r ( d i ~ p ) ~ ]4,+ ,1113 IrC7ZH57P5 [Ir(PPh3){P(C6H4PPh,-2),}]~. 4, 1135 IrC7,H,,BrPS IrHBr(PPh3){P(C,H4PPh,-2),}.4. 1135 IrCnH6002P4 [Ir(O,)(PPh,),l+. 4, 1138 I~C~ZH~OP~ [Ir(PPh,),j3+, 4, 113H lG2116101zP4 I~H{F'(OPII)~)~, 4. 1120 I rO7& J ' 4 IrH(PPh,),, 4, I I19 IrC,sH,,N2P, [Ir(CNB~'),(dppm)~]+. 4, 1163 IrCIF, [IrCIF5]2-,4, 1166 IrCIZO,,S4 [Ir(S03)4C12]7-,2,638 IrCI4O6S2 [Ir(S03)2C14]5--, 2,638 IrCI6 [IrCk]'-, 1,336,4116: 3. 1236; 4, 1157; 5,289.398.500; 6, 17,97,517.75XI 8U8,823 [IrC1J3-, 1,336; 2.887;4. 1149.1157; 6 , 16,495,496, 808,823 [IrC16]4 , 4, 1123 IrCUC16H25P2 [IrH3(PMe2Ph)2Cul 4,1 lfd I~CUC~~H~~C~~N~OP [IrCl(PPh,) { fi=NC(py-2)=CHCH=Cpy-2} (vNO)CuCI]Z+.5.653 IrF, IrF,, 2,680 IrF, [IrFJ, 4, 1158 [IrF,IZ-, 4, 1157 TrFe2C38H30104P2 IrI(FePPh2(C0)2Cp),,4 . 1 I 1 1 IrFe2C,8H3004P2 [Ir{FePPh2(CO),CpjZ]'4, 1 I 1 I IrFeZC39H3nBr05P2 [IrBr(CO){FcPPh2(COj,Cp)zl-. 4, 1111

+.

~

[Ir(CO)(FePPh,(CO),Cp},CI,4,1111 IrFe2C,IH300,P2 [Ir(C0)3{FePPhz(CO)2Cp},]+,4, 1111 IrGeC3,H3,CIOP IrHCl(GePh,)(COj(PPh,), 4, 1126 IrGeC40H,,0P, TrH2(GeMe3)(CO)(PPh,),,4, 1126 IrGeC41H,,02Pz IrH2(C0)2(GeMe3)(PPh3),, 2, 19 IrHC1,O Ii-CL(OIJ), 4, t 149 IrHFIZP4 1rH(PF3)+ 4,1120 IrH2Br,0 [IrBr5(HzOj]z-,4, 1157 IrH,C1,0 [IrCis(H20)]-.4, 1157 [IrCls(HzO)]z~. 4, 1149, 1157 IrH2C16 IrC&H,. 4. 1166 IrH4Cl,0z IrC14(HzO),,4, 1157 [IrC1,(H20),]-. 4, 1149 IrH, [IrHj] ,2,693 IrH,CI,O, I I Q ~ ( H ~ O3,) ~1149 , IrHbO, [Ir(OH),]Z ,4, 1156 [Ir(OH),13 ,4, 1138 TrH,06 [Ir(OH)5(H,0)]2-, 4, 1138 IrH9N,0,S3 [Ir(S03)3(NH3)313-,2,638 1rHl2TZN4 [Ir12(NH3)al+, 4, 1128 lrfi14iNao- [IrI(H,0)(NH,),]2+, 4, 1128 IrHI5BrN, [Ir3r(NH,),j2+, 1128 IrH, ,ClN, [IrCI(NH3)5]2I , 4. 1128 IrHtBNS Ir(NH,),, 4, 1LOO 1rH15N602 [Ir(N0,)(NH,)s]2+. 4, 1143 [Ir(ONO)(KH,),]2+, 4, 1143 IrHIsNp [Ir(N;j(NH3),IZ+,1,406;4, 1128, 1133 TrHI6NSO [Ir(NH3)5(OH)J2+, 6,435 IrH17CIN6 [Ir(VH,Cl)(NH,),I3+, 4, 1128, 1133 IrTII7Ns [IrH2(NH,j,]3+, 4, 1128 lrll,7N50 [Ir(H,O)(NH,),]? ' , 4 , 9 5 8 , 1128 IrH18N6 [Tr(NH3j6l7+,1,400; 4,1128 IrHl8N60 [Ir(NH,0H)(NH3),]3+, 4, 1133 TrHgC7HlsBr30Pz (IrCOBr,(PMe3)2}HgBr, 1, 123 IrHgC37H30BrzCIOP2 IrB rCl(HgBr)(COj( PPh3)*,4, 1124 IrHgC3,H3&IN,0P, {IiCI(CO)(PPh3),)Hg(NO3),, 4, 1125 IrHgC37H30CI30P2 IrCl(HgCl,)(CO)(PPh3)z~ 4, I125 IrCI,(HgCl)(CO)(PPh,),, 4, 1124. 1127 IrtIgC39H,oC'IN20P, IrCI(CN)(HgCN)(CO)(PPh,),, 4, 1125

IrHgC,9H,,C13F,NP,

TrCl2(HgCl)(NCFZCHFCF3)(PPh3j1. 4. 1124 IrHgC53H40CIOP2 IrCI(HgC=CPh)(CO)(PPh,),(CCPh), ~rHg3CllIH90C1303P6

IrH,(SnCI,)(CO)(PPh,)~,4, 1127 IrSnC38H33C1,0P2 IrC1(SnCl3Me)(C0j(PPh,),, 4, 1128

4.1124

[{IrCI(CO)(PPh,),}3Hg]z+, 4, 1125

Ir(CO),(SnPh,)(PPh,), 4. 1103 IrSnC39H&130P2

Ir(SnC13)(C,H,)(CO)(PPh3)z, 4, 1103

IrH&48H120C1404P8

[{IrCl(CO)(PPh,),),Hg]z+, 4. 1125 I ~ I ~ , 4 , 1149 IrN601s llr(N03)6]z-, 2, 303;4, 1156

[tr(N0,),l3-, 4, 1147 IrN 18 [Lr(N3)6]3i, 4 , 1133 IrOs3C29HlsOl,P O S , H ~ ( C O {) Ir(PPh,)}, ~~ 4, 1166 IrPdCzaHzsCINzOPZ

Pd(CN),(y-dpprn)Ir(CO)CI,5.1164

IrSnC,9H,,CI,0P,

Ir(snCl3)(C~H4)(C0)(PPh3),~ 4, 1103 IrSnC54H46C141'3 IrtIC:I(SnCI,)(I'Ph,),, 4, 1127 IrSn2Brlo [IrBr4(S~iB13)2]-.4 , 1127 IrWC,,H,2P2 [IrH(PPh3),(u-H),(T1-o:1-5-rl-C,H4WCp]'. 4.I152 IrWC54H4006P3 IrW(y-PPh2)(CO)6(PPh3)2,4, 1163 IrWC&,,OsP4

IrWH(CO)5(p-PPh,),(PPh3)2, 4,1163 Tr2As6C80H72C1202

IrPdC,oH40C12N50P2

[Ir(N0){(2'-py),pyridaz1ne}(E'Ph~)~(PdCl,)]~+, 4,1161

Ir,CI,(C0)3{PhAs(CH,AsPhz),}2.4. 1164 IrZAs6PdCa0H72C130,

IrPtB9C42H5aP4

Pt(PMe,),(PPh3)(Ph2PC6fT4)HlrR9Hlo. 5.372 IrPtC24H64P4

[P~H[PE~&L-H),I~H(PE~,),~' . 4 . 1152 [Pt(PEi9),(~-H),IrH,(PE1,),1'. 4, I152

[Ir2PdC13(COj,(PhAs(CH2AsPh,)2}z]+r 4, 1164 Ir2B2C30H44C14N12 { I r ~ l , { H B ( ~ N = C ~ l e C H - = ~ M t ) 3 }4, } 21134 r

IrzRrg [lr2Srg]3 , 4 , 1149

IiPtC30H68P4

'

PtPh(T'Et3)(v-H)21rH(PEt3)3, 5 , 363 IrPtC',,I 152C14P4 [IrC'12(PMe,Ph)2(~r-C'I,)Pt(PPh3)~]~, 4. 1 156 IrPtC,,H4,C1N,0P4 lrC~(CO)(u-dpp~n)~Pt(CN)~, 4,1i62 IrPtC66HS4C1P4 Pt(C-CPh),(k-dpprn)21rCI, 4,1112. IrPtC,9H58CIOP4

Pt(C=CC6H4Me-4)2(p-dppm)21rC1(CO), 4, 1112 IrRhCZ4H6,CIP4

Ir2C,II,,Cl,F,N,P, {IrCl(PFNMc2}2,4.1163 Ir2C8H37K803 I{Ir(en),(H,O j 2 (

2, 305

Ir,(CO),(SPh),. 4. 1121 Ir2Cl6Hz4Cl2 {IrCl(cod)),, 4. 1159. 1160,1167

IrH,(PEt3)z(p-Cl)(p-H)Rh(~€t3)2. 4. 1074,1151, 1164 ~rRhC'l,H,,,P4 Rh(dppe)(p-~I)zIrl12(PPr11)2, 4, 107-1, 1151 TrRhC44H7,CIPs

[IrH(PEt,),(p-CI)(p-H)Rh(dppc)] ' .4.1164

I TKhC'44H72Ps

[Rh(dppe)( p-H)31r(PEt3)3]+ . 4. 1075, 1151 IrSb3C&d, [Ir(C0)2(SbPh3)3]+, 4, 1111 IrSiC16H&1 IrH,CI(CSMe5)(SiEt3). 4. 1166 IrSiC,,H350P2

fr(CO)(PPh2CH,CH2SiMe,)(PPh3). 4. 116.1 IrSiZC2,H4, IrH,(C,Me,)(SiEt,),, 4, 1166 IrSi,C,,H,,INP, Ir~(~e)~N(SiMe,CHPPh,),1, 4, 1161 ..

IrSi,C 13H39iNOPZ

IrHI{SiH,N(SiH,),}(CO)(PEr,),. 4, 1126 IrSilC13H3910P3

IrHI{SiH,P(SiH,),}(CO)(PEt,)z.4. 1126 IrSnC24H2403P Ir(CO),(SnMe,)(PPh,). 4,1103 IrSnC36H31C14P2 IrHC1(SnC13)(PPh3)2,4, 1103 IrSnC,,HI2Cl4OP, IrH,(SnCl,)(CO)(PPh,),, 4, 1103 IrSnC,,H,,,CI,OP, IrUI(SnC1,)(CO)(PPh,),. 4, 1103 IrSnC,7H30C150P2 trCl(SnCI,)(TO)(PPh3),. 4. 11% lrSnC,,H,,C140P,

IrHC1(SnC1,)(CO)(PPh,)2,4,1103,1127 IrSnC3,H3ZC130P2

. ..

lr,CI,(CI-Cl)t(S~tZ)4.4: 1145 Ir,C:I,(I'-CI)(Ii-SEtz)(SEt,)3, 4,1 145 lr2C16(SEtZ)1.4. 1 \ 4 5 Ir2C,7H381ZOBP2S2. { IrI(CO)(r(-S3ut){ P(OMe),}},(p-CH,), 4. I 1 65 IrZC20H30C14 {IrCl2(CjMe5)},~ 4. 1159 Ir2CzOH3, {IrH3(C5Me5j)2.4, 1166 Ir,CzzH30~4 {Ir(cud)(ll-r;JN=CrlCH=~H)},, 4, 1161,1167 Ir,C,,H,,O,P Ir,(CO),(PPh,), 4.1101 Ir2C2sH2,,N02P {Ir,(Co),(PPh,)Ipy)j.. 4.1100 ITZC26H5 1p2 [(Ir~l(C,Me5)(I'lvle3~},(p-H)]+,4, 1166 11-2C32H40N8

[Ir,{rrteso-NC~HCH,CHCN[~H,)3~4]2+. 4, 1102

Ir2C3ZH4004 {Ir(cod)},{ 1.4-{ (MeCO),C}C,H,), 4, 1165 Ir,C3ZH4JjP4 [Ir215(PMe2Ph)J, 4, 1156 Ir2C36H30C12NZ03P2 {Ir(NO)Cl(PPh,))2(~-0), 2, 301;4. 1105 IrZC36H3012NiZ03P2 {lrl(NO)(PPh,)},O, 4, I101 I~IC~WNZUIPZ {Ir(NO)(PPh,))20. 4, 1100 IrIC3,H.30N404

Ir,(NO)4(PPh3)z. 2, 113 Ir2C38H44N406

{Ir(CO,)}z(~-octaethylporphyrin), 4.1155

409

Cumulative Formula Index

.

.

{IrC1(C0)3}2(N-methyloctaethylporphyrin),4, 1120 Ir2C44H34C14N402PZ { IrCI(CO) (PPh3j { p-rl'?J=CHC(CI)=c H} } 2 , 4, 1161 I~zC~~H~~IZN~~ZPZ {IrI(CO)(PPh,)(~-r;JN=CHCH=~H~}*, 4, 1161

IrzC4,H5,)OzPzS2 {IrH(Coj(PPh,)(p-S~ut)}~ 4.I12 1, t 122 IrZC46H5102P2S2 [ { IrH(CO)(PPh,)( ~ - S B U ' ) ) ~ H4. ] +1. 122 1r2C47H37N206P2S

[{Ir(CO),(PPh3)},(p-N2C6H4kle-4)(p-S0,)It, 4. 1107 1r?C47H38N206P2S

[ { Ir(CO),(PPh,)},(p-N=h HC6H4~le-4)(y-SOZ)]Z+, 4, 1107 I~ZC~SH~&ZOZP& Ir2Br2(CO)z(PPh3)2(tetrathionaphthalene), 4, 1121 IrZC48H4S04PZSz Ir2(C0)4(PPh3)2(SBu')2> 4. 1122 IrK52H4402P4S Ir,(~-S)(C'C))z(p-dppni)z.4. 1 I59 Ir,C5J~44C107P4 [Ir,CI(CO)3(dpp~ii),]+, 4, 11 12 1r2c53H44c1203p4

Irz(~-Cl)(~-CO)(~Oj2~~-d~~m)zl*, 4, 1113 IrzCdLC104P4 [Ir,(p-CI)(p-CO)(CO)3(~i-dpprn)2]-. 4,1113 I~zCS~H&~Z~ZP~ {IrCI(CO){Ph,P(CH2)2CH2))2. 4. 11 13 Ir2C58H53CIN03P4 [Ir2C1(CNBu')(C0)3(dpprn)z]t. 4 1I02 IrZC59H4505P3 Ir2(CO)5(PPh,)3+ 4, 1101 Ir2C62H62CINZOZP4 [Ir2CI(CNBut)2(CO)z(dppm),] ' .4, 1102

I~~c~~~I~~cIA

[f4~40H430*P4

KAs~Wdi40 [KAs4W400140]27-, 3, 1042 KBC32H40F1208

BK(CF3COCHCOBu')4, 3, 1219 KCCIS2 K(S2CCI), 2,591 KCH30 KOMe, 2,348 KC,F,O K{OCF(CF3),}, 2,343 KCaHTNtOS K(SCN)(AcNHMe), 2,492 KC4H90 KOBu', 2, 348 KC5H702 K(acac), 3,2h KC,H,,NSi, K{N(SiMe,),}, 2,168, 170 KCaHiJNA KI(AczNH)Z, 3, 15 KCioHmN&S K(HOCH2CH2CH(CH2NCH2)3CH2fi(NCS), 3,42 KC10H2005

[K([l5]crown-5)]+, 2,931

KC&z,OA [K[18)cmwn-O4S2)1+,2,93 I KCizHzaO, [K(l8-crown-6)]', I , 444; 2,931: 3.38 KC12H26N204

[K([18]crown-N,0,)1+, 2,931 KCizHz,O6 [K{MeO(CH,CH20)5Me)]t, 2.931 KCI:H~JO~SZ K{~(CH2CH2O),CH2cH,}(NCS). 3,41 K C I ~ H Z ~ N , ~ ~ K { HN(CH2CH20CHZCHZOCH2CH2)2NH} (NCS), 3 , 41 KCi,HiiN,O, K(2-OC6H4NO,)(PhCOCH=NOH). 3,3U KC i 4H2& 7 [K([Zl]crown-7)] ', 2, 931 KC,,H,,NO,Si, K{ N(SiMe3)2}(OCH2C€120CH2cH2)Z, 2, I 7 1 KCi,H,iINO, K(MeOCH,CH,fl(CH,CHzO)5CHz~H2}I, 3,41 KCiJLzNzOs .. _ _ [K(cryptand(2.2.1])]+, 2,938 KCi,H,iOa K(18-crown-6)(acac), 3. 38 KCI~HJ'J~O,S K([2.2.l]cryptand)(NCS), 3,16 KClsf-I36N206 [K(cryptand[2.2.2])]+, 2, 938; 3.46 KCzoHigOiz K{2-(H02CCHzO)C~H40CH2CO~} { 2C,H4(OCH,CO,H),), 1,525 KCmHwO,

[K(dibcnzo[l8]crown-h)l ' ,a, 931 KC20H3604 [ K(dicyclnhexano[l8]crown-6)]+, 2,Y3 1 KC,oHA'207 IK(crvptandl3.2.21)1-, . _ - 2,938 K C ~ ~ H ~ ~ N ~ O ~ ~ [K{cH(CONMe2)(OCH2CH2)20CH(CONMe2)~ CH(CONMe,MOCH,CH,LOcH- _ _ (CONMe,)}F.3.55 KC28HJOm KI(PhCOCH20~=CHOC(CH20H)=CH~O},. 3.15 KCmbJO~ii K(benzo- 15-crown-S),I, 3 , 39 K~,,H4,O,, IK(benzo-15-crown-S)21L, 3,39 KCJLoNO,nS K(d1benzo-30-crown 10)(NCS), 3,40 KCz&LoNOizS K(4'-HO-benz0-15-crown-5)~(NCS), 3,42 KC~~HS~N~O~ [K(enniatm B)]-. 3 , 63 KC40H56012 [K(nonactin)]-. 3. 64 KC44fr640i? [K(tetranactm)]+,3.64 KC54HdWiB [K(valinomyon)j '362 KCdCI3 [K(CdCl,)].,, 1. 125 KCeC28H4406

K{ O(CH2CH20Me)2}2Ce(cot)2,3, 17 KCOCi6Hi4Nz02 Co (salen)K. 4,637 KCOC~~H~~N~O~ Co(Pr-salen)K(CO,)(THF), 3, 16 { Co(Pr,salen) K(CO,)(THF)},, ,4,638 KHItO, KI03(HI03),3-31 KHl,O, [KW2O)sI + 3 . 3 KZCZOh KzCA06,2,449 KZCZ6H32N20BS2 K2(d~benzo-21-crown-8)(NCS)2, 3,40 KzC~~HI~N~ K,(phthalocqanine), 2,863 K2Mo04 K(Mo04)K, 3,1377 K3CioH13N208 K,(Hedta), 2.790 K3N K3N, 1,110 KrF [KrF] ',3 , 3 13 Kr2F3

[Kt,F,] ' ,3.313

410

LaBr, [kdBr,l3-, 3,1068 LaC&N06 La{N(CH,C02)3}. 2.789 LaCloHlzN208 [La(edta)12-, 2,784 LaCloH13NzO~ [La(Hedta)]-, 2,784 LaCloHI8NzO11 [La(H,O),(edta)]-, 2,783: 3.1088 LaCloH,lN,O Iz La(H,O),(Hcdta), 2,783: 3. 108X LaCIIH14NA [La(tmta)l2-, 2,784 LaCllHl5N2U8 [La(Htmta)]-, 2,784 L~C~ZHI~NZ~S [La(teta)l2-, 2,784 LaC12H17N208 [La(Hreta)]-, 2, 784 LaC12Hz4N3015 La(N0,~,(18-cro~n-h). 3.1092 L~C~;H,~C~~OI~S, [La(C10,),(H20)(1, 10-dithia-18-crown-61 , 3 , 1087, 1092, 1093

LaC36H45hT10 La(octaethylporphyrin)(OH), 2,822 J.aC,,H,,N,OPSi, La{Ii[Si%l.le3)2)3(0PPh3),3, 1072, 1083 LaC3,H5,CI2N20, LaC12(CPh3)(2.2,2-crgptate),3, 1098 LaC40H3zKsOs (La(bipydioxide),I3+, 3, 1081 LaC40H40N808 [La(py ?V-oxide),13', 2,496; 3, 1081 LaC,,H,,Cl,Y,O La(C104)3(phen),. 3, 1069 LZtC,:,BH,,,C)flP5S6 La{S2P(OEt)2}J(OPPh3)2, 3, 1083

,

LaC56H64016

~La{OC(CHcMe),0},l3+, 1,84 LG5H63P6 La{HC(PPh,),),. 2, 1041 LaC13 LaCI,, 3. 1106 LaH,NjOl, [La(N03)5(OH,)Z]z-,2,306 LaHlnN30q4 La(N03)3(H,0),, 1,99; 2,306 LaH, 2C13018 La(CIO,),(H,O),. 3, 1074 LaH,*O,

LaCisHz106 La(acac),, 2,373: 3. 1077 LaCi&i,C13N,O, LaCl,(salenH,), 2, 733 LaCi&008P4Ss [La{(EtO),PS2}4]-. 2.644 LaCisH36N309 [La(NO3)(2,2.2-cryptate)l2+. 3. 1098 L~CISH~~N~OIZ [La(N03),(2,2,2-cryptatc)]-, 3,1UY8 LaC18%&015 La(N03),(2,2,2-cryptate). 3,1097 L~CZ~IH~~N~OY La(NO,),(bipy),, 3. 1069 LaC,oH40N4S8 [La(S,CNEt,),]-, 3, 11187 LaCz1Hl8N3O9 La(2-OC6H4CONHOH),.2. 507 L~C,ZHZ~N;IOY La(N03),{~=CMe(2.6-py)C(Me)=NCH,CH,N= CMe(2,6-py)C(Me)=NCHzcH2}.3, 1095 .. ~. LaC2,H3&i3N' 0 1 4 La(C104),&CMe(2 ,6-py)C(Me)=NCH2CH,N= CMe(2,6-py)C(Me)=NCHz~l I,}(l IZO),, 3, ~

1..n9h . .

LaC23Hz1N8011

La{PhC(OH)=NN=CMet=CHCH=CHcC(Me)= NN=C(OH)Ph)(NO,),. 3, 1090 LaC24Hd120J'4 [La(HMPA)4]3+,3, 1084 L~C~OH,OFZIO, La(CF3CF2CF2COCHCOBu')3.3. 1078

[K~(ti~0)~]~'+. 3, 1068 Lal, La(I3)>?I . 110 LaN 0, [La(N0,),13-. 1, 101; 3, 1068 La,C60HlozN,04P,Sis 3, 1072- 1083 {Laz{N(SiMe3)2),(OPPh3)}2(p-Oz), La2~I,80,1S3 LaT(S04)3(HZ0)913. 1076 La4Re20,, La4Ke2OI0,1,177 LasRe4OlS La6Re4OiB.4. 177 LiAgC:2H16NR AgLi(phthalacyanine) 2,868 LiAICsHzoOz LiAIH4(THF)z. 3. 124 LiAlH, LiAIH,, 3,174 LiA12H, LiA12H7.3.124 LiAmO, LiAmO,. 3, 1216 LiBC,,H,,O, Li{(2,4,h-Me3C6H3)2BHz}(MeOCH,CH,0Me), 3. i 4 LiBMoCl,F120T2N703 Mo { HI3 (fl;JN=CMeCH=c Me)3}(NO)I,Li( OEt), 3. 1280 LiCH,O LiOMc, 2.348 LiC2H302 LiOAc, 2,438 IX,H,IN,O, LiI(H2NCONH2)z,3 , 6 ~

41 1

LiC4H90 LiC4H90 LiOBu', 2,345 LiC4HloN LiNEt,, 2, 182 LiC4H16C1N4 LiCl(en),, 3, 11 LiC5H702 Li(acac), 3,26 LiC,H,,,CIO LiCl(dioxane), 3 , 6 LiCSHT2N3 LiN=C(NMc,),, 2,284 LiC,HI4BrN,O, LiBr(alanylgly~ine)()1,0),, 3, 6 LiC6HlsNSiz Li{N(SiMe,),), 2, 168, 170.173.184 LiCbH2,1N6 LiI(en),, 3, 11 LiC9H16N04S Li(l2-crown-4)(NCS), 3,40 LiC,H2,BrN3 LiBr{MeN(CHZCH,NMe2)2]. 3, I1 LiC,oHiZCINZO LiCl(HzO)(py)2, 3, S LiCloHl404 [Li(acac)z]-, 3,25

Li(hfacac)(TMEDA), 2, 370; 3, 13 LiC,2H28C1N404 LiCI(AcNHMe),, 2,492: 3 , 4 LiC13H24N04S L1(16-crown-4)(NCS),3,40 LiC14Hi,N0,S Li{2-~C6H,0CH2C~i2O(C~I2)~0CI l,cHz}(NCS), 3, 40 L1C14Hz10 Li(OCbH3Bu')z-2,6,2,352 LiC14HzHNz04 [Li(cryptand[2.1.1])] ',2, 938 LiC16H32N20S [Li(cryptand[2.2.1])]' ,2,93X LiC,,l l9F,N2O2 . . Ll(hfacac)(phen), 3, 13 LiCl9HzON0,S Li{ 2-~C,H,0(CH,),-2-OC,H40 (cH2)3}(NCS), 3,40 LiC20Hd4 I L i ( b i p ~ ) ~ l3,13 +, LiC2,,H17BrOP LiBr(PhCHZCOPPh2),3 , 1 5 I.iC22H,oN0 Li(NHC6H2But3-2,4,6)(OEt2). 2. 164 LiC23H55N3Si3 Li{(Me,Si),Cp} { MeN(CH,CH,h'Mc,),). 3, 12 LiCwHw06 ILi[spherand)l+, 3 , 4 3

[Li(antamanide)]+, 3,64 LLC~OH~~~SPS LiI(Ph3PO),, 2,498; 3 . 4 LICOC~~H~~N~O~ Co(salen)Li, 3, 16 LiCrS, LiCrS,, 3,882 LiCuC32H16N8 CuLi(phtha1ocyanine). 2,868 hFeC45H9605

FeLi(OCIIBu',)4(110CHBu'2). 4.227 LiH12N4 [L1(NH3)41t, 3 , 4

412

Cumulative Formula Index LiHfC64H12002 P5 Hf{P(C6H1,)*),Li(DME),2, 1055 LiMnC7H,N20, MnCp(CO),(NWLi), 2, 133 LiMnCl3Hl0N2O2 MnCp(COlz(N,Ph)Li, 2, 130 LiSi6C36H8604 [Li{C( SiMe,)3}2](THF),. 3 , 4 LiZC,H702 [Li,(a~ac)]+,3~25

Li2C32H,6~s Li,(phthalocyanine), 2,863 Li2C44H80N202

{L~(~L-NHC,H,BU',-~,~,~)(OE~~))~, 2, 173 Li2RuC47H6002PJ

RuHMe(PPh3)2(LiMeOEt2)2, 4,454 Li2SnCloHB Sn(C&Li)?, 3 . 2 1 8 Liz LJC611 laO, Li,U(OMc),, 3,1147 LiZU2C80HBoNh04 [UO(Ph,N)3Li(OEt,j]2, 3 , 1141 Li2WC8HL4 Li,W(Me)*. 3. 976 Li,AIHb Li3A1H6,3. 124 Li3Am04 Li,AmO,, 3, 1219 Li3C18Hj4N3Si6 [Li{N(SiMe,),}],. 2, 1173 Li3Cr4C120H180C13012 jCr(l-adarnanty~oxy),),(l.iC:l),,

3,930

Li3Ni2C:731172Ns02

LnF, [LnF6I3-. 6.846 Ln0& [Ln(SO&]* '. 6 . 854 Ln4He201i 1,n4Re20,1.4, I92 LnhRe4OlH Ln6Re40,,. 4, 192 LuC6H6N06 Lu{N(CH,CO,),}, 2,789 LuC8Hl I N 0 6 [Lu{EtO,CCH,N(CH,CO,),}]+. L~CISHZIO, Lu(acac),. 2.387

6,422

413

Cumulative Formula hdex

LUCwH64N06

Lu(Bu'C0CHCOBut),(3-picoline), 1, 81; 3, 1080 LuC43H3sNs.02

Lu(phthalocyanine)(Bu'COCHCOBu'). 2. 865 Luc16 [LuCI6l3-, 3,1099

COC 7-N'

LuH,O, [Lu(OH),I4-, 3, 1076 LUH12C1206 [LuCI,(OH,),]+, 2,297 LG32 [Lu9'F3,]'-, 3,1099

414

415

Cumulative Formula h d e x

MnC2HSN305S

Mn0-87Cu0.26PS3

Mno.B7C~.26PS3, 5,690 MnAgaSb,S6 MnAg4Sb2S6,3,265 MnAlC12H36BrzP4

[Mg
M~I(AIH~)(M~~PCH~CH~PM~~)~, 4,32 MnAlC12H36P4

Mn(A1H4)(Me2PCH,CH,PMe,),,4 , 9 MnA1G4Hs60p Mn(AI(OPr')4}2: 4 , 3 7 MnA12Ha Mn(A1H4)2,4. dl MnAsC,H,,Br2N MnBrz(2-H,NC,H4AsMcz), 4, 34 MnAsC13Hl,CI0, [Mn(C104)(Ph2MeAs04)]+,4,40 MnAsCI,H,Nz [Mn(2-H2NC6H4AsMe,)z]z+, 4,34 MnAsCz7HZ5N, Mn (2-( MezAs)C6H4N=CPhC(Ph)=NNHpyridyl-2}. 4,34 M~A~XI,HI&ZPZ MnBr2(CO)l(diars), 4?31 MnAs,C,,H,,BrO, [MnBr(CO)j(AsMeZI~h)z]+~ 4 , 3I MnAs2C3,H3UC1302 M ~ C I J P ~ , A S O 4) ~, 9, 0 MnAsZF2,N,S, Mn(AsF,),(NSF,),, 4,22,60 MnAs4C12H36CIZU12 M~(CIO,),(OASM~,)~, 2,500 MnAs4C,,H60C108 [Mn(C10,)(Ph,A~0)~]+, 4,47 M~A~~C,ZH~OCIZOIZ Mn(C104)2(0AsPh3)4,2,500 M ~ A s ~ C ~ ~ H ~ ~ O ~ [M~(MC,ASO)~]~', 4,40 M ~ A U C ~ ~ H ~ ~ O ~ P Au{Mn(CO),j(PPh,), 5,903 MnAu,C5,t-1,,04P, ( A u ( P P ~ ~ ) } ~ M ~ (5,905 CO)~, MnB03 [MnBOJ. 4,42 MnB204 MnBI04, 4,42 MnBz05 MnBIOj, 4.42 MnB40, MnB,O,, 4*42 MnB6OI0 MnB,Olo, 4,42 MnBeW, IHZ040 [BeW11Mn(OHz)039]7-r 3,1048 Mn Br CI [MnBr,Cl,l2-, 4,59 MnBr,I, [MnBr,I2l2 , 4 , 5 9 MnBr, [ M ~ B T , ] ~4.11,58 -, MnBr, [MnBr614-, 4,59 MnCH4ClZNzS MnClZ(H2NCSNHz),4,54 MnCN304 Mn(CO)(NO),. 1.290; 2,106; 4,7 MnCN,03 [Mn(CN)(NO),J , 4 , 8 MnC0,P [Mn(C%)[PO,)I'-, 4,41 MnC1H3N403 Mn(CNMe)(NO),,4,8 MnC2H5N3OSS Mn(SO,)(H,O)(triazole), 4,21

,

,2,477

MnC2N04

Cumulutive Formulu Index

MnC,NO,

MnC,Hs17P Mn13(PMe3),2,1040 MnC,N* Mn(CN),, 4,83, 102 [Mn(CN),]-, 4, 11, 12 MnCaH205 Mn(02CCOCH2C02),6,455 !d/InC,H206 [Mn{02CCH(0)CH(O)C0,)]2-, 4.51 MnC,H,O, Mn(malatc), 4,51 hlnC4H5N04 Mn{HN(CH,C02)Z},4, 66 MnC,I&NzS4 Mn(SZCNHCH2CH2NHCS2). 6,1016 MnC4H60, Mn(glycollatc),, 4, 51 MnC,HeN204 Mn(H2NCH2COZ)2, 4,63 MnC&N6S4 Mn{(H2N)2CS)2(NCS)2,2,639 MnC,Hs07 Mn{(S)-02CCH2CH(OH)C02)(H20)2.2.475 MnC4HsS4 4. 53,90 [Mn(SCH2CH2S)Z]Z-. MnC4Hl0Cl2N2O2 h4nCI2(HCONHMe),,2,492 MnC,Hl0CI,N6O4 MnC12(H2NCONHCONH2)2.4,62 MnC,HloN20RS MnS04(l~,NCl12C02H),, 4,62 MnC4HloN4010 Mn(N03)2(H2NCH2COzH)2. 4.62 MnC4HI2 [MnMe4I2-, 4,13 MnC4HI4N4 M~(CZH)Z(NH,),,4, 14 MnC4H16N404PZ Mn{0zP(CHNL)z)2, 4 6 4 MnC4K05 Mn(CO)*(NO), 1,290; 2, 103, 105.109: 4.7 MnC,N,O, [Mn(CN)(CO),(NO)I , 4 , 8 MnC4N404 [Mn(NC0),]2-, 4,22 MnCaN4S4 [Mn(NCS),I2-, 4,22 MnC,N4Se4 [Mn(NCSe),lZ-, 4,22 MnC4N50 [Mn(CN)4(N0)14-,4 , s MnC404S,

MnRr(CO),, 1. 290; 2,204. 280.587, SYO MnC5HNS0 [Mn(CN),(OH)I4-, 4.11 [Mn(CN),(OH)JS-, 4.8 hlnCSHO,

MnH(CO),, 2,697,701,707 MnC5H3N204 Mn(CNMe)(CO),(NO), 4, 8 MnC5H4C12N0 MnC12(2-pyridone).4, 61 MnCSH5Cl2N MnCldpy), 4,18 MnCsH5NOS2 {MnCp(NO)(S,)},, 2,534 M ; ~ ~ ~ ~ H C O z H ) ( H , O ) , l4 ,Zh 'l , MnCdNs IMn(CN)511-, 4, 12 -_ M ~ C N ~ S ~ [Mn(NCS),I3-, 4,22 MnCiN,O [Mn(CN)5(NO)]2-, 4, 12, 83 [Mn(CN),(N0)I3-, 2,103; 4,12 MnC jN602 [Mn(CN),(NO,)]j-, 1,12,83 MnCj05 [Mn(CO),]-. 2.210,215 Nln(C,O,), 2.455 MnC,H,NO, [Mtl(CO),(Cr.i;Mc)j-, 2,212 MnC6H41\lh Mn(CNH),(CK),. 4, 12 MnCdW14 IMn(C2O&(H2O),1-, 4,89 MnC6H,N04S Mn(OSCNMe,)(CO),, 2.587 MnC6H6YOfi [Mn{N(CHIC02),]]-, 2,789 bhC.&N& Mn( NCS),(triazole), , 4 , 2 1 MnC&lsC!>", M~~C,I~(pyaznle)~, 4,X MnCsHsOs Mn(L-lactrtrelz.4, 51 MnC,H,N,O, [Mn(ON=CMcNO),] , 4 , 6 3 MnC6H12N202S2 Mn(NCS)2(EtOH)2,4,22 MnC6H1308 Mn(OAc),rH20)2, 4,88 MnC6HlaBrNzOsPz MnBr(NO)2{P(OMe),}z, 4 , 9 M~C~HIBI~PZ MnI,(Phle,),. 4.85 MnC6Hd206 [Mn{n.L-MeCH(NH,)CO,H} 2(H20)2]t,2.745 MnGH24N, [Mn(en)3]*+.4,23 M n C 8 z . d1 2 0 6 [Mn(I12YCONt12),13t, 4, 90 MnC6N307 [Mn(cN),(CO),l2-, 4 , 7 , 8 MnC6N,02 [Mn(CN),(C0)z]3-, 4 , 7 , 8 MnC6N6 [Mn(CN),12--.4.5,102 [Mn(CN),I3-. 4.5,83 [Mn(CN),14-. 1.272; 4,5,7,11 [Mn(CN)J-. 4 . 8 MnC6N,S6 [Mn(YCS),l4-. 4,11. 22 MnC6N,Sc6 [Mn(NCSe),14 4.22

414

Cumulative Formula Index

4 17

[Mn(CZ04)3]3-,1,409; 4.89 MnC7H40,P Mn(CO),(PCH=CHCH=CH). 2.1044 MnC7H70ZSe Mn(CO),Cp(SeCH,), 2,665 MnC8H4 [MII(C~H)~I’-, 4,14 MnC8H502S Mn(C0)2(CS)Cp, 2,581 MnC8H502S2 Mn(C0)2(CS2)Cp,2,581 MnC,H,O, Mn(CO),Cp, 1, 131 MnC8H6N06S Mn(OSCNMe,)(CO)r, 2,587 MnC&,O6 [Mn(CO)4(CH2CO)z]-. 2.396 MnC8HloC1ZN602 MnCl,(cytosine),, 4,62 MnC8Hll12P MnI,(PMe,Ph), 4,32,59 MnC8H14CIZNZ02 MnC1,(8-quinolinol)2, 4 , 6 1 MnC8H16CI,02 MnC12(THF)2,4, 38 MnC,H,,Cl,O,P, Mn(P02C12)2(EtOAc)2.4. 39 MnC8H1802 Mn(OBu1),,4, 37 MnCsN4S4 [Mn{S,C,(CN)Z)21’~, 4,54 MnC.N,OSd [Mn{S,C~(CN),},(N0)]2~-.4.54 MnC804S4 [Mn{S~=C(S)CO~O},]z-,4.53 MnC9HF,0, Mn(hfa&)(C0)4, 2, 375 MnC9H803P Mn( CO),(PCH=CMeCMe=C H) 2 1043 MnC,H 1503s6 [Mn(S2COEt)l]-.-.4.55 MnC9HZ1ClZN3O3 MnCI,(H2NCOHt),, 4, 39 MnC9HZ4BrZN6O3 MnBr,(MeNHCONHMe),,I. 39 MnCloH8CI2N2O2 Mn(bipy dioxide)CI,, 4 , 5 1 MnCloHsCl4N2 MnCl,(bipy), 4,103, 108 MnCloH8N509 Mn(N03)&ipy), 4,84 Mn(O,NO),(bipy), 2.423 MnCloHloC1?NZ MnC12(py),, 4, 18 MnCloHloClA08 Mn(C104)2(py)2,4 , 1 9 MnCloHlzNz08 [Mn(edta)]-, 2,783 [Mn(edta)lz-, 2,784 MGOHd208 [Mn(Hedta)]-, 2,784 MnCloH14C10, Mn(acac)2C1,4,89 I

~

MnC10H14N209

[Mn(edta)(H,O)]-, 4,69,96 [Mn(H,0)(edta)]2-l 2,783 MnCl,,H14Nt04 Mn(acac)2(N3), 2.230; 4 8 9 MnCl0Hl4O4 Mn(acac),, 2,388,402; 4.49; 6 , 28% 1016 MnCloHI4O6 MnO,(acac),, 6 , 121 MnCloH15N60

MnC13H19NZ()8

[M~I(CNM~)~(NO)]’-, 4, 12 MnCloHI6Br2O4 MnBrZ(MeCOCH,COMe),, 2,402 MnCl0Hl6CI2N4 MnCI,(1 .2-di-Me-imidazole)2,4,20 MnCloH1606 [Mn ( a~ ac) ~ ( H ,O ) ~4,90 ]’, MnC,oH,8Nj09 Mn(NO,),(bipy), 4 8 7 MnCloHlB04 Mn(02CBu‘)Z, 4,43 MnCJ Ila06 Mn(acac)2(t120)2,2,388; 4, I I , 49 MnC,,H,&S4 Mn(S,CNEt,),, 4,54 MnC10H22Br2N206 M ~ { D . L - ~ H ( C H , ) ~ ~ H C O Z H ) , B ~2.745 ~(H~O)~, MnC10H24N204S6 Mn(NCS)2(DMS0)4, 2,641 MnCloHZ4N4 [MnCI, HfSCH2CH2NH(CH2)3NHCH2CH2k H & } ] + , 4, 100 h.lnCloHzsPz MnMe4(Mc,PCH,CH,PMc,), 4,34,103 Mnr10fT30P2

MnMe4(PMc3)2,4, 103 MnC, 1H14N04S Mn(acac),(NCS), 2,227; 4,89 MnC, 1H14N204S2 Mn(a~ac),(NcS)~, 2,230 MnCl1Hl4W& [Mn(tmta)I2-, 2,784 MnCI,H,,IG208 [Mn(Htmta)]-. 2,784 MnC12F1809 [Mn{(CF3)2COC02)313-, 4.89 MnClzHaBrzN4Sz Mn(NCS)2(3-Br-py),, 4,19 MnCl21IloO2 .Un(OPh),, 2.345 MnC12iT14N04

Mn{2-UChE14ClI=N(CH2)30}(OAc), 4, 93 MnCIZH1408 Mn(02CC(Me)=C(Me)C02H)2,4,50 MnClzH16N208 [Mn(teta)12-. 2.784 MnCIzH,7N20s [Mn(Hteta)]-, 2,784 M ~ C ~ ZH ~ ~ C I ~ N ~ MnCI,(2-Me-imida~ole)~, 4, 19 MI~CI~HZ~OI~ Mn(D-gluconate)2, 4,51,6,534 MnC, 2H2,Br,P MnBr,(PBu,), 4,32 I MnC12H2712P MnI,(PBu,), 4, 32

h.lnClztI,,O‘ [Mn(DME)3]2C,4,47 MnC12HdW4 MnBr2(Me,PCH,PMez)2, 4,32 MnC12H34N2017

[Mn(N0,)(H,0),](N03)(18-crown-6), 4,SO MnC12H3,P4 MnH3(Me2PCH2CH2PMe2)2, 4,93 MnC12H36C1016

[Mn(H20)6](C104)(18-crown-6), 4,80 MnC12H36N2Si4 Mn{N(SiMe,)2}2, 4, 17 MnC12N6S6

[Mn(S,C,(CN),),]2-, 4,107 MnC1&8NA [Mn(peta)]’-, 2,784 MnCl3H1&08

Mn(acac),(CH,=CHCH,NH,),, 2,388

[Mn(Hpeta)]-, 2,784 MnCi3HuNOs [Mn(l8-crown-6)(MeNO,)12+, 4.80 MnCI4H8N6S4 [Mn(NCS),(bipy)lZ-, 4,22 MnCi4Hs06 Mn(2-HOC6H4CO&, 4 5 1 MnC14Hlo04 Mn(tropolonate),, 4,48 MnC14Hlo0, Mn(2-02CC6H40H),, 2,469 MnCI4Hl2Br2N20 MnBrz(H,0){2-(2-pyridyl)quinolinc). 4.24 Mnc14l-L ZNZOZ [ M ~ I ( M ~ C ~ ) ( C O ) ~ ( N' .2.131 ,P~)] MnC,,HI2S4 [Mn(SZC6H3Me),]-, 2,606

MnCleH3zBr60s Mn(12-crown-4),(Bt3),, 4, 80 MnC16H36C12N4 I

Mn((2-OC,H4CH=NCH2),CH,J(OH),4,95 MIIC~~H,,N,O~S~ MnC3,H2,N6SZ Mn(NCS { H S (CH2),N=CMe-2,6-pyC(Me)= &H7L).4. 77 MnC17H27ClN5 [MnCl H h CH2 ,N=CMe-2,6-pyC(Me)= &€I&)]+, 478 MnCI8CIl2S6 [Mn(S2C6C14),]Z-,4: 107 MnClsHI2K2O2 Mn(8-quinolinolate)2. 1, 528; 4,64 MnCdh2N306 Mn(2-pyCO& 4,93 MnCl8H,&O, ~Mn(2-OC,H4CH=NCH2CC2),~~~, 4,94 MnCI8Hl5N3P Mn(PPh,)(N,), 2,230 MnC18H1604P Mn(CO),Cp(PhPOC(=CH,)CH=CMe~),2,369 MnCl8Hl7NZO4 Mn(salen)(OAc). 4, 5.67, 95 MnClSHl8C1N3P [Mn{(2-pyridylCH2),P}CI]+, 4,34 MnC18H18NzOzS4 Mn(S2COE1)2(phen),4,55 MnC,,H,2N,02 Mn(salen)(en). 4, 66 MnC gH24N, Mn(2-CH,C6&NMe2),. 4, 14 -,I,

96

Mn(C0)5{Si(SiMe3)3}, 2, 19 MnC14H37P4 MnH(H2CFCH2)(Me2PC~12CH2PMe,)2, 4,93 MnC 4Hd'4

MnMez(Me2PCH,CH,PMe,),.4,34.1U3 MnG~HllCW303 MnClz(terpy trioxide), 4 , 5 2 MnC15dl'1F3N202 [Mn(MeCp)( CO),( N2C6H,CF3-2)]+, 2, 131, 136 MnCi5HizCI2N4 MnC12~(2-pyridyl)3N},4, 27 MnC15H15Br3N3 [MnBr3(py),l-, 4,19 MnCi5Hl5C13N3 MnCl&y)3,4,84 MnC15H2106 Mn(acac),, 2,210,371, 379,386; 4,5,89; 6,1016 MnC,.iH,,CIN4 MnCl{Hh CHz ,N=CMe-2,6-pyC(Me)= &&I, 4- 77

[M;(Ei%C),]+. 1.336 [Mn(EtNC)6]2f. 1.336 MnClsHj4NsSi6 Mn{N(SiMe,),},: 4,84

Mn(NO3),(1:8-naphthyridine),. 4.25 MG6H14N202 Mn(salen), 4,5, 11,66; 6. 379 MnC16H16N202 Mn(2-OC6H4CH=NMe)2,4,64 MnC1,Hl,N,0,S4 Mn(S,COEt),(bipy), 4, 55 MnC26H24Br2N8

MnBr2(5-methylpyrazole)~,4, 19 MnCi6Hdz04

MnlBu'N=CHCH=NBu'L. ,- 2.210 MnC2bHd4 4,33 Mn{2-(CH2)2C6H4}(Me2PCH,CH2PMe2)2, MnC,,,H4&0? Mn(0Ac HhCH CH NHCMe,CH2CHMeNHCH2U l - l M e ) , 4,77 MnC,,H, ,NO.P

Cumulative Formulu Index

419

MnC,,H,,N,

MnC30H30Nb [Mn(p~)~l'' 4,5 MnC3,H3,0P Mn(CjMe5)(Ph2PC6H4COMe),2, 1056 MnC30H43P khPhz(P(C6Hii)3}, 4, 13,33 MnC3zH16ClN8 Mn(phthalocyanine)CI, 2,866; 4.99 M~C~~HI~NB Mn(phthalocyanine), 1,273; 2,861,866,870: 4. 5.75. I

W;6, 1016

MnCz2Hz2C1N, MnC1{2 f i C H N-CMeCH=CMeN-2-C6H,N= -Me), 4, 101 MnCZ,H3,O4"

Mn(CHzPh)z(dCHzCH,0CH2~H2)2, 4, 13 MnC,aH,2F906 _ . .[Mn(furylCdCIICOCF,),]-, 4 , W MnC24HlsC12N202 MnC1z(2-pyCOPh)z.4.60 MnC2J%~N5 MnN(tetramcthy1porphyrin). 2.845 MnC2&,N7 Mn(N,)(tetramethyIporphyrin), 2. 845 MnCZJh0P2 Mn(PPhz)z,4,34 MnCzJLoS4 [Mn(SPh),],-, 2,525; 4,53 MnCZ4Hz4N3O3S3 Mn{ONMeC(S)Ph},, 4.96 MnCz4Hz9N3Pz M ~ ( P P ~ z ) z ( N H4,34 ~)~, MnCz4H4~06 [Mn(THF),12+, 4,38

"_

-"

(-)-MnH(SiMePhNp-l)(C0)2(C5H4Me), 2, 19 MnCz6H16N602 Mn(CNO)z(phen),, 4, 14 MnCz6HZON2OZ Mn(2-OC6H4CH=NPh)2, 4,64 MnCz6HzsN6Sz Mn(NCS)z(5-Me-pq),. 4.19

[Mn(phthalocyanine)1-, 2,866 [Mti(phthalocyariine)l"-, 2, 870 MnC12H,,N@ MnO(phtha1ocyanine). 4 , 5 MnC32H16N8 0 2 Mn(phthalocyanine)(O,), 2,866; 4,76 MnC3zH16N90 Mn(phthalocyanine)(NO). 2,866 MnC32H,7N902 Mn(phthalocyanine)(NO)(OH), 2,866 MnCdLNa [Mn(l.8-naphthyridine),j2+, 4,25 MnC32H2BN602 [Mn{(2-p~.ridq.I)~COH},], 4,66 [Mn{(2-p~ridyl)~COH}z~z+, 4,27 MnCilI13,N7 [Mn({(2-pyridylCHz)2NCHz}2}]zc, 4,30 MnC33H17N&2 Mn(nhthalocvanine)(OCOI1). 2. 866 MnC,~H,,O,P . Mn(C0) 5 ( PCPh=CPhCP h=cP h) ,2,1043 MnC3,H19N804 Mn(phthalocyanine)(OCOH)(HCO,H),2,866 MnC34H35N5 Mn(sapphyrin), 2,889 MnC3SH19N10 Mn(phthalocyanine)(HhICH=NCH=cH), 4.76 h.inC36H24Nb [Mn(phen),12+, 4 , 2 3 MnC,,,I-I3,QsO,P2 MnC13(P113PO)Z. 4,90 MiiC36H30P3 [Mn(PPh2)sl-, 4,34 MnC36H44N402 Mn(octaethylporphyrin)Oz, 2,827; 4,73 MnC3,YI,, N 9 0 z , \

Mn(8-quin0ltnolate)~,1,64.93 M~CZBHZOF~NSO~

Mn(NCOCF3)(tetramcthylporphyrln)(OzCCF,),2, 845 MnC28H37N5

Mn{2-C6H4(N=CMeCH=CMeN),C,H4-2}(NEt3), 4,

77 MnCz8H4202 Mn(OC6H3But2-2,6)2,2.345 MnC28H44 Mn(norbornyl),, 4, I03 MnC30HZ2N6O6 [Mn(terpy trioxide),l2+. 4,51,52. 106 MncJoH z4 N6 Mn(bipyh, 4,25 [Mn(bipy)J, 4.25 [Mn(bipy)J2+, 4,23,25 MnC3oHmN606 [Mn(bipy dioxide)3]zi, 4. 106 [Mn(bipy dioxide)3]3+. 4.40

M~c,,H,,cIN~ MnCl(tctraphenylporphytin), 2,827,845; 4,72,97,98; 6.375,376,377,378 MnC,,H,,CIN,O MnO(tetraphenylporphyrin)CI, 2,845 MnC tI LIN I Mn(tetrapheny1porphyrin). 4,72

Curnulutive Formulu Index

MnC44H2SN4

[Mn(tetraphenylporphyrin)]' , 4 , 9 9 MnC44Hz8N40~ Mn(O,)(tetraphenylporphyrh). 2,'317,827; 4,73 MnC44HZ8N5 MnN(tetraphenylporphyrin), 2, 828; 4, 110 M~C~~HZENSO Mn(tetraphenylporphyrin)(NO) 2.827 MnC44H28N7 Mn(N,)(tetraphenylporphyrin), 4$98;6, 377 MnC44H&'10 Mn(N3)Z(tetraphenylporphyrin),2, 828; 4, 108 MnC44HmNzOzPz Mn(CO)z(N2Ph)(PPh3)2,2,132 MnC45H30N4

Mn(N-methyltetraphenylporphyrin) 2,849 MnC&3iN40z Mn(OAc)(tetraphenylporphyrin)?6,375,377,378 MnC46H34N402 Mn(OMe)z(tetraphenylporphyrin)l 4, 108 MnC46H36N40~ [Mn(tetraphenylp~rphyrin)(MeOH)~]+, 4, 97 MnC47H31N6 Mn(tetraphenylporphyrin)(imidazolare). 4,97 MnC48H32C12N8

MnCIZ(phen),, 4,25 MnC,,H,,N, Mn( tetraphcnylporphyrin)( 1-mcthyEmidazolc), 2,826; 4,72 MGsH~oNzP~S~ Mn(N(PPhZS)zlz,4,54 MnC411H40P4 [Mn(PPh,),]*-, 4,34 MnCwH46NzP4 [Mn(PPhz)4(NH3)zlZ-, 4,34 MnC49H33C1N5 MnCl(tetraphenylporphyrin)(py) 4>97 MnC49H33N5 Mn(tetraphenylporphyrin)(py), 4 , 7 3 MnC,,H33N5CI Mn( tetraphenylporphyrin) Cl(py), 2, 828 MnCsoH32N6 Mn(tetraphenylporphyrin)(4-CN-py), 2,827 MnC50H34N8 [Mn(tetraphenylporphyrin)(imida~olate)~], 4 , 9 7 M~CSOH~IN~O Mn(tetraphenylporphyrin)(NO)(j-methq.lpiperidine), 2, 827 MnC52H36N303 Mn(2-OC6H4CH=NCHZF'h),, 4.93 MnC52H48C12P4 [MnClz(diphos),]+, 4,85 I [MnC12(diphos)z]z+,4,104 MnCdWJ3P3 [Mn(2-pyridylCH2PPh2),J2 , 4 - 34 M~CS~H~~C~ZP~ MnClz(diphos)2, 4,32 [MnC12(diphos)Z]+,4,32 4, 32 [RlnCl,(diph~s)~]~+~, MnC60H46IzN406 Mn(tetraphenylporphyrin){OI(OAc)Ph) *, 6, 378 MnC68H44Niz04' Mn(rneso-a,a,a,a-tetrakis(2nicotinamidophenyl)porphyrin}, 4 , 98 MnC72H60C1&1ZP4 Mn(C104)z(0PPh3)4,2, SO0 MnCnH60I04P4 [MnI(Ph3PO),]+, 4,40 MnC7,H4,N1sO {Mn(phthalocyanine)(py)}20, 4 , 5 , 7 4 I

+

'

MnC88H56N140

{ Mn(tetraphenylporpbyrin)(N3)}20, 2.828 MnC10, Mn03CI, 4,110

420

MnC10,S MnO,SO,CI, 4,110 MnClzIz [MnC121z]2-14. 59 MnCl2O2 MnO2Cl2.4: 110 MnC1208 Mn(C10&. 4,47 MnC13 MnCI,, 4,91 [MnCI,] , 4 , 5 7 MnCI,O MnC)CI,,4; I10 MnC1, MnCI,, 4. 108 [MIICI,]~-,1, 272;4+5 . 1 1 , s . 58 MnC1404P, Mn(C12P02)2.4 . 4 5 MnCl, [MIIC~,]~-, 4. 91,92 MnC1, [MnC1612-,4.108 [MnCI,l3-, 4,91 [MnCl6I4-, 4,%: 6,846 MnCoC.,,H,,O,PS, (Me3.1')CpCo(CS,)Mn(C:C)),C:p, 2, 582 MIJCOC~~H~~O~P~S~ Co(triphos)(pCS2)Mn(CO),Cp, 2, 582; 4,646 MnCr,S, MnCr2S,* 3- 833 MnCuC,,H,,N,O, Cu{ O2CCH,NCOCHZN=CHC,H3{ Mn(CO),}CH2NMez},6,209 MnCuC18HZoN306 Cu{ 02CCHMeICOCHMeN=CHC5H3 { Mn(C0) 3}CH,NMe2), 6,209 MnFO, MnO,F, 4, 110 MnFO,P Mn(PO3F). 4.45 MnFd MnF,, 4, 107 [MnF,1-. 4>91 MnF, [MnFj]-. 4> 107 lMnFslZ-, 4>91 .~ M~F, [MnF,I2-, 4 . 5 - 107 [MnF6]'-- 4.91 [MIIF,I~--. 4,56 MnFeC,,I Fc~nn(Bu'NCIfCHI;JHBu'), 2,215 MnFcCIIH90,PS2 ( MeJ)(OC)2Fe(CS,)Mn( CO)<,2,582 MnFeC, ,H,,,WC),S, (ON)CpMn(CS2jFc(CO),Cp, 2,583 MnFeC,,H140ePSz {(MeO)3P}(OC),Fe(CS,)Mn(CO)3Cp, 2,582 MnFeC24H1B05PS2 (Ph,MeP)(OC)zFe(CS2)Mn(C0)3Cp, 2,582 MnGaCllHZ3NSO3 Mn(3,5-dimethylpyrazole)(N0)2(Me2NCHzCH20GaMe2), 4,9 MnGeCz5HZ3O, (S)-(-)-Mn(CO),(CMe(OEt)}(GeMePhNp-1). 2. 19 MnHClO Mn(OH)Cl, 4,35 MnHI MnH1,4,60 MnHO, MnO(0H). 4. Xh MnH0,P MnHP03, 4,45

42 1

Cumulutive Formula Itidex

MnHO,P MnHPO,, 4 , 4 5 MnHO,Sc, MnH(SeO,)(Se,O,). 4.88 MnH, MnH,, 2,693; 4 , 6 0 MnH2C150 [Mn(H,O)CI,I3--, 1.50 MnH, MnH,, 4 , 9 3 MnH,0,P2 MnH,P,O,, 4,87 MnH4F402 [MnF4(H20)J 4.92 M n H4N Mi1(NIH2),. 4, l h MnH,O, [Mn(OH),]*-, 4 , 3 5 MnH408P2 Mn(H2P04),, 4,45 MnH606 [Mn(OH),I2-, 4,104 [Mn(OH),I3-, 4 , 8 h [Mn(OH)6]4-, 4,35 MnH,O,,P, [Mn(H,Pz07)3]3.. 4. X7 MnH,CI,N, MnC12(N2H4)2,4,17

,

MnH,N,

[Mn(NH2),]"~,4, 16 MnHl106 [Mn(OH)(H,O),]+. 4.35 MnHl2CI2N, MnCI2(NH3),, 4,15 MnHI2O6 [Mn(H20)6]2+.1.33.272.284.300; 4. 11,35,60; 5. 682; 6.859 [Mn(H,0),I3 ' , 1,253; 4.85 MnH,,N, [Mn(NH3),JZ+,4, 15; 5. hH9 MnHgC4N4S, HgMn(SCN),, 4,22 MnHgC,H702 Hg(C0)2Mn(,rlS-hIrC5H,)I5 , 1085 MnHgCllH8CIZN3O5 (OC)SMnHg{N3(2-CIC6H,)2}2 . I MnIz06 Mn(IO,),, 4, 46,37 Mn13 [MnIJ, 4,59 MnI3OI8 [Mn(I06)3111-,4, 105 MnI, (Mnl,12-,4, 11, 59 MI11 5 0 is

[Mn(I03),12 , 4 . 88 Mnl,O,, [Mn(lO3),l2-. 4, 105 MnInC4,H4,N405 In(octaethylporphyrin)Mn(CO),,2.843 MnK,O,S, K2Mn(S04)2,4 , 4 6 MnLiC7H5N,0, MnCp(CO),(NNLi), 2. 133 MnLiC13HloN202 MnCp(CO),(N,Ph)Li. 2. 130 MnMo04 MnMoO,, 3, 1376 MnN40x 4.44 [M~I(NU,),~~-, MnN4012

[ Mn(NO,),] .4.87 [Mn(NOj),]'-, 4. 44

MnV 13%

M nN& III [Mn(Fi02)5]3-. 4.44 MnN6 Mn(N3),. 4.23 blr~N,~ [Mn(N3),IZ-. 4 , 2 3 hinNa2OsSe, NazMn(Se04),. 4 4 6 MnNiC,O,S, MnNi(S2C2O,),. 5 , 182 MnO,S MnSO, 4 - 3 6 MnO;Se MnScU,. 4,46 Mn03Si MnSiO,, 1,41 hrnO,Te MnTeO,, 4, 46 MnO, [MnOJ. 1.336,539,553; 2,296,414; 4, 109.525.6. 351.493.517, 1016 [Mn04]*-. 1.336; 4,109 IMn0,j3-. 4,109 [moJ-. 4.104 MnO,P Mnk3,. 4,X7 .VnO,S hfnSO,. 4 , 4 h IlnC),S, [hIn(SO,),]~+,2,635 Mn0,Se hfnSe04, 4 4 6 MnO, [MnO5J3-.4.109 Mn05Sel hInSe20j,4,46 Mn06S3 [h.In(S03)2]2 ,4,46 Mn0,5e2 Mn(SeO,),, 4 , G . 102,105 [hIn(Sc0,),]-, 4, 88 MriO, IMn(02)30]4-.4,105 Mn0,P2 [MnP207] .4.87; 6 , 125 MnO, pm(o,),j4-, 4,105 MnOsPl (h,ln(P0,),]2-, 4. 105 IMn(PO4),I3-, 4,87 Mn08S2 [Mn(SOpj,]-. 4,87 {Mn(SO,),]+. 4,86 MnO,P,

Mn(PU3);. 4,87 MnO 8'I'e3 lMn(TeUh)3114-, 4 , IO5 MnPtC, ,H,,O,PS [ M ~ P ~ ( ~ L - C S M ~ ) ( C O ) , ( P M C' ,.5.385 P~)C~] MnRuCj4H4006P, RuMn(:i-PPh2)(C0)6(PPh3)2. 4, 373 MnRuC,,H,,CIO,P, RuMnCl( p-dppm),( pCO),(CO),, 4, 373 MnSnC,H,Oj Mn(CO),(SnMe,), 2, 19 MnSnCIsHl7O, Mn(CO)2(C5H4Me)(SnCp2),2, 17,3,219 MnSnC,?H, (OC),Mn(CS,)SnPh,, 2.583 hiinTi2C20H2DC14 (TiCp,Cl),MnCl2, 2, (778

Curnularive Formula Index

422

MnZC32H2008SiZ Mn2(CO)8(SiPh2)2,2, 19 MnZC32H28N40S {Mn(salen)O},O,. 4.67 Mn2C34H36N106 { Mn{(2-OC6H4CH=~CH,),CH2}(H20)}2, 6,498 MnzC36H&I& Mn2C14(2.2'-biquinolyl),. 4.24 M~zC~OH;~N@~ Mn202(bipy),. 4 >1(13 [Mn202(hipy)4]3'.4 . 84: 6.498 [ M r ~ , O ~ ( b i p y ) ~6.] ~398 -. Mn2C,,H,2N,02 Mn,O,(phen),* 4, 103 MnZC64H36N.160 {Mn(phthalocyanine)}20. 4,76 Mn,C6,H400sP2 { Mn(CO),(PCPh=CPhCPh=cPh)},, 2, 1033 Mn2C74H.12N {Mn(phthalocq.anine)(py)}20, 4,99 M ~ ~ C ~ S H ~ ~ N I ~ O { Mn(N3)(tetraphenylporphyrin)}20, 4.98. 108; 6.378 Mn2C700H66CIZIZN803 {Mn(tetrapht.nq.lprirphyrin){C)T(Ph)CI}),O, 6.378 Mn,CdCloOlo C ~ { M I ~ ( C O ) 5,988 ~),. Mn,CI04P Mn2C1P0,, 4. 45 Mn2CIi [Mn,CI,l3-. 4.58 MnzErHd Mn,ErH,, 4.60 MnP5 MnzFs, 4.91 Mn2F9 [Mn,F,]-. 4,107 Mn,H,CI@, Mn,(OH),CI. 4. 35 Mn,HgSnC,,M,,N4Og Sn(tetraphenylporphyrin)Mn(CO),HgMn(CO),* 2.843 {Mn(CO),(OSCNMeZ)}2,2,5XX MnZK,O,S, Mn,C,,H,,O,S, {Mn(C0)3(0SCNMrz))2,2,587 K,Mn,(S03)3. 4. 46 Mn2K2012S3 Mn2C12H14016 K,Mn,(SO,),. 1.46 2,479 [Mn{ 0zCCHzC(OH)(C02)CH2C0,)(H,@)]2z~, Mn204Si Mn2CI3Fl2N2O7 Mn2Si04. 4.41 Mn2(C0)7{NC(CF3)2}2.2, 126. i28. 280 Mn206 M n K , 4H100,s~ [Mt1,0~]~-.4.87. 109 {MnCp(CO),}Z(S,). 2.534 Mn207 MnZCi4H1~O4Se~ Mn20i, 4, 110 {Mn(CO)zCp}z(Cl?-Se2),2,667 Mn2O7P2 Mn2C14H36NioOz Mn2P207,4 , 1 5 [Mn,(tren)2(NCO)212'. 2,230

M~,C~~H~,,O,S, Cp(CO),Mn(CS,)Mn(CO),Cp. 2.582 Mn,C, 5H,204Te {Mn(Cd)zCp}z(p2-TeCH2)r2,671 Mn~C18HnN906 [Mn,Cl(isonicotinyl h y d r a ~ i d e ) ~ ( H ~ O )4~, 6] ~3 + , MGi9H25Ni& Mnz(NCS)4(4-Metriazole),. 4. 21 MnzCmHioN408 {Mn(NzPh)(CO)4}2.2, 132. 137.280 MnzCzoHz6N4Oi6 Mn3{(02CCHz)2NCH2CH2N(CH2COz)(CH2C02H)}2.4.70 MnZC24HZ6N16

Mn,(irnida~olate)~(irnidazole),. 4.21 M ~ ~ C Z ~ H ~ A S ~ S Mn,{N(SiMe3),},. 2. 174: 4. 17 Mn2C2dLZN2O8 Mn,(acac),(H,NCH2CH=CH&. 4.49 MnZC30H46NZOS Mn2(0zCBu')4(py),. 4 , 4 3

Mn,O,Se, Mn,(SeO,),, 4.88 MnzO1?S3 Mn2(S04),, 4 8 7 M112PdC2OH ioNzO1o Pd{Mn(CO)S),py,. 5 . 1108 Mn,ScH4 MnzScH4,4, bo Mn2WC401 MnZ(C204)2W03. 4.50 MntZrF8 Mn,ZrF,, 3.428 MnzZrH, Mn,ZrH,, 4 - 6 0 Mn3A~C24HIBOl8 Al{Mn(CO),(MeCO),),, 2,3Y6; 3, 1'15 Mn3AIC42H30018 AI { Mn( CO),(MeCO ) (PhCH,CO)} 3 , 2,397 Mn3As3Au3C26H2702S {AuMn(CO),)3{(Me2AsCH,),CMe}, 5,905 Mn3BH604

423

Cumulative Formuh Index

Mn3(OH),{B(OH),}. 4.42 Mn.$206 Mn3(B0d2,4,42 Mn3C12H3012 Mn,H,(CO),,, 2.703 Mn3Cl2HlOOl4 Mn,(citrate),, 4,51 Mn3C13H3N2012 Mn3(CO)12(N2Me).2. 136 Mn3C13HloFOl Mn3(p3-OEt)2(pF)(C0)9-1. 145 Mn3ClSHlsN4O4 Mn3Cp3(NO),, 2, 108. I16 Mn3ClhH25017

Mn,O(OAc),(HOAc). 4.88 Mn3CiaHziN404 M n , ( M e c ~ ) , ( N o ) ~2, 117 Mn3ClsH22N403 [Mn,(MeCp),(NO),( NH)]-.. 2 . I 17 Mn3ClsH22N404 [Mn3(MeCp),(NO),(NOH)]+. 2. 117 M~~C~IHI@~T~ {Mn(CO)2C~h(ln3-Te). 2.671 Mn3C21H1506Te2 {Mn(CO)2Cp},Te2. 2.671 Mn,Cz7H,lCIdW~, Mn30(OAc),(3-Clpy),, 1. 145 Mn3C27H33N3013

M ~ , O ( O A C ) ~ ( ~1.~ 145; ) , . 4, 5 [Mn,O(OAc)6(p)'),]'. 4 . 88 Mn3GeC21H1506 {Mn(CO)2Cp},Ge, 2, 19 Mn3I2OIo Mn,(IOS),, 4,47 Mn,O,Te Mn3Te06,4,46 Mn308P2

MndPO,),, 4,45 Mn3SnCl5C1OIs {Mn(CO),},SnCI. 2,19 Mn&i@isL Mn,(S,),(CO),,. 3. 512, 533 M%C~,H~~NI~O~ [Mn,(p-O),( 1,4,7-triaza~yclotionane),]~', 1, 151 Mn4C24H60N1206 [Mn,06{ H&(CH2CH2NH),CH2~H2j,]4',4, 103 Mn4C6oHsoSio [Mn4(SPh)lo]2-.1, 151: 1 . 5 3 Mn4Cii~Hi600ih Mn4(3,5-Bu'Z-l.2-02C6HL)81 4?106 Mn4Hg4CJ%&h Hg,Mn,(CO),(r15-MeC,H4)11 5 , 1049 Mn4Na2Ol5SS Na,Mn,(SO,),, 4,46 Mn4Sn,C2,H2O2, {M~I(CO),}~S~,H,. 2- 19 M~&,H~,CIIOO.I, MnSCllo(EtOH)14,4 , 3 7 MnsH4012P2 Mn,(OH)4(P04)2,4.45

Mn12C32H5h048 1. 169; 4, 88 Mn120,2(0Ac)16(H20)4. MoAgCNS, [AgCN(MoSl)j2-, 2 , 5 W MoAgS, [Ag(MoS4)]-,2.565 [Ag(MoS4)l2-,2.566 [A~(MOS,)]~-., 2. 568 MOAg&iH4sP3S~

MOSa(Ag(PPh,),}(AgPPh,). 2.566; 3. 1422 MoAg&2HmP& Agz(MoS4)(PPhs),, 2,567 MOA&C72H6oP?Ss ( A ~ ~ M O ~ S ~ ) ( P P 2,567 ~,)~SZ, MoAIC, 1 H , 5 0 , MoH(CO),Cp(COAIMe,), 2,697 MoAIC,~H~, MOHICP~(AIMC~). 2. 697 MOAIC~~H~,N~P~ h l ~ ( ~ ~ A I M e , ) ( N , ) ( d p p e3, ) , ,1270 MOAlsOz, [ A I I C I O ~ O ~ 3, ~]~ ", 117 MOASCisH~~O, h?IoCp(CO)2(AsBuLl),2, 1052 MoAsCOFCWC~H~S CoFeMoWS(AsMe,), 4,832 MOAS,C,oH16CI2?1202 MoCI,(NO),(diars). 3, 1274 MOAS,C~~H,,I,O, Mo12(CO)2(diars),3, 1281 MOAs~C11H1~F~N0, Mo(O,PF,)(NO)( CO)(diars) , 3 , 1276 MoAs,C~,1H16N0, lMo(?lO)(CO)(
-.

MoBCqH 1nC12N70

Cumulative Formula Index

424

MO(NO){HB(~~N=CM~CH=~M~)~)(OMC)(NH~),~, 1287 MoBC~~H~~N~O~ Mo(N,Ph) (HB(fiN=CHCH=cH),} (CO)2, 3,1294 MoBC,,H,,N,O, ., -. -

-

Mo{Et,B(fiN=CHCH=CH),}(CO),Cp, 2,250

MoBC~~H~~N~O~S

Mo(NO){HB(fiN=CHCH=cH)3}Br(OEt),3,1287

Mo(CO),(NS)(HB(&N=CMeCH=cMe),}, 2,121 MoBC,,H,,N,O, Mo{HB(fiN=CMcCH=tMc),} (NO)(CO),. 3.1276 MoBC~~H~~CIN~O~ MorNOII HB(hN=CMeCH=CMeL \CI(OEt), 3, 1287 MoBC, 7H271N70S Mo(N0){€lB(fiX=CMcCH=~Mc)~)I(SEt), 3, 12x8 MoBCi7H271N701 M o ( N O ) r H B ( f i N = C M e C H = ~ M ~ ~ ~ ~ I ( 3,1292 OEt~ MOBC~,H;~C~N~O Mo(NO){HB(fiN=CMeCH=(?Me),} CI(NHEt). 3. 1”1

MoCI, HfiN=CHCH=cH)(HS(Nr= b H ) , ) . 3,1331

~

I

1287 Mo( NO) {HB(hN=CMeCH=cMe),)Cl(NMe,). 3.

1287 MoHiBHJ)iPMe,),, .., . . 3,1284,1438 MOBC,~H ,7Nh~1 MO{I IR(AN=c;HCH=~H),(CO),~~~~-AC) 2,249 %foBC14H,,N,0, M~{B(A N=CHCH=-C?H),} ( NO)(CO):. 3,1276 Mo3CISHI5CIN8 Mo(N,Ph){HB(&N=CHCH=cH),}Cl. 3, 1295 MOBC~~HI~CIN~O Mo(N0) { HB(&N=CHCH=c Hjj}Cl(N2Ph),3,1288,

1294 MoBCISHI~N~O~ Mo{HB(&N=CHCH=cH),) (CO)2(il3-C4H7),2,256 MoBC~SH,~N~O Mo{H,B(6JN=CMeCH=cMe)2) (C0)2(t13-CH2CH= CH,). 2. 246 MoBC ,,H,,r;kb; Mo(Et,B(&-N=CHCH=tH),} (N?)(CO),(q”CH,= CHCH2),2,249

MoBC17HZ91N90 Mo{HB(&N=CMeCH=tMe),} (NO)I(NHNMe,) , Z 1 151 Mo(N0) { I IR( k N=CMeCH=c Me),} I( N HNMe,) 3.

1288 MoBCI8Hz2N6O3 IMo{HB(fiN=CMeCH=cMe),} (CO),l-, 2,249 M~BC,,H,,CIN,O, Mo(NO){HB(HN=CMeCH=cMe),)CI(OPr’), 3,

1287 MoBCisH3iN~0z Mo(NO){HB(fiN=CMeCH=cMe),}(OEt)NHMe),

3.1287

M O { E ~ ~ ~ ( ~ ~ N = C H C H ~ H ) ~ ) ( C ~2,250 )~(~~-C~H, MoBC ,,H,,N,O

’

[Mn{I fB(hN=CMeCH=c;Me)3}(NO)(MeCN)2]. 3, 1279

MoBC19H31C1N70S

Mo(No){HB(&N=CMeCH=~Me),}Cl(SBu), 3,1288 MoCl,(NO) { HB(&N=ChleCH=~Me),), 3. 1287 MoBCI5H2,CI,N6 MoCI,{ HB(fiN=CMeCH=eMe),). 3.1342 IMoCI,{HB(&N=CMeCH=cMe),)l-. 2,256; 3,1331

MOBC~~H~~N~O~

Mo(NO){HB(&N==CMeCH=~Me),}(OEt)z, 3,1287 MoBC~~H~~N~OZ Mo(N0) {HB(fiN=CMeCH=cMe),)

(OEt)(NHEt)

3.1287 MoBC19Hi4N90

Mo(NO){HB(&N=CMeCH=cMe),)(NHEt),. 3. MOBC1sH241N80 1288 ( ~ H ~ ) , MoBC,,,H,,N,,O, MO(NO){H B ( & N = c M ~ c H = ~ ~ ~ ~ ) , ) I3,1287 Mo(N,Ph){B(fiN=CHC€l=eH)4)(CO),,3,1294 M0BCisHd703, Mu(NO){HB(NN=CMeCmMe),}(OH)z, 3, 1287 MoBC~~H~~N~O~ Mo(N0) (HB(&N=CMcCH=tMc),} (OEt)(OPr’), 3. MoBC~SHZ~IN~O 1287 Mo{HB(Me,C,NII,),)I(NO), 3, 1279 MoBC~~H~~IN~O 1287,1292

Mo(NO){HB(fiN=CMeCH=~hk),}I(NHNHZ),3, 1288

CH,CPhCH,). 2.250 MoBC~~H,~CIN,OS Mo(N0) { HB( &N=CMeCH=cMe),)Cl(SPh), 3,1288 MoBC~~H~~IN~OS Mo(NO){HB(flN=CMeCH=cMe),}I(SPh),3,1288 MOBC~~H~,IN,O, Mo(NO) { HB(hN=CMeCH=C Me),) I(OPh), 3,1287 Mo{B(P;[N=CHCH=cl I),) (NO)(CO)(EtNC), 3,1276 MoBC,,H2,C1N,0 MoBC,,H,,CIN,O M C ~ ( N O ) { H B ( ~ ~ N = C M ~ C H = ~ M ~ ) ~ ) C I ( N H M ~Mo( ) , ~NO)( , HB(fl N=CMeCH=c Me),)CI(NHPh), 3,

12x7

1288

MOBC16HiiTN90

MOBC~IHZ~INSO MO(NO)(HB(~~N=CM~CH=CM~)~}I(NHNHM~),~, Mo(NO){HB(NN=CMeCH=CMe),}l(NHPh), 3.

1288

1288 MoBCZ,H,JNsOS

Cumulative Formula Index

425

MoC~H,~N,O,S

MO(NO){HB(;~~N=CM~CH=~M~),)I(NHC,H,SH), [MoBr,j3-! 3,1330 MoBr12N4 3,1288 (MoNBr,),, 3,1394 MOBCZ~H~~IN~O~ Mo(NO){HB(fiN=CMeCH=~Me),)I(NHC,H,OH), MoCCIIIN MoCl,(NCI), 3, 13.54 3,1288,1293 MoCH303 [MoMeOJ. 3.1380 MoC2H,C1,0, MoCl,(OMe),, 3, 1355 MoBC2lE 1331N70S [MoCI,(OMe),] , 3 , 1354 Mo(NO){HH(fi I\;=CMeCH=t‘ Me)3}l(SC,H, 3, MoC2H,N0, 1288 M00[0:),(Cily-0)(1 I Z O ) , 3.1399.1400 MoBC,,H, ,FN,S MoC2H8C,I3N4O2 Mo(N C H F 4)(SC,H,Me-~)(HB(~N=CH8&-H)3:, 2.136 MoC12(NO),(en). 3, 1272.1274 MoC2H,N,0, MOBC~~H~~IN~O Mo(NO){HB(fiN=CMeCH=~Me),}I(NHNMePh), MoO,(ONHMe),, 3,1391,1393,1405 MoC2N,04 3,1288 Mo(C204)N4,2,444 MOBC,,H~~CIN~O Mo(NO){HB(&N=CMeCH=c \Te),}CI(NHMoC2O4S5 ~ ~ ~ o O ( S ~ ) ~ ( C ~2,532,533.805 O~S)]~-, C6H4Me-4).3. 1288 [MoO&),(O,CCOS)]~~,3, 1392 MOBC~~H;OIN~OZ Mo(N0) { HB(&N=CMCCH=C‘M~)~} MoCZOg T(NHCJI,OMc-3). 3.1288 [M00(02)2(C304)]’-, 2,319; 3,1261,1399. 1400 MoC& MoBCZ~I~~ON~C)~ M o ( N O ) { H B ( ~ N = C ~ e C F ~ ~ ~ ~ ~ , } ( 0 P ~3, ) ( O M[ M c )o,S ( C S ~ ) ~ ],2, ’ S46; 3, 1344,1432 MoCY>FTTNZO~SZ 1287 MoO(ONHMe)(ONMeCS,), 3,13Y4 M O B C ~ ~,N,OS H; Mo(N0) {HB(fiN=Ch.lcClI=~I\le)3}(NHMe)(SPh), MoC3f-ll;Ox 3,128X M O O ( O ~ C C H ~ C O ~ ) ( H3,~1337 O)~. MoC3H,0S3Si MoBC231T,,N7O,S .MoS3(OSiMe3).3,1378 Mo(N0) { HB(&N=CMeCH=tMe),} (OEt)(SPh), 3, MOC;H12CI;N& 1288 Mo{(H,N),CS}~CI~, 2,639 MoC4Hbi;,02 [MoO(OH)(CN),I3-, 3,1249,1335.1337>1338.1345 MoC4H,N,02 MoBC~~H~ZN~OS~ [MoO(H,0)(CN),]2-, 3,1248,1335,1337, 1338,1335 [IMoO(OH,)(CN),~~-, 2,296 Mo(NO){HB(h”=CMeCH=Ch4ej3}(SPh),, 3,1288 MoC4H2N,02S4 MoBCZ,H,jNyO Mo( NO){ HH(fiN=CMeC€k=CMe),} (NH Ph)2, 3, [Mo(NO)(H,NOj(NCS),]2 ,3,1291 MoC,H,CI~N,C)~ 1288 M o B C ~ ~ H ~ ~ I N ~ ~ ~ l o C I z ( N 0 ) 2 ( M e C N ) z3, , ‘I272 Mo(NO)(HB(AN=CMeCH=CMe),)R/IoC4H6C1,N2S MoSCI,(NCMe),, 3,1354 I(NHC6H,CH2C,H4NH2),3,1292 M0C,H6CI3?I30 MOBGYHZ~N~O~ Mo(NO)C13(MeCN),,3,1286 Mo{P~,B(~~N=CHCH=CH),(CO),(T~~CH,CPhCH,). 2.250 MOC~H~C~N~ MoCl,(NCMe),, 3, 1346 MoBC~~H~~N~OP M O ( N & H ~ M ~HB( ) { I ~ N = C H C H = ~ H ) ,(}CO)MoC~H~N, (PPh,), 3,1294 Mo(CY)I(NH,)2.3, 1345 MoC4H*0, MoBL~C,,H~~,I~N~O~ Mo { HB(&N=CMeCH=hk),](NO)I,Li(OEt),, 3, M o O ~ { O ( C H ~ C H ~ O3, ) ~1381 },

MoBC,,H29INyO

Mo(NO){HB(6IN=CMeCH&Me),}I(NHNHPh),3, 1288,1293

1280 MnBBi2C8HIZ04P2 (HiMe),Mo(CO),(PMe)l. 3.283 MoBrC1,O [MoOC1,BrI2-, 3,1349 MoBr2C12N202 [MoC12Br2(N0)2]2-,3.1273 MoBr,O, MoO,Br,, 3,1380,1387 MoBr, MoBr3,3,1330 MoBr30 MoOBr,, 3,1348 MoRr, MoBr,, 3,1334 MoBr,O MoOBr,, 3,1392 MoBr,O [MoOBr,]*-, 3,1398 MoBr, [MOBr,]’ , 3 , 1342

MoU,II,O, MoO(OAc),(H?O), 3,1337 MoC4H,oC1402 [MoCl,(OEt),]-, 3,1354 MoC,H,,O, MoO2(0CH,CH2OH),, .~ 3,1381 h.loC4H, ~N,0.,$2 MoO(ONHMe),{S2CN(0)Me}, 3,1392 MoC,H,,Br,N,O,S, M O B ~ ~ ( N O ) ~ ( M3, ~ ,1272 S)~, MoC4H1,Br,N204S2 MoBr2(NO)2(DMSO)2,3,1272,1274 MoC4Hl2Br4S2 [M~Br,(S?vle,),]~,3,1330 I?OC~Il l 2 C I Z N > 0 4 MoCI,(NO),(FtOl I)?. 3. 1272 MoC,H ,CI,NO,S, Mo(NO)CI,(DMSO),, 3,1286 MoC~H~~N~OZS~ M O O ~ ( S C H , C H ~ N H3, ~1387 )~, MOC~H~~N~O~S ~

MOC~HI~N~O~S

Cumulative Formula Index

MoO(ONHMe),{ONMeC(S)NH}, 3,1392,1405 MOGHIZN,OIO [ M O ( N O ) ~ ( M ~ N O , ) ~1273 ]~+,~. MOC~H~~O, Mo(OMe),, 3, 1344 MoC,HI,N,O MoO(dien), 2,47 MOC~HI~N,~, MoC),(dien), 3, 1256,1379 MoCd1304 [Mo(C0)413]-? 1,149 MoC,N,O,o [Mo(NO),(C,O,),]' , 3 , 1273 hlOC4N402 [MoO,(CN),I4-. 1,53; 2,296;3, 1219. 1335. 1336.

1338,1345 MoCjN,O,S, [Mo02(NCS)4]'-, 3, 1387
426

[MoO(NCSe),JZ-. 3.1351 MoC~NSO [Mo(CN),(NO)JZ-, 3, 1290 [Mo(CN),(NO)J3-, 3,1279 [Mo(CN),(NO)]'-. 3,1276 MOC~H~CL~NSO~ Mo(NO)CI~(DMF)~, 3,1286 MOCgHaNO, [M00(01),(2-~vC0,)]-, 3, 1399; 6,332 MoC,H,NO, [MOO,(N(C~I,CO,),}]~-, 3, 1379 MoChHhN209 Mo(o)(NNMe,)(CIO,),, 2 , 146 MOC6HfiO&z [MoSz(Me02CC=CC02Me)]~~, 2,546 MOC6HhOi 2 [Mo0(02)1(citrate)j~~, 3,1400 IMo(O,CH),~~-. ~- 3. 1235 M&&S6 Mo(S2CZH2);. I , 63:2.597;3,1413 MoC6H,N03 ~ o { M c N c ( H ) M ~ ) ~ o ( c o ) ,2,204 , ,

MOC~N~O,

[ Mo(CN),(NO),]' , 3 , 1273 MoC,N,0zS4 [Mo(CPJS),(N0),l2-. 3. I273 h.lOC,O 6 MOO,(CO)~,3, 1336,1339 MO C,F;O, [MOO,(O~C(CF~)~CO 3.1380 ~}]~~. MoCGHCI~F~O? - . . MoOCl,(hfacac), 2,679 MoC,H,CIO, MoO,CICp, 3, 1387 MOC~H~CI~NS IMoSCl,(py)] , 3 , 1354

MoC,H,CI,O, [MoCl,(OEt),]-, 3, I354 MoCsHsNii MoN(N,),(py), 2,230;3, 1394 MoC5H6BrZN2O4 [MoBr,(NO){ON=C(COMe),}]-. 3. 1289 MoC5H6Cl2N2O4 [MoCI,(NO){ ON=C(COMe),}]+ 3. 1289 bIoCSH6FN02S2 [Mo(S,CNMe,)F(CO),]-. 3. 1282 MoC5H,CI20, [MoO,Cl,(acac)]-, 3, 1387 I\;loC,H,Cl,O, [MoOCl,(acac)l-, 3, 1349

MoC,H,,NOzS, Mo0,(S2CNEt7). 3, 1337

MoO(O,)z ((S)-MeCH(OH)CONMe,) .3. 1399 MoC5HllN0, MoO(O,)Z{Me,NCOCH(OH)Me]. 2.319;6,329 MoGH 13N 5 0 4 s 2 Moo(ONt~Me){oNMeC(S)~J I){ONMeC(S)NH2),3, 1392 MoCjNjO [Mo0(CN),l7-, 3, 1339 MuC5N50S, [MoO(NCS)512-,3,1235.1249.1351.1352 hloC,N,OSe,

Mo(N0)2(S2CNMe,)2,3,1272, 1274 MoC,H,,OS, [MUO(SCH2CH?CH3S)Z]-. 3, 1350 MoC,H.,,N0,S3

Mo02(SCH2CHzNHCHZCH2SCH2CHZS), 3,1382 MO'Z~I+~~C:IZNZO~ MoO,CI,(DMF),, 3, 138.1, 1387;6 , 351 MoC6H14K02S MoOz(SCMezCHzNMe,),3, 1405 MoC,Hi,O, MoO,(OPr'),, 3. 1315 MoC6HI5BrN5O2 [MoBr(NO)2(l,4.7-triazacyclononane)]+,3, 1272 MoC6H15C13N3 MoC13(1,4,7-triazacyclononane), 3,1333 MoC6Hl&,02 M0(1,4.7-triazac~clononane)(NO)~, 3, 1272 MoC,HdsOz [MoH( NO),( 1,4.7-triazacyclononane)113, 1272 MOC~H.,~N~O~ Mo02(ONMe3),,3,1383 MoC~H~~N~O~P Mo0(02)2(HMPA).2. 328;3, 1403 MOCciHi806 Mo(OMe),, 3.1413 MoC6HisO6P& Mo{S,P(OMe),),, 3. 1331 MOC~H~&IJ, Mo(NMe2),CI3,2. 163 MoC~H,,N~O,P MoO(O,)(HMPA)(H,O), 2,319 MOC~H~~N~O,P Moo(o2),(r-1MPA)(H,o).3 . 1399; 6,321,329.330 MoC6HZ4Nb [Mo(cn),j?+. 3.1330 MoC6NOl3 Mo(NO)(C~OA)~. 3, 1290 MoC~N~

Cumulative Formula Index

427

[MCI(CN),]~-,3, 1283 MOC6N6S6 [Mo(NCS)6]2-, 3, 1235.1344.1346 [MO(NCS)6]3-, 3, 1235.1331 MOC6N6Se6 [Mo(NCSe),13-. 3. 1331 M0C606 Mo(CO),, 1, 145; 2,237.264.275,355; 3, 1230; 6,342, 343,346 MoC7F307 Mo(CO)S(OzCCF3), 2.143 MoC7HN7 (MoH(CN),l4-, 3, 1345. 1439 MoC,H,FNO, [MOO(O,)F{ 2,6-py(C02), J- , 2, 319 MoC~H~NO, [Mo(CO),(Me3CN)]'. 2.265 MoC,HqNO7 MoO(O,){2,6-py(CO,),] 6 . 331 M0C7H307 Mo(C0MOAc). 2,438 MoC,H,N03 ' MoCp(CO),(NO), 2, 115.237; 3, 1275, 1276 MoC,H
[Mo(NO)(MeZCNO)(NCS)4]Z-.3, 1201 MOC~H~CI~N~ MoCln(NNMePh), 2, 114. 148 MoC7Hl,C1N205

[MoCl(NO)(OEt){ON=C(COM~)2}~ ' , 3 , 1289 MoC,Hi
MoCqHl~05P~S

MoC8HI,CI,0, MoC14(THF)z.2. 698 [MoCI,(THF),]-, 3.1330 MOC~HI~N~O~ MoO,(ONEtAc)2,3, 1387 MOC~HI~NZ~~SZ MoO2{SCH2CH(NH2)CO2Me},,3,1256,1382.1387, 1392 MOCBHWPZS~ Mo{SCH~CH~)ZP}~, 3,1344 M G H& Mo{(SCHZCH,)~S}Z,3, 1344 MoCeHiaN202S2 3, 1382, 1391 1392 Mo02{(SCH2CH2NMeCH2)2}, MoO2{(S~H,CHZ),NCH,CH,NMeZ),3,1387 MOCSH~SN~OS~ MoO(NNMez)(SzCNMe2)2,2, 144,146: 3.1397

M 0 0 ~ ( 0 B u ' ) 2,350 ~, MOCBHZOC~ZO~ Mo02C12(DME)2.3,1381 MoC*H,oC1402 MOCI,(OEt,)z, 3. 1342 MOC~H~~N~O~S~ M o O ~ ( S C H ~ C M C , N H3,~ )1382 ~, Mo0,(SCMe,CH,NH2),, 3, 1387 MoO,(SCMe,NHMe),, 3,1382 MoC~J~ONZO~ MoO~(ONEtz)z,3. 1391 MoCsHzoNsS4

Mo(N2Me)(NHNHMe)(S2CNMe,),,2,132 MoC~H,OOP~S~ MoO(SzPEt2),. 3,1339 MoC&H,oOS? [MoO(SEt),]-, 3, 1350 MOCSH2004 Mo(OEt),, 2,347 MOC~H~~O~PZS~ MoO,{S,P(OEt),},, 3, 1388 M~CBHNN, Mo(NMe,),, 2,163, 169,172,177,178,339,352; 3. 1343 1346 MoC8HzsN4 Mo(NMe,),. 3.1344 MoC8Ne [Mo(CN),]~-, 1,251,336; 2,8, 11; 3,1354, 1355 [Mo(CN),I4-, 1,32,84,86,252,336,406; 2,s. 11; 3. 1248, 1338, 1345, 1346 MoC,H,CI,NO, [MoOCI,(&-quinolinolate)]-, 3, 1349 MoC9Hs03 MoMeCp(CO)?, 2,203 MoC9119CIN,O, [MOCI(NO)~(H~C=CHCN)~]+, 3,1272 hfOcgHc~N303

Mo(CO)~(M~~CN),, 2,264 MoCgHjoN03S Moo, {ON MeC( S)C6H4Me-4},3, 1381 MoGH*iOz Moo2(C6H2Me3-2,4,6),3, 1389 MoC~H~,N,O,S~ M O ( C O ) ~ ( S ~ C N M3,1282 ~~)~, M o C d 13N404 [Mo(acac)(NO),(MeCN),]+, 3, 1272 MGHd303 Mo(CO),(l.4.7-triazacyclononane), 3, 1289 MoC~HI sN70 Mo(C?J),(NO)( 1,4,7-triazacyclononane)+3. 1289 MoC~H,~O~P~S Mo(CO),(drnpe)(q'-SO,), 3. 1278 Mo( CO),( dmpe)(qz-SO2),3. 1278

MoCsHlsN40Ss

Cumulative Formula Index

MOC~HI~N~OS~ Mo(NO)(S2CNMe2),, 3, 1289,1290 MOC,HI~N& MoN(S2CNMe,)3, 3, 1394,1395 MOCgHlsN4S7 M o ( N S ) ( S ~ C N M ~2,~ )119-121: ~, 3. 1290 MoCPH~ROJ’~S, Mo(S~CO)(CO)z(PMe,)z,3. 1278 M0CqH19C1302 Mo(CBu‘)CI,(DME), 3, 1407 MoCqHzoN20& MOO~((SCH,CH~NMCCH~)~CH~). 3, 13x2, 1391 Mo02{(SCH2CH~)2N(CH2)3NMe,J1 3, 1382 MoC9H2,Br,N,0 MoBr;(NO)( 1,4,7-trimethyl- 1.4,7-triazacq~clooonane). 3. 1279 MoCgHZ1Br3N3 [MoBr3(l,4,7-Me3-1,4,7-triaza~yclononane)]~, 3, 1342 MoC~H~~CIN~O~ Mo02CI(1,4,7-trimethyl-l,4,7-triazac~clononane), 3, 1387 M0CioH703 Mo(CO),(C,H7), 1,121 MoClOH8Br2N2O2 MoOzRr2(hipy), 3, 1381, 1388. 1405 MoCIOH8Br2N3 MoNBr,(bipy), 3, 1353 MoC,oH,Cl,N,O? MoOzC12(bipy),3, 1387 MoC,oHsCI,N3 MoNC12(bipy),3, 1353 MOCioHsCIzN4Oz MoCI,(NO),(bipy), 3, 1274 MOC,oHsC13N20 MoOCl,(bipy), 3, 1350 MoC~~H~CI~N~ MoKCI,(bipy), 3, 1394, 1395 MnCloHSCI3N30 MoCI,(NO)(bipy), 3,12S8 MoCloIT8Ci4Nz MoCl,(bipy), 3, 1342 MoGoHsN~02S2 Mo(2-pyS),(NO)z, 3, 1272 MoC10H8N6 MoN(N,)(bipy), 3, 1296 M~CioHsNiz MoN(N,),(bipy), 3, 1394, 1395 MoCIoHIoCI, MoC12Cp2,3,1346 MoCioHloC12N402 MoCI*(NO)2(py),, 3, 1272, 1175 MoC~OH~OCI~N~O~ MoCI,(NO),(py N-oxide),, 3, 1272 M o r ioHi,,CI,N,O MuCl,(NQ)(py)z, 3, 1288 ~ocIoHIosz

MoCpZS2, 2,533.537.545;3, 1435 MoCioHi0S4 MoCp2S4,2,542,545,546; 3.1435 MoCioH11N02S2 Moot{ C,H,N-2,6-(CH,CH2S)z}, 3. 1381 MoCioHiiNO3 Milo(ON=CMe,)(CO),Cp, 2,270 MOCIOHIZ MoH,Cp,, 2,697; 3, 1346 MOC~~H~~CI~NO~ MoOCl,(acac)(py), 3, 1349 MGOH12N2014 [ M~,O,(edta)]~-.,3, 1256 MoCIOHI~NSO~ [Mo(NO)(H,NO),(bipy)]+, 3,1291 M0CioH22P2 MoCp,(HP=PH), 2,1045

428

Mo(NO)(acac){ON=C(COMe),),3, 1289 MoCloHi,CIO, MoOCl(acac),. 3. 1352 MoCIOHI~C~~O~ MoCl,(acac),l 3, 1336 MoCioHidzO, Mo(NO),(acac),, 3.1272. 1274 Mo(acac),O,, 1.57: 3. 1381, 1387, 1391 MoC, ,H .I,?F4N MoF4(h’Et2PPh).3, 1342 M0CioH15KibO [ M O ( ~ \ ’ O ) ( M ~ C N ) , ]1279 ~-~,~, MoCloH&IN20SI MoOCI(S,CNEtl),, 3.1352 MOC~~H~~CI~K;?OS~ MoOClz(SzCNEtzj2.3. 1392 MoC~OH~OF~N~OSI MoOF2(S2CNEt2)2.3, 1392 M’oC~~H~~N~OS~ MoC)(S2C:YEt.t2)2.3,1336,1339, 1391 MOC~OH~ON~OS~ 2.539 MoO(S~)(S,CNEIL)~, Mo(SzO)(SzCNEt;?)?. 2,63h MoC1oH2,h’ 2OzSz MOS~{ONTR~~~),),, 3.1404 MoCIoI 12oN2OzS4 Mo02(S2CI\’Et2)2,1,57; 3, 1256, 1381, 1387, 1390-1392: 6. 351,354 MOC,~H~~N,O~S~ M o O S e { O h ~ H 2 j 5 j 23,. 1404 MoC,oH2oN?04 M o 0 2 { 0 N ~ H z ) , } , ,3, 1404,1405 MoCloHzoN206Sz Mo02(SCH,CH(NH,)CO,Et),, 3,1390,1391 MoC1oH;oN,O,Sq Mo(N,CO,M~)(NHNHCO,MC)(S,CNM~,)~, 3, 1341 MoC,(,II~(,N~OS~ [Mo(NO)(N,),(S,CNEt2),12-, 3, 128h MOC~OHZINSSL Mo(NNMe)(S2CNMe,),, 2,130 ’

M O ( N O ) ( H ~ N O ) ( S ~ C N E3,1291 ~~)~, MoCioH24NzOzSz MoO,(SC,~ezCH,NHMe),. 2,530; 3,1382 MOC~~HJN~O[MoCp(NO)I(NH,NHPh)]+, 2,101 MoC ,Hi?NO MoCp;(Me)(NO). 2 , 103 MOC~IH I$?I,NO Mo(NC,tI,Me-.1)C14(THF). 3, 1396 MOCllIIZ~CIN402S4 [Mo(NO)(NCO)(S,CVEt2j2Ci]-,3,1290 MoC<*H,nN,O,Sd [MO(NO)(NCO)( N3) (S2CNEt2),]-, 3,1290 MOC~~H~IN~O~PS~ Mo(SzCNMel)z(CO)z(PMe3), 3,1282 MoCtiH,iN40, [Mo(NO)(CO),( 1.4,7-trimethyl-l,4,7triazacyclononane)]+, 3,1276 MoC I ,H,,KaOJ‘ MoO(O,)(HMPA)(py), 2,31Y MOC~~H~~N~O~P Mr~o(O,),QrMFA)(py), 3, 13Y9; 6,331 MoCii Hz3N502S~ Mo(N0 )(NCO)(S,CNEt,),(NH,), 3, 1290 MOC~~H~&IZO~P~ MoC1z(CO)2(PMe3j3.3. 1281

MOC.,ZCI~N~OZS~ [Mo(S&CI~)~(NO),]-,3, 1273 [ M o ( S ~ C ~ C I ~ ) ~ ( N O )3, ~ 1273 ]'h'fOC12Fi&, M o { S ~ C Z ( C F ~ )1~. }63; ~ , 2.600: 3. 1436 MoC12F18Se6 M o { S ~ , C ~ ( C F ~ )2,607 ~},, MoC12HsCIN30; MoCI(CO),(NO)(bipy). 3. 1275 MoCl,H,CI,N,O, MoO,Cl,(phcn). 3. I38i MOC~~HRCI~N~OZ MoCI,(NC)),(phen), 3, 12711 MoC~~HRN~O~S~ [MO(NO),(C~,H,S>)~]', 3 . 1273 MoCJW2Os MoO(0,)2(phen), 3, 1399. 1400 MOC12HsN206S2 Mo(CO),(bipy)(SO,),. 2.635 MoCl,H,NsOS2 Mo(NCS),(NO)(bipy), 3, 1279 MoC~~H~N~OZS~ Mo(NCS),(NO),(hil,y). 3. 1272 MoCI,H,OS, [MoO(S,CC,H4),]-. 3 , 1350 MoC.,,H,O, [Mo02(02C6H4)212'-. 3, 1381; 3. 1389 MoC1ZHloCI2NZ02 MoCI2(CO),(py)l, 3, 1281 MoC1,I llON602S2 Mo( NO) (H,NO) (NCS),(bipf), 3 . 1291 MoCi2HioNci0, MO(NO)(H,NO)(~-~~CO~~?~~. 1291

[Mo(NO)(H,NO),(phm)]-. 3. 1286 MoCilHiZNhOL 3. 1273 [Mo(NO),(H2C.I;CHCU),12 MoCi,I I iiN8 Mo(CN)J(CNMe),, 3. 1745. 1346 I

M°C12H1203

Mo(1 ,3,5-Mr3C,H;)(CO), 1.116 MoCi,Hi,O$4 [ M O O ( S ~ C , ( C O ~ M ~ ) .3.1337 ,}~]~ MoC~~H~~CIN~O~ [ MoCI(NO),( MeCN)(py),]+. 3. 1372 MoC~ZH~~N~OZ MoO,Me,(bipy). 3. 1406 MoC~~H~SNO~ Mo(C,Me,)(NO)(CO),. 3,1176 MoC12FI16CIZN~OS~ MoOCIZ(SLCNH~C~H~):. 3,1392

MoC1,H2,CLN40hP MOO(O,)CI(~~CO,)(HMPA). 3.1399 MoCi,HnN"OSs Moo( SZCNMe,)(p-N,CS2Et)2Mo(S2CNMe2),3, 1341

MOC12HL3NS02Sb Mo(N2C02Etl(S,CNMe2)3.2. 136 MoC~~H~,CI,O; MoC13(IHF)3,3, 1331 MOC~~H~JN~O,S~ Mo02{SCMe~CH(NH2)C02Me},. 3. 1256. 1382 hIOC12H21N406 MoO,(ONMeCONBu'),. 3. 1405 kIOCizHzjN6S8 MO(N,CS,Et)(H,NNC S,Et)(&CNMC2)2. 2 . 136: 3. 1341

hlo(',:1 I&&

[MoO(SH)( lh]nneS,)] ', 2 . 5 I Y (MOO(1,5.9,13-tetrathiacyclohcxadccane)(SH)] . 3 . 1335,1337 MOC ,2H16C1*N06P Mo02C12{(Pr'0)2P(0)CH,CONEt2},3, 1381 R.IoC~,H~~CI~N~O, h I o C l , ( N O ) ~ ( C ~ H I i N H 3, ~ ) 1272 ~, MOC12H26N6O2S5 hIo(NO)(N,)(S2CNEt,)2(DMSO), 3. 1290 ~~oC;,II,,CINOS, [MoCI(NO)(SBU~)~]-, 3, 1289 MOC 12H27NO'P3S2 klo(COMr)(S,CNMe2)(CO)(PMe3),. 3.283 M o r 1ZHL7045i [ M 0 0 , ( 0 S i R u ' ~ ) ] - . 3, 1380 hloC 1 >lI I H I i L 0 2 S I hloO,(SCMeZCH,NMe,),, 3, 13x2. 1387 MoC,~H,BO,P~S, hlo02(S,PPr'2)2. 3, 1387 MoCi2H280.1 IvIo(OPr'),. 3. 1334 MoC,~H,~CI,N,O,P, Mo0,C12(HMPA)2.3, 1381 MOC>,H;~CI~N~O~P, Mo (NO)CI,( HhlPA), ,3,1286 MoC, ,H,,CI,P, M U C L ( P M C ~3. ) ~ 1283 . MoC 1ZHj,,CIjh'~03P~ MIJOCI;(HMPA)~, 3. 134(J MoCI2H3Glzl'q

MuI2(PhleJj4,3, 1283 MoC~~H~~NJP~ \Io(N,),(PMe3),, 3. 1268 MOCI~N~S~ [Mo(S,C~(C?J)~},J~-, I , 63,3, 1436 MoC 13H5FixS4 h4oCp{S2C2(CF,),},, 2.604 MoC, JijIi4S4 [hloCp{SLC,(CN),},]-. 3. 1437 MoCiJLNhO Mo(CN),iYO)(hipy). 3, 1289 MoC:i,H ION201 MoCp(CO),(N,Ph). 2, 130. 133 MoC13H,,V,S, [Mo{S,C,(CN),},(S,CNEt2)]-,3, 1437 MoCiJHLZNlOS

[ M o O ( O & { ~ , ~ - ~ ~ ( C O ~, 2) .~319 },] M o C I ~ H os O [MoO,(alizarin red-S)]*-, 3. 1380

MoC ,,H,Cl,O,

Cumulative Formula Index

M0Ci4HsC1204

MoOzC1,(9,10-phenanthroquinone). 3. 1382 MoC~~HSN~OZS~ Mo(2-rnercaptobenzothiazolate),(N0)2, 3. 1272 MOCI,HSN~OS, Mo(NCS),(NO)(phen), 3, 1279 MOC~&N~OZ Mo(CN)z(NO)z(phen),3.1272 MoCi&N6OzSz Mo(NCS)2(N0)2(phen),3. 1272 MoC,,H,N,S4 Mo(NCS),(bipy). 3. 1344 MOCI~HIOC~ZN~OZ MoClZ(NO)z(PhCN)2,3,1272 MoCI,(NO),(PhNC),, 3, 1272 MoC14HioN2Sz MoCpz{SzCz(CN),), 3, 1437 MOC~~H~~N~OZS? Mo(NO)(H,NO)(NCS),(phen). 3. 1291 MoG~HYo~zSZ MoCp(CO)z(SZCPh),3, 1435 MG4HiiN302 [Mo(CO),(bipy)(MeCN)l2+,3. 1281 MoCt4H12CIOS4 M~OCI((~-SC,H,SCHZ)?), 3, 1337. 1349 MOC~~H~~NZOZS~ [ M O ( S , C ~ H ~ M ~ ) ~ ( N 3, O )1273 ~]-, MoC14H1202 MdCO),CdC7H7), 1,121 ,- . , MoCI&Hl2O2S4 MOOZ{(~-SC~H,SCHZ)~}, 3.1337. 1382. 1387

MkI4HZ5CINO4P2S4 Mo(NPh)Cl{SzP(OEt)2}2,3, 1353 MoCi,Hz&lzN~OS, MoOCI,(S,CNPr,),, 3, 1392 MOC14HZHNZ0S4 MoO(S,CNPr,),, 3, 1335. 13% MoCi,HmNzOS6 MaOSz(S,CNPr,)2, 2,533; 3, 1392. 1393.1431 MoCi4HmNzOzS4 Mo02(S2CNPrz)2, 1,57; 3, 1381. 1390 MoC14H36N,0zSi, Mo(NBut)z(0SiMe3)2,2, 167 MOCi4HxN80d'zSz Mo02(NCS)Z(HMPA)2,3, 1381 MOCI~H~~O~'~ Mo(C0z)2(PMe3)4, 3, 1277 MoCiJHvF?Oi4P, MoH(O,CCF,){P(OMC)~},.3, 1285 ~oCi&LnOzP4 MoH(OAc)(PMe,),,3, 1284 MoC15HsN20sS Mo(C0)3(phen)(SOz),2.635 MoCISHgNsO [M~O(CN)~(phen)l-, 3. 1339 MOC15HsN6O Mo(CN),(NO)(phen), 3, 1289

430

MOCisHiiClN i o MoN(N,),Cl(rerpy), 3, 1394 M0CitiHiiN130 Mo(NO)(N,),(terpy). 3, 1289 MoCi~HiiO6 Mo(PhCOCHCOPh)20z,1,57 MoCISHIJ'JZO+ MoO2(OC6H4NCHMeCtIzNC62I,O), 3, 1381 MOC~;HI&I~K~ MoCl,(py),. 3. 1331. 1332 MoCisH I s C ~ , N ~ MoSCl,(py)3, 3. 1354 MoCI~HISN~G [MO(NO)(H~NO)(H~O)(~~~~~)]~', 3. 1291 MoCI~H~~NS,~~ [Mo(N0)(H2NO),(terpy)]+, 3, 1291 MOCi5Hi6N20sS MoO,(OC,H4CHNHCOpy)(DMSO), 3, 1387 MoCisHi6y603 Mo(NO)(H2NOH)(H,NO)(terpy), 3, 1291 MoCi sH2i0 6 Mo(acac),, 1. h 5 ; 2 : 371,375; 3. 1331, 1332 MoC~SHZ~N~SZ Mo(N2Ph)(S2CNMez)3. 2, 136 MoCI,H23lrl5S6 Mo(N,Ph)(S,CNMe,),. 1 , 82; 2, 134, 140 MoC.lsHZjNaOS1 Mo(N2C6H40Mc-3)((SCH,CHZNMeCH&). 2. 136 MoC,5H,,ClN3S6 MoCI(SZCNEtZ);, 3. 1331 MoCISH~ON~OS~ MoO(S,CNEt,),, 3.1352 [ M O O ( S ~ C N E ~ ~3,) ~ 1392, ] + , 1393 MoC~~H~~N~OZS~ Mo(S2CNEt2)3(11'-SOl), 3. 1331 MoCisHmN,OS6 Mo(NO)(S,Ch'Et,),, 3, 1289 MoCisHmKA, MoN(SZCNEtz),, 3. 1395 MoCls H31It3s7 Mo(SII)(SZCNEt,),. 3. 1343 MoC 35H33C1 0 MoOCI(CH,But),. 3, 1407 MoCisH33S3 M o ( S C ~ H ~3.~1330 )~, MOC~SH~~NO~P~ Mo(C0z)2(Ph?e3)3(CNPri),3, 1277 MoC1sH3RCI02P3Si MoC1(q2-COCHzSiMe3)(CO)(PMe3)3. 3, 1283 MoC H45NzP5 Mo(N2)(PMe3),,3. 1268 MoC I s&~'J I SPF MoH,{P(OMe),},, 3, 1285 MoCi5H4iPs MoH,(PMe,)j, 3, 12x5, 1438 MOC16F3605 MoO(OC4F,),. I . 44

{MoCp(CO),}z, 2. 203 MoCI6Hl,N6O2 Mo( NO)(HNO)(CN) (terpy), 3, 1291 MOC,,HI,CIK,O~ MoOCl(sa1en).3 , 1349 MoC,,~1,,CIN,O> Mo(NO)Cl(salcn). 3. 1289 MoC ,6H14C12?J202 MoCl,(salen), 3, 1342, 1346 MoCir,Hi,N,O, Mo02(salen).3. 1387. 1389 MOCI~H~~CI~N~OJ M O C ~ ~ ( ~ - O C ~ H ~ C H =3,N1342 M~)~,

Cumulative Formula ladex

43 1

M O I , ( N N H ~ ) ( P M ~ , P3, ~ )1341 ~. MoCI~HZ~NZO~ M o 0 { O N ~ H z ) 5 } 1,2-02C,H4), z( 3, 1392, 1405 MOCI~HZ~C~~N~S~ MO(NPh)Cl,(S,CNEt,),. 2.167

MoClsH&lFN402 Mo(N2C,H4F-4)(bipy)(cO),CI. 3, 1294 MOCISH~~CINZOS~ MoOC1(8-quinolinothiolate)2, 3. 1350 MoC 18H12C1N203 MoOC1(8-quinolinolate)2. 3. 1350. 1352 MoCiSHi ,CIN,O, M0Cl(pyC0~)~, 3, 1346 MOC~~H,~N~O~S~ Mo0,(8-quinolinothiolatc)2. 3. 1256 MoC 18 I11~ N ~ O J Mo0,(8-quinotinolatc),. 1, 528; 3, 13x1. 13H7 MoCiHHi 3 1 0 5 MoO(O1)!X-quinolinol~~e)l, 3. 1401 M0CtSH.i2 - Y 1 0 1 Mo(X-quinolinolate)2(NO)2.3, 1272 MoCisHi2Sn [Mo(S,CC~H,),]~-.3,1343 Mo(S&H,)~. 1.63; 3, 1413 MoCinHi& M O H ( ~ . ~ - S ~ C , 3. H ~1439 )~, [MoHII .Z-SZChH4)3]3 -,3, 1437 MoC~~H~~CIF~N~ M ~ ( M ~ C P ) ( N ~ C ~ H ~2. F -136 ~),~I. MnC: ,ST I ,CI 1P {,hTKIz(PPh3)],,,3, 1319 MoC]81-11,C1,01JS MoOCI,(SPPh,), 3. 1349 MGnHid’”S3 Mo(n’HC6H4S),,1.63; 3. 1413 MoC18H1504Si [Mo03(OSiPh5j]-, 3, 1380 hfoCisHi5S3 Mo(SPh),. 3. 1330 ~~oCisHinOi,S6 [Mo~S2C2(C02Me)2}?]2-, 1,63; 3, 1432 MoC IBHz2N2OI M O O , ( O C ~ H , C H N M ~3~, )1381 ~, MoC, ,H2?02 MoOZ(C,;HZMc3-2,4,6)?.3, 1407 M O C ~ ~ H ~ ~ N ~ O ~ Mo(CO)2(py),(OPr’)2,3, 12x2 ~~IC,,H,,NO,I’~S, R;m(NPh)(S,P(OEt),},, 3 , 1353 hfOc MoO:(S~CYBU~)~. 3, 1387 MoC I ~ L s P ~ R.lo(dmpe),.3, 1277 [Mo(dmpe)J‘. 3, 1280 MoC I J L 4 0isP6 \ ~ I I ~ { P ( O M ~3,) ~1277 }~, MoC sH54P, Mo(PMe,),. 3. 1277 MocLXfM)lSP6 [MoH{P(OMc),},]’. 3. 1285 MoC1,Hl2FK40, [ ~ . ~ 0 ( ~ ~ C , H ~ F ) ~ b ; p y ) ( 3, C 01294 ),1+, MoCi,Hi2N20s Mo(C0)5(PhN=CHCH=NPh), 2,208 MoGdi4N303 MoH(CO),{ tris(27-pyridylmethane)}, 2. 704 M0Ci9H15ClN.102 Mo(N2C,HJfe-4)(hipy)(CO),CI. 3. 1294 M0CwHi5Xi302 MoCp(PhNNNPh)(CO)2.2,203 MoCIVH~RNJOS>

,

Mo(SBU‘)~, 2, 172.526.531: 3. 1344, 1346 MoCihH4oN4 M O ( N E ~ J3, ~ ,1341 MG&oNzO~SI, Mo(OSiMe,),(HNMe,),, 2.339. 352: 3. 1344 MOCI~HI,N,O~S Mo(phen)(CO),{MeC(S)h’H:). 3, 647 MoCI~HISN~O [MoCp(NO)(PhNNNPh)]’. 2.203 MoCI7Hl6CIN,O3 MoOC1{2-OC,H4CH=NCHI)zCH,) 3, 1349 MuCI~HI~N& Mo0z(0C6H4CH”CH2CHMeNCHC6H40). 3,1381 MoCi7Hi&z MoCpz(SZC6H3Me-4), 3, 1437 MoCi7HinNzO4 [MoO(salen)(MeOH)]’. 3, 1351 MoG,HmN3S4 Mo(S,CNEt,)(NHC,H,S)23 3, 1354, 1355 MOCI~HZ~NJOS~I M o O ( N C ~ H ~ M ~ - I ) ( S ~ C3,N1341 E~~)~. MG7H27N3S4 M o ( N C ~ H ~ M ~ - ~ ) ( S , C ~ 3, ’ E1341 ~~):. MoC17H4005 Mo,Et(OPr’),, 3, 1309 MOCI~H,IOI,P~ Mo{P(OMe)z}{P(OMe),}5,3. 1285 I

Mo(CO)(NNCMePh)(S,CNEt,),, 2.

147

MOC,~H~~C)~ MoC19A,,NOP4 MoH(PhI\’CHO)(PMe,),, 3, 1285 MOC&,~NO, Mo(CO)z(N=CPh2)Cp, 2. 126. 129,281

MOC~,H,~NOS~ Mo(NO)(SC,Ii,SVe),, 3- 128.5 MOC~IH~~N~S~ Mo(HNNHCSPh),. 3 1413 MoGiH3,NA [Mo(YMeNMeFh)(NIMePh)(S,C".

2, 1 1

MoC22H16ClN402 [MoCI(CO)?(bipy),l+,3,1281 MoCzzHIbNaOZ Mo(CO),(bipj),. 3 1277 [Mo(CO),(bipylz] 3, 1278 MoC',,H ,qNO,P MoC)(S-q~~nol~noIar~-)(PPh,Mc), 3, 1340

MOC~~H~~N~O~PS~ Mo(NCO)(S,CNMe,)(Ol'I'h,), 3, 1279 MOC2~H2aCl~N~02S~

[MoO(NNMe,)(SPh),]-, 2,146;3. 1350,1397

MoO(S,CNPr,),(TCNE). 3. 1336 MoCxpH,,N,S, Mo(NNMePh),(S,CNMe2),, 2, 1-18.150 Mo(S2CNMe2)2(MeN=KPh)Z.1.57 MoC~OH~~N~S~ [ M o ( N N M c P h ) ( N H N h l e P h ) ( S ~ ~ ~ ~2, ~ c150, ~jz] +.

151;3, 1397,1398 Mo(-:2,f 13,1C14P2

MoC:14(PEt2Ph),. 3. 134h ~~OCIUHBOP~ { Mo(C,Me,)} ,( pq6-P,). 2. 106I MoC2,,H31CIN,U2

MoC1(q3-CH2C(Me)CH2)(CO),(C,H , N=CHCH=

NC6HlI). 2.209 I\iloC20H34P4 MoH2(diphos),. 3,1439 b1OC20H36S12 [Mo(S,CSBu'),]', 3, 13.54 MoC?,JI,,N& bIo(SzCNEtz),, 3, 1343.I346 [Mo(S2CNEtZ),]-.3, 1355 IMo(S,CNEt,),l+. 1-94;3. 1354. 1355 MOC~~H~~NO~ Mo(CH)(OBu1)3(quinuclidine), 3. 1407 MOCZOH~~ MO(CBU')(CII,UU')~,3. 1407 MOC~~H~~O MoO(CH,Bu'),, 3, 1407 MoCXIH~~N~P~ Mo(N,),(depe), 3, 1269 Mo(N,),(depe),, 2, 145 MOC21H15CIN40z Mo(N2C,H,Me-4)(phen)(CO),CI. 3. 1294

MoCZ1H15C1NsOz [MoCI(NO)>(PhCN)31+. 3. 1272 MUC,,H,,S, MO(S&H~MC)~, 2,601,605:3. 1436:6. 1015 , 3 . 1436 [.Mo(S,C~H~MC-~)~]Z MoCzlH,,N,O, MuCp(CO),{MeCH(Ph)&=CH(C5€f5N)j, 1 , 133

MOC~,(CO)?(~-~~CSNHBU)~, 3, 1281 MoC,~H~,,N~O~S, Mo203(SPh),(S2CNEt2)2,3, 1365 MoCZ~H~DN~S~ Mo(S2CNEi,),(Azb), 1, 57 Mo(IPh)2(SzCNEt,)2.2. 175 MoCZ~H~LN~PZS~ 3, 1397 Mo(h"Me,){ (SCHZCH2)LPPh}2, MoC~~H,,P, Mo(C,I Ij)(diphos),, 3,I438 MoCXJWLOBS~ M(i(Et02CNYC02Et)2(S2CNEt,),,3, 1296 MoC2,H,,N,0S, Mo(SzCNBu&(NO). 2, 103 MoC23Hl1Fj,NIO: MoCp(3 .5-(F3C)2H,NNNC6Hq(CF1)z-3,5}(C0 2, 204 MoC~~H,,CI~N~OP MoOCIZ(bipy)(fPh,Me), 3,1339 MoC2aF36Se12 Mo {Se2Cz(CF&) 6.3, 1437 MOC~~H~~T?~~ [Mol,lphen),]+. 3. 1330 Mo~~~II&& [Mo(NCs)(H,~O)(pher1)112*,3, 129 1

MoC&xiNOS, [Mo(YO)(SPh),l-, 2. 357; 3, 1289 MoCZ4H2,Y02P Mo(X-Cp)(CO)(NO)(Pph,). 2, 115 MoCZ~H~OOS~ [MoO(SPh),J-.2.526,3, 1350,1352,1353 [MoO(SPh)4]z-.2.531 MoC2,HzOOSe, [MoO(SePh),]-. 3. I350 MoC~~H,,O~P,S~ M001(S~PPh2)~,3. 1387,1390 MoC~~H~~NH [Mo(NNMe,),(hip~),]+,3,1397 [M~o(NNMc,)z(h~py),]'' . 2 , 146, 148

MOC,,H,<,N,O, MoO,((OC,H?(Bu')CHNCH,)2)

3. 1382

MOC~~H~~N& Mo { S,Cc:--C(NH,) (C HZ)3) 4 , 3, 1343 MoC,,H;,CI,OP, MoOCi2(PMe,Ph),. 3,1335,1338,1339 MoC,~H,~CI~NOP~ MOCI~(NO)(PM~~P~)~, 3, 1289 MoCMH~~C~~P~ MoC1,(PMezPh),, 3, 1342 MoC,,H,,O,Si, MuO2(0SiBur3),.3. 1389 MoCz4Hs6CI4Os MnCl,(OPr'),. 3, 1319

MoC,,M2,CI2h',OP MoOCl,(phcn) (PPh,hlc).3, 1340

MoC2,H,2ClOaPZ Mu(acac)CI(CO)z(PPh3),.

3, 1281

433

Cumulative Formda Index

MoC~~H~J~P~

MoCzsH4007 [MoO(O:)( 1.2-0~-3,5-Bu'~C~H~),]*~, 3, 1401 MOCZ~H~~N~OSI MoO(NNPh,){ (SCH2CH2NMeCH2),},, 3. 1397 M O C ~ ~ H ~ ~ N ~ S ~ MOCSB~')~(CNBU')~, 2,531; 3, 1283, 1344 MOC~~H,,O~P, MO(PBU;)~(CO)~, 1, 53 MOC29HZ11203P2 Mo(diphos)I, (CO),, 1.7X MoCI,H,,N0,P2 [Mo(NO)(CO),(dppc)]*, 3, 1276 MoCz,Hz,OsP,S Mo(COj,(dppe)(SO,), 2,635 MoC.2gHjlK40 MoO(diethylhexamethylcorrole), 2, 876 [Moo(diethylhexamethylcorrole)]- .2.876 [MoO(dIethylhexarnethylcorrole)]+. 2.876 [M~O(diethylhexamethylcorrole)]~+, 2.876 MoC~~H,,N,O, Mo(OBut),(N,CPh2), 3, 13 16 MoC?oH,10, MoO,(PhCOCHCOPhl,. 3. 1381. 1392

MOC~,H,;CIN~O~P~

Mo(CPh)(OBu')3(quinuclidine), 3, 1107 MoC ,,HI ,,N,OS, MoC)(X:quinolinothiul~i~)~~ 3. 1350 MOC~~~.I~~C:INO~PZ MnCI(NC))(C:C)),(dppm) 3: 1276 MoC,,H,,F,~OP~ Mu(CO)(PF,),(dppe), 3, 1266 MOC~~H~~NO~P, [Mo(NO)(CO)(dppe)]'. 3. 1276 MoC27H31N703 [ Mo(N0)(3,5-MezC,N,H3)3(OC,H40)]-, 3, 1292 MoCnHs4N4OSs MO(NO)(S~CNBU,)~. 3. 1289 MoC27H69P3 MoH,(PPr',),, 3. 1339 MoCzsHi,NsO2 [ Mo(CO),(phcn),( MeCN)]" , 3 , 128.1 MoC,~H~,N~O, [Mo(NO),(PhCN)4]". 3, 1273 M~C~RHZOS~ Mo(S,CPh),, 1 , 9 4 ;3, 1313 MOC~~H~~CINO~P~ M0Cl(N0)(CO),(dppe)~ 3. 1276 MoC~~HZ~N,OZP~SZ Mo(NCS),(NO),(dppej, 3. 1272 MoC2&2402S, M O O ~ { ~ - ( ~ - S C ~ H ~ S C H , C H , S ) C6,658 ~H,~),, MoCZsH270PS4 MoO(PPh,Et){ (2-SC6H,SCH&}. 3, 1337 MoC~NH~~OPZS~ M o O ( S C H 2 C H ~ P P h ~3.) ~1337 . MoCZnHq IC12N03P2 MoC)(NH)C12(OPEtPh2)2.3. I396 MoCZ~H~SN~O~PSJ M o O ( S ~ C N E L ~ ) ~ ( O P 3. P ~1336 >). MoC28H3506P3S4 Mo{S2P(OEt)2},(CO)~(PPh~). 3, 1281

MoCI(K,COPh)(NHNCOPh)(PMe,Ph),, 2. 136 MoC;~H,~CI,NOP~ M&?14jNPPrPh,j(OPPrPh2). 2. 125; 3, 1354 hlo(N1),( l'MelPli)2(PhSCHZCH2SI'h),3, 12h9 MoC,,,t I,,CI,C)P, Moll)Cl2(PEt2PI1),. 3, 133s. 1338 MoC30H45N4P3 Mo(N,)2(PEt2Ph)3.3, 1268 MoC30H,4BrN6 [Mo(CYBu),Br]+. 1.73 MoC,,H j41N6 [Mo(CNBu),I]+, 1,73; 3. 1283 MoC,oH561N, [MOI(C?JHBU')~(CNBUI),]+. 3. 1283 MoC;IH,,KO~S~ Mo0,{(SCPhz)2py}.3, 1391 hIwC,,H2,N& Mo(NNMePh)(SPh)4.2, 148 M D C ~ ~ H ~ ~ N ~ ~ ~ P ~ S ~ Mo( S2CK Me>)(NO)(CO)2(dppe), 3, 1276 MOC31H33C)4P3SZ Mo(CO)2(dppe)(PMe3)(q1-S02), 3,1278 MoC,,H~~O~P Mo02(C6H2Me3-2,4,6){ C(PBu3)C6H2Me3-2.4.6) 3.

1407 MOC~~H~~CI~N~ Mo(phthalocyanine)CI,, 2,866 MoC3,HI6&O MoO(phthalocyanine), 3, 1338 ~IoC~,H,,N~O~ Ir/Io(phthalocv3nine)(C),), 2,866

Mo(OC,H,h.le-Sj4(NHMe,),,3. 1344 MoC32TJ,,C12PI

M O C L ( P M ~ , P ~3,) ~1283 , Mo'LH-LJ'U" Mo(N2)2(PMe2Ph)4, 3. 1268

MOC32H4RP4

Cutnulutive Formulu index

MoC,,H,,CI,P, ~MoC11(Ph2PCH2CH2PPliCH,~l~,P1 [Ph,)]', 3, 1284 MoC,,H,,CI,NP, M;(NC,H,Me~4)CI,(PEtPh2), 3. 1353 MOC~~H~TNSP~ [Mo(dppm)(CNMe),12+. 1.77 MoC3sHaN7 ~MO(CNBU)~]*+, 1,72 MOC36H28N402P [Mo(N2Ph)(bipy)(C0,)(PPh3)]-. 3. 1294 MoC36H3oBrZ04PZ MoO,Br,(OPPh,),, 3, 1381 ~ V I O C ~ ~ H ~ ~ C I ~ N ~ ~ P ~ MtjCI3(NO)(OPPh3)2,3: 1788 MOC~~H~~CI~NP~ MoNCI,(PPh3),, 3, 1353 MOC~,,H~~CI~N~O~P~ MoCI,(NO)z(PPh3)2,2, 104, 106: 3, 1272. 1274, 1275 MoGJ~wC~~~OJ', MoCI,(N0)2(0PPh3)2,3. 1272 \"!OC36H3&1204P2 MoO~Cl2(OPPh3)2,2,498,500; 3. 1381. 1387 MOC~,H~~CI~NOP~ Mo(NO)C13(PPh3)2,3, I286 ~IOC~~H~&I~NO~P~ MoNC13(01Th3)2,3. I394 hfOC36H30C1302PZ M O O C I ~ ( O P P I ~3.~ '1349 )~.

434

1414 MO<~40t~3(rN~04P~ [Mu(No)2(MeCN)2(OPPl~3),~2+, 3, 1273 MoC4,,H4,C1N4P2 [ M O C I ( N N M ~ ~ ) ~ ( P P2,~ 146, ~ ) ~ 148; ] + , 3, 1397 MOC~OH~~Y~P, Mo(NZ)z(PEt2Ph),, 3, 1268 MoC4,Hj9Br3P3 MoBr,(triphos). 6. 719 MoC41H43hT4P3S Mo(N2),(PPh,Me),(Ph2PCH2CH2SMe), 3, 1269 MOC~~HZ~O~, Mo(O,C~,,H,),.J. 1413 MOC~ZHWNJO~ Mo(OC,H3Pril-2,6),(NMe,)(NHMc),, 3. 1341 MoC,J%O, M~(~.~-O~-~.~-BU'Z 3,C141 ~ H1 Z ) ~ . MOC42H67NO4 Mo( I-adamantoxo),(Me,KH), 1.44; 3, 1344 MOC,,H~,NO~P, Mo(NCO)(n-Cp)(CO)(PPh3)2,2,115,237 MoC4,H2,BrNJ0 MoOBr(tetraphenylporphyrinate), 3, 1351 MoC,,H,,Br,N, MoN(tetraphcnyIporphyrin)(Br,), 2, 826 MOC,~H~~CIN~O [ MoOCl( tetraphenylphenylporl-rhyrinatt.)l-, 3, 1338 MoOCl(tetraphenylporpbyrinate), 2, 820; 3, 1351 MoC~~H~~~CIZN~ MoCIZ(tetraplien~lporphyririate),2,826: 3, 1338 M~G.IHZHN, Mo(tetrnphcnylporphyrin), 2.826 MoC44HdbO MoO(tetraphenylporphyrinate), 2,826; 3, 1338, 1351 MoCUH~,OI Mo(O),(tetraphenylporphyrin), 2, 826 MOC~~H,~K~O~ [MoO(tetraphenyIporphyrinate)(O2)]- , 3 , 1338 MOC44H2sN404

Mo(02)2(tetraphenylporphyrin). 2 , 319, 325,826: 6. 329 MoC~~H~RN~O~

Mo(WO),(retraphenylporphyrin), 2,826 MoCJSHL9N& MoO(tetraphcnylporphyrinate)(OH),2, 325; 3, 1351. 1352 MOCwHd MoIl(CO)*{PhP(C6HjPPh2-2)2), 3, 1281 MoC~~H~~NSP~ Mo(N 2)2(py)(PPh,Me)3. 3. 1269 MoC44Hed2P.1 Mo(N,),(triphos)(PMe,), 3, 1268 MoC~SH~OO~P~ M O ( O C ~ H , M ~ - ~ ) , ( P M ~2, , P341 ~)~, MoC+~H~~N~O~ M o o ( tetraphenylporphyrinate)(OMe). 3, 135 MoC,sH,I%O, Mu( letraphcnylporphq.rin)(NO)(HOMe). 2,826 MoC~SHUW; Mo(PhCOCHCSI'h),: 3. 1331 MoC~SH,~CINO,P~

435

Cumulutive Formula Index

MOC56Ei45N40P2

MoC:52H49BrN2P4 MoCl(NO)(CO)(PPha)(dppe). 3, 1276 .. Mo(N,H)Br(dppe)2, 3, 1293 MOC45H50N3P3 [MoH,(PM~P~,),(NCM~)~]~+. 3. 1439 MOCS~HWFNZP~ Mo(NzH)F(dppe)*, 3,1293 MoCA~H~~CIZNO~P, MoC12(NO)(PPrPh2)2( OPPrPh,). 3, 1279 MoCS~H~~NO~P~ Mo(OH)(NO)(dppe),, 3, 1275 MOC&&'~S~O M O ( N O ) ( N H ~ ) ( S C ~ H ~3,P 1289 ~'~)~, MoCszH4@ 2P4 [MoO(dppe),(OH)]+, 3,1337 MOC.+~H~OCIN~O~P~ MOC~~HS~CIN~P~ MoCI(NO)(CO) (PPh3)i(py),. 3, 1276 [MoCI(NNH,)(dppe),]+, 2,146, 147 MOCd7H6902S3 [Mo(CO)*(SC6H2Pr3)3]~, 1.45; 2.526 MOC,IH=,,,CI~P, MoH,Cl,(dppc),, 3, 1284, 1439 MOCg~f136C12N4 MoCS?H~~FN~P~ MoClz(tetratolylporphyrmate), 3, 1342 [MoF(N N H,)(dppe),]+, 2, 145 MoCasf436N4Oz Mo02(tetra-4-tolylporphyrinate). 3. 1382, 1390, 1400 MoC52H,,P, MnH,(dppe),, 3, 1284 MOC~SH~~N~O~ MoC~~HS~N~P~ M0(0~)~(tetra-4-toIylporphvrinate), 3, 1399, 1400 . . . . MOC,+~H;,~NS Mo(N,),(PPh,Me),, 3, 1267 [MoN(tetra-4-tolylporphyrinate)]. 3, 1395 MOC,~HSIP, [MoN(tetra-4-tolylporphyrinate)]+, 3, 1394 M ~ H , ( d p p e ) 2,702. ~, 1026; 3, 1284 MOC&3.$"02 MGZHsJ'4 Mo(tetra-4-tolylporphyrinate)(l\lO),, 3, 1272, 1274 M O H , ( P M ~ P ~3,~ 1439 )~, MoCj 2H77NsS3 MoCnnH.&4P, Mo(CO)~(~,~,~-M~~C~ , 2, H1048 ~ P = C P ~ , ) ~ Mo(N2Ph)(MeCN)(SC,HZPrl,),, 2, 136 MoC,,H44ClNOP, MoC,,H,,CINO,P, MoCI(NO) (PPh2H)4.3. t 276 MoCl(NO)(CO)(dppc),, 3, 1276 MoC~~H~BNZOP~ MOC4SH76N4P4 Mo(N2)2(PPr2Ph)4r 3. 1268 Mo(N,)(CO)(dppe),, 3. 1269 MG~H,EN,P, M°C48H66P4 MO{P(cgH11)2)4, 2. 1053 Mu(CN)(NJ(dppe),, 3,1269 MOC~~H~~N~P~S MoC~~H~SN~ [Mo(CNPh),12+. 1.72 Mo(SCN)(N,)(~PP~)~, 3,1279 MoC~~~ONSO~ MoCS~H~~OP~ Mo(tetra-4-tolylporphyrinate)(NO)(MeOH),3, 1279 Mo(CO)(dppe),, 3, 1266 M0Cj3H,,Ih',P4 MOC~OH~&"P~ Mo(N,Me)I(dppe),, 3, 1294 M ~ ( N ~ ) ~ ( d p p r3,n 1269 )~, MoC,,H~,CIN~P, MG&L7N& [MOCI(NNM~P~)~(PP~~)~]+~ 2. 144 Mo( N2Ph)(SC,H2Pr',-2,4.6),(NCMcj, 3, 1340 MOC51H550P5 MOCSJ~N~OP~ MO(CO){P~P(CH~CH~PF~~)~}~FM~~P~),, 3, 1266 Mo(NzC,H4Me)(hipy)(CO)(PPh3)2, 3, 1294 M o C ~ I,,FO,P, ~F MoC=,~ILN~P~ Mo(N,),(PPh,Me)2(dppe), 3.1268 [MuF(CO),(dppc),]'. 3, 1281 MoC~~H~~OLP~ MoCS~H~~C~~O~P~ MoC1,(CO),(dppm)z, 3,1281 Mo(CO),(dppe),, 3, 1266 [ M o t C O ) , ( d ~ p e ) ~3, l ~1278 , M o C ~ U O ~ P ~ [ M ~ I ( C O ) ~ ( d p p r n )3. ~ ]128i +, [ M ~ ( C O ) ~ ( d p p e4,31 )~l~~, MoCS~H~~NJ'~ MoCSJLEOJ'~ Mo(N~)~(P~~PCH=CHPP~~)~. 3. 1269 M ~ ( C O ~ ) ~ ( d p 3,1277 pe)~. MoC~~HS,CIN~OP~ MoC~~H~~B~NP~ Mo(N,COMe)Cl(dppe),, 3, 1294 MoBr(N)(dppe),, 3, 1341 MoC~~H~~NZOP~ MOC~~H~~B~NP~S MoBr(NS)(dppe)?, 2. 119. 121 [Mo(NO)(MeCN)(dppc),]+, 3, 1275, 1276 [ M ~ ( N o ) ( M e C N ) ( d p p c ),3, ~ ] ~1279 ' MOC~~H,,B~,P, [MoBr,(dppc)], 3,1331 MoC~~HS~N~P~ MoC~~H~RCINOP~ Mo(N,)(MeCN)(dppe),. 3, 1269 MoCI(NO)(dppe),, 3.1276 MoC,,H,,BrN2P4 [ MoCI(NO)(dppe),]- , 3. 1279 Mo(N,Et)Br(dppe),, 3, 1294 MOC~~H~ECIN~P, MoCI(N,)(dppe),, 3, 1278 MoC~~H~~CIOP~ [M~OCl(dppe)~]+. 3. 1335. 1338 MOCS~H~EC~~P~ MoCl,(dppe),, 1,493; 3. 1266. 1284 [MoCl,(dppe),]+. 1.493 MOCI~(P~P(CH,CH~PP~~):}(PP~,), 3. 1284 MoCVJLJ'J~OZP~ [Mo(NO),(dpp~),]2~. 3. 1273 Mo(N~-CO,Et)Cl(dppe),. 3, 1294 MOC52H48N4P4 MoC55H,,P?S MoH(SPr')(dppc)z. 3. 1284 Mo(N)(N,)(dppe),, 3, 1342 Mo(N,),(dppe)2, 2, 147.707; 3, 1266, 1269, 1293 MOCS~H~SNX Mo(N,Ph),(tetraphenyIporphyrin), 2, 133. 136 [Mo(N,),(dppe)J-, 3. 1278 MoC~~H&LOP, MOC~,H.,~B~NP, [MoBr(NH)(dppe),]+. 3. 1341 Mo(N2C6hMe)(phen)(c O ) (PPh3),, 3, 1294

MOCS~H~F~N,O~P, Mo(N2COCF3)(02CCF,)(dppe),. 3. 1294 MOCsJLNOJ'4 [Mo(CO)Z(MeCN)(dppe),]2-. 3. 128i MOC~~H~~CINZP, [MoCI(CNMe),(dppe),]+. 3 . 1283 k1oCsbH5&"P4 Mo(CNMe),(dppe),, 3, 1266. 1277. 1283 hfOC56H55N3P4 Mo(N,)(PrCN)(dppe),, 3, 1269 MoC,Ji,,Hr,P2 MoBr2(Ph2PC:HMeC~iMePPh2)2.3. 1284 *~OCF~HS~N~PJ Mo(N2),(dppb),, 3, 1269 kWkHsJ'4 Mo(H2C==CH2)2(dppe)2,2 , 707 MoCS~H~~INZP~ Mo(N,Bu)I(dppe),, 3, 1294 MoCdbP4 [Mo(H2GCH2)(dppe)2Et]i,2,707 MoCS7Hj60zP4 MoH(acac)(dppe),, 2,375 MoC~~H~~N~P, Mo(N,Bu)(CN)(dppc),, 3, 1293 MoC5,HS7N3P4S Mo(N,Bu)(CNS)(dppt)2, 3, 1294 Mo( N,Bu)( SCN)(dppe j2, 3. 1204 MoC~~H~:%CINZOP~ Mo(N,COPh)Cl(dppe),, 3. 1294 MoCSSH~~NJP~ Mo(N,)(PhCN)(dppc),, 3, 1269 MOC,~H,~B~N~OP~ Mo(N,CONHPh)Br(dppe),. 3. 1294 MoC~~H~~INP~ Mo(NC6H11)I(dppe)2, 3 . 1294 MOCS~HS~IN~P~ R;ZoI(N,C6J11,)(dppe),, 2. 136 MOCS~HS~CINZOP~ MoCI(NZCOPh j( dppe),, 2, 136 MoC,,H,,N,OP, [Mo(NO)(PhCN)(dppc),]2++3. 1279 MoC:59H54N4P4 Mo(Nl),(triphos)(l'l'h,), 3. 1268 bioCS,H56C:I N, P, [!vloCI(NNI I,)(tril.'iios)(PPh,,]t, 2. 146 FV~OC~OH~OF~~N~P~ Mo(N,),(dmpte)2. 3, 1269 MoC60H4404S4 Mo(PhCOCHCSPh),, 3, 1243. 1346 MoCb0Hj5NP4 [Mo(CNC,H,Me)(dppe j,]'. 3, 1278 MOC~OH~~P~S? Mo(SBuj,(dppe),, 3, 1284 MoC,oH77NsP, [Mo(dppm)(CNC,FI,,),12;. 1,77 .\/IoC,,H,,0S4 I M o O ( S C ~ H , P ~ ' ~ - ~,,2,~ 531; , ~ ) ~3.] 1350 MoC,,H9,S, M O ( S C ~ H ~ P ~ ' ~ - ~3,. ~1344 ,(,),, MOC~~H~~NOZP~ [Mo(C0),(PhCN)(dppej212t,3 . 1281 R/IoC~~H~,N,P~ Mo(N2)(triphos) (dppm) , 3 , 126X Mo(N,)(triphos)(dppe), 3, 1268 MoC~~H~~NZO~P~ [ M O ( N O ) ~ ( O P P ~, 3~. )1273 ~J~' MOC~~H~ZCI~N~O~P~ hInCI3(NO),(dppe),, 3. 1289 MOC,~H,~P~ Mo(dppc),. 3, 1277 MoCIO, [MoCIO,]-. 3, 1380

MoClS MoSCl, 3, 1320 MoC12F; MoFiC1,. 3. 1348 MoCI~UZO, MoCI,(NO),. 3. I271 MoCI,O MoOC12,3. 1331 MoCI,O, Mo02CI,, 3. 1377, 1383, 1387, 1389 MoCI,S MoSCI,, 3. 1334 MoCl3N MoNC'I,, 3 , 1395 MoCI,NO MoCI,(NO). 3. 1285 MoCI,O MoOCI,, 2,678: 3. 1318 MoCI,N [MoNCl,]-. 1.44.3. 1394 [MoNCI4I2 3. 1350 MoC14N0 [MoCI,(NO)]-, 3.1289, 1290 MoCI,N,O> [MoCI~(NO),]~-.3, 1 2 3 MoC14N2S2 MoCl,(h'SNS). 3. 1413 MoT140 MoOCI~.3. 1392 [MoOCI~] . 1.44; 3 , 1249, 1250, 1348, 1350, 1352 MoC1402 [Mo02C14]'-. 3, 1387 MoCI,N [MoNCI,];-. 3. 1250 MoC15iX0 MoC1,mOI. 3.1288 [MoCi;(KO)j2-. 3. 1288,1290 MoC15C) [MOOCI,]~- I SO: 3 1249, 1250, 1254, 1337. 1348, 1349.13.52. MoCI, MoClh, 3, 1413 [MoCI,]-. 3. 1353, 1355 [MoCI6]? ,3.1342, 1346 [MoCIJ-, 3. 1230,1234, 1304, 1330. 1332 MoC16N03P [MoCl4(N0)(0,PCI,)J~.3, 1290 MoCI,NO,P, MoNC13(P0,C1,j2. 3. 1394 MoC19N0;P2 MoCl,(NO) (OPCl,),, 3, 1289 MOCOC,~H~VIOO~ [Co(CN).q004100(OH2)(CN)s]5+,4.780 MoCoFeCl3H5OBS C:oFeMoS(CO),Cp, 4,832 M O C ~ F ~ C ~ ~ I ~ ~ ~ O ~ S C:oFeMoS(CO),Cp(P~ePrPh),4.832 MoCoH, z N 4 0 4 [Co(NH,),(MoO,)]+, 3, 1377, 1379 MoCoH, jNjO, [ C O ( N H ~ ) , ( ~ , ~ O O3,~1377, ) ] + , 1379 [CO(I~H~)~(OMOO,)]+, 1 . 291; 4,825 MoCrC,H1208 CrMo(OAc),, 3,735.737, 1231, 1307 , MoCrC,,H ,2N20 [Cr(edta)(Mo04)13-, 3. 1377, 1379

.

MOC~C~~H~,N,O,

CrMol&=CMeCH=CHCH=60),. ,- 3.747.1307 MoCuCGS, [CuCN(MoS,)12 -,2,S65-5h7,570,571.575 MoCuC:,I 15Ss [CuSPh(h?oS,)]z-. 2,566.3, 1421 [Cu(SPh)(SZ~~loS,)l'-.5,572

Cumulative Formulu Index

431

MoCuC28H54BrN4S2 Mo(CNBu‘)4(p-SBu‘)2CuBr. 3, 1283, 1424 MoCUS, [CuMoS,];-, 3, 1421 [Cu(MoS,)]-, 2,565, 566 M~CU,C~N,S, [(CUCN),(MOS,)]~-,2,566. 567 MoCu,C,7HinSh - ._ .- . [ { CU(SPh)),( SzMoS,)] *-, 5 572 [(CuSPh),(MoS,)]’-. 2.566: 3, 1421 MOCU,c 36H& Pzs3 MoOS~CuZ(PPh3)~,3. 1422 MoCu2CS,H4,OP3S3 (CuPPh3){ Cu(PPh,),} (MOOS,), 2,568 (CUZMOS3)(PPh3)30:2,566 MOCUZCS~H~~P~S~ Cu2(MoS4)(PPh3)3.2- 562,566,567;3. 1422 MoCU~CIZOS~ [ ( M O O S ~ ) ( C U C5,572 ~)~~~~, MoCu3Br,S4 [(CUB~),(MOS,)~-, 2: 566 MoCU~C,~H,~BTOP~S~ (Cu3MoS,Br)(PPh3)30,2,566 M o C U ~ I4sCIOP3S3 C~~~ (CuPPh3),(MoOS3)C1,2 . 5 6 8 (Cu,MoS3C1)(PPh,),C), 2,566, 3: 1422 MoCU~C~~H~~CIP~~ (Cu3MoS,C1)(PPh,),S, 2,566,567: 3. 1422 MoCU~CI~OS~ [ ( C U C I ) ~ ( M O O S ~2? ) ]566,568; ~-~ 3,1422 MoCu3CI3S, [(CuCl),(MoS,)]’-, 2,566. 569; 3, 1421; 5,572 MoCu4Cl4S4 [MOS~(CUCI),]~-, 3,1421 MoF2O2 MoO,F,, 3,1387, 1389 MoF,N [MoNF4]-, 3, 1394 MoF40 MoOF,, 2,678; 3, 1392 MoF~OP~S~ MOO(S,PF~)~, 3, 1337 M0F402 [Mo02F4lZ-, 3: 1381.1387 MoF,03 [MOOF,(O,)]~-,2,317, 319; 3,1399 MoF4S , MoSF,, 3, 1394, 1413 MoF4Se MoSeF,, 3,1394, 1413 MoFs MoFS, 2,678, hX0 MoF,O [MoOF5]z-, 3, 1348 MOF6 MoF,, 3, 1412, 1413 [MoF,]-, 1,498; 3,1353 [M0F6lz-, 3, 1342 [MoF6I3-;3, 1330 MOF6P3S6 Mo(S2PF2),,3, 133011332 MoF, [MoF81z-,3,1413 MOFI?NZO~P~ Mo(NO)z(PF,),, 3, 1274 MoFeCIZH,,,OzS, [Fe(OPh),S2MoS,j2-~3. 1426 MoFcCl2HlOS6 [F~(SP~),(MOS,)]~-, 2,565 { M O ( S ~ ) ~ F ~ ( S P 6.722 ~)~]*-. COC 7

4

MoHzN , 4 0 2

MOF~C~~H~~CI~N~S~ Mo(CN t3uL),(p-SBu‘),FeCI,, 3,1425 MOF~C~~H~~N~P,

[Mo(~16-C6H5Me)(PPh,),(Nz)FeCp(dmpe)] .3.1270 +

MoFeCI,0S3 [FeC12(MoOS3)]2-,2,565 MoFeCl,OS, [FeClz(MoOS4)]z-, 2,566 [FeC1zS2MoO(Sz)]z~, 2,570 MoFeC1202S, [F~CI,(MOO,S,)]~-, 2,565 MoFeCl,S4 [F~CI,(MOS,)]~,2,565,570,575 MoFeN202S4 [Fc(NO),(MoS,)I2-, 2,566 MoFeS, IFe(MoS,)1-, ,. 2,565 MoFeS, [F~(S,)(MOS,)]~-, 2,542,565 MoFe2Cl2HIDO2S4 [Fe2(OPh),(MoS4)]2-,2,565 MoFezC,,Hl0S8 [FeSz(SPh)zFeSzMoS2]2-,3,1426 MoFe2C14H&

[F~(SC~H,MC-~),(~-S~)F~(MOS~)]~ - , 2,566 MoFe2CZZHlMO2S4 Mo02(S2CC5H4FeCp),,3,1388 MoFe2C14H3608SS MoFe,(SBu‘),(CO),, 3,1424 M o F ~ & ~ HiN4o6PS2 , Fe,(CO)&Mo(NNMePh),(PPh,), MoFeZCl3S4 IMoSaFe,C1,12-. 3.1426 -_

2.148

MGF~~C~,SI

[(F~CI,),(MOS,)]~-,2,562,565,574; 3,1426 IMoFezSdCl,12-.4,242 MoFe,ChO,S, [MOS~FCS,F~,(CO),]~-, 3,1428 MoFe3C10H4Y402S4 [Fe,MoS,(CN),( 1,2-O2C6H4)]’-,3, 1428 MoFe,S, Fe,MoS,. 3, 1426 MoFe,C,,H,,06S, [Fe,MoS,(SEt),( 1.2-0zC6H4)3]3-,3, 1428;4.241 MoFe~CizOi& ~MoOFe,S,(C0)lz~2-, 3,1429 MoGaCI4Hl5N60~ Mo{ Me,Ga NN=CHCH=CH),(CO),(“H= A H ) , 2,256 MoGaCISH,,N6Oz Mo{ MeGa( flN=CHCH=cH),} (CO)Z(q3-CH2CH= CI 12). 2.256 MOHO [Mo(OH)IZ+.2, 296 MOHO, [MoHO3lf,3, 1030,1259 MOHO? [MoO~(OH)],3,1256 [MoO,H]-. 3,1259,1260 MOHO, [MOO(O~),(O,H)]~-, 2,323,324; 6,330 MoH,Br,O [MoBr,(HzO)]Z-, 3, 1330 MoHzCljNOz [MoCI,(NO)(OH,)1’-, 3,1279 M~H,c~,N~o, [MOCI,(NO)(H,NO)]”-, 3,1291 MoH,CI40, ~MOOCI,(H,O)]-,3, 1249, 1250, 1348. 1352 MOH~C~~O

[MoCI,(H,O)]~-, 3,1234,1330,1332 MoHzNri02 [Mo(NO)(HZNO)(N3),]*-, 2,230; 3, 1291

MOH,ClzN,O,

Cumulative Formula index

M0HqC12N204 M O C I ~ ( N O ) ~ ( H ~3,O1272 )~, MoH~CI~O~ M o O ~ C I ~ ( H ~3, O )1381 ~, MOH,N,O, [Mo(OH),(NO),]’-, 3, 1273 M0H407 MoO(O2)2(H20)2,3, 1399 [MOO(02)2(H20),12-, 3, 1261 MOH606 Mt)(OH),r,, 3, 1256; 6,944 MoH806 [Mo(OH),(H,O),]’ ’ ,3, 1256 [MoO~(H,O),]’+, 3, 1256, 1376 MoHIzO~ (Ma(H2O),I3+, 1,309; 3, 1230, 1134-1238. 1242, 1244

MOHI~OIO (Mo,0,(H,0)61Z+, 3,1236 MOHgC8HsCI CpMo(CO),HgCI, 2.3 MOHgCwHmS2 Cp,Mo(HgSEt),, 2 , l MoHg04 HgM004,5,1068 MoHgKi,H2oSz Cp,Mo(HgSEt),, 2 , 3 MoTzOz

M0021,,3, 1387 MoIIIC,J 149NdO3 In(octaethylporphyriii)MoCp(CO),. 2.841 M0K204

K(MoO,)K, 3,1377 MoMg04 MgMoO,, 3, 1376 MoMn0, MnMoO,, 3, 1376 MoNI~ [ M O N ( N ~ ) ~3, ] - ,1394 MoNdReOx Nd(O,MoO,)(O,ReO,). 2,426 MoNICSHInNS, (MoS,)Ni( S2CNEt2),3, I422 MolViC,,H,,P,S, Ni(Me2PCH2CH2PMe2)(SMr)Zh.lo(cud)25. 169 I

MON104

NiMoO,, 3,1376 MoOSSe, [MoOSSe2J2-,2,521 MoOSzSe iMoOS,Se12-, 2,521 , MAOS, [MoOS,12-. 2,521,545.560,561; 3, 1260.1377, 1378. 1424

MOO& [MOO(S,),]~-,2,545; 3, I431 Moose, [MoOSe,l*-, 2,521 .. MOO, MOO,. 3. 1316. 1334 MOO^]^+, 3, 1030 M002S2

[Mo02S,]-, 3, 1383 [Mo02S212-,2,521.537,560,563; 3. 1260. 1377, 1379, 1380, 1424 MOO,& 2, 532 [Mo202Sz(S~)~12-, MoO,Se, /MOO,S~,]~-, 2,521; 3,1380 MOO~S [Mo0,S12-, 2,521; 3, 1260, 1377. 1379 Mo03Se

[MoO,Se]*-, 2,521 MOO,

438

[M0(02)2)~-,3,1377 MOO,]^-^ I. 145*151; 2,296,413,970; 3, 1030, 1229. 1230,1238.1242. 1256-1260, 1376-1379; 6,328. 805,806, 828,860,872, 1015 Moos [MO(O,),]~-, 1,94: 3, 1261, 1398, 1399, 1402 MoPdCSHiONS6 (MoS4)Pd(SzCNEt2). 3, 1422 MoPdCss€IjjN,C)3€‘4

Pd(CN)2(~-dppm)~Mo(CO)~, 5, 1164 MOP~ZCS:H*~CIO~P~ Pd,MoCp(CO),Cl(dppm)?, 5, 11 10 MoRcC2.,H.,,N20,

MoCp(CO),(&NC6H4Me-4)keCp(CO)2, 2, 136 MoKeC26H36C16N ?P3 KeNC~,(PMe,Ph),MoCl,(NCMe), 4,189 MOR~C~~H,,C~~N~~P~ MoCl,(OMe){(Y2)ReC1(PMe2Ph),},4,133 MORe&,&8C16N4P8 M O C I ~ { ( N ~ ) R ~ C ~ ( P M4,~133 ~P~)~}~, MORhC46HdZP2 Rh(PPh3),(~~-H),MoCp,.4, 1076 MORUC~~H~~N~S~ MnS4Ru(bipy)z.3. 1122; 4, 352 MORUZC~OH~~NBS~ [MoS,{Ru(bip~)2)1JZ+, 3,1422; 4,361 MoRu&C,,H,,O.i2 (BU‘CL)R~~(CO)~H~MOCP 2 ,(2C O ) ~ , MoSSe3 [MoSSe,12-. 2, 521 MoS2Se, [MOS,S~,]~--. 2.521 MoS,Se [MoS3Se12-,2.521 MoS, [MoS,]-. 2,561 (MoS4]2-, 2+521,524,525,545,56&563,571; 3. 12tiO. 1261: 1377-1379,1424, 1426, 1431; 4,241; 6$657, 805,828 ( Z ~ ( M O S ~ ) ~ ]2,572 ”-, MoS,

[MoS(S,)]’-. 2.545 MoS, [MoS(S,)?]’-, 2, 546 [MoS9I2-, 3,1431 MoSe4 [hfoSe,12-. 2.521 MoSnC2H60, SnMe,(MoO,)+ 3,1376 MOS~C,~H~,CI~N~ [Mo(CNBu),(SnCI,)]+, 1,73; 2, 19 MoSnzCll0 [MoCl4(SNCI3),J2-,3, 1342 MoTajCIi, [Tai;MoC1,,]3’ 3, 1321 Mo’I‘IISCITB \{~d,MOCl,z)Cl6]’-. 1, 160 MoTiC 4H2,N406 Mo(C0)5{C(NMe2)OTi(NMe,)3}, 2. 182 MOWCBHI~OB MoW(OAc),, 3, 1307 MOWC~UH;~~~ MoW(O,CBu‘),. 3.999,1232 [MoW(O,CBu’),]-, 3, 1009 MOWC~~H~~N~OJ M o W ( ~ = C % l e C H 4 H C H = ~ O ) ,3,. 1009. 1307 MoWC,~HSLCI,P, MoWCl,(PMePh,),,3, 1308 MoWHCI, [MoWCI8HI3-. 3. 1316 MoWHClq [MoWCI,H13 .3.999 MoW11040Si I

439

[ ~ ~ o ~ O ~ ( C ~ O ~ )2,444; ~ ( H3, ~ 1256, O ) ~I408 ]~-, MoZC4H6CI4O4 [ M O ~ ( O A C ) ~ C3, ~ ~1302, ] ~ - ,1303 Mo,C,H,Cl,O,S,

.

.

EH)OH},. 2,250 M02B4C40H64N16 MoZ{Et,B(r;rN=Cr~CH=~H),J,, 3, 1305 MozB~~N202S, [MoS,(~-S),MOB~,(NO)~]-. 3. 1333 Mo,BrzN,OA [Mo,B~,(NO),]~-.3. 1275 MozBr6 [MOzBr6]-,3,1316 kf02Br6N404 [{MoBrz(NO),},(y-Br)2jz-. 3. 1347 MozBr8 [MozBrsI4-,3, 1230, 1303. 1306; 6.196 Mo,Br, [ M O ~ B ~ , ]2,684; ~ - , 3. 1313. 1316 MozCzC140h Mo,O,CI,(C,O,), 3. 1358 Mo2C2HAN2O2Sh MOZO~(CLL-S)~(S 3.~13MI. CNI~ 1361 ~)~~

MoZCZH6Br3S5 [MuS2(~-S)2MoBr?(SMc2~12-. 3, 1333 MoZC2N,0S, [{MO(NCS)},(CL-O)(U-S)14-. 2,302

MoZC4Br4F6O4 [ M O ~ ( O ~ C C F ~ )3.~ 1302 B~~]~ M02CaF12012Sa Mo,(O,SCF3)4. 3, 1232. 1304 Mo~C~H~CIO~ [Mo,(O,CH)~CI] , 3, 1312, 1303 Mo~C~H~OR M02(02CH)4.3, 1302, 1303 Mo~C~H~OIZS~ [Moz02S~(Cz04)~(H~0)2]2-, 3. 1250. 1255

M02CsH20C1407

Cumulative Formula Index M02CioH24NzS6 Mo,S,(SCMe,CH,KHMe),.

MO2C~N40 ] 1s, ~ M O ~ O , ( N C S ) ~ ( C ~ O3.1253. ~ ) ~ ] ~1357 -.

[(Mo0,),(cdta)14--, 3. 1024. 1379. 1408 MOZC1OHlJNOZ [Mo2Cp{r-fiH(CH,),cHCO2}]*. 2.745 ~~2Cl~H18N2012 Mo2(OH)z(H20)2(edta).3. 1239 MoKinH?nNL& 3.1360 Moz0S(~-S)2(S2CNEt2)2, Mo2C10H20NZ02Se4 MoOz(SezCNEtz)2,3, 1390 MO~CIOH~&"~~S~ MOZO4(S2CNEt2)Z13,1252,1360 Mo2C1oH,oN,OaS2 Mo204{SCH2CH(NH,)C0,Er),, 3, 1361 M~zCloHzoNzSi MoZ(SZCNEtZ)2,3, 1305 MozC10H20N2Ss Mo2S4(SzCNEt2)2,3, 1252. 1360 MOZCIOH~~NZO~S~ Mo203{(SCH2CH2)2NMe}z.3. 1357

440 3, 1361

441

Cumulative Formula Index

M O ~ ( M ~ N C H ~ C H ~ N2,165: MC)~ 3.1310, , 1313 MO~Ci2H3oN604 Mo2O4(l,4,7-triazacyclononane),. 3, 1251, 1361 [Mo204(l,4,7-triazacyclononane)~2+. 3, 1241, 1358 MO~CI~H~IB~~N~O [ { MoBr(1,4,7-triazacy~Iononane)}~@-Br)(p-OH)IZ-, 3, 1333 M%CI~H~~CI~N~O~ [{MoCI(l,4,7-triazacyclono1iane))~(~-OH),~~~, 3, 1242, 1333 MOIC~~H~~CI~P~ M O , C I ~ ( M ~ ~ ~ ~ C H ~ C H3.~1308. P P V1309 IC~)~. MO~CIZH,,CI,N,P, Mo2C13(NMe2)3(PMe3)2. 3. 1313 Mo2C12H36C14P4

Mo2C14(PMe3)4, 3, 1308, 1309 MOZCI~H~~N~ Mo,(NMe,),, 2, 163, 169, 175: 177.180, 181; 3, 1310, 1311, 1313, 1314 M02Ci2H36N604 [Mo2(OH),(H20),( 1.4.7-triaza~yclononane)]~+,3, 1241, 1251 Mo,C., ,N., ,S {Mo(CN)6)2S,2,522 [ Mo,S(CN),,16 ,2,524; 3, 1296, 1333 [Mo~S(CN)~,]"' , 2 , 524 Mo~CI,HI~'J~OI~ [Mo2(p-OH),(k-Ohc){(02CCH,)N(CH,),N(CH,C9,),)1,3,1333 I M02C13H32N605 [Mo2(OH)2(C03)(1,4.7-triazacyclononane),]2+, 3, 1241 MO~CI~H~FNZOI~ [ { MoO(O2){2,6-py(COZ')2))2F]~,2.3 19; 3,1402 MozCi4Hio04 Mo,Cp,(CO),, 3, 1316 MoKI~HIoOJ', {MoCp(CO),},P,, 2, 1047. 1059 M02C14H1308

Mo,(OAc),(acac),, 3,750 Mo2C,J I&

Mo,(C5114Me)2(C1-S),(p-SCH,C'H2s), 3, 1435 MoKi4H2n08 Mo,(acac),(OAc),, 2, 377: 3. 1302, 1308 MozC.14HmS4 M O ~ C ~ , ( ~ - S 3. M 1435 ~)~. Mo~CI~H~SN~W, Mo202(p-0)( p-S)(S2CNPr2)2.3. 1360 k102C14H28NZS4 M o ~ ( S ~ C N P ~3, ' , )1305 ~, Mo2C14H3201U

Mo,04(l,5,9-triazacyclododecane),, 3, 1251 {Mo02(OCMe2CAMe20H)),(~i-OMe),, 3, 141I [Mo,O,(l ,S,Y-triazacyclododeca~ic)~]~+, 3- 1358 Mo~CI~H~SN,O, I{Mo( 1,J,7-triazacycl ono~i~~~e ) } ~~~- OH) ,( lr - +, Mo2ClRH42P;h05 3, 1241, 1333 Mo,0s(l,4,7-tritncthyl-l ,4,7-triazacyclononan~)~. 3. MO~C.,,H~~CI,N~P, 1408 M o ~ C I ~ ( N M ~ ~ ) ~ ( M ~ . ~ P C3,H13 ~ 13 C H ~ P M ~ ~ )MoZC1BH4204 . Mo2Mel(OBu')4. 2, 165; 3, 1313 ~10zCisHioN04 [CP~MO~(CO)~(CN)I 2.8 M0zCia&1-1206 Mo2(OPr'),, 1. 148; 2, 199,340,346,356: 3. 1313-1316 MO:CisHisF60~ Mo,0,(acac)2(hfacac)I 3. 1356 Mo2ClsH4604P2Si2 MO~(OAC)~(CH~S~M~~ 3,)1307 ~(PM~~)~, Mo~CISH~BN~ Mo2(NMeEt)6,3,1310

Mo~CZ~H~~N~O~S

Cumulative Formula Index

442

, 3 , 1365

1253

136.1 M%C24HioP& M O , ( ~ - L - S ) ~ ( S R ~ ' ) ~ ( P M3,~ 1344 ,P~)~, Mo2C2,IlsoSlo [ {Mo(SH)(l.S,9.13-tetraihiacyclohe~adecane)}~~~-. 3. 1347 IMu2(SH)2(l16]iincS1)2]zi , 2 , 518,519 MozCZ~HS~O~ Mo,(OBu')b, 2,355,356,358; 3, 1001, 1313-1315. 1317. 1407 Mo,C,~H,,P~ , 3 , 1303 Mo,( ~-PBIJ'~)~(PBu'), M02C?&608 Mo,(OPr'),. 2.347.349; 3, 1316 Mo2C24H60N6 MOz(NEtl),. 3. 1310 Mo2C24HwOs Moz(OPr')4(HOPri)4.2, 349; 3, 1303 MoZCz,H,,Si, Mo2(CJlzSiMe,),.3. .13'111, '1311, 1314 Mo2C2FFXR7F3N206PLS6 Mo2(NC6H4Me-4)2S( SMe) { S2P(OEt)z)2(0,CCF3). 3, 1364 MoXzsH,40, Mo,(OBu'),(@-CO), 2, 355; 3, 1315, 1317 MOzCxH16~405S: Mo20S(,phen),iNCSj2, 3 , 1408 MozCXH~~S~ Mo2Cpz(i'-S2C6H,Me2),. 3, 1435 MOZCZ~H~~Y~SZ { M o C ~ ( N B ~ ' ) ~3,) ~ 1361 S~, Mo2(2,4,h-~~e,C6H,S),rNMe,),,3,1314 MOZC26H54010 Mo,(OBu'),(O,COBu'),, 3. 1310, 1313

M o ~ C J1,,c)l, Mo2(OPr')B(C0)2,2, 356 Mo2C26H,8N4Si8 M o , { S ~ ( S ~ M ~ ~ J , } ~ ( ~3,V 1314 M~~),. MoZC~~H~~N~O~

MO~(~~-C~M~~)~(CO)~(N=CM~~)(NCO), 2,238 MozCz8H~09 Mo,O,(phenanthroquinone),, 2,398 MoIC~SH~OC~~ {.MoC14(PhCCPh)}2,3, 1347 MOZC28HZ0012 MoZ(02CC6H,0H),, 3, 1302, 1303 kla,C2,H,&, Mo,(S,CPh),, 3. 1303 MOJ&H~~O~SC~ Mo2(r17-C,H,)(CO),(p,-SePh), ,2,663 MoX28H28NA Mo2(C5H4Me),(u-S2CNCH2Ph),, 3,1435 M02C28H30F1208P2 Moz(p-02CCF3)2(02CCF3)2(PPhEtz)2, 3 , 1303 Mo2C28H36ic'204 Moz(q5-C,Me,),(C0),(N=CMe2)(NCO),2.238 M

o ~ C ~ ~ H ~ ~ ~ ~ Mo~O,(1.2-02-3,5-But2C,H2)2, 3, 1401

Mo2C28HNt09

[Mo,O,( I .2-0~-3,5-R~'~C~11~)~]z-, 3 , 1410, 1412 MoZC~HH~~O~PS~ [Mo*(SzCPEt,)(O,UBu'),(OPEt,)l', 3, 1304 Mo2Me2(OBu'j4(py),, 3, 1313 Mo~CZ~H~~O~P~

[Mo~(~,~-M~,C,H~O)~(PM~,)~]+. 3, 1309

443

Cumulutive Formula Index

MozC130HlZZ

~o,(COj,{u-~=C:Phz},Cp,, 2,280 Mo&sH&Oz% Mo,O,(SPh),(MeCN), 2,531 h~ozCmHsoO6

M0~(OPr'j~(OC~H~Me~-2,6,)~,2.340 M0ZC38H5406

M O ~ ( O P ~ ' ) ~ ( ~ . ~ - M 3, ~ ~1313 C~H~O)~, M ~ K ~ ~ H ~ s N O ~ MU:( OCH~BU'),( p-C,H.+)(py),3. 1315, 1317 MoZC40H44014

Mo,{(R)-0,CCH(OH)Ph}4(~HF)Z, 2,474 ti,*0,S4 Mo,jOPr'),(SC,H,Me,),, 3, 1310 .~ . Mo,C'~~H,~O,S, [ M O , O ~ ( S C ~ H ~ M ~ - ~ ) ~ ( 3,1365 OM~)]-, MO,C,,

~

MOZC30H6606 Mo,(OCH,BU')~. 3,1310, 1311. 1315

Mo2{Me&H3N=C(NI 1)$}4.3,1303 MOZC32H36012 Mo,{2,6-( MeC)),C,H,O} j. 3.1303

[ { Mo(CO)4(PMePhz)}2(p-H)]-, 3, 1438

M0z(oZc6ci4)6r 3,1308.1-111,i413 MozC36Hz.+N407 M0,0,(8-quinolinolate)~. 3. 1357 M02C36H40NS06 Mo2(NZPh)4(acac)z(OMe)2. 2, 136 MozC36Hs,Nio

Mo2(NMe2)4(MeChH,NNNCbH4Me)2, 2, 19Y; 3, 1313 M02C36H58N604

Moz(OPr')4(PhNNNPhj2,2. 199 MozC~~H,INO~P~S~O { M O O ( C ~ H ~ P S ~ ) ~2.80 OS}~~~. MozC~~H~ON~OZ

. .

. .

~(~203(tetraphenylporphyrinatc)z, 2, 8261 3. 1253. 1357; 6,616

Cumulative Formula Index

M02C1404 Mo2C1404 [Mo~O,CI,]~-,3, 1360 MO~CI,S,

[Mo&J-, 1,148 [Mo2C1814-, 1,403; 3, 123G1232. 1302-1304, 1306, 1308, 1309

[~Io;(S,)~CI,]~, 3 , 1362 Mo2CI, [MozCI9j3-, 2,684; 3,1232,1242,1304. 1309.1316 Mo2CIlo Mo2CII0,2,683; 3, 1354,1355 [ M O , C I ~ ~3,1347 ]~~, MozC1iA04Pz {MOC~~(NO)(OPC~,))~, 3, 1289 MOZC~I~O~PZ M0202C16(OPC13)~.3, 1362 M0,COO*S6 [Co(MoOS,)Z12-, 2,575 Mo2Co04S4 [CO(MOO,S,)~]~’ ,2,574,575 [ C U ( M O O ~ S ~, 2) ,~575 ]~ Mo,CuS, (CO(MOS,),]~--, 2,573,575 [Co(MoS4),13-, 2,566,575;3.1.122, 1124 Mo~CU~CZ~H~~CI~N~O~S, ( M O { O N ~ H , ) ~ } , S ~ C U3,C 1425: ~ ] ~ , 5. 572 MOZCU~C~ZH~O~ZP~S~ (CuPPh3)4(MoOS3)2,2, 568 MozDyOs [Dy(MoO4)J, 3,1376 MozF604 [M0zF6O4IZ-,2, 681; 3. 1392 MozFq MozF9,3, 1334 MozFA

[Mo~OZF~]-, 3, 1412 MO~F~C~H~S.,~

[F~S,{MOS(SCH,CH,S)},]~-, 3. 1430 MozFeClsHsOloP2

Fe(PCH=CHCH=~H),{Mo(CO)5)z. 2, 1044 Mo2FeCzzH3002S4 Mo,(C5Me5)2S4Fe(CO)2,3, 1430 M02FeC23H3003S4 i Mo,(C5Me5),S2(S,CO)Fe(CO)z:3,1430 Mo,FeS, {Fe(MoS4),J2-, 2,574,575 [Fe(MoS4)2]3-,2,564,56S1 566.573, 574,575.576 [Fe(SZMoSZ)2]3-,3,1426 [Mo(S,),Fe(S,)Mo(S,)l~- 6,722 [Mo,F~S,]~-, 4,242 MOZFC~C.I~HIOO& MOzCp,FC2(y,-S)i(lr-s)~(co)61 3. 1429 M02Fe2C18H1008S~ MOZCPZF~Z(~~-S)~(~-~O)~(~O)~. 3, 1429 MO~F~ZCISHI~~~S~ M O ~ ( C ~ H ~ M ~ ) ~ F3,~ 1430 ~(CO)~S~~ M o ~ F ~ ~ C ~ ~ H ~ O N ~ ~ ~ S ~ M O ~ ( C ~ M ~ ~ ) ~ F ~3.1429 ~S~(NO)~, Mo2FeZC24H3004S4 M O ~ ( C ~ M ~Fe(CO),} ~ ) ~ S ~2 1{3. 1130 MoZFehCdClhOdSh [Fe6SI,CI6{Mo(CO),J21J .3>1430 ~

M02Fe6C16H40S17

3,] 1429; [F~,MO&(SE~)~ ~ ~ , 4. ‘I243 M02FebCltlH45S17 [Fe,Mo&(SEt)g]”, 3,1427,1429 MOZF~~C~~HZ~C~~SI~

[ M O ~ ( H ~ O ) , ,6.496 ]~+. Mo2I2OI6 [Mo,I~O,~]~-. 3. 1411 Mo2NiC,,H3,S, [N1(SIv1e),(h?oCp~)~]~+, 5 , 168 Mo2Ni0,S6 [Ni(MuOS,),]2-. 2. 575 Mo,NiC),S, [N~(MoO,S,),]~ .2,575 Mo2NiS4 [Ni(MoS4)J-, 5 , 175 Mo,NiSs [Ni(MoS4),I2-. 2.564,566,570,571,575

444

445

Cumulative Formula Index

Mo20S4 [MoO(MoS,)]*~-,2,562 Mo,0S9 [ M ~ ( S ~ ) ( S ) ( S ~ ) M O ( S ) ( ~2.546 ~O)~~-, [MozS4(Sz)(S30)]’-, 3, 1431 Mo202S6 [ M O , O ~ S ~ ( S ~ 2,533.537,539,563; )~]~-. 3, 1432 M0202S10 [MozQZSz(S4)Z12-,2,546 Mo204 [M0204]’+, 2,296; 3,1249 M0204S7

[Mo(S,)(0)(S),Mo(O)(S;O2)]~-, 2,546 M0207 [Mo2U7]-. 6,806 [Mo2O7I2-,1, 148; 3, 1030. 1032, 1257. 1258, 1376, 1408; 6, 1015 MoZO16S4 [ M O ~ ( S O ~ ) 3, ~ ] 1232. ~ - , 1309 [Mo,(S0,),14-, 3, 1232.1233, 1303, 1308, 1309; 6,496

COC 7 4 .

M03H2401ZS4

Cumulative Formula Index

M03A24012S4

[MO~S,(H,O),,]~+', 3, 1247 Mo3HfOi2 IHf(M004),1*-, 3,408 -_ MO,OS, [MOO(MOS~)Z]~-, 3. 1422 IMoqOSRIZ-, 2,565 ,

[MO;O,~]~-,3, 1032 M083 {MoS,]-, 3,1319 Mo3S9 [Mo3S9]2-, 2,563,565; 3, 1122 MoS,, [ M O . ~ ( ~ ~ - S ) ( ~ L - S , ) , ( 1. S ~14.1; ) ~ ] ~2.523, -. 535-539; 3. 1318, 1431

-

. I

Mo4Br4S4 Mo4SlBr4, 1,154 MojcH~Ois [MO~O,~(O~CH,)(OH ~ . 3) .] 1054.1376 . 3 . 1054

1411 2.476

}2.

119; 3. 1254

MO.+CiJ'Ji& [Mo4S4(CN),2]S-,1. 151: 3, 1248.1321. 1433 IMo,S4(CN),,1"-. 2.521

Mo4F2o IMoF,).. 3. 1347. 1355 M ~ , H ~ , 2~ ~ 4O [MO,S,(H~O),Z]~, 3 . 1248 [M0,S,(11~0),,]~+,3. 1248 Moa17 [Mo,I;]~-. 2.685 Mdii [MoJll]' . 1. 149; 3. 1319. 1321 Mo~NOS,, [MOj(NO)(S2)SS3]4 . 2 . 532

444

447

Cumulative Formula ladex

M06019 [M0601,]~-, 1, 160; 3, 1024,1030, 1031, 1258.1259 (M060,,]3-. 3, 1052, 1259 lMo601914-,3,1259 M~,o,T~. I T ~ M O ~ O ~3, ~1043, ] ~ - 1044 ,

Mo& [ M O ~ C I , ] ~2,685 +, MosC113 IMo,CI,,12-, 1, 155:3. 1321

[Hf(Mo04),lX-. 3.408 Mo.5IOz4

Cumulative Forrnulu Index

448

NaAs3Sh6Wz1086 [ NaSb6A~3W2108h]1n-. 3, 1042 Na CCISz Na(S,CCl), 2, 591 YaCHO, NaO,CH, 2,437 NaCH,O NaOMe, 2,348 NaCH6C1N202 NaCI(H2NCONH2)(H20),3 . 6 NaC3F70 Na{OCF(CF,)2}, 2,343 NaC,H,,,BrN20Z NaBr(AcNH,),, 3, 5 NaC4H121N20S NaI(glycine)2(€420),3 , 6 NaCSH702 Na(acac), 2,370; 3.25 NaC6H14ClN206 Na(CIO,)(AcNHMe),, 2, 492 NaC6H18BrN4 NaBr{H,N(CH,CH,NH)2CH2CH2NH2}. 3 , l l NaBr{N(CH2CH2NH&}, 3, 11 NaC6H18NSi, Na{N(SiMe,),}, 2, 168, 173 NaC',H,,lN, NaI(cn),. 3, I I NaC,H,,BrN,O, NaBr(Ac2NH)2,3, 15 NaC9H1,10, NaI(Me,CO),, 3 , 4 NaC9H2]IN03 NaI{N(CH,CH20Me),}. 3,23 NaC9HZ1IN3O3 NaI(DMF),, 3 , 4 NaCloH1304 Na(OH,),(PhCOCHCOMe). 3 . 2 NaCloH14N209 [Na(H,Oj(edtajl3-, 2.783 NaC10H20Ns0S Na{t IC)C:H,CH2t'H(CH21U'CH,)3CII,A}(NCS), 3,42 hraCloHzOOs [Na[lS]crown-5]~', 2 . 931 VaC, 2H240h [Na[l8]crown-6]+, 2. 931 N aCl,HZ6Br0 NaBr(sucrose)(H20)2,3, 25 NaCizHxO6 [Na(MeO(CH2CH20)sMe)]-:2.931 NaC13HZ4N05SZ Na{S(CH,CH20)5CH2cH,}(KCS). 3.41 NaCl3HZ4No6S Na(18-crown-6)(SCN). 3. 37 NaCI4H2,IOG Na(henzo- 1 5-crow n-S)1 (H,O). 3.41 NaCI4Hz2O6 [Na(benzo-1S-crown-5)(H20)j ' .3,39

NaC,,E-12,07 [Na[2l]crown-7]+,2. 931 NaC1.5H3F1806

[Na(hfacac),12-, 1.65; 2, 366,370

NaCj5H1102 Nn(PhC0CHCOPh). 3, 14,2h NaC 16H,,N205 [Na(cryptand[2.2.1])]+, 2,938; 3,46 NaCl6H,,N2O6

[Na{HOCH2CH2N(CH2CH20CHzCHzOCHzCH~)~NCH,CH,OH}]+, 3,42 NaC,,H, IF6N203 Na(hfacac)(phen)(H,O), 3, 13 NaCisH,&O6 [Ya(cryptand[2.2.2])]+, 2,938; 3, 46 NaC20H240b

[Na(dibenzoll8~crown-6)1+,2,931 NaC10H26Br07 Na(dibenzo- 1X-crown-h)Bi-(H,O), 3,41 NaC,,H,,O, ~Na(dicyclohcxano[l8]crown-6)~+, 2,931 NaCLoH,oti20, (Na(cryptand[3.2.2])] +,2, 938 NaC,,H,,N,O, -_ ." [Na{~CH,N(CF12CH20CH2CHz)zNCH~]~}]~, 3.46 NaC2,H2,Y06S Na { (3-h/IeOC6H,0CH,CH,0CH,)2} (SCN), 3.19 NaC,,Hl2Fl2N?OS ._. . . . Na(hfacac),(phen)(H,O), 3, 13 NaC,,H,,O, [Ndsphcrand)]', 3,43 NaC24H3aC1012 Na(dil.renzo-24-cruwn-H)(CIO,), 3 , 4 0 NaC,,H2,B~0,P2 I\;aBr(Ph2P(0)CH,P(O)Pli2}, 3, 15 NaCZ8H281012

NaI{PhCOCH,0~=CHOC(CH~OH)=CH~O)2( H z O ) ~3,, 15 NaC28H40CIO14 Na(benzo- 15-crown-5),(C104), 3, 39 NaC28H40010 [Na( dibenzo[30]crown-10)]+, 2,931 NaC30H20Nj03 Ma(2-0,NC6ti,0)(phen),, 3, 13 NaC3~116~N~010

[Na ( O {CH2CHIN(CH2CH20CH2CH20CH2CH2)2YCH,CH,),O}]', 3,46 NaC3JL08 Na(laso1ocid). 3.67 NaCjtiH6,0, Na(rnonensin), 3,66 XaC3,H6,Ol [Na(monensin)]+.3,M NaC37H42N40G [Na(spherand)]+,3,43 NaC40H56012 [Na(nnnactin)]+,3,65 NG4H64012 [Na(tetranactin)]-, 3,6S NaC,,H,,N,,,O,,, INa(antnrnanide')l-, 3,64 NaCoC,,H,,N,O, Co(salen)Na('THF), 3, 16 NaCo2C40H44N,0s [ {Co(salen)),Na(THF),]+, 3.16

449

NaC03C40H36N409

{Co(saten)},NaCo(CO),(THF).3. I6 NaCuC4H9CIN07 Cu{ OCH,C(NH,)( CH20H)CHZO}Na(C1O4),3,17 N~CU~C~~H~~CIN~O~ {Cu(salen)}2Na(CI04),3, 16 NaEuCI8Hs4N3Si6 NaEu(N(SiMe,),},, 3, 1111 NaFeC31H40N06P NaHzN NaNH,, 2, 162, 164 NaH,,N, [Na(NH3hI+,3 , 4 Nab206

[Na(H20),]+,3 , 4 NaMgCI5Hz1O6 NaMg(acac),, 3,27 NaNiZC36H34N604 [ {Ni(salen)},Na(MeCN),]t, 3.16: 5 . 197 NaRbZCI5H3Fl8O6 RbJNa(hfacac),l, 3,27

[(V0[1,2-(2-OC6H4CH=~)2C6H?j)2Na]-,3,534 NaW2CZ4Hs7O8 NaW,(H)(OPr'),, 2,359 NaW3001 [NaW300110P5]14-,3, 1039-1011 NaYbCl8HS4N3Si6 NaYb{N(SiMe,),},, 3, 1111 NaYbCzoH,6N202Si4 NaYb{N(SiMe3)2},(OEt,),. 3,1111 NazB4H409 Na-B4Oq(OH)4,2,298 ' Na&F120z Na2(OC(CF3),C(CF3),C)}, 2.343 NazC,H,07

-

I,

Na2C44H~8N4 Na,(tetraphenylporphyrin). 2.820 Na2Fe2C34H57N407 FezE\la2{{ MeCOCHC( Me)=NCH,}z) ,(OEt)(THF),, 4,1238 Na,Mn08Se2 Na,Mn(SeO,),, 4,46 NazMn4OlsSs Na2Mn4(S03)5.4,46 Naz03S Na,SO,, 2,638 N~~CGH~NO~ Na3{N(CH2C02)3},2.790 Na3C10H13NZ08

[Na(cryptand[2.1.1])]+, 2,938 NbAlCl8 NbAIC1,: 3.591 NbAsC,,H,,C15 NbCI,(AsPh,), 3,600 NbAsC18H1SCISN [NbCIs(NA5Ph,)]-. 2 , 122; 3,620 Nb As4Czol13?Br4 NbBr4(diars)l. 3. 642 N~As~CZOH~~CL NbC14(diars),, I , 88; 3,644 [NbCl,(diars)J'. 1. 88; 3, 599 NbBC9HIOCl5N6 -, 3,622 [NbCIS{ (p~;razolyl)~BH}] NbBr,O NbOBr,, 3.626 NbBr4 NbBr4,3.640 NbBr,N [NbBr,NIZ-. 3, (120 NhRr, NbBrS, 3.589.590 NbBr,N, [NbBr,NJl 3: 619 NbBr,O [NbOBr5]*-. 3.627 NbBr, [NbBr,]-.3.594.6;10 NbCCIS'U [NbCI,(CN)]-. 3,623 NbCHCISN NbCI,(HCN): 3,598,623 NbCH3CISO [NbClj(OMe)l2-: 3,649 NbC2CI3O4 NbCI3(C2O4).3.606 NbC2H3C14N20 hhC1,(NO)(MeCN)I 3, 655 NhC2H3ClsN NbCI,(MeCN): 3,595 NbC2HSCl40 NbCI*(OEt). 3,606 NbCzH,Cl,O [NbCI,(OEt)]-. 3,606 NbC,H6Br4S2 NbBr4(SMe)2,3.643 NbC?H,jCl,N,O, NbC1,(ON(Me)NO)Z, 3,623 NbC3H2CI5N2 NbCI,(NCCfI,CN). 3, 597 NbC3H9CI,03 NbCI,(OMe),. 3,606 NbC4F20, [NbO(C204)2F2]3-,3,633 NbC4HDii [NbO(C204)2(OH)(HzO)]2-, 3,634 NbGH40ii [ N ~ O ( C Z O ~ ) , ( H , O )3,634 ]~. NbC4H6C13NzO NbOC13(MeCN),I 3,630 NbC,H,Cl4NZ NbCI,(MeCN),, 3,641 NbC4H9CIZ02 NbOCI,(OCMe3),3,1r31 NbC,H,,Br,S NbBr,(SEt,), 3! 596 NbC4H,oCI,Sz NbCI,(MeSCH,CH,SMe). 3,596

Cumulative Formula Index

45 1

NbC4H12C1303S2 NbOCI3(DMS0),. 2. 488: 3,630 NbC4Oiz [Nb(0,)z(C,0,),]3-. 2,319; 3.635; 6.329 NbCSH3N05 [Nb(CO)dNH3)]-, 3,685 NbC5HSC102 NbCI(Cp)(O,), 2.319 NbC,H5CI, NbCI,(Cp), 3, 682 N bC5H5NS3 NbS,(py), 3,654 NbC5H,oC14NO NbCI,(CN)(OEl,), 3, 623 NbC~HisN606 NbMeZ{ON(Me)N0)3,3.623 NbC5H150s Nb(OMe),, 2,349; 3,601 NbC5N50S5 [NbO(NCS)5]2-, 2,229: 3,634 NbC505 [Nb(C0),l3-, 3,684 NbC6Br01, [NbO(C204)3Br]4-,3,634 NbChH909 NbO(OH),(nscorba!e), 3. 631 N~C~HIZC~NZSZ NbCI3{NMcC(S)Me),, 3.623 NbCbH18C106PzS4 Nb(OMe),CI{S2P(OMe),)1, 3.607 NbC6HI9Cl3N2 Nb(NMe,),CI,, 2. 163 NbC6N6S6 [Nb(NCS),j-, 3,624 [Nb(NCS),]*-, 3,645 [Nb(SCN),]-, 3,624 NbC6N6Seb [Nb(NCSe),] ,3,624 [Nb(NCSe)6]2 ,3,645 NbC,O, [Nb(CO),]-, 3,684 bC601

3

[Nb(C,0,)30]1-, 1.82; 3. 634 NbCsBrsO, NbBrS(MeCO,Ph). 3.603 NbC8H~CI3F3O3S [NbOCl3(CF3COCHCO&=CHCH=CH~)]-, 3,633 NbCRHsC1203 NbCG(CO),(Cp), 3,666 NbCsHJ203 NbI,(CO),(Cp), .~ . . 3,666 NbC8H;03 [Nb(CO),(Cp)lz-, 3; 685 N bCRH6Br4NZ N~B~~(M~C 3,642 N),, NbCsH603 [NbH(CO),(Cp)]-, 3,685 NbCsHizSs Nb(S2CMe),, 3,651 NbCsHi6Br2S3 3. 626 NbSBrZ(-H2),. N bC8H16Br4S4 NbBr4(SCH2CH2SCH2CH2)23.644 NbCsHi6CI,O5 NbC13(OMe),(acac), 3.6117 NbC,HI,Cl,OZ NbCI,(THF),, 3,641.644 NbCSHl6CI4S4 NbCI4($CH2CH2SCH2CH2)z. 3,644 NbCsni614S4 Nb14(sCHzCH2SCH2(?Hz)z.3.643 NbCsHl8CI304 NbCI,(OEt),(AcOEt). 3. hob

NbC,H,,C15Nz NbCI,(NEt,)(MeCN), 3, 597 NbCSH&lO, NbCl(OEt),. 3.606 NbCaHmO, Nb(OEtI4, 3,649 NbCsNs [Nb(CN)8]4-. 2.9, 11; 3,644,645 [Nb(CN),IS- 2 - 9 11; 3,666 NbC,H,O, Nh(CO),(Cpj, 3,682 NbC, ,H,Cl,N1O NbOU13(bipy),3, 629 NhCioH&I,N, NbCI,(bipy), 3, 597 NbC,,,Hl0Br,N2 NbBrJpy),. 3,641 NbCloHIoCIO NbOCI(Cp),. 3.632 KbCl0HloC10, Nb(0,)CI(Cpj2, 3,636,6,321,329 NbCloHloCISz NbCp,(S,)CI, 2,533,539 YhCl,lEl,~lClz NbC12(Cp)Z.3.632 NhCinH ioF4N2 NbF4(py)2,3, 640 N~CIOHI~CJZO~ NbC12(acac)l, 3,650 NbCiuH1405 YbO(acac),. 3, 644.646 NbCloH23ClN04 NbCl(OEt),(MeCK), 3,606 NbCioHz,Os Nb(OEt)S, 3.600 NbCioIim% Nb(NBu1)(NMe,),, 2, 165; 3,613 "JCIOH~ON~ Nb(YMe,)+ 1.40; 2, 163, 164,168, 172, 179; 3,6419 NbCi i H oNS2 Nb(SiICN(Cph, 3,638 . . . N bC H; N~CU,(COIH. 5.931 NbCllH;3N203 YbO(ONMeNOj(Cp)z, 3,632 NbCiiHi3Sz NbCp,(S,)Me, 2,533; 3,638 NbC11HT3Se2 Nb(Se,)Me(Cp),. 3.638 NbCi I H ~ &

Nh(NNMe2)(SZCNMe2)3,3,614 NhC12HBN206

[Nb(O,),(phen)J ,2,319,3,63.5 NbCl zHxNz08 IN~(U,),(Z-P~.CO,),]-,6 , 329 NbC12HIOliIOZ Nb(CNO),(Cp),, 3. h45 hbGzHwNS, Nb(SCYjZ(Cp),. 3,645 NbC12HliC15N3 NbCl,(bipy)(MeCN), 3,596 NbCizH12 Nb(q6-C6H6)2,3,683 NbC12Hj3CIzN20 NbOCI,(OEt)(bipy), 3,632 NbCl2Hi4Cl4N2 NbCI,(4-pi~oline)~,3,644 UhC,,t 1,,NO NbMc,(Cp)z(NO), 3, 632 NbCiZH,,S? Nb(SMe),(Cp),. 3.652 N bC,,H2dN20i2 [Nb(N03),( 18-crown-6)]+,3, 1092

Nb(NCS),(bipy),. 3,645 NbCzsHwNs Nb(NCjH,o)j. 1 . K N~C,~HZ~CI~F NbCl,(dppej, 3, 600 NbC2,Hi8Br2M3O3 NbBr2(8-quinolinolate),, 3, 606 NbCzaHzoOs [Nh(tropolonate),]", 3, 604 NbC28H30C14P2 NbCI4(PPhzEt),, 3,642 NbC,,H,,N,O, (NbtBu)(Cp)zJ,(rV'2)(02), 3,655 NbGoH2505 Nb(OPh)5, 2.340: 3- 6113 N bC3oHaSOg Nb(OEt)(tmpolnnatej,, 3, 604 NbC3,HI6Br3N8 Nb(phthalocyanine)Br,. 2,861,865 NbC32H16C12Xs Nb(phthalocyanine)Cl,, 2.865 NbC33H~706 Nb(Bn'COCHCOBu'),, 2, 373 N~C~~H~OCI~O~P~ NbOCI,(OPPh3),, 2,501; 3,630 NbC39H30N30?

NbO{PhC(OjN(O)Ph},, 3,632 NbCI,,I-I,,04 Nb( 1 -adamantyloxy),. 3, 650 NbC44H2aBr2N, NbBr,(tetraphenylporphyriri), 2, 325 NbC44Hz8Br2N402 NbBr,(tetraphenylporphyrinj(O,), 2, 323 NbC44H2aC1,N4 Nb(tetraphenylporphyrin)Cl,, 2,825 NbC44H28C13N4 Nb(tetraphenylporphyrin)CI,, 2,825 NbC44H7608

Nb(Bu'COCHCOBu'),, I , 93,94; 3,650 NbC,hH3lN,O3 NbO(tetraphcnyIporphyrinaro)(OAcj, 2,825; 3,633 NbCd8HSP4 Nb(P(C6H11)2)4r3,653 NbC4SH88P4 Nb{P(C.8ii)z)4.3,665 NbC4&3jN403

453

Cumirlative Formula Index

NbO(tetraphenylporphyrinato)(acac). 2. 825; 3,621 NbCIz0 NbOCI,, 3,646 NbCIzSZ Nb(SZ)CIz,3,646 NbC130 NbOCI3,2,488; 3,625 NbCI3O2 [NbOZCl3]“, 3,628 NbC13S NbSCIl, 3,626 NbCI, NbCI,, 3,640 NbC1,O [NhOC14]-. 3,606, 628 NbCI,S [NbSCI4]-,3,596 NbCI, NbCI5, 3, 589,590,625 NbCI5N3 [NbCI,N,]-, 2,229; 3,619 NbC1,O [NbOC15]2-,3,603,627 [NbOCl,l3-, 3,646 NbCI, [NbCI6]-, 3.590,593 [NhCI6l2-, 1,271; 3,644 NbFO, NW2F, 3,625 [NbO,F]-, 3,646 NbFzN NbF2N, 3,620 NbF30, [Nb(Oz)zF31Z-,3.637 NbF, NbF,, 3,640 [NbF,]“, 3, 592 NbF,O [NbOF,]-, 3,627 NbF5 NhF5,2,680; 3, 589, S90 NhF,O [NhOF5]z-,1 , SO; 3,591,626;6. 813 NbF,02 [Nb(O,)F,IZ-, 1, 76; 2,319: 3. 637 N bF, [NbF6]-, 3,592; 6,813 [NbF6I2-,6, 854 NbF,O [NbOF,l3-, 1,73; 3,626 NbF,02 [Nb(0,)E613 ,3,636 NhF, [NbF,]’-, 1,72; 3,591 [NbF,13-, 3, 64U NbhsP, [Nb(PF3),]-, 3,684 WbGaCls NbGaCls, 3,593 NbH2CI,0, [NbOC1,(H,O)]Z~,3,643.636 NbHZF403 [Nb(Oz)F,(HzO)I-, 3,636 NbH,O, Nb(O,)(OH)z, 3,635 NbH50, Nb(C)Ii)s,6,944 NbHg3C25114oN3S6 Nb(Cp)Z(HgSZCNEt2)3.2.3:3.639 NbIN NbNI, 3,654 NbIzO NbOlz, 3,626,646

NbZC9H2709

NbI3 NbI,. 3: 655 Nb130 NbO13,3,626 NbI, NbI,. 3.640 NbIS Nb15. 3.589.590 NbMgOB [MgNb(n,),]-. 2,319 NbN4C),3 NbO(NO,),. 3.638 NbOS3 [NbOS3]”-, 2, 524; 3,626,638 NbO& [ ~ b o , s , j 3 - ,3,626,638

Pl;b05P NbOP04, 3,639 NbOs [Nb(O,),]”, 3,635 NbOgSz [Nb(SO,)z]-, 3,666 NbS, NbS,, 3.654 NbS, iNhX,J3-. 2,524 NbS,TI, Tl3NbS4,2,521 NbSbCl ,o NbSbCl,,. 3. 591 N bSbF, NbF5-SbF5.2.678 NbSe, NbSez. 3, 654 NbSe, NbSe,, 3, 654 NbSe,TI, ‘Tl,NbSe,: 2.521 N bSiC,oH29N, Nh(NMe,),(Ct IISIMc3),3,653 NbSiC17112501

Nb(CH,Sihle,)(~’-CO,)(~~s-CpMe),. 3,666 NbSnC,,K,,O KbCp,(CO)(SnPh,), 2, 19 NbTaCloH,,O,, NbTa(OMe),,, 3,601 NbTaF,, [NbTaF,,]-. 3: 592 NbZnC15H17 NbH,(Cp),Zn(Cp), 3,639 Nb,AsaC20H,2C1, Nb,CI,(diars),, 3,656 N b,Br, [Kh2Hr,l3-, 3,655 Nh2C,F608 [Nb,[02)2F,(Cz04)12-,3,636 N b,C,H,CI,,jNiSi NbzClio{I‘-C2H4(SCN),}, 3,624 Nb2C4H8C18S 3,655 [NbzCb{WEEHz}]’, Nb2C6H,,CI,S, Nb2C[6(SMez)3, 3,657 Nb2C8Cl,0s [Nb,(CO),CI,]-, 3,681 Nb,C8H,,CI,N,S, { NbSC12(McCN)z}2, 3, 647 Nh2C,H IZC1GN4

(NbCl,(?vleNC)),(NCMeCMeN), 2, 168 N b2C8H,2CI,N4

INb2ClH(MeCN),(p-NCMeCMeN)I2. 3 , hl5 NbX8HizN4 (MeCN)Nb{NC(Me)C(Me)N)”(MeCN): 2,265 NbZC9H2709

Cumulative Formula Index [Nb,(OMe),]-, 3, 649 NWioHzoC1ioS4 NbzCllo(tetrathia[ 14]crown-4), 2,934; 3.596 Nb~CioH30010 {Nb(OMe),},, 2,347,348 N~~CI~HBCI&

INbCI,(1,2-SZC6H4)12,3,652

[Nb3(11-C1)6(116-C,Me6)311, +,143 [Nb3C16(C6Me6)3]z-. 3, 669 Nb3C4zH78017 [Nb302(02CBut)6(THF)3]+, 3,664 Nb3C107 Nb307CI,3,626 Nb,CI,Se, Nb3SesU1,, 3.647 Nb3CI8 Nb3C18. 3.667 Nb3F0, Nb307F, 3,625 Nb3H60z9Ss [N~~O~(SO~)~(OH 1, Z145; ) ~ 3,668 ]~-, Nb318 Nb&, 3, 667 Nb3RhW9CRH12040Si [Rh(cod)(SiW,Nb,0,,)]6-, 3, 1047 Nb3RhWyC10H15040Si [Kh(CSMeS)(SiW9Nb3O4U)j5, 3, 1047 Nb4C8kTlZRrloN,Se3 Nb4Br,o(Scz)(Se)(McCN)4,2, 667; 3,648 Nb4C8Hl,Br Nb4(MeCIV),Br10Seq, 2, 667 Nbd&H4&112

{NbC13(PhC=CPh)}4.3,656,659

454

455

[Nd{2.6-(0,C),py)3]3--,3, lo90 NdC,,H3ON,O, LNd(NO3)(H2O),(fi=CMe&CHCH=CHCC(Me)=

NCH2CH2N=CMe(2,6-py)C(Me)=NCHz. .

eH2}l2-,3, 1096 NdC&5JsOs [Nd(DMF)J3+,1,285; 3, 1086 NdCz7H6d909 [Nd(DMF),j3-, 1,285 NdC2sH50N30 Nd(NPr',),(THF). 3, 1072 NdC33H46N901

2

Nd(N03)3(0C3HN2Me2Ph),, 1, Y7 NdC:&&!qO Nd(octacthylporphyrin)(OH), 2, 822 NdGcH,odic@J', [Nd(HMPA)6]3t, 3.1084 N~C~OH~ONSOS [ N d ( p y W o ~ i d e ) ~ ]1,84; ~ + , 2,496; 3,1081 NdC54H33F909P&

Nd($CH=CHCH=cCOCF3)3(OPPh3)2. 3,1083 NdCuH33Ni6 Nd(phthalocyanine)(H-phthalocyanine), 2.865: 3.1095 NdCI, NdCI3,3: 1110 NdCI30 Nd(C104)3.3. 1108 NdF4

Nb90zsP Nb902jP,3,639 Nbioozs [Nb,,,0,,]6~~, 3, 1029 Nb12NiOJR [NiNb12038]'2-.5, 296 NdC,H,O, Nd(O,CH),, 3. 1131 NdC6r*i,N,Oi,

Nd(N03)3{H(OCH2CH2)30H}I 3 , 1093 NdC"H1,CIZO2 NdCI,(THF),, 3. 11 10

[NdF,]-, 3.1 I35 NdF7 [NdF,I3-* 3, 1115, 1116 NdH06P2 NdHP206.3. 1076 NdHBN301 Nd(NO,),(H20)4, 3, 1086 NdH1~Cl20~ (NdCl2(0H,),] +,2,297 NdH,,Br,O,, Yd(BJ&)(Ii2cl)9, 3, 1074 NdHwO, INd(H,0),13"', 3, 1074 NdI,O, N L I ( I O ~3, ) ~1076 , NdMoReO, Nd(02Mo02)(02Re02), 2,426 NdN309 Nd(NO&. 3. 1108 N~NsOIS [Nd(NO3),IZ-, 3, 1076 ~

'

Nd014P5

Nd(P50,,), 6, 1027 NdzCioHiJ'Jto02a [Nd,(N03)s(H20)4(bipy)]2-, 3. 1086 N~~G~HMNu Nd,(phthaIogat~inc)~. 3, 1095 N&OuS, Nd,(SO,),, 1,2061 NdAOi2 Ndx(S04)3,3, 1086

N~~C~IH~I~CIOI~

Cumulative Formula Index

456

[Ni(diars),Cl]+. 5 - 6 7 N~~S,C,~H~~C~, [NiCl,(diars),]+, 5- 5 , 289,299 [NiCI,(diar~)~l~+. 5,289 N ~ ; ~ S ~ C J & I ~-; NiI,(diars),, 5. 124, 125 NiAs4C21H32N [Ni(CN)(diars)?]+, 5, 118 NiAs4CdL02 Ni(CO),(diars),, 5, 11 NiAs&~Hd,3r [NiBr(McPhhsCH2CH2AsPhMe),l', 5,119 N iAs4C,,Hd4 Ni(AsMeiPh),, 5,4 NiAs4C,oH,,CI, NiCl, { 2,2'-(MeAs),biphenyl) 2 , 5 , 124 NiAs4C44H40N8 ,~

NiAsC,H,,N,S [Ni(NCS) { N(CH2CH2NEt2)2(CH2CH&Ph2)}] *,5, 135 NiAsC2XH42NSS2 Ni{Ph2AsCH,CH2N(CH2CHlNEt2)2}(NCS)2, 5,64 NihsCqaHiaPS? -. - . [Ni{MeAs(CiH4SMe-2),} {PPh2(C6H4SMe-2))]2f, 5, 66,67 NiAs2C6HI4Cl2 NiCI,(Me,AsCH=CHAsMe,) 5,119 N~AS,C~~H,~S~ 5,130 [Ni{(Me2AsCH2CH2CH2SCH2)2CH2)]*--, ?JiAs2CI8HZ9N2P Ni(CN)2{PhP(CHzCH2CH2AsMe2)2}> 5.67, 125 NiAs2C,,H,,N,

[Ni{(Ph2AsCH2CHzNMeCH2j2}12+, 5.130 N~ASZC~~H~~S~ Ni(2-SC,,H4AsPh2),, 1, 432 NiCl,(OAsPh3),, 5,62, 159 N~AS,C~~H~,O~ Ni,(acac),(OAsPh,). 5 . 143 NiAs2C42H38NZ02 PG(~-OC~H~CH=NCHZCH~ASP~&, 5 - 190 NiAs2FeC15H20120 NiI,(CO){Fe(qS-Me,AsC,H,)2}, 5 , 124 NiA& 1H27Br2 5 , 67,125 NiBr,{ MeAs(CH2CH2CH2AsR;ie2)2}. NiAs,C,,H,,+J,N NiCI,{N(CII,C~-I,AsMe,)~},5, 54 NiAs3C13H27NLS2 Ni(NCS),(MeC(CH,AsMe,),), 5 , 133 xiAS3C15H36CIP lNiCl(P(CH2CH2CH2AsMe2)3)j+l 5?66 NiAs3C,6H36NP [Ni(CN){P(CH2CH2CH2AsMe2),)]' 5 : 135 NiAs,C,,H,,BrN

5 , 43 [N~{N(CH2CH2AsPhZ)3}]'. NiAs3C,,H44N0 [Ni(COMe){N(CH,CI~,AsPh,),)l+, 5 , 138 NIAS~C~~H~~N [NiPh{ N(CH,CH,AsPh,),] . 5 . 138 Y~AS~C~OH~~NP [Ni{N(CH2CH2AsPh2)3}(PPh,)]+. 5.41. 42 NiAs3SbC,,H,,CI [Ni{Sb(C6H4AsMe2-2)3}Cl]+, 5,66 N~AS,S~C,~H~~NS [Ni { Sb(C6H4AsMe2-2),}(NCS)]+. 5.66 NiAs4CI2Hz8Br2 NiBr(MezAsCH=CHAsMe,)z7 5 , 119 NiAs4CIZH&I2O Ni(CI04),(OAsMc3)4, 2,500 NiAs4C1SH36CI [NiCI{As(CH,CH,CH,AsMe,),)l ' , 5 , 6 6 N~AS.,C~~I-~~~ Ni(diars),, 5 , 9 [Ni(diar~)~]~', 5,66,289 N~AS~C~~H~~CI +

[N~(M~P~ASCH,CH,ASP~M~),(TCNE),]~+, 5 . 1 19 N~AS,C~~H~~NO~ [Ni( 0ASPh,Me),(KO,)]-, 5 , 6 5 N~As~C~~H;,CIO~ [Ni(OAsPh,Me),(ClO,)]+, 5,51,64 NiAs4CS4H4,Br [NIBr(As(C,tl,AsPh,-2),)11,5,66, 133 NiAs4C,,H,,CI [NiCI{As(C6H,AsPh,-2),)1', 5 , 66 NiAs,C,,H,, Ni(AsPh&, 5 . 9 NiAs4C7,H,,CL0, [NI(CIO,)(OAsPh,),]-, 5.64, 152 NiAs4C7,H,,C1,0,, Ni(C104)2(OAsPh3)412,500 NiAssC,,H4,0s [Ni(OAsMe,),12+, 2,499; 5.3,64, 159

[Ni(diars){MeAs(C,H,AsMe,-2),}]*+,5,66,67, 128 Niks6C2,H5& N ~ C I , { M C C ( C H , A S M ~ ~5, ) ~133 )~. NiAS&7&1h606 [Ni{(OAsPh,)2CH2),]2+, 5,161

NiB2C HY2F4N,6i

Ni{d=CMeC(Me)=NOBF,ON=CMeC(

m). 6. 185

Me)=N-

NiB,C12H16N- ' Ni{H2B(N=H),),, 2,252; 5 , 102 NiB2C16H2& Ni{ H,B(&N==CHCH=cH)(NN=CMeCH=chk)} '

5.102 -, ---

Ni { Me,B( &N=CHCH=cH),},, 2,252 NiB2C1~H~ON12 Ni{HB(~N=CHCH=f?H),},, 5,102 NiB2CZOH& Ni{Et2B(N*H),}2, 2,246,252; 5 . 102. NiB2C2.,H2 N B Ni{B(N-H),), 5, 102 NiB2C32H32N404 Ni{fi=CMeC Me)=NOBPh,ON=CMcC(Me)=N6 , I85

d),

,

457

Cumulative Formula Zrzdex

Ni(Ph2B(~N=CHCH=tH)2}z, 2,252; 5 , 102 NiB3Cl8Hz4N12 [Ni{H,B(fiN=CHCH=tH)2}3, 5 , 102

NiBaO, BaNi03, 5,297 NiBrNO NiBr(NO), S, 13 NiBr3 INiBr,]" , 5 , 187 NiRr, [NiBr412-,5,187 NiCH3C10 Ni(OMe)Cl, 5 , 140 NiCH5N04 Ni(OMe)(OH)2(NO)I 5,107 NiCN60 Ni(CO)(N,),, 1. 28 NiCzF602Pz Ni(CO)Z(PF3)Z,5, 11 NiC,F,O,S, Ni(03SCFR)2,5 , 154 NiC2H2O4 Ni(O,CH),, 5, 155 NiCZH2S2 Ni(SlC2HJ, 5.67 NiCZH30Z [Ni(OAc)]+, 5,155 NiC2H4N,S4 Ni(S2CNHz)2,5 , 67 NiC2H4N402S4 Ni{SN=SNCH(OH)CH(OH)NS==NS}, 1,446 NiC2H5CIzNS NiCI,(MeC:(S)NH,), 2,647 NiC&,C120S Ni(DMSO)CI,, 2,641 NiC2H6N4S4 Ni(SZN2Mc),,5,212 NiC2H602 Ni(OMe)2, 5 , 140 NiCJ I6O6S2 Ni(03SMe),, 5,154 NiC2H6S2 Ni(SMe),, 5 , 168 NiC2H8N2 [Ni(en)l", 1,553 NiC2H,NBS2 Ni{H2NNC(S)NH,}z, 5,210 NiC2H9N5SZ Ni(NCS)2(NH3)3,5 , 70 NiC2H.,oC1,N,0~S2 Ni{H,NC(S)NHNH,},(ClO&, 2.803 NiC2HloCI2N6S2 Ni{ €i2NC(S)NHNH2)2C12, 2,803 NiCZH,,N6S2 [Ni{H2NNHC(S)NH,)2]2-, 5,210 NiC,HlnP2 Ni(PH3),(C2H4), 5 . 17 NiC2Ht2CIzN4 NiC12(MeNHNH2)2.5,77

Ni(en)(H,O),(SO,). 5 . 106 NiC2N,S2 Ni(NCS),, 2,227 NiCzS6 [Ni(CS3),12-, 2,646; 5, 172. 176

NiC2SB [Ni(CS4),IZ-, 2,646 NiC3H3S2 Ni(HCSCHCHS). 5,67 NiC3H4CI2N2 Ni(HfiCH=NCH=~H)Cl,, 5 , 8 3 NiC3HI8Cl2N6S3 Ni{SC(NHNH2)2}3C1z,2,803 N iC IO [YiI(CO),]-. 6,279 NiC3N203 Ni(CO),(N,), 5 , 2 8 NiC3N, [Ni(CN),]'-. 5 . 37 NiC3N3S3 {Ni(NCS),]-, 5, 104 NiC3N40 [Ni(CN),(NO)]'-, 2,111; 5,6,37,107 NiC4C12N4 [Ni(CN)4C12]3-.5.290 [Ni(CN)4C12]5-.5.290 NiC,FI,N,OA [Ni(S,CCHYO,),I2-, 5,176 NiC4E3,05 Ni(02CCOCH2C02),6,455 NiC,HaCI,N 1 o i%{ IJ,NC(=~'rr,I)N~~C(=NH)NH,},Cl,]+,5.291 NiC4H4N402S4 [Ni(NCS),(H20),lZ-, 5, 104 KiC4H4010 [Ni(C20&(OHz),]2-, 5.158 NiC4H4S4 Ni(S2C2H2),, 2,596,614,617,620,621,631; 5 . 179 [Ni(SzC2H2)2]2-,2,596 [Ni(S2C2H2)2]4i,2,596 NiCaI16C12N2 N i ( M e ~ ~ , ~ = N C H = ~ H ) C 5,83 l,, Ni(IkCMeNHCH&H)CI,, 5,83 NiC,H,Cl,N,O, Ni(CIC)4)2(McCN),,5 , 152 Ni(02CI02)2(MeCN),, 5 , 105 NiC4H6N2Sa lNi(MeN=~(s)C(s)=NMe)],, 1,126 NiC4H6N4O4 Ni(HON=CHCH=N0)2, 5,99 NiC4H6N604 [Ni(HNCONHCONH)2]2-,5 , 165 NiC4H602SZ Ni(AcS),, 2,645 NiC4H604 Ni(OAc)2, 6 . 1019 NiC4H,N203 [Ni(H2NCH2CONHCH2C02)]+, 2.760 NiC4HBN2O2S2 Ni(SOCCH,NH2'),, . . . 5,219 NiC4H8N6S4 ~i{SC(NH,)=NC(NI~z)~}z, 2,640 Ni{(H2N)2CS),(NCS),, 2,639; 5 , 185 NiC,H802S2 Ni{MeC(S)=NOH},, 5,214 NiC4H8O7 Yi{(S)-0,CCH2CH(OH)C02}(H20)2, 2,475 NiC4H8S4 [Ni(SCH2CH2S)2]z--,5,170 NiC4H9N06 Ni(0,CCH(NH2)CH,COz}(H,0),. 5.220 NICAH I , C l 2 f r i 2 0 2 NiCIJHCONHMc),, 2,492 NiC4Hi&&N6O4 Ni(H2NCONHCONH2)2C12,5,165 NiC,HlnN,O, [Ni(gONCOCH2NH2)2]Z+, 5,165 NiC4HloN8O2 -

*

I

NiC4HloNsOz

4%

Cumulative Formula lndex

[Ni{H,NC(GNH)NC(0)YH,)21+: . . . ~ _ ~3,291 _ Nk4Hl&,S4' Ni(HzNC(S)NHNHz},(SCN),, 2. 803 NiC,H,,O,P,S, [Ni{S~P(0)Et}2]Z-, 5, 172 NiC4Hl0O,S Ni{ (OzCCH2)zS}(HzO),,5,216 NiC4HIOS2 Ni(SEt),, 5, 168 NiC,H.,,CI,O, Ni(02CCHZC1)2(OH2)4. S, 155 NiC4HI2ClEP4 Ni(PCI,Me),, 5 , 8 NiC,I-I,2Nz0, Ni(Gly-O)z(H,O)z, 5,219 N iC,H 12N2SZ Ni(SCH2CH2NH2),, 1,417,445; 2?554. 799; 5,208,209 NiC4Hl2O4PZS4 Ni{(Me0)2PS2}2.2,644; 5, 175 NiC4Hlz0,P2 Ni{O,P(OMe),),, 5, 154 NiC4Hl4N,OZ [Ni(HOCHZCHZNH2)z]Z', 5,214 PiiC4HI4N4O4 Ni(Gly-O),(NH,),, 5,219 NiC,H,,NI, [Ni{ H,NC(=NH)NHC(=NH)NH,}3]z*22,284 NiC4R40, Ni(OAc),(H,O),, 5, 155 NiC4HI6ClZN4 [Ni(en),CI,]+, 5,290 NiC4HI6Cl2N8S4 Ki(H2NCSNH2)4C12, 2, 639; 5,59.61. 185 NiC4Hi6N4 [Ni(en),I2+, 1,553; 2,33.902: 5 . 7 2 , 823; 6,150, 163 NiC,H,,N,O,S, Ni(S203)(H2NCSNH2)4,5. 153 NiC1H16N502 Ni(en),(ONC)), 2, 32 [hl(N02)(en)2]', 5. 72, 151 NCHiJ'Jd), [Ni(NO,)(en),1", 5, 149 NC,H,,N,O, Ni(N02)2(cn)2,2,32; 5, 72. 150 NiC4Hl,N,0, Ni(N~O,),(en),, 5, 149 NiC,H,,N,O,S, Ni(tu)4(0Sz02).2,431 NiC4HL0N4O2 [Ni(~n),(H,0),]~+,5,72 NiC4N202 [Ni(CN)z(C0),12-, 5 , h NiC4N4 [Ni(CN),]-, 5,290 [Ni(CN)# , 2 , 9 , 10, 12; 5,4.h . 7.67. Ir8.69.70,290: 6 , 110,822,873 [Ni(CN)d]'-, 5, 37 INi(CN),I4-, 5 , 6 , 7 KiC,N,O, [Ni(CNO),IZ-, 2, 13 NiC,N4S4 [Ni(NCS),I2-, 5, 104 [Ni(NCS),I4-, 1. 470 [Ni{S,CN(CN)},IZ-, 5, 175 NiC4NJSel [E;i(NCSe)4]2-,5 , 104 NiC,O, Ni(CO),, I , 288,289: 2,452; 5,6: 6.768 Ni(C404),2,455 YiC404S4 (Ni(S,C202)212-.2,645; 5, 181 NiC5H5Br3N [NiBr3(py)]-. 5,78

NiC5HSCI,N NiClJpy), 5.78 NiC,H5N0 NiCp(NO), 2: 103 NiC5H9Nz0, [Ni (H2NCH2CONHCH(Me)C0,}]+, 2,760 [Ni(H2NCH2CONHCH2CH2COz)]+, 2,760 NiC,N, [Ni(CN),13-. 1,10.206,207; 2 , 9 , 10; 5,3,69,70 NiC,H,N, [Ni(2-pSCK)l2', 6,453 NiC6,11hNOh [Ni{N(CH,CO,),}1-. 2.789; 5,219 Nk,H6N4 Ni(flCH=NCH=CHJ,. 5,86 Ni($TN=CHCH=cH),. , - 5,82 NiC,H,S, Ni(HCSCHSCHh. 2.617.621 _

-

I

_

[Ni{H2K(CH2CONH)2CH,C0,)I+,2.761 NiC6HION4S4 Ni(H2NCSCHCSNH2)2,5 , 183 Ni{MeC(S)NH,)l(~CS),, 2, 047 NiC61I,,O,S, Ni(SC(S)OEtj2. 2,588 NiC,H,nOzSe, Ni(Se2COEt),, 5. t73 NiC6HllN3 Ni(CN),(Et,NH), 5- 70 NiC,H, lNiO

[Ni{MeC(=NO)C(hle)=NCH2CH2NH}]2+, 5,294 NiC6H,,N,0,SI Ni{HSCH,Cfi(NH,)CO,},, NiC,H,,YJ,O

2,746

[N~{MCC(=NO)C(M~)=NCH,CH~CH~NH,}]~+. 5,244 NiC6HI2N3O6 [Ni(Gly-O),]-, 5. 219 Ni(02C:C~12NCOCH2NCCCH2NI 12)(t-120)2, 5,291 NiC6HI6NZO6 Ni(O,CCH,CH,NH,)z(H,O),. 5,219 Ni(02CCH2NHMe)2(H20)z, 5,220 NiC6Hl6N2O6 Ni { OzCCH(NHJ CH,OH} 2( H20)2,5,219 NiC6H16N402 Ni(G1y-O),(en), 5,219 NiC6HI6N4O4 Ni(O,N),(TMEDA), 5,151 NlC6 H16 N 4 0 6 Ni(N0,)2(Mereri), 5 , 149 NiChHI6N6S2 Ni(en),(NCS),, 2 , 3 2 ; 5,59,72 N iCBHI& [Ni{i HN=C(NH2)NHC(NH2)=NCH,),)]2-,5,101 NiCd l,&rN, [Ni{N(C~.I,CH,NI13)3}Br]+,5,75 NiC6H18BrZN202 NiBr2(ONMe3),, 5, 164 NiC6H18Br2P2 NiBr2(PMe,)2, 5, 110 NiC6Hi8Cl3P2 Ni(PMe3)2C13.5.299 NiC6Hl8T2N1S2 Ni(MeSCH2CH2NH,),I,. 5,208 NiC,H *N2O3P2 Ni(N0,)(€iO)(PMeS)2. 5, 14 NiC6Hi8N4 [Ni(H,NCH,CH2NHCH2CH2NHCHzCH2NH2)]+ 2, ~

~

54

[N~{H,NCH~CH~NHCH~CH~NHCH,CH,N~~,).]~+, 2, 54

459

Cumulative Formula Index

NiC8H24N2P4S4

[Ni{(H2NCH,CH2NHCH2)s}]2+, 5,74,76 NiC6WisN60i2 [Ni(MeN02)6]2+, 5 , 141 NiC6H2&l3N4 Ni(~n)~Cl,, 6, 150 NiC6H2& [ N ~ { H Z N ( C H ~ ) ~ N H ~2.4s }Z]~+, NiC6H20N@2 [Ni(Gly-O)(en),]+. 5,219 NiC6HZiN303 [Ni(HOCH,CH,NH,),]", 5,214 NiCbW24Br2Ni2S6 Ni(H2NCSNF1,),Br2, 5 , 184 NiC6H24N402 i2I2l2+, 2,45 [Ni{H2N(CH2)3NH2}2(01 NiC6H24N6 [Ni(en),]", 1,450.553; 2.32.901; 5, 3,60,71,95, 106, 226; 6,163,164 INi(en)?l3+'.2, 33

NiCaH,,Br2N4 Ni(r;[==CMeNHCH=cH)2Br2, 5 , 8 3 NiCSHl2CI2N4 Ni(HfiN=CHCH=cMe)2C12, 5,83 Ni(Me&CH=NCH=cH)2C12, 5,83 NiC8H1,CIZN40s Ni(C104)z(MeCN)4,5 , 152 NiCsHl2NI& {Ni(NCSh(NHd}4.5,70 NiCaHltS4 Ni(S2C2MeZ)2r2,614 [ N I { S ~ C ~ M 5,45 ~~)~~~-, NiC8HI2S9 Ni,(S,CMe)(S,CMe),, 5 , 174 NiC8Hl3N4O5

[Ni(Nco),],-, 5, 104 NiCBN& [Ni(NCS),I4- ,5 , 104 NiC6N6Se6 [Ni(NCSe)6]4-,5,104 NiC60i2 [Ni(C2O4),I4-,5 , 5 8 NiC6SI0 Ni(S2C2S2CS)2r 2,621.625; 5. 181 [Ni(S2C2S2CS)2]-,2,624 [Ni(S2C2S2CS)2]2-, 2,624 NiC,H,,ITe NiCo(TeMe7U.2,669 -, NiC,H,;N,O, Ni(C404)(H$JCH=NCfl=~I1)2(H20)2,5, 159 NiC,H,,CI,OP, N/CI;(CO)(PM~,),,5.112 NiC,H1810P2 Ni12(CO)(PMeq)2,5. 112 NiC7HZ0N4 [Ni{(H2NCH2CH2NHCH2),CH2}I2+. 5,74,76 NiCsFI2S4 Ni{S2C2(CF3)2}Zr 2,614; 5.178, 179.180 [Ni{S,C,(CF,),},]-, 5, 179. 180. 299 N
N k a H l~ci104P2s4

Ni{ oN=C( Me)C(Me)=N OBF20N=C( Me)C(Me)= m F z } . 1.453

[Ni{H2N(CH2CONH)3CH2C02}]2-, 2,763 NiC,H,,N,S Ni{(SCH,CH,N=CMe),}, 5,207 NiCaHi,N404 Ni(HDMG)2, 1, 120,453,525;2,271,798; 5,4.99: 6, 185 NiCsH14N406 Ni(H,NCH2CONHCH2COZj2,2,760 [Ni(H,NCH2CONHCH2C0212-, 2,763 ~. NiC(ClCH,Cn,~),PS,},, 2,644 NiC8HI6NZO4SZ Ni(02CCH2SCH2CH2NHJ2,1,445; 5,208 NiC8H1&,SZ Ni(NCS)2{(H2NCHzCH2NHCH2)2}, 5,74,76 Ni(NCSI2{N(CH2CH2NH2)3},5,74 NiCsHI8O2P2 Ni(COI+(PMed2, - 5, 11 NiC,fI,,P& h'i(PMe3){SC(S)$C(PMe,)$}, 5,26 NiC.H,,N,O, INi { O,CCH,N (CH,CH,CF),NH) (H20)2]+.5,221 [Ni ( 02CCH2N(CH2),NH( H2)3)(H20)2Jf, 5,157 NiCsH20Br204Sz NiRr,{(l-10CH2CH2)2S}2, 5,216 NiC,H~,1,N,04~ 2,270 NiCl, 1N(OHl=CHMe NiC,H;iCl;K,S4 NiCI2{MeC(S)NH2},,2,647 NiC8HZ0NZS2 Ni(SCH2CH2NMe2),, ~. 5,209 NiC8H20Ni ~Ni(l,4,7110-tetraazacyclododecane)~3+, 5.296 . ,

,

I

.

~

~

[Ni(3HCH2CH2NHCH2CH2NHCH2CHlNHCH2cH2)]2+,2,912 NiCsHzoN4S4 [Ni{MeC(S)NH2},]2'. 2,647 NiCsH2,,N6O4 Ni(MeNHCHZCH,NHMe),(ONO),, 2,418 P;iCSHZ0O4P2S4 M((Et0)2PS2)2.2,644; 5, 67, 172 NiC8H2003PZSe4 Ni(Se2P(OEt)2}2,5,174 NiCBH2oP2S4 Ni(S2PEt2)2.5, 172 NiCBHz,CIOP, NiCl(COMe)(PMe,),, 5,112, 114

5,216 N;Bri{(H2NCH2CH2)2S}2, NiCsH24C12N408 Ni(Ct04)2(MeNHCH2Cl12NHMe),, 5. 152 NiCRH24C1204 NiCI,(EtOH),, 5,140 NiC,H,,F8N4P4 Ni(PFZNMe2).,,5 , 9 N iCsH24N2P4S4

~

~

NiC8H24N2P4S4

Cumulutive Formula Index

Ni{Me,P(S)NP(S)Me,},, 5 . 183 NiCsH24N406 [N~(AcNH,)~(H,O),]*+. 2.492; 5 , 165 NiC8H24N604 Ni(ON0)2(Me,NCH2CH2NH2)2. 5 , 150 NiC8HZ6N6 [Ni(dien),I2+, 1,553; 5,74,75 NiC8N4SZSe2 Ni{SeC(S)=C(CN)Z)2,2, SO8 NiC N S Ni{S,C,(CN),},, 2,616 [Ni(S,C,(CN),),]-, 2,623,627: 5, 179, 180,299; 6, 147 [Ni(S2C2(CN),},]~~ , 2 , h10,613. 617.623; 5 , 175, 179, 180: 6. 147 [Ni{S,C,(CN),},]3-, 5.44, 179 NiC,O,S, Ni(S2C402),,5, 182 NiC9H7Br3N NiBr,(quinoline), 5,62, 187 NiC9HaCI2N, Ni(8-aminoquino1ine)Cl2,5 , 84 NiC9H10N3S4 [Ni(S2C,(CN),}(S2CNEt2).2,610 NiC9HlJ%O* [Ni{ N(CH,CXl,),} (H,NCH,CO,Mc)]-, 6 , 4 18 NiC9HI3N4O3 [Ni { fi=CHNHCH=k CH,CH( NHCOCH,CH,NH,)CO,}J+, 2.7M NiC,H17N306 Ni{H2NCH2CH2N(CH2C02)2}(H2NCH2C02Me), 6, 418 NiC9H17Te2 [NiCp(TeMe,),]+, 2,669 NiC9H2,N4 [Ni(&HCH2CH2NHCH,CH2NHCH2CH2NHCH,CH&H,)IZ+, 2,912 Ni&HZ4BrN4 [NiBr{N(CH,NMe,),}]+. 5.3.5 I , 65 NiC,I~I,,N,O,

460

NiCInHl2Y6 [Ni{2,9-(HzN~H),bipy}],+, 5,9h [Ni{3.3'-(H,NNH),bipy)lz+, 6, 184 NiCloH13N20a [Ni(Hedta)]-, 2.784 NiC1nH,4N20SP2 Ni(0,PHz)2(py)2.5. 154 NiC10H14N504 [Ni{ P(T=CHNHCH4CH2CH( NHCOCH,NHC0CH,NH,)CO7)1 ' ,2,761

NiCl0HI40S3 Ni(MeCOCHCSMe)(MeCSCHCSMe), 5, 183 NiCl0HI4O2S2 Ni(MeCOCHCShle),, 5,67, 183 Ni{SC(Me)=CHCCOMe},, 6,112 NiCIOH1404 Ni(acac),, 1. 187; 2,371.378,379; 5, 142, 144; 6,205. 248 NiC,,,H& Ni(MeCSCHCShlc),. 5 , 67, 183 [Ni(McCSCHCSMe),]' , 5 , 45 NiCIOHl6Br2O4 Ni(flacac)2RrZ.2,402; 5 . 143 NiCloHl6CIN0P2 Ni(NO)Cl(diphos). 2, 113 NiCloH~6CIN02P2 Ni(NO,)Cl(diphos). 2. 113 NiC1,,Hl6C1,Y4 Ni(HfiN=CMeCH=cMe),CI,, 5,83 Ni(r(l=CMeNMeCH=CH),Cl,, 5,83 NG,Hl&O, Ni{O,CCH,K(CH,CH,CH,),NCH,CO,), 5.22 I NiCloH16N&S Ni(bipy)(H,@),(SO,), 5, 106 NiC, ,&O1 /Ni{(H2NCH2CH2NHCH2)2}(H2NCH2C02Me)]2+, 6, Ni(HZO)(Hlzdta),2.783: 5,218 418 NiCIOHI6N4O4 [Ni{N(CH2CH2NH2),}(H2NCH2CO2Me)l2 ' ,6,418 Ni{ON=CMeC(Et)=NO},, 5.67 NiCBH,,Br,P3 NiBr2(PMe3),,1,45: 5, 66. 110 NiClOHl& Ni(CNBu'),. 5. 7 NiC9H271Z09P3 NiClbHlSN2O2 NiI,{P(OMe),},, 1,45; 5, 115 Ni(O,)(CNBu'),. 2.318,319,320; 5,7,27,28; 6.321. NiC9H27N506S 329 Ni{MeN{P(0)(NMe,),},)(S04)~ 5. 161 NiC,H30C12N60s Ni {H2N(CH2)3NH2}3(C104)2r 571 NiC9H30N6 [Ni(pn),I2+,5,227; 6 , 165 [Ni{H2N(CH2)3NE-12}3]z+. 1.439; 2.45:5,9h,227 NiCloH5N2C) [Ni(Z-cyano-8-quinoIinolate)l-, 6, 453 PJiCl&F6O& Ni(MeC(S)=CHCOCF,J,, 2,642.651 NiCi oHiaNi Ni{MeC(=NH)CHC(=NH)Me},, 5 , 9 8 NiClOHlO NiCl JI, sK 406 NiCp,, 1,274; 2,217,218 Ni(ON02)2(CNBu')2,5,29 NiC1,,HloC12N2 Ni{H,NCH,CONHCHMeC02}2, 2,760 NiCI,(py),, 5,59,78 NI(H~NCH~CONHCH~CH~CO)Z, 2,760 NiCd10N408 Ni(O,NO),(pyridine N-oxide),. 2,497 N1GoHi&'a Ni(&NCHKNCHMeCHMeNNCHNNCHMeCHMe). 5.257 Ni(fiNHCH,NUCMeCMeNNHCH,=Me), 5, [ NiCp(C,H,)] +,2,669 257 NiCloH I IN40aP NiCl,lH,,O, Ni(inosine-5'-monophosphate).5. 59 Ni(~cac),(H~O),. 2, 370, 372,402; 5 , 142 NiCIoHIRPiS2 NiClJIlzN,O& Ni(SH),(diphos), 2, 518 Ni(SO,)(bipy)(H,O),, 5 . 153 %iCl0HI2N2O8 NiC1&,N204S2 [Ni(edta)]*-, 2,783.784; 5,219 Ni{HSCMe2CH(NH,)CO,},, 2.746

Cumulative Formula Index

46 1

Ni{ D-MeSCH,CH,CH( NH2)CO2}(I.MeSCH,CH2CH(NHZ)CO2),2,754 Ni{L-MeSCHzCH2CH(NH2)COz},,2,754 :. 5: 220 Ni{OZCCH(NH2)CH2CH2SMe} NiCloHdzS4 Ni(S,CNEt,),, 5,67.68, 172: 6, 1021 NiCl0HZ0N2Se4 Ni(Se2CNEt&, 5 , 172 NiCdLoN, [Ni{h=CHCH=N(CH&N HCHzCH2NH((?Hz)3]Z+, 5,229 NiClOHZ,~N8 [ Ni{ m=CMeC( Me)=NNHCI i2NHN=CMeC(Mc)= NNHCI-I,NH)]2’.2, YU4:5,230,257; 6 , 182 NiCloH2006 [Ni(Hacac)z(H,O),]”, 2,402: 5 > 143 NiCloH,oS4 [Ni(1,4,8,11-tetrathiacycl0tetradecane)]~+,5, 171,258 Ni(tetrathia[l4]crown-4), 2.934 NiCloH24C12N4 5,234 NiCI2(1,4,8,1l-tetraazacyc~otetradecane), 5,296 [NiCI,( 1,4,8,1I-tetraaza~yclotetradecane)]~, NiC10H24C13N402 Ni(H2NCHzCH2NMe2)3(CCI CO Ni(MeN1 ICHzCH2NIIMe),(CCI, $3,5y ,02), 5,59 NiCIOHZ4IN4 lNiUl.4.8,l I-tetraazacvclotetradecane)l’t,5,238 NikloH2,N202S [Ni($CH2CHzSCH2CI12NHCH2CH,0CH,CH,NHCH2CH2)(H,0)]z+’.5,262

NiC,,H,,CI,N,

[Ni(h=CMcC. Me)=NCH=CHNN==CMeC(Me)= d ) I z ..+ , 6, 182 NiCllHl8NZO3 Ni(OC0,)(CNBut12, , - 5,29 NiC,;H,,N,

[Ni(N=CHCMe2CH2NHCH2CH2NHCH2CH,NHCH2cH2)12+. 6.164 -,_ NiC, 1H26K*;4 [Ni(6,6-dimethyl-l,4,8,1 l-tetraazacyclotridecane)j2”, 5, 711 111

[Ki(fiHCH,CHZNHCH$H CH,NHCH, C H 2 C H 2 N I ~ C H 2 C ~ , ~ H’ ,,2,912 )I2 NiC,,I. IZiN20,P3 Ni(CN),{P(OMe),},, 5, 115 NiC, ,H2,CIOP2Si NiCI(COCH,SiMe3)(PMe3)z, 5,112 NiC,2C1804 [Ni(02C6C14)2]2-, 5, 146 NiC,2HgNz04 Ni(2-pyCOz),. 5 . 106 NiClZH804 Ni[1;2-O2C6H4),,5 >146 5, 146 [Ni(l.2-02C6H4)2]2-r NiCl2H,S4 [Ni(S2CC5H,j,12-, 5, ‘175 Ni(l.2-S2C6H&, 2, 6’15 [Ni(l .2-S2C6H4)2]-r 5, 179 NiCl2HSSel [Ni(I.2-Se&H4)2]-, 2,607 NiC12H.,oI052N404 Ni(benzoquinone dioxime),I,,,,, 6 , 144 NiCl2HloN2O2 [Ni(2-OC6H4NH)z]2-,5,214 NiC10H24N4 NiCY2HlnNZ04S4 [Ni{HP(’CH,CH2NH(C~)3[Ni{SzC=C(CN)COzEt}212-, 6,112 1.198,336,417; 2, NHCHICH,NH( H2)3)12A. NiGZHioN2S2 912; 5,239,289 Ni(2-SC,H,NH)2, 2,800 [Ni(HhCHZCH2NH(CH,),[Ni(2-SChH4NH)2j2, 5,212 NHCH2CH,NH(~H,j,}]”, I . 336 NiCl2HYoN4 lNi{l I ~ C H 2 C H 2 N t l ( ~ H 2 j5.77 J}~~2+~ N i ( l - ~ y c H = N ) ~1,423 , [Ni{H,N(CH,),N(CH,CH2)zN(CI I,)3NH2}]k ’ , 5 , 7 4 NiC12H,,K,02 [ N I ( ~ H C H ~ C H ~ N H C HNHCH,~CH Ni(Z-pyCONH),, 5,98 CHzCH,NHCH2CHz~H2)l2+, 2,912 NiC ,2H1uN.10 [Ni(hHCHzCHzNHCH,CH2NHCH2NI(HON=&H=CHCH=CHc=NO),, 5,991 6,143 C H ~ N H C H ~ C H ~ C H ~ C H2,912 ~))Z+. NiC12H,oS2 NiCIOHZ4N5S Ni(SPh),, 5. 168 [Ni(NCS){N(CH2NMez)3}]+.5 6 5 NiC,;Hl2N2O6 NiCl0HZ4N6o6 Ni(Z-pyC02)z(HzO)2,5,221 [Ni(l,4,8,1l-tetraazacyclotetradecanc)(N03)z]+,5,289 NiCI2Hl,hi2Ol2 NiC10Hd$& [Ni{N(CH2C02)3}2]4-,5,219 Ni{Et(Pr’O)PS2)z,2,643 NICT~II~ZN~S~ NiCloH2,BrN,0 Ni(C4Me4){S2CZ(CN),), 2,604,009 [NiBr(1,7-dimethyl-1,4,7,10-tetraazac~clodadec~ne)Ni(2-SC6H4NH&,2,799; 5,20Y (H,0)1+, 5,232 NiClZH12N4 NiC.,nH26P4 Ni{1,2-(HN)2C6H4)z,5,97; 6, 112 [NiBr { (MeHPCH,CH2PMeC1.1,) 2 ) ] 2 + , 5 , 130 [N1{112-(HN)zCJL}2] ,5,97 NiCIIIH2,BrOP, [Nill,2-(HN),C,H4},]+, 5 9 7 [NiBr(CO)(PMe,),]+, 5, 112 [Ni{l.2-(HN)2C6H4}2]2-. 5,97 NiClOHzgBrN,S2 lNiF1,2-(HN)2CsH4}212+, 5,97 [NiBr{N(CH2CH2NEtz)(CHzCH2SMe)z}]+, 5,216 NiCl0HZ8N4O2 [Ni(l ,4,8,11-tetraazacyclotetradecane)(HzO)z]z+, 5, 239 Ni(q5~C5H4Me)2, 1. 127 NiCloH28N6 NiC,2H,412N2 }]~ [Ni{(H2NCH2CI1 2 ) z I I ; C H I C H 2 N ( C H z C : ~ ~ ~’ ,z ~ ~ ~ ) 2Ni12(2-Mepv),, 1, 3-07 1,553 NiCl ,H,,O& NiCloH,,CIPZSi Ni(OzSPh)Z(HzO)n, 5,154 5. 112 NiCI(CH2SiMe3)(PMc3)2. NiC, ,H,,O6Sc2 NiC, ,HI4N~O8 Ni~(O,SePh)~(H,O),,5, 154 [Ni(tmta)l2-, 2, 784 NiC12HlhBr2N8 NiCllHISNZOB Ni(HfiN=CHCH=CH)4Br2, 5,49,82 [Ni(Htmta)]-, 2,784 NiC12H16C12NB NiCI,(H&N=CHCH=CH),, 2,75; 5,58,83 I NiCllH15N7 ’

Chmulative Formula Index

NiCl2HI6Cl2N8

462

[Ni(2,4.4-trimethyl-1,5,9-triazacyclododec-l-ene)12'. 5 . Ni(H&CH=NCH=kH)4Clz, 5.83 241 NiC12HI6NZ08 NiC12H26N206 [Ni(teta)]'-, 2,784 Ni{(S)-02CCH(OH)Me}2(TMEDA), 2,473 2,787 [Nil (02CCH2)zNCHzCH2N(CH2CH2COz)2}]z-, NiCl2HI6N4 Ni(2-pyCH2NH2)2,1,430 [Ni{l,3-(H2N)2C6H4}2]2+, 5 , 77 [Ni { H?dCH,CH,NHCH,C( Me)( NO,)CH,NHCH,NiCizH16N404 CHINHCH,C(Mc) (N02)CH2}]Z+1 2,902 [ N ~ ( ~ - ~ ~ C O N H Z ) Z ( H5.106 ~O)~]~+ NiC,,H,,Br,P NiC,,H,xN60a [NiBr3(PRut3)] , 2 . 1025; 5, I I O Ni(DL-histidine)z,5,59,220 NiCdJ% INi(H,NCH,CH,N=CHCMe,Cl IPr'NHCH,CH,NH2)I2' . 6 . 161 NiC1ZH27N6U [Ni{MeC(=NO)C(ICle)= N(CH2CH2NH)3CHzCH2NHz}I2+,5,291 [Ni(Hteta)]-, 2,784 NiC,2H28C12N4 NiC IZHI &lzN 608 Ni{H2NkH(CH2)4~HNH2}zClz, 6, 150 Ni(MeCN)6(CI04)2,5 , 5 6 , 58 NiClzH18N20z Ni(C0)2(CNBu')2, 5,29 Ni{(MeCOCH=CMeNCH,),},l,422 N1C12HlsNzS2 Ni{(MeCSCI ICMeNCH2)2}.5,206 Ni{MeC(S)=CHC(Mc)=NCH,CH2N=CbleCH= NiCI,H,,,Br2P2 C(SIMe), , , , 6, 112 NiBr2(PEt3),, 5, 110 NGH& NiC1ZH30Br3PZ Ni{cH2CH2N=CHCH=CiMeNCH,CH2NC(Me)= NiBr,(PEt>),. S,5, 288 CHI I=& } , 1,423 NiC12H30N204P2 Ni(IbCHCH=CMeNCH,CH,N=CMeCH= Ni(NO,)(NO)(PEt,),, 2 , 109 CHNCH&H,), 5,255 NiCI2H3,,N6 [Ni(1,4,7-triaza~yclononane)~]~+, 5,232 [ N i ( H N ~ H 2 ) 6 ] 25.70 +. NiC12H3& [Ni(sepulchrate)j2+,5, 271 NiCI2H3006 [Ni(DMG),IZ-, 2,271; 5,289,291 [Ni(DME),I2', 5 . 142 NiC1,H,oBr,N,S2 NiCl ZH900SS6 Ni( 1,2-(H2NCH2CH2SCH2)2C~H,)Br,, 5,2W [Ni{MeS(O)Ckl,Ct 12S(0)Me},]z', 5,164 NiC1,HZ&12N404 NiCI2tlR2Br2NBS4 2. 2,271 NiCI,{HON=-=NOH} Ni(McNHCSNHMc),BrZ,5,184 NiC12H20N608 NiC,zH32Cl,N, NilH,N(CHzCONH)2(CHzCO~}~, 2,761 Ni(EtNHCH,CH2NHEt)zC12,5,59 NiC,;H,,,N802~ NiCI2H32N6 [Ni( H&CH=NCH=cH) 4( H,0)2]z+. 5.59 [Ni(l,4.8?1I-tetraazacy~lotetradecane)(en)]~+,5,239 NiC12HzlN303 NiC1ZH32P4 INi(AcfiCHZCHzNAcCH,CH2NAcCH2CH2)]2+, 5, Ni(Me2PCH2CH2PMez)2, 5,9 296 NiC~zHdh NICIZHZIN~O, [Ni{HN(CH2CH2CH2NHz)z}z]+, 5,74 [Ni(H2NCH2CONHCH2C0,)~]-.2.760 [Ni{H2N(CHz)3NH(CHz)3NHz}2]*+, 2,47.49; 5,75 NiCIZHJ3rZN& NiC,,H,,BrO,,P, Ni{fiHC(S)NHCH2cH2}oBr2. 2,639 [ N ~ B ~ { P ( O M C ) ~ 5, } ~115 ]'. NiC,,H&I2N4Ox NiC12H36BrP4 Ni@( CH2)3fi(CH2)3}2(C104)z.5.67 [NiBr(Pkle,),]-. I . 44: 5. '1.10 NiCl2HZ4CI2NSS4 NiC:l,H36C1,0,,S6 Ni{fiHC(S)NHCHzcHz}4C12.2.639 Ni(DMS0)6(C104)2,5,58 NiC12H24ClzS4 NiC12H,6N,Si, NiC12{$(CH2),S(Cfi2)3}2, 5.59. 171 Ni{N(SiMe3)2)2.5.107 NiC12H24LN8S4 NiC12H36N404 Ni{fiHC(S)NHCH2cH2},IZ.2.639 [Ni(ONMe,),lz-. 5 . 164 NiC12H36N603 NiCl2H24N4 [Ni(fi=CMeCH2C(Me)=NCH,CH,KH(CH2)3[Ni{H2NCH2CH2N(0)Me2}3]2+, 5 , 164 NHCH,CH2I2+,6.167 NiC12H36N806P2 Ni(HMPA)2(N02)Z,5 , 159 NiCl2H24N8S4 [Ni{fiHC(S)NHCH&H-r,}412f,2.639 NiC,,H,,O,S, NiC,,Hza04 [Ni(DMSO),12-. 5.60, 164 [Ni(Me2COCH2CMe20H)2]2+5.11 I NiC.12HRh06Sc6 [Ni(OSeMe,),l~z.,5 , 164 NiCi>H2406 [Ni(MeCH0)6]24, 5 , 142 NiC12H36012P4 Ni{P(OMe)3}4.5 , 9, 115 NiC12H24012 [ N ~ ( H O A C ) ~5] ,~142. + , 155 NiC,2H36P4 Ni(PMe3)4,5 , 9 NiCI2H25N3 I

I_

.I

I

463

Cumulative Formula Index

[Ni(PMe,),l+, 5,41,42

N~C,,H,,N~

[Ni{HN(CH2CHZNH,)z)3]2+. 5.58 NiC12H4,N,06P, [Ni(HMPA)z(OH2)4]2+. 5. 161 NiC12N6Se6 [Ni{Se,CC(CN),}3]-, 5.300 [Ni{Se2CC(CN)z)3]2-,5,299 NiC13H7N3 INi(2-NCphen)12'-. 6.450,453

Ni{&=CMeC NO2 - HNCH2CH2NCH=Ca H , ) , ) . 6, 173

[Ni{o-&=CHNHCH=~CH,CH(NH,)CO,Me} {Dfi=CHNHCH=cCH,CH(NHZ)CO,)1+, 6,424 [Ni { D-fl=CHNHCH=CCH,CH(NH,)CO,Me){ L - N L CHNHCH=CCH2CH(NH2)C02}] ' ,6,424 NiC13HZON~QZ Ni({MeCOCHC(Me)=NCH,~,CH,), 5,205

NiC14H128N604Se2

NiC,4H12ClzNz NiC1,(2.9-Me2phen), 1, 187 NiCl4Hl2CI2?.J4 Ni(benzimidazole),CI,, 5,83 NiCl4HI2I2NZ NiI2(2.4-Me,phen), 5, 81 NiCq4H,,N202 Ni(X-quinuIinolate),, 5,214 KiCl4HI2N2O4 Ki(2-OC,H4CH=NOH),, 5,215; 6,118,800,801 NiC,,H,,S, Ni(S,C,H,Me),. 2, 606 [Ni(SZChH3Me),]-,2,606 [Ni(S,C,H3Me)2]2-, 2,606 YiCI4Hl4N6O2 Ni(2-pyCH2NHCONH2)2,1,430 NiCI,Hl6Br2N3 NiBr2{(&=CMeCH=CHCH=cCH2)2N).5 - 87 NiC14H16NZ04 Ni(OAc),(py),, 5 , 155 NiC1qHj&\i6 [Ni{2-pyNHN=CMeC(Me)=NNHpy-2}l2+. 5$94 NiC,,H,,CI,N, Ni(Me,py),CI,, 5,62 Vi(3-Et py)?Cl2,5 , 59 NiC,,H,,N,

Ni($JCH=CHN=CMeCH=CMeNCH=CHN=

NiCI3HZ0O2 Ni(Hacac)(cod), 5 , 14-1 NiC13H22N402 Ni{ HON=CMeCMe,Y=CHCH=CHNCMe,C(Me)=NO), 1,456:6.185 NiCl3Hz5N4O2 [Ni { ON=CMeCMe2NH(CH2)3N KCMe,C(Me)=NOH}l+, 6 , 1x5 NiCI3H2,N4C); [Ni{HON=CMeCMe,NHC~ 12CM2C112NtKMe2C(Me)=NO)]'. 1.456 .. NiC1,H,,BrF,P, NiBr(CF3)(PEt,),, 5. 114 NiC13H39P4 [NiMe(PMe,),]+. 1,44; 5.42, 112, 113,114 NiCl4H4F1& Ni{SZCZ(CF,),}2(tetrathiafd~~alene),5 , 179 NiCl,H,N4Ss Ni{S,C,(CN),}2(tetrathiafuvalene), 5. 180 NiC14H6N208 [Ni{2 , 6 - ~ y ( C O ~ ) , } ~S1 ] ~221 NiCj4HSN2OR Ni{2,6-py(C0,H)C02},. 5.221 NiC14HlOF12S4 Ni{SC(CF,)C( CF,)SCH,C(Me)=),, 5, 181 NiC!4H1oNA NI{(~-SC~H~N=CH)Z). 5.208 NiC1&10N10S4 Ni(NCS)4(HfiCH=NCH=cCH2CH2NH3)z, 2,82 NiC14HloOzS2 Ni(PhCOS)z, 2.645: 5.213 NiC14H1004 Ni(tropolonate),. 2. 397 Ni(2-OC6H4CHO)2.5. 188 Ni(O,CPh),, , - 5, 155 NiC1iH;OOh Ni(2-0,CC6H,0H),. 2.469 NiC14H10S4 5 , 181 Ni{S=( cCH=CHCH=CHCH=CS)),, Ni(S,CPh),, 2.646 NiCj4H,,,S6 Ni(S,CPh),,, 5 , 176

CMeCH=CMe), 2,906 [Ni{h=CHCH=NC( Me)=CHC(Me)=NCH=CHN= CMeCH=tMe}l2 ' ,2,906 NiCllHIBNID [X{2 .6-(HZNN=CH)py},l2+, 5,90 NiC14H20C12N4 Ni(2-pyCH,CH2NH2)2C12,5, 86 NiC14H20N,04P2S, Ni{(MeO),PS,},(bipy), 2,644; 5,80 NiC,,H,,N,O, Ni(OAc),(H20),(py),, 5, 59, 78, 155 NiCl,HzoN20, [ ~Ui{(O~CCH2CH2)2NCH2CC12N(CI-IzC:H?CC)2)~]2-, 2.781 NiC laH20Y2S2 Ni(benzo(14]crown-N2S2}, 2.925 NG,H,uO& 5 , 172 ~Ni{S,C(COzEt)z}z]Z-, NiC1,H2& Ni(S,CPh)(S,CPh), 5 , 176 NiC,,H2zC12N40s Ni(C10,),(S17,12.14-tetramethyl-l,4,8, 11tetraazacyclotetradecane),5. 152 NiCI4HI2NZO2 Ni(D,)(CNC,H,,),, 2, 320

NiC14Haa02P Ni(P(C6H,lM(CO)2,5-40 NiC,4H24N, [Ni { &=CMeC(Me)=N(CH,),N=CMeC(Me)= N(CH,),}IZ+, 5,229 NiC,,H,,O,S, Ni{MeCSCHC(OEt)Me},, 5,67 NiC,,H,,?O. [N~(MkOCH2COMe),(AcOH),12+.2,402 NiC14H2,N,02 INi { MeC(=NO)C(Me)=NCH2CHzNHCHz) 2]2', 5 , 294 NiC14H27N602

[Ni{MeC(=NOH)C(Me)=NCH,CH,NMCH,CI&NHCH2CH2N=CMcC(=NO)Mc}]*+. 5,294 N1C14Hd604Sez

Cumulative Formula index

NiCI4H2&O4Se2

Ni(NCSc)2(DMF)4.2,227; 5, 104. 165 NiC14H30C13N, [Ni{N(CH2CH2)3NMe}zC13]+.1.45 NiC14H30N6 [Ni(1,4,8,11-tetraazacycI0tetradecane)(MeCN),]~+,5 , 289

NiCdLNh [Ni{H,NN=CMeCH,CMe,NHCH,CH,NHCMe,CH2C(Mc)=NNH2}]"-,2, 904 ~Ni(:H2NN=CMcCH2CMe2NHCH1)?)12' , 6 , 181 NiC:14H32N6S2 T\ii(EtNHCti2~~t~2Nt.lEt),(NCS),. 5,50 Ni(1 [,NCII,Ci T,NEt,),( NCS), , 5,59

NiCI4H3,N7 [Ni(l~4,8,11-tetramethyl1,4,8,11tetraazacyclotetradecane)(N3)j-, 5,239 ;ViCI4H3,P2 Ni(PEt3)2(H,C==CH2),5, 16 NiC14H36N204PZS4 Ni(S,P(OEt)),(TMEDA), 5,174 NiC14H36N60Z Ni(tren),(NCO),, 2,233 NiC.,,H,aN,0,P,S2 Ni(HMPA),(NCS),, 5, 161

-14

Ni(tctraazaporphyrin). 2, X5X NiC16HloF,0,S4 Ni { $CH=CHCH=c C(.S)=CHCOCHF,} 2 , 2.653 _ NiC16HloN4S4 Ni { (c 6 H 4 N = CS)C( ( S)=& H),},5, 182 NiCdI0N8 Ni{N=CHC Me =CHNC(CN)=C(CN)N=CHC6,166 *CNJ, ,. .

Ni( 1 ,X-naphthyridine)2(N03)2.5,80 NiC IhH141iz07Ni(salen), 1,531; 3.735; 5 , 197 Ni{(2-OC,H,CH=;UCHz)2}, 5, 192; 6, 85 NiClbHI4N2SZ Ni{ (2-SC,H4CH=NCH2)2},5, 193

Ni{2-SC6H,{N=CMeC(Me)=N}C6H4S}, 6 , 112 NiCdW, Ni(S,CCH,Ph),, 2,646 NiC16H16N& Ni(2-OC6H4CH=NMe),, 5, 189 NiC16H16N204 Ni(2-OC,H,C(M~)=NOH),, 6 , 1021 NiCl6Hl6N4

Ni(2-NHC6H4CH=NCH2CH2N=CH-2-C6H4NH). I I

445 NiC16Fi18N104 Ni{OlCCH(NH2)CH2py-2)2,5,220 NiCI6HI8N6 Ni(CNBu'),(TCNE). 5, 17.29 NiCI6Hl9CIN, [Ni{HN(CH2CH,NCHpy),}Cl]~',5.59 NiC16H20N20~

Ni(2-OC,fZCH=NMe)(2-HOC,H4CHNHMe), 5 . 20 NiC,,H2,N,0~P,S, Ni{(MeO),PS,},(phen), 2,644 NiC16H20N6 [Ni{3;3'-(~le,C~NNH),bipy}12+, 6, 184 NiCI6HZON6S2

,97

Ni(NCS)2(2-pyCH2CH2NH2)2, 5,87

[Ni(MeCOCH2COMe)3]2+.2.402 ?;iCliHZ,NO, Ni(a&c),(piperidine), 2, 38h NiCISH~WM" [Ni{P(OCH,)3CMe}3(NO)]+~ 5.14 NiC1&7N30~S Ni(CNBu'),(SOz), 5,30 NiC,,t I Z ~ N ~ O ,

[Ni{H2NCH2CONHCHMeC02)3] ,2.760 [Ni(H2NCH2CONHCH2CH2C02)]2 , 7 W NiC.,,H,,O,S, 1Ni(S,COBu'),]-, 5, 172 NiC15H30BrN3S6 Ni(S2CNEt2)3Br,1,410 N~CISH~ON~S~ Ni(S2CNEt,),, 5,299 [Ni(S2CNEt2)3]+, 5,300 NiC,,H3,BrN3S [NiBr{ N(CH,CH,NEt,),( CH2CH2SMe)}]+,5 : 216 NiCISH4505PS [N~(OPMC,),]~+, 564 NiCl5H4SOd's (Ni{P(OMe),},J2+,5, 115 NiC.,,H F 0 S4 Ni ( S ~ ~ = ~ l ~ c I - i = ~ C ( S ) = C H C O C ,2,651,652, F~)*, 653 NiC I 6HBN4S4 [Ni(quino~aline-2,3-dithiolate)~]~ - 5 %182 NiCl6HsN8 I

'

364

NiC,6H22Br2P2 NiBr2(PMe2Ph)2.5 , 110 N~CI~H~~B~~P, Ni(PMe2Ph)2Br3,5,298 NiC16H,,S, [Ni{(2-pyCHzCH2NHCH2)2)12t,5 , 8 8 NiCI6H22N402 Ni{&CHC COMe)CMeNCH,CH,NCMeC(COMe)&H!), 5,269 N~CI~HZZNB~~ Ni{~ = C H N ~ C H ~ C ~ - r , C IHCOCH2NH2)C02) -I(N 2. 2,760

N~{I~CHNHCH=~CH,CH(NH~)CONHCH~CO,J 2. 2,760

NiCJL NilcodL. 2.218.221.582: 6.295.305 NiiH&N=CHC Ni(MefiCH=N , Ni(&=CMeNHCH=cH),Cl,, , - 5,83 NiC16H25C150~P2 Ni(AcO)(C6C15)(PPhMe,),, 5 , 114 NiC ,6HzsNzOz NiiMeCOCHC(=NPr')MeL, 5,205 NiCl,H2,N4 [Ni{~=CHCH,N=CMeCH,CMe,N=CHCH2N= CMeCH,tMe,lZ-. 1.455: 2,905; 5,228; 6. 165 I -

[Ni(&=CMeCH,CMe,NHCH,CH2N=CMeCH,CMe3N=CHcH7112-.6.165 NiCI6H32N4 -I,

[Ni(5,7,7,12,12,14-hexamethyl-l~4,8,11tetraaza~yclotetradeca-j.l4-diene)]~+,1, 420, 450; 2,901,906; 5,227,228,249,296; 6, 163 [Ni(5,7,7,12,14,14-hexamethyl-l14,8,1 1tetraazacyclotetradeca-4,1l-diene)]z+, 1,455; 2, 901,906,908; 5 , 227,228,239,296; 6 , 163, 16s Ni(EtNCHMcCHCHNEt),. 5 , 107 NiC16Hd5 INi{H$JCH,CH,NHChk CH T(Me)-NN= C'MeC3 I,C:Me,Nl ICIIL H2)12'. 2,905 .. NiC 16H34N206 Cu{ (S)-O,CCH( OH)Me},(Et2NCH2CH2Et2),2,474 NiCI6H34N4 [Ni(fi=CMeCH2CMe2YHCH,CH2NHCHMeCH,CMe,NHCH,~H,)I2+. 6.165 NiC16H36Br2f2PZ NiBr,(PFBu'2)2, 5. 110 NiC16H3& [Ni(5,7,7,12,14,14-hexarnethyl-l..1,8,11tetraazacycloretradecane)j2i, 1. 204,455; 5,228, 239; 6, 165 NiCi6Hd402 INi(H,NCH,CH,NHCMe,CllzCOMe)2]L', 2, 901; 6 . 163 h'iCI6H39NOI'~ Ni(PEt3)Z(Bu'NO), 5 , 19 NiCI7HllN5S2 Ni(terpy)(NCS),, 5 , 82 NiC17H18N4 Ni(2-NHC6H,CH=NCH,CHMeN=CHC6H4NH-2), 5, 98 NiCI7Hl8O2P2 Ni(CO),{PhPH(CH2)3PHPh,). 5, 11 NiC17H20NZS2 NiCI2{2-~6H4CH,NH(CH2)3NHCH2-2C,H,SCH,CH2}, 5 ; 259

-y -,l

NiC18Hlj13P [NiI;(PPh;)]-, 5 , 110, 187 NiCIsH,6NaO2 Ni{PhC(O)=NNCMe},, 5,203 NiCIaHiBBr2N20, Ni(2-OC6H,CH=NCH,CH,Br),,

NiClSHlBS2O2S Ni{(2-C)T6~IJCII=NCH,CH,),S), 5 , 194 NiC1 t b N 4 Ni(N=CHC6H,NCH,CH2NC6H,C:I I=NCH&H,), 116.435,456; 5,22H; 6, 'I77 NiU18H22N204 Ni{ 1,2-{MeCOCH(COMe)CH,N),C,,K-I4j. 5,228 NiC18Kz2N6 [Ni{2,6-(MeN=CH)py},l2+, 5,90 NiC18H,Br2N6P2 NiBr,{P(CH,CH,CN),},, 2,262; 5, 111 NiC1&4C12N6Pz TiiCl,tP(CH,CH,CN),}~, 5, 110

Ni(NCS)2{N(CH,CH2NEt2)2(CH2CH2SMc)}, 5,216

NiC17H3,NOP3 [Ni{MeC(CH,PEt,),}(NO)l+, 5 , 12

N~'c,~H,F,,o,s,

Ni{$CH=CHCH=CC(S)=CHCOC2F5},,2,653 NiCl8Hl0N2S4 Ni(S2C2Ph2){SZCZ(CN),).2,601 NiCl8Hl2Br2N2 5.62 Ni(2,2'-biquinolyl)Brz. . . NiC,,H,,N,O, Ni(8-quinolinolatc),, I, 528 NiC18H12N2SZ Ni(X-quinolinothiolat~~~, 2+800; 5,683

250 NiCI8Hl5Br3P [NiBr,(PPh,)]-, 5,62, 110, 187

I,

Ni{S,~'~C)Me.),},(2,9-Mc,phen), 5, 80, 174 NiCIBI124Ti,0H

Ni{4-HOC6H4CH2CH(NH,)C02}2(HzO)~ 2. 745; 5 , 720 NiC 24E [Yi(?-pyCHzNH2J3]2+, 5 , 5 8 , 86 [Ui{1;2-(H2N)2C6H,}3]2+,2,59 NiC, *H,,N,P [%( Pip.),} {N(CH,NH2)3}]Zi~,5, 58 NiC18H24N12 [Ni(H$ICH=NCH=cHLl2' ,2.75

,..~ ..,-. NiC17H2,NI',S, Ni(S,PEt,),(quinoline), 5 . 78 NiC17H33N502 Ni(NC0)2{HNTH2)5)3.5. 70 NiCI7H3,PS NiCp(SH)(PBu,), 5 . 166 NiC17H35ClP2S2 Ni(MeCSCHCSMe)CI(PEl:)l, 5, 183 NiC17H35N5S3

1,445

.

.

.

N i { ~==CMeC.'(COMc)=CHN(CH,),NCI I= C(COh;re)C(Me)=N(~.H,),), 6,172 NiClnH,,Ki N~(c~B;'),(B~'N=c=c(cN),), s,20,22,23 NiC18H28h'2PZ Ni(PMe3)z(PhN=NPh), 5.22 NiClaH2,N2P2S4 Yi(S,Ph.Ie2)2(2.9-Me,phen), 5,64 NiC18H1RN402

[Ni{$J=CMeCH(COMe)CH=N(CI-I,),N=CHCH(COM~)C(MC)=N(~H,)~}]~', 6, 172

NI(CH,SiM&),(py),, 5,79 NiCIgH32N3PSZ Ni(PBu3)Cp(S2CN3), 2,588 NiCI8H3&P Ni{P(C6Hl1)3)(W, 5,27 "iCIaH3&

[Ni{fiHCH2CH2NHCMe2CH,C(Mc =NN= CMeC(Me)=NN=C:MeCH, .Mel)la+,2,904 NiCIBH&l2N lzO& Ni(HACSN1 ICI IZ~H2)6(C104)2r 5,59 NiC181-136XN2S4 Ni(S,CNBu,),I. 5,299 NiC,,H,,NOS Ni(OSCY3u2)z.2. 587 NiC1BH36N2S4 Ni(S,CNBu2)2, 6, 1020

Cumulative Formula Index NiCisH 6N,

[Ni(d=CMeCH,CMe2NH(CH2),N= CMeCH,CMe2NH(CH,'),}]*-. 5.227 - .NiC18H3606 [Ni(Me2C0)6]2+,5 , 141 N1CisH36S6 [Ni(l ,5.9-trithiacycloundecane),12 '. 5. 171

NiHCi(PPr,),, 2, 703 NiClsH4J', Ni(PEt3),, 5,32 NiC1BH48Br2N6PZ Ni{P(CHZCH,CH,NHL)3)LB~~, I, 27 -UIC1&SN1206

INi(MeNHCONHMe)6]2t, 1.470 NiC18H48P4Si2 Ni(PEt3)Z(PSiMe3)2,5,23 N~CIBH&NIO~~ 5, 161 Ni { MeN{P( 0)(NMe2)2}2}212, NiC18H5qN~2 [Ni(trien),14+, 6, 164 NiCI9Hl3N4 (Ni(cictadehydroct)I-l-in)l+,2: 879, 882. 888 hriCI9Hl4N40 Ni{2-OC,I14N=NC(Ph)=NNl'h). 6. 78 NiC19H-i5PS2 Ni(PPh,)(CS,j, 5.25 NiC,,H,,N, [Ni { 2-flC6H,CH=NCH2CH,N=CH-2-C,H,N= CHCH=cH}]+, 1,456: 6.177 NiC19H19b liiCp(4-MeC6H4N=NN=NC6H,hle-l), 2,218,220, 224 NiC19H20N4 Ni { 2-fiC,H4CH=NCH2CH2N=CH-2-C6H,NCH,CH,CH,J, 1,456; 6.177 NiC19H24P2S2 5, 130 Ni( (SCHZCHzPPhCH2)zCH2), NiC,,H,,PS Nkp(SEt)(PBu3),5 , 169 N1C'l~lI,,N,O, [NI{ fi=CI IC{=CMe( C)Me)}C(hIe)=~CFI,CH,CH,N=CMeC {=CMe ( 0-Me)} CW= =H,,1*'. -, 2.907: 6. 169 NiC19H,5CIOP2 NiC1(PhCO)(PEtJ2, 5 , 114 NGoHsF1402S4 Ni{$CH=CHCH=cC(S)=CHCOC,F,) 2 , 2,653 ~

>

NT{SZb2(CF;),},(phenothiazine), 5. 179 NiC,,,H,F,,NOS, Ni(S,C2(C'F,),),(phenux;l7.ine), 5 : ,179 NiC20Hlo~r2F602S2 Ni{4-BrC,H,C(S)=CHCOCF3)2, 2.651, 652 N~C&~OC~~F~OZSZ Ni{3-CIC6H4C(S)=CHCOCF,}2. 2.652 N~C~OH,OF~O,S~ Ni{4-FC6H4C(S)=CHCOCF3),. 2: 652 NiC20HION202S4 [Ni{S,CC(CN)COPh},]z. 5 . 176 N~C~OHI~F~O~S~ Ki{PhC(S)=CHCOCF,},. 2,65 1-653 NiC& ,,Fi,,N4 Ni(cod)(C6FSN=NN=NChFs). 2.217.218.220,222, 223; 5 , 2 3 NiC,,H,,N,O, Ni( l-nitroso-2-naphthol~t~)2. 5. 211 NiC20H12N4 Ni(porphyrin), 6. 198

4666

NiC2,H 14F,0zS, Ni{PhC(S)=CHCOCHF,),, 2,653 NiC2~HI4NZOZ Ni{ 1,2-(2-OC6H,CH=N)2C6H4},5 , 197 NiC20H14N, Ni(methyloctadehq.drocorrin), 6, 198 NiC2,Hl4N,O2 Ni{2-0,CC,H4N=NC(Ph)=NNPh}, 6,79 NiC,,H Ni(bipy):? 6 6N ,SI NiCZ0H1 [Ni{S,Cz(CN)2J(Ph,N,C2Me2)1-, 5 , 179 NiC&1II6N8 Ni(tetramethy1tetraazaporphyrin). . . _ ,2, 859 NiCZ~,H18N20 Ni{l ,2-{-=CHN}2C6H4}, 6. 169 NiC,nHlnNa07Sn N~(NCS),(~20)z(quinoline)2,5,78 NiCZOHls0,S2 Ni{MeC(S)=CHCOPh} 2 , 2, 65 1 NiC2,H191,PSI Ni12{(2-MeSC6H,)2PPh). 5, 128 NiC2,HI9PS2 NiI2{PhP(C,H,SMe-2),). 5, 170 NiC2,,HZOCl2N4 NiCl,(py),, 5,58.78.79 NiC7nH,,Cl,h-d08 Ni(C10,j2(py)4, 5 , 152 NiC20H201ZN40d NiI,(pyridine N-oxide),, 2, 496 NiC2,1 Iz0N, [Ni{3,3'-(3=CMeCH=CMefi),bipy)lZ+, 6, 184 N~C20Hzo~lo Ni(py),(N3),, 5 , 5 8 NiCZoH20h2 [Ni{HC(fiN=CHCH=cH),),]z+,5, 102 NiC,oHzlC1,N,O, 5.194 Ni{ (2-C)-i-CIC6H3CH=NCH2CH2CH2)2NH}, NiCZOHZ3 (NiCp)4(w3-H)3>2,702 NiC2,,H2,N20z Ni(I-OC,I I,CII=NPr'),, 5 . 62 NiC10H24NZ04 Ni(acac),(py),. 2: 388; 5 , 143 NiC20H2,N,06 Ni(acacj2(py N-oxide),, 2, 388; 5 , 143 NiC20H24N40z Ni(2-0C,H,CH=NPri),, 5, 189 [Ni(py)4(H,0)212fl 5: 59 NiC,,H2,N606S2 Ni(py),(NH,SOA 5.59 NiC,oH24N8P,S2 Ni(NCS),{P(CH.zCH,CN)3},, 5 , I 1 1 NiC,,,H,,S, [Ni(lr2-S2CGM~4)2]2-, 6,127 NiCZUHZ6N4S2 N ~ { Z - { H U N = C ( S ) ) ~ ~6, } ~112 , NGoHnN@* fii{NPhC(O)OcHPh}(TMEDA),5,32 NiC20H26P;204P& Ni{S,P(OEt))2(phen), 5, 174 NiC20HzsN,0s Ni{H,N(CH,)3NH,}2(4-0,NC6H4C0,)2, 2,45 NiCZOH30N404 Ni(camphorquinone oxime oximate),, 5,214 ~

NiC,;,I 1&12NR Ni(fi=CMeNMeCH=tH),C1,, NiC,,Hs2CI,P, INiClz(diphosjz]+.5,289,299 [NiC1i(diphos),i2+. 5,289 NiC,,H,,N,O,

5,83

Cumulative Formula Index

467

NiC,,H,,N,S,

[Ni{fi=CMeC{=C(NHEt)Me}CH=NCH,CH,N= CHC{=C(NHEt)Me)C( Me)=N(~H,),}jZ+, 6 , 169 NiCtlH43N402 [Ni(5,7,7112.14,14-hexamethyl-l ,4,8,11tetraazacyclotetradecane)(acac)]+, 5,239 NiC&l~F~~OzS~ Ni{PhC(S)=CHCOC2F5}2,2,653 NiC22Hi,F,OzS, Ni{4-MeC6H4C(S)-CHCOCF,J,, 2,651,652 CHC(=N(NHMe)MelC(Mc)=N(CH,),}Iz+,6, NiC,,H,,F,O,S, Nil 4-McOC,H,C(S)=CHC0CF3},, 2,652 I70 NiCzzHds NiC20H36N4 Ni {2-p?lCH=NN=C5NCH=CHCH=CH)2.6? 180 Ni(CNBu'),, 2,218; 5 , 7.29 NiC22H1BN& NGnH370izP4 Ni { 3-i~oquinolinylCH=NN=C(S)NH,)~,5,203 [NiH{P(OCH,),CMe),]-, 5,115 NiC22H,0Br,N,S2 NiCZ0H3,PS3 Ni{ l-naphthglNHC(S)NH,},Br,, 2,640 NiCp(S,CSEt)(PBu,), 5, 177 NiC22H20C12N4SZ NiCZ0H4,,N4 Ni{ 1-nap hthylNHC( S)NH2},CI2, 2,640 [Ni{&=CEtCH2CMeEtNHCH2CH2N=CEtNiCZ2H20N8 CH2CMeEtNHCH2CH2}]*', 6. 163 [Ni{2-pyCH=NNHpy-2}2]2+, 6,180 NiCz2HHzzN4 Ni(&=CMeCH=CMeNC,H,N=CMeCH=Cm , H , I . 6 , 167 Ni(oAc)~(Me4en),(0H2),5 : 157 NiC20H48C12NSS4 Ni(EtNHCSNlIEt),Cl2. 5 , I84 NiC20H48~P4 NiI(depe),, 5, 124 [NiI(depe),]+, 5, 119 NiCZ2Hz3P NiCzaH4&'4 Ni(PPh,)(H,C=CH,),, 5, 16 [Ni(depe),12+, 5, 118 NG~Hz~NIoP~S~ NiCZoHs5P3Si4 [Ni(NCS)4{P(CH2CH,CN)3}2]z-, 5, 110, 111 Ni(PMe3),{(Me3Si),CHP=C(SiMe3),}, 2, 1049;5,21 NiC22H26C12Pz NiCzlH14C12N,0,S NICI2(PhCH2f'CHzCH=CH~H2),, 5,110 [Ni {2-{2-O-5-CIC6H3NCH=C(N=NC6H?S(),NH2)NiC22H26N106S2 Ni(O,SMeMpvL, .,- 5 , 154 NiC22Hi8N4 Ni(CNBu'),(PhNNPb), 5,22 NICzzHzsN402 N i ( 2 - H O C 6 H 4 C H = N C H 2 C H 2 N ~ H 2.735 ~)~, NiC2;HI7N4 NiCz2HZsNl4 Ni(trans-1, t9-Me2octadehydrocorrin). 2.882 Ni(CXBut),(PhN=NPh), 5,22 NiCz1Hi7N4O4 NiCZ2H3,S4 [Ni(tribenzo[b,f,j][lS ,9]triazacyclododecine)(HzO){Ni(CsMeS))2(S2CZS2), 2,604 (NO3)]+,5,241 NiC22H34N404 NiCZ1HZON2S2 Ni{H2N(CH2)3NH2}2(4-MeC6H4C02)2, 2,45 Ni{CH2(CH2NCH=CPhCHS),). 6. 168 NiC22H3804 NiCzlHzlBrPSe3 Ki(Bu'COCHCOBu'),, 5,4,67,143 [NiBr{P(C6H4SeMe-2),}1+-5.66 NiC,,H,,N,S, NiczlH~~C I P S ~ Ni(NCS)I{HNTHp)S}4,5 7 0 [NiCI{(2-McSC,H4),P}]-. 5.66,133, 170 NiCdhN3 NICZIHZZO~P~ Ni(bipy)(Ph,CNH), 5,20 Ni(C0)3(2.4,6-Me3C,I i2P=PC',I12Me2-2.4,6). 2, 1045 NiC2JW&, NiC21H23CINP [~"~{~,~-~~(CM~=NNHCOP~),)(HZO)~]~', 5,199 NiCI(PPh,)(Me,NCH,). 5. 20 NiCl3HZ6N4 NiC21H25N302 Ni(CNBu'),(diazafluorene), 5,22 Ni{MeN(CH2CH,CH,N=CHc6H~o-2~2},5 , 6 4 NiC23HzsN5 NiC2,HZ8N4O2 [Ki((2-pyCHzCH2)2NCHzCHzNHCH2CH2py-2}]z+, 5. Ni{ N=CMeC{ C( OMe)=CH,)=CHNCH,CH,88 __ NCH=C{ C(OMe)=CH,}C(Mej=N(cH2),), NiC23H36N40z 6,169 Ni { fi=CMeC( CH2CH2C02Et)=CHNCH2CH2NiC21H33BrN7 NCH=C( CH2CH2C0,Et)C(Me)=N(cH2)3}, Me)?) I + ,.5,88 NiBr/N(CH,CH,&N=CMeCH=C 6, 173 -_ NiCzlH~,N402 NiC2&hF1402S2 [Ni{h===CMeC{=C(OEt)Me)CH==NCH,CH2N= Ni{PhC(S)=CHCOC3F7)2. 2,653 CI K{=C(OEt)Me)C( Me)=h'( CH,),)]", 6, NICMHI~~ 169 [Ni(phen),12+, 2,615 NiC2,H,,N, Ni(meso-tetrarnethylporphyrin), 2. 852 N I ( %=CMeC{ C( Me)=NEt }=C11UCH~CH2NCH= NiC24H &I2N6Os C ( C ( M e ) = ~ E t ) C ~ ~ l c ) = N ( ~ H62, )169 ~I. Ni(l.8-naphthyridine)3(C1O4),, 5.80 NiC24H18N4S2

[Ni{&=CHC(=CMeOMe)C(Me)=N(CH2)3N= CMCC(=CM~OM~)CH=N(~H,)~}]~', 5,256, 270:~,6. 170 NiC20H32N6 Ni{fl=CMeC{ C(Me)=NMe)=CHN( CH,),NCH= C{C(Me)=NMe)C(hfe)=N(cHz)3}, 6,170 NiC20H32P4 INi(diDhosL12'. 5.289 . NiCCZOHq4Nh [Ni(fi=CMeC{=C( NHMe)Me} CH=N( CHZ)3N= ~

I-.

-

r

Cumulative Formula Index

NG4H1&S2 [NiCl{2-(2-pyCH=N)C,H,S}2] ‘ , 5 1 9 9 NiC24H,,C1,P4 Ni(PPhCl&, 1,418 N ~ G ~ H Z ~ F ~ P ~ Ni(PPhF2)4,1,418 NiC H IN Ni(tetramethylporphyrin)I, 6, 147 NiCz4HZoN4 Ni(tetramethylporphyrin), 5,274 NiC24H3004PZ Ni(02PPh2)Z,5,154 NiC,,H,,,P,Se, Ni(Se2PPh2),,5,172 NiC24HZOS4 [Ni(SPh)4]2 ,2,526: 5, 167 NiCz4HZzN4 Ni(tetramethylchlorin), 2,892; 5,275 NiCz4H23C15P2 Ni(c~CH)(C6C1,)(PMe,Ph),, 5. 114 NiC,,H2,02P Ni(acac)(Me)(PPh,), 5 , 144 NiC24H26N402

,

NiCzaHzsC12N4 Ni(MaNl’h)4CIZ, 5,59 NiC2,H,&N40* Ni(C104)z(PhNHz)4,5, 59, 152 NiC,,H,*N, [Ni(4-Mepy),I2+,2,80 NiCZ4Hz& Ni{SzC2H(C6H,Bu-4)},,2,611. 626 NiC24H30N202 Ni(2-O-4-MeC6H3C==NBu)2. 6 , 1020 NiCL4H32NJ02 INi(Hz0)2(3-Mepy)4]Z+. 5.78 NiC,4H12Nh

Ni(CNBut),(4-MeC,H,N=NN=NC,H,Me-4), 2,218, 221

-

.

NH2)C02},]-, 2,760 NiC21H36C12N12 Ni(HfiCH=NCH=tMe),CI,, 5: 83 Ni(mN=CHCH=cMe)6C12, 5: 83 NilMefiCH=NCH=cHLCL. 5.83 ,FiiC2~H36CIZN1208 Ni(HfiN=CHCH=cMe),(ClO,)z. 5.56 ~

NiC,,H,,CI,N,,O,,P, Ni{ I ( M e J W ” 0 ) 1,O} 3(C104)2,5 5 8 NiC24H7~N12P4S4 [Ni{(hfe2N)3PS},]Z+, 2,642 NiC25HZ1N604 [Ni{4-{4-MeOC6H4C(O)=NNCH=C(N=NPh)CH= I\I”=C(0))C6H40Me}]-, 6,83 NiC2,HZ7O2P Ni(acac)(Bt)(PPh3).2 , 391; 5, 112, 143 NGH31N403 [Ni(camphorquinonemonot)ximate)(py),(H,0)1’. 5, 215 NiC2,H4,0P2 Ni(I’Et&(OCPh,). 5,20 NIC~,H~,N, [Ni(2-NCphen)z]2+,5 . 106 NiC,,H,,N,O, -. ~. Ni(NCO),(phen),. 2,233 NiC2,HI8N2S1 Ni(S,C,Ph,)(phen). 2.615 NiCt6HZ0 Ni(C3Ph3)Cp,5.33 NiC26H24BrN,S2 Ni( PhNHCSNHPh)2Brz, 5, 184 NiC,,F12,CI,P2 NiCl,{dppe)*5: 119 NiC26H24N204 Ni( 02CPh),(2-Mepy)z,5, ‘I 57 NiC26€-124h’6P2 Ni(N,),(dppe). 5 , 105 NiC26H26NOPz [Ni(NO)(PPh,Me),]+, 5 , 13 NiC26H26?1204 Ni{(PhCOCK2COCHCMeNCH2)z}, 3,561 N ~ C Z ~ H ~ ~ P ~ Z Ni(SH)ddiphos). 5, 118. 166 NiC26H3;06 Ni(2-0-3, 5-Pr’2CbH2C02)z, 6, 1021 NiC,,H,,N,P, -.. . .. . .. Ni(CN)z(PPhMc,),, 5 , 110 NiC26H36C12N40z Ni(~-CI-2-OC6H3CH=NCHzCH2NEt2)~, 5, 65 Ni(2-0-3-C1C,H3CH=NCH,CH,NEt,),, 5,189 NiC26H36N6 I

Ni(3.5-Me2C6H3N=NN=NC6H3Mez-3,5)(CNBu‘)2. 2: 221 NiC2,H,,C1N3P ’,5,64 [Ni{Ph2PCH2CH2N(CH2CH2NEt2),}C1] NiC26H40NP Ni(P(C6H,,),)(,.c-PhCH2CN), 520 NiC27HZ202P2

5.56 Ni(MeNCH=NCH=CH)&10,),. NiC24HJoP2SZ Ni(SPh),(PEt,),, 5, 169 NiC,4H43ClP2 NiCI{ ~ , ~ - ( B U ~ ~ P C H ~5.)119 ~C~H~). 12.143

270

468

Ni(CO),(dppm), 5 , 11 NiCZ7HZ4Cl3N6 Ni(8-aminoquinnline),CI,, 5 , 84 NiC.z71Z2,CI,02P, NiCI2{(0PPh2CH&CH2}, 5, 161 NiCZ7HZ7N4 [N~(octameth~lcorrole)]~, 2, 873 NiC27H31N5 Ni{ hle,(NC)didehydrocorin} ,6,201 NiCZ7H3,N4 [Ni{2,6-(Me,NCHz),C6H3}{4-MeC6H4N= CHNHC,H,Me-4)]+, 2,198 NiC27H51P2 NiH{(C,HI,)2P(CH2),P(C6H11)z}. 5,42, 44 N~CZ~HS~N~S~ [Ni(S2CM3~2)3J+: 5,300 NiCz,H54N,Se6 [Ni(Sc2CN3u2),]’, 5,300 NiCz7H7,C12N,z014 Ni(H,CIP(o)(NMe,),},),(C10,),, 5. 161 NiC27H81Clz?J15014 Ni { MeK {P(O)(NMe,),} 2}3(C104)2.5,161

Cumulative I Tormula Index

469 NiCz7HSIN,P3Siy Ni{(Me3Si)ZNP=NSiMe3)3. 2. 1051 NiCZ8Hl2F12S4 Ni{S2C,(CF,),J2(perylene), 5, 179 NiC28H,6Br204 Ni(phenanthrenequinone)2Brz,5, 146 NiCzRH16F60zS2 Ni{2-C,oH7C(S)=CHCOCF3}29 2,653 NiC,,H1604 Ni(02C14H8)2,5 , 146 [Ni(02C14Ha)21L. , 5 , 146 NiCZ,HZolN4(3, 5, 294 Ni{ PhC(=NC))C:(=NO)l'h},I NiC,JL,PL I

[Ni(fi=CHC,H4N=CHC,,H4N=CHC6H4N= m , H 4 ) ] 2 ' , I - 334,439: 5.229,269; 6, 173 NiCZ8Hz0N4O4 Ni{PhC(=NO)C(=NO)Ph}2. 5.294 NiC28Hzu04S4 [Ni(PhCOS),lZ-, 2,645 NiCZ8HZOS4 Ni(S2C2Ph2),,2. 608,610,613-617,627; 5, 180;6,530, 1021 [Ni(S2C2Ph&--, 2 , 608: 5 , 179 NiCZRHz2BrN4O4 6 . 144 Ni (ON-CPhC(Ph)=NOH},Br, NiC2g.H22IN404 Ni{H0N=CPhC(Ph)=YO)21~ 5 , 100,294; 6, 143, 144 NiC28H22N404 Ni{ HON=CPhC(Ph)=NO) ?.5,100 NiC28H2,C12N8 Ni(benzimidazole),CI,, 5. 83 NiCz8H24N202P2 Ni(NCO),(dppe), 5. 105 NiCZ8Hz4N4O2 [Ni{PhCOC(Ph)=NNH,) ,I2+. 2. 904 NiCzfiH2,CIsFJ'z Ni(Cc,Fs)(CbCl.5){ PMePh2)>,5 , I12 NiCZ8HZhNZO2P2 Ni(CN),(PPh,(CH,0H)}2, 5 , 111 NiC2,H2,N2PZS, Ni(NCS),(PPh,hle),, 2,233: jl 110 NiC28H28C120P2 5 , 6 2 , 124 NiC12{(PhZPCHzCH2)20). NiCz8H28N8 Ni(4-MeC6H4N=NN=NC6H4Me-4),, 2,218,220,224

Ni(acac)2(PPh3).5 . 143 NiC2,H,,BrZP2 NiBrZ(PEtPh2)2,1. 470 NiC2sHd4 Ni(Me,hexahydrocorrin). 6.199 [Ni(HZNCHPhCHPhh'H2),1'-. 5,72 NiCz8H34N4 Ni(Me,tetradehydrocorrm). 6.202 NiC28H36C12N408 Ni(C10,),(3,5-Me2py),. 5. 76? 152 NiC2,H,,N4 [Ni(3,4-M~,py),,1~+. 5.76

Ni(l,2:0,C6HzBu'z-3.5)Z, 5 . 135 NiC2SH40P2 Ni(C-CPh)z(PEt3)2, 5 , 112. 1 I3 COC 7-P

NiC31H273iY2P

NiC28H42NSPS2 Ni (Ph2PCH2CH2N(CHZCH2NEt2)2} ( NCS),. 5 , 6 4 NiC28H440~P2 Ni{PBur2(C6H,O)),, 5, 114 NiC28H,oN,P2Si6 Nit bipg) { (Me,Si),NPN( SiMe,)P( NSiMe,)= N{SiMe,)). 2, 1051

Ni I SKH,) 3 1(dppc) ,5,119 NiCdhLN4 INi(ciiethylhexamerhylcorrclle)]~ ,2,876 NiC29H32N4 M(H-diethylhexamethylcorrole), 2,875,876 NiC29H41CkN202S Ni{2-{ 2-S-5-(C1,H,,O2C)C6H3N=CH)py) Cl, 6 , 112 NiC30H16Flo02S2 Ni{2-CloH,C(S)=CHC0C2F5},, 2,653 YiC30HZ2N6 [Ni(terpy)#+. 5,81 NGoHz202S~ Ni{PhC(S)=CHCOPh},, 2,651 NiC,,I IZ4Br2N6 Ni(bipy),Br2, 5,SX NiC,,H,,K, Ni(bipy),. 5 3 7 [Ni(bipy),]"-, 5,37 [Ni(bipy),]+. 5.37 [Ni(bipy)3]Ztl 1,24,64,466; 5,60,80 [ N i ( b i p ~ ) ~ ]5,290 ~+. NiC30H2JY606 [Ni(bipy NIN'-dioxide),I2+, 5, 162 NiC30H24N8 [Ni(2-py3N),I2', 5,84 NiC30H27N9 [Vi(2-py3NH),IZ+,5, 84 NiC30H28N6SZ Ni(4-pyCH=CH2)4(NCS)2, 5 , 5 9 N i L J 13u&N&14 Ni(py N-oxide),(C10,),, 5 6 1 NiC30H30Nh [Ni(py),l2+,5 5 8 ~iC,,H3,N,0, [Ni(p!; N - ~ x i d e ) ~ ]2,496; ~ + , 5,58,162 NiC30H31C15N0P2 [ Ni (HN=C(OMe)Ph) (PPhMe,)(C,CI,)] +,2.277 NiC30H,,NOP2 fii(COCH,CH, Me) (dppe) , 1.12 1 NiC3uH3,h'zPz Ni(&C(Me)=CHCH=CMe),(PPh,) , 5 , 107 IiiC,,H,21,02P2 NiI,((Fh,PCH2CH2OCH2),},5, 124 NiC30H343r2P2 NiBr2(PP?Ph&. 1,470 NiC,,t I &1 NP,Si2 NiCI(N(SiMe2CH2PPh2)z},5, 129 NiC,,H, 0 {Ni(acac)Z}3.2,399 IGC30H45015P5 [NiCP(OCH)3(CH2)3}512+.5,115 NiC30H47C12020 Ni(acac),(CIO,),, 5,58 YiC30H49Pz NiIP(C,H,,),}CP(C,H,,),Ph},5,4O NiC,,,H,,CI,N , O A Ni(EtHNCSNHEt),(CIO,),, 5, 59 NiC31HzsC1Nz Ni(C,Ph,)(py),Cl, .5,33,34 NiC, ,H,,N,02

hi{OC(Ph)=CPhN=NCMe,N=NC(Ph)=C(Ph)O}

2,904; 6 , 181 NiC31H27N2P

Cumulative Formiilu Index

NiC31H2,N2P Ni(hipy)(2,6-Me,C,H,P=CPh,), NiC31H;;C1202P2 ~~

2. 105(1

NiC12(Ph2PCH2CHOCMe20~HCH2PPh2), 5 , 125 -ViCllH3,BrP2S2

[I\liBr{(Ph2PCHzCH2SCH2),CH2)]+. 5.130 NiC31H34P,S, [Ni{(Ph,PCH2CH,SCH,),CH,) NI'C3,H36P,

5, 130

[Ei{(PhPHCH2CH2PPhCH2)2CH2}]z++ 1,446 Ni{{PhPHCH,CH,P(Ph)CH,},}. 2.926 NiC1ZH16F~40~S~ Ni{2-ClmFI,C(S)=CIlC:UC,F,),, 2. h53 NiC-,?H ,,IN, Ni(phthdocyaninc)I, 5.274 NiC32Hi& Ni(phthalocyanine), 2,863, 868; 5 , 106. 271; 6 . 91, 193 [Ni(phthalocyanine)]"-, 2,870 NiC3&2N402 Ni(2-OC6H4CH=NC9H6N),,1,419 Ni{ 1-(PhN=N)-2-OC,oH6J216,42 NiC3~H,~Cl,N808 Ni(1 ,8-naphthyridine),(CIO4),+ 5,79 NiC32H2& [Ni(bipy),(phen)12+,5, 81 Ni(l-(PhN=N)-2-HNC,~H6}2, 6, 44 NiC32H&rF5P2 NiBr(CbF,)(PMePh2)2,5, 112 EiC32H26NzS2 Ni(SPh),(hipy),, 5 , 168 NiC32H28N2S4)CbH4)2.6. 1070 Ni{ 4-MezNC6H4C(S)C(S NiC32H2g04S4 Ni{ 4-{4-MeOC6H,C(S)=C(S j}C6H40Me},.6, 112 NiCjZH30N2S4 Ni(S,C,Ph(C6H,NMe,-4)},, 2,625 NiC32H32N202P2S2 Ni(NCS)Z{Ph2PCH,CHz0CH7)2}. 5 ? 124 NiC3zH,2N, Ni(PhNCHMcC1IMcNPh),, 5,97 NiC3,H3,BrNZP2 1 Ni((Ph,PCH,CH,N=C'he~~}Brl', 5.207 ~

_. ..

.

Ni(deoxophyl1oerythroetioporphyrin) 6,864 NiC32H36N~ Ni(3,5-Me2C6H3N=NN=NC6H,Me2-3,5)2. 2,220, 221; 5 , 2 4 NiC32H3EBrN2P, [NiBr{(Ph2PCH2CH,NMeCH2)2}]+.5. 130 NiC32H38N2P2 [Ni((Ph2PCH,CH,NMeCH2)2)]z+. 5 , 130 NiC32H39NP2 Ni(C,Me,)(PPh3j(P=NHur), 2; 1051 N~C~ZI.J~&"P~ Ni(PPhEtz)z(PhN-NPh), 5 , 22 NiC32H44S4 Ni{S ~ C ~ H ( C ~ H A C } z,~2H60 ~ I~ - ~ ) NiC&45N206P3 Ni(CN),{PPh(OEt),),, 5 , 115 N~C~~H~SN~O~PZ &i(NPhC(O)NPhC(O)rPh}(PEt,),. 5.32 NiC3,H50NO2S Ni(NHBu){{2-0-5-(Bu'CH2CMe,)C6H3)2 S ) , 6, 1020 NiCxH6oP2 Ni(dcpe)(Me,G=CMe,), 5 , 17

NIC~~H;,B~,II~ {NIB~(P~'~CHN==CHCH=NCHP~',))~, 2 . 2 11 NiC~IH,,OAP, Ni{0,&C,HI7),},, 5, 154 NiC32H6E08P2 Ni { OP(O j ( OCH,CHEtBu ) 2 } 2 , 6.792 NiC3BH2EN02P,

470

Ni(CO),(Ph,PC1I,~=CHCI~=CHC(=&H)CH,PPh,). 5 , 129 NiC33H30N6 Ni(&C Ph =CPhN=NCMe,N=NC(Ph)= h H 7 - ) . 2,904; 6, 181 NiC33H38P;S2. [Ni{(Ph2PCH,CH,CH2SCH,),CH,}]2+, 5,130 NiC34H2LN802 Ni(dehydrophthalocyanine)(OMe),, 6,90 -I

Ni{$=CPhCHPhNH(CH,),N=CPhCHPhNH(CH,),) I", 6,165 NiC,,H,,N,P,S, .. . ... . .Ni(NCS),{Ph2PCH,CH,NMeCH,)2},5, 130 NiC,,Ho,IN,P, [NiI{N(CH2CH2NEt2)(CH2CH2PPh2),}]+, 5, 135 NiC34H44N2P2S [Ni(SR){N( CHzCl12PPh2)2( CH2CH,NHEt2)12+,5 , 137 NiC34Hs6082 Ni{0P(0)(OEt)(CH2C6H20H-4-But,-3,5)}z, 6, 1020 NiC3,H3602P3S [Ni(O,Shle) {FhP(CH2CH2PPh,),}]+,5, 128 NiCISHSiN,P3SeSi3 Ni{ (Me,Si),NP(Se )=NSiMe3} (dppe), 2, 1051 NiC3SHsiNZP3Si3 Ni{(Me3Si)2NP=NSihk3}3(dppe),2, 1051 NiCJ6Hr6IN8 Ni(phthalocyaninej1,6, 144 NiCI3824N6

[Ni(phen),l2+.1.24,64,466,467.539; 5 , X O I N i ( y I i ~ n ) ~ ]5.~ + 29U . NiC.36H24N60, [Ni(phen :V,:V'-dio~ide),]~+, 5, 162 NiC3,HZEP2Se2 Ni(2-Ph,PC6H4Se),. 5 , 124 NiC,,H3,BrKOP2 NiBr(NO)(PPh,),. 2, 109 NiC36H30BrP2 NiBr(PPh,),. 5,40 NiC3,H3"Br2P2 NiBr,(PPh,),, 5 , 110; 6, 3U5 NiC36H30Clh'OPz NiCI(NO)(PPh,),, 5 . 13 NiC3,HJ,,C1P, NiCI(PPh,),, 5 , 37 NiC36H130C1202PZ NiCI,(OPPh:)?, 5.62: 159 NiC3,H3&12P2 IViC12(PPh3)2, 5 : 62. 110; 6,279,306 N~C~~H~OIZPZ Ni12(PPh3j2,6.248 NiC36H30NOPZ [Ni(NO)(PPh&]'. 5, 13 NiC36H30N~02P~ Ni(NO),(PPhd,, 5 , 13 NiC36F130N203P2 Ni(liO,)[NO)(PPh,),, 5 , 13 NiC3iH3,$iOPi Ni(N,)(NO)(PPh,),. 2, 103, 107,233; 5 , 14 NiC-,hH?n02P2 _ _ .. . . Ni(PPh,),(O,). 5 , 28 NiC,,H3,O,P,Sz ~~

Cumulative Formula Index

47 1

NiC4ZH3HNZP2

Ni(PPh,),(SO,),, 5,30 NiC36H3006P2S Ni(S04)(0PPh3)2,5,153 NiC36H3oPz Ni(PPh3),, 5 , 9 NiC36H321NZPZ NiI(2-pyCHzPPh2),, 5 , 124 1020

NiC36H3312P3

NiI,(PHPh&, 5 , 110 NiC36Hd8 [Ni{(2-pyCH,)3N)Z]2' 5,88 NiC36H39Br08P4 NiBr(HO,CCH,PPhCI jzCl I,PPhCH,CO,H)(H02CCH2PPhCH2CH2PPhCH2Co,),5,125 NiC36H40N4S4 Ni{S,C,(C6H4NMe2-4),},, 2,625 NiC3;H4,N6 Ni{&=CHC6H4NCH(NEt2 C6H4N= CHChH4NCH(NEtZ) 6H4}, 5,270

Ni(octaethylporphyrin), 2,841; 5,274 NiC36H44P4Sz [Ni{S(CH2CH2PPhCH2CH2PPhCH2CH2)2S)12', 5,264 NiC36b154018P6 [Ni{P(OC~~),(C~l,),},IZ, 5 . 115 NiC3JLPM" Ni(PBu,),(PhN=NPh). 5.22 NiC36H66P2 Ni{P(C6Hii)3}zr5,32 NiC36H67C1P2 5 , 112 NiHCI{P(C6H11)3}2, NiC36N44N4 Ni(octaethy1porphyrin).6.147 NiC37Hi71N7 Ni(triazatetrabenzoporphyrin)I. (1. 744 NiC37H30N20PZS Ni(NCS)(NO)(PPh,),, 2,233: 5 : 14 NiC37H6602P~ Ni{P(C,HI1)A}2(CO2).2.452; 5,5,24.25

Ni(PPh,),(H,C=C=CH,), I\;iC39H39BrP3 NiBr(PPh,Me),. 5,40 NiC H ?.P

5, 15

Ni{2-~H2C6H4CH2P(Ph)CHzCH2P(Ph)(CH,),P(Ph)CH,CH,PPh), 1.446: 2.926.935 ~. NiC40H201N4 Ni(tetrabenzoporphyrin)I, 6, 144 NiC,,H,P, Ni{ P(C,H,,),),(MeCH=CHMe), 5 , 15 N~C~OH~OF~PZS~ Ni{S,C,(CF,),}(PPh,),, 5 , 178 ~

Nii+H30F8PZ

I{ Fddl(PPh3)z. 5 , 15 NiC40H,oN2P2S2 Yi{S2C,(CN)Z}(PPh,),, 5, 178 NiC40H34P2S2 [Ni(S,C,Ph,)(dppe)]- ,5,179 Ni(SzCzPh2)(dppe).2,613 NiC40H38PzS, [Ni{PhP(C6H4SMe-2)2}2]2+, 5, 171 NiC40H40NZPZ N i( PEtPh,) 2( PhN-NPh), 5,22 NiC,,HC,PdS, . _ __ . [Ni{S(CH2CHzCH2PPhCH2CH2PPhCH2CfTICA2)2S}I2*: 5,264

NiC40H78N404

Ni{ON=C(C17H3j)C(Me)=NOH}2, 6,112 NiC,,Hq,N2P, . . . Ni(CK)z(9-Me-9-phosphafluorene),, 5 , 110 NiC4iH39ClP3 YiClttriphos), 5,37,41 NiC41H39C)ZP3 NiCl,(triphos), 5 , 133 Ni C, ,H3JPj NiI(triphos), 5 . 42 Ni C, H,,NO P3 [Ni(NO)(triphos)]+,5 , 13 NiC41H39K203P3 Ni(CN)2{PPh2(CH20H)}3,5, 110,111 NiC4,H3902P3S Ni(SO,)(triphos). 5,5,2Y NiC41H3904P3S Ni(SO,)(triphos), 5.64, 133, 153 NiC41H3904P3Se Ni(SeO,)(triphos), 2,425; 5, 153 NiC41H39P6 [Ni(triphos)(q3-P3)]+,5 , 33,36 NiC41H40P3S Ni(SH)(triphos)? 5.41,42 NiC,&LFi A P z Ni(PPh~),C(F3C)2CNNC(~F3)2}, 5,21 NiC42H35C1P2 NiCI(Ph)(PPh,),. - , - 5,32 NiC42Ef36N2'F2 Ni(PPh,),(CH,CHCN),, 5 , 15 NiC42H38NZPZ Ni(bipy)(PPh,),, 5,32 ~

N~(O~Cl~H8),(py),, 2,398: 5.146 NiC38H30CIF3P2 NiCI(C,F,)(PPh,),. 5. 114 NiC38H30F4P2 Ni(PPh3),(C,F4), 5, 15 NiC7aH7nN206P2 Ni(CN),{P(OPh),},, 6.296 NiC38H3AJ" Ni(CN)2(PPh,)2,5 . 45 ~

NiC38H30N8

Ni(NPhN=CPhN=NPh)2, 6.78 N~C~SH~ONI& Ni{SC(=NNHPh)N=NNPh},jphen). 1,547,552 NiC38H3002P2 Ni(C0),(PPh3),. 5, 11; 6,279 NiC38H3002P4 Ni(CO)(PPh,),, 5 , 11 NiC38H30P~S4 Ni(CS2)2(PPh3)2,2, 582 NiC38H34Br2P2 NiBr2{P(CHzPh)Phz},.1,207; 5 . 110 NiC38H34PZ Ni(PPh3)2(H2C=CH2), 5 , 15. 16. 17, 18 NiGdhP2Sz Ni(SPh),(diphos), 5 , 169 NiC38H3502P Ni(acac)(PhC=CPhMc)(PPh,), 5 , 112, 113 NiC38H40NP3S2 Ni{N(CH2CH2PPh2)2(CHzCHzPPhCS,Me)}, 5,26

NiC,zH390P3 Ni(CO)(triphos), 5 , 10 NiC42H3P3S~ Ni(triphos)(CS,), 5,25,26 NiC42H3J'3S3 Si(S?C)(triphos),5, 178 NiC5~HdoO,P2 Ni(PPh3),(CH2=CMeC02Et). 5. 17 NiC,,Hd1CLP, N l ~ l z { ~ c C ( C ' H z P P h , ) 2 ( C ~ , C ~ , P P5, l ~133 ,)), NiC42H42BrNP3 1NiBr{N(CH2CH2PPh,),1]C: 5.3:hh NiC,,H,,CINP, NiCI{N(CH2CH2PPhz)3},5,37.41 (NiC~{,N(CH,CH,I'Ph,)~}~ .5.hb NiC42H421NP3 Nil{N(CH2CH2PPh2)3},5,5,32 [NiI{N (CH2CH2PPh2)3}] 5.135 NiC4ZH42NOZP3S Ni{N(CH2CH2PPh2)3} ( SOz),5,29 NiC4,HdZNP3 Ni{N(CH2CH2PPh2)3},5,30: 31 5 . 4 1 , 4 3 , 136 [Ni{N(CH,CH2PPh2)3}]++ NiC42H42NP7 Ni~N(CHZCHZPPh2)9).(rl'-P,). 2, 10%: 5 , 30 +

.

N~C,;H,,NP,S~ Ni { N( CH2CI12PPh2)3} (ri ' - P 4 S ~ )5.3 r 1 NIC~,H~~N,OP~ [N;(N(CH2CH2PPh2),}(NO)] I , 5 . 5 , 12. 14 N IC',k I5,P4 [ N I { P ( C H ~ C H , P P ~ ~ ) ~5.42.43 }]+, [Ni{(Ph2PCHZCH2PPhCHz)z)]'-. 5,130 N I C ~ ~ H ~ ~ N P ~ [NiH{N(CH2CH2PPh2)3}]-,5 , 3 0 . 136 NIC~~H~~NP~S [Ni(SH){ N(CH2CH2PPh2)3}J+. 5 . 166

~ ~ ( N ( S I M C ~ ) ~ ) ( P5,43, P I I ~1U7 )~, KiC4,H39F4P3 Ni(triphos)(C,F,), 5, 15 NiC43H3&~P3 Ni(CN),(triphos). 5, 133 YiC43H52NOP3 Ni(CO){N(CHzCH,PPh,)3}. 5 , 11.31, 41 [Ni(CO){N(CH,CH,PPh,);)lt. 5.138 NiC43H4~P3S3 (Ni(S2CSMe)(triphos)l', 5 , 178 NiC,,H,,NO,P,S [Ni'(S&(OMc)} {N(CH2CH2PPh2)3)] +.5 . 138 NiC43H45NP3 jNiMe{N(CH,CH,I'Ph,),}]-. 5,13K NiT,,Ht7( )P7

Ni~P(~,II;,),},(PhC~IO), 5,20 NiC44H18CIN404 Ni(tetraphenylporphyrin)(OCIO,). 2,841 NiC4,Hd4 Ni(tetraphenylporphyrin), 2,841 NG4N3& Ni(octamethyltetrabenzoporphyrinate),5,274 NiC45H4~P2 Ni(PPh,),(cod), 5, 15 NiC14H440P3SZ [Ni(S,COEt)(triplios)]+, 5, 178 ?iiC,JI,,NOP3 [Y~(COMC){N(CH,CH,PP~~)~}]~, 5 , 139 NiC54H&,Pz N i { P( 0C,H4Me-2),} 2 ( H&==CH;). 5. 17 NiC44H4rN03P3S [Ni{S0,(OEt)}{N(CH,CH,PPh2,3)]'i , 5. 138

NiC44H73NP2 Ni{P(C,H, ,),},(a-PhCH,CN), 5,20 NIC,SH~FSP, Ni(triphos)(C2F4)2.5. 17 NiC,,H,,YO,P,

.

.

NiBi-(MeC;=C:R.lzPh)(P~h3)2, 5 , 114 NiC:,6114sN,P2 Ni(C:NDuL)2(PPIi,)2, 5 : 29 NiC,,€IJqNP,S, [Ni(S,CNE~,)(viphos)]', 5. 178 NiC,,H,,N,O,S, Ni(7--HN-4-(,C,6H330zC)CgH3S),6, 112 NiC47H.1003P2 Ni(PPh3)2(PhCOCH=CHCOzMe), 5,17 NiC47N34N11 Ni(N-methyltetrapyridylporphyrin)(imidazole)2,2. 841 N G S H ~ OnFNI 3 z IG(C6FjNNNNC,Fs)(Pph;),, 5.23 NiC48H30F,8P2 Ni(PPh,)l(C,(CF,)6}, 5, 16 NiC.,sH3,N40z Ni (etliuxycarbor~yl)tt:traplietiylliom~porpliyrin), 2 85 1 NiC4JLJ~.d4 Ni(octarnethy1tetrabcnzoporphyrin)lI 6 , i46 NiC48H40N2P2 Ni(PPh,),(PhN=%Th), 5 , 21,22 NiC48H44NP3S Ni(triphos)(PhNCS), 5,25 NiC48H44Pf Ni(PHPh&. 5 - 9 NiC48H54P4S2 [Ni(S,CPEt,)(tripho~)]~+, 5 , 178 NiC'lRH10004P2S4 Ni{S2P(OC,zH,,)2)2, 6, 112 NiC48H108C12012P4 Ni(Bu3PO)4(C104)2. 5 . 159 NiCjJ1421'2 Ni(pPh,),(PhC.~H=CHPlI), 5 , IS NiCSoII,,NP, Ni(PPh,)2(C,hteSP=NBu'), 2, 1051 NiC&66yiP4Si3 Ni{(Me,Si),NP=~SiRe~}3(triphos),2, 1051 NiCjoH,,P2 Ni{P(C6Hll:)3}2(l.2-q2-anthracene), 5, 15, 17 NiC50H92P4 Ni{CHz{P(C6H11)2}~)2, 5 , 10 NiC51Hj5N502S Ni{N-(,tosylamino)tetraphenylporphyrin,2, Si19 NiCSJL5N [Ni { tctrakis(%iV-mcthv1pyridyl)porphyrin ) ( f I N r = R F R Z H ) ~ ] ~1 ,5,274 NiC:52H4sN203P4 Ni(NOZ)(K:O)(dppe),. 5 , 14 NiC52H4sP4 Ni(dppe)2, 5,6,9,31,118 NiCSzH;,CI08P4 [Ni(OPPh,h.ze)d(CIO,)!+, 5,64 NiCF,H42P4 Ni(PMePh,)?. 5. 9 NiCs2H62N304 [Ni(NPh,),(THf)4] , 2 , 171 NiC54H430P4 [Ni(otl){2-Ph2PC,H,),P)li, 5, 136 NiC,,II,,OP, [NI(HIO)((2-PhIPChH4)RP)]2+, 5, 136 NiC,,H,,BrP, NiBr(PPh3)3. 5.5, 32 NiC54H4SCINOP, Ni(NO)Cl(PPh,),. 4> 1067

473

Curnulutive Formidla ladex

NiH12Br20h

NiCI, [NiC13]-*5, 56, 187 NiC1, [NiC14JZ-.1.255.274; 5,61,62, 186, 187, 595 NiC140,P2 Ni(02PC12)2.5, 154 NiCl, [NiCI,]". 5. 186 NiCl,,P4 Ni(PCI,&, 1,418; 2, 1030; 5 , 9 NiCoC,,,H,,N,O, ICO(?*'H~)~{(O?CCH~)~NCH~C~~,N(CH~~~~~)~}Ni(HIO)] , S , 219 NiCrCsH,&rK8 CrBrlen),(y-NC)Ni(CN),, 3, 778 NiCrC8HI6C1N8 CrCl(en)2(p.-NC)Ni(CN),, 3,778 NiCrC,oH20FN8 CrF(pn),(u-NC)Ni(CN),, 3,778 CrF( HZN(CHz),NH2} z( y-NC)Ni(CN),, 3.778 NiCuC4HB0 N ~ C U [ C ~ O ~ ) ~ ( H5,690 ,O)~. NiF3 5 , 287 N iF4 [NiFaI2-,5, 187 NiFh [NiFJ-. 5, 2% NiC62H54P3 [YiF,I3-. 5 , 296 [Ni(C,Ph,)(lriphos)]'. 5.33.31 [ I\IiF,I4-. 5. 186 NiC6,HS7OP, NiF,Si 5, [Ni(C,Ph,){ P(CH2CH2PPh2),(CH,CHzPOPhz)}]+, NiSiF,. 5.56 34 NiFI2P4 NiC63Hs7P4 [Ni(C3Ph3){P(CH2CH,PPh2)3}]-. 5,34.43 Ni(PF3)4.1, 318; 5,8,9,10 NiGa2CI6HZ4N8 NiC64H40N8 N i { M e G a ( N ~ H ~ H ) , ) 5, . ,102 Ni(octapheny1tetraazaporphyrin). 2, 858 NiGeC2,H2,,C1,P NiC64H50PZS4 NiCp(C;eCI,)(PPh,), 2, 19 Ni(S2CzPh2)2(PPh3)2, 2.617 NIC7ZHbOC108P4 NiFIN& Ni(S,N,H)(S,N), 5,212 [Ni(ClO,)(OPPh,),] ' . 5.04. 152 NiHN4S, NiC72H60C1z012P4 [Ni(S,N,H)(N,S,)]-, 5,212 Ni(C10A)2(0PPh3)4. 2. 500; 5 159 NiH02 NiO(OH), 5,297 NiHZN4S4 Ni(HS2N,),. 1.446; 2,120,799; 5,212 Ni(PPh,),, 5.32; 6.290, 305 NiH3NOI [Ni(PPh,),]+, 5 , 4 0 Ni(OH),(NO). 5. 107 NiC74H60Nz04P4S2 Ni(NCS),(OPPh,),, 2. 500 NiH4C12010 h'i(C104)2(H,0)2,5 , 152 NiC,sH,,OJ'h NiH4N208 [Ni{(OPPh,),CH,) ;I2'. 5 , 161 Ni(N0,)2(t120)2,5, 14Y NiC78H7206P6 NiH,O, [Ni{(OPPhZCH,),},]". 5. 161 [Ni(OH),]'-. 5 . 139 NGzHd'6 NiE&O,P, Ni(triphos),, 5, Y Ni(H,PO,),, 5. 154 NiH40,P2S4 Ni(S,P(OH)2)z, 5 6 7 NiH6ClzN2 N-i(NH&CL2,5, 59 NiH6Nz [tG(NH,),]2+I6.829 NiCdC4HiN6 NiH606 Cd(NH3)2Ni(CN)4,5, 932 [Ni(OH),14-. 5. 139 NiCdC12H16N402S4 NiH,N,O, NiCd(SCN),(THF),, 5.988 Ni(GHj(NH3),(NO), 5, 107 NiCdCl4Hl0NG Nil T,CIIN, Cd(py)zNi(CN)4,5.932 NiCI,(N,H,),, 5 , 7 7 NiCde;,H,,N, Cd(en)Ni(CN)4(pyrrult.)2.9,932 NiHsN20zrl NiC1,NO {~CI,(NO)),,,5. 107 NiClzOs Ni(C104),, 2,414

NiCS4H4XIP, NiCI(PPh3)3,5,40 NiCs4H4s02P3S~ Ni(PPh,),(SO,), 5. 30 NiC54H4sP3 Ni(PPh3),, 5 , 9 NiCs4H46BrP3 NiHBr(PPh3)3,5, 112 NiC54H52N2P2 Ni{P(C6~-I,Me-4),},(I'hNNPh). 5.22 Nit&HQ9P3 Ni{P(ChH,M3,5 , 9 NiC1ssH4s0d'3 Ni(CO){P(OPh),},, 5. I 1 N~CS~H~~NPR NiH(CN)(PI'h?)?, 5, 112 N~CS~HS~PZ 5, 17 Ni{P(C6H4Me-4)3}2(PhCH=CHPh), NIC _ _ ~ __L O A S ? Ni (3-{2-O-J-(Bu'CH2CMe2)C6H3S}-4HOC6H3CMe2CH,Bu'},, 6, 1021 NlCs7H4sPz [Ni(C3Ph3)(PPh3),lt,5 , 3 3 NiCs7Hs60P4 Ni(CO)(dpph)2, 5, I 1 NiC,,H,,,NP, Ni(PPh,),(PhCN), 5.20

NI€I,,Br2O6

Cumulative Formula inndm

Ni(HzO)6Brz, 5,61 NiH1ZBr201z Ni(H20)6(Brodz, 5,60 NiHI2Cl2N6 Ni(N2H4)3C12,5.58 NiH,,CI,O,, Ni(H20)6(C104)2,5,61, 152 NiH*ZNZOIZ Ni(H20),(N03)z, 5,61 NJjH,,N4 [Ni(NH3),I2+, 1,27; 5, 595 NiHI2N6O4 Ni(Nli9)4(N02)2,2,28.418; 5, SY. 61. 150,595

474

NiN,s {Ni(N&]*-, 5 , 104 NiNa2C36H34Nb04 [{ Ni(~alen)),Na(?vieCN)~]+, 5 , 197 NiNb1203B [NiNb12038]12-,5,296 Ni02 [NiOJ. 5.297 Ni(02), 5 , 29 NiO, Ni(O&, 5, 29 Ni04S2 [Ni(S0,),j2', 2,635 NiPbN,O,, [PbNi(N0,)6]z . 2 , 418: 5,691,701 NiPtC38H46N10

Ni(4-MeC,H4N=NN=NC6H4Me-4),Pt(CNBu')2, 2, 221

NiPtCSSH4,C1,P3S2

(Ph3P)CINi(CS,)PtCI(PPh3),,2,583

NiH,Ni [Ni(N2H4)6]2',5,77 NilOb [Ni(061)]-, 2,418,431 Ni13 INiI,1-, -_ 5 5 8 Nii, [NiI,IZ-, 5 , 187 NiMnCAOASA M n N i ( S ~ C ~ 0 2 )52, ,182 NiMoC,HloNS6 (MoS,)Ni(S,CNEt,), 3,1423N~MOC~~H~,P~S~ Ni(Me,PCn,CH,PMe,)(SMtt),Moood),, NiMuO, NiMoO,, 3, 1376 NiMo2C24H32S4 [Ni(SMe),(MoCp2),J2+, 5.168 NiMO@& [N~(MOOS,),]~--, 2,575 NiMo204S4 [N~(MOO,S~),]~-, 2,575 N iM o S [N~(MOS,),]~-,5 , 175 Niblo& [Ni(MoS,),]*-, 2,564,566,570,571,575 NiMo9O3, ( N ~ M o , ~ , , ] ~3,~1045; ' , 5,296 NiN,O,

,

Ni(S3N)2, 5, 176,212 NiN306 [Ni(NO,),]-, 5 , 150 NiN402 Ni(N&O,, 1,28; 5,29 NiN4OI2 [Ni(N03)4]Z-,5, 148 NiN4S4 [Ni(N,S2)z1Z-,5,212 NiNSO [Ni(N0,),I3 , 5 , 150 NiN60i, INi(NO,),(ONO),]'-, 5 , 150 [ N i ( N 0 ~ ) 6 ] ~ 5- , 150 NiN8 Ni(N2)4, I , 28; 5 2 8

5, 16Y

NiPt&H5601zP8 [Ni{Pt{ OP(OMe)2)2(diphos)}2]2+,5, 155 NiReCsOs Ke(CO)5Ni(C0)3. 1. 123 NiSs [Ni(S&I2-, 2,541,546.5. 167 NiSbC,Cl,O, Ni(CO)3SbC13, 3,271 NiSbC72H60 Ni(SbI'h,),. 5, 9 NiS bSrO, SrNiSbO,, 5,297 NiSnC,C1,04S4 [Ni(S2C,0,)2(SnC1,)]2-, 5 , 182 NiSnCbOHs7NP, [Ni(SnPh,) { N(CH2CH2PPh2),)]', 5, 139 NiSnH12C1606 Ni(H20)6(SnC16),5,61 NiSn2C.4C1804S, [Ni(S,c,0,Sn~l,),12-, 5, 182 NiSrN,O,, [SrNi(N0,),I2-. 5,701 NiVC16HZ2N2U5 Ni(V0) ((MeCOCHCOCHCMeNCH2),}, 3,562 NiVC26H24Nz05

Ni(VO){(PhCOCHC0CHCMeNCH2),}, 3,561 NiV13038 [NiV1303s]7-, 5,297 NiWS, [Ni(WS4)I2-* 6. 112 NiW,O,S, [Ni(WOS,)2]z-l 2, 575 NiW.,O,S, [Ni(W02S,),]2- , 2,570,575 NiW& [Ni(WS,),I2-, 2.564.566,570,571,575 NiWhHh071 [ N ; W ~ H ~ 0 2 , ] 4 -3., 1044 NIW60z4 [NiW602+]'-. 3.1044 NiWl1H20,,Si [W,lSiNi(OH2)039]6-. 3, 1048 NiZnC.,H& Zn(NH3)2Ni(CN)4,5,932 NiZnC404S4 ZnNi(SzC,Oz),, 5, 182 NiZnCZoH32N904S4 NiZn(NCS),(THF),, 5,988 NiZnC,lH,lN,O, NiZn{(PhCOCHCOCHCHMeNCH,),)(py), NiZrF, NiZrF6, 5.61 Ni2A~3C4i H d 3

5,968

Cumulative Formula Index

475

[Ni,(triphos)(q3-As3)] ' .5.36 INi2(triphos)(r13-As9)12f.5,36 Ni;As3C4;H4,IN [NizI{N ( C H ~ C H ~ A S P ~ .5.42 ~)~}] Ni2As6c38 H 5 8N4 NiZ(TCNE){PhAs(CH2CH2CH2AsMe2)z}2, 5,128 Ni2(TCNE2-)(PhAs(CH,CHzCH2AsMez),) ,I2+, 2,263 Ni2AshCR4HR51N2 ~Ni[N(CH2CH2AsPh2)3])z(u-I), 2.681 Ni2A~6C85f18412N2 [NiZI{N(CH,CF12AsPh,)3)2lt. 5 4 3 NiZA~qC48Hs90 Ni,(H20) { PhAs( CH,CH,CH,AsMe,)2} 3,5, 128 Ni2Au2C20HJ6N40& [Au2Ni,(SCMe2CH(NH,)C0,},]-, 5.877 Ni2BZC14H42N10 [{Ni(NCBH3){N(CH2CH,NH,),)}~J2', 5,75 NizBazO5 Ba2Niz05,5,297 NiZC2HZ4Br3N70S Ni(NH,),Br{ p-MeCOS}Ni(NH,),&r,. 1, 123 +

Ni2C4nH42N,&

{Ni{S2C2(CN),},J,. 2,617 Ni2CI7Hl5F3N2O3

Ni2(py)2(CF3COCHCOCHCOMe),2,399 I\:i2C18H26N,S2 [{Ni(2-pyCH2CH2NHCH2CH,S)},]*+,5 2 16 NiZC18H3sN806 [ N ~ ~ ( C ~ H ~ ~ ~ ) { N ( C H Z C H5.74 ~NH~)~}ZI~+~ Ni2C181154C14N Ni2{(H2~C:H2CH2NHCHZ)2J3C14, 5,227 Ni2C18H54Nll [Ni,{(H,NCH,CH,NHCH,),}3]4' ,2,54: 5,76 Ni,C ,,H,,P,Si, {,Ni{P(SiMe,),}(PMe,)},, 5,42,43 Ni&&d16 {Yi(&!NCHKNCMeCMcNNCHNNCMeeMe), 5,257 NiZC20H48P6 {Ni(depe)},P2, 2,1047 . Ni&2H32C1,N, { Ni (HzC(fiN=CMeCH=~Me),}CI,} ,, 5,102.280 Ni2C24HzsN80s Ni2(~0,)4(4%epy),. 5, 151 Ni2C24H48S12 [Ni,(l.4.7, lO-tetrathiacycl~undecane)~]~~~, 5, 171 Ni2C24H5,Nc;0, ~

fNi,(S,7-dimethyl-l,4,8,11tetraazacyclotridecane),(C,~~)I2'*~ 5.233 NiZC21H66P4Si4 ~'iz(l'Et3)2{P(SiMe3),),,5,23 NizCz4l-f7,P,Si4 {Ni(P(SiMe,),}(PMe,),),, 5,40 Ni2C25H33N08 Ni,(acac),(py), 2,386; 5. 143 NiZC2&4010 Ni,(acac),(Pr'OH),, 5, 143 NiZC28H16N1Lh {Ni(NCO),(3-pyCN),},, 5, 104 Ni,CzsH20Slu Ni,(S,CPh),S,. 2,646 NI,Cl o ~ , 4 ~ ~ , ~ 2 Ni,C,,I 1,4C14N., [Ni21(~N=CMcCH=~Mc),(NO),] . 5 , 14 (Ni(2,9-Mc2phcn)CI,),, 2,679; 5,80,8'1 NIZC10Hf4N603 5.14 Ni(r(l-Me)(NO)},, Ni Z C ~ d L04t o Ni,(tropolonate),(H,O),, 5, 145 Ni2C10H20S8 Ni,(SEt),(S,CSEt),. 5. 177 Ni2G&4N17 [Ni,( l;?,S,l l-tetramethyl-1,4,8,11Ni,C~oH,,N,~ tetraazacyclotetradecane),(N,),lf . 5 +240 Ni,{(SCH,CH2)zNMe},. 1.147 NiZC28H66N602 Ni,CloHq,NRO, [{Ni{N(CH2CH,iXEt,),(CH,CH,0H)}}2]z-~ 5,217 [Ni,(C0,),(en)4]2+, 5,72 Ni2C30H260& [Niz(Cz05)(en)412t,5,158 Ni,(OSCPh),(EtOH), 5,148 NiZC10H32N10S~ [{Ni(NCS)(en)2}2]", 5, 72 N i 2 C d b 8I R Ni2(SCH,Ph),(S2CSCH,Ph)2,2,527 NiZCIZH18018 INi{0,CCH,C(OH)(C0,)CH,C0,}(H,0),],2-,2,477 Ni2C30Hd208 _, Ni,(acac),{HN(L H2IS}, 5, 143 Ni2CI2HJ6Nl4 [Ni2(trcn)2(N3)2]2+, 2,233: 5 7 4 , 104,282 Ni&J%&rd% [Ni,(l18-naphthyridinc)413rz1+, 2,92; $79,283 Ni2C12H39N606 Ni,C32H2sS8 [Ni,(OCH,CH,NH,)3(HOCH2CH2NF~2)312+7 2,795 (Ni(S2CCH2Ph),},, 5, 172, 174 Ni;C1iH22N202S2 Ki2C32H30N808 {Ni{MeCOCHC(Me)=NCH,CH,S}},, 5,222 Ni,(CO,),(py),(NO,),, 5,78 NiZC14H32C12N309 Ni2{OCH2CH2N(CH2CH2NEt2),) (C104)2r5,64 Ni2C36H&LN4 {Ni(biquinolyl)CI,},, 5,280 NiZC14H32N13 [NiZ(N3)3( Ni2C36H301ZN202P2 1,4,8,1l-tetramethyl-l,4,8,11{Ni1(NO)(PPh3)},. 5 , 13 tetraazacyclotetradecane)]+, 5, 104 NizC~,H,,,NHO, Ni2C14H,6N 10°2 INi,(NCO),(trcn),l". Ni,(C,O4)(0NO),(py),. 5, 158 ~. 2.227; 5,74, 104, 282 Ni;C1iH36N1,& NiZC38H30P2S4 2,582; 5, 25 Ni2(CS2)2(PPh3)2, [Ni~{N(CH~CH2NHZ)~}z(NCS)2]2C, 5,282 & C d d A N~zCI~H~~N~O~ Ni,(02CBu')J(quinoline)2, 5,282 [NiZ{1,4-{(H2NCHICH2)2NCH2}ZChH4}(H,0),]4+, 5, 226 N i2C40H3sPS { Ni(SCH2CHZS)(PPh,)}2 . 5, 170 Ni,C16H,,Br,0R [(NiBr(EtOH)4},]2+. 5. 140 Ni&oHdi& Ni2(NCS),(4-Mepy),, 5,282 NizCi6NaSs

Ni&& [Ni,(CN),I4-, 5, 37 Ni2C8H16S6 Ni,(SCH2CH,SCH2CI12S),. 2.529.5.170 Ni,C8Hz6CI,N6 {NiCl,(dien)},, 5.74 Ni2C8H3,Br,Ns [Ni2(en),Br,12+, 5. 280 Ni,C8H3,CI,N8 [{NiCl(en),}z]2+, 5, 72, 277 NizCsH32Nio04 ~Ni(en)2(0,N)1Z*-,2,427; 5.72, 151

Ni2GOH54N2O8

.

Cumulative Formula h d e x

476

. .

[Ni2C18]4-,2,680 Ni,H4CLR02 [Ni2(H20)2C18]4~, 5,280 Ni2Li3C73H72Ns02

Ni2(Ph2CNH)2(Ph2CNLi)3(OEt2)25 5.20 KI2NaC&34N604 [{Ni(~alen))~Na(MeCN)~]+, 3, 16 Ni203 Ni203,5,297 1 8 N~zVCIRHR ~ 4O VO~{C)P(OMe)2j,NiCp}zJ, 3,567 Ni3AbC60H90N12012

{Ni(camphorquinone oxime oxirnate)ZAg)3,5,214 Ni,B,O, Ni3(03B)2,2,430 Ni3Ba308 Ba3Ni30a,5,297 Ni3C7HI9F3Ol1 Ni3(0H)2(H20)6(CF3COCHCOCHCOMe)2, 2,399 Ni3C8H24C12N4S4 Ni3(SCH2CH2NH2)4C12, 5,209 NLCBH~'G, ~Ni3(SCH2CH2NH2),]z+. 1.417; 2.799 Ni3C.,2H30NP3 ~Ni,{N(CH,CH,PMe,),)]~' ,k.135 NiC H N 0 :N;~~(&N-H),(OH,)~~~I . 5 , 86

Ni&28H56016 Ni4(OMe),(acac)4(MeOH),, 5, 140,286 Ni4C,6H440,z Ni4(2-OC6H,CHO),(EtOH),, 5,286 Ni4C36Ha016 N L , ( O M ~ ) ~ ( ~ - O C ~ H ~ C H O ) ~ ( M5,286 ~OH),,, Ni4C40Hj6016 Ni4(OMe),(2-OC6H,CHO),(EtOH),, 5, 140 Ni4C4BH32N808

[N~,(OM~),(OAC),(CNCM~,CH,CH~CH~CM~,NC)~]~ 5.

157 Ni4C48H96N8SB {Ni($CHCH2CHaNMeCH2~H,j,},,1, 148,5, I68

Ni3C12H48N1506

Ni4C,00H80N4p4

{Ni(en)z(NOd)j, 5,287 Ni3C14H28S8

{Ni(PPh3)(PhCN)>,. 2.262; 5,20 N~~CIIZ%&

477

COC 1-P.

Cumulative Formulu Index

NPOlOS2

NpRhHio0.l KDRhHqnO,

Cumulative Formula Index

0 OSAIC~~I~~,CI~N~P~ Os(NNA1Me3)(PEt2Ph),C12. 4.555 OSAS~C~~H~~CI~ Os(AsMe,Ph),CI,, 4,577 OSAS~CI~H~~CI~ Os(AsPr,),CI,, 4,577 OSAS~C,,H~~CI~ Os(dpam)CI,, 4,579 OSAS~C~,H~~CI~P Os{PPh(CHzCHzAsPh2),)C13,4,579 OsAs2C36H30Br4 Os(AsPh3),Br4,4,577 OSASZC~~H~(JJNO Os(NO)CI(AsPh,),, 4,550 C)sAs2C3,H3,CI3NS OsCI,(NS)(AsPh3),, 2. 114, OSA~~CXH~,C~, Os(AsMe,Ph),CI,, 4.577 OSAS~C,,H~~CI~ Os(AsPr3),C13,4,577 OSAS~C~~H~~ Os(AsEtPh,),H,, 4,576 OSAS~C~~H~~CI~NZ Os (As(C6H,Me-4),) 3C12(N2H4), 4,556 OSAS~H~~C,~H,~C~, O S ( A S P ~ ~ ) ~ C I .4.~S25 H~C~~. OSAS~C~~H~~CINO [Os(NO)(diars),CI]’+, 4.537 OSAS~C~~I~~ZCIN~ [O~(N~)(diars)~ClI 4,5 5 5 - 565 O S A ~ ~ C ~ H ~ C ~ N ~ Os(N,)(diar~)~CI. 4,565 OSAS~C~~H~~CI~ [ O s ( d i a r ~ ) ~ C l4, ~ ]579 ~+, OSAS~CZZH~~N~SZ Os(diars),(SCN),, 4,566 OSAS~C~OH~ON~ [Os(bipy)(diars),12’. 4.540 C)SAS~C~OH~, Os(AsEt,Ph),H,. 4. 576 OSAS~C~~H~~N~S~ Os(dpam)2(SCN)2,4: 566

~.

[OsBrJ. 4, 6.15 [OsBr,l2-, 4,613,614 [OsBr,13-, 4,613 OsCC1,NS [Os(NCS)CI5]*-,4,566 [OS(SCN)CI~]~-, 4,566 OsCH12N60 4, 555 [OS(N~)(NH~)~(CO)]”, OsCHlSCl,Ns0 Os(NH,),(CO)CI,, 4. 528 OsCH,,FSks’O,S [Os(03SCF,)(NH,),12+,4,529,536,600 OsCH,,NiO [Os(NH3),(CO)]Z’.4,529 ~ O S ( N ~ I , ) , ( C O )4,529 ~~+, [C)S(NH~)~(CC))]~+, 4, 528 0SC2C1~O4 ~os(c20,)c1,]~-, 4,601 OsC2H2N204 [OSO,(OH)~(CN),]*-,4, 526 OsC2H3Br, N [Os(NCMe)BrJ, 4,567 OSC~H~NO~ [OSN(C~O,)(OH)~(H,O)]-, 4,562 OsC2H4N2O4 [ O S ( C ~ ‘ ; ) ~ ( O H ) 4,526 ~]~-, OsC,t.I,Br,N, Os(en)Br,. 4,530 OsC,H,Cl,N2 Os(en)CI,, 4,531 [Os(en)C1,1-. 4,531 OSC~HRN~O~S~ [O S O ~ ( H ~ N C S N H ~4,584 )~]~+, OsC2H808 [OSO~(OH)~(OCH~CH~OH)]*-, 4,593 OsC,H,d,oOz [OS(N~)(NH~),(CO),I‘~, 4,529 osc3c1305 [os(c,u,)(co)c13]’-, 4,6U1 OSC~CIIZN~ [Os{NC(CC1,)NCCICCl3}CI,~,4,558 OsC4HZNO9 [OsN(C,O,),(H,O)]-. 4, S62 OsCqHZN402 [ O S ( C Y ) ~ ( O H ) ,~4],~526 OSC~H~N,O [OsN(CN),(H,O)]-, 4,525,562 OsC4HBN20, O~Oz(Gly-0)2.4,583 0sC,H805 0~0(02CzH4)2,4,585 OSC4H8O6 [ O S O , ( O , C ~ H ~ )4,~ ]585 ~~, OsC4HqNOs OSO~(NRU‘), 2. 182; 4,558 OsC4HluC1202Sez OsO2Cl,(MeSeUHzCH2SeMe),4,609 OsC,H, ,CI,O,S, O S O ~ C I ~ ( S M 4, C ~584 )~. OsCJHl2NlOOl OsOZ{HN=C(NHZ)NC(NH2)=NH),, 4,568 ~

479

Curnulutive Formitla index

OSC4~1206

OsC,Hl,06 [ O S O ~ ( O M ~ ) , ]4,580,582,585.5Yh ~-, OsC,H,,NO,S [OS(SCH,CH,NMe,)(OH),]-, 4,607 OsGHi4NioO, [OSO2{HN=C(NH,)NHC(NH2)=NH)21',

[OsOz{HN=C(NH,)NHC(NH2)=NH} ,I2',

OsC,H,,N

11

4,568 4,568

0

[OsON(HN=C(NH,)NHC(NH~j=VH},]'-,4,563 OsC,H.,,CIN,

[OS(~~=CHCH=NCH=CH)(NH,)~CI]~ ' .4,535

480

OsC,H&', [ O S ( H ~ N C H ~ C H ~ N H' ,4,530,532 )(~~)~]~ [ O S ( H ~ N C H , C H , N H ) ( ~ ~ )4,532 ,~~+, [Os(H,NCH2CH21iH)2(en)]2+, 4,531 OSC~ZJZN~ [ O s ( e r ~ ) ~ I ~4,531 ]~-. OSC~HZJN~ [O~(en),]~'.4.531 [0s(en):j3-. 4.53&532 0 S c : 6 k 3 2.tN I &

[Os(I12NCSNI12)c]2+. 4.608 [ O S ( H ~ N C S K H '~ )4, ~ (rOR ]~ OsLIRNb [Os(CK),]'-, 4,525.526 [oS(cK;)6]"-.4. 525,526 OsC,N6S6 [Os(NCS),13-, 4,566 j(NH3),IZ+,4, 535 OsC7H,,N0, OsO,(quinuclidine). 4. 592 OS{N(CH,CH,)~CH)O,, 1 ,4 4 OsC8H,,N03 OsO3(N(CH2),Me}. 4,558 OsC8H1 ~ o s ( ~ ; ~ = c H c H ~ ~ 4,536 c ~ ~ ~ ( ~ H ~ ) &1,S3 ~ ~ ~ ~ . Os { S( CH2CH2CH?SMe)2}C13, 4,603 [os(H=cHcH=NcH=CH)(NH,),~~-. 4,535 OSC~~H,,K~~~, OsO,(NBu'),, 4, 559

OsC,H16C1,N, [Os(en)2Cl,] ' .4,530, 531 OSC,H,~N~O, [CkO,(en),]z+, 4,583 0~CqH16N8 [Os(H=CHCH=NCH=CH)(h', OGHi6NsOA [Os02(H*NCSNH2)41'+,4,608 OS'C,H~~N,[0~H,(en)~]",4,530, 531 OSc4H 19N7

OsCJ I,,N,

[Os(IIN=C(Me)C(Me)=NH}Z(NH3)2]2+, 1. 446: 6.

[Os(NS)(NCS),12-,2, 119; 4,553.562.566 OsChH,N,S [OS(H,NCSNH~)(CN),]~-, 4,608 OsC,H,NsOS [OS(NO)(CN),(H~NCSNH~)]~-. 4.608 OsC6H,Oio 4.582 [Os02(O~CCH2C02)2j2-. OsC,H,CI,NO

. .

[Os(HN=CHCH2NH2)(en)2j2-.4.532 [O S ( H ~ N C H ~ C H ~ N H ) ~ 4.532 (~~)]+. [Os(H,NCH2CH2NH)2(en)j2+. 4.532

1YO OSC.~H~,N~ Os(NH3)2(HN=CMeCMeNH)2,4,533 OSCBH~~N, [ O S ( H ~ N C H ~ C H ~ N H )4,533 ,]~+, OsCpH2gYS [Os(H2NCH,CH,KH),( en)),', 4,533 OSCqH27P&6 Os(PMe3),S6.4.603 OSC,H~~P,S, OS(PMYIC3)3S7r4>603 C)sC,,,HSCIJ2 [Os(hipy)CI,] . 4 . 541 OSCl@II,, OsCp,, 1 . 1.27 OsCloHioC13N3S Os(NS)C13(pyj2,4,553 OsCioHid'W3 osO,py,, 2.980: 4 . 5 8 5 , ~ ~ OSCioHioN203 OsO,(py),, 4.592

OsC,oH,,CI,OJ Cls(acac),CI,, 4,597 O K loH.l,Ni,O, Os0,(1.2-0,C,H4)(p);),, 4,598 OsCi,,H,,NzOg Os(H,O)(edta). 2,783 OsC1oHijN OsO,(X-l-adamantyl), 4.558 OGJLOi, OsH3(!~-OH)(C0)12,2,297 OsC12H806 [ 0 ~ 0 2 ( 137-02C6H4)Z]2-,4,582,597 OsCi,H i"C:IZNZ02 os(py),(c:o),c'I,. 4,533 OSC,,H~~N~~, OsO,(OH),(phen'). 4 , 583 OsC12H., 2C12Y30L Os(bipyj(G1y-O)CI,, 4,602 OSC12Ht213N6 OS(H=CHCH=NCH=CH),I,. 4,535

Clrinulalive Forrnulu Lndex

48 1

Os(YS)C13(PMeZPh),,4,553 OsCl,H2*C],PZ Os(PMe,Ph),CI,. 4.574

osc12H;4N,oz

Os02{HN=C(NH2)NC(NH,)=NH)(bipy)]+, 4,568 OsCizH140 OsCp(v5-CjH4CH2CH20H).1. 127

OsO,(tropolonate),, 4. 597 OsC14H1,Os

{0~0(1,2-0~-4-MeC~H~)~}~, 4 . 598 OSCi4Hi6N404 [Os(bipy)(Gly-O),] , 4 , 602 OSC~~HZZNOP~S~ Os(PMe,Ph),( S,CNMe,) (S2COEt),4,605 OSCi4HwN6 [Os(bipy)eti,]2t, 4, 540 OG.+H2J'J,O, Os02(NBu'CH(C02Me)CH(C02Me)NBuf}, 4,557 +

0SC15H12N303

OsO,(terpy)(OH), 4,544 O S C ~1,5CI,N3 ~I Os(py),C'I,, 4.534 OSC15H1513N3 OS(PY),I,, 4,534 OSCi5Hi6N406 OsO,(thymine)py,, 4.586 OsC15H2106 Os(acac),, 4,597 IOs(acac),l-, 4,597 Os{MeC(S)CHC(S)Mej3,4,606 OsC, ,H,,,CIN,S,

Os(PEt2Ph)3H4,4,571 OsC,,H,,CIO, jPj [OS(P(OE~)~}&I]',4,575 OSC32H16CINs Os(phthalocyanine)Cl, 2, 867 OSC~~H,&~ {Os(phthalocganine)},,, 4,618 OG2HlbN802 Os(O),(phthalocyanine j , 2,867

OSC,,H,,N,O,S

O~(C204)(phen)2, 4,601 O~CXHZ~C~ZPZ Os(PMePh2)zH2C12.,4.570 OSC26H38C120P3 0~(PMe,Ph)~Cl,(0Et), 4, 596 OSC~~H~~CIP~S~ Os(PMe,Ph),(S,PMe,)CI, 4,606 OsCz7HI 8N3S3 O~(8-quinolinothiolate)~. 4. 617 OsC,,H,,C10P3S2 Os(PMeZPh),(S2COEt)C1. 4.605 OSC~~H~~CINP~S~ Os(PMe2Ph)3(S2CNMeZ)C1, 4. Clr).l OSC~,H&I,OP~

[ O S ( P M ~ ~ F ~ ) ~ C I , ( O C M4.598 ~~)]+. OSC2BH2ZNM

Os(phthalocyaninc)(SO,). 2,867 { Os(phthalocyanine)S04},2,4, 619 OSC~ZHZ~N~ [Os(bipyj,(phen)]?+, 4, 537 OSC32Hz8N6 [ O ~ ( p h e n ) ( p y ) ~ 4. ] ~540 -. O S C ~ ~ H ~ ~ N ~ P ~ O S ( N ~ ) ~ ( P M ~ * 4.565 P~),. OsC3zHd', O S ~ P M ~ ~ P I4.571 I)~H~~ OSC~;H,~N~O. Os(phthalocvanine)(CO), 2,867 OsC38H30C12N3P Os(py),(PPh3)C12. 4, 534 [Os(py)dPPh3jCI~]+,4,534 [O~(py)~(P€'h,)Cl~]~+, 4,534 OSC33H48C13N15

[Os(pal~drine),]~+. 4.567 [O~(paludrine),]~',4: 568 OSC~~H~ON~

[O~(bipy),(4-pyCH=CH,)~]~+, 4,542 OSC36Hz& [0s(phen)J2-, 1 , @ ; 4.537,538 [Os(phen),13', 4.437,538 [Os(phcn)#+. 4.539 OSC~~H~~CI~F~P~ OS(PF~)~[PP~~ 4,576 )~CI~, OSC,,H&I~NOP, Os(NO)C12(PPh3)2r4,549 OSC&30C12NP2S OsC13(NS)(PPh3),. 2, 121

483

Cumulative Formula Index

OsC,,H,,N,OP,

Os(Se2)(C0)2(PPh3)2, 2,667 OSC38H3004P2 O~(CO)z(Oz)(PPh3)l,2.320;4,596; 6. 329 OSC~BH~~P~S~ Os(PPh3)2(&CH)2,4.608 OSC~,H~~B~,NP~ Os(NCMe)Br3(PPh3)2, 4,567 OSC~~H~~CI~NP~ Os(NCMe)~13(rJ11h3),, 4, 567 OSC~SH~~CI~O~P~ OS(PP~.I)~CI~[OM 4,596 C)~, OGJL,N,O, Os(oclaethqIporhyrin)(CO)(McOH),4, 595 OSC~~HSON~O~ Os(octaethylporphyrin)(OMe)2,4, 6 I8 OsC3,1 I,,N,O, OSO~(O~C~~H 4,586 ~~)PY~. OSC~~H~~O~P~SZ [ O S ( C O ) ~ ( P P ~ ~ ) ~ ( ~ * - 4, S ~1121; M ~ )6,350 ]+, OSC~&~C~J'~ Os(PMePh2),HC13.4,570 OsC,oHmCIN,, 04phlhalocyanine)CI{ 1,2-(NC)2C6H4J, 4,619

Os(octaethylporphyrin)Br,, 4.618 OSC~~H~~C~ZN~ Os(octaethyIporphyrin)C1,. 4. 618 OSC36H44FNs OsN(octaethy1porphyrin)F. 4.562 OSC36H44FNsO Os(NO)F(octaethylporphqrin), 4,548 O~C~&,N~OZ OsO,(octacthylporphyrin). 2.837; 4,583.618 OSC36H44N602 Os(NO)Z(octaethylporphvrin).2.837; 4,551 OSC36HmN402 Os(octaethylporphyrinj(OMe),, 2.837 .. . . OSC36HsoN6 Os(octaethylporphyrin)(NH,),, 2, 837 OSC36H90018P6 [Os{P(OEt),},12+, 4.575 OSC~~H~OCINO~PZ OsCI(CO)(NO)(PPh,j,, 2, 111:4. 548,550,596

OSC~~H~~NOZP, Os(NO)H(CO)(PPh,),, 4.550 .~ OSC~;H,,CINO~P~ OSCl(NO)(CH2SO2)(PPh,),. 4, 1165 OsC,,H,,ClN,O Oi(octaethylporphyrin)(CO)Cl. 4.618 OG7H47NsO OsN(octaethy1porphynn)(OMe), 2,837 OG7H47NsOz Os(NO)(OMe)(octaethy.Iporphyrin) 4. 548 OSC~,H~~C~~~PZ OS(Oz)(CO)HCI{P(C,H,,),),. 4.596 OGsHnN& Os(phthalocyanine)(py)(CO) 2 , 867 OsC3,H3,C120Te OsCI,(PPh,),(CO)(CTe), 2, 671 OSC~~H~OJ', [Os(CO)2(NO)(PPh,)z]'. 2. 103, 105, 112; 4,550

OS(NO)~(PP~~),(O,CCF~)~, 4,547 OsC4,H3,C140,P, OS~O(OAC)~CI~(P 4,595 P~~)~, [ O S ~ O ( O A C ) ~ C I ~ ( P P4,595 ~~)~]-, 0'3C4OH37 C12N303P2 Os(N,){N( OH)CHC02Et}(PPh3),C1,, 4.555 OSC~OH~~N~O Os(octaethylporphyrin)(N2)(THF), 2,837; 4.618 OGoH63P1 [Os(FEt,Ph),H,]+. 4,571 OGiH39CLP3 Os(triphos)CI,, 4,579 OSC~~H~~CI~P~ Os{PPh(~'HjPPhz-2)2}ZCIZ, 4,579 O S C ~13jC13NZPZ ~I Os(N2Ph)(PPh3)2C13, 4,551 OSC~~H~~YZP~S~ Os(PPh3)2(S2CNMe2)2, 4,604 OSC&42P& Os{S2P(C6H4Me-4),),, 4,608 OSC~~H~SCI~NO~P~ Os{NP(OEt)Ph~}Cl~{P(OEt)Ph~}~. 4,568 OsC4,HJ9Y50 Os(octaethylporphyrin)(CO)(py), 2, 837; 4- 471.617 OSC~~H~~N~S Os(octaeth ylporphyrin)(CS)(py), 2,837 OGIHWPS OsH,(PEtPh2)31 6. 250 OsC,,H5,YS, Os(SC6HMe,-2.3,5,6),(NCMe), 4, 607 OSCJZHJ'L~J'Z Os(octaeth ylporphyrin) { P(OMe),} 2 , 4.61 8 OSC~~H~IN~OP~ OSH(CO)(N2Ph)(PPh3)2,2, 136 O S C ~ ~ H ~ ~ B ~ ~ O ~ P ~ Os(02CPh)Br,(PPh3)2,4,600 OsC,3H&lN" Os(NCPh)CI,(PPh,),, 4,567

OsH(~O),(N,Ph)(PPh3)2.2, 132 OSC,~H,~N,OP,

OsH(CO)(PPh,),{CH,=C(Me)NC(H)NPr'J,2.205 OSC~~H~~NZOP~

Cumulative Formula Index

4x4

Os(PPh,),CI,. 4.572 OsCIBrF, [OsF,CIBr]-. 4.610 OsClO4 [0sO4C1]-. 4. 592. osclo,ss, [os(so,)jcl]’-. 4.599 OsCI,F, [OSF~CI~ 4:]610 ~~,

OsCI,Hi,N, [Os(N,)(NH,),CI,]+, 4, 555 OSC120~ [Os03Clz]’~, 4,583 OSC1,O ,,s4 [Os(so3)1c12]~ .4.599 OSCI~F~ [OsF,C1,]2-, 4,610 OsCI,NO {Os(NO)C13},,.4. 546 osc130zP oso2(Pc13),4 , 576 OSCI~FZ [ O S F ~ C ~4.~ 610 ]~-~. OsC1,N [OsNCI,]-, 1,44;4,560 OSCl,h‘O (Os(NO)Cl,j-. 4,546: 548 OsCL,N2S2 OS(NS)~CI~, 4.553 osc1,o OSOC1,, 4,5Sl OSCl4O2 [0sO2Cl4]*-,4,583 osc140,2s4 [OS(S03)4C14]8-r 4* 599 OsCI,N [OsNCI,]?-. 1-50:4,560 OsCI,NO [Os(NO)CI,] 4,545 [OS(NO)CIS]2 ,4.546 OsCISNS [oscl,(~s)]2, 12’1,4, 553 OsC15NzS2 [OsCI,(NS)(NSCl)]-. 2,120 [OS(NS)~CI.CI~]4,552 OSCI, [0sCl6]-, 4,615 [oSc16]’-, 4, 613,6141 6, 823 [OSCI,]~-,4,613 OSClgN2S2 Os(NSC1),C14, 4, 553 OSCI,O [OsOCl,]-. 4! 584 (jsc:lhP OsCI,(PCI,), 4,576 OsFO, [OsO,F]-. 4: 592 OsF203 Os03F,, 4,593> 596 OsF204 [OsOqF2]*-,4.592 OsF302 O S O ~ F4,588.596 ~, OsF303 [OsO3F3I3-!4.593 OsF304P OsO,(PF,), 4,576 OsF, OsF,, 4,609 OsF,O OsOF,, 4,584 OsF, OsF,, 2,680; 4.611 ’

OsH{4-MeC6H4NC(H)NC6H,Me-4}(CO)(PPh3)2, 2, 204 OSC~ZH~~CI~’~ Os(dppe),CI,, 4,579 OSC~~H~~NOP~ Os(NO)(dppe),, 4,551 [Os(NO)(dppe),]-, 4,550, 551 [O~(NO)(dppe)~l’ ,4,550 0SCj2H54P4 Os(PMePh2)4H2,4,570 OG4H36N, [0~(2,2’-biquinoline),]~+, 4,542 OSC~~H~~CINOP~ Os(NO)CI(PPh,),, 4,550 OSC~~H~SC~ZP~ Os(PPh3)3C12,4,572 OSC,~H~SCI~NP, OsCI,(NPPh3)(PPh3)2,2, 123, 125.1, 568 OSC54H45C13P3 Os(PPh,)TCI,, 4,574 OsC,,H,,CIP, Os(PPh,),HCI, 4, 570 OSC,~H,~NOP, Os(NO)H(PPh,),, 4,550 OSCSJL~F~P~ O S ( P F ~ ) ( P P ~ ~4,576 )~H~, O~C54H4d’3 OsH4(PPh3)3,2,204 OSC~~H~~CIP~ [OS{PhZP( CHz)3PPh2}2CI]+.4.579 OSC55H470P3 OsHZ(CO)(PPh9)3,2,205 OSC&~@ZP~ Os(OAc)H(PPh,),, 4, W0 O~CWHM Os(PEtPh&,H2, 4,571 0SC56H62P4

OSHz(PEtPh2)4, 6, 250 OSC58H46N6

Os(tetra(4-t0lyl)porphyrin)(py)~). 4.618 OSC60H4804S4 Os(SOCi,Hiz)4,4,607 OSC~~JH~ON~PZ Os(PhNNNPh)2(PPh3)2,4,565 OSC~IH&I~NOP~ Os(PhCONPPh,)CI,(PPhj),, 4,569 OSCS~H~SNS~ Os(SC6H,Pr’,-2,4,6),(NCMc).4, h07 C~SC?&OB~~P~ Os(PPh,),Br,, 4, 573 OsC72H60CIZo12P4 Os{P(OPhj3}CI2,4,575 OSC~~H~OC~ZP~

I

I

Ciirnidative Formula lndex

485

OsF,NO [ O S ( N O ) F ~ ]4.546,548 ~-, OsF,O OsOF,, 4,588 OsF, OsF,, 4,611 [OsF,]-, 4,611 [OsF6]*-,4,610 [OsF6I3-, 1,498 OsF, OsF,, 4,612 [OsF,]-, 4,612 OsF, OsF8, 4,612 OsF,,P, O S F ~ ( P F ~4,) 610 ~, OSFI~P~ [Os(PF,),]*-, 4, 575 OSFisPs Os(PF,),. 1,41; 4. 576 OsFeC4HZ6N4O7 [Fe(H20)500sO(en)2]4+. 4.583 OSHCI~O [OsCl,(OH)]*-, 4,594,615 OsHNO, OsN(OC1)02,4, 562 OsHNsOio [OS(NO)(OH)(NO,),]~-,4.546,548,598 OsHO, [OsO,(OH)J-, 4,591 OsHO, [Osz(OH)O,]-, 4,579 OsH,Br,NO [OSNB~,(H,O)]~-. 4. 561 OsH2C1303 [OsO,Cl,(H,O)]-, 1.583 OsHLCI,NO [OSNCI,(H,O)]~-,4,561 OsH,CI,NOS [Os(NS)CI,(H,O)] , 2 . 120: 4.553 OsHzCI,N03S [OS(NH~SO~)C'I~]~-, 4. h l h OsH,C1,0 [OsCI,(H,O)]-, 4,615 OSH~F~NOZ [Os(NO)F,(H,O)]-, 4.546 OsHzFiJ'4 Os(PFX),H2, . -4,576 OsH206 [Os04(OH),]Z-,2,296; 4.579.591,592 [OsO,(H,O)]-, 4,588.591.592 OSH~OIOS~ [OS(SO,)~(OH),]'-. 4,549 OsH2OI2S2 4. 599 CISO~(OH),(SO~)~. os11201Gss [ O S ( S O ~ ) ~ ( H ~ 4.599 O)~~-, OsH,BrC1N20z [OsBrCI(NO,)(NH,}]-. 1. 177 OSH~CI~N [Os(NH,)CI5]-, 4, 528 [0s(NH3)C1,]*~, 4. 528,529 OsH306 [OSO~(OH)~]-. 4,592 [OSO,(OH),]~-,4.580 os€i4c1,o* OsC14(H,0)2,4, 615 OsH4FzN03 [OsNF,(OH),(H,O)] .4.562 OsH,O, Os02(OH),, 4,593 [OSO,(OH),]~-,2,296; 4,525.579,580,581, 591 OsH6OIZS3

Osl,N

[OS(SO,),(H,O),]' -,2,638; 4, 599 OsH60,$, [or(HS0,),]4-. 4,600 OsH,S6 [Os(SH),IZ-, 4,603 OsH9Cl2N5 OS(N,)(NH~)~CI~, 4,555 [OS(N,)(NH~),CI~]+, 4,555 OsH9Cl3N3 Os(NH3)3C13,4,528 [OsWH3)3C131+4,528,529 OsH,N,O,S, [Os(S0,),(KH,)3]4 , 2 , K U OsH10BrZN40Z ()s(NO)( Ot I)(NH3)3BrZ,4. 549 CkH,, QN40? Os(NO)(H20)(NH,),CI, 4,549 [Os(NO)(H~O)(NH3),Cl]2+, 4,546 OsHl2ClN,O3S Os(SO,)(YH,),CI, 4,599 OsHI2Cl2K4 [Os(NH3),C1,]+. 4,528,529 [ O S ( N H ~ ) ~ C I 4,528,529 ~]~-, OsHI2lN, [Os(N2)(NH,),II+, 4,555 C)sHIIN,O, [OSO,(NH,),]~+.4,528, 5x3 OsH,,N, ~

[Os(NO)rOH)(NH,),]2', 4,546,548 OSH,~N,O [OsN(NH3),(H,O)l3+, 4,562 OsH&,O [OS(KO)(NH~)(NH~)~]*+, 4,546,557 OsH,,N, [OS(N,)(NH~)(NH~)~]'+, 4,554 OsH15ClNS [Os(NtI,),C'l~Z+,4,528,529

OsHijN7 I-, 4,528,554 [OS(NZ)(I'~H~)S]~ [Os("'JH3)5]3', 4,555 [OS(N~)(NH,),]~+, 4,555 OsHI6Nj0 [Os(NH3)j(OH)I2', 4,528 [ O S ( N H , ) ~ ( O H ) ]4,529 ~~, OsHI7N50 [OS(NH~),(H,O)]~+, 4,528,529 OsH,,N,, [Os(NH,)(?rH,),J3+, 4,557 (ISH,e& [ O S ( N H ~ ) ~4,528 ]~+. [Os(NH,)J3+.4, 528; 6 , 190

~

0~(PPh&C1~2HgCl,,4,525 osr4K

Cumulative Fortniilu Ifidex

486

[OsN141-, 4,560 Osl, [os16]2-,4,613 OsNO, [OSO~NI-,4,561,562 OsN20, [OS03(N02)2]'-, 4,583 OsN,O,, [O~O>NOZ)4]2 -,4,598 OsN,O,, [OSOZ(NO,)~(NO~)~]~-. 4.598 OsN,01n [Os(N02),]2i, 4, 598

O~N~,O [Os(NO)(N3)s]Z-,4.546 OsNm [Os(N,),] ,4,565 Os04 [Os04]-, 4,588 [0sO4]2-, 4,580 [Os0,j3-, 4,580

oso,

O S ~ C ~ H X I11C ~ N

[OS~(&=CHCH=NCH=~H)(NH,)~C~]~+, 4,535 [ O S ~ ( ~ = C H C H = Y C H = ~ H ) ( N H , ) , C ~4,535 ~~+, O&C4H34N12

[OS~(~'=CHCH=NCH=~H)(NH,),,)~~, 4,535

[0sO5l3-, 4,588 [ O S O ~ ] ~4,580 -, Osob [osob]5-, 4, 580, 588 [OS06l6 , 4 , 580 [os06]'-, 4,580 0SOPS?

[os(so,),]4-.4,599

oso14s4

{OSO~(SO,)~]~-, 4,583 [OSO,(SO,),]~-, 2,638; 4, 591,599,600 OSO,,S6 [Os(SO3),l8-, 4,591.599 OsRhC4Hs4NiZ

[OsRh(fl=CHCH=NCH=ekJ)(NHs)io]6+, 4,535. 956 ...

0~RuC,BrC1~0~Si Os(CO),BrRu(SiCI,)(C0),, 4,285

[OsRu(2,2'-bipyrirnidine)(bipy),j'+. 4,537 OSRUC~~H~OCI~OP~ Ru(CO)(PPh3)2(p-CI),0sCl(l'Ph3)2. 4,411 OSRUC~~H~~N~ OsRu(octaethylporphyrin),, 4,618 OsRuH,,N,, 0

OsSb&4Hi5Br3 Os(SbPh,),Br,, 4,577 OSS~~C~~H~SCI~ Os(SbPh,),CI,, 4,577 OSS~~C~~H~OCI~ Os(SbPh,),CI,, 4, 577 OsSnCS4H4&l5P3 Os(SnCl3)(PPh,),CI2, 4. 527 OrSnCI, (0~(SnCl,)Cl,]~-,4,527 OSSIIZCRH&~,~N~S, 2.647 OS{M~C(S)NH,},(S~CI,)~, OsSn,C19N0 [O~(NO)CI,(S~ICI,)~]~ , 4, 518 [Os(NO)C13(SnC13)2]2+, 4,549 OsSn5Br16 [0~(SnBr,),Br]~-,4,527

[OS,(~~=CHCH=NCH&H)(NH,)~~]~ ' ,4,535 [Os~(fl=CHCH=NCH=~H)(NH3)io]'+. 4,535

487

Os3CBiHI6N2O9

Cumulative Formula Index

488

P P ~ A s ~ C ~ ~ H ~ ~ C ~ ~ PaCl,(diars), 3. 1144 PaAs3CI8Hl8Ol1 PaH30Z(PhAs03)31 3,1182 PaBr,O PaOBr,, 3,1185 PaBr, PaBr,, 3, 1173 PaBr, PaBr,.". 3. 1185 PaBr, [PaBr,12"-, 3, 1175 PaC,H,O, Pa(O,CH),, 3, 1154 PaC10H14C1J04 PaCl,(acac),, 3, 1182 PaCi8H15CI,PSe PaCI,(Ph,PSe), 3,1185 PaC2aH,&IN& Pa(Et2NCSJ4CI, 3, 1184 PaCzsHZoClOs Pa(tropolonate),CI. 3. 1182

PaIiloOd'~ PaO(II,P04),(H,0)2, 3, 1182 Par5 PaI,. 3,1185 PaN30i0 PaO(N03)3, 6,957 PaN50i5 Pa(NO&. 6,957 PaN60T8 [Pa(NO,),]-, 3, 1182 PaOd'3 PaO(P03)3.3. 1182 Pa,C4Hd ,,,O,, Pa,0(N0,)8(MeCN)z, 3, 1179 Pa2CIB0 Pa,OCI,. 3, 1 I85 Pa2F9 Pa2F9.3,1185 P a A Pa2U5,3.1180

PaCZ8H2008

Pa(tropolonate),. 3- 1149 PaCioH~6C10$

Pa(tropolonate),Cl(DMSO)s 3. 1184 PaC35H2sOl~~ Pa(tropolonate),. 3, 1182 [Pa(tropolonate),l-, 3, 1150 PaC1*0 PaOCI,. 3,1173 PaCI, PaCI,, 3, 1173 PaCI, PaCI,, 3, 1185 PaC1,O [PaOCI,IZ-, 3. 1186 PaF, PaF,, 3, 1185

PbC,I-I,O,

PaF, [PaFJ ,3, 1186

FdCpCl, 3,218 PbCjH9N02S Ph{D-SCMEZCH(NH,)CO2}, 2,745 PhC5H1202 PbMe,(UAc), 3,210 PbC,H&I, [PbPhCI4]-, 3,200 PbC6HjCls [PbPhCIjl2-, 3,200 PbC6HsNO6 [Pb{N(CH2C02),}]-, 2,789 PbC6H60z PbPh(OH)O, 3,206 PbGH,,Ni 2 S f i [Pb(SC(NH,)2},]2', 3, 188 PbC7HI4N2O2 PbMe,(C(N,)(CO,Et}, 3,205 PbC8HIINOfi Pb{EtO2CCH2N(CH2CO2),), 6,422 PbC&i,O, Pb(OAc),, 3,212 PbCBH180

PaF, [PaF,12 , 3 , 1186 PaF, [PaFJ-, 1,24:3. 1132. 1186 PaHN6O:s PaH(NO&. 3. 1182 PaH09S2 PaHO(SO,),, 3, 1182 PaH2N0, [Pa(0H),(NO,)I2+, 6,956 PaH?N,O, [Pa(Oil),(N0,)2]*, 6,956 PaH2N301 Pa(OH)z(N03)3.6.956-957 PaHZN,O,, [Pa(OH),(N01)4]--, 6.956 PaH3OI3S3 PaH,O(SO,),, 3, 1182 PaH,O,,Se, PaH,0(Se04),, 3, 1182

Pb(O,CH),, 3.222 PbC2HsCI2N4S2 Pb{(H2N)ZCS}2C12.2,639 PbC206 [Pb(C03)2]2-, 6,853 PbC3H309 [Pb(HCO,),]-, 6,853 PbC3H9N3 PbMefN3, 3,210

489

FbCBH 1 8 0

Cumulative Formula Index

490

PbSut2O. 3,206 Pb(tetraphenylporphyrin)CI,, 2,822 PhC,H,OO,P,S, PbC,,kI,,N, Pb(meso-tetraphenylporphyrin), 2,822 Pb{S2P(OEt)z}2,3,222 PbC8N4S4 PbC48H32CIN804 [Pb(phen),(ClO,)]+, 1 , 9 7 [Pb{SzCz(CN),},IZ-, 2,617 PbC9H1503S6 PbC66H72NlZ06 [Pb(a n t i ~ y r i n e ) ~ ]3~ +188 [Pb(S,COEt),]-. 1,82 PbCI3 PbCioHio [PbCI,].., 6, 851. 853 PbCp,. 1, 151; 3,218 PbCI4 PbCi o H , J W " [Pb(cdta)12-,2,784 [PbCI4l2 , 6 , 847.851.853 PbCoN6012 PbCioH,J'J208 [PIK:O(N~~),]'-.5,691 [Pb(Hedta)] ,2,784 PbCrC36H:,n04 PhC10H14N209 Cr0,(OPbPh3),1 3,912 [Pb(H,O)(edta)]2-, 2 , 7 8 3 PhCuFe,H,O,,S, PbCiiHidzOa [Pb(trnta)],-, 2, 784 PbCuFez(S04),(OH),, 6 , 827 PbCuN601z PbCiiHisNz08 [Pb(Htrnta)]-, 2,784 [PbCu(N02)J-. 5-656,663,669,690,691,698,700, 701,702>704,707 PbCizHi6N&h1 [Pb(teta)]*-, 2,784 PbF6 2,787 [Pb{(02CCH2)2NCHzCH2N(CH2CHzCOz)2}]z-. [PbF6I2-, 3,200 PbFeCl0H,,O2 PbC,,H,,NzO, FeCp(CO),(Pbhle,), 2, 16 [Pb(Hreta)]-, 2,784 PbFcN,O,, PhCltHZ804PZS4 [PbFe(NO2),l2. 5, h91 Pb(SZP(OPr1)2}Z, 3,222 PhHBrCI2O PbC, ,H,,N,Si, [Ph(C)t-I)BrCI,]Z-.6, 853 Pb{N(SiMe&),, 3,220 PbHBr,C10 PbCmHizNzO, Pb(8-quinolinolate),, 1,528 [Pb(OH)Br,CI]-, 6, S53 PbHz08P, PbCi&i60 PbPh,(OH), 3,210 Pb(03POH)2,2.427 PbH3N PbCiaH1906 [Pb(02CMe)3Ph,]-, 1,90; 3.211 [Pb(NH,)]'+, 6.853 PbH3S3 PbCI8Hz8Cl2N3OP PbPh2C12(hmpt),3,200 [Pb(HS),]-. 6 . 853 PbH& PbC i d 1 ,NO PbH(HS),. 6 , 8 5 3 PbPh,(NCO), 3,210 PblI,N, PbCi826NsS PbEt,(SC(=NNHPh)N=NNPh}, 1. 530 [Pb(NH3),]2'1 6,853 PbIN7012 PbCmH lsoz PhPh,(OAc), 3.210 [PbNI(NO2),jZ-,2: 426 Pb13 PbC,oH,6O Pb( CsH3Etz-2 ,6),0, 3, 206 [PbI,)-, 3, 195 PbMo,C,,H,,O, PbC2OH3O (MoHCp2),Pb(OAc)z, 2.16, 19 Pb(C,Me,),, 3,218 PbCZ4Hi9BrS PbN6 Pb(N3)2,I . 1063 PbPh3(SC6H,Br-2). 3,213 PbNiN6012 PbC14HZ004PZS4 [PbNi(NOz)6]Z-.2: 418; 5,691, 701 Pb{SzP(OPh)z}2,3.222 PbC,,H,,CIN,OP PbO, PbPh,Cl(hmpt). 3,200 [Pb02]-, 3,205 PhC:,,H,,S, Pb03 [I'bC),j2? 3,204 Pb(SC61i,Pr'-2,h),, 3,220 PbC14H38C)4PZS4 PhOJ PbPti,{SzP(OPr'),}z, 3. 215 [PbO4I4-,2 , 295; 3: 204 PbC,,H,,ClzN,O,P2 PbOsSz PbPh2C12(hrnpt)2,3,200 [Pb(S0,),]2-. 6 , 85 1 PbPtC39H39CIPz PbC~6HnNioS2 Pb{SC(=NNHPh)N=NNPh}?, 1.530 PtCI(PbMe3)(PPh3),. 2, 16 PbPtCS4H4,CIP2 PbGoH32NioSz PbEt,{SC(=NNHPh)N=NNPh)Z. 1 . 5 3 1 PtCI(PbPh3)(PPh,)?. 5.420 PbPtC60H50Pz PbC3oH4602 Pb(OC6H2Me-4-Bu',-2,6)2,3. 220 PtPh(PbPhJ(PPh,):. 2, 16.20 PbCjrH2sNOz PbSiC&,,O Pb(ONPhCOPh)Ph,. 2. 507 PbPh3(0SiPh3). 3,206.208 PbSi4C14H38 PhC32Hi6Ns ~'b(phthalocyanine),2, 8A3, 8b.l. 868 Pb{CH(Sihle,),)z. 3.217 PbC3,H3,,0zSi, PhWC,,H,,O, Pb(OSiPh3)1. 3.220 (WHCpJ,Pb(OAc)>. 2. 16 PbC36H44CIlN4 PbZnH121,0,, Pb(octaethylporphyrin)C12, 2 , 822 Zll{Pb(I03)6)(H20)6. 5,961 PbC4,HZ8CIzN, Pb2C,CI06 ~

~

~

49 1

Cumulative Formula Index

PdC2HsN20&

Pd A s ~ hHjeC12 C~

Pb2FeRcO6 FePb2Re06,1,111

Ph,Ga>54

PdC12(Me2As(CH2)12AsMe2}, 5 , 1163 PdASZCZGH24C12 PdCI,(PhzAsCH2CHzAsPh2), 5, I162 P~AS~C~~H~JCI~ PdC14(PhzASCH,CH,AsPh2), 5, 1124 P~As~CZ~H~~N~S~ Pd(SCN),(AsBu,),, 5 , 1141 P~AS,C,~H~~N~S~~ P~(SIXN),(P~~ASCH~CH~A 5,1139 SP~,), P~AS~C~OI-~~~CIZ PdCII{ 1.2-(PhzA~)2CfiH,),5, 1162 PdASdL,oC& PdC12(AsBu'2(C6H4Me-2)}~, 5, 1167 P~AS~C~~H~~CIT' [ P ~ C I { P ~ P ( C I ~ ~ C H ~ A S5,1166 P~~),)~', P~As~C~~H~~CIZS~

Pb2CJa2S4,3, 137 Pb208 [pblos14-, 3,205 [Pb2OHI8-,2,302 PbZPtC7ZH60Pz PtPh(Pb2Ph5)(PPh3)2,2. 16 Pb,RuCioHisO, Pd{Ph3A~S)?C12,2,644 Ru(PbMe,),(CO),. 4.289 PdAs,C,6Hq6CIz Pb304 PdC12{AsBuc(C6H4Me-2)2}2, 5, 1167 Pb304,3,202 P~AszC~~H~ONZSZ Pb3014 Pd(NCS)2(AsPh3)2,5,1139, 1140, 1141 [Pb3Ol4]I6-,2, 302; 3,205 Pd(SCN),(ASPh,),, 5, 1139,1140 Pb3SbCgH27 P ~ A s, C ~ ~ H , , T, S ~ Sb(PbMe3)3,3,259 Pdl,(2-Ph~AsC6H4SMe),. 5. 1165 Pb4Clo,H,,,0,Si, PdAsIC42HJ;T Pb40(OSiPhl)h. 1. 151; 3,221 Pdl(Ph)(AsPh,),, 6,283 Pb4H4CI4O4 PdAs3C11H2,Br Pb4(0H)4CI4,6,853 [P~B~{McAs(CH,CH,CH~ASM~~)~}]+, 5,1166 PbJ I,O, [Pb4(OH),I4+, 1. 151; 2.300; 3,202 PdAs3C,SH23CI [ P ~ C ~ ( M ~ A S ( C ~ H , A S5 M , 1166 ~~-~)~}, PbS PdAS&,H3,CI2 [Pb5l2-,3,46 [PdCll(diars)2]2+,2. 1040; 5, 1123 Pb6H,07 PdA~JC20H3212 [Pb6O(OH)6lt, 2,304 Pd12(diars),. 5 , 1163 [Pb6O(OH),l4+,1, 157: 2.304: 3.202 P ~ A S ~ C ~ ~ H ~ ~ N S Pb607 [Pd(NCS){As(C6H,AsMe,-2),)1 '.,5 , 1141 [Pb607]*-, 2,302 PdAs,C2,H,,NS Pb8HIZC14012 'I41 [Pd(NCS){ ~ , X . ( M C ~ A S ) ~ C I O H5~,}l Z] +~ Pb,(OH),,CI,, 6,853 PdA~qCjdH42C12 PbeO [PdC12{As(C6H4AsPh2-2)3}]2+, 5 , 1123 [Pb,OPh,l*'. 1 , 163 P~AS~CJSH~~ P ~ ~ T I B ~ ~ o ~ ~ TIPb,O,Br,. 1. 163; 2,314 [P~{M~As(C,H,ASM~,-~)~}~]~+, 5 , 1166 PdAs6TrZCB,,H72C1302 PbyBrl,O; ' [ Ir2PdC13(CO),{ PhAs(CH2AsPh,),J2]+.4. 1164 Pb9O4Brl0. 1 . 163 PdAuC2,,F,,K2S2 Pb8tC36H3oPz [AU(C~FS)(~-SCN)~P~(C~FS)~]~-, 5, 874 [PtPby(PPh,)2]4-15,121 P~AsC~H~SCI~~ PdBCajH, BNgO [PdClS(AsEt3)]-.5 . 1123 Pd{ B(&=CHCH=cH),} { HON=CPhC,H,}. 2,252 PdBeC20H2,CIN,O, PdASC23H16F602 Be(acac){ MeCOCH,COCH,PdCl{bipy}} 3.26 [Pd(hfacac)(AsPh,)l+ 5 . 1114 PdBr, P~ASC~~HZ~N~PSZ [PdBr6]? 5. 1122 P ~ ( S C N ) ( N C S ) { P ~ Z A ~ ( C ~ H , P 5, P ~I139 ~-~)) PdCCLO PdAsC,,H,,N2PSe2 Pd(SeCN)2{Ph~lZs(C',H4PPhl-2)j,5. 1139 PdAsC3,H3,C12 PdClz(AsPh3)2.5 , 1158.6.282 PdC2H4N2S4 PdAsIrCl9H3,CI5P2 P~CI(ASM~~)(~-CI)~I~CI~(PM~~P~)~. 5, 1162 Pd(SZCNH2)2,5, 1147 P ~As ~ C ~ H~ ~ C I ~ PdC2HeCI3OS [PdCI,(DMSO)]-, 5, 1142 Pdcl,(A~Me,)~, 5, 1161 PdAs2C7HlsCId PdC2H6C13S PdCl,{Me,As(CH,),AsMe>}. 5. 1124 [PdCI,(SMe,)]-, 5, 1145 PdAsZCloH,,C14 PdCZH6CISS PdCl,(diars), 5, 1124 [PdCI,(SMe,)]-, 5, 1124 PdAs,C,,Hl,N2S, PdC,II,N,S, Pd(SCN)>(NH3):, 5 , 1139 Pd(NCSj(SCN)(diars).5 . 1163 PdCiHBCliNi P~ASZCIZH~OS~ Pd(SCH,CH,S)(dim). 5. 1149 PdCI,(en). 5, 1116 PdC2H&I,N, PdAs2C12H&, P~CL,(ASE~,)~, PdCl,(en). 5. 1123 5 , 1123 PdCzHSN103Sz P~AS~C~~H~OS~ Pd(S,O,)(en), 5 , 1136 Pd(2-Me2AsC,H4S)2.5. 1165

Cumulative Formula Index PdC,H,N,O6S, [Pd(Sz03)z(en)]z-,5, 11 16. 1136 PdC2H&40& [Pd(S~03)z(HzNCSNHz)z]2-,5, 1136 PdC*H,nN,O.& P~(s;O~)(H~O)(H~NCSN 5.1136 H~)~. PdC& [Pd(CS,)z]2-, 2,646 [Pd(S,C)z]2-, 5, 1147 PdC3H6C120S PdCI,(CO)(SMe,), 5, I142 PdC;H,CI,O,S PdCI,(CO)(DMSO), 5 , 1142 PdC,HgCl,N [PdCI,(NMe,)l-, 5 , 1116 PdC,H,CI,N [PdCI,(NMe3)] , 5 , 1123 PdC3HloCIzNz [PdCl,(pn)lZ+, 5, 1123 PdC3HloCI2NZO PdC12{HzNCHzCH(OH)CH,KHz}. 5. 1116 PdC3H12ClN4 [Pd((H2NCH,)3N}CI]+, 2,52 PdCaHdS, Pd(S2CzHz)z,2,621; 5, 1148 FdC4H6CINqO2 PdCI(MeCN)2(NC),), 6,372 PdC4HbClzNZ PdCI,(NCMe),, 2,201; 5 , 1 I21 PdC?HbIN,O, Pd(ON=CHCH=NOH),I.6.llJ PdC4k&.+S2 Pd(NH3),{SZC2(CN),}, 2.603 PdCdHbOj Pd(OAc),, 6,281,285.286. 287,788.290,301.307 PdCqH6Sa Fd(S,CMe)*, 5, 1147 PdC,H,N,O, Pd(Gly-O)Z, 5, 1115 PdCaHsN6Sa pd{SC(NH,)=NC(NHz)S)2. 2.640 Pd{H,NC(S)NC(S)NH,),, 5 . 1149 Pd(SCN)2(H2NCSNH2)2, 5 , 1139 PdC4H,,C1,0,S, PdCI,(DMSO),, 2,489,640.641.5. 1142. 1143 PdC4HlzC14Sz PdCI4(SMeJ2, 5. 1124 PdC,H1zN20&2 Pd(N03)z(DMS0)2,5, 1113, 1112 PdGHi2N2Sz Pd (HZNCHZCHZS),, 2,799 P~C~HIZO~S~ Pd(SO,)(DMSC)),, 5, 1142 PdC4H1208S4 [Pd(OzSMe),lz ,5,I135 P~C,II,,RTN, [PdBr(dien)]'. 2. 47 PdC4H13CIN3 [Pd(dien)CI]+, 1,505 [Pd(iea)CI]+, 1.505 PdC,Hi3N,Oz fPd(NO,)dien]+, 2,47 PdC~Hid6 [Pd(N3)(dien)]+,2.47 PdC4HI6Br2N4 [PdBr,(en),]Z+, 5, 1123 PdC,H,,CI,N, PdCl,(cn),, 5, 1123 IPdC12(cn),]2' , 5. 1123 PdC1H16N4 [Pd(en),I2+,2,33; 5, 1 1 16; 6 , % 150 P~C~HI~N& [Pd{(H2N)ZCS},lZ+,2,639,s. 1134

PdC,N, [Pd(CN),IZ-. 2 . 12 PdC,N,S, [Pd(SCN),]'-. 5.1138; 6,98 [Pd(S,CNCN),I2-. 5 , 1147 PdC4N4Se4 [Pd(SeCY),I2--. 5. 1139 PdC404 Pd(CO),. 5.1100 PdC,O,Sa [Pd(SC(0)C(O)S),J2 ,2,h45; 5. I149 PdC408 [ P d ( C 2 0 & ] 7 5.1111;6,113, 117 PdCSFIsUISN [PdClSpyl-, 5,1123 PdC,HIIN,U,

[Pd{MeO2CCHzNC(O)CHZNHZ}(H2O)]', 6,423 PdCSH13N,S [Pd(SCN)(dien)]-. 5,1140 PdC,H7,N,Se [Pd(SeCN)(dien)]+, 5, 1139, 1142 PdCSHISN3O2 [Pd(en)(H,NCH,C02Mc)]2+, 6,424 PdC61 ISCIS (PdCI(SPh)),,. 5 , 1137 PdChH6N4 { l'd(fiCI I=NCH=c I I),},, , 5 , 1I 17 PdC6H654 Pd(HCSCHSCH),, 2,621 PdC6HYF3Od Pd(OOBu')(O,CCF,), 6,347,348 PdC6HioCI2 PdC1z(q3-C3Hj)2,5 , 1102 PdC6HtoOz Pd(OAc)(l13-C,HT). 6,296 P~C~HIIIS, Pd(SCH=CHSMe),, 5, 1146 PdCGT1izNzO6 Pd{L-HOCH,CHINHz)COz}z, 2,745

PdCL2(DMF)2.6.248 T'dChH14S2 Pd(SPr),, 5. 1136 PdC6H14Si { Pd(SCH2CH2CH2SMe),}n, 5, 1146 PdChH,,Cl,P, PdC1,(MezPCH2CHZPh?e2),5, 1124 PdC6HI7K3O2 [Pd(en){a-hleCH(NH2)C0,M~}]2+, 6,424 PdC6HisC12P2 PdCI,(PMe,)2. 5. 1 I58 PdCGH18N4 [I'd{(H,NC'IIzCIIaNH~'t12),}]2+, 2, 54: 5 . I l l h PdC',Hlk,NJC)S [Pd(d~cr~)(DhlSO)j'.2 488 [Pd(dien)(DMSO)l2', 5.1143

PdCli(nbd). 6.288 PdC,H,,N,O,S [Pd(en){HSCH,CH(IdH,)CO,Et}]Z+, 6,424 PdC,FIrSa

492

Cumulutive Formula Index

493

PdCSH14N404 Pd(HDMG),, 5, I l l 8 PdCsH16C120& PdCl,{:TH2k} ,, 543:; PdCI,( CH CH OCH- Hz),, 5 , 1145 PdCSHi6C12SZ PdCI,{S(CH,),},, 5, 1143 PdCsHlsCI,Se, {PdCI2{MeSe(CH,),SeMej},,. 5. 1151 PdCsHlsC12S~3 PdC12{(McScCH2),CMe}.5, 1151 PdC12(Se(CH,CHZCH~SCMc)2], 5,1151 PdCsHjOCl2SC2 PdCl2(SeEt2j2,5 , 1144 PdC,HmO,PA Pd{(Et0)2PS2}2,2,644 PdCsHzoPSSe Pd{SP(Se)Et2}2, 5,1150 PdCsH20PSe2 Pd(Se,PEt,),, 5, 1150 PdCsH22CIZP, PdCI?(PEt,H)2,5. 1161 PdC8H;;NP2S, [Pd(S2CNHMe)(PMe3),]+.5.1117 PdC,H,,O,S, [Ph(DMSO),lZ', 2,490,641: 5. 1 112, 1143 IJdCsN4S4 [Pd{S2C,(CN),),]- ,2.623,5. I l O I , 1148; 6, 147 [Pd{S,C2(C:N),},]' - 5 , 1147. 1148 PdCyHiyNSOZ

PdC12H2B04P4

PdC ioH iJ'JLh Pd(O,)(CNBu')2.2,320 PdCIOHisPZS2 Pd(SH),(diphos). 2 , 5 18 PdCloH20N2S2Se2 Pd{SC(Se)NEt2Jz, 5, 1150 PdCioHzoS4 IPd(l.1.8.1 I-tetrathiacvclotetradecane)l+. 5 . 1150

Pd{Me?H(CH,)3PHMe},, 2,926 PdCioOio [Pd(CjOs),]*-, 2,455 PdCiiHioFPO2 Pd(CF,COCHCOMe)(NHPh), 2,390 PdCI2H8N2O3S Pd(S03)(phen),2,638; 5. 1133 PdCI2HBN2O6S2 [Pd(S03)2(phen)]z , 5 , 1133 PdC.,,H,N,S, Pd(NCS),(bipy), 5, 1139 T'd(SCN),(bipy), 5,1139 PdCI2HsN4Se2 [P~(~I~)(~=CHNHCH=~CH~CH(NH,)CO~M~}]'~ Pd(SeCK),(bipy). 5, 1139 6,424 PdCiZH9F12N04 PdCgH23CIP3 Pd(hfacac),(NHMe,), 5, 1114 [PdCl{MeP(CH2CH2PMe,)2}]+. 5 . 1 166 PdC12HloClK;O PdCQH7,ClNb Pd(2-O-3-MeC6H4N=Npy-2)CI, 1,448 [Pd{(Me,NCH,)3NH}CI]'t. 2. 52 PdC1ZH I oC12OqS2 PdCioHzF1?04 [PdC12(02SPh)212-,5, 1134 Pd(hfacac)L,2,347,375. 379.380,385.388,394; 5, PdC.l2HloCI,P2 1114, 1115 I'dC12(PPhC12):, 1,418 PdCloH,Cl,Br,N, I'dCl,Hlolo,;N404 Pd(4-CI-yy),Rr,, 1,314 Pd(henmquinons dioxime)ll,,5, 6, 'I44 PdCioHsC12N2 P~CIIH~ONIOA PdCl,(hipy), 6,305 Pd(benzoquinone dioxime),, 6 , 143 PdCioHsC14N2 Pd(4-Cl-py),Cl,, 1,314 PdCi#inN& Pd(SCN),(py),, 5, 1139 PdCl,(bipy), 5, 1123 PdCi2HioS2 PdCioHsF,O,S4 Pd(SPh),, 5.1136 Pd(MeC(S)=CHCOCF3JZ. 2.65 I . 652 PdC,,HloTe PdC,,H8F604 {Pd(TePh,)},, 2,669 Pd(CF,C0CHCOMel7, 2.389.390: 5. 1115 PdCi~HIICIN20~ PdClbHl,C1212N2 PdCI(OH)(phen)(H20), 6,305 PdIZCI2py2,5, 1123 PdC 1 ZH 1iCl,N, PdCloHloCIZNz P ~ ~ ~ - I M c C ~ H ~ N = N1,448 ~~-~)C~,, PdCI*(py)>,1,314; 6, 98.290 PdC.IZHttN303S PdClJ 11"CYdNj Pd(S03)(NH,)( p hcn) , 5 , 1133 PdCllpyz, 5,112'3 PdCIzH,2CI0,S PdCloHl lC1N202 [PdCI(O,SPh)i(H,O)]-, 5, 1134 PdCI(OH)(bipy)(H,O). 6.305 PdCi,Hi,N,O, PdC1oHi2C13N405 Pd(2-pyCH=NOH)z, 1,419 [PdCl,(inos~ne)]-, 5 , 1117 PdCi2Hi40& PdCioHi3C13N505 Pd(O,SPh),(H,O),, 5,1134 [PdC13(guanosine)]-, 5. 1117 -~ PdC12H& PdCioHi404 (Pd(1,4.7.10.13,16-hexathiacyclooctadecane)]2*. 5 , Pd(acac),, 2,379,380. 389-391; 5. 1101, 1114; 6,248, 1150 288 [Pd(l,4.7-trithia~yclononane)~]~' , 5 , 1150 PdCiJ I,,& PdCIZHZh04S2 Pd(McCSC1IC:SMe)>, 5. 1119 Pd(OAc),(SEt,),, 5,475 PdCIOHlSBrSP PdC12H&I2Sz [PdBr,(PEt,Ph)]-. 5. 1123 PdClJSPr,),. 1.314: 2.556 PdCioHi,CI,N,O, PdC *H;804P4PdCl,(camphorquinone dioxirne), 5, 11 19 Pd{P(Me j(CH,)3P(Me)CH(OH)CH(OH)P(Me)PdCiJfi,N30, (CH,),P(Me)CH(OH)kHOH}, 2,931 [Pd(en)(2-pyC02Et)12I . 6.424 ~

,

Cumulative Formula index

PdClzH29CIN3 PdC1zHZ,ClN3

[PdCI{(Et2NCHzCHz)2NH}]A, 1,505.605; 2.24; 6,113 ,

. ~ . _

PdC12H30C1N4 [PdC1{N(CH2CHzNMez)3}]+,5 , 1116 PdCi JLoC1zPz fdC12(PBu'Mez)z,5, 1158 PdCIZH3 IClP2 PdHCl(PEt,),, 5 , 1160 PdC12H31C1ZP2

PdHCI2(PEt3),, 2, 1026 PdCi2H3zCW4

[PdC12(MezPCHzCHzPMe2)2]z+. 5 , 1124 P~CI~H~~CIZN~PZSZ Pd{(Me2N)3PS}2C1z,2,642 PdC12H36C12N6P2Se~ PdClz{(SeP(NMeZ),},, 5 , 1144 PdCi3HizNO& [Pd(CNS)(OzSPh)z(HzO)]-, 5.1134 PdCi3Hi902 [Pd(acac)(cod)]+, 2,393 PdClJHZON204 Pd(ONPhCOPh)2, 6,366 PdC I,H,qIP2S2 PdI(S,CPh)(PMe3)z, 5, I147 PdC,,HZ3N3O; [Pd(en){PhCHzCH(NH2)CO2Et)l2+.6,424 PdCiXH2712OP PdIz(CO)(PBu3), 6,289 P~CI,HZ~W [Pd(NCS)(Et,dien)]+, 5, 1139, l14001 1141 [Pd(SCN)(Et4dien)]+, 5,1139 PdC13H29N4Se [Pd(NCSe)(Et,dien)] . 5 , 1139.1142 [Pd( SeCN)(Et,dien)] , 5 ; 1139. 1111 PdCi3H3iC1N3 [PdCI(EtzNCHzCHzNMeCHzCH2NEt2)], 2,24 P~C~~HBN~SZ Pd(SCN)&hen), 5,1139 PdCuHioCIZNz PdCIZ(PhCN)Z,6,285,293,369 PdC&i& Pd(dithiotropolonate)z, 5 , 1149 Pd(SzCPh)z, 2,646; 5,1147 PdCi4H12N404 Pd(N02)z(2,9-Mezphen),5, 1116 PdC14Hi3CIN3 [PdCl(dien)]+, 5,1116 PdCi4Hi3IN3 [PdI(dien)l+, 5,1116

494

PdCi5HisCLN202 PdCl(acac)(bipv), 2,390.391 PdCl5HI6KPSZ Pd(S,CNPh)(PMe,Ph), 5 . 1147 . I ,

Pd(tetraazaporphvrin), 2, 858 PdCiJIi34 Pd(S2CCH2Ph)2,2,646 P d C i 8 IW% 5 , I101 [Pd(SzC6HZhleZ)2]-, PdC16H18NZ

Pd(PhCH=NMe),. 2.718 PdC16HisN2Od PdH(acac)(PhNO,)(py). ,, - _ . _ ,6,248 PdC1&& [Pd{2-MeSC,H4SCH2)z}]Z+,5,1149 PdCi6HzoCIzO,Sz PdC12{MeS(0)C6H,Me-4}z, 5,1145 PdC16HzzCIzP2 PdC12(P.MezPh)2.1,515; 2,1026; 6,285,288 PdC16HzzIzPz Pd12(PMe2Ph)Z,5, 1167

~, ~

+

+

:

Pd(SC,H4SMe-2)Z,5. 1146 P~CI~HI,N& [Pd(dien)(H,O)]*+, 5, 1116 PdCi4HiaC1zN204 [PdCI2(4-ethoxypyridineN-oxide)z. 2,496 PdC14Hi9N02 Pd(acac){2-(MezNCH2)C6H4],2, 394 PdCi&oC12Nz04 {PdCI(C7H1oON0)}2,6,374 PdCi&6N80s [Pd(dien)(guanosine)I2+, 5, 1117 P~C~~H~ON~PZS~ Pd(NCS),(PEt3),, 5, 1139 PdC14H33NOP2 Pd(OMe)(CN)(PEt,),, 5,1113

PdC16Hi60,P;Pd{ P(Me)(CH,),P(Me)C(Me)(OH)C(Me)(OH)P(Me)rCH,LP(Me)C(Me)(OH)c(Me)OH, 2,935 PdC17FIllFIZN04 ' Pd(hfacac),(2,6-pyMe2), 5, 1114 PdC17H,,CI,NjO PdClz( (2-py),NCOPh}, 1,423 PdC17H210PIS2 Pd(SZCO)@Me21'h)2,2,646 PdC18H8F1002S4 Pd { SCH=CHCH=I:C(S)=CHCOCzF,} 2,2,653 PdCl~HIZN2O2 Pdf8-auinolinolateh. 1. 528 PdC18H;4FJA 2,393 Pd{ OCMeCH(COMe)C(CF3)=CCF3}z, I-

PdC18H4004P4 Pd{P(Me)(CH2)3P(Me)C(OH)Me)C(OH)MeP(Me)(CH,),P(Me)C(OH)Me (OH)Me}, 2,926

PdCisH~FisN6 F e ( h f a ~ a c )2,389 ~, PdCisHi4N~02 Pd(CH,COCHCOMe)(bipy), 2.369, 390

Pd(hfacac)z(PhCH2NMe2),2,394

495

Cumulative Formula Index

PdC,,H,,ClNa

PdCi9Hd3PSz Pd(NCS)(SCN){ Ph2P(CH2)3KMe2}. 2,233 PdCZOH~Fi40zS4

Pd{$CH=CHCH=&(S)=CHCOC3F7},,

[Pd(bipy),lz+. 5, 1116. 1117 PdC,oHl~N6~ Pd(2-pvN=cNCH=CHCH=cH),, PdC,bH;,N3 [PdPh(dien)]+, 5 , 1116 PdC,oHis% [Pd{(2-py)2NH}J2+, 1,423 Pdc20H180*sz Pd(MeC(S)=CHCOPh),, 2.651

2,653

1,423

PdC26GZbN202 Pd(2-OC,HaCH=NPh),.,.. 5.1118 PdCz~Hz3C~2N30z PdCIz(?-HOC6H4CH=NPh)z, 5 , 11 18 PLIC~~H~~CI~OP~ PdCl~(PhZPCH,~H,P(O)Ph2}, 5, 1167 PdCa6H23CI21'2 PdCl,(dppe).S. 1112, 1132, 1162;6,248.303 PdC,+,H,,CI,P2 PdCl,(dppe), 5,1124

PdS4(dppe).5.1132 PdC26H25C12NPI PdC12{(Ph2P)2NEtj15 , 1167 PdC26H26C12P2 PdCI,(PMePh,),, 1,515,6,285 PdCxH&zP,S, Pd(SC~)(~CS)(PhPCH=CMeCMe=~H)z, 5. 1141 PdC26H26P2S2

PdCzzHzsN4 Pd(flCHMeCH,CHILleC,H,NCHMeCH2CHMeNc6H,). 5.1121 PdCzzH34NzPzS2 Pd(NCS),(Bu'PCH=CMeCMe=CH),, __ Pd(PPh,)Cl(acac), 2.367 PdC2 4F2 oSa [Pd(SC6F5)4]Z-.5. 1137 P~CZ~HI~FI~OZSZ Pd{PhC(S)=CHCOC3F,} 2 . 2,653 P~CZ~H~OCU'~ PdCIZ(PPhzC1)2, I, 418 PdCz4HzoN6 Pd(PhNNNPh)2. 2.201 PdCz4HzoO& [Pd(0,SPh),12 . 5 . 1135 PdCZ,Hz&, Pd(CPh,)(acac), 3.3Y5 PdCz4H38CINzP2 [PdCI(PEt,),(phen))*, 5. 1117 PdC24HJ2P, PdIZ(PB~3)2,6,287 PdCz4H,,O& [Pd(OSPrz)4]2i,5 , 1143

5 , 1141

Pd(SH),(dppe), 5, I132 PdC2SH26P2Se2 Pd(SeH),(dppe). 5,1132 P~CZ~Z,OZP~SZ Pd(PPh,O) {PPh2(0H)}(S2PMe,), 5.1167 PdC26H2sCIP Pd CI (PPh,)(q 3-Ct3His), 6,248 PdC2,Hj4N2P2Se2 Pd(NCSe)z(PBu3)z,5,1141 P~CZ~HS~C~~PZ PdClZ(Bu',P(CHZ),oPBu'Z}, 5 , 1163 PdC&dbS4 IPd{S3CN(UII,CHZNHEt~)z}~]4' , 5 , I147 PcICZ~H~~NZP~SZ Pd(SCN),(dpprn), 1, 185; 2,227,233; 5, I IM. I lh2 PdCz,H,6CI,0Pz PdC12(PhzP(CHz)3P(O)Ph,), 5,1167 PdC27H260PzSz Pd&CO)(PMePh,),, 5,1147 PdCxH27N4 [Pd(octamethylcorrole)]-, 2,873 PdC27H3SN4 IPd{2,6-(Me,NCHz),C6H3}{4-MeC6H,N= CHNHC6H4Me-4)]' , 2 , 198 PdC27H39CliP3 PdC12{PMe2(CH2Ph))3, 5, 1 I60

PdCzsHzok

P~(I~=CHC~H~N=CHC,H~N=CHC~H,N= m , H , ) . 5.1121

Cumulative Formula Index

PdC28H2ACIN4

[PdCI(2,9-Me2phen)2]C,5, 1117 P ~ C W H ~ ~ N ~ P ~ Z Pd(NCS)(SCN)(dppe), 1, 185; 2.233: 5 . 1139, 1140, 1162 PdC28Hz7CIP2 PdC1(q3-C3H5)(dppm),5 , 1164 PdCmH27Pz [Pd(r13-C,H,)(dppm)l+, 5, 1164 PdC,sH&I,P, PdCl,(dpph), 6,285 PdC28H2904P Pd(acac),(Pl'h,), 2, 390 PdC,8H30CIC)P,S [PdCl(dppe)(DMSO)] I , 5. 1112, 1143 PdCz,H,[,CIP,S [PdCl(dppe)(SMe),]+, 5 , 11 I2 PdC28H35C12N2P PdCl2(PPh3)(Bu'N=CHCH=N3u') 2.206.208 PdCzsH36N4 Pd(Me,corphin), 6,202 P~C~H~~C~ZPZ , 1161 P ~ C I , ( P P ~ B U5 ~ ~)~, PdCz81.14602P2 Pd(OZ)(PPhBUt2)2,2,31Y: 6.321, 329 PdCz&LJ'z Pd(PBu',Ph),, 2, 1026; 5, 1102

Pd(NCS)2{Ph2P(CH2)3PI'hZ]: 1, 185; 2.233; 5, 1140, 1162 ?dC29H3zN4 Pd(H-diethylhexamethylct,rr~)le~. 2: 875 PdC30H16F1002S2 Pd{2-Cll,H7C(S)=CHC02F,}27 2 653 PdC,,,H.,,CI,F,,N,O, Pd(4-Clpy),(hfacac),, 2,367 PdC3UH20C12F6P2 PdCIZ(Ph,PC-CCF3),, 1,452; 3,1168 PdCZQH,,CI,Frj PdCI, { Ph,PCH=CCl(CF,)J 2 5 , 1168 . PdC,OH2;0& Pd IPhC(SkCHCOPhl7. 2.65 1 PdC3~H23F3NzP,Sz Pd( SCN)*{Ph2PCH2C(CF3)=CHP Ph,} ,5,1168 ~

I -

PdC'12TPhNNNPh)(PPh,).5. 1 I I8 PdC30H27F3NOZP

Pd(CF3COCHCOCH2)(2,6-Me2py)(PPh3), 2,390 PdC30H28F3N0zP Pd(F3CCOCHCOMe)(PPh3)(2.6-Mezpy).5. 1115 P~C~OH~OC~ZO~PZ PdC12{PPhZ(CH,OAc)]2,5, 1158 P ~ C ~ O H ~ ~ ~ ~ P Z S Z [Pd(dppe)(DMSO),]*+. 5. 1112. 1143 PdC30H45P3 Pd(PPh3)(PEt3),, 5, 1102 PdC,iH&izO,P Pd(hfacac),{P(C,~I,Me-2),}, 2. 367; 5 , 1114

496

PdC3ZH16NS Pd(phtha1ocyanine). 2.861,863.868 P~C~ZHZ~CLP~ PdC12{PhP(CHzPPh2)Z],5, 1104 PdC3~H3oC1d'2 PdC1z{PPh2(C=CEt)}2,5, 1158 PdC32H31BrPZ PdBr(Ph)( PMePh&, 6,285 PdC3ZHJ'a

[Pd(PhMcPCH2CH2PMcPh)JZ+, 5, 1163 PdC3ZH66PZ

Pd(PPr',rnenthpl),, 3,1026 PdCS2H,,O4S, [Pd(OSBu,),l2+, 5,1112,1143 P~CS~H~~F~NP~S Pd(C6Fj)(YCS)(PPh,Me),. 5,1139 PdC34HmCW2P2 PdClz(Ph2PpF)z. 5, 11W PdC34Hzs02 Pd{OC(CH=CHPh),},, 6.280,290,293,295,296.301 PdC34H33IP3 [PdI{PhP(CHZCH,PPh,),)1 ,5,1166 PdC3,H4"N,P,S, Pd(SC(NEt,)=NP(S)Ph,),, 2,640; 5, 1149 PdCwHw CLP, P~C14{PBu'(CoH4Pr'-2)}z, 5 , 1I61 PdCJboNd'2 ,5,1164 [Pd(CNB~')~(dppm)]*' PdC,,Hdr,P, PdBr2(PPh3)2,6.281 PdC36H3oCl2Pz PdCIZ(PPh&. 5.1101,1112, 1158, 1159; 6,280.290, 302,303,306.369 PdC36H30ClZPzS2 PdCI2(SPPh3)2. 2,641; 5, 1143 PdC36I 13QC12P2Se, PdClz(SePPh3)z, 2 , 604 PdC36H30ChP1 PdCIa(PPh,)2.5, 1123 PdC3Pw12P2 PdJZ(PPh3)2,5, 1167; 6,282 PdCd30Nz06P2 Pd(N03)2(PPh3)2,5, 1113 PdC36113oNsP2 Pd(N3)z(PPh3)2,5,1103, 1121, 1160 PdC36H3002P2 Pd(OZ)(PPh3)2,2.320,432: 5,1103, 1113; 6,329,337. 348 PdC36H3004P2S Pd(SO,)(PPh,),. 5,1113 PdC36H32PzS2 Pd(SH),(PPh3)2.5,1132 PdC36H38C12Pt PdC1z{PPh*(C~CBu')}z,5,1158 PdC36H,,N, Pd( octaeth ylporphyrin) , 2,841 +

PdC36H66PZ

Pd(P(C6H,,)3}2, 2, 1026; 5 , 1102 PdC,,H,,CIP, "- ,[PdCl{P{ CH2CHzP(CHzBu')z]3}]+,5,1166 PdC37H3oOPZ Pd(CO)(PPh,)z. 6,281,282,284

497

Cumulative Formula Index

PdH3C13N

Pd(diphos),, 5, 1162; 6,280,290,295,296 [ P d ( d i p h o ~ ) ~ ]6,248 ~+, PdC&&J'4 [Pd (P(OMe)Phz}4]Zf,5,1167 PdC53Hd4 [Pdh3-C3HS)(d~~m)z1+, 5 , 1164 PdC53H10805P4 Pd,(CO),(PBu,),, 5 , 1111 PdC54HdbP3 Pd{P(OPh)3);. 5, 1102 PdCJLsP, Pd(PPh3)3.5,1102 PdCs4H52P4 Pd{T'hzP(CHz)3PPh2}Z, 5, 1162 PdC54I w 3 Pd{P(C&Ill)j}3,5. 1102 PdCjjHq50P3 Pd(CO)(PPh,),, 6,281,282,290 PdC56H46C12F6P~ #'dClz { Ph2PCH2C(CF3)=CH#' Phz)*, 5, 1168 PdCmHd'4 [Pd(1,2-(PhzP)2C6H4}2]'+,5,1163 Pd{(i-C5H11)LS0)4.2.641; 5,1112 PdC4iHwOP, Pd(McCHCHCOCH,)(PPh3)2. 2, 390 ~'&iHwO&'z [Pd(acac)(PPh,),]+, 5,1114 PdC,211,5BrPz PdBr(Ph)(PPh3)2, 6 . 281 PdC4zHJPz PdI(Ph)(PPh,)z, 6.281,284,285 PdC4zH3603PzS Pd(OH)( OzSPh)(PPh3)2,5,1134 PdC42H39Br~P3 PdBr,(l-Et-dibenzophosphole),. 5 , 1160 PdBrz(2-Ph-isophosphinoline);, 5 , 1160 PdC4TH4ZC12P2 PdCl,{ (4-MeC6H4)3P)I.6,285,288

Pd(SzC2Phi)(PPh3)2, 2,613 PdCSOH44ClN3Pz

PdC1(4-MeC6H4NNNC6H4Me-4)(PPh3)2, 2, 196 PdC&44P4 Pd(dppt>I),, 5 , 1105; 6,296

PdC6@H50N6P2

Pd(PhNNNPh)Z(PPh,),, 5,1118 PdC62H6404P2 Pd(diop),, 6,298 PdC64Hv,04Pd P d { P ( 0 3 ~ ) P h ~5), ~1167 , PdC72H60012P4 Pd(P(OPh),},, 6,298 [Pd{P(OPh)3}4]2+.5 , 1160 PdCnH6oP4 Pd(PPh3)?, 2, 1026; 5,1101, 1102,1103,1104: 6,280. 290,298,300,301,303,307 [Pd(PPh3j4]2+,5,1160 PdCdC6N6 CdPd(CN)S, 5,989 PdCI,03S [ PdCI3(SO,)j3 , 5 , 1133 PdC1, {PdC1412-.1. 16,314; 5,717; 6, I I , 97, 113,290,392. 807.823 PdC16 [PdC16]2-s5,1122; 6,97 PdClBH46P3 [PdH(PEt,),]-, 6,496 PdCozCisH~oNzOs Pd{Co(CO)i)zpyz, 5,1108 PdCrC8H16BrN8 CrBr(en),(p-NC)Pd(CN),, 3,778 PdCrC,H,6ClNa CrCl(en),(pNC)Pd(CN),, 3,778 PdCrC, OH20FNX CrF(pn)l(p-NC)Pd(CN),, 3,778 CrF{H,N(CH,),I\;H,),(p-NC)Pd(CN),,3,778 PdCrZC,oFT,oY,O, Pd{ CrCp(CO),) 2(NCPh),, 5,1108 PdFdPzS, Pd(SZPF2)z. 5,1148 . . PdF6 [PdFJ, 5,1100 [PdF6]*-, 5,1122 PdF6018S6 [Pd(SO,F),]*-, 5, 1124 PdFePtCi4H,,04P4 PdFePt(dppm),(CO),, 5,457 PdFc&&i, fFe,Pd(C0),,]2-, 5 , 1111 PdHN3S5 Pd(SNS2)JSZNzH).5, 1149 PdH2N208 Pd(N03)2(OH)2. 5 , 1124 PdHsCI3N

PdH3C13N

Cumulative Formula Index

[PdCl,(NH,)]-, 5 , 1116 PdKN-Os Pd(Nb3\z(HzO)z,5 , 1113 PdH405S Pd(SO3)(HzO)z,5, 1133 PdHGC17N2 PdCIZ(NH3),,6, 11,98,807 [PdC1z(NH3)z]t,5, 1123 PdHhCI4Nz PdCI,(NH,),, 5,1123 [PdC14(NH3)z1-,5, 1123 PdH6NZ06SZ Pd(S03)2(NH3)z,5. 1116 [Pd(S03)z(NH,)z1Z-,5,1133 PdH6NzOeS4 [Pd(Sz03),(NH3)z]z-, 5, 1136 PdH606 [Pd(OH),]'-, 5, 1124 PdH606S Pd(SO,)(H,O),, 5,1133 PdHsN204Sz Pd(SZO,)(NH3MH~O),5,1136 PdH80i [Pd(H20)4]2+.I , 310 PdHqN,O,S Pd(Sb,)(N113)3,2,638; 5 , 1133 [Pd(SO,)(NH,),]+, 5,1116 PdHqN,O,S, Pd(SzO?)(NH?),, 5, 1136

[Pdk12(NH,),IZ+,5, 1123 PdHizW [Pd(NH3)41Zt,2,27; 5, 1115, 1116; 6. 11, 113. SO7 PdHizN403Sz (Pd(NH3)41Sz03,5, 1136 PdHgCs2HaC12N2P4 Pd(CN)2(CL-dppm),HgC12,5, 1164

Pd06S4 [Pd(S,0,),Iz-, 5, 1136 PdOizS, [Pd(S0,),]6-. 2.318.638; 5, 1133, 1134 Pd01&6 [Pd(so,),j]z-. 5, 1124 PdPtCI2Hl8K6 [PdPt(CNMe)6]z-. 5. 1104 PdPtC34H,sClzN,P> PdPtCl,(Ph,Ppy)?, 5 , 1107 PdPtC4x€14nCLP2Sz Pt(PPh,),(u-SPh),PdCl*, 5, 1138 PdPtC50H44C12P4 PtPdCl,(p-dppm),, 5,458, 1104

PdRhCl,(CO)(I'h,Pp~), 5 , 1 IOX PdRhC21HtoCI,Y3P [ PdRhCIZ(UNMe),(PhlPpy)]+, 5, 1108 PdRhC28H22CllizOP, Pd(CN),(u-dppm)Rh(CO)CI,5 , 1164 PdRhC7,H2&l,N20P2 PdRhC13(CO)(PhzPpY)2,5,1107 PdRhC38H34CltNdP2 PdRhC12(NCMe)z(PhzPpy)z, 5,1107 [PdRhClz(NCMe)z(Ph2Ppy)z]+, 5,1107 PdRhC&44CINzOP, PdRh(CN),(CO)(C!)(dppm),, 5,1105 P~RUC,~HZ~CI,N,O~P, RuPdCIz(CO)~(PhzPp~)z, 5,1107 PdSs [Pd(S4),I2-. 2,541,546 I'dS [PdSll]2 .2,.i45 PdSbZCGHjsC14 PdC14(SbMe,),, 5, 1123 PdSb,CzUH3,Cl,K, PdClZ~2-MelSbC,H,?JMcz)z,5,1165 PdSbzC2,HZ6Cl2 PdCIz{Ph,Sb(CHzj3SbPh2}, 5,1162 PdSb&?hHqnCI, PdCI,(SbPh,),. 5 , 1158 PdSbzC&3oN,Sz Pd(SCN)z(SbPhz)z.5,1139 PdShZC42H4zC1, PdCI, { Sb(C6H4Me-2)3} 5, 1158 PdCl,(Sb(C,H,Me-3),}2. 5, 1158 PdCIi{Sb(Cp,H,Me-I),} 2,s. 1158 PdSb,C,,Hb,P, Pd(PPh3)2(SbPh3)2,5. 1102 PdSeC13H29N4 [Pd(NCSe)(Et,dien)]', 2,227 [Pd(SeCN)(€t4dien)]+,2,227 PdSi4Te2C26H,oN2Sz

,,

Pd(SCN)z{Te(CH2CHzCHzSiMe3)2}zr 5,1144 PdTe2OI2 5.1124 [Pd(Te06)2]B-, PdTlCi,H,,Ol, TIPd(OAc),, 3,173 PdVCi,H,4O,P,

VO(aca~)[{0P(0Me),)~PdCp], 3,567 PdW2C3oH2(rK20+ Pd{WCp(CO),},(NCPh),, 5 , 1108 PdW2SB [Pd(WS4)*]2-.2. 575 PdZrC14HloN4

498

499 {Pd(CN)4ZrCpz),, 5,375 Pd2As2C4H18Br4 P ~ , B ~ , ( A S M ~5,1161 ,)~, PdzAszCizHzoC14 PdZC14(A~Et3)2,5,1161 Pd& [PdzBr6lZ-,6,290 Pd2CzC1402 [PdzC14(CO)z]'-, 5 . 1111; 6.290 PdzCzH6Br406s2 [PdzBr4(S020Mc)2]2-, 5,1135 Pd,CzW,CI,O,Sz [ P ~ ~ C I ~ ( S O , O M C 5, ) , ~11~13 -. PdZC4Hl2Br4S2 PdzBr4(SMez)2,5 , 1146 PdzC4HlzCIzOzSz {PdCIz(DMSO)}z,5. 1142 Pd&HizC1z {PdC1(q3-allyl)}z,2,201 P~zC~HZ~N~O~S~ Pdz(Sz03)z(en)3,5, 1136 Pd,GHi,O, Pdz(~~-OAc)z(ri3-C3H5)z. 5. 1113 PdZC8H8Cl4Te2

{PdCl(TeCH=CHCH=CH))2(uT1),,2,670 PdzGHTzSw {Pd(S,CMc),},, 5, I147 PdZCaH14C12 PdzCl,(CHzC(Me)=CH,)2. 2.682 PdzCiHJzCIzN8 [ Pd(en)zC1zPd(en)z]4-,5,1123 PdzC,HzoC14Se4 (PdCI&{p-{C(CHzSeMe),)), 5, 1151 (PdCI&{ p-{(MeSeCH2CH2SeCH,)2CHz}},5, 1151 PdzCioHi4CIzO4 {Pd(acac)CI},, 2,390 Pd2C10H14NZS2

Pd,(NCS),(HzCCMeCH2),, 5, 1141

{Pd(l,3-q3-C4H,)(MeNNNMe)},. 2,200, 201 PdzCizHwCLPz Pd2C14(PEt3)z,5, 1161

_.

PdzC18H34Ci2NZ

[PdCl(q3-C4H,)]z(B~'N=CHCH=NB~f). 2,208 PdzCisH36S8 {Pd(SzCSBu')(SBu')}z,5, 1147

Pd~C54H44N4P4

Cumulative Forrnulu inde.r

so 1

Cumulative Formuh Index

PrC16H400J'& [Pr{(EtO)zPSz}4]-, 2,644 PrCl8HS4Cl3N9O3P3 PrC13(HMPA)3,3, 1084 PrCmH36C130ia

Pr(C104)3(dicyclohexpl-18-crown-6). 3. 1093 PrC,aHzoO8 [Pr(tropolonate),]-, 2, 397 PrC3of13oFziO6 Pr(CF3C'F2CF2COCHCOBu')l.3. 1079,1104 PCC&16F12(>& [Pr(then0ylCHCOCF~)~12.373 PrC3,H5,06 Pr(Bu'COCHCOBut)3, 1.408 I'rC36H45N40 Pr(octaethylporphvrin)(OH). 2,822

PtB,IrC 13&70P4

P~AszC~SHM Pt(C2H4)(AsPh3)2, 5,410 PtAs4CzoH32 [Pt(diars),j'+. 5,498 PtAs4C20H32C12 [PtClz(diars)z]z+.5,498 PtAs4Cz4H30CI [Pt{(2-Me,AsC6H,),As}C1]+, 1,321 PtA~4C72Hm Pt(AsPh&, 5,440,463 PtAuC,,H,,CI,P, AuPt(PEt3)3(C&I,), 5,364 P~AIIC~~H~~C!~P~ Au(PEt,)(p-H)Pt(C,jCls)(PEt,),, 5,869 PtBCqH17N4 Pt{H2B(fiN==CHCH=CH),)Me3, 2,253 PtBC,,H;3N60

Pr(Bu'COCHCOBu'),(bomeol). 3. 1101 PrC4&36Niz IPr(na~hthyridine)~l~+, 1,101; 3. 1070 PrCS1H7~O7P Pr(Bu'COCHCOBu'),( OPPh)3, 3. 1080 PrCRsHqA" .. . . PrH(tetraphcnylporphyrin),. 2,823 PtC:I, PrC11,3, 1105, I117 PrF, [PrF6I2-, 3,1115 PrF, [PrF,I3-, 3, 1115 PrHla09 [ P T ( H , O ) ~ ] ~3,+ 1074 , Pr2Clo020 [Pr2(C204)S]4-,3, 1076 PrzC34H48C160zo Pr,{ Oc=CClC( O)C( O)=ClcO) ,(EtOH),, 3,1085 PrZC45H1 I lF18N7015 Pr,(DMF),(3-trinuoroacetSI-( +)-camphor),, 2, 49 1 ~ ' ~ Z C ~ O H I~2 O F ~ Z O Pr2(CF3CF2CF2COCHCOBu')6. 2. 373; 3, 1078 pr2C'66t'114012 Pr,(Bu'COCHCOBu'),. 2.373; 3,1077 Pr2C%5H141F1a018 Pr2(3-CF3CO-(+)-carnphor),(Bu'COCHCOBu'),, 3, 1080 Pr.&oH90H63018 Pr,(CF,CF,CF,COCHCOBu'),. 3,1078 Pr6Fq1 [PC6F3,l7-,3, 1115 PtAsC6H,,C1, [Pt(AsEt3)C13] , I , 314 PtA&,8HLaM2S [PtC1(MeNSNMe)(AsMe,I'h)2] I , 2 , 191 PtAsC20H17C12 PtClz(2-PhzASC'6~[4CtI=[:II,). 5.406 PIAsC~~H~~C~~P PtCl,(PEt,)(AsPh,). 5.445 PtAsC24H31ClP PtHCl(PEt,)(AsPh,), 5.445 PtAsZCloH270 [PtMe{C(0Me)Me) (AsMe,),] .5.383 PtAStCiZH16NZSZ Pt(SCN),(diars), 5 , 1163 PtAsZC12H&IZ PtCl,(AsEt,),, 5 . 497 PtAs2C,2H30C14 PtCI,(AsEt,),, 5 , 463 PtAs,C,,H,oI, PtI,(AsEt,),, 5, 463 Pt A s z C ~ ~ H ~ O P Z Pt(C=CPh)2(AsEt3)2.5.388 +

COC 7

4

Pt{HB(fiN=CHCH=cH),}(Me)(CO), 2,253 PfBCiiHi6N6 PtMe,{ HB(~N-CHCII=~H),}, . . 2,254 PtBC12Hi9N6 Pt{HB(fiN=CHCH=cH),)Me,. 2.253

PtBC15H,z%PS,

P~M~(CN~U')(HB($IN=CHCH=~H)~}, 2,253; 5, 380.132 PtBC17H25N404 Pt { Et,B(hN=CHCH=eH),} CCO,Me), 2,253

(MeO,CCMe=

PtCl(BPht)(PEt,),, 3,100; 5,372 PtBC,,€l,,N, (Mc)(PhC=CPh), 2. Pt { Et,B(hN=CHCH=CH),) 254 PtBC3,H3,F6N4P Pt { Et,B($lN=CHCH=cH),) { C(CF3)=C(CF3)Me)-

~

PtWkJL

Cumulative Formulu index

PtB9CzoHj,Pz (PtC,B9H9)Mez(PMe2Ph),, 5,373 PtB91rC4,H58P4

Pt(PMe3)z(PPh3)(PhzPC6H4)HIrB9H~o, 5,372

PtB 1 zCsJLsCIi3PJ (PtCl(PPh3)3}B,2CIi,, 5 , 446 Pt B M C ~ , H ~ O P ,

(PtB,6H18)(PMe*Ph)2,5,372 PtBisCi6Hd2 (PtB18Hzo)(PMezPh)2,5,372 PtB20C28H41CIP2

PtCI(PhZPCzBloHio)(Ph~PC~B~oHj I ) , 5,374 PtBr, PtBr,. 5,488 [PtBr,J2-, 5,488,490,499 PtBr, [PtBr,Iz-, 5,488,491,499 I'tCCI,O [PtCI,(CO)] ,5,377,378,379 PtCCI50 [Pt(CO)Cl,] ,5,378 PtCHzC120 Pt(CO)H,CI,, 5,378 PtCHZCI30 [Pt(CO)H,CI,]-, 5,362,378 PtCHSC140 [PtMeCI,(OH,)]-, 2,297 PtCH7CI,N,S PtCI,(NH,){SC(NH,),}. 5.480 PtCH, ,ClN [PtkI(Nl i3),(NH,Mc)]+, 1, 127 PtCHlSF3N503S [Pt(OSOzCFn)(NH3)513c. 5.470 PtC2Cl,Oz PtCI,(CO),. 5,378, 379 PtC,H,CI,N PtCI,(MeCN), 5,436 PtCzH,CIzNO, [PtCI,(Gly-O)]-, 5,427 PtC2HdC13 [PtCI,(CzH,)]-, 1,3,21,407; 5,403,405,407 408,451 PtCZH4NZS4 Pt(S,CNHz),, 5,481 PtC2k{#jCI,OS [PtC'I,(DMSO)]-, 1,314; 5,479 PtCIH6CI3S [Pt(Me,S)CI,]-. 1,314 PtC,H,N, Pt(NH,),(CN)Z, 5, 375, 377 PtCZH6SZ Pt(SMe),, 2,554 PtCzH7CIzN PtC12(NH3)(C2Ha), 1, 121,5,403 PtCzH8Cl2N2 PtCl,(en), 5,422 PtC2H8CIzN,02 PtCl,(€IzNCONH~)~. 2,491 PtCZHeN20ZS Pt(02CCH2S)(NH3)2,5,474 PtC2H,,CIN, [PtCI(NH,)(cn)]' + 5.479 PtC2H, ,ClNsS2 [PtCl(NH,){SC(NIlz)2},]+, 5,480 PtC2Hi,CI2N4 [PtCI,(N~13),(en)12+,5.428

PtC,Hi+N& [Pt(NH3)2{(H2N),CS}2]z+,2,639 PtC2N, [Pt(CN),\?-. 5.375 PtC2N208 [Pt(N02),(C,O,)I2-. 5,466 PtC,S, [Pt(CS,),]*-, 2,646 PtC,H,CI,O,P [Pt{P(Okfe),)C13]-. 1.314 PtC3H9CI3P [Pt(FMe,)CIql-. 1 , 3 I 3 PtC,I rl,,ci2b, PtCl,(pn). 5.425 PtC,H,,CIN,S, [PtCI{SC(NH21,) 3]', 5,480 PtC3N308S [Pt(NO,)z(SCN)(C204)I3 ,5,466 PtC4Br,N4 [Pt(CN),Br2]". 2. 10 PtC4CIzN4 [Pt(CN)4C12]2-.2. 10 PtC,H,S, Pt(S,C,H,)I. 2,521 PtC4H611N2 Pt12(CNMe),. 5.380 PtC4H,h6 Pt(C"),(NH,),. 5. 37: PtCaHhS, Pt(S,CMe),. 5.181 PtC4H8N205 Pt(Gly-O)z. 1.407,2.745,5,427 PtC.&N6& Pt{SC(NH,)=NC(NHZ)$},, 2,640 PtC,HloCI,N20, Pt(H,NCH,CO2H),CI2. 2, 745 PtC4H.,&12K*;2S2 PtCI2{MeC:(S)NH,},, 2, 647 PtC4H,,CI,N, [PtCI2(McHNCP;HNHCNHMc)lZ*. 5,381 PtCdH loC1,Sz PtCI,(MeSCH,CH,SMe), 2,555 PtC,H ,2ClK2S [PtCl{S(CH,CH,KH,),}] ",5.478 PtC4H lzClzIi 2 PtCI,(H,NCHMeCH,NHMe), 5,425 PtC4Hi2C1202S2 PtCl2(DMS0)2,1,319. 320; 2,640; 5,429,479 PtC,Hi,CI,Sz PtCl,(Me,S),, l I288.314,318,321; 5,430 PtC4Hl,BrN3 [YtBr(dien)J' 5.424,476.494 PtC41[&IN3 [Pt(dicn)Cl]'. 2.47; 5,1117 PtC,H,,Cl,N,S [PtCl2(H2XH2CH2SCH2CH2NH3)J ',5478 PtC4HiaC13N3 [Pt(dien)CI;]'. 2, 47 PtC4H,,C14N,S [PtC14(HzI*;CH2CHzSCHzCH~NH3)]+, 5,478 PtC4H131N3 [Pt(dien)I]+. 2>47- 48 PtC,H,3N& [Pt(NO,)(dien)]+, 2,47; 5,494 PtC,H,,CIN,OS [PtCI(DMSO)(en)]+,5,425 PtC4H,,CI3K2S [PtC13{S(CH2CH2NH,),~].',5,477 PtC,Hl5CI2N20S 5,425 [~'tC12(DMSO)(enH)I+. PtC,H,,N,O [Pt(dien)(H2O)l2+.1. 310; 5,496 PtC4H,,Br2N,

502

Cumulative Formula index

503

PtC7H&13N

[Pt(SCN)(dien)]+,5,494 PtCsHIjCIS2 PtCIMe(SMe,),. 5.392 PIC5Hy.&12N3 PtC12{(H2NCH2CH2)ZNMe}, 5,425 PtCSHisIN3

[Pt(MeNHCH2CH2NHCH2CHzNHz)I]’, 2,48 PtC,H,,N,OS [Pt(SMe,)(en)(H,0)]2+. 5: 376 PGHiJJ4 [Pt(en)2]2+,1,337; 2,33; 5,423,424, 500 PtCaHi,NaO, [Pt(Gly-0)2(NH3)2]z+. 5,466 PtCaHiJ‘!& [Pt{SC(NH,),}4]2+,2,639: 5.380 PtCqH17N40 [Pt(OH)(en),]Zt,5.423 PtC4HisCINzOS [PtCl(DMSO)(en)]+.5.479 PtC4HisNzSz [Pt(NH,),(Me,S),]+. I. 317 PtC4H19CINs [ P t C l ( d i e r ~ ) ( N H ~2.37 )~]~~, PtC4HZoC12N4 [P~CI,(MCNH,)~]~+, 5.428 PtCdHzON4 [Pt(NH2Me),12+,2,28 Ptc4H~oN6

IPt{HN=C(Me)C(Me)=NH}(NH3)4]3’, 1,446 PtC41;N4 [Pt(CN),I,]’-, 2. 10 PtC,N306S, [Pt(NO,)( SCN)z(CZOA)]’-. 5.366 PtC4N4 [Pt(CN)4]’”-, 5,376 [Pt(CN),]’-, 1,3, 396; 2, 10. 12; 5.375.437; 6, 136, 1022 PtC4N40, [Pt(CNO),J2-, 2, 17 [Pt(NCO),P-, 5,4h9 PrC4N4S, [Pt(SCN)412-,5,487 PtC4N,Se4 [Pt(ScCN),l2-, 5.488 .~ PtC4N10 [Pt(CN)4(N3)2]2-,5,437 PtCaOa

PtC,H,CI,FbS, PtC1,(F3CSCHMeCHlSCF3).5,477 PtC,H,CI,O, [PtCl,(acaE)] ,5.467 PtCSH,BrCIIN30, Pt(Nkl,)(py)CIBrl(NO,). 1.26 PtCSHlOCl3N3O PtCl,(a-pyridonato)(NH&. 5.335 PtCSH11CIN3O [ P t C l ( ~ - p y r i d o n e ) ( N H ~ )5.435 ~]+. PtCSHiyC12NOZS Pt { D, L-M~SCH,CH,CH(NH,) C 0 2 H )CI 2 , 2,749 Pt{L-M&CH2CH2CH(NH2)CO,H)Cl2,2,749

PtC,H,,N4 [Pt(CN)(dien)] PtCsHl,N4S

+ ,

5,494

PtCSHicC12N3

[PtC12(Me2EI:CH,CHz(NH2)CHzNH,}]+, 1, 121 PtCSHZIN, IPtrNH,),(HN=C:MeCH=CMcNH)j”~.

6. 190

[Pt(NH,),{MeC(NH)CHC(NH)Me}]3L, 5.429 PtC6HaClaN2 Pt(4-CNpy)CIz. 1. SOX PiC,Hc,S, Pt(HCSCHSCH),. 2,621 PtC6HIZNZOI P t ( N H 3 ) 2 { ( 0 2 C ) 2 ~ H z6,757 }, PtC,HI2N,O, [Pt(Gly-O),]-. 5,427 PtC&I,,CIN,O, [PtCI(Me,CNU)(Me,CNOH)]-, 5,426 PtC6Hl4CI2N2 P t C 1 z ( H , N ~ 1 3 ~ )5,424 2, PtC6H,4C12NZOL PtC12[Me2C:NOI1)2, 5,426 PtCJ ItaNzCl7 P t { H 2 N . m H. N H z ) C I , ,6,774 PtC,H ,,CI,P [Pt(PEtZ)C13]-. 1,314 PtC6Hl,0P [Pt(HZO)(PEt3)l2+, 6.498 PtCeHisCIS3 [Pt(%le,S),C1]+,1,318 PtC6H18CIZNZ PtCI,(NMe&, 5, 460 PtCaHisClZNd PtC1,{(J-I,PiCH3CHzj3N},5,425 PtC6HIBCIIP2 PtCl,(PMe,),. 1: 319; 5,448 Ptc~,H,,m Ptl,(PMe,),* 5,448 PtC6HisSz PtMe2(SMe2)21 1,321; 5,3Y2 Pt C6H20Br,N [Pt{H2N(CH2)3NH2} 2Br2]2+,2,45 PtC,H,oCl,N4,+ [PtCl,(pn),]- S ?500 [Pt { Hz”(CH,)3NH,}2Cl,]2+, 2,45 PtC6H&4 [Pt(pn),J2+.ZI34; 5,425 [Pt{H2N(CH2)3KH2}2]z+, 2,45 PtC6NiOsSz [Pt(C,0,),(SCN),]4- , 5,466 PtC,Ni,Sz [Pt(S,C,(CN)2}(CN),I.-, 2,6’17 PtC&$, [Pt{ S,C( CY),) $-, 5,481 PtCsN, [Pt(CN)6]2-, 2. 9; 5, 377 Ptc6N 6s6 [Pt(SCN),]’-, 5.487 PtC6N6Se, [Pt(SeCr*j)6]2-,5,488 PtC7HSCI3NO PtCI,(2-p$OCHCI). 5,386 PtC,H,CIN,S [Pt(4-CNp>r)CI(H,NCSNHz)]’ , 1, SOX PtC7H,CI,N PtCI,(C,H,)(py). 5 : 407 PtCTHgC12NO PtCL,(C,H,)(py N-oxide), 5,407 PtC7H9CI,N

Cumulutive Formulu Index

PtC7H9C13N [PtCI3(2,6-Me,py)]-, 2,27: 5,430 PtC7H1oCIZN2S PtC12{MeC(S)NH2}(py),2,447 PtC7Hi iClOz PtC1(C,H4)(acac), 5,404 PtC7HIIC103 PtCI(CH,=CHOH)(acac), 5 : 404

PtC7H1302 PMe,(acac), 2,392 PtCTHiSClS4

PtCIMe{(MeS),C=C(SMe),}.2. 612; 5,477 PtC7Hl,BrCIN4 [Pt(en)(py)(NH,)ClBr]* 1 , 2 6 PtC~Hi6C12N4 [PtCI,(NH,)(en)(py)]*+, 1,26: 5.428 PtC7HZiIP2 PtIMe(PMe3),, 5, 394 PtC,HJ’J,O, [P~(C~)~{L-H,NCH,CH(NH~)C~,}]~+. 5,428 PiCsHdNs ~’t(~rN==C(CN)C(CN)=NH),.5,438 PtC78H&I~N4 PtCI2(2,2‘-bipyrimidyl) 5. 433 PtC,H,CIzN4 PtCl,(pyrimidine),, 5.432 PtCsHgCIzN P ~ C I ~ ( ~ - P ~ C H ~ C H =5.406 CH~), PtCI, ( ~ - H ~ N C ~ H ~ C H Z C5 H406 ~). PtC8HI2Br2 ftBr,(cod), 5,404 PtCsHizC12 YtCl,(cod), 5, 3 4 PFCsH 12C12NZO +.

I

Yt(HDMG),, 6, 143 PtCsHISN, [Pt{CNMe),(MeHNC=NNHCNHMe)lt. 5 . 381 Ptc8HI6Br2OZSe2 PtBr2{SeCH2CH20CH&H2),. 2.661 PtCsHI6BrzS Pt($CH2CH,CH,cHZ)ZBr,. 1,468 PtCsHi6N20~ I’t(02CCH2COZ){(HzNCIT,)zTMed} 5.425 PtCBII1bN408 [Pt(Crly-O),]2 5,427 PtCp.lI~~Cl~N~ P t C 1 2 ( H Z N m H 2 ) 3 ) 25,424 , PtCpH1sS4 PtMe2{(MeS),C=C(SMe),). 2. 612 PtC8HZoC12S2 PtCI,(SEt,),, 5,475 PtCaHzo04PzS4 Pt{S,P(OEt),},, 5,482 PtCsH24C12N4P4 PtC1,(~=PMe,N=PMe2\1=Pn.le,N=P Mez), 2.82 PtCSH24012P4 [Pt{OP(OMe),},12-, 5.460 P t C,H,,O I ,P,

[Pt(en),j4+, 5,428

504

PtCsN4S, [Pt{SK,(CN)2}&. 6 , 14s [Pt{S,C,(CN),),]’-. 2,617; 5,484; 6 , 148 [Pt{S2C2(CN)2},’J3-.5.485 PtC&iiCI,NOS PtCI2(2-pyCOCHSMe2).5,386 PtC9HI4I2N4 Pt { H2C(fiK=CHCH=cH),} Me212,2,253 PtCqHl,Cl PtCl(cod)Mc, 2>278 PtC9Hi&303 Pt(ON=C~le,),(HOk-CMe,), 2, 270 PtCJ I,,CI,N,P PtC12{Cy(NHhfe),}(PEt,), 5, 383 PtCgH23C14NZP PtCl,{C(NHMe),}(PEt,). 5, 383 PtCgH27CIP3 [PtCl(PMe,),]+. I , 319: 5,448 PtCioH,FizO, Pt(hfacac),. 2. 376, 389 PtCioH,CIZN, PtCL(bipy), 1: 314.508; 5,378 PtCl,,H“F604 Pt(CF,COCHCOMe),, 2 , 3SY PtCiliHsNa0,j T’t(NO,),(hipyj: 5: 4hil t’t(::.,oHqN?c), Pt(OH)(NO,)(bipy): 5.469 PtCloHioCIN30, PtC1(NOz)(p)7)z.1,288; 5,430 PtCloHioC1,Nz PtCl,(py),> 1,312,407;5,429,430,495 PtCinHioI32 Pt12(py),>5: 429 PtCIOHizN?Oz [Pt[bipy)(H,O),]”’, 5.431 PtCIoHi3Cl2N PtC:lz{2-\lel lNC:6€f4C(Me)=Cl I,}, 5, 406 PtCl0fl14c:lo4 [Pt.Cl(acac),].-. 2.367,392; 5,467 PtCwHi,CI,O, [PtClZ(acsc),]*-, 2, 392 PtCioHiJ204 Pt12(acac),, 2,386 PtCioH1404 Pt(acac),. 2.366.380,390; 3, 1104; 5,390,467.469 PtCIOH1SCIOj PtCl(acac)(MeCOCH,COMe), 2,380 PtCl(acac)(MeCOCH=CMeOH), 5,467

[PtCl,(en)(hip~)]a-, 5,437 PtC,”13,,K‘,C)2 l~t(cr-pyiidone),(NH,),1” ’ , 5,435 I’tC loHlBCIaY2 PtC1,(BuLCN)2. 5. 451 PtC,oHzoN2S, Pt(S,CNEt,),. 5.481 PtCloH&,Se4 Pt(Se,CNEt,),. 5.482 PtCloH22C12IU’202S, PtCI, { SC(OEt)=NMe ,} ,, 5,481 PtCioH22CI2NlS P ~ C I , ( R U ‘ N S ~ ~ ~ ‘ ) ~ ~ ~ - C H ,2,= C 191 H?),

Pt(CO)Cl(hipy), 5 , 37X PtCIIHsCl2N20 PtC12((2-pq)2CO),5,433 PtC,,TI,,Cl?r4S [Pt(bipy)C1(H2NCSNH2)J+,1,508; 5,480

505

Cumulative Formula Index

PtCIIH lsc12P PtClZ(H2GC=CH2)(PMezPh),5,404 PtCiiHi,CI,N 5+405 Pt&(EtMeCHCH=CH,)(py) PtCiiHmCIzNz PtCI,{ 1,2-(H2N)ZC6H4}{(S)-hle2C=CHMe)}, 5,405 PtCl2H8Br2N2 PtBr,(phen), 5,430,499 PtCI2HRBr,CIN, PtBr,Cl(phen). 5,499 PtCl2H8C.IzN2 PtCl,(phen), 5,430 PtC‘,,t18CI,N4 PtCIz(4-NCpy),, 5,430 PtC12H812N2 PtI,(phen), 5,430 PtCl2H8N4Se2 Pt(SeCN),(bipy), 5,488 PG~HRS~ [Pt(S2CC,H4)2I2--,5,481 PtCizHizN402 Pt(2-pyCH=NOH)z. I. 419

PtC,4H,,CI,N,

PtH?(PEt,),, 5,362 PtClzH,,P,S, Pt(SH),(PEt,),. 2.518 PtC1,H3,iPzSe PtH,I(SeH)(PEt3)z. 5,356 PtC12H?4P2Se2 ~

PtC13H2212NI Pt { H,C( flN=CMeCH==c Me),} Mez12, 2.253 PLC13H2ZNfiORP

[Pt{H2N(CH,),NH,}(inosine-5’-phosphato)]’, 2 , l i

PtC,,lI,,O [Pt(Me)(cod)(Me,(’O)]’, 2. 3 3 PtC,,H,,CI,S, Pt(PT,S),Cl,, 1,314 PtCizHmIN3 [PtI(Et4dien)]+,5,424 PtC12H30Br2PZ PtBr,(PEt,),, 5,388,448 PtCizH,oBr& PtBr4(PEt3),, 5,499 PtC1ZH30CIFzP3 PtCI(PFz)(PEt3)2,5,357 PtC,,H,,CI,Br,l’, PtCIZBrz(PCt,),, 5, 4 W PtCl2H&I2P2 PtCI,(PEt,),, 1,407; 5,448.494 PtC1ZH,oCIzPzS, Pt(Et3PS)2CIz, 2, 641 PtCi2H3oC1.P~ PtC&(PEts)i, 5,462,499 P~CI~H~ONZO~PZ Pt(NO,)(NO)(PEt,),, 5,436 P~CIZH~~NZO~P~ Pt(NOz),(PEt3)2,5.436 PtCIZH31BrP2 PtHBr(PEt3)Z,2,700; 5.448 PtC12H31CIP2 PtHCI(PEt,),, 2,690; 5.354. 359,367,370,494

PtCI3H2,0;PS Pt(CO),( SEtz)(PE t3), 5,358 PtC13H3,CIOPz [PtCI(CO)(PEt3),]-, 5,378,448 PtC13H31C102Pz PtCl(CO,H)(PEt,),, 5.397 PtCI,H3,NOP, (Et,P),l’t(H)(CNO), 2, 13 IN’,3H31NPL PtfI(CN)(PEt,),, 5, M Y , 370 PtCIl3lI,,NP2S PtH(SCK)(PEt,),. 5,361 PtC,,H,,OP, [PtH(CO){PEt,),]+. 5,361,367 PtC13H3,CINP2 PtH,Cl(CN)(PEt3)z,5, 356 Pt c,,H,,CIO,P,S PtC1(S02Xle)(PEt3),, 5,470 PtC13H33Clf2 PtClMe(PEt&, 5,391.400,494 PtC,,Il,,OP, PtH(OMc)(PEt,),, 5,361 PtCiJWi2N2 P~(cod){NC(CF,),},,2, 126 Pt c ,,H ,Cl,N, PtClZ(CNPh)z, 5,380,434,436 PtCI,(PhCN),, 2,264 PtC14Hi002S2 (Pt(SCOPh),),, 5,480 PtCi,Hio& Pt(&CPh)Z, 2,646 PtCI4HIiClYzO PtCI(Z-HNCsH4CH=NCsH4CHO-2), 1,437 PtC14H12N402 Pt(2-p]CH2C=N0)2, 5, 430 l’tC14H

14rlZk2SZ

PtC:l,{PhC(S)NI 12}2. PtC14H,*Clt02S2

2,647

Pt{PhS(O)CH~CH,S(O)Ph}Cl~,l, 314 PtC IIHI& PtMe2(phen), 2,342 I’tC,4Hl,CI,Nz Pt(C4&)Clz(Py)z, 5,390

PtC r4HzzSz

Cumulative Formula Index

Pt(hfb)(PEt,),, 5% 417 PtCl6H35CINP P't(N\lHBu'CH2~=CHz)CI(PPr~), 5, 409 PtC16H35CINPzS [PtCI(PEi,),{CkZ(Me)=CHfiH)]+. 5,382

PtC14H35CIP2 Pt(Et)CI(PEts)z, 5, 365

[PtH(MelCO)(PEt,)2] ' ,5,366,367 P~CI~H~SPSOIS [Pt{P(OMe)3}5]2' ,5,447 PtC16H8F602S4 Pt{SCH=CHCH=CC(S)=CHCOCF,),, PtCi6Hi2Ns [Pt(2,2'-bipyrtm1dyl),~~+. 5. 433 PtC16H14S4 Pt(SZCCH?Ph)Z,2,646 PfCibHi6N60

2,651,652

Pt{PhN=NC(Me)=NO}{PhN=NC[Me)=N}, 1,455 PtC16H!GN602 Pt{PhN=NC(Me)=NO)2 1 . 455 PtC16HlsCIlOS PtC12{(S)-4-MeC,H,SOh.le) {(R)-PhCH=CH2}. 5,405 PtC,e,H,oCI2O2S2 PtClZ{PhCH,S(O)Me},. 5.179 P~CI~HZZ h{CH(CH=CH,)CH2CH2cHCH=CH2}(cod),5,397 PtC16H2ZCIZPZ PtC12(PMe,Ph)2,2,646; 5, 419.172 PtC?6H22C14P~ PtC14(PPhMe2)z,5,462 PtCi~tJz2N4 5.423 [Pt(NI1,),{ (S)-H,NCH,CH(~H,)Bur~I2~. PtC1bH220tS2 PtPh,(DMS0)2, I , 321 PtCI6H,,CIP2 PtHCI(PMe,Ph),, 5,371 PtC16H24 Pt(cod),, 2,219,221; 5.397.31 I , 439

209 PtC:,sH,,P, PtMez(PMelPh)z. 5.398 PtCISH31CI5P2

PtH(C'6Clj)(PEt3)2.5.86Y PtC1BH34CIFN2P2 PtCl(N&HqF-4)(PEt3)2,2, 136 PtClaH3,BrP2 PtBr(Ph)(P€t,),. 5 . 399 PtC 1 sH35CIN2P2 PtCI(N,Ph)(PEt&. 2. 130, 134 PtCisH35CIP2 PtClPh(PEt,),. 1.317; 5,399,494,496 PtC,,T13,N2Se4 Pt(SzZCNBu't),, 5,482 PtCleH,,CIFN,P2 [PtUl(H,N?WC6H,F-4)(PEt3)2]t. 5,438 PtC18H42Cl2Pz PtCI,(PPr& 5, 462 PtC,,H,,CI,P,

506

Cumulative Formula index

507 Pt2C1z(~-C1)2(PPr3)2, 5,448.462 PtCisH4zPz P~(PPT'~ 5,441 )~. PtCiiH44PZ PtHz(PPri3)z,5, 361 PtCidLP3 Pt(PEt3)3, 5,444 PfC18H46P3 [PtH(PEt,),] ,5,357 [PtH(PEt,)i] ', 5,357: 6.496.197,533 PtC18H47C1P1 [PtHzC1(PEt,),]+, 5,333 PtCl,H,,P, PtHz(PEI3)3, 5,359,444 PtC19H,,C1 PtC1(q3-CPh3),5,418 PtC19H15CIzO PtCI,(CO)(PPh,), 5,378

[P~(x~H,CCH=CH2)(PR/Ie,Ph),]i, 5,418 P~G~HJINOZPZ Pt(NOZ)Me3(PMe2Ph),.5.392 PtC,qH,,FNPz Pt(CN)(C,H4F)(PEt,),, 5,389 PtCigH87CIPz [Pt(PEtl),(m-C6H,Me)Cl]. 1.510

PtC24B31C"P

Pt{(CH2)PBut2}2,5, 386 PtC2,H2,TP PhG(2-PhzPC,H,CH=CHz), 5,406 PtC21HzII2PS2 Pt{C(SMe),}(PPh,)I,, 2, 581 PtC2;H13PS2 PtH(SCH2CH2SMe)(PPh3), 5,355 PtC,,HI,NOP,S [Pt(?-& ,V-oxide)(PMe,Ph),]*, 5 , 474 PtC, ,HZ7CI,N3OJ IPiCI;(Z.h-lutidine N-oxide),l+,2,496 PtCl,H, ,OP, [PtMe(PPhMc2),(CCH2CH,CH20)] ,5,384 PtC,IH3,C182 PtCI2(PPr,)(PHPh,), 5,456 PfCziH330P2 [PtMe(PMe,Ph),(THF)]+, 5.447 PtC21H,lBrP2 PtBr(2.4,6-h1e3C6H,)(PEt3),, 5,399 PtC2lH46C12PZ [PtC12{Bu'zP(CH,)5PBUt~}],,,5,451 P~C~?HI~F~O~S~ Pt(4-hleC6H,C(S)=CHCOCF,),, 2,651.652 PtC2ZH16F604SZ Pt(4-MeOC6H4C(S)=CHCOCF3)L. 2,052 PtU221117FhP Pt (CF,) ,( ?-Ph, Pc',I IdCl k C H , ) , 5, 406 PtC,,H,~F,;O,P~ Pt { (CF3),C( O)C(O)(CF3),} (PPhMe,),. 5 47 1 PtCZ2H2TP P6fer(2-PhzPC6H4CH=CH,), 5,406 ~

P;{3-CIC,H4C(S)=CHCOCF,),. 2,652 PtCzoHioFsOzSz Pt{4-FChH4C(S)=CHCOCFsJ2.2,652

PtC12H45C104P2 P~C1(09CCH2PBu'L)(EtO~CCH~PButz) 5 , 455 PtC:22H52P2 Pt(CH,Bu'),(PEt,),, 5, 396 PtC2,H,,Cl,K03P PtCl2(py){P(OPh)3}, 5,404 PtC2,Hz,CkzP PtC12(Me2C==C=CHz)(PPh3),5,408 PtCZ3Hz5CINPS2 PtCI(SzCNEtZ)(PPh3),5,481 PtC2,HZ5C1NPSe2 PtC1(Se2CNEtz)(PPh3),5,482 PtC23H25C1N4Pz PtMeCI(rCNE)(PMcZPh),, 5,402 PtC,,H2,1[\i We, PtJ(SeLCNEt,)(PPh3), 5,482 PtC23H34BrC'1N4 Pt{2,h-(Me2NCH2)zC6H,}{4-MeC,H,NC(H)NPr') , 2 , 202 PtC23H38NOP2 [Pthfe(PPhMe2)2{(NMe2)(CH2CHzCH20H)}]+q 5.384 PfCdi6N4 [Pt(phen),]"-, 5,431 PtC2,H2&I2Se2 PtCll(SePh2),, 2,672 PtC24H2202 Pt(acac)(+CPh,), 5,418 PtCZ4Hl8NPSe2 PtMe(Sc,CNEt,)(PPh,), 5,482 PLC~~H~~PS~ Pt(SCH?CH,Shle),(PPh,), 5,474 ~

..

PtCzoHz4Pz Pt(C=CH),(PMe,Ph)2. 5.402 PtCzoH3oIzPz Pt(CHZ)41z(PMezPh)2,5.395 PtCzoH3zPz PtEt2(PMezPh)z,5.398

Pt{C,(CF3),}(PEt3),, 5,443 PtCzaH31ClNzP

PtC24H31ClN2P

Cumulative Formula Index

~t(NMczCHzNMez~Hz)Cl(PPh3) 5.413 PfCz4H3zN6

Pt(4-MeC6H4N=NN=NC6H4Me-4)(CNBu'),, 2,221 PtCz4Hd', PtMe(4-MeC6H,)(PMezPh),, 5,398 PfC24H3SClNZP2 [PtCl(phen)(PEt3)2]+,5,431 PtCz&of'z PtPh,(PEt,)z, 5,399 PtC24H4,CIPz PtC1(2,6-(But,PCH~)2C6H3),5.454 PtC24H4BP2 PtH2{(But2PCH2)&H4},5,361 PtC24H43CIP Pt{CH,C(Me)=CHPBu Ci(Bu~2PcHzcHz&~zj. 5,446 PtC24HjoClZPz P t C 1 z ( B u ' 2 P C H z ~ H H 25.336 )2r P~CZ~H~~C~ZPZ P~CI~(PBU~)Z, 1,319; 5,449; 4.303 PtCz4H5402P2S Pt(S02)(PBu13)2,5,485 PtC24H54P2

F't(PBu',),, 5,441 PtCzJi,,CIP2 PtHCI(PBu',),, 5. 355,441 I'tC,,Hd', [PtH(PBu',),]+, 5,360 P~CL&~PZ P ~ H , ( P B U ' ~5,362 )~, P~CZ~H~OOI,P~ Pt{P(OEt),},, 5,442 PtCZ4H60P4 Pt(PEt3)4,2,1026,5,418.441 ptC~~H6iP4 [PtH(PEt,),]+, 5,357 Ptc~H63P4 5, 364 IPt2~1(~-H)z(PEt3)4]+, PtCZSH54F31Pz P~I(CF~)(PBU~)L,S. 387 PG,H24CI,P, PtCl,(dppe), 2,355; 5,432,133 PfCL+jH&IP2 PtCIMe(dppm), 5,457 PtC26H25C13PzS1 Pt(dppe)(H)(SiCl,), 2, 16 PtCz6Hz7BrPz PtHBr(PMePh,),, 5,366 PtC26Hz7NOJ'z PtH(N03)(PMePh&, 5,366 PfCnHz4PzSz Pt(CSz)(dppe), 5,472 PtC2,H2,C1Pz PtMeCI(PMcPh,),, 5,387 PrC2,H2,CIPz Pt(dppe)CI(Me), 2,354 PfCZ7II*@PZ Pt(OH)(Me)(dppe), 5,389,454 PtCz3zsPz PtMe,(dppm), 5,450,457 PtCz7H35N4 {4-MeC6H,N= [Pt { 2,6-(Me2NCHZ),C6H3} CHNHC6H4Me-4}]*,2. 198 P~CZ~HS~N~S~ [Pt(SezCNBu'z)3]+,5,482 PtC27H63P3

Pt(PPr'>),, 5,441,442 PtC,,H2,,S4Pf(SZCzPh2)2, 2,608,613; 5,485 PtC28H28C12N4S4

PtC12{PhC(S)NHz}4, 2,647 PtC,,H,,TP, PtMeI{Ph2P(CH2)3PPhz},5,450

SO8

PtC28H2904P Pt(acac)z(PPIi3).2,390 PtC,sH300P2 Pt(dppe)(OMe)Me, 2,354

PtMe,(dppe). 5.400.150 PtC2sH31C1P2 PtHCl(PPh,Et),, 5.448 PtC,HII,,IP, PtMe,I(dppin). 5.450 PtCZsH3iPZ [PtH(C,H,)(PMePh,),1-, 5,366 PtCzsH4oPz Pt(C=CPh)z(PEt,),, 2,219; 5,439 PtCz8H430zPZ Pt(OZ)(PPhBu'z)z. 2.319 PtCzsH46CIzPz PtCI2(PBut2Ph),,2, 1026; 5,448 PtCzsH& Pt(PPhBu',),, -, - 5,410.441 PtC ' H P *K;(PBu3),, 5,395 PtC,*H,,,I', PtEt,(PBu,),, 5, 395 ~~

PtMe&dppe)> 5 : 450 PtC30HzoClzF6Pz PtC12(PhZPCECCF3)2,5,446,452 PtC30H21C14F6P2 PtCI, { PhZPCH=C(Cl)CF3},, 5,446 PtC30HZ202S2 Pt{PhCOCH=C(S)Ph},, 2,651; 5,483 PGoH,~FJ'J,PzS, Pt(NCS)(SCN)(PhZl'CH,CCF,CHPTJhz),5,488 PtC3oH30F40P2

Pt(dppe)Mc((::F,C:F,C)Me), 2,354 PtC3OH300?P2 Pt(dppe)(C02Me)2,2. 355 PtCwH,iCIP2 PtHCI(PPh&. 5- 359 PtCioHdz [PtEt(C,H4)(PMePh2),]+, 5,366 PtC3oHw02P Pt(C2H4){ OcC( Me)=CMeCOC(Me)=c Me}-

Pt{4-{4-MeOC6HC4(S)=C(S)}C6H40Me),, 6 . 127 PtC32HmNd'z Pt(fiN=CHCH=CH),(dppe), 5,432 .. PGzH32Pz Pt(C,H,)(diphos). 6,304 PtC3JLP4 Pt(PMe2Ph),. 2.1026; 5.440,442 PtC32H46ClZP2 PtC12(Bu'2PC=CPh)2,5,446 PtC3zH 03Pz P t ( l i ~ O ) ( P P h B u ' , ) , ,5,410 PGzHwN~~JPL Pt { cHC(PEt,)H(CH,),CHCHCH,CH,} (PEt,)(402NC,H,N=NN=NC,r-r4NC)Z-4), 2, 219, 220. 224

509

Cumulative Formula Index

PtC33H34Pz PtMePh(PMePh,L., -,- 5.398 PtC33H37CIP2Si

PtC36H32P2S

PI(H)(SH)(PPh,)Z, 2,516; 5,473 Pt(SHI)(PPh3)2.2.516; 5,473

(+)-PtC1(SiMePhNp-1)(PMezPh)2, 2. 79 PG4H3W2 PtMe(NMePh)(dppe), 2, 177

( P h 3 P ) z ~ ( d N O ) 22,, 13 PfC-gH30N\iZP2 (Ph,P)ZPt(CN)2.2,13 PtC37H300P2S Pt(COS)(PPh,),, 5,472,486 PtC37H3oOPzSz Pt(SzCO)(PPh3)z,2,583; 5,486

Pt(N03)z(PPh,)z. 5,469 lW236H30N2PL P ~ ( ~ - P ~ ~ P C ~ H5.455 ~NH)Z. P~C~~II~ONZPZSZ Pt(S2NZ)(PPh3)2, 2. 120 PtC36H3oN6Pz Pt(N3)z(PPh3)2,5,437 PfC36H300zPz Pt(Oz)(PPh3)z, 2,318-320. 3?8.329,798,5.443,464, 465,469; 6,321,329.335.337,349 PtC3,H,oOzP2S Pt(SOz)(PPh3)2,5.485 YtCxH3004P2Sz Pt(SOz)2(PPh3)Z95 , 4 8 PtC'Jl,oP2 Pt(PPhj)z, 5 , 3h9,440 PtC36H30PZS

(PtS(PPh3)2),1,5,477 PtC36H30PzS4 Pt(S4)(PPh3)2,2,546,5, 472 PtC36H30P2Se {PtSe(PPh3)2},,,5.472 PtC36H30P2Se4 PtSe4(PPh3)2,5.472 PtC36H31CIP2 PtHCI(PPh,)z, 2,696; 5.356.362.367; 6,263 PtC&,,F,O,P, Pt(OOH)(O,CCF,)(PFh,),. 6.324

Pt(O3C)(fPh3)z,5,448,468 PtGHwOJ'2 Pt(C04)(PPh3)2,2,449; 5,468 PtC37H30P*SSC Pt(SCSe)(PPh3)2, 5,486 PtC37H30PZSZ Pt(CSz)(P€'h3)2,2,580,581; 5,412,486 P~G~H~OPZS~ Pt(S?CS)(PPh3)2,5,472 PtC371J30P2Se2 Pt(CSe2)(PPh3)z,2, 664; 5,412 PtC,7H,qCIP& PtCl(SCHS)(PPh,),, 5,369 P~C~~H~IFJ'~ PtH(CF3)(PPh3)2,5,360 PtC3,H,,NOP, PtH(CNO)(PPh3),, 5,389 PtC3,H3,NPZS PtH{SC(PPh,)=NPh)(PPh,), 5,356 PtC3,H3,NPZSe PtH(SeCN)(PPh3)2, 5,488 PtC37H3zCLP2 PtC1(CH2CI)(PPh3),, 5,389 PtC3&.3CM'z PtMeC1(PPh3),, 5.387 PtC,7H,J02P2S

Pt(CH,)(tSOt)(PPh3)2,2,635 PfCwHJPT PtI(Me)(PPh3)2,5,388 PtC37If33, PtH(Me)(PPh,),. 5,360 PtC3TH; ,CIP4S2

PtC37H51CIP&

5 10

Cumulative Formula Index

PtC38H29CIO;P2

PtC1(2-PhzPC,H4CO)(2-PhzPC,H,CHO),5,456

PtClaHlnBrFzP, _ _ __ Pt(CEZ=CFBr)(PPh,),, 5,414

Pt(NCO)i(PPh&, 5 , 389,169 P~C~~H~ONZPZ Pt(CN),(PPh,),, .~5 , 389 PtC38H30N2P2S Pt( NCS)( CN)(PPh3)2,5, 488 P~CX~~ON~PA Pt(NCS)Z(PPh3)2, 5,389 PtC38H300P2

PtC38H34P2 Pt(C,H,)(PPh,),, 2, 194,644; 5 . 355. 390,410,411,413, 414,415,419,466 PtC38H34PZS3 Pt(SCH2SCH,$)(PPh3),. 5.474 PtC,,H,4P, Pt(PhP=PYh)(dppe). 5.443 PtC3,H,,C1P2S PtCI(CH2SMe)(PPh3)2,5 . 389 PtC38H36P~ PtMe,(PPh,),, 5,398 P~CWH~SNZP~SZ Pt(Ph2PC=CBur)2(NCS)(SCN).2.233 PtC39H3OCIFsOP2 PtCI(CF2COCF3)(PPh3)2, 5.412 PtC39H&IF,NP2 PtCl{NC(CF3)z}(PPh;)~,2. 126 PtC39H30C12F40P2 PtCI(CF2COCF2CI)(PPh3)2.5.389 P~C~~H~OF~OP, Pt{(CF,),CO}(PPh,),, 5,412 ~ G Y 0F60zP2 H 2.329 -}(PPh,),, PtC39H30FP2 Pt(CF3CF=CF2)(PPh3)2. 5.41 3 P~C~~H~OF~PJ Pt(PCF3Ph2)3,5,440 PtC39~30OzP2

PtC,,F~I,,CIP, P t C 1 ( C H a H 2 ) ( P P h 3 ) 2 5,388 , PtC3yH3,C102P2S PtCl(02SCH=CHMe)(PPh3)2, 5,419 PtC39H35CIPZ PtCl(CH?CH=CH,)(PPh,)z, 5,419

[Pt{C(SMe),}(PPh,),Iji, 2,581 PtC H 0 P 2, 329 -)(PPh3l2, PtC39H370P2 [PtH(Me,CO)(PPh,),] ' 5,343,368 PtC3,I 13&IP2S [PtCI(CH,SMc,)(PPh,),]', 5,389 PtC39H3sP2 PtMeEt(PPh,L. 5.394

.

PtC4bH3,'FBN3PZ (Ph,P),Pt~N=C(CF,)N=C(CF,)~H}, 2,265 . .

.

PtC.iH,,CIOP, PtC1(COCH=CHMe)(PPhqL, 5,419

PtC,oHwN,OP,

[Pt(CNMe)(PPh,),(CONHMe)j',5,383

PtCnnHanN ,P,

Pt( 2-CH2C6H4PPh2)(2-McC6H4CH2)(2-MeC6H4PPh2).

5.397 P~C~GH~~N~PZ

[Pt(CNMe)(PPh3)z{C(NHPh)NHMe}]z+. 5.383

Pt C,, Hi8Pz P t ( M e m H , ) ( P P h , ) , . 5.411 PtCa,HwP, Pt(P=CBu')(PPh,),, 5 , 443 PtC4 lH3$6 IPt(triphds)(r13-P,)1-, 5. 445 .~ Pti',li34bCINiP; [PtC1(PPh3)Z(cNMeCHzCH,NMe)] + ,5,382 PtGiH4zP2 PtEtPr(PPh3)?, 5,394

PtBr(Ph)(PPh,f,, 5.3XX PtC42H35NOPz Pt(PhNO)(PPh,),. 5.437 PfGzH3sPzS PtH(SPh)(PPh3)2, 5, 355 PIC~~H~~NZOZPZ Pt{OOCMe2~(CN),}(PPh,j2,6.336 464

PtC46H440zPz P ~ P ~ ( O O B U ' ) ( P P ~5,465; , ) ~ , 6,330,349 PtC46H4eNzIPZ [PtI(CNBu'),(PPh,),]+, 5,380 P~C~~HWNZPI Pt(CN3urjZ(PPh3)z, 5 , 380 PtC47H41N02PLSz Pt(SSPr')(phthalimide)(PPh,),, 5,475 PtC,aCImF,oxPJ Pt{PF(OPh),},, 5,442 PtC48H40P2

PtPhT(PPh3)z. 5,394 PGeH410P; PtH(OPPh,)(PPh,),, 5,371 P~C~SH~L'J'~ Pt{(OPPh2j,Hz}, 5,460 PtC50C40P2 Pt(CzPhZ)(PPh,)z, 5,369 PtC5oH,,N2O,P2 Pt(4-0,NC,H4CH=CHC6H,NOr-4)(PPh,)z, 5.413 PtC,"H,,OP, Pt(Ph2C=CO)(PPh3)2, 5,412 I'tCsoH4,04Pz Pt(OzCPh),(PPh3)2.5,465 PtC50H40PZ

Pt(PhC=CPh)(PPh3)2, 5,415 PfCsoH42P4 Pt(PhlPCHPPhz)z, 5,452 PtC50H43P4 [Pt(Ph,PCHPPh,)(dppm)]+, 5,452 PtCqnH44CINqP,

P;C1(4-MeC6H4NNNC6H4Me-4)(PPh,)2, 2, 196.1026 PtCjoH4&02PZSZ

Pt(PPh,),(4-MeC,H4SOzN=NN=NSOZC,H,Me-4),2. 222 PtC5oHwP2 P ~ ( ~ - M C C ~ H ~ ) 5,394 ~(PP~~)~, Pt CmHuP4 [Pt(dppm),la+,5 , 452,458 PtCSoH,SNzPz

PtH(il-MeC6H?NNNC6H4Me-4)(PPh3)z. 2. 196. 198 PtCsOH48C1204P2 PtC1,(2-Ph,PC,H4COCHCOBu')2, 2,402

*

PtC43H3iN4P2 Pt{C(CN)ZCHzc(CN),} (PPh3)2, 5, 390 PtC H N03Pz m } ( P P h 3 ) 2 .5.137 PtC43H43CIOPZ P ~ C I ( O C C ~ H I ~ ) ( P6,264 P~~)Z, PtCuH~tlN4 Pt(tetraphenylporphyrin), 2,841 PtC44H37BrPZ PtBr(HC=CHPh)(PPh,),, 5.388 P~C~~H~XPZ PtBu,(PPh3)z, 2,328: 5.393 PtC45HiiP3S2 Pt,(~-S)(CS)(PPh,)(dppe). 5.472 PtC4,Ha,Br02Pz

__ .. - . Pr(CN),(dppm)2, 5 , 458 PtC H N P S ~ ~ H - 4 . 6 - M c Z C 6 H 2 ) ( 3 , S - M c , C , H ,(PPh&. )) 2. 194

Cumulative Formula index

PtC54HS40P4 Pt(dppe),(OMe)Me, 2,351

PtC55H45Br02P2 Pt(OOCPh,)Br(PPh,),, 6, 322

[Pt2(y:SMe)(CO)(PPh),

I-,

512

P ~ F BisSn O [Pt(S03F)J. 5.470 PtF804P4 [Pt(PFzO),]’-. 5, I60 PtFizP4 Pt(PF,),. 5.441 PtFeC4,H3,0ZP,S2 (Ph,P),Pt(CS,)Fe(CO),Cp, 2,583 PtFePdC,,H,,04P, FePtPd(dppm),(CO),. 5.4.57

5,472

__

.. PtH(PPh3),(CF3COz),H, 5,355 PIC58H51P3

Pt(2,4,6-Me3C6H2P=CPhz)(PPh3)2. 5.143 PtC59H54P4 Pt(triphos)(PPh,), 5,442 P~C~OH~N~PZ Pt(PhNNNPh)z(PPh3)2,2, 196 PtC62H6404P4 Pt(dir>p),, 5,442 PfCnH6oP4 Pt(PPh>),,l, 142; 2,265.583; 5,355. 430; 6,240 PtC,JI,,,P,S PtZS(PPh3)4,2,522 PtC73H60P4

PtCI2(PF,),, 5,445 PtC1,03S2 [Pt(S,O,)C1,]2-, 2,637 PtCI, PtCl,, 5,488,489 (PtC1,]2-. 1,2,3, 16, 187,390: 5,403.406, 4OS, 414, 418,425,430,436,551,463, 465.467.474,479, 480,483,488,490,495,499, 500; 6 . Y7,150,292 492,506,507,513,823, 830 PtCI, [PtCIJ-, 1, 16,385,5,42X, 429,445.488.490,491, 500;6, 11,250,291,553.52h,XO8.823 PtCIsH,,BrP2 Pt(PEt,),(Ph)Br, 1,318 P~COC~SH~~CI~NZP~ COC~~(~-P~C=CP~-~)P~(PP~~)Z, 5,116 PtCo2CZ6H1508P PtCoz(CO),(p-CO)(PPh,), 5. 462 PtCrC7H5 PtCr(p-CPh), 5,385

PtCrC,lI1,CIN, CrCl(sn),(p-NC)Pt(CN),, 3,778 PtCrC,oH20FN8 CrF(pn)*(p-NC)Pt(CN),, 3, 778

CrF{H,N(CH,),NH,},(p-NC)Pt(CN),. 3, 778 PtCuCSoH,SC1204PZ CUP~CI~(~-P~,PCOCHCOBU’),. 2.402 [CUP~CI~(~-P~~PCOCHCOBU~)J”. 2.402 PtCuHI2CI4N4 Cu(NH3)4PtC14,5,652 Pt(NH3)4CuC14,5, 653 PtF401S4 Pr(SO,F),, 5,470 Ptf, PtF,. 2,680; 5,491 PtF, PtF,, 5,4Y I {PtF,]-, 5,4Y1 [PtF6I2-,5,488,491 PtFGO, (PtF6)02,5,491

Fe2Pl(CO),(PPh,),. I. 124 PtGeC ,5H39CIPZ PtCI(GeMe,)(PEt,),, 5,420 PtGeC,8H49FP3 5,358 [PtH2(GeH2F)(PEt3),]+, PtGeC,,H4,0P2 Pt(OH)(GePh,)(P€t,),. 5.465 PtGeZC60H32F?OP2

PtH{Ge(C6F,)2HGe(C,F5)z}(PPh3)Z, 5,358 PtGezCl,o [PtC:l,(CieCl,),j’.-, 5, 421 PtGe,HgC,,I 160P1

Pt(GcPh~)(HgG~Ph,)(PRl13)z. 5,421 PtGe,CI,, [Pt(GcC13)513-,5,421 PtGe5HC115 [PtH(GeCI,),]*-. 5.421 PtHBrJO [PtBr,I(OH)]’-. 5.499 PtHCI2O6S [Pt{(S0,)2H)C1z]3-.2,638 PtHCl30 [~tci,(on)12-, 5.495 PtHNzSs Pt(S,N,H)(S,N), 5 - 472 PtH,BrCI,O [PtC14Rr(H10j] 5: 499 PtH2Br4CI0 [FtSr,Cl(fl,O)]-. 5.409 PtH2Br,lU [PtBr,I(H,O)-. 5,499 PtH2Br,0 [PtBr5(HzO)]-,5,499 PtHKXO [ k 1 3 ( H 2 0 ) ] - . 5.403.495 PtH2C16 PtH,CI,, 2,699.709 PtH,P;,S, Pt(SZN2H)l. 2 120.5.472 PtH,C12N PtC‘L(NH,). 5.422 PtH,CI,N [PtCI;(NH,)] -1. 187,5,465 PtH,Br,O, PtBr,(H,O),, 5,399 PtH4C12N0 [PtCI,(NH,)(OH)]-. 5.465 PtH4CI2O1 PtC12(H20)2.5.495 PtH4C1302 [PtC13(H20)Z]-, 5 ?495 PtHsC1,NO PtCI,(KH,)(H,O). 5,165 I’tH,Br,N,O, PtHrz(N02)2(NH3)2, 1, 195 Pti I,U2Nz PtCI2(NH3),. 1. 3. 17, 120, 180. 187; 2,93,039.980.5. 422,423.424.465.471,495, 1117; 6,756,757 PtH6ClZN404 PtC1Z(N02)I(NH3)zI1 . 195 ~

Curniillrtive Formula index

513

PtH,N, [Pt(NH3)J2+, 2 , 9 3 PtH,N,O, Pt(NH,),(NOz),, 6 . 11 PtH6N406 Pt(NH3)2(N03)2,2,27; 5,123 PtHGOS [Pt(OH),I2-, 2,296; 5,466;6 . 11 PtH7ClPz PtHCI(PH3)2,5,367 PtH,CI,N,OJ PtCI,(OH),(NII,),, 5 , 465 PtH,O, [Pt(H,O),l2+. 1,310. 321; 5,479.496 PtHsPz PtH,(PH3)2, 5,354 PtH,CIN, [PtCI(NH,),]+, 1, 187 PtH9CI3N3 [PtCI3(NH,),]+, 5, 428 PtH9CI,Ns [PtC1(NC12)2(NH3)3]+, 5.429 PtH,N303S Pt(S03)(NH3)3, 5,470 Pt H 1ON101 [pt(N~13),(H,0),]2’, 5 . 391. 423,134,471 PfH12Br2N4 [ P I ( N H ~ ) , B ~ ~2,27 ]~+, PtH,,CIN, [KCI(NH,),]+, 5,427 PtHlZClN50 PtCI(NO)(NH,),. 5 . 436 PtHIZCIN7 [PtCI(N3)(NH,),]z+, 5,137 PtH,,CI,N, [Pt?I,(NH,),I2+, 5, 428.398 PtHi,N, [Pt(NH3),] ‘. 5, 423 [Pt(NH&], I . 1 , 2 , 3 , 16. 187;2,27,5,422,123,427, 433,498,6, 98. 150 PtH,,N,OSS, Pt(S04)Z(NH3)4.5 . 470 PtHi,Nt, [Pt(NH&l2-, 5,429 PtHi3N4 [PtH(NH3),]*+,5,423 PtH13N405S [PtOH(SO,)(NH,),]+. 5.465.370 PtHI,N,O, [Pt(OH),(NH3)4]Z-,5,422 Ptl1 &IN5 [PtC1(NH3)5]3+,1 , 366: 5,42X. 429,49X, 49‘4 PfHi5N40z ’ .5.423 [Pt(OH)(H,O)(h-Ii~),]z P~HI~NSOJS [Pt(NH3)s(S0,)]2f. 5.470 PtHi5N602 [Pt(NH3)5(N0,)14-, 5,470 PtH,,N,O [6(NH3)5(H,0)]4+.5,470 PtHisN6 [Pt(NH3),]*+, 5,129 IPt(NH,),l4’, 1,446; 5,429; 6 , 190 PtkgCz3H3:BrC1N4 PtHg(2,6-(MezNCH,),~~~~3)BrC~{ 4MeC,H,NC(H)NPr’}. 2.202 Ptlfg,CI, [Hg,PtC1,]2-, 5. 1061 PtHg3C110 [Hg,PtCllo]* , 5 , 1061 Ptl, [ P t I , y , 5,499 Pt1rCZ4H6,P4 ~

PtSiC 10H19C103

[I’tH(PEt,)(~-Fl),IrH,(PEt3)3]+, 4, 1152 [Pt(PEt3)Z(p-H),IrHz(PEt3)2]+, 4, 1152 PtIrC30H68P, PtPh(PEt3)(p-H)21rH(PEt3)3, 5,363 PtIrCS2Hs2Cl4P4 [IrC12(PMe2Ph),(u-CI,)Pt(PPh3),1’, 4, 1156 PfId&H54CIP4 Pt(C~CPh)2(~-dppm),IrCI, 4, 1112 PtIrC~.4H&10P, _,

__

Pt(C=CC,H4Me-4),(p-dppm),IrCI(C0). 4. 1I12 I’tMnC,,H ,gO,PS

[MnPt(p-CSMe)(C:O),(PMc,Ph)Cp] ’ ,5,385 PthIO2SR [Pt(MoS,),]Z-, 2, 575 PLN’,O, P;(O,)(N,). 5,422 PtN&

[Pt(N,),]2-, 5.437 PtN,, [Pl(N3)6]z-.5.437 PtNiC,,H,,CI2P3S2 (Ph,P)CINi(CSJPtCI(PPh,),, PtO,S, [Pt(S03),IZ-, 2,638 PtOS,

2,583

[Pt(SO3),jh- . 2.638 PtOlZS8 [rl(s,o,),~b .2,h37 I’t c ) ,8S6

[Pt(S0,),l6 2.638 PtPbC39H39C1P2 PtCI(PbMe3)(PPh,),, 2, 16 PtPbC54H45CIP2 PtCI(PbPh3)(PPh3),, 5,420 PtPbC,,H,,P, PtPh(PbPh,)(PPh3),, 2,16,20 PtPb,C7,HsoP2 PtPh(Pb,Ph5)(PPh3),, 2, 16 PtPb9Cj6H30P2 [PtPb,(PPh;)2/4-, 5,421 PtPdC,zlllsN~ [PdPt(CNMc)J2*, 5 , 1104 PtPdC,,H,*CI,N,P, FrjPtCl,(Ph~Ppy~, 5, 1107 PtPdC48HjoCIzP2S2 Pt(PPh3)2(~-SPh)?PdClz, 5, 1138 I’tPdCsOH4,Cl2P4 PtPdCI,(p-dppm),, 5.458, 1104 PtPdC55H4jC12P3SZ

(Ph,P)ClPd(CS,)PtCl(PPh3)2,2,583 PfRuC26H29?19

[R~(Cr)(bipy),(u-CN)Pt(dien)]~+, 4,283 PtRU2C3aHZ+08P2 Ru,Pt(CO),(dppe), 4,374 PIS,, [Pt(s,),lz .2.542,546 PIS I 5 ~ P t ( S ~ ) > ]1’ -26; ~ 2,542,546: 5,472 PtSW,,HJ‘, Pt(PPh3)&3bPh3),, 5,463 PtSiC,,Hl9C1O~ PtCl(CH,-CHOSiMe,)(acac), 5,404

5 14

Cumulative Formula index

PtSiC,,H,,I,P,

[Pt(SnCI,j,(cod)l-, 2,20 PtSn,C7,Hp,0,P PtH(Sn(C6H4Me-4)2) { Sn(C6H4Me-4),}(OMe),(PEt,), 5, 358 PtSn4HCI,, [PtH(SnCI4),l3-. 5,371 PtSn5C1,, [Pt(SnCI,),]-. 2, 19 [Pt(SnCl,),]3-, 5,421 PtSn,C3,1 I,$,

PtSiC14H3412P2 PtHI,(SiH,C=CH)(PEt,),, 5. 357 ptsic,,H,,cI~ PtCI(SiMePhnp)(PMe,Ph). 5.420 PtSiCz,H&IPz PtC?i(S<MePh,)(PMe,Ph)z7 5.420 PtSiC,4H35F3P2 PtH{Si(C6H4F-4)3}(PMe,Ph),. 5.357 PtSiC,,H,,,P, P ~ H ( S ~ H ~ ) { P ( C B H5,358 II)~)~. PtSiC40H4P P t HiMe( { A HZ),}(PPh3),. 5 , 357 PtSiC47F157N2P3S ~~

Pt{Bu'N=P(S)NBu'(SiMe,)}(Ph,P)21 5.433 PtSiC53H4J'~ PtH(SiMePhnp)(PPh,),, 5>420 PfSiC54H46P~ PtH(SiPh3)(PPh3),, 5,357 PtSi2C30H36C1NPZ PtC1{N(SiMezCH,PPh2)z},5,453 PtSi2C30H3,C12NP2 PtC12{HN(SiMe,CHzPPh2)2} 5>453 PtSlzC38H36C14Pz Pt(SiMeC12)2(PPh3)2,5,419 PtSiZC40H440P2 PtH(Mc,SiOSiMc,H)(PPh,), . 5 . 357 PtSizC42H4,P, Pt(SiMePh2),(PMeZPh),. 5 , 420 PtSi2CI4HSZPZ Pt(CHzSiMe3),(PPh3)2.5.393 PtSi2C46H46P~ Pt{l,2-(Me2Si)ZC6H4}(PPh3)2, 5.420 PtSi3C33H81N6P3 Pt {Bu'N=PNBu'(SiMe,) }, , 5 - 443 PtSi4C84H70P2 (PPh3)z , 5,420 Pt { (SiPh2)3SiPh2} PtSnC19Hi6CI30P PtH(SnC13)(CO)(PPh3), 6. 264 PtSnC31H32CI402Pz PtCI( SnCI3)(diopj ,6,266 PtSnC36H,oC1,Pz PtCl(SnCI,)(PPh,),, 6,248 PtSnC36H31C13PZ PtH(SnCl,)(PPh,),, 5,358, 371; 6,248,263 PtSnC37H30C1,0P, PtH(SnCI,)(CO)(PPh,),, 5 , 371 PtSnC37H31C130P2 PtH( SnCI,)( CO)(PPh,) ,, 6,263 PtSnC39H39CIP2 PtMe(SnMe,CI)(PPh,),. 2, 180 PtSnC40H37C130P2 Pt(SnCI3)(COPr)(PPh3)2.6.264 PtSnC42H35C13PZ Pt(SnC13)Ph(PPhl)Z,5,400 P tSnC,,H,,FbNP, Pt( SnMe,){NC( CF,),} (PPh&. 2- 126 PtSnC54H45C1P2 PtCl(SnPh,)(PPh,),, 5,420 ~ . , PtSnC56H4,PZS2 Pt{MeSC(S)SnPh,J(PPh,),, 5,487 PtSnzClzH31ClnPZ [PtH(SnCI,),(PEt,),]-. 5,371 PtSn2C36H30C1606P2 Pt(SnC13)z{P(OPh)3},,2, 19 PtSll2C36H30C16P2 [ P ~ ( S ~ I C I ~ ) ~ ( P P5.42 ~ , ) ,1] , PtSn,C,,H,,P, PtH2(SnPh3)2(PMezPh)2, 5.358

,

PtC1,(TEEtz)),,5,476 PtTeZC28Hz8CiZ PtCI,{Te(CH,Ph),},, 5,476 PtW,S, [Pt(WS,)Z]Z-. 2.575 PtW6H3024 [PtW6H302J]5-.3, 1044 PtWA4 [PtW,0,,18-. 3.1044 Pt;AgC~OH3~N130, Ag[Pt(NH,),( I-methylthymine),],NO,, 5, 7XY

[Pt2(COjzC1~]2-,5,378 Pt2C2H6Br4S Pt,Br4(SMez), 1, 122 Pt2C4H8C14 PtzClz(~-Cl),(C2H4)*,5, 390,407, 490 PtzC4HiJ4OzSz PtJ,(P-I)z(DMSO)s, 5,479 PtzCsH12Cl2Ss Pt2(S2CMe)4C12. 5.480 PtzCpHi& Pt,(S,CMe)n, . . 5.480 Pt2C8H& [Ptz(KH3)4(2.2'-bipyrirnidyl)]4 ' ,5,433 Pt?CgHzUBr,S1 2,552; 5, 476, 1146 Pt2Br4(SEt2)21

PtSn2C5bH5808PZ

Pt{Sn(acac),},(PPh3),, 2. 18; 5.421 PtSnzCI, [PtC12(SnC13)2]2-, 5,421; 6,250 PtSn3C8Hl2CI9

5.43s

515 PtzCI4(SPrZjz,5,476 PtzClzH30BrzS4

(PtMe3Br)z{(MeS)zC=C(S.Me)z}. 2,612; 5,477 PtzCizH30C14Pz PtzClZ(~-Cl)z(PEt3)z.~5.477~490 PtzCizH4zN6 [Pt,(en),Me6lZ+, 2,30 P~zCI~HZZC~~PZ Pt2C14(PMe2Ph)2,5 , 404 PtZC16H3204

{PtMe,(acac)},, 5 , 467 Pf~Ci6H4oC140 1nP4 PtZCI4( (EtO)ZPOP(OEt),),, 5 . 459 PtzC16H56CIZN8[ {Pt(NHzEt)4}{PtCIz(NH2Et),}]+.1, 187

..

Pt;CS2H48NP4 [PI,H(MeCN) (dppm),]' ,5,355

141

Ptz(p-SPPhz)*(PPh3)z.5,461 Pt,C, H N P S e N -J,5-MezC,H,)] (p-PPhZ)(PPh,),(Ph). 2. 1Y4

Cumulative Formula Index

[ Ni{Pt { OP( O M ~ ) ~ } ~ ( d i p h o s )5. ) ~155 ]~-. Pt,PdCHz,N,O, [Ptz(Pd(NH3)(H2NMt))(p-OH)3(NH,)4J3+.1 + 125

516

517 Pt,CI,,, 1, 159; 5.489

Cumulative Formula Index PuF~O PuOF,. 3. 1211 PuF6 PuF6, 3.1210 PuE; [PuF,I2-, 3, 1132, 1186 PuFeC6N6 PU[Fe(CN)6], 3, 11% PuH204 PuO>[OH)2,6,942 PUH2O8PZ PU(HPO?)~. 3.1152 PuH,O, P u ( O H ) ~3. . 1133, 1134 PUHi&1,06 PUCl3(H20)6,3. 1133 Pur3 PuI,, 3, 1132 PuNzOs PUO~(NO~ 6,937,938 )~, PUN6018 [PLI(NO~),]~-. 6,925,947 PUOZ [PuO,jz’. 2,301 PU0,P PuPO,. 3. 1133 PUO,S, [Pu(SO,),]-, 3, 1134 PUS2 PUS,, 3, 1135 PU2C30, Puz(C03)3. 3, 1134 PU2C60,2 P u ~ ( C ~ O *3,) ~1134 . PuzF, [Pu2F7]-,3,1136 Pu,HO 12p3 Pu,H(PO,), 3, 1152 PU,O,S PU2C>,S,3, 1135 PU,O,S, P u ~ O ~3,S 1171 ~, pUzo3

PuF4 [ P u F ~ ], 3 , 1135

Pu2O3?3.1133 pU,o9& P~2(S03)3.3,1133 Pu201sS7 [Pu,(SO,),]~-, 3, 1132 PUIS3 PU2S,. 3,1133 Pu&H&II PU(OH)~PU~(CO,),, 6,940 PU3016P4 Pu3(P04)+3, 1152 pu3s4 Pu~S,.3, 1135

ReAs,CLoH&I, RbCClSz Re3C19(diars)2.4, 162 Rb(SzCCI), 2,591 R~AS~C~~H~~CI, RbCgH90 ReCI,(diars),. 4. 136 RbOBu', 2,348 [ReCl,(diars),l+. 4. I48 RbCaH607 Rb{02CCHZC(OH)(C02H)CH&Oz) 2,477 R ~ A s ~ C ~ ~ H ~ ~ ReH3(PhzAsCH2CH2AsPhz)z, 4, 150 RbC I 3Hz4N05S2 ReAuC31H27N;202P R~{S(CH,CH,O),CH,CH,}(NCS). 3.11 ReCp(CO)(N2C6H,0Me-4)(AuPPh,j, 2, 136 RbC16HzdN404 ReBBr7N Rb{NCCH~N(CH~CH~OCH~CH~OCH~CHZ)~[Re(NBBr,)Br,]-. 4, 194 NCH,CN}I, 3 , 4 2 RcBCgHioCIzN60 fZbCi~Hgd'J,Os Re{HB(AN=CHCH=C-~1)3(0)CI,, 2,251 [Rh(cryptand[2.2.l])]', 2, 938 ReBC27Hz5C12N,P RbC1BH36NZ06 ReCI,(PPh,)( HB(hN=CHCH=CH),), 2,251 ;4, 154 [Rb(crypand[2.2.2])]'. 2,938; 3 , 4 h ReB2C5H605 RbCdLoN20, [Rb(cryptand)[3.2.2])]+,2,938 [Re(BZH6)(CO),I - 3 , 101 ReBr,N,O, R bC2,H2,N06S Re(NO),Br,. 4,204 Rb(dibenz0-18-crown-6)(NCS)~ 3.38 ReBr,N RbCzzHzoN203 [ReNBr,]-. 4.194 [Rb { (8-quinolinylOCHZCHZ),0)1T 3. 19 ReBr,O R~CZ~H~SNZO~ ReOBr,, 4, 195 [Rb{[8-quin0linyl(OCH~CH~)~],O}]+. 3, 19 [ReOBr,]-, 4 . 164 RbCdLoNOioS ReBr,NO Rb(dibenzo-30-crown-lO)(NCS), 3,40 [Re(NO)Br,lZ-. 4.202 RbC3oHJ'Js03 ReBr,O Rb(2-0,NC,H40)(phen),, 3, 13 [ReOBr,] , 4 , 195 RbC33H57N309 [ReOBr,12 , 4 , 1x3. 195 [Rb(enniatin B)]+,3, 63 ReRr, RhC44H64012 [Rb(tetrdnactin)]+,3,65 [ReBr61z-,4,lb4, 172 ReCH3C14N0, RbC4&8zOi, ReCI,(MeNO,). 4. 171 [Rb{[g-quinolinyl(OCH,CHz),]zO) I-. 3. 19 ReCH3C1,0 R ~ C S ~ H ~ O N ~ ~ ~ S [ReCI,(0Me)lz-, 4, 173 [Rb(valinomycin)]+,3,63 ReCH304 RbYbF3 ReO,(OMe), 4. 198 RbYbFg, 3,1112 ReCH4C15NzS RWZ~HJSN~OIZSZ ReCI,{(H,N),CS}. 4, 171 (Rb(lS-crown-6)(SCN)},, 3>38 ReCH6C1,N,02S ReAsCZ6HZ4Cl4P [ReOCl,{(H2N)2CS)(H20)]+,4, 182 ReCl,(arphos), 4, 169 ReCH,CI3N2O2S R~As&H,~CI~F~ ReOCl,{(H,N),CS}(H,O), 4, 182 ReCI,(Me,AsCH=C(AsMe2)CF,CHF,),, 4, 170 ReC2Cl6N20PS2 ReAs2C9HI2Cl4E6 Re(NCS),CI,(POCI,), 4, 194 ReC1,(MezAsC=C(AsMez)CFzCFz~F2). 4. 170 ReC2C1,0N kASzCyoH&IgO [Re(NC2C1,)CI5]-.4,194 ReOC13(diars),4, 181 ReC2CIl2NOP R ~ A s ~ C ~ ~ H ~ ~ C ~ ~ Re(NC2Cl5)Cl4(POCl,),4, 194 ReCl,(diars), 4, 170 ReC2HZCl60, [Re(02CH)2C16]2-,4, 160 ReCI,(AsEt,Ph),, 4, 147 ReC,H3BrN0 R~As~C~~H~~CI~P, [ReOBr(NCMe)l-. 47183 ReC14(arphos),, 4, 169 ReC,H,Cl,N,O, ReAs2C,,HS,P~ Re(NO),CI,(NCMe). 4,204 ReH3(PPh3)z(Ph,AsCH2CI AsPh?). 150 KeCZH3Cl4N20 ReAs,C,,H,o ReH,(AsEtPh,),, 4, 192 Re(NO)CI,(NCMe). 4.203 RcC,H,CI,N ReAs4C20H,,CI, [ReCI,(CNMej]-. 4,166 [ReClz(diars)z]+,4, 162 ReCzH4N08 R ~ A S ~ C ~ ~ H ~ ~ C I ~ [ReCl,(diars),]+, 4, 193 [Re(NO)(Cz04)(OH),(H,0)lt, 4,203 I

518

519 ReC2H5CI4N2O2 [Re(NO)CI,(H,NAc)]-. 4.2114 ReC2H6Br4NOZ [Re(NO)Br,(EtOH)]-. 4.202 ReC2H6CI@S [ReCIS(DMSO)]-, 4, 171 ReC2H8CI3N,O ReOCl,(en), 4, 177 ReCzHgClzN2O2 ReO(OH)Cl,(en). 4. 178 RcCZH,oCIzN20, [Re(OH),Clx(cn)]', 4 , 178 ReC3Cl2N3OS5 [ReOC12(NCS)312 , 4 , 179 R;C3H2FN3Q2 [Reo(H,O) (CN),F]-, 4. 177 ReC3HZN402S3 [Re(NO)(NCS),(H20)1-- 4.203 ReC,H,CINO, ReC3HiCl;NO4 [ReO,CI,(DMF)]-, 4, 199 ReC,H,CI,NO, R~OCI,(DMF),4,178 ReC,H,CI,NO [RcCl,(DMF)]-, 4,171 ReC3Hq02 ReO,Me,, 2,296 ReC,Hy,C13N6S3 ReC13(W2NCSNHz)3. 4. 150 ReC4HN402 [ReO(OH)(CN),I2-, 4, 177. 185 ReC,H,O, FeH,(CO),, 2,700 ReC4H6CI4N, ReCI,(MeCN),, 2,277; 4.147. 167,169 [ReCI,(MeCN),]-, 1.406: 4. 146 ReC4Hb03S4 IReO(SCH2COSH)21 . 4 , 183

ReC,H,OS, ~ReO(SCH,CH,S)21-. ~- 4+ 182 R~,H,S, [ReS(SCH,CH,S),]-, 2.529.531: 4. 192 ReCaH,,CI,NO (ReOCl,(Et,NH)]-. 4.178 ReC4H,,I04S2 Re021(DMSO),, 4. 187 ReC4H,,N,02 [ReO,(en),]', 4, 1Hh ReC4H16NROZS4 Re02{(H2N)zCS),,4. 187 ReC4HY7N,O, [ReO(OH)(en),j2-, 4, 178 ReC,N,O, [Re0,(CN),13 , 1.53,4. 185 ReC,N,O2S, IRe02(CNS)413-,4, 187 R~C,N, [ReN(CN),I2 .4.189 ReC40,S4 [ReO(CzS202)z]~~. 4. 182 ReCSC1O5 ReCI(CO),, 4, 172 ReC5FNOsS [Re(CO),(NSFjI', 4, 204 ReC,H,Cl3N1 ReNCl,(py). 4. 194 ReC,H,CI,N,O [Re(NO)Cl,(py)]-. 4. 202 ~

~

ReC5HjC15N [KeCl,(py)]-, 4, 173 ReCjHIOCl4hS2 [ReC1,(S,CNEt,)]2~. 4, 171 ReC5Ha3CIN5 [Re(NMe)(NHzMe)4CI]z+, 4, 190 ReCSNO5S [Re(CO),(NS)IZ+,2, 119; 4,204 ReC5N50Sj [ReO(NCS)jl-, 4, I67 [ReO(NCS)5]'- . 4 , 179 ReC,N, [ ReN(C?4)5]3-,4, 189 ReC,N,O [Re(CN),(NO)li-. 4, 128 ReCiN6S, [ReN(NCS)5]2-,4, 194 ReC,O,

[Re(CO)5],2,210 ReC6H9CI3N3 ReCI,(NChle),, 4, 147 ReGH,A Re03(OAc)(THF),4, 199 ReC6H,,CI,0S, ReOC1,(EiSCH2CH,SEt), 4, 182 RKbH 14C14tizO2 RcCll(HN=C(OMt.)Mt.)2, 2,277; 4, lh7 KeC,5HT4NO3

ReO,(NPr'z), 4, 197 ReC,H,,CI,O,S, ReO(OH)Cl2(E:SCH2CH2SEt),4, 182 ReC,Hi&6 Re(OMe),. 4, 196 ReC& [Re(CN),l5-, 4, 128 [Re(CN),16-, 4, 128 ReC,N,0S6 [ReO(NCS)61z , 4 , 167 KeC,N60, [Re(l"C))h]2-. 4. 166 [Rc(OCN)hl-, . ~. 4, 193 Rk,N,S6 IRe(NCS),IZ-, 4,146, 156, 167, 179 IRe(KCS)61J-.4. 146 ReC,012 [Re(C20,)3]z-.1,171 ReC,H, CI 0, [ReOC13(2-OC6H,CHO)]-,4, 184 ReC,H,NO, ReO,(OAc)(?-HOpy), 4, 199 ReC,HI9N204 ReO,(OMe)(TMED), 4, 199 RcC7H,,ClN,O Rt(0Mc) {(NC),C=C(NH,)CH,C(N ti2)=N}(NH3)4CL,4,147 ReC,N, [Re(CN),]' . 1,72: 4,135, 143 ReC,H j03 [ReCp(CO)3]', 2,237 ReC,H,,Br,N, ReBr,(CNMe),, 4, 143 ReC8H16Br402S2 ReBr,($CH,CH,OCH,~Hz),. 4, 171

Cumulative Formula index ReCgH,O,Si ReO,(OSiMe,), 4, 198 ReC,oH8Br3CIN, ReCIBr,(bipy), 4. 166 ReCloH8Br3N20 ReOBr,(bipy), 4, 178 ReCloH8C1N2O3 ReO,Cl(bipy), 4, 199 ReC inHK1,N, ReCl,(bipy), 4, 156 KeCloH6C13N20 ReOCl,(bipy), 4, 177 RcClol18CI,N, Rel\lCl,(bipy), 4, 194 ReC,,H,CI,N, ReCl,(bipy), 4. 166 ReC,oH,oBr3N20 ReOBr,(py),, 4. 172. 178 ReCloH,,CIN202 Re03Cl(py),, 4,199 ReCloHloC13N20 ReOC13(py),, 4, 177 ReC,,H,"CI,N, ReCl,(py),, 4, I66 RcC~,,H,,CI,N,C) Re(NO)Cl,(py),, 4,203 ReCloHl,I,N, ReIdpy),, 4, 166 ReCJL ReHCp,, 2,690,696,707 ReCIoHIIBr,N,O2 ReO(OH)Br,(py),, 4, 178 ReCloHIIC12N202 ReO(OH)CI,(py),, 4, 178 ReCl,H12 {ReHzCp,]', 2,696 RcCiOH12FN203 Re02(py),(H20)F,4, 186 RcC1JI12N203 [ReOZ(py),(HlC))]' , 4 , 180 R c G J Ji,N 2 0 1 I [RCOx{ ozCCH,),NCH,CH,N~CH,c02H) CH,C02}]z--.4,198 ReCloH14C1204 Re(acac),CI,, 2,376; 4. 119. 170 [Re(acac),CI,]-. 4, 149 ReCioH,& [Re{(SCH,),CMe),]-, 2,530: 4,192 ReCloH2,CI2N2S4 ReCI,(S2CNEt,),. 4, 171 ReCdLON3S4 ReN(S,CNEt,),, 4, 189 RcC.,,,H,,CI,OP, ReOCl,(dcpe), 4, 181 ReC11H19N203

KeO,(py)(NPr',), 4, 199 ReCI,Hz3N2O2S4 ReO(OMe)(S2CNEt,),, 4, 183. 188 ReCllH27CIOZP3 ReCI(CO),(PMe,),, 4, 134 ReCi 1H29F3011P3 ReH2{P(OMe)3}3(0,CCF3),4, 152 ReC I H3,C1N,09P, ReCI(N,)(CNMe){ P(OMe),), , 4 , 130 ReC12H8CIN,03 Re03Cl(phen),4, 199 ReC,2H6C.14NZ ReCl,(phen), 4, I66 ReC ,,IIyCI,N20 Rc(OH)Cl,(phen), 4, 166 ReCizHi3NzOzSz 4 , 188 RzO(OH)(~-SC~H,NH,)~, ReCtzHiD"05

KeO,(X-quinolinolate)(DMF). 4, 199 ReCl2HI5Cl2N2O2 ReO(OEt)Cl,(py),. 4, 178 ReC12H22N4021 Re,(NO),( OAc),O( OH),. 4.203 ReCi2H2,O4Si Re0,(0SiB~',)~4. 198 ReC12H30NP2 ReH,(NHPh)(PMe,),, 4,202 ReC12H36CIN2012P4 KeCI(N2){P(OMe)3}4,4, 130 RcC,,I 7390,zP4 RcH,{P(OMe),),, 4, 151 RCC~,H,~P, ReH,(PMe,),, 4. 134, 151 RGJLoP? [ReH,(PMe,),]+, 4,152, 193 ReCI3HlZN2O2 [ReCp(Cb),(NHNHPh)]-, 2, 145 ReC13H,oO14P5 ReH{P(OMe),},( (MeO),POP(OMe),}, 4, 135 ReC14H120S4 [Re0(3,4-S,C,H3Me),]-, 4, 182 ReCI4Hl3N2O2 ReCp(CO),(NNMePh), 2, 144 KeCl4Hl,N2O, ReCp(CC1),(NN1iC6fI~~Me), 2, 146 ReC15H3F1806 Re(hfacac),, 4. 149 ReCjSHjSC13NR ReCl,(py),, 4- 144 ReC15H15FN,0z ReO,(py),F, 4,186 ReC15H15N203 ReCp(CO),(NNMeC,H,OMe), 2, 149 ReClSH2,06 Re(acac),, 2,376; 4, 149 RCC15I I,,CI?O3P RcOCI,( acac)(PEt,Ph), 4, 181 ReC,,H2,N,0S, Re(NC,H4Me-4)(S,CNhle,),(OEt), 4, 190 ReC.15H30N30S6 Re(S2CNEt2),C0.4, 150 R~CI~H~ON~S~ Re(S,CNEt,),, 4, 150 ReCl5H3,CI2NP3 Re(NPh)Cl,(PMe&, 4, 166 ReCi5H3sO6 [ReO(OPr'),]-. 4.196 RcCl5H3,N3OSi RC(NBU')~(OS~MC~). 4. 197 R~CI~H~J'~ Ke(llZ-CH,PMe,)(PMe,),, 4. 134 ReC H45CIPs ReCI(PMe3)5,4. 134 ReClsH4sN20~Si5 Re{N(SiMe&)(NSiMe3)(OSiMe3),. 4, 197 ReC15H45Ws [Re(N2)(PMe3)5]+.4,132 ReC15H46CIP5 [ReHCI(PMe,),j-l 4, 151 R~CI&~OI~P, ReH(P(OMe),}5, 4, 135 ReC15HJ'5 ReH(PMe,),. 4. 131 ReC15H47O1d'5 IReH,{P(OW,),l+, 4, 152 ReC.16H10N304 [Rc(CO),(PhNNNPh)] . 2 , 2 0 4 ~eC1,H,,C~,N,O, KeCl,(salen), 4. 175 ReC16H16CIN203 ReOCl(2-OC6H,CH=NMe),, 4, 184

520

521

Cumulative Formula index

ReC16H16C314N,Oz ReCl,(salenH,), 4. 176 ReC16HzzC14Pz ReCl,(PMe,Ph),, 4, 118. 168 ReCI6HZ,C1N3S4 Re( NP h)Cl(SzCNEtz)a,4,190 ReC16Hz7Pz ReH,(PMe,Ph),. 4. 193 ReC, 6H29PZ ReH,(PMe,Ph),, 4.152,201 ReCL6H30N4PZS4

[Re(NCS),(PEt,),]- ,4,14A ReC,6tI3,NOzf3 Rc(NHPh)(q2-C02)(PMe3),,4, 132 ReC16H360s ReO(OBu‘)4, 4, 196 ReC16H4sPs ReMe(PMe,),, 4, 134 R~CI~HSIOISP~ ReOP( OMe),{ P(OMe),),. 4. 135 ReClSHl2C12N202 ReCl,(S-quinoIinolate),,, - 4. 176 ReClsHI2Ci3N3S3 Re(2-(WN)-4-ClC,H3S),, 4.192, 196 [Rc { 2-(HN)-4-CIC,H,S),J’, 4.201 [Re{2-(HN)-4-CIC6H,S),]-, 4, 192 ReC18H13CINZ03 RerOTI)C1(8-uuinolinoIarei,. 4. 176 ReCl~Hl4ClNzO~ Re03C1(8-quinolinol),, 4, 199 ReCl8HI4N3S3 Re(2-NC6H4S)(2-HNC6H4S)2. 4,201 ReCIsHl,C140P [ReOCI4(PPh3)]-, 4,179. 183 ReClsH,,C1,P [ReCI,(PPh,)] ,4, 173 ReC1dhN3S3 Re(2-HNC6H4S)3.4, 192, 1% [Rc(2-HNC,tl,S)q]-, 4, 142 [Rc(~-HNC~H,S)~]-, 4.201 ReC,,H,,INP, [Re(NHPh)I(PMe,),]+, 4.132. 144 ReCI8H4JU” Re(NHPh)(N2)(PMe3)4.4.130, 152 ReClsH44NP4 ReHz(NHPh)(PMe3).,. 4. 151. 152 ReC18H45C1309P3 ReCI,{P(OEt),},, 4. 149 ReC18H45C13P3 ReCI,(PEt,),, 4, 147 RCC18H54N30S16 ReO{N(SiMc3)2}3.4. 179 ReCl9HI5Cl4NZ ReCI4(PhC(NPh),},2,276 ReCI9HzzClO3P, ReCI(CO),(PMe,Ph),. 4, 157 ReCI9H&12N3 (NHC6H1 I)( N H ~ C ~IH ) , I4, 190 Rc(NC6H4Me-4)C12 ReCI9H4,C1N2P3 ReC1(CNBu‘)2(PMe3)3, 4, 129 ReC19H46C1NZPi [ReCl(CNBu‘)(CNHBul)(PMe,),l+. 4, 129 ReC2,HI7N4O2 [ReO(OH)(bipy),]2’, 4,178 ReC20H18C1N202P Re(NO)CI(Phd’O)(NCMe), 4,203 ReC20HlsClsNP ReCI,(NCMe)(PPh,). 4. 168 R~CzoHzoN40z [ReO,(py),]+, I , 53:4,178, 186, 199 ReC20H21C1302PS ReOC13(PPh3)(DMSO).4. 181 R~CZOH~OB~~OZPZ I -

ReCZ5H&I,P,

ReOBr3(PEt2Ph)(OPEt,Ph),4, 180 ReCzoH,nC13NP,S ReCI,(NS)(PEt,Ph),, 2, 119, 121 ReC20H30C130Pz ReOCl,(PEr,Ph),, 4, 169,179 ReCZOH30Cl:0ZPZ ReOCl,(PEt,Ph)( OPEt,Ph), 4, 180 ReC2,H: 1C13OP, Re(OH)C13(PEtzPh)Z, 4, 169, 179 ReCmH37P2 ReH,(PEt,Ph),, 4. 202 ReC,,,H,,,N,S, [Rc(SICNEt2),l2+,4, 171 RcCzoH,,C120,P, ReC12(C0)2(PPr3)z,4, 136 Rt%Hi& Re(3.+S2C6H3Me)3,4, 196 ReC2,H22CIJOzP ReOCl,(PPh,)(DMF), 4,180, 181 ReC2,H2,Br2N3 ReBr2(HzNC6H,Me-4),.4, 144 ReC, iH45CIN3PZ ReC1(CNBuc),(PMe,),,4, 129 RcC~,H~~NP~ ReH{NtIPh)(ql-Cl I,PMe,)(PMc,),, 4, 152 KeC2,11,,C‘I,N,P, ReC‘12(~\;2Pl~)(NH,)(PMe2Ph),, 4, 145 ReCz2H,1C12N3P2 IReCl,(NNHPh)(NH,)(PMe,Ph)] ’ , 4 , 115 ReCZ2H,JW”S4 ReH(S2CNh.iez)2(PMe2Ph),,4, 151 ReC23H20C13NP ReCL(py)(PPh,), 4, 166 ReC2,H2,C1,03P ReOCl,(acac)(PPh,), 4, 180,181 ReC,,H,,Cl,NOS,P RcOCI,(S,CNEt,)(PPh,), 4. 1x3 RCCZJH~~C~~~~O Re(KO)Cl,(phen),, 4,203 ReC24H20C13N021’ ReCl,(PhNO)(Ph,PO), 4, 190 ReC34H20NS, ReN(SPh).,. 4. 197 ReC H 0S [ReO(SPh)J. 2,526; 4, 182 ReCz4HZoOSe4 [ReO(SePh),]-, 4, 182 ReC2,H,4Cl,h’3P ReCI,(CNMe),(PPh,), 4, 143 RcC,,H,,CI,NP, ReNCI,(PMe,Ph),, 4, 189 ReC34H33C13P3 ReCI,(Ph.le,Ph),. 4, 147, 148 [ReCI,(PMezPh)3]’, 4, 148 KeC24H35C13PJ ReH,C1,(PMe2Ph),, 4, 193 RcC-dLJ’, ReH,(PMe,Ph),, 2,703; 4, 152, 153, 193 ReCZ4H4,PL ReH,(PPr’,Ph),, 4,201 ReC25H20C13Nz0Pz ReCI3(N=NCOPh)(PPh3),, 4, 166 ReC35H2ZBr4P2 ReBr4(dppm), 4, 169 ReCzsHzzClzNOzP ReCI2(4-MeC6H4NO)(Ph3PO), 4, 190 ReC25H,,C1,NP { Rc(NC,H,Mc-4) C13(I’I’h3)} ,,, 4 , 190 ReCz5H22C130P2 ReOCll(dppm), 4,181 ReC,,H,,CI;~OP Re(NC6H,Me-4)C1,(Ph3PO), 4, 194 ReC25H22CllPZ

,,,

ReCdb2C14P2

Cumulative Formulu Index

ReCl,(dppm), 4, 169 ReC2,H3,CI2NP3 ReC12(NCH2)(PMe2Ph)3. 2. 127 ReC2SH36C12NP3 [Re(NMe)C12(PMe2Ph)3]+, 4, 190 ReC25H37C1202P2 ReCl,(acac)(PEt,Ph),, 4, 149 ReC25H,SCIN5 ReCl(CNBu'),. 4, 129 RcC2,fI,,CI,N, [Re(CNBu'),CI,]', 4, 143 KeC'25H4512NS [Ke(CNBut),I,]+, 4, 143 ReC26H22C13NOP Re(NC6H4Me-4)CI,(CO)(PPh3), 4. 191 ReC26H24Br30P2 ReOBr,(dppe), 4, 180 ReC&&I,P, (ReCl,(dppe)j+, 4, 162 R~c,,H,,CI;NO, ReOC13(2-HOC6H4CH=NMe)(PPh3).4, 181 ReC2cH,,C1,0P, ReOci,(dppcj, 4,180,181 KeC26H24C14P2 ReCl,(dppe), 4, IO9 ReC26H&l2N4P [ReCl,ICNMe),(PPh,)]', 4. 143 RecmH~Pz RcH,(dppc), 4,201 ReC26H36C12NP3 [KeC12(PMe2Ph)3(NCMe)]+, 4, 148 ReC26H36CI2N20P3 ReCI,(N,COMe)(PMe,Ph),, 4, 131 ReC2,H21C13NOP ReCI,(S-quinolinolate)(PPh,), 4, 176 ReC27H29C13NP2 ReCI,(NMe)(PPh,Me),, 2,280 ReC2,H40C1NP3S2 ReHCl(S2CNMe2)(PMe2Ph),, 4> 151 ReC,,H,,CIN,O,P, RcCWd(PPh3) {P(OMc),I 3,4, 130 ReC28H23C13N2P ReCl,(bipy)(PPh,), 4, 144 ReC28f125C13N,P R c C ~ ( P Y ) ~ ( P 4, P ~144 ~), ReC28H27C13NP2 ReCI,(CNMe)(dppe), 4, 143. 146 ReCI,(NCMe)(dppe), 4, 148 ReC2sH2712N02P ReO(OEt)12(PPh3)(CNC6H,Me-4) 4. 177 ReC2sH29C104P ReCl(acac),(PPh,), 4, 149 ReC28H30C14C)4P2

ReCI,(OP(OEtjPh,),, 4. 171 ReCZ9Ht2CIN20, Re.(C0)3CI (4-PhCH=CI-l P Y ) ~ 6 . 27 ReCz9HzzN,PZS4 [Re(NCS),(dppm)]-, 4,146 ReC29H33C13NPZ Re(NMe)C13(PEtPh2)?,4. 189 ReC29H38CIN3P3 ReC1(N2)(py)(PMe,Ph)314. 130 ReC29H43N3P3SZ Re(S2CNEtz)(N,)(PMezPh);. 4. 130. 193 ReC29H45CINP3S2 [ReCI(S2CNEtZ)H2(PMe2Ph),12+, 2, 691 ReC,oHzZC1204 ReCI,(PhL'OCI.lCOPh),, 4, 171 RcCWHWNJ'~S, [Re(NCS),(dppe)] , 4 , 14h ReC,,H,,N, Re(hipy),, 4,202 ReC30H28C12N2S4

5 22

4, 171 ReC12(SICN(CH2Ph)2)2, ReC30H38C12NZF3 ReCI2(N2Ph)(PMe,Ph),.2, 133, 136; 4, 145 ReC30H3804Pf Re(OPh),(PMe,),. 4. 17C ReC3JL4P3 Re(r16-C6H6)H,(PMe,Ph),,4, 193 ReC30H,SCI,NP3 ReNCI,(PEr,Ph),, 4, 188 KeC,,,I I,,CI,NP,S ReCI,(NS)(PEt,Ph),, 2, 121 RCC~,,H~~IO~P~ ReO,I(PEt,Ph),, 4, 186 ReCdL3fi [Re(CNBu'),] ' . 4 . 129 ReC3,,H,,ClN6 [Re(CNBu'),CIIZ+.4, 143 ReC31H3BC12NIOP3 ReCl,(N,COPh)(PMe,Ph),, 2, 133, 136; 4, 144 ReC31H3BC12N20;P3 ReC12(N2COPh)(PPh3){P(OMe)3}2, 4, 130 ReC,,H16Ns Rcfphthalocyanine), 2,866 ReC3,H1,ClNs0 Re(phthalocq.anine)(LlH)CI,2, 866 ReC3,1-I2,CI3O2P ReU13(9,lO-phennnthroquii~one)(PPh,), 4, 150 ReC3,HzsCl2O2P ReCI,(PhCOCOPh)(PPh,), 4, 150 ReC32H28Br3N4 RcBr,(CNC6H4h€e-4),.4, 143 ReC32H3,CI,N2P ,~

~

Re(NC6H,Me-4)CI2(4-H2NC6H4Me)(PPh3), 4, 191 ReC32H33C12N2P2 ReCI2(I\;=CH,)(py)(PMePh2),, 2,280; 4, 144 ReC32H43N2P4 Re(N2)(PMe2Ph)3{PMe2(C6114)}, 4, 130 ReC3,II,,CIN,P, ReCI(N,)(PMe,Ph),, 3,329; 4,129, 131, 132 [ReCI(N,)(PMe,Ph),]+, 4.131, 136 ReC,,H,,L'I,P, RcC12(PMc2Ph)4. 4.136 ReC32H47P4 ReH3(PMe2Ph)4,4. 151 ReC32HS0N60SB {Re(NPh)(S,CNEt,),),O, 4. 190 ReC33H2005P Re(CO),(PcPh=CPhCPh=cPh), 2,1043 ReC33H30N302P [ReO2(py),(PPhdl+, 4, 186 ReC3,H2&I2N30P

Re(NO)C12(4-CNC6H,Me)2(PPh3j, 4,203 ReCwH37C12NOP3 Rc(NO)CI,(PMe,Ph),(PPh3), 4,203 RcCz4H5CI 2N4P [Re(CNBut)4(PE.tPh,)Cl,~'4, 143 KeC,,H, ,I N, Re(CNPh),I, 4. 129 ReC3,H2,N, Re(phen),. 4.202 ReC36H30BrC!3P2 ReCI,Br(PPh,),, 4. 168 ReC36H30Br2C12P, ReC12Brz(PPh3),l4. 168 ReC3GH3oCIN202P2 Re(NO)2CI(PPh3)z.4.204 ReC36H3,)C!210P, KeOCI,l(PPh,),, 3, 179 RcC36H.30C1212P2 ReCI2I2(PPh3j2~ 4 - 168 ReC3,H,oCI,NY2 ReNCI,(PPh&. 4. 188 ReC36H30C12N202P2

Cumulative Formula index

523 Re(NO),Cl2(PPh3),. 4.204 ReC3,H30C1,0P, [ReOCI,(PPh3)z]Z', 4,181 ReC36H30C13IP2 ReCI,I(PPh,),, 4,168 ReC36H30C13NOP2 Re(NO)CI,(PPh,),, 4.203 ReC,,HJoCI3NPZ ReNC13(PPh3)2,4,194 ReC&&l,NPzS Re(NS)CI,(PPh;),. 4. 203 ReC36H30C13NZOZP2

ReCl,(NO)(NPPh,)(OPPh3)q2, 124; 4,204 ReC36H30C130P2 ReOC11(PPh3)2,4,148,178,179 ReC36H30C130~P2 ReOCI3(0PPh3)(PPh3),4.148.181 ReC36H,oC14NP, ReCl,(NPPh,)(PPh,). 2,123:4, 197 ReC36H3oC140zP2 ReCI,(OPPh3),. 4.171 R~C,~H,OC~~Z RcCl4(PPh3),,4,154,166,168 ReC36H3aI0zPz Re021(PPh3),, 2, 296:4,186, 193 ReC36H31FNOP2 Re(NO)HF(PPh3)2,4,203 ReC&31N202Pz ReH(NO),(PPh&. 4,203 ReC36H32NOP2 ReH2(NO)(PPh3),, 4.203 ReC36H35C13P3 ReCl,(dppe)( PE t,P h) .4.147 ReCd37Pz ReH7(PPh3),. 4,201 R~C~~H~~NZP~SZ Re(S2PPl~2)(N2)(PMe2Ph)r. 4, 131

Rc(NO)C1,(OMe)(PPh3),. 4. 203 ReC37H331~0~P? ReO12(0Me)(PPh3}214,180 ReC38H30CIN,0PzS, ReOCI(NCS)2(PPh,)2.4,179 ReC38H30N03PZ Re(NO)(CO),(PPh,),, 4,200.203 ReC38H30N20ZP2S2 \Re02(NCS)2(PPh3)2]-, 4, 187 ReC3sH31N202P2S2 ReO(OH)(NCS),(PPh,),. 4.179 ReC3,H33C13NP2 ReCI,(CNMe)(PPh,),, 4, 143> 146 ReCI,(NCMe)(PPh,),, 4,146. 147, 148 ReC38H33NPS3 Re(SPh),(,NCMe)(,PPh,).4,150 ReC38H35C1202P2 ReOCI,(OEt)(PPh,),. 4. 180 ReC38H351ZOZP2 ReOI,(OEt)(PPh,),, 4.180 ReC38H46N3P4S2

Re(q1-S2PPhz)(N,)(CNMe)(PMe2Ph)3, 4,131 ReC39H30C103P2 ReCl(CO),(PPh&+ 2,204;4.191 ReC39H3~N30PZS3 ReO(SCN),(PPh,),, 4,179 R~C~YHWNIS~ Re(S,CNPh,),, 4.150 ReC39H3

1

ReH(CO),(PPh,),, 4,191 ReC39H39Br,P3 ReBr,(PMePh,),, 4, 147 ReC39H39N3P3S3

Re( NCS)3(PEt,Ph)(dppe), 2,230 ReC40HblN$'4 ReH(N,)(PEt,Ph),, 4,130 ReCiiH31ChF60zPz ReCl,(hfacac)(PPh,),, 4,149 ReC41H37C1202P2 ReC12(acac)(PPh3),,2,377;4,149 ReC4,H37CIz03Pz ReOCl,(acac)(PPh,),, 2,377; 4,149 ReGIH3,P2 ReH,(Cp)(PPh,),, 4,1163 ReC4,H3BCIzOJ'2 ReHCl,(acac)(PPh,),, 4,174 ReC4,H,,Cl3OP1 ReOC13{(Ph2PCH2)3CMe}, 4,181 ReC41H39C1&'3 ReCl,(triphos). 4,149 ReC41H40C12NP2S2 ReC1z(SzCNEt2)(PPh3)2, 4,150 ReC41H51C12N3P2 [Re(CNBu'),(dppe)CI,]+, 4,143 ReC&&lN6 [Re(CNPh),CIIZ', 4,143 ReC4zHdk [Re(CNPh),l+, 4,129 ReC,,H,,S, h{SCIPh)=C(Ph)$13. 1.24.63;4,196 .~ ReC4;H34C13NQPZ ReCI3(C6H4N4)(PPh3),, 4,147 ReC42H35BrN30P2 ReBr(NO)(N,Ph)(PPh,),, 2,140 ReC42H35NPS4 Re(NPPh3)(SPh),. 2, 124;4,197 ReC4zH37C12NZP2 Re(N=CH2)C12(PPh3)2(py),4,190 ReC4zH370~P~S~ Re(acac)(CS,)(PPh,),, 2,376 ReG2H&13P4 { ReCl3(Ph2PCW2CH,PPhCH2CH2PPhCH2CH2PPhZ)),,,4,162

{ReCI,[(Ph,PCH,CH,),P]},,,4,162 ReCd,H4,N402 ReO(OPh)(octaethylporphyrin),4,185 ReC42H50P3 ReHS(PEtPh,),, 4,192 ReC,3H,,C12N20P2 ReCl2(N2COPh)(PPh3),,2,140;4,130,144 ReC43H35C1LV'2 ReOCl,(2-OC,H,CHO)(PPh,)z, 4,184 ReC43H3&302P2 ReC13(2-HOC6H4CHO)(PPh3),,4,153 ReC4,H,,C13NP, Re(NC,H4Me-4)Cl,(PPh3),, 4,190 RcC~.H~#~P~ Re(acac)(CO)Z(PPh3)2,2,376 ReC4&Cl2NP~ ~, ~

Re(NC6H4Me-4)HCI2(PPh3),, 4,190 ReC43H,sN2P2 _. - . Re.(N=CHMe)( PPh3),(py) ,4,190 ReC43H41C1~0~P3

ReO(OEt)CI2{(PhzPCH,),CMe}, 4,181

ReC,H3,Nz0,P, Re( CO),( N2Ph)(PPh3),,2,140 ReC44H37Ch02PZ ReCI,(2-OC6H,COMe)(PPh3),, 4,154 ReC-J4Hf9102P3 ReO,I(dppe)(PPh,), 4, 186 ReC,,H,,CI,NOP, Re(NC6H4Me-4)C1,(OMe)(PPh,),, 4,190 ReC,,H,,CINOP,

Re(NC6H4Me-4)HCI(OMe)(PPh,),,4,190 ReC44H43Nd'~

[ReH(NCMe)4(PPh3)2]2+,4. 152

ReG4Kd3

Cumulative Formula Index

ReC H P ReH,(PPh,)(dppe), 4, 192 ReC45H43C1NOP2

Re(NC,H,Me-4)HCl(OEt)(PPh3),, 4, 190 ReG6H4~N202P2 tRe02(~~)2(PPh3)21t, 4,186 ReC46H421N02P2 [ R e o (OEt)I(PPh,),( CNC6H,Me-4)]+, 4, 177 ReCd&CIzOJ'2 4 , 149 ReCl,(a~ac)~(PPh,)~. R~G~H~HN~O, Rc( CO),( tetraphcnylporphyrin), 2, 828 ReC47H45N3P2 [ReH(NCMe),(PPh,),(py)lZ' ,J. 174 ReC4,H4,Hr2N4P2 [ R ~ B I ~ ( N ~ P ~ ) , ( P P ~2, , ) ,133 ]+, ReCj8H&IN4P2 ReC1(N2Ph)2(PPh3)2,2, 132, 140 ReC48H,&12N30P2 ReC12(py)(q1-N2COPh)(PPh3)2. 2.132 ReC48H47BrJU" ReBr2(N2Ph)(N2HPh)(PPh3)2. 2.136. 146 ReCdLCIJV" ReCl,(NNHPh)(N,Ph)(PPh,),. 2.140. 141 ReClHH42C12NZP4 [ReCI,{ I!N(PPh2),},]+, 4, 148 RcCJSH~P~ [k(cNC6H&fC-4)6]" , 4 , 136 ReC48H43C12P4

ReCI2(PPh2)(PHPh2),, 4, 149 ReCj8H8,P4 [RetP(CsH11)2)41-. 4,149 ReCJ9H39C1202P2 ReC12(2-OC6H4COPh)(PPh3)2,4 154 ReC50H33N402 ReO(tetraphenylporphyrin)(OPh). 2. 828 ReCsOHJ3Cl2N4O2P2

ReCi,(NHNHCOPh)(NNHCOPh)(PPh,),, 2, 151 KeCSOH44C1ZN3PZ

ReC1,(4-MeC,H,NNNC,H4Me-4)(PPh,),.

4. I45

ReCSUH,,CI4P, RcCl,(dppm),, 4, 169 ReC5aHs4N&P2 ~

IRe(CNBut),(NCMe),(PPh,)J2+, 4, 135 ReC,,H,,C1,P4 .. [ReCI,(Ph2PCH=CHPPh2)2]+, 4, 148 ReCSZH42WM"

Re(?-MeC,H,NNNC6H,Me-4)(CO)z(PPh,)2, 2,204 ReCS2H,&1NP4S [Re(NS)Cl(dppe),]+, 4,204 ReC52H48C1N2P4 ReC1(N2)(dppe),, 4, 129. 132 [RcCl(N,)(dppe),]+, 4, 132, 136 ReCS2HJBCIP4 ReCl(dppc),, 4, 134 [ReCl(dppe),lz+,4, 148 ReC52H48C12NP4 [ReNC12(dppe)2]' , 4 . 189 ReC52Hd2P4 [ReCl,(dppe),]+, 1,498; 4, 118 ReC52H1802P4 [ R e O , ( d ~ p e ) ~ ] 4, + , 186 ReCS2H4&l2P4 ReHC12(dppe),, 4, 152 ReC52H49N2P4 ReH(N,)(dppe),, 4. 130 ReC32H4J'4 ReH(dppe)?, 4, 134 ReC5ZH50ClP4 ReCIH,(dppe),. 4, 134, 150 RcCFLH~ON~P~ [ R ~ H A N d d p p c ) ~, 4] '. 152 ReCszHs I P,

524

Reti,(dppc),. 4, 134. 151 ReC521152P4 [ReH,(dppe),]+. 4: 193 ReC52Hs3P1 ReH,(dppe),, 4> 192 ReCS3H&IOP4 ReCI(CO)(dppe),l 4* 134 ReC54H45C12NOP3 Re(NC))C12(PPh3)3,4,203 ReC54H45I309P3 Re13(P(OPh)3}3,4. 149 RcC&I~~NOP~ Re1 I,(NO)(PPh3)B.4+203 RcCS~KUIP, RcH41(PPh3)3:4: 193 ReC54H50P3 ReHs(PPh3),, 4,153. 192 ReCs4H5,CINOP4 ReCl(MeNCO)(dppe),, 4,145 ReCS4Hs,CINP4 ReC1(CNMe)(dppe)2, 4. 132 ReCS4Hs1N3P4 [Rr(N,)(NCMe)(dppe),] - , 4,132 R~CS,HSZCM'~ [ R C C I , ( P ~ X P ( C H ~ ) ~ P' ,P4~, ~148 )~] ReC55H45FNOZP., [Re(NO)F(C:O) (PPh, )J . 4, 203 R C C ~ ~ H ~ ~ P Z 1,153, 175 [RC(CNB~'),(PP~,)~]+, ReCs8H60C12P6 [ReCIz{(PhzPCH2CH2)2PCH2CH2P4. 162 (CH2CH2PPh2)2}]+. ReCS9Hs3C1OZP3 ReHCl(acac)(PPh,),. 2.376; 4, 150 ReCS9K4O2P3 ReH,(acac)(PPh,),. 2, 376; 4. 150 ReC6zH,,P, ReH,(PPhMdppe), 4: 150 ReCBZH5RP4 [RcH4(PPh,),(dppe)] ' - 4 , 193 RG6H58W4 [Kt.(CNPh),(dppe),]+, 4.132 ReC,,FI,,O,P, ReH3(PPh3), { P(OPh)3}2;4, 152 ReC72%309P4 ReH,(PPh,){P(OPh),},, 4, 152 ReC72H63P4 ReH3(PPh3),, 4. 151, 153 ReCnH684 Re2H8(PPh3),, 4. 175 ReCqoH,sC1015PS ReCI(P(OPh),},. 4. 135 ReCIF,N ReF,(NCI), , 4, iY7 RcCIO, Re0,CI. 4. 199. 200 ReCIS, ReS,Cl, 2,520 ReCI3NO Re(NO)Cl,, 4,203 ReCl3N2O2 Re(NO),CI,, 4,204 ReC1,03 [Re03C13]Z-.4.200 ReCI,N ReNCI,, 4, 197 [ReNCI,I-. 1.44; 4 191 ReC1,NU Re(NO)CI4, 4.203 ReC14N,0, [Rc(NO),CI,]-. 4- 204 ReCI40 ReOCI,, 6,855 +

Cumulative Formula Index

525

[ReOCI,]-, I, 44; 4, 183 ReCI4O2 [ReO2CI4] ,4,200 ReCI, {[ReCIsl-l,,, 4,173 ReCI,, 6,298 ReCI,NO Re(NO)CI,, 4,203 [RC(NO)C~,]~-, 4,202 ReC:I,NS [Re(NS)Cl,]-, 2, 120 ReCI5N2S2 [ReCI4(NS)( NSCI)J 2 - , 2, 120 ReCI50 [ReOCI,J-, 4. 195 [ReOClSl2-,4, 195 ReC1, [ReCI,]-, 4,192 [R&16]'-, 2,296; 4, 163, 16.1.172.173; 6,98 ReC16NzS2 [ReCI,(NSCl),]--, 4, 197 ReC1,NOPS Re(NSCI)CI4(POCl3),4. 193 ReClsOP ReCI,(OPCI,), 4, 192 RtCoHI5N,O4 [CO(OR~O,)(NH,),]~',4, 198. 826 ReCrC40H60C14N202P4 CrC1,(TI-IF)2((N2)ReC1(PMe2Ph)4}, 4. 133 RCCUC~,H~~P~ [ReH,(PPh,Me),Cu]+, 5,585 ReFO, Re03F,4,199 ReFO, [ReO,F]'-, 4,200 ReF303 [ReO,F,]'-, 4,200 ReF,O2 [ReO,F,]-, 4,200 RcFs RcF,, 2,680 ReF,NO [Re(NO)F,I2 ,4,202 ReF,O [ReOF,]-, 4,195 [ReOFS12-,4, 195 ReF6 [ReF,]-, 1,498; 4, 192,201 [ReF6IZ-,4, 172 ReF,N ReF,(NF), 4,197 ReF40' [ReOFJ, 4,200 KeF, [ReF,]-, 4, 105 RcF, [ReF,]-, 4,201 {ReF8]*-,4, 195 ReF,,O,Te, Re02(0TeF5)3,4, 198 ReFeC8HI7N2 Feke(Pr'NCHCHfl HPr'). 2 . 215 ReFecl2H5o6SZ (OC),Re(CS,)Fe(CO),Cp. 2. 5S3 ReFeCl,Hl,N,O ReFeH(CO),(Pr'N=CHCH=NPr'),2,215 ReFcPb,O, FcPb,ReO,, 1,11 I ReGdH,O,,> [Gd(OReO,),(OH,),]-. 2,418,124 ReHCI,O [ReC1,(OH)]Z-, 4,173 ReHF204 '

ReTiC36H52CISN20P4

[ReO3(0H)F2IZ-4,200 ReH2Br402 [ReOBr,(H20)] , 4 , 183 ReH2CI20, [ReO,Cl,(H,O)]~, 4,200 ReH,CI,N ReC1,(NH2), 4, 166 ReH,C1,02 ReOC1,(HZO), 4,195 [ReOCI,(H,O)]-, 4.183 ReH2C150 (ReCI,(H,O)J-, 4,173 ReH,CI,N ReC14(NH3).4,166 ReH,Cl,NO [ReOCl,(NH,)]-, 4, 177 ReH3NU, Re(NO)(OH)+ 4,203 ReH4F603 [Re02(OH)(HF2)31-,4,200 ReH6C13N20 ReOC13(NH3)2,4, 177 ReFIBCINjO [ReO(YlH,),CI]-, 4,194 RcH9 {ReH,I2-, 2,690,h91,696,702,703,705; 4,201 I

R ~ H ~ ~ c I ~ N ~ ReC13(NH2)2(NH,)Z, 4, 193 Re1,NO [Re(NO)ISl2-,4,202 Re I, 0 [Re0I5I2-,4.183 ReI, IReI,lZ-. 4.172

MOC~(CO)~(&NC~H,M~-~)~\~C~(CO),. 2, 136 ReMoCz6H34C14NzP,

ReNCI2(PMe2Ph),MoC1,(NCMe),4, 189 RelrfoC33€~4,C15NzOP, MoCl,(OMe){ (N,)KeCI(PMc,Ph),), 4,133 RGNO, [RcO3Nl2-.4, 196 RcN blW4Cj022 [Re(CO),(h'b,W,C),,)I3-, 1, 162; 3, 1047 ReNiCsOs Re(CO),Nr(CO),. 1, 123 ReOClj [ReOCl,]'-, 4,183 ReOS, [ R e o & - , 2.521 ReOzS2 [ R e o & - . 2,521 Reo$ [Reo&] ,2,521: 4,200 KeO,

[Reo,]-, 1,531 ; 2,296,413,696; 4, 196,197 [Re0,I27 4,196 Reo, [ReO,I3-, 4,198 Reo, [ReO6I5-, 2,296; 4, 198 ReO,,S, [R:O;(SO,),]-, 4,198 Res, [ReS,]-- 2.521,561; 4,200 RcSb2CJLCM'JzOz Re(NO)2Clz(SbPh3)Z, 4,204 ReSnC2,H,50,S2 (OC)4Re(CS2)SnPh3,2,583 ReSnC24H,,05S2 (OC)5Re(CS,)SnPh,, 2,583 ReTiC,,H,,CI,N,OP, {ReC1(&)(PPhMe2),}(TiC1,)(THF), 3,329; 4, i33

ReTi2C36H54C17NzOz

Cumulative Formula lndex

RCT~~C~~H~~CI~NZOZ

(ReCI(N2)(PPhMe2)4}(Ti2C160)(EtzO) 3.329 ReTiZC3bH54C17N202P4 TizOC16(EtzO){(N2)ReC1(PMe2Ph),}, 4,133 ReWi1040P [RePWi1040]4-,4, 192 RezAS4C72H68 RezH8(AsPh3)4,4, 174 Re2Br2C16 [Re2C1,Brz]2-, 4, 156 Re2Br4CI4 [Re2C14Br4]z~'~, 4, 156 Re,Br,Cl, [ R C ~ C I ~ B 4, ~ ~156 ]~-. Re28r6C1, [Re2C12Br6]2-,4,156 Re2Br8 [ReZBr8lZ-,1, 123; 4, 155 Re2Br, [Re,Brg]-, 4, 176 Re~C&C1604 [Re2(02CH)zC16]z~, 4, 159 ReZCZH6F2Oii 4, 188 [ReZO(C2o4)(oH)~Fz1'-, R%C,H3C1@b Re2(OZCH)3C13r 4, 160 R&&Br404 Re,(OAc),Br,, 4, 159 RC&&,C1,04 Re2(OAc)zC14,4,159,160 Re&H&14N403 Re203C14(en)2,4, 187 Re&HgC1306 Re2(OAc)3C13,4, 160 RezC6Hi809 R e o ( O M C ) ~p-O)( ( p-OMe) ,Reo( OMe) 2 350; 4, 196 1

Re2C8H208

Re2H2(C0)8,2,706 Rr,C,H,Br,O,S, Rc,Br,(CO),(S,Me,), 2,553 Re2C8HI2Br2OH Re,(OAc),Br,, 4, 160 Re2C8Hi2C1208

Re2(OA~)4C12, 4,129, 159 R~&IHI~CISS~

Re2C15{SCH2S(CHZ)2~H2)2. 4,142

I

Rez(CO)lo.2.237 Re2C12H30C16P2 Re2Cl6(PEt3)2.4. 157 R~~CIZH~~CIJP~ Re2C14(PMe3)+4. 136 Re2CI4Hl0I4O4 Rez(O2CPh)J4. 4. 159 Re2Ci4HI6Br2O8 { Re(CO),(Tt 1F)}(1.12-Rr)2, 2, 663 Rc2Ci5I-Il5N2OB {Rcz(CO),}(~H)(u-p~)(Me,"), 2,4Y7 Re,Ci32,CI,O, Re,(O,CBu'),CI;, 4, 159, 160 ReZC16H14C16N204 [(ReOC13)2(sa12en)]2, 4 , 184 KezC16Ht6C1aK204 [(ReOCl,)2(sa12enH2)]z-, 4, 184 Re2Ci6HzzC16Pz Re2C16(PMezPh)z.4, 157 R~~CI~H,OC~~O& Re20C16(SEt2)4,4, 170 RCzCisHioBrz06Se2 {Re(CO),}2(pz-PhSeSePh)(p-Br)z, 2,663 Re2ClsHioBr20GTe3 {Re(C0)3)z(1"-Rr)r(C-~h~Te2), 2,669 R~~CIJLW% {ReO,(NPr',)},(T~ED). 4, 199 RcZCl,H,,C14N, Rc,Cl,{PhC(NPh),). 2.276 Re2C20Hi6C12N40.1

Re2(f4=C(0)CH=CHCH=~H)4C12, 4,160 Re2C2~H20C~4N403 Re20,C14(py)l. 4. 178.187 Re2C20H28C1408 {Re(acac)zC12}2.2.377 Re2CzoH36C1208 Re2(OZCBu'),CI2. 4, 159 ReXzoH40N40& Rc,O,(S,CNEt,),. 4. 188 RCZCZ~HHNJO~S~ Re203(2-SC6H,UHz)4,4, 188 Ke2C24H60C14 Ke,Cl,(PEt,), 4 1% Re2Cz&oChP, Re2C14(PEt3)4.4. 138 Re2C28H20C1208

Re2(02CPh),C12, 4,153 Re2C28H&!& Re2CI4(PhN=CMeNPh), 2, 199,200,276,4, 157 RezC2sH3oNd'& [Re,(NCS)8(PEt2Ph)2]2-,4, 146 Re2C28H7?N40SS14,,

Re,O~NBut),(ObtMe,),, 4, 197 Ke2C30H20Br201.P2 Re,Br,(CO),(P,Ph,), 2,683 RC2C30H28N702S5

Re,O,S{ SZCN(CH2Ph),}, , 4 , 188 RezCmH900soP10 Rez{P(OMe),},o. 4,128 Re2C3zH44C14N20P4 ReOC13{{N2)ReC1(PMe2Ph)4}, 4, 134 Re2C32H44C14P4 Re2C14(PMe2Ph)4.4,138 [RezCI4(PMelPh),]' . 4 , 139, 157 [Re,CI,(PMe2Ph),]2+, 4, 139, 157 RC~CJZH~ON~OSB (Re(NPh)(S,CNEr,),},O, 2, 166 Re2C32HS2P4

Kc,H,(PMe,Ph),, 4, t93 Re2C331.127K06P2 Re,H(CO),(NCHMe)(dppm), 2, 128 R~zC~JH~OC~~NZPZ RezCl6(Ph2Pp))2.4. 157, 160

526

RC2CwHzz0iu

Rc2(PhCOCHCOPh)z(CO)6.2.375 Re2C36H30Ch.p~ RezC16(PPh3)z,4,136,138 RezC36H44C1zN8 Re2{(MeN)zCPh}4C12. 2.199,200; 4, 157 RezC37H5zC14P4 RezC1,(PEt3)2(dppm),4, 141 R~zC~~H~OCI~N~ Re2{(PhN)2CPh}2C14, 2, 199.200: 4 157 Re2C39H35C1503PL RezOC15(02CEt)(PPh3)2. 4. 176 RezC4,1€I,lP5 RezHJPMe2Ph),,4,153 Re2CinHk8P4 Re,H,(PEt,Ph),(p-H),: 2,702;4. 174 ReZC42H35NZOZS7 [Re2(NO)2(SPh)7)-,4.203 ~

Re2C17FN2 [Re2FN2Cl7I2-,4,194 Re2C16 [Re~Ck8]-,4,1% [RezCls]'-, 1,406; 2,199,276; 3, 1230;4,129, I138. 154.

172 RezC1803 [Re,03CI,]Z-. 4, 195 ReZCl9 [Re2Cl,j-, 4,176 [Re2Clr]2-,4, 138 RczC1,,, Rc2CI,,, 2,683 Re2Cl,o0 [Re20ClIol3" ,4. 171 [Ke20ClloJ4-.4.171 Re2QlOOlZ4 {Re03(0zPC1z)(POC13)}2, 4,199 Re2CoC5aH2JW6 Co(tetraphenylporphyrin){Re(CO)3}2, 2.844 Re2CuCI2H6Ol2 { Re(CO)4}2(OAc)zCu,5 , 652 Re2CuC,GH,20,2 Cu { Re (CO)4(MeC0)2}2 , 2,397 Re2CuC26H3,P2 [~ReH,(PMePh2))ZCu1+, 5,572 ReZC:u2C201 I2.,I2 ((RcHCp2Cu)(li-I))2 , 5 , 572 Re38 [Re2F8j2-.4,155 R G i1 [Re,F,,]-, 4 . 192 Re2Hz08 Re206(0H),. 4, 198 ReZHl6N8O2 {ReO(NH,),),. 4,194 Re2HfC,,H1,012 Hf{(OC),Re(MeCO),),, 3,402 Rc2Hg@,o Hg,Rc,O.,,, 5, 1050,10h9 Re218 [Re2I,l2-, 4 . 155 Re2L401,

La,Re,Olol 4.177 Re2Ln40 I Ln,Re,Oll, 4,192 RezMgC38Hi6Ns06 {Re(CO)3)zMg(phthalocyanine),2,868 Re2MgC5~H2&06 Mg(tetraphenylporphyrin){Re(CO)3},I 2.844 Re,MoC64H8,C16N4P, MoC14{(N2)ReCI(PMe,Ph)4}2,4, 133 Re&hCmHioBr,O lop* (MoCp(C0)2)zPZ{Ke(C:O),},Br,, 2, 1047 Re2M04Cj~H2UBr2C),IP4 { (MoCp~C0)z}2P2}2{Re(CO)3Br)2~ 2, 1047 Re20, Rt.Z07,4>197;6,351,356.806 Rez0.16S4 IRe2(S01)412-,4,158 RezSnC3sH,6N806 {Re(CO)3}zSn(phthalocyanine),2, 868 R~IS~C~OHZ~N~O~ Sn(tetraphenyIporphyrin){Re(CO),),, 2.844 Re,Te, Ke,Te,. 4, 1M

Re,TiC,,H,,CI,N,P, { R C C I ( N ~ ) ( P P ~ M ~ ~ ) ~3,} 329; ~ ( T4. ~ C133 ~~), Re22nC3sHjh N a 0 6 { Re(CO),I,Zn(phthalocyanine), 2. 868 Re2ZnC,aH,8N,0, Zn(tetraphenylporphyrin){ Re(CO),},, 2, 844 Re2ZrCl8H,&hz

Re,ZrC HH"0

Cumulative Formula Index

Zr{,(OC),Re(MeCO),},, 3,402 Re3AszC16H18Br30 Re3Br3(As04)Z(DMS0)3,4, 162 R~~AS~C~SH~~C~~PZ Re3C19{(PhzAsCH2CH2)2PPh)2. 4. 162 Re3Br6CI3 Re3C13Br6,4, 160 Re3% Re,Br,, I, 28; 4, 162 Rc3Br11 [Re3Brl112-~, 4, 163 Re, Hr ., [Re,Br.,2]3-, 4, I63 Re,C,CI,N, [Re3ClY(CN),J3 , 4 , 161 R~~C~HIZC~YS~ Re3C19(SCH,S(CH2),~H2),.5, 4, 163 R~~CEHZ~C~~OS~ Re3C19(Et2S)2(H20), 4, 163 Re3C9C13N9 [Re3C13(CN)9]3-,4, 161 Re3C9H3OI0 [Re30(H)3(CO)9]2-,2,303 R23CloI 13<),0

[ R C ~ H ~ ( C : O ) ~2, ~ ]692 ", RG&20iz [Re,H4CO),zI-, 2,700 ReJCl O., Re3H3(CO)12,2,703 Ke3Ct&t CbO 10 {Re,(02CPr')3CI,}Re04, 4, 160 Re3Cl2HZ4Cl9O3 Re3C19(THF)3,4, 162 Re3C12H24C190&3 Re3Cl9($CH2CH2OCH2cH2),.4. 163 Re3Cl2NIZSl2 [Re3(NCS)12]3-,4,161 RQCI~HI~CLN~ Re3C16(py)3,4, 142 Ke3Cl5Hl5CI9N3 Ke,C19(py)3. 4,161 Re,ClsI i21Cl&6 Re,Cl,(acac),, 4. 162 Re3C15H30C16N3S6 Re3CI6(SZCNEt,),, 4, 163 Re3C18H30C13N6S9 4,163 Re3C13(NCS)3(S2CNEt2)3, Re3CI9Hz3Cl3F9O6Si

Re3(CF3COCHCOMe)3C13(CH2SiMe3j, 2,378 Re3C31H3906 Re3Me6(acac)3,2, 378 ReX2dMWhSi3 Re,O,( p3-0)(p-0)(p-OSiMe, j (NB 4s Rc3C30H45C19P3 Re3C19(PEt2Ph)3.4, 162

OSihle,)z 1,

Re3C39H36C19P3

Re3C19(dppe)l.5,4, 162 Re3C41H39C19P3 Re3C19(triphos), 4, 162 Re3C44H34C1903P3 Re3CI9(1,2,5-triphenyl phosphole oxide),, 4, 162 Re3C54H45Br9P3 Re3Br9(PPh3)3,1, 143 Re3CeeH66C19P6 Re,C19{(Ph,PCH2CH,),PPh),14, 162 Re3C84H84C19P8

Re~C19{(PhZPCH2C€~Z)3~'}z, 4, 162 Rc~CI, [ R P ~ C ~ ~4,] 142 ~-, Re,Cl, 4,160, 172 Re3C19W309

~

[Re3C19(N03),j3-, 4, 163 Re3ClI [Re3C111]2-,4, 163 Re3Cl12 [Re3CIl2l3-, 1, 124. 133.4163 R%C~CZ~HIEOI, Cr{(OCMe),Re(CO),},, 3,861 Re,H,Br,Cl,O, [Re3C13Br7(H20)2]. 4 , 164 Ke3H1,CI,N6 4. 161 Re,CI,(hl L)3(NH3)3, ReJ9 Re&,, 4,161 Re4Brl,CI, [Re4C16Brl2I5 . 3 . 164 Re&,, [Re4Br14]2-.4.163 Re4C61806 Re,I,(CO),. 4. 155 Re4CI2H4Ol6 {Re(OH)(CO),),. 2.297.300 Re& .H,O [ R C ~ H ~ ( C O ) , , ]2,692 ~-, Re4C12N1,S4 [K~,(CL~-S)?(CN),,]",I , 154; 4, 165 Re4CI2Nl2Se4 [Rej(l,l~-Se)4(CN)11]4-.'. 1. 154; 4,165 Re4Cl,H,2012S4 {Rc(CO),(SMc)],, 1, 154: 2: 529 R~~CI~H~BOI~ 4, 159 {Re2(02CPr)4}(Re04j2, Re4ClEOY Re203C16(Re03C1),, 4, 195 Re4ClZ4N4O4P4 {ReNC13(POC13)),I4, 194 Ke4La6Ola La6Re4018,4. 177 Re4Ln6OI8 LnhRe401r,4,192 R c ~ C J ~ HI 2~ Z F ~ ~ ~ RcgMc.i,(hficac),. 2, 378 Re6ClzSe8 Ke6Se8Clz,1,163 Re6Szo [(Re6Ss)S6.2]4-.4,164 Re& [(Re6S8)S4,,(S,),,,~-. 4: 164 ResC33H44C18Ns { Re,Cl,(MeN=CPhNMe)),, 2,276 RhAsC9H1,CIdS RhC14(2-McSC,H,AsMe,)]-, 4,101 5 KhAsCT2H6.,P3 RhH(PPh3)3(AsPh3),4, 921 924 KhAszCzuH3ZClzNz [RhC1,(2-Me,NC,~~I,AsMe,),~+, 4, 1024 RhAs2C20H32C13N2 RhC1,(2-Me,NC,H,AsMe2),, 4, 1023 R~As~C,~H~,CI~N RhCl,(AsMe,Ph),(py), 4. 1031 RhAS2C26H,,CI,NO, RhC12(N03)(AsMePh2),, 4, 1022 RhAs2C33H3SC13N RhCl,(AsEtPh,),(pg). 4, 1031 R~As~C~~H~OC~~NO Rh(NO)C12(AsPh,),, 4, 1072 RhAs,C,,H,,I,NO Rh(NO)12(AsPh3)2.4, 1072 RhAs2C36H31CII KhHCI,(AsPh,),, 4. Il)'Ib: R~As~C,~H,,CI RhH,Cl(hsPh,),, 4,1018 RhASzC36H34C12Nz [RhCI2(AsMePh2),(bipy)]+, 4,1034

528

Cumulative Forrnulra hidex

529

R ~ A s ~ C ~ ~ H ~ ~ C I N ~ [RhHCl(AsMePh,)2(bipy)] . 4 , 1033 RhAS2C36H66C13 RhCI3(AS(C6H11)3}2,4.1022 RhASZC38H34ClzNZ [RhClz(AsMePhz),( phen)] .4,1034 R ~ A s ~ C ~ ~ H ~ ~ C I N ~ [RhHCl(AsMePh,),(phenj]+. 4.1033 RhASZC38H38ClzNz [RhCl,( A~EtPh2)2(b1py)]-,4. 1034 RhAjZC38H39CIN2 [RhHCl(AsEtPh,),(bipy)l-, 4. 1033 K~ASXC~~H~~N~O [Rh(NO)(MeCN)2(AsPh;)2] *-, 4,1072 RhAsZC4oH3&12Nz [RhCIZ(AsEtPhZ),(phen)]+. 4.1034 RhAs2C,oH42ClzNz [RhCl,(AsPh,Pr),(bipyj]+. 4. 1034 RhAszC4oH4qCIN2 [RhHa(ASPh,Pr),(bipy)]+. 4, 1033 RhASZC42H30N402 [kh{OOC(CN)z~(CN)2)(AsPh,),]t, 6,339 RhAS2C42H42ClzN2 IRhClz(AsPh2Prjz(phenj]+. 4.1034 Rh As,C,,H,,CIN, [RhHC$AsPh,Pr),(phcn))+, 4. 1033 RhAs2C42H46BrZNZ [KhBrz(AsBuPh2)Z(bipy)]’ ,1.1034 RhAS2c44ki++6BrzN~ [RhBr,(AsBuPh,),(phen)]-. 4, 1034 RhAs,GeC,9H40C1 RhHCl(GeMe,)(AsPh,),. 4, 1020 RhAszSiC36H31C14 RhHCI(SiCl,)(AsP h3),, 4. 1020 R~AS~S~C,,H,~C~~~ RhHCI{ Si(OEt),} ASP^,)^, 4, 1020 +

RhAS3C16H29

RhCl{PhAs(CHZCH2CH2AsMeZ)Z), 4,1041

KlrBr,

RhCI>(HgF)(AsMcPh,)3,4, 1076 RhA~3H&39H&13 RhCl,(HgCI)(AsMePh,),, 4, 1076 RhAS3HEC4iH42C1202 RhCl,(HgOAc)(AsMePh,),, 4, 1076 RhAsaC2oH;2ClNO, [RhCI(NO,)( diars),]+ , 4 , 1040 R~AS?C~OH;~CI~ [RhC12(diars)2]+, 4, 1039, 1040 RhAs,C,,H&,S [Rh(SU4)(diars)2]+,4, 1040 RIIAs~C~~H,,CI [KkHCl(diars),l+, 4,1037 Rhhs,C,., H,,CIO,S [RhC1(02SMc)(diars)2]”’,4, 1040 RhAs,C,,H,,CINO,S [RhC1(3-OzSC6H,N0,)(diars),], 4, 1040 RhAsiCz6H,7ClOzS [RhCl(O,SPh) (diars),]+ .4,1040 RhAslC,7H39ClOzS [RhC1(4-02SC6H,Me)(diars)2]+, 4, 1040 RhA~dkH440z {Rh(O2)(,AsMe2Ph),1+, 2,320; 6,329 RhASqCS2H44Sg [ K ~ ( P ~ ~ A S C H = C H A S P I ~ 2,533; ~ ) , ~ ~ 4. ’ , 1037 RhAs4CS2HJ5CI [KhtiCI(Ph~AsCH=CII A s P ~ ~ ) ~4,] 1037 +. RllASqCsZHqg [RhHz(Ph2AsCH=CHAsPh,)z]+, 4, 1037 RhAS~C53H~7C102S [R~CI(O,SM~)(P~,ASCH=CHA~P~~)~] -,4, 1030 R~As&~~H,~CIO~S [RhCl(O,SPh)( PhzAsCH=CHAsPhz)l]--. 4. 1040 RhAs,C,9HssC102S [RhCl[3-OzSC6H4Me)(Ph2AsCHzCH2AsPhz)zl+, 4, 1030 RhAS,C72H6,02 IRh(Oz)(AsPh,),]+, 6,337 RhAs&34H16 ,),]~+ [Rh ( M E A ~ ( C ~ H ~ A S M ~ ~ -4,~ )1U44 RhAuClsHl5FlZPj Kh(PF,),,4uPPh3, 4, 904 RhRC9H,,CI,N6 [Rh{HB(~N=CHCH=cH),}CIzH] ~,4,I012 ~

Rh(0,)Cl~PhAs(CHZCH,CH2AsMe2)2}, 4,1042 RhAs,C16H,,C10,S

RhC1(SO,){PhAs(CH,CHzCH,AsMe,)z},2,635 RhAs3C,,H,,Br3

R~B~,{M~AS(C,H,ASM~~-~)~}, 4.1043 RhA~3CI7H23Cl3

RhC13{MeAs(C6H,AsMez-2)z}, 4, 1043 R~AS~CI~HZ~N~OY

Rh(N0,)3{MeAs(C6H,AsMe2-2)2}. 4, 1043 RhAs3CiJ%Kl, RhCI,(AsEt,),, 4,1031 R~As~CZ~H~~CI~ RhCI,(AsMe,Ph),. 4. 1031 R~As~C~,,H.,~B~~ RhBr3{AsMe,( C:H,=CMPh))3, 4, 1031 RhAS3C36H63Cl~ RhCl,(AsBu3)3,4, 1031 RhAs3C39H39Br, RhBr,(AsMePh,),, 4. 1027 RhA~jC39H39Cl3 RhCl,(AsMePh,),, 4.1031 RhAs3C39H40Br RhHBr(AsMePh,),. 4,1027 RhAstC3yH4oClz RhHCI,(AsMePh,),, 4, 1026 RhAs,C,,H, iC1, RhCl,(AsPh,Pr),, 4. 1031 RhAs,C,,H,,CI, RhHCI,(AsPh,Pr), ,4,1026 RhAS3C72H61P RhH(AsPh3)3(PPh3). 4.921 RhA~3HgC39H39ClzF

RhBC,oH;4C12N60 Rh{HB(Ih’=CHCH=cH)3}Clz(MeOH). 4.1013. RhBCuHisN6 Rh{HB(hN=CHCH=cH),) (HZCrCHZ)Z, 2,252

.

-,

RhBC 16HliNB

Rh{B($JN=CHCH=cH),}(H2C=-CH,)I.2.252 RhBClsH, N Rh{B(N=H),)(nbd), RhBCzoH24Ns

2,252

Rh{B(gN=CHCH=cH),}(cod), 2.252 RhBC22H24Ns02 Rh (B(flN=CHCH=cH),}

(duroquinone), 2,252

Cumulative Formula Index RhCC12N205 [RhCI,(CO)(NO),]-, 6,277 RhCHiZCIN, IRh(NH,),(CN)CI]’, 4,986 RhCH12N503S Rh(SO,)(CN)(NH,),, 2,638 RhCHI,N50 [Rh(NH,),(OH)(CN)]+, 4,961 RhCH,,NSO [Rh(XH3),(CN)(H20)]z’,4,964. 986 RhCHI5F3N5O3S [Rll(NII~),(OS(12C‘F,)~Z+, 4 , 956. 961 RhCH, j N 5 0 3 [ R ~ ( N H ~ ) S ( C O ~4,960 )I+, RhCHl,N6 {Rh(NH3),(CN)]Z*,4,986 RhCHiSN60 [Rh(NCO)(NH,),]*+, 1, 186,4,956.962 RhCH15N6S [Rh(NH,),(NCS)I2+, 1,504 RhCH16NjOz [Rh(NH3),(O,CH)I2+,4, 960 RhCH,c.N, [Rh(NH”3)s(HCN)]3++, 4,960 RhCH,,N,O IRh(NH3)5(H2NCONH2)]3 ’ , 1, 186. 430: 4,957,960, 96 1 [Rh(CO),Cl,] , 2 , 114; 6,277 RhC7H7CI,N [RhCI5(MeCN)J2-,4, 1005 RhC2H,CI,N2 Rh(en)CI,, 6,492 RhC2Hl,C13N,O, [Rh(NH3)5(02CCC1,)]2f,4,960 R ~ C ~ H M F ~ N ~ ~ [Rh(NH3)5(02CCF3)]*+, 4,957,959.960 RhCZH15N504 [Kh(NH3)5(C204)]+,4, 956 RhU2tII6F2N5O2 IRh( NH,),(O,CCHF,)]”, 4.960 RhCzH,,FN,O, [Rh(NH,),(O,CCH,F)]”. 4.960 RhC,H,,N,O, [Rh(NH3),(0Ac)lZC, 4,957,959.960 RhCzHxJ’J, [Rh(NH,),(NCMe)l3’, 6. 449,450 RhCZHZoN6 I R h ( N H 3 ) 5 ( H N w H z ) ] 3 -4,961 . RhC2HZoN60 [ R ~ ( N H ~ ) ~ ( I I ~ N A4,964 c)]~+, RhC21202 [RhI,(CO),]-, 6,272,275 RhC3HloC14N2 IRh(pn)CI,] 4,981 RhCaH I ~ N & Rh(H2NC(S)NHNH},, 2,803 RhGHi9N7 [Kh(?lH3)5(imidazole)]3T,4,964 RhC3HzzN6O [Rh(NH3),(DMF)I3+,6,433 RhCJCI2Os [Rh(C204)2C12I3-,4, 1049 RhC4HN402 [Rh(CN),(O0H)l3-, 6,330 RhCjH3N403 IRh(OOH)(CN)4(H20)]’-, 4, 1052 RhC,€I,O Io [Rh(C@4),(HB),] ,4. 1049 KhC4H6C14N2 [RhCI,(MeCN),]-, 4, 1005 RhC,H,Br,N,O RhBr3(MeCN),(H2O), 4. 1005

-.

5 30

KhC,H,,CI,S, Rh(MeSCH,CH,SMe)CI,, 4, 1055 RhC4HloC14S2 [Rh(MeSCH2CH2SMe)Cl4]-,4, 1056 RhC4Hl2CI4Y2 [Rh(H2NCHhleCHMeNH,)C14]-, 4, 981 RhC,Hi,CI4O,S, [Rh(Dh.ISO)zC14]-l2.641; 4, 1053 RhC4H 14C1303S2 RhCI,(DMSO),(H,O). 2,490 RhC,H,,BrCIK, [Kh(en),CIBr].”.4. 968 RhC,H,,BrIN, [Rh(cn),BrI]’, 4,968 RhC4H16Br,K, [Rh(en),Br,l-, 4, 988 RhC4H16CIIN4 [Rh(en)2ClI]+.4,968 RhC,HI,CIN,O, [Rh(en)2(NOz)Cl]+.4.969 RhC4H16CINT [Rh(en),C1(N3)]+.4,968 RhC4HI6Cl2H, [RhCl,(en)J, I , 400 RhC,H IhCIZN3 Rh(en),Cl,: 4.967 [Rh(en),CI,]’, I , 299- 483,505; 4,966,968,972-974, 981,982, 9r)8?1004. 1(:)05;6,492 RhC4HI6I2N4 [Rh(en),I,] ’ , 1.799 RhC4HiJW4 [Rh(en),(NO,)(Oz)]+. 4.1052 R~C~HI~N~OJ [Rh(en),(NO,)J+, 4.969,970, 1052 RhC4Hi6N1o [Rh(en)dN3),1+,4,969 RhC4H,,CIN4 [ R h ( ~ n ) ~ H C l4.969 l+, KhC4H17CIN40 [Kh(en),(Cl)(C)H)]+,4,968,974 RhC:4HI:IN40 [Rh(e1i)~(OH)1]+, 1. 299 RhC4Hl,C1N,0 [Rh(e.n),Cl(H,O)]+, 4,968 [Rh(en),C1(H,O)jz+, 4,968.972,973,978 RhC4HI8N4 [Rh(en),H,!’. 4.966.969 RhC4HlRN40 [RhH(en)2(OH)]+,4,969, 1004 RhGHisN40z [Rh(en),(OI-t),]+. 4.969,971,978,979, 1004 RhC4F 118 N40, [Rh(cll)z(OH)(OOH)1’, 4,1004 RhC4H19CIYs [Rh(en)Z(NH,)C1]Z-,4,969,971,972 RhC4H,,N40 [RhH(en),(H,0)]2 ’ ,4, 1004 KhC&i&”02 [Kh(en),(OH)(II,O)]’+. 4,969, Y71,974,979 RhC4HI0N4O2 [Rh(en)z(H20)2]3+. 4.967,969,971,973,974,979.988 RhC4H2,NsO [R~(~II),(KH,)(OH,)]~+, 4,969 RhC4H22N6 [Rh(en)2(NH3)z]3-.4.969,971,974 RhC4012 [Rh(CO;),J4-, 4.938 RhC5CIN, [Rh(CK),CI]’-. 4.952 RhCsHNs [Rh(CN),H]””. 4.952 RhC,HN,O [Rh(CN),(0H)j3-, 4, 952

531 RhCsH2N50 [Rh(CN)s(HzO)]Z-,4,952 RhCSH,F,OzPz Rh(acac)(PF3)z,4.910 RhC5H16CIN403 Rh(en),CI(C03), 4,969.978 RhC5Hi6CIN5S [Rh(en),(NCS)CI]+, 1.299;4.969 RhC.5H16N403

[Rh(en),(CO,)I+, 4,977 RhC5H16N406 IRh(en)z(OCC)z)21 4,969 RhC,Hi7ClN,O, Rh(en),CI(C03H), 4,979 - I

RhCSH17N404

Rh(en),(CO,)(OH), 4,969 [Rh(en)z(C03)(0H)]+.4,979 RhC,H,,N,O, [ R h ( ~ ~ ) z ~ C 0 3 ) ( H 2 4,969.978 0)]-. RhCsHi9N404 [Rh(en),(CO3H)(H20)]-, 4,978 RhCJLoN, [Rh(fiH&(py)13+. 4,985 RhGHz4NsOz [Rh(NH3)5(02CBu1)]2-,4.957 KhCSHZSCIN5 965 [Kh(NH,Me)5C1J2' ,4,961, RhC5Hz7N,O [Rh(NHZMe),(HZ0)J3', 4,964 RhC5N5S5 [Rh(SCN),IZ-, 4,1054 RhC6HgClN4O [Rh(NO)CI(MeCN),] -,4,1072 RhC6H9CI3N3 RhCl;(MeCN)?, 4,1005

2,32;4,902,965,966.970-972, [Rh(en),13+,1,417; 981,985,994,995,998 RhC6N6 [Rh(CN),I3-, 4.952 RhC6N6S6 [Rh(SCN)613-.4,1055,1056 RhC6N,See [Rh(SeCN),l3-, 4.1055,1056 RhCbOII [Rh(C204)3]3-,4,964,977, 1049,1050 RhC7H3N6 [Rh(CPT),(MeCN)]2-,4,952 RhC?H,NClOz RhCI(CO),(Py), 6,276 RhC,H,O, Rh(acac)(CO),. 6,275 RhC7H902S RhCp(S02)(qZ-CH2=CHz), 2, 191 RhC7HihO4P RhH(PMe,)(OAc),, 4,948 RhC7Hz&IzN4

[Rh(H2NCH2CHzNHzCH2)~CH2}(31~]+, 4,990.991 Rh(Gly-0),, 4,1044 RhC6HI,CI,N, Rh(HNCH,CH,)3CI,, 4.964 RhC,H &I3N3S3 RhCI,{MeC(S)NH,),, 2,647 RhC6Hi6N404 [Rh(en)2(C204)]f,4,967,970.976 RhC6Hi6N406 IRh(enMC03)21-,4,978 RCC~H~~CIN, [Rh(en)2(en-H)C1]3t,4.969 RhCbHlsCIZN4

[Rh((HZNCHzCHZNHCH,),}CIz]' I , 299;4,989, 1003, 100s [Rh((H2NCH2CH2),N)CIz]-,4.990-991 RhChH1RCI3O;S; RhCI,(DMSO),, 2,490.641 4. 1053 RhC6H,sCI,S, RhC13(SMe2)3,4,1054 RhC6His06P3Sb Rh(S,P(OMe)2\;, 4,1040 RhC6hi9dlN4 [Rh{(HzNCHzCHzNHCH2)2)HCl]+,4,990 RhCAHmCINaO [Rh{(HzNCH2CH2)3N}Cl(H20)]2+, 4,992 RhC6H20CIZN2 [Rh{HzN(CHz)3NHz),CI,1-. 1,299 KhC6H20ClZN4 4,981 [Rh(pn)ZC121+, [Rh{I1,N(CH2)3NH,},TI~lt. 4.979,YX5.988 RhC6HmN502 [Rh(en)Z(O-Gly)12' , 4 . 970.'171 RhC,HzoN, [Rh(en - 2H)(en H)J. 4.966 RhC6HziClN40 ~

RhC7HZoN6 [Rh(NH,),(NCPh)]3+,4,960,962 KhC,I l z z N 6 0 [Rh(NH3)5(H2NCOPh)J3+, 4,964 RhCsH6CIN4S4 Rh(hC(S)CH=CHNHCS},CI, 4,1048 RhCsH6N402

[Rh(Co)2(H&'CH=CHN=cc=NCH=CHhH)]+ 90

2.

RhGHic"08 [Rh{HN(CHZCOZ)Z} z]-, 4,1046 RhC& z C I ~ N ~ O ~ [Rh(DMG)zCI,]-, 4.995 RhCsHiPb Kh(N,)(c~d),2,237 RhCsHi2N4 [Rh(CNMe)4]+,6. 151 RhCaHiINsO [Rh(NO)(MeCN),]*+. 4,1072 RhC8HiZNjOz [Rh(MeCN)4(N0z)]Z+, 6,374 RhCsHi4CIZN204

[Rh(DzCCH2CHzNHCH2CHzNHCHzCH2CO2)ClJ, 4,1047 RhCsH,jCIZN,04 [Rh(HDMG)zCIJ, 4,1014 RhCsHi I C I ~ S ~ [Rh(S2CPr)zClzj-,4,1054 RhC8HiiClZNjO4 Rh(H,DMCi)(HDMG)Cl,. 4,1014 RhCsH16ClN~06 [Rh(HzDMG)2(NOz)CI]-. I, 505 KhCsnibNJ2 [RhI,(aziridine),]+, 2, 28 RhCSH,,ClNsO,

Cumulative Formula index

RhC8Hl7CIN504

Rh(HDMG),(HN,)Cl, 4,1014 RhC~HisF308Pz Rh(02CCF3){P(OMe),}2,4,908 RhC8H,oClZN4 [Rh(HNWH,)4Cl2]+, 4,964 RhCaHZoCI& [Rh(MeSCH2CH2SMe)2C12]+, 4.1055 RhCsHmNaOa IRlh{H,N(CH2)3NH2}2(C2~4)~+, 4.979 RdC8HZOS4 [Rh(MeSCH,CH,SMe),]+, 4, 1056 RhCsEIz4ClFxN4Pa RhC1(PF2NMez)4,4,924 RhCsHa4CIzN4 [Rh(H1NCHMeCHMeNH2)&l2]', 4,981 RhCsHJ8N4P4 [Rh(PF2NMeJ4]-, 4,905 RhCsHz4N6 [Rh(dien - H),]+, 4,966 RhCsHd'4Sz RhS2(PMe2)4,4,1038 RhC&J'J, [Rh(die~~)~ 4,966 ]~+, RhC8H28N6

[Rh(en)(en-Me),13' ,4,970 RhCaHdx03

I{Kh(en),(t120)}2(~-oH)IIC. 4.970 RhC9Hi5O2 Rh(acac)(CH,=CH,),, 2,376.394; 6.300 RhGHi& [Rh(SzCEl),, 4, 1054,1056 RhC9H16PTe RhCp(PMe3)(q2-TeCH2).2.671 RhC9H17C13NS2 Rh(py)(SMez)zC13,4,1054 RhC9Hi7Nz03 Rh(DMG),(Me)(H,O), 1, 299 RhC,kI,,CINiO,S Rh(HDMG)2C1(H2NCSNH2),4, 1014 RhCqHi RNqO, Rh(O~CCH(NH,jMe),,4, 1044 RhC,HlsN,S6 Rh(S2CNMe2),,4, 1054, 1063 RhC9HlsN4OSh [Rh(NO)(S2CNMe2)3]+,4,1072 RhC9Hi9N40s Rh(HDMG),(H,O)(Me), 4,1014 RhC9H21CINS [Rh(en)2Cl(~y)12+, 4,974 RhCgH27CIP3 RhCl(PMe,),, 1, 166; 4,917>918 RhC9H,,CI,O9P3 RhCIj{P(CHzOH)3}3,4, I028 RhC9€127CI,P3 RhC13(PMe3)3,4, 102s RhCrHnP3 [Rh(PMeJ,l+, 4,921 RhCgH2xC12Pz RhHCl,(PMe& 4. 1027 RhGH3oNcj [Rh(en-Me),13+,4,970 [Rh(pn),13+,4,980 [ R ~ { H Z N ( C H Z ) ~ N H 4.980 ~}~]~+, RhCgH43C12PZ RhHC12(PBu',Mc), . 4 , 1018 RhCioHzF12C104 Rh(hfacac)2CI,2,376 RhCloHsCIF1207 RhCl(hfa~~)2(H20)3.4, IO5 1 RhCioHsF604 Rh(CF3COCHCOMe),. 2,384 RhCit,H1XlJ'Jz Rh(p~)&13,4,995 '

~

'

532

KhCioHIzNzO, [Rh{OzCCHzCH(COZ)NHCHZCIIzNHCI I(CO2)CH,C02}]-, 4,1045 RhCioH1,Nz09 [Rh{02CCHZCH(COz)NHCH2CH2NHCH(CO2)CH,CO2}(OH)I2-, 4, 1045 RhCloHi4C12NZOs [Rh(H,edta)ClJ, 4.1004. 1044 RhCioHi4NzOa [Rh{MeN(CHzCO:),),]-, 4,1046 RhCLOH14N209 [Rh{02CCHpCH(CU?)NHCH2CH2NHCH(COz)Ct+~CO~)(ItzO)l-, 4, 1045 [Rh{~02CCHI)IEICH2CH2N(CH,Co,),)(lI&))]-, 4,

Io41 RhC10H14PS4

Rh(C,S,)(PMe,)Cp, 2,582

Rh(qS~C,Me5)(N,),.2,237 RhCioHisN306 Rh(OzCCH2CH2NHCH2CH2NHCH2CH,Co,) (Gly-0),4.1046 RhC1,,H1,N,O4S Rh(DMG),(Me) { S(NH& j , 1,299 RhC1UH20C12S4 [Rh( I 14.8,'~1-tetrathi~cyclotetrsdccane)CI,)' , 4 , 1056 RhCloI~I,lClzK402

RhCl,(ON=CMeCMe2NH)(HON=CMeCMe2N~T), 4, 1013 RhCloHZ2N4O4 [Rh(O2CCH2CH2NHCH2CH2NHCH2CH2CO2)(en)lf 4, 1047 RhCioH24C12N4 [Rh(l,4,7,10-tetraazacyclotetradecane)C12]~~ 4.993 [Rh( 1.4,8,1l-tetraazacyclotetradecane)C12]+.1.400; 4. 991 992 RhCioHuN,Oa [Rh(l.4,8,1l - t c t r a n z a c y c l o t c t r a d c c ~ ~ e ) ( N ~4,993 ~)~]'~. R K o H J ' JI o [Rh(l,4,fi11l-letraazacvclotelradec~n~)(N,)Z1+, 4,993 RhCloH,,TIN,O [Rh(1.4,8.1l-tetraazacyclotetradecanej(Cl)(OH)I+.4, 993 RhCloH25ClNj [ R h ( H N m H 2 ) s C l ] 2 +4,964 , RhC10H25N70 [ Rh( 1,4,8.ll-tetraazacyclotetradecane)(N3)(OH)]~,4, 993 RhC ,,,H2,CIN40 [Rh(l,4,8,1l-tctraazacyclotctradecane)CI(H20)]' .4. 993 RhCloHzbh',O [Rh(l ,4,8,1l-tetraazacy~lotetradecane)(N~)(~~O)~ ' ,4. 993 RhCloH27NaO2 [Rh(l,4,8.1 I-retra~a~yclotetradecane)(OH)(H~O)]~ ', 4.993 RhCioH3oC105S5 IRh(DMSO)iCI\+,2,641 RhC,,H,,Cl,N~Se; Rh(SeCNCH2CH2biCSe)CI3(4-H2NC6H4hfe), 4,1057 RhCiiHi,NzOn [Rh{0,CCH~)2N(CH,),N(CH,C0,),)I-, 4,1045 RhCiiHi6Nz0g 4, [Rh{O?CCH~),NCHMCCH~N(CH~CO~)~}(HZO)]~, ~

1045

RhCl j i l z o h 3 0 6

R~(O~CCH~CH~NHCHZCH~NHCH~CH~CO~){O,CCH(NH,)Me}, 4, 1046 RhC1,HZ3CIN404P Rh(HDMG)ZCl(PMc,), 4, 1014

533

Cumulative Formda Index

RhC16H2sCI

RhCl3H19OZ WacacHcod), 2,394,396; 6,266 RhC1;HI9O4 Rh(CO),(Bu'COCHCOBu'), 2, 394 RhC,,H,,ClN,O RhCI(C0) (CH,=CH,)(Bu'N=CHCH=NBu'). 2 2 10 RhCI,Hz,CI,N402 RhC12{ON=CMeCMezN(CHz)3NCMe,CMe==NOH}, 4,1013 RhCi3HnFaN@zPz Rh(acac)(PF,(NEt,)},, 4,908 RhC14H6N20S

RhC1iH24C1LO$3 RhCI,($CH,CH,OCH,~H,),, 4,1054, 1055 RhC,,HiaNh ._ _ . [Rh(1,4,X, I I-teiraazacyclotetradecane)(CN),1', 4,993

R ~ c ~ ~ H ~ ~ N ~ s ~ Rh(1,4,8,1 l-tetraazacydotctradeca~ie)(NCS)~]+, 4,993 RhC,,H,4& Rh((MeS),C,H,},, 2,610 R~CIZHZJJIZ Rh(l,l,7,7-Et4dien)(N,),,2,232:4.991 RhC12H30CIzNOPZ Rh(NO)Cl2(PEt,),, 4,1070 RhC12H3oC13S3 RhC13(SEtz)3,2.552;4,1054;6.245 RhC12H3oN8 [Rh(sepulchrat~)]~+. 4.991 [Rh(sepulchratc)]V . 4.994 RhC'izI13006P3s6 Rh{S2P(C)Et),}?,4.1054 RhC1ZH31Pz RhH(PEt4)l. 4,920 RhCl2H1,Br2P4 [RhBr2(Me2PCHiCH2PMe2)z]+, 4,1035 RhC12H32C12P4 [RhC12(Me2PCH2CHzPMez)2~-, 4,1035, 1039 RhCi2H32P4S2 [RhSz(MezPCH2CH2PMe2)2]+, 2,533,4, 1037,1039 RhC12H32P4SeZ IRhSez(Me2PCH2CH,PMe2)z~+. 4,1037 RI~C~~H~~CIP~ [RhHCI(Me2PCHzCH2PMe2)2]+. 4,1036, 1037 RhC,,HwP, +,4,1036,1037 [RhH2(MeZPCH2CH2PMeJ2] RhC1ZH36Br20d4 [RhBr,{P(OMc),),]+. 4.1U34 RhC12H34N6

[Rh(l-12NCHMeCHMeNH,)3]3-, 4,981 [Rh(MeNHCHzCHzNHMe)3]3-, 1,417

RhCizH360& [Rh(DMS0)6]3+, 4,1053 RhC12H36P4 [Rh(PMe,),]+,4,920,921,926, 1041 RhCI2H3,BrOl2P4 [RhHBr{P(OMe),],l+. 4,1033 RhC12H37P4

RhH(PMe3)4,4,924 R~C~ZH~XOIZP~ [RhHz{P(C)Me)3)41' 4.1032 R ~ c ~ ~ N ~ S ~ 4, 1063 [Rh{SzC==C(CN)2},]2-, RhC12N6Se6 [Rh{Se2C2(CN),}J3-, 4,1057 COC 7-R

~~~~~,~-PY(CO,)Z},~-, 4,1047 RhC,,H,oC1,N2 [RhCl,(PhCN),]-, 4,1005 RhC14H14F304 Rh(C0)2(3-trifluoroacetylcamphorate),1,561 RhC14H16Cl RhCl(nbd),, 6,277 RhC14HisN2S2 Rh(cod){(MeS),C,(CN),}, 2,604 RhC14H29CIP3 RhC1(PMe3),(PMe2Ph), 4,920 RhCisHJ,NO, 4,1050,1051 Rh(hfacac),, I , 351;2,376; [Rh(hEacac),l , 1, 351 RhC15H12F906

Rh(CF3COCWCOMe)3, 4,1050,1051,1052 RhCliH&lIN3 Rh(py)qCIq, 4,995,1003; 6,274 RhG~HisN3012 Rh{MeCOC(NOz)COMe},, 4,1050 R~CI,HI&~~O~ Rh(acac)(MeCOCClCOMe),, .~ 6,205 RhCI;HZ1N6O3S3 [Rh(&=C(OH)CH=CMeNcS}3]3+q 4,1048 RhCidl2106 Rh(acac),, 1,421;4,1050,1051; 6,205,273,277 RhCd21Sb Rh(MeCSCHCSMe),,4,1056 RhC,,H,,ClO, Rh(C,Me,)Cl(acac), 2,393 Rh'&H3oN30&3 Rh{02CCH(NHz)CHzCH2SMe}3, 4,1044 RhCisH3oN& Rh{S2CNEt,),, 4,1054 RhCliH45015P~ [R~I{P(OM~)~},]+, 4,929,930, 1033 RhCi814N2Oz Rh(salcn). 4,943 R~G~HI~NZOJ Rh(salen)O,, 4,943 RhC16H 17N60

[Rh(NO)(MeCN),(bipy)]2', 4,1072 RhCiaH20C1306 Rh(MeCOCClCOMe),{MeCOC(CH,Cl)COMe),6, 205

RhCi6Hzr07 Rh(acac),(MeCOC(CHO)COMe},6,205 R~C~~H~ZCI~NO~P~ RhClz(N03)(PMe,Ph),,4,1022 RhC16HzzC13N2S Rh(blp~.)(SPrz)CI3,41 ,054 R~CI~HZZCI~PZ [RhCl4(PMeZPh),]-, 4,1016 RhC,,H,,CI RhCl(codL 6.252 RhC1SH2i24Ci2k8 IRh(Me~CCtI=NCH=CH),CI,l+, 4.996 '

RhC16H40CIF&J"

Cumidntive Formula Index

RhC18H38CI,NzPz RhC13(PEt3)z(PhNHNH2),4, 1029 RhC18H42ClNzP2 RhC1(NZ)(PPr'Jz, 4,920 RhCiJLzCIOzP, RhCI(Oz)(PPr',),, 2, 320 RhC18H4zC102P3 RhCI(O,)(PPr',),, 2,319 RK&zCId'z RhCI,(PBu',Me),, 4,932 RhClsM4zCI7St RhCI,(SPr,),, 4, 1054 RhC18H43CIP2 RhH,CI(PBu',Me),, 4, 1018 RhCiaHdWZ RhHClz(PBu'2Me)2, 4,932 R~~CTJLNZPZ RhH(N2)(PPr'3)2,4,920

RhCI3(PEt3),, 4, 1028 RhC, 8H~sN603 [Rh,( 1,4,7-Mc3-l,4,7-triazacyclononane),(y-OH),l"i, 4,993 RhC,sH4,CIN,Pz RhCI(N2)(PPr',),, 4,919 RhC,8H4,CI02PzS RhCI(S02)(PPri3)z,4,920 RhCiaHaO$'z tRhHz(PPr13)2(Hz0)21+1 4, 1033 [RhH2(PPr'3)2(Hz0)Z]2+, 6,496 RhCwHisS, RhCp(SzCzPhz), 2,611 RhCi9H2&1zOPzSz RhC12(SzCOEt)(PMe2Ph)2,4, 1022 RhC19H28C12NPZS2 RhCIz(SzCNMeZ)(PMe2Ph)z, 4, 1022 R~CI~H~~IPZ [Rh(nbd)(PEt,),]+, 6,241 RhCiJLOzPz Rh(OH)(CO)(PPr',),, 6,275 R~CI~HASOJ'~ RhH2(PPr'3)Z(qZ-02COH). 6.242.262, 275 RhC,,H,5CIOzP RhGl[CO),(PPhX), 6,261

534

[Rh(py),BrzlBr.FfBr2H,0. 4,996. RGOHZ,OJ'~S~ Rh(S2CO)(S2C0Et)(PMe,Ph),,4, 1022 RhCmHz,O, Rh(C,Mc,)(acac),, 2,393 R ~ C ~ O H ~ ~ N ~ O [Rh(NO)(Bu'CN),]2', 4, 1072 RhCZOH4tCWZ Kht~CI,(PRu'Prz),,4,1018 RhC21H15C13N3 RhCI3(PhCN),> 4. 1005 RhCziHi& Rh(SzCPh)3. 2.646 RhC,IHi9CLN302 Rh(sa1en)pyCl. 4,1047 RhCziHi9N302 Rh(salen)py. 4.943. 1047 RhC21H361\;9S, R h {lizNC(S)NN=m I.Iz)s}>, 4, 1048 RhC,;H,,N$S, ' I R h { H z N C ( S ) N H ~ = ~ H 2 ) ~ } 3 l 4,1048 3+. RhC,, HAnP7 [RF;(nb~)(Pri2PCH2CH2PPr'2)l',6,241 RhC2iH&IPz RhHCl(C(CH2CKzPBu'2)2}, 2,698 RhC,iH,,ClOP2 RhCI(CO)(PBu',Et),, 2, 1039 RhCzlH4,CIP2 RhHCl(CH(CH,CH,PBu',)2},2,698 RhCzzHzzN30Z RhMe(salen)py, 4. 1047 [RhMe(aalen)pyj+.4. I002 KhC:22H,,Si2 RhH(C5Me5)(S~Et,)2,2. 19 RhC,,H,,Si, RhH,(C~SIe5)(SiEt?)?,2, 16 RhCz2HSOCl2NP2 RhHCl2(PButPrz),(MeCN), 4, 1027 RhCZ3HZ0PS5 RhCp(PPh3)(Sj). 2.545 RhC23H47C13NP2 RhCl,(Pf~-,)~(py).4. 1029

~ hSCH=CHCH=~C(S)=CHCOCF,}, { RhC,,H,,CI,N, [Rh(phcn)?Ciz]', 4,997,998 RhCwHi6N4 [Rh(phen),I+. 4.982 KhCz,H,oClZN404 [ R ~ ( ~ - P Y C H O ) ~ C4,996 I~]+. RhCz4H2iS6 Rh(S2CCH2Ph)3, 2.646 RhC,,H,,CI2N4 [Rh(3,3'-Mezbipy),CI2]+, 4,999 RhCZ4H3,,Cl3S3 RhC13(PhSEt)B,4, 1054 RhCZ4H,iNz025

, 2, 652

Rh(C0)z{2.4.6-AMe3C,H2)NS(Bu')N(2,4,6-Me,C6H2). 2, 194 RhC2,H,,BrCI,P3 RhCI,Br(PMe2Yh)3, 4, 1029 RhC24H&IP, RhCl(PMe,),(PPh,). 4,920

535

Cumulative Formula Lndex

RhC1z(N3)(PMezPh)3, 4, 1029 R~CZ~H~~CM'~ RhCI,(PMe2Ph),, 4, 1028.1030. 1034 RhC24H33N9Pi Rh(N3)3(PMe2Ph)3,4, 1029 RhC24HwCIP3 RhHC1z(PMe2Ph)3,4,1026 R~CZ~H&~,OP~ [RhC12(PMe2Ph)3(0Hz)]+, 4, 1034 RhCdhN2Pz

RhH(N2)(PRu'3)2,4.919,920 RhC24H56CIP2 RhH2CI(PBu'3)2,4, 1018 RhC24H61012P4 RhH{P(OEt)3}4,4,921 RhCz5H33C12NOP3 RhClz(NCO)(PMe2Ph),. 4.1029 RhC2sH33CIzNP3S RhClz(NCS)(PMezPh),, 4. 1029 RhCI,(SCN)(PMe,Ph),. 4 1029 RhC,,H&isP, [Rh{P(OCH,),CMe},]+, 4.929 RhCz,H4pCINOPZS RhC1(PPr1&(4-MeC6H4NSO).2, 191.4.920 RhC25H54CIOP2 R~CI(CO)(PBU~ 6,276 )~. R~C~~HZ~CIN~O~PZ Rh(NO)CI(N02)(dppe), 4,1070 RhC26H24C1zPz RhCl,(dppe), 4,929,933 R~CZ~H~~CIN~O~P Rh(DMG)2(PPh3)CI,4.950 RhCz6H29CIN404P RhCI(HDMG),(PPh,), 2,271: 4.1014 RhCp,H&lN,O4Sb Rh(HDME),CI(SbPh3), 4, 1014 RhCZ6HZ9CIO4P RhCl(acac),(PPh,). 4, 1017 R~C~~H~OCIN~O~P [Rh(HDMG)(HzDMG)CI(PPh,)]' , 4, 1014 RhCxH30N404P Rh(HDMG),H(PPh,). 4.1014 RhCz6H39C12P4S2 RhC12(SzPMe2)(PMe2Ph)3. 4. 1030 RhC2;Hz;N40,

Rh(diethyldirnethyldioxacorrole)(CO)2, 2, 877 RhC27H24CIOP2 RhCI(CO)(dppc), 4,926 RhCz7H33N3W3 Rh(NCO),(PMe,Ph),, 4. 1029 RhCnHnNd'3S3 Rh(SCN),(PMe,Ph),, 4. 1029 R~CZ~H~~CI~NP~SZ RhC12(S2CNMe2)(PMezPh)3, 4. 1030 RhC27H63C1303P3 R~CI,(PBU,)~{P(OM~),}, 4. 1028 RhC27H63C13P3 RhC13(PPr3)3,4, 1029 RhCnH64P3 RhH(PPf3)3, 6,242.497 RhC2sHzoN4 [Rh(CNPh),]', 6. I51 RhCzsHozClzP2h RhClz(S,PPh2)(PMe,Ph)2.4. 1022

RhH{P(OCH,),CPr},, 4* 921

RhC,,H,,O,P,

RhC29HZsClNzPST RhCI(CSz)(py)z(PPh3),2,581 RhC29H38CIzNP3 [RhC12(PMe2Ph)3( py)]+,4, 1034 RhC29H63Cl3P3 R~CI~{BU'CHZP( CH2CH2P(CH2But)2}Z}.4,1042 RhC,oHiJizO&

Rh{rl-FC6H4C(S)=CHCOCF3}3,2,6.52 RhC3oHiaF9Wh

Rh{PhC(S)=CHCOCF3}3,2,652 RhC3oH22N6 [Rh(terpy)2]3+, 4,997 RhGoHdJ, [Rh(bipy),12-, 4,93U, 1000, 1001; 6,507 [Rh(bipy)J]3+.4.997-1001; 6,276,506,507 RhC3oH3d' Rh(C2H,)(C,Me,)(PPh3), 2, 1026 RhC30H38B06Pz [Rh(BPh,)UWMe)3)z, 4,930 R~C~OH~SCU'~ RhCI3(PEtzPh),, 4,1028 RhC3oH&,P& Rh{SzP(0Et),},(PPh3), 4, 1017 RhC30H46C12P3

RhHC12(PEt2Ph),,4, 1026 RhC3oH&l>NtPt RhC12(PBu2)2(PhNHNH,), 4, 1029 R~CJOH~OC~~P~ RhHCI2(PBu'PrJ3, 4, 1027 RhC30H7j012'~ [Rh(P(OEt),),]+. 4,929 RhCaiH33CI2FsNP3 [RhC1z(PMe,Ph)3(NCC6Fs)]+, 4, 1034 R~C~IH,~NG Rh(H,-diethylhexarnethyIcorrole)(CO j2. 2,875 RhC32H16C1NB Rh(phthalocyanine)CI, 2,868,870; 4, 1011 RhCxHid&8 Rh(phthalocyanine)(SO,H), 2,868 RhC32HZ4N6 [Rh(bipy)2(phen)]3',4,999 RhC3ZH2sN4

[Rh(CNC6H,Me-4),]', 4.943 RhC32H29N50jPSz

Rh(NO)(PPh3)(4-MeC,H4S02N=NN= NSOzC6H4Me-4),2,218,222 RhC32H3zC103PZ RhCI(CO)(diop), 6,266 R~C~ZH~JCLO~P~ [RhC12(Ph2PCH,C0,Et)z]+, 4, 1039 RhC3ZH34C1304P2

RhC13(Ph2PCHZCOzEt)Z,4, 1023 RhC3zH35N402 Rh(H,-diethg Ipentarnethylcorrole)(CO),, 2,875 RhC~t&Od'zSz [Rh0,(Ph,PCHzCHzSEt)2]+, 4, 1037 R~C~~H~OCLP~ [RhC12(PhMePCH2CH2PMePh)2]+, 4,1039 RhC3zH4002P4 [Rh02(PhMePCH2CH2PMePh)2]+,4.1038 R~C~ZHWO~P~S [Rh(O2SO2)(PhMePCH2CH2PMePh),J+,4.1038 RhC~z~~oOJW" [Rh(ONO,),(PhMePCH2CHZPMePh),]+, 4, 1038 RhC3zH4,NO4Pa [Rh(OH)(NO3)(PhMcPCH2CH2PMePh),lt 4.1039 RhCs2HA2BrOP2S RhBr(DMSO)(PPh,),, 2,641 RhC32H,zCIOP2S RhCI(DMSO)(PPh,),, 2,641 RhC,&LCI,P, [RhCI,(PMe,Ph),]+, 4, 1034 RhGzH4402P4

Cumulative Formula Index Rh{3,4-(Me0)&H3C(S)=CHCOCF3}3, 2,652

[Rh(OZ)(PMe2Ph)4]’,2,319,320: 4.1034;6,321 R~C~ZH&~ZPZ RhClz(PhCECPBu‘z)z, 4.932 RhC33HZoClNsO Rh(phthalocyanine)(MeOH)Cl. 4,1011 RhC33Hz4F903S3

RhC36H3oI2NOPa Rh(NO)I2(€‘Fh3),. 4, 1070 RhC36H30NOPZ

Rh(5-methyl-8-quinolinolate)(Ph,PCH=CHPPh2). 4. 914 Rh(NO)(PPh,),. 4. 1068

Rh(4-MeC6H4C(S)=CHCOCF3}3. 2.652 R~C&Z~F@~S~ Rh{4-MeOC6HdC(S)=CIICOCF, j3, 2,652

KhCmH32Pz [Rh(nbd)(diphos)]+,6,275 RhC.13H42C10P2Si2

RhCl(CO)(Ph,PCHZSiMc3)2, 6.261 RhC3,H42IOPZSiz RhI(CO)(PhzPCHzSiMe,),, 6,261 RhC?qH43ClO2P,S ~

[RhC1(02SMe)(PhMePCHzCHzPMePh)z]t, 4,1039 RhC33H4506 Rh {3-(hydroxymethylene )camphorate),. 4.1053 . , . RhC3;H;8C1,N,; [Rh{4-ClC6H,NHC(=NH)NHC(=NHPr’),l4” 1063

5 36

4,

RhC36H3oNO3PzS Rh(hOl(PPh3)2(SO,I, 2,635;4,1067,1068 RhC36H30N05P2S Rh(NO)(SO,)(PPh,),, 4, 1068,10711 R~G,H,oN,OLP: Rh(NO)z(Pl’hSjz, 6,277 [Rh[NO)L(Pl’h3)1] ’ .4.1067,1073,1074 KhC&wNdhPz Kh(NO)(N03)2(PPh3)2. 4,1067,1070 RhC3&3oP& Rh(SzPPhz),, 4,1055 RhC36H31CIZPZ RhHC12(PPh3)2.4. 1018 RhC36H31Pz RhH(PPh3)2.4-970 RhC36H32CIP2 RhH2C1(PPh,)2.4.1018 RhC,,H,,CIP,S’ RhHCl(HSI(PPh,l,. ,,- 4.. 1018 RhC3hH3;C13Pi RhC13(PHPh2)3.4. 1028, 1029 RhC36FIj6V6 [Kh(3,3’-Mezbipy)3jjC,4, 999 RhC3bW37C102P3 ~

RhC1(02)(PhP(CHzCH2CH2PPh2)Z}, 2,320; 4,1042 RhCI(Ph,Ppy),(CO), 5,1107 fiC3jHd2

[Rh(nbd)(S,S-Ph,PCHMeCHMePPhz)], 6,257 RhC36Hz4N6 [Rh(~hen)~]~ 4,1000 ’, I R h ( ~ h e n ) ~ l4,998,999, ~+, 1001

[RL(CpPh,CO),]’ ,6,339 RhC3,H30BrCINC)P, * Rh(NO)C1Br(PPh3)z,4,1070 RhC36H30BrzNOPz Rh(NO)Br,(PPh,),, 4,1069 R hC36H30BrZN07PZ Rh(NO)Brz{P(OPh)3}z,4,1069 R ~ C ~ ~ H ~ O B ~ Z ~ ~ P Z RhBrz{P(OPh)3}2,4,1070 RhC36H30Br4P2 {RhBr4(PPh,),] ,4,1016 R~C~~HJOCIF~P~ KhCI(PF3)(PPh3),, 4,910,918 RhC,6H3oCINzO3Pz Rh(NO)Cl(NO,)(PPh,),, 4. 1070. 1071 RhC?hH3nClN,P, RhCI(N,)(PPh,),, 4,919 R~C,~H~OC~O~PZ

RhCl(Oz)(PPh3)2,2,319.320: 4. 1021;6.340 RhC;6H3&1OzPzS RhCI(SOz)(PPh3)z,4,911,918 RhC36H30C1P2 RhCI(PPh3)z,4,906 RhG,H3nCIP, RhC1(Pa)(PPh3)2,4,920 RhC3,H30C12NOP~ Rh(NO)C12(PPh3)z,2, 104; 4,1M7, 1068, 1069, 1073

RhC36H&lOJ’3S RhCI(SO,){ PhP(CHzCH2CHzPPh,),}, 4,1041 RhC36H,,CIO,P3S

R~(SOI)CI{P~P(CH~CH~CHZPP~~)Z}, 4,1042 RhC36H37ClP?

RhCl{PhP(CHZCHaCH,PPh,),}, 4,1041 RhC36H3,CIP3S2 Rh(S2)Cl{PhP(CI1 ~ C I i ~ C H ~ P P h ~ 2,533; ) Z } , 4, 1042 RhC,,H,,CI,P, RhCI~(PhP(CHICI12CFIZPPhz)Z}, 4,1043 RhC,,H,,NOP,

Rh(NO)(PhF(CHzCHzCHzPPhz)~}, 4.1067 RhC36H38C1P3 RhHCI(PhP{CH&H,CHzPPh,),}, 4,1043

[Rn(nbd){ S.S-(Ph2PCHMe)ZCHz}]’~, 6,257

-_

..

Rfi(octaethvlporphyrin)C1,2,839; 4, 1007,1009 RhC36H44C1N50 Rh(octaethylporphyrin)Cl(NO). 4,1007 RhC36LN4 [Rh(octaethylporphynn)]-, 2,839; 4,1007 RhC36HuN&02Rh(octaethylporphyrin)(Oz), 4,1007,1052

Rh(octaeih$porphyrin)(NO),, 4,1008 RhGdLNo RhH(octacthylDorphyrin), 4,943,1007

537

Curnulutive Formula Index

RhC3,H30C10Pz RhCI(CO)(PPh,),, 6,259- 261.273,274,276,277,303 RhCq7H&IO,Pz RhCI(CO){P(OPh),},, 6, 276 RhC37H3oIOPz RhI(CO)(PPh,),, 6,273 RhC333oNOzPz Rh(CN)(O,)(PPh,),, 4, 1021 [Rh(NO)(CO)(PPh,),]'+~ 4.1073 RhC,,H3oO,P, [Rh(CO)(PPh3),(0,)]+. 2*320 RhC,,H,,OP,S Rh(CO)(PPh,)z(SH)+2.583 RhCmH, I OzP, Rh(OH)(CO)(PPh,)z, 6.304 RhC37H3N" RhHz(CN)(PPh3)2,4. 1018 RhC37H33C1202PzS RhClz(S02Me)(PPh3),, 4, 1022 RhC37H33IzP2 RhMe(PPh3)J2, 4, 1007 RhC37H37C103P3 Rh(CO,)CI{PhP(CI 12CH,CH2PPh2)2}. 4, 1042 RhCdL7N4 RhMe(octaethylporphyrin), 2,839; 4>1007, 1009 RhC38H30N30PZS2 Rh(NO)(CNS),(PPh,)2>4, 1070 Rh(NO)(NCS)Z(PPh,)?, 4. 1067 R~C~~H~ON~PZS~ Rh(NCS)3(PPh3),,4,1022 RhC38H3102P RhH(CO)Z(PPh3)2,6,260 RhC38H3ZClNZPZ RhHCl(CN)(PPh3j2(HCN). 4, 1022 RhC38H33CINOzP2 RhCI(O,)(PPh,),(MeNC), 2,320 RhC38H,3CINP, RhCI(PPh,),(MeCN), 4,920 RhC38H33CIN20P2 [Rh(NO)CI(MeCN)(PPh,),1'. 4. 1072 R~C~SHMN~PZ [Rh(NCMe)z(Ph,Ppy)z]+,5,1107 RhC3sH350zPz RhHz(OAc)(PPh3),, 6, 243

RhC41fI39C13P3

RhC3sH36CIP2 RhClH,(H,C=CHZ)(PPh3),, 2,710 RhC3sH38C12N2P2 [RhC12(PEtPh2)2(bipy)]+,4, 1034 RhC38H39CIN2P2 [RhHCI(PEtPh,),(bipy)]+, 4, 1033 RhC3sH,,NP3 [Rh(MeCru'){PhP(CHzCH2CHZPPhz),}]+, 4, 1041 RhCdLn02P? ." - . [Rh(nbd)(diop)]', 2,709,710 RhC3aH44C.IN04P1S [RhCI(4-02SC,H,NOz)( PhMePCH,CH,PMcPh), ]', 4, 1035, RhC38HwN404 Rh(mesoporphyrin IX diethylester), 4, 1006 RhC39H30F6NP2 Rh{N=C(CF,)z}(PPh,),, 4,907 RhC39H3303Pz Rh(OAc)(CO)(PPh,)Z, 6,262 RhC39H36CINzOP2S RhCI(CO)(MeNSNMe)(PPh,),, 2, 192 fiC3JLNOzPA Rh(O,)(S2CNMeZ)(PPh3),,4, 1021 RhC39H36N20PzS [Rh(CO)(PPh3),(MeNSNMe)]+. 2, SY I RhC3,H,,CI,P3 KhCI3(PMePhJ3,4. 1029 RhC,,H,,NOP, Rh(NO)(PMePh,),, 4, 1067 RhCdLCLP3 RhHC12(PMePhZ)3, 4, 1026 RhC39H47C102P4S [RhC1(4-02SC6H4Me)(PhMePCH2CH2PMePh)2]T 4. 1039 RhC4oH3,F,NO,P, ,4,1070 Rh(NO)( OzCCF3)z(PPh3)2 RhC4,A,,N,PIS, [Rh(NCS),(PPh,),]-, 4,1016 [Ilh(SCN)4(PPh,),]-, 4, 1015 RhC~oH3JYO~P~ Rh(NO)(OAc),(PPh,),, 4, 1070, 1071 RhCa0H36N30P2 [Rh(NO)(MeCN)Z(PPh,)2]z+, 4, 1072 RhCaoH3sClzN~Pz [RhCI,(P€rPh,),(phen)]+, 4,1034 RKoH3aNzPz [RhH2(PPh3)2(MeCN),]+, 4, 1032 RhC40H3802PZs2 [Rh02(Ph2PCHzCH2SPh)2]+, 4, 1037 RhCaoH,,CIN2PI [RhHCI(PEtPh,),(pheii)]+, 4, 1033 RhCaoH4402Pz [RhHz(PPh~)2(EtOH)z]+,4,1032 RhCdLmCIOsP4 RhCI(PPh(OEt),},, 4,924 RhGoHsiOsP4 RhH{PPh(OEt)2}4.4,923 UC~OH~JZPZ [RhH,IP(C6H,,)3}z(MeCN);1+, 4,1032 RhC,,H3,Cl04Pz Rh(PPh,),(OH)Cl(acac), 4,1051 RhC4iH42P2 Rh(acac)(PPh,),, 4,908 RhC4iH370sPz

Rh(aCd~)(P(OPh)3)~,4,908 RhC,,H3,C102P2 RhCl(acac)( OOH)(PPhJZ,6,330 RhC,,H,,CIO,P, Rh(PPh,),( 0 0 H ) C I ( ~ a c )4, , 1051 RhC41H39C1N01P1 Rh(0,)CI(Bu'NC)(PPh3)2, 6,329 RhC41H39C13P3 RhCI3{MeC(CH2PPh2),},4, 1043

Cumulative Formula Index

RhC4 1H39NOP3

533

Rh(Oz)(tetraphenylporphyrln),2,326; 4, 1052 RhC44HzsNdOiSA [Rh{4-U,SC6H4)4porphyrin}(OH2)z]3~, 2, 839; 4, 1008. 1009 RhC44H28NsO Rh(tetraphenylporphyrin)(NO), 2, 839; 4, 1007 RhC44H29N4 Rh(tetraphenylporphyrrn)H, 2, 83Y RhC44H30Nio Rh(phthalocyanine)(H2NPh),, 2,868 RhC4J 134N50 Rh(tetraphenylporphyi-in)(CONEt2),4, 1009 RhCuHsoFbNd' Rh{C(NiYreCH,)2)(NC(CF3)2}(PPh,),. 2, 128 R~C~~H~UFCJ~PZ Rh{N=C(CF,),} { C(NMcCHz)z)(PPh,),, 4,907 RhC44H4006P2S~ [Rh(COd)( ~ - O ~ S C ~ H ~ P-,P6,275 ~Z)Z] RhC44HaPz [Rh(cod)(PPh,),]+, 6.263 RhC44H43CINPz RhHzC1(PPh3)(PhCHMeNHz), 4, 3026

RhC41H39NOP3 Rh(NO){MCC(CH,PPh,)3), 4, 1068 RhGiH4oNzOPzSz [Rh(NO)(S,CNEt,)(PPh,),]+, 4, 1072 RhC4iHdJW2

[Rh{PhCH=C(NHAc)CO2Et}(S,S(Ph,PCHMeCHMePPh,)l-, - 6,255 RhC47Hs~N2P2 [Rh(nbd)(PhzPCH2CHzNMe3)z]3+. 6,263 RhCdiH,2CIzNPz RhHCg{P(C,H,,),},(py), 4. 1019 RhCmHd903S3 Rh(2-CjoH7C(S)=CHCOCFn ) 3 , 2 6S2 RhCaH,oCWzPz RhCI(C6C140,)(PPh3),,4, 1022 RhC4ZH3SCIZNZPZ RhC12(NzPh)(PPh3)2,2,130; 4. IO22 RhC42HgsOP2 Rh(OPh)(PPh,),, 4, 907 RhC42H36C13N3P3 RhC13(Ph2PCH2CN)3, 4,1023 RhCaH36N6 IRh(4,4'-Me,phe11),1~+,4,1002 ~,

Rh(NO)(0,CEt),(PPh3)2, 4, 1071 RhC4,H4,CINzP, [ RhCI(N,Ph) { PhP(CHzCHzCHzPPh2)2} 1' 2, 134,136 Rh(N,Ph)CI{PhP(CHZCHzCFizPPhz)2}, 4, 1043 RhC4zH4zClzNOPz Rh(NO)(Cl,){P(C,H4Me-4)3}2. 4. 1068 R~C~ZH~~C~~PZ RhCl, { P( C6H4Me-2),}2 , 4,932 RhGzH42CG3 RhC13{S(CHIPh)2)3,6,245 I

RhC42H4ZN30ZPZSZ

Rh(Oz){MezNC(S)NC(S)NMe2) (PPh,),, 4,1021 R~C~ZH~~OZPZ [ RhH,(PPh3j2(Me2CO),]+:4,1032 mC42H45ClJP3 RhCI3(PEtPhz),, 4,1027, 1029 RhC,,H4,CIP2Si RhH(CI)(SiEt,)(PPh,),. 6 : 299 R~C~ZH~~C~ZP~ RhHClz(PEtPhz)3,4, 1026, 1027 RhC42H47ClP3 RhH,CI(PEtPh,),, 4,1026 RhC4&&1$'3 RhCI,(PBuZPh),, 4, 1028 RhC4,H&lNOJ', Rh(NO)CI(PhCO)(PPh,),, 4,1U67, 1U70 RhC43H37CIzOzP2S RhC12(02SC6H4Me-4)(PPh3)2, 4 , 1022 RhCj3H&IP,S RhNC1(4-SC6H4Me)(PPh3)2. 4! 1018 RhC43H3sP2 [Rh(nbd)(PPh,),J+, 2,709 RhC44Hz4N40izS4 Rh{tetra-(4-~ulfonatophenyl)porphyrin}4. 1008 R ~ C ~ ~ H Z ~ N ~ O I ~ S ~ (H20)J3-,4, [Rh{tetra-(4-~uIfonatophenyl)porphyrin) 1007 R ~ C ~ ~ H Z ~ N ~ O I ~ S ~ [Rh{tetra-(4-sulfonatophenyl)porphyrin) (OH),J5-, 4. 1008 RhC4jH2&INj Rh(tetraphcnylporphyrin)Cl, 2.83Y; 4,1007 RhC44HzJNa Rh(tctraphenylporphyrin)I+ 2,845 RhC44HmN4 [Rh(tetraphenylporphyrin)]- ,2,839 RhC~HzsN40z ~

Rh(NO)(OzCC6Fs),(PPh,),, 4, 1070 RhCwH23ClNs

539

Cumulative Forrnulu index

RhCl(PhCOCHCOPh)(PPh3)2. 4, 1022 RhC5,H44ClNZO5PzSz RhCl{(4-MeC6H4S02N)rCO}(PPh3),, 2,286 R~CSI&N~O~PZSZ Rh{ (4-MeC6H4S0,N),CO) (NO)(PPh3),, 2,285 R~CS~H~~N~SPZ Rh(N0)(4-02CC6H4Me)Z(PPh3)2r 4, 1070, 1071 RhCs2H4sClP4 [RhHCl(PhzPCH=CHPPh&]+, 4,1037 RhC<2HanC12Pa [RhCl,(dpp~)~]+. 4.1039 RhC,,H4,NOP4 [Rh(NO)(dppe),I2+, 4.1072 RhCszH480zP4 [Rh(dppe)z(Oz)]+,2,319; 4. 1037, 1038; 6,339 [RhO,(PhzPCHMePPhz)z]f. 4, 1037 RhCszH48P4 Rh(dppe),, 4,906 [Rh(dppe),]+, 4,906.924.926,928 R~CS~H~~'~SZ [RhSz(+pe)J+, 4,1037 RhCSZH49CIP4 [RhHCl(dppe),] ' , 4 , 1037, 1039 [RhHCl(Ph,PCHMePPh,)2]+, 4,1037 RhCszH49P4 RhH(dppe),, 4,906.924 RhC5zH53C104P4 [RhHCl(PPh,(OMe)},]+, 4,1033 RhC52H53P4 RhH(PPh,Me),, 4,921.924 RhC54CIF45P3 RhCI{P(C6F5)3}3.4.9lj RhC54H36F9NOP3 Rh(NO){P(C6H4F-4)o)3,4, 1066 RhC54H4nP3 , RhH( I-phenyldibcnzophosphole),,4,924 RhC54H44P3 Rh(C&PPhz-4)(PPh,)2,2, 699 RhC54H45BrP3 RhBr(PPh,),, 4,917 RhC54H45ClNOP3 IRh(NO)C1(PPh3)31+,4. 1072 RhC54H45C1NO~P3 [RhC1(N02)(PPh3)3]f,4. 1033 RhC,4H4,CIO,P3 RhCI(O,)(PPh,),, 4, 1030: 6, 1019 RhC54H45C109P3 RhCl{P(OPh)3}3,4,916 RhC54H45CI09P3St RhC1(3-HO,SC,H,PPh,),. 6,243 RhCs4H45CIP3 RhCI(PPh?)?, 2,709; 4,903.905,90h, Y 13,914, 916-918,920.1017. 1021. 1026, 1030, 1041; 6, 239,241,242.250,259,273.274.275,277,294, 299,303,337.349. 1019 RhCs4H45CW3 RhC13(PPh3)3,4, 1029 RhC54H45NOP3 Rh(NO)(PPh3)3,2,111,218; 4. 10661068; 6,244 RhC54H45NOzP3S Rh(O,){ SC(=NPh)PPh,}( PPh3)2,4, 1021 RhCs4H4sP3 [Rh(PPh,),]", 4,914 RhC54H45P4S6 Rh(SzPPhz)3(PPh,), 4, 1017 R~CS~H~~C~ZP~ RhHCIp(PPh3)3.4, 1026

[RhH{P(OPh,},]-, 4,923

RhF4

RhC5&6P3 RhH(PPh,),. 4, 916-918 RhCsqH47ClP3 RhHZCl(PPh3),, 4, 1026 RhCj4Hj202Pj [Rh{HOCH2CH(PPh2)CH2PPhz}*]+,4,928 [RhOz{PhzP(CH2)3PPhz}z]+, 4, 1037 RhC54H52ClP4 [RhHCl{ Ph,P(CH,),PPh,),]+, 4, 1037 RhC.wH,,P, [RhH,{,PH2F(CH,)3PPhz}*l+, 4, 1037 RG4H&I3P3 R~CUP(C,H,,M,, 4,1029 KhC55H45NOP3S Rh(SC(=NPh)P(O)Ph,}(PPh3),, 4, 1021 RhC5,H4sN03P3S Rh(O2) {SC(=NPh)P(O)Ph,}(PPh3)2,4, 1021 RhCS5H4,NP3S Rh{SC(=NPh)PPh,} (PPh3)2,4, 1021 RhCssH460P3 RhH(CO)(PPh,),, 6,243,259,260,261,262,264.266, 273- 276 RhCssH,,O,,SJ'x

RhH(C0)(3-H03SC6H4PPhz)3,6.2h3 R G s H ~ ~ RhH(CO)(PPh,),, 6,265 RhC55Hd3 RhMe(PPh,),, 2, 699 RhCdL02P3 Rh(OAC)(PPh,);, 4,916; 6,243 RhC57HJ': Rh(PPh3)3(v3-C3HS),6,243 RhC6ofIjoClNsPz RhC1(PhNNNPh)z(PPh3),, 4, 1017 RhCsoHmOd's [Rh{P(OBu),}i]+. 4,929 RhChiWsoO,P, Rh(OlCPh)(PPh3)3,4,916,917 RhCmH6504P4 RhH(diop),, 4, 925 RhC6&&J'4 [RhH,(diop),]-, 4, 1037 RhC63H&OP3 Rh(NO)(P(C6H,Me-4),},, 4, 1067, 1068 RhC&d'J30

RhH(CO){N(CH,Ph)3}3,6,263 Rhc&j~N,oP3

Rh(?rO)(PhNNNPh)(PPh3)3, 4,1067 R ~ G J W S RhH( l-phenyldibenzophosphole)4,4. Y24 RhH(5-phenyldibenzopbospholc)4, 6,242 RhCnHGiOizP4 RhH{P(OPh),},, 4,923 . RhC,ZH,,P4 RhH(PPh,),, 2,583,701; 4,921-923. 1019; 6.241.242 R h C n H ssh O , (Rh(octaethi Iporphyrin)},O,, 4, 1008 RhCi&,zoPs {Rh(PPh3)4}z.4.905 RhCIN202 (RhCl(NO)z},, 4, 1066 RhCI,F6P2 [RhCIZ(PF3)2]-. 4,906 RhCI3 RhCI3. 2. 697 RhCI,I, [RhC1,ISj3 , 4 , 1058 RhC16 [RhC1,]Z-, 4,1061. 1062 [RhC1,I3-, 4,964, 1057-1060; 6,340,823 RhCll&2C102P2S RhCI(SO,)(PPr',)z, 4,920 RhF,

Cumulutive Formula Index

RhF4 RhF4,4,1062,1065 RhF5 RhF5,2,680; 4, 1063 mF6 RhF,, 4,1064, 1065 [RhF6]-. 4,1063 [RhF61Z-, 4,1061 (RhF613-, 4,1058 RGF,P,S, Rh(SzPF2)3,4, 1055 RhF,NOP, Rh(NO)(PF3)3, 4,1066 RhFi2P4 IRh(PF,),]-, 4,904,923 RhFeC,H, ,N,O,

[Rh(HDMG)(HDMG-Fe)(HzO)Me]z+,4, 1015 RhGeC36H31Ci4Pz RhHCI(GeC13)(PPh3)z, 4, 1020 RhGeC39H40C1Pz RhHC1(GeMe3)(PPh3)Z,4,1020 RhGe,CI,, [Rh(GecI,),]-, 4,1019 RhHFiJ’4 RhH(PF3)4,4,904,921,922,923 RhH,CI,O IRhC1,(H20)]Z-, I , 50; 4,1058-106U; 6.801, [RhC1,(HZ0)l3-, 6,299 RhHaC1402 [RhCl,(H,O),]-, 4, 1058-1060 RWOiiP3 Rh(HzO)(HzP30io), 4,1053 RhHbC1303 RhCI,(HZO),, 4,1058-1060 RhH8Cl2O4 [RhC1z(H,0)4]+, 4, 1058-1060 RhH,N,O,S,

~ R k l ( H ~ O ) s ] 4,943,948 ’, ~RhCI(HZO)S]Z+,4, 10.58-IOh0 RhHllO6 [Rh(HzO),(OH)]Z’, 4, 1049 RbHIZC1N7 [WNH3)4(N3)Cl]+, 4,987 RhHiZCIzN, [Rh(NH3)4C1z]+,1,299,400,401: 4.954,959,987,988 WHizIzN4

[Rh(NH3)4Iz]+, 4,982 RhH1206

[Rh(HZ0)J3+, 4,948,1049,1053,1058-1060 RhH,3ClN4O [RhCI(OH)(NH,),]+, 1,401 RhHI4CIN40 [RhCl(H,0)(NH3)4]2 , 4,961,988 RhH14N40Z [Rh(NH3)4(OH)zIz+, 4,964 RhH15BrN5 [Rh(NH3)sBr]2+,1,400; 4,958,959,964,981,982,985 RhHi5ClN5 [RhCI(NH,),]+, 4,930 [RhCI(NH3)5]Z+,1,395.400,402; 4, W2,948.953,954, 956958,960,965,982,985,988,995; 6.274 RhHlJN5 [RhI(NH3),]2+, 1,400; 4,958,982

’

RhH15N402

~ R ~ ( N H , ) ~ ( O H ) ( ~ Z ~4,963 )]”, RhHISNsO4S [~(NHJ)S(SO,)I+, 4,957,960 RhH1SN60Z

[RII(NH~)~(NO~)]~+, 4,957,959-961 [Rh(NH3),(ON0)]z+, 4,961

540

RhHisN603 [Rh(NH3)s(N0,)l2+. 4,957,959,960 RhHiJ’Js [Rh(NH3)5(N3)jz-, 1,406; 4,959,960,986 RhHl,N,OZ [Rh(NH3)4(H20)2I3’. 4.964 RhHi6Ns Rh(NH?)sH. 2,697 [Rh(NH,),H]-, 2 , 693 [Rh(NH3)sH]2’.2.691; 4,954,963 RhH16NS0 [Rh(NHj),(OH)JZ-. 4, 960, 963 RhIl,,N,O [Rh(NH3),(Hz0)]3’. 1.299, 309; 4,954,957,958.960. 964,985.986 RhH.,N,CI

[Rh(NH3)6I3+. 1,186,400,430; 4,956,962,984 RhHgCz4HdW3 RhCl3(PMezFh),(HgCl2). 4, 1076 RhHgCl,(PMe,Ph),, 4,1076 RhIrC,,H,,CIP, IrH2(PEt,)2(p-Cl)(p-H)Rh(PEt3)2, 4,1074, 1151, 1164 RhIrC44H,$1 Kh(dppe)(~-11)21rI-12(PPr’3)2, 4, 1074, 1151 RhIrC44W71C1P5 [IrH(PEt3)3(u-Cl)(~~-H)Rh(dppe)] ’ , 4, 1164 RhIrC,,H,,P. _. [Rh(dppc)(p-H),Ir(PEt3)3]+., 4,1075, 1151 R~MOC~~H~ZP, Rh(PPh~)z(~-H)zMoCpz, 4, 1076 RhN60iz [Rh(N0,),I3-. 4.1012 RhNbW4CioH&i, [Rh(C5MeS)(Nb,W,019)]z~, 3, 1047 RhNb3W,C8H,20,0Si [Rh(cod)( SiW9Nb3040)]6-.3, 1047 R h N h W L Jh5GS [Rh(CsMc,)(SiWgNb30,0)]5 , 3 , 1047 RhNPHlOOl [Rh(H,0),0NpO]4+, 4, 1053

KhO [Rh0I3+. 4,1063

Rho, RhOz, 4.1062 [Rhoz]+. 4,1063 Rho3 Rho3,4,1065 [Rh03]-. 4.1063 [Rho3]*-, 4.1062 RhoI [RhO4I2-,4, 10@, 1065 [Rh04]’-. 4,1063 Rho, 4, 1062 Rho$, [Rh(SO3),l3-, 2,638 Rho,& [Rh(SO4),I4--. 4; 944 R~OSC~H~~N~,

[Rh(NH3)5(U-h=CHCH=NCH=~H)O~(NH3)5]6-. 4,53.5,956 RhOsiC,,HcnO,, RhOjs~h2(aca~)(CO),,.2,394 RhPdC1,H14CI,NOP PdRhCI,(CO)(Ph,Ppy): 5, 1108 RhPdCllHZoCIzN,P [PdRhC12(CNMe)z(PhfPpy)]+, 5, 1108 RhPdC28H22C1Nz0P2 Pd(CN),( p-dppm)Rh(CO)CI, 5,1164 RhPdC35H28C13NzOPz PdRhClS(CO)(PhzPpy)z. 5.1107

Cumulative Formula index

541

RhPdCmH34C12NJ'Z PdRhC12(NCMe)2(Ph2Ppy),.5 , 1107 [PdRhC12(NCMe)2(Ph2Ppy)2]+, 5, 1107 RhPdC53H44ClN20P4 PdRh(CN),( CO)( Cl)( dppm), 5 . 1105 RhRuCSiH44CIOP4 RuRhCI(p-CO)(dppm),. 4.373 RhRUC52H46CIOZP4 RuRhH,Cl(p-CO)(CO)(dppm),. 4.462 RhRuC7zH,"C:I,P, RhCI(PPh3)2(p-CI),KuCI(PPh3)2 4, 1076 RhSi5 [Rh(S,),J3-, 2,542 RhShCZIH2iC12 RhC12{Sb(C6H4Me-2)1}r4,933 RhSbSnC54H4sC15 RhC12(SnC13)(SbPh3)3,4, 1032 RhSb2C36HsiC12 RhHC12(SbPh3),, 4,1018 RhSbzC36H32CI RhH2C1(ShPh3),, 4, 1018 RhSb3C54H45C13 RhCI,(SbPh3)3,4, lU32 RhSb3C55H45C12NS RhC1Z(NCS)(ShlJh,)3,4,1032 RhSiC,,H, IC14Pz RhHC1(SiCI,)(PPhi)z. 4. 1020 K hSiC37H34C13P2 RhHCI(SiCl,Mc)(PPh&, 4, 1020 RhSiCJ 137C12Pz RhHC1(SiC1Me2)(PPh&, 4>1020 RhSiC3,H40ClP2 RhHCl(SiMe3)(PPh3j2.4.1020 RhSiC,9H4,0,P, RhH2{Si(OMe)3}(PPh,),, 4.1018 RhSiC40H43P2 RhH,(SiHEt,)(PPh,),. 4. 1018 RhSiC4iH46C101P2 RhHCl{ Si( OEt),} (PPhl)2. 4. 1020 RhSIC:,, Hd.+CIP? RhHCI(SiEt3)(I~Ph3),,3. 1020 RhSiC,,H,,CIP, RhHCI(SiPh,)(PPh,),. 4, 1020 RhSi,C33H45NP3 Rh{N(SiMe2CH2PPh2j2} (PMe,), 4, 1041 RhSi2C42H4sNP2 Rh{N(SiMe3),}(PPh3),. 4,907 RhSi2C48H51NP3 Rh{N(SiMe2CH2PPh2)2)(PPh3) 4: 1041 RhSnCI8HISFIZP4 Rh(PF,),SnPh,. 4; 904 RhSnC4,H4,CIP2Si2 RhC1(PPh3),Sn{CH(Sihle,)2}. 4,920 RhSnzCllo [RhC14(SnC13)2]3-,4, 453 RhSn3Cli2 [RhC13(SnC13),]3-,4, 953 RhSn7HsFI9O4 [Rh {SnF2(H20)2 1,(Sn,F, d - , 4,953 RhWCdW'2 Rh (PPh3)2 (p-H) 2WCp2.4 1076 [WCp,(p-H)zRh(PPh3)2]'. 2,692 R~zAS~C~~H~OC~~ {RhCl,(AsEt,),),, 4, 1025 RhZAS4CilH44C1L0 Rh,ClZ(p-CO)(dpam),. 4,941 RhZAS4CSII 14SCI3O Rh,CI,(~-H)(Ir-CO)(dparn),,4: 941 RhZAs4C52H44C12IZ02 Rhz(CO),Cl2I2(dpam),. 4,941 RhlAS4C52H44C1202 Rhz(CO),Cl,(dpam),, 4- 941 R~ZAS~C~SH~ZC~

RhZC8H36NB04

I

~

~

~

COC 7-R'

Rh,(OAc)(HNCOMc),, 4,950 Rh,CSH,,CI, (RhCl(CzH,)z},, 6,266.277 RhzCsHi6N~04 Rh,(HNCOMe),, 4,950 RhzC~Hi601o Rh,(OAc),(H,O),, 2,297; 3,1231; 4,934,944,945 Rh&HisCI~NL'2 [Rh2C16(Me2NCOMe)2]2-,4,944 Rh2 BHZ0C16S4 Rh2(MeSCH2CHZSMe),CI6,4, 1056 Rh2CnH32Cl2N802

[Rh,(OAc);{ 2-(2-pyridyi)-l,S-naphthyridine;}I+, 4.,941 KhKmHsNs04 { Rh(CO)2}2(tetraazaporphyrin),2, 858 Rh,C2ofIi,CI4N,O,

Rh,(OAc),( theophylline)2, 4, 936 Rh2Cz3Hi~C14~604

Rh,(fi=CCICH=CHCH=CO),(imidazole),

4,939

R~zC?~H~RN~OS

Rh2(OAc)2(fi=CMeCH=CHCH=~O)z(imidazole). 4, 941 Rh,C?4H&I,FJd,P, Rh2C12(PF3)2(PhNNPh),+4,90Y KhLC24H21N406 [ Rh,(OAc),{ 2.7-his(2-pyridyl)-l ,X-naphthyridine}]' , 4 . 94 1

{RhCl(cod)}Z, 2,210,682,710; 6.257, 265,275.277

Kh2(0,CCF,),{Me,~(CH,),CMe2~O},, 4,937,938 Rh2C,,H7 N 0 R h , ( ~ ~ C ~ ~ C H = C H C ~ O ) , ( i m i d a z 4. o l 939 e),

543

Cumulative Formula Index

Rh*C*8&6%

Rh2C88H64P4

544

Cumulative Formula Index Rh6C16016

Rh,(cO)16~6. 274 R~~CU~CI~HSN~~IS 5, 572 Cu2Rh6(CO)15(NCMe)2, Rh6CuzC3zH16018 Cu2Rh6(CO),a(PhMe)2,5,572 RhsGiOziP [Rhy(C0)21P]2-:2.1060 RhlllC22027S [Rh,,,S(CO)J- 2,522 ~

Rh12C30030

[Rhq2(CO)3oI2 .2.697 Rh,,C,4%S, [Rh.,,(S),(CO),,]3~ 2.522 Rh55C144H324C1d'iZ Rh5,(PBu',),,CI,,. 1- 139, 170 RuAsC,H,O, Ru(CO),(AsMe,). 2, 1038 RuAsCzzHi jO4 Ru(C0)4(AsPh3), 2, 1038; 4,371 RuAsC~~H~&IZP {RuCI,(AsPh,)(PPh,)},,, 4, 379 RuAsC~,H~,C~N, [RuCl(bipq.),(AsPh,)]+, 4. 392 RUASC:~,H~~F~~~P~

Ru(O,CCF,)(COj(PPhR)(arphos), 6,235 RuAs,C,,H,,CINC)~ 4,36X, 394 RuCI(?~O)(ASP~~)Z, RuAs~C,~H~,,CI~ {KuCI,(AsPh,),},. 4.379 RUAS~C~~H~~CI~NO~ RuCI3(NO)(AsPh3)(0AsPh3),4,394 RuAs~C,~H~OCI~NPZ RuC13N(PPhj)2,4,419 RuAs2C36H31Br2 RuHBr2(AsPh3),. 4,461,462 RuAs~C~,H,,CI~O RuCI,(AsPIi,),(~leOrl), 4,379,416 RuAs2C3BH36Br30S RuBr,(AsPh,),(DMSO), 4,439 KUAS,C,,,H,.,ClOzP,Si RuHCI(DMSO),(AsPh,),, 4,458 RuAsGoH~N~O~S~ [RuH(h',)(DhiiSO),(AsPh,),l*, 4,459 RUAS~C~~H~~F~OP& Ru{szCz(CF3)2}(Co)(AsPh,),, 4,406 RuAs~C~,H&IP~ RuHCI(PPh3)2(Ph2AsCH2CHZAsPh2), 4,453 RuA4s2C72H7,N, [Ru(octaethylp~rphyrin)(AsPh,)~]+,4,471 RiiAs3C24H3,C.13 RuC13(AsMe2Ph)3,4,379 R~AS~C~~H~~CI~NO RuCI,(NO)(AsMePh,),. 4, 374 R U A S ~ C ~ ~ H ~ ~ K ~ O ~ S ~ [KUH(~\~~)(DMSC~)~(A~M~P~,),]'~, 4,459 145CIzOz RuAs~C~ J RuCl,(hsPh,),(O,), 4,416 RuAs~C&~SC~~ RuC13(AsPh3)3,4, 379,416 RuAs~C~~0 H~~CI~ RuC13(AsPh3)2(OAsPhsj , 4,416 RuAs4C20H31CiK [RuCl(NH,j(diar~)~]+, 4,391 RUAS~C~~H~~CIWO [RuC1(NO)(diars)ZlzC? 2. 111; 4, 394 RuAs4C,,,H3,CIN0, RuCI(NO,)(diars),, 4,394 RUAS~C~~H~~CIN~ [RuC:I(N2)(diars)2j"~r 4, 391, 394 KuAs,C,,H,,CIN3 RuC1(N,)(diars)2, 4, 394 RUAS~C~OH~~CI,

545 RuCl,(diars),, 4,379 [ R ~ C I ~ ( d i a r s ) ,4,418 ]~, RuAs~C~~H~~INO [R~I(NO)(diars),]~+, 4,394 RUAS~CZOH~ZN~ Ru(N,),(diars),, 4.394 RuAs4CzlH35CI RuCIMe(diars), 4:386 RuAs~C~LPIS~ Ru(S,PMe,),(diars),, 4,405 RUAS~C~~H~~CI~ RuCl,(AsMe,Ph)+ 4.37rl RuAs~C~~H~~C~~NO RuCI,(NO)(dparn),, 4.393 RuAS~CS~H~~CL RuClz(Ph,AsCH=CHAsPh2)z. 4.379 RuAs4C,,H44CIz0, RuCl,(CO),(dpam),, 4,383 RuAs~C,,H~~CI

RuHCI(Ph2ASCH2CHzAsPh2)z-4.353 RuAs4CS4H4,Br2

R u B ~ ~ { A s ( C & I ~ A S P 4,380 ~~-~)~},

Cuniulative Formula Index

RuC,H,CISNO

[Ru(CO)(NH3)dOH,)I2 ’ ,4,292 RUCH,~F~K~O;S 4,304,305,307 [Ru(O,SCF~)(NH,),]~+, RuCH,,N,O [RU(CO)(NH,),]~+. 4.291 RuCH,,N, [Ru(CN)(NH,),]+. 4,282 RuCHl,N60 [Ku(XO)(NII,),]~+,4,301, 303 KuC‘FI,,N,S [Ru(NCS)(VH,)s]’+, 4,301,318 [Ru(SCN)(NH3),]’, 4,301,318 RuCHi6NS02 [ R ~ ( N H ~ ~ ( O Z C H1,377 )I-, RuCHI6Nb [Ru(NCH)(NH,),]+, 4,282 RuCH17N, [ R U ( N H , ) ~ ( N ~ H ~ 4,299 )]~+, RuCHlaN602 [Ru(H2NC02H)(NH3),I3+,4,303 RuCH,&O

[Ru(NH3),(H,NCONH2)]3+,6,471

KuCH,1NsUS Ru(CN),(Ph,ASCH=CHAsPh,),, 4.282 [ R ~ ~ ( N H ~ ) ~ ( D M S 04, ) ]3206 +, RUAS~CG~H,,CIP, RuC,C1,0, [RuCI{1. ~ - ( P ~ , A s C ~ - I , C ~ ~ ~ ) ~ F ’-,C4,I377 ~~}*~~H ~}~ {RuCI,(CO),},, 4,143 RuAsbC75HbsClzPs RuC~CI~NO~ RuCI,(Ph,AsCH,AsPh,),. 4.3811 [RuCI,(C,U,)(NO)]’-, 4,429 RuAuCO~C~~H~~O~ZP KuC2Cl,0, C O ~ R U ( C O ) ~ ( C I ~ - C O ) ~ ( C L5,~908 -AUPP~~)~ [RUCI,(CO),]~-,4,443 RuBCHlsN6 RuC,H,N,O, [Ru(BH,CN)(NH,),]+, 4:281 [Ru(OH),(GI~-O)(NO)]-,4,362,466 [Ru(BH,CN)(NH,),]?+, 4,282 RuC,H,O, RuBC&fd’, [Ru(CzO4)(OH,LI+, 4,429 [ R U H ( $ - B H ~ ) ( P M ~4.454 ~)~. RuC,Hl,U,OJ RuBC~~H~OCINGO~ [ R U ( C , O ~ ) ( N H ~ )4,305,306,308 ~]+, R ~ { H B ( ~ ~ N = C H C H = ~}H ), (CO),CI, 2-251 RuC,H 12N6S2 [Ru(NCS),(NH,),]+, 4,301 RuCIHl,N,O, [RU(C,O,H)(NH,),]~ ’ ,4,30h RuC~HI~N~O~ [Ru(NH~)4(02CCONH,)]2+, 4, 311 RuH(r12-Bt14)(PMePh,)2. 4,154 RuC,H, cNiO, [R~(OAE)(NO)(NH3)4]z+, 4,298 RuBC36Hd3 RuH(v2-BH4){ PhP( CH,CHzCHzPPh2)2}, 4,454 RuC2Hl7C1N5O2 RuBC37H,IOPZ [RU(O,CCH~C~)(NH,),]~+, 4,306 RuH(BH~)(CO)(P(C,H~~)~),. 4.157 RuC2HliN603 RuBC~~H~~NO~P~ [Ru(NH;)S(HNCOCO,H)IZ+,4,303 RuH(BH3CN)(CO),(5-Ph-dibenzophosphole),, 4,457 RUC~H~SN~O~ [RU(OAC)(NH,),]~+, 4,306 RuBCS~HSOP~ RuH(BH,)(PPh,),. 4.451 RuC,H,aN, [Ru(NM,),(NCMe)]*+,4,301;6,449,450.-?58,496 RuBC,~H~OP, RuH(BH,)(CO)(PPh,),. 4,457 [Ru(NH,);(NCMe)l3+, 4,302; 6,449,450.452 R~BIoC~GH~>NZP~S nuCzH,,,N,% K U H ~ ( N ~ B ~ ~ H ~ S M ~4.451 ~)(PP~~)~, [RU(NH~)~(NH~CH~CO,H)]~+,~,~~O RuBr, [RU(NH~)~(O~CCH,NH,)]~+, 4,310 [RuBr,]”, 4,447 RuC~H~IK~OS [RuBr,13-, 4,445 [RU(NH,),(DMSO)]~+,1, 186;4,307,439 RuCBrO RuCZHZlNjS {RuBr(CO)},, 4,440 [Ru(NH3),(HSEt)12+,4,307 RuCCI,O [RU(NH,)~(SM~,)]~+. 4,307,432 [RUC~,(CO)]~-, 4.292.443,146 [Ru(NH,)~(SM~,)]~+, 4,308 RuCHCISO, RUC~I~O~ [RUCL,(O,CH)]~-,4,429 {RuIz(CO),},. 4,440 RuCH2Cl40, RuC,CI,O, [RuCl,(CO),] .4,443 [RuCI,(CO)(OH~)]~4,292,443 RuC3FJ0, R~CH3C1403 [RuCl,(O,CH)(OH >)]*-, 4.429 RuF3(C0)3,4,442 RuCH,,N, [RuF,(CO),]-, 4.446 [RU(CN)(NH~)~],”+.~.~XZ RuC3H50, RuCH12N602 lRu(O,CHh(OH,)l-, 4,426 4,298 [RU(NCO)(NO)(NH,),]~+, RuC3H,CljNO RuCH14N40, [RuCl,(DMF)]-, 4,447

RuAs~C~~H~~N~

Cumulative Formula Index

RuC~H~~CIN~

[RUCI(NH,),(H~~CH=NCH=~H)]~+. 4.296 R;C3Hl6N50;S Ru(NOz){HzNCSNC(=NH)NH,) (OH2)3-4.468

RGHi9N7

[RU(NH,),(N=CHNHCH=~H)]~-, 4,295

544

RUC,H~~N,O~ [RU(~~)~(OH~)~]~’ .4.323 [RU(~~)~(OH?)~]~+. 4.323 RuC~HZON~ [RU{HN=C(M~)C(M~)=NH}(NH,),]~+, 1.446; 6. 190 RUC~H,~N,O, [RU(NH~)~(NCCO~E~)J~~,~,~O~ RuC~H~~N~ [Ru(NH,),(HikCHCH=NCH=cH)]”, 4.326 RuC4H2,N603 IRu(NH,)i(FINCOCO,Et)l~’ ,4,303 ,308

fRL(CO),(NO)]’, 2 , 118 RuC4BrC1304Si R~3r(SiCl,)(C0)~,4,285 RuC~BK~O, RuBr,(CO),, 4,443 RuC4C1NO9 [RUCI(C~O~)~(NO)]~-, 4,429 RUC~C~~O~S~Z Ru(SiCI,),(CO),, 4,285 R~CaH204 RuH,fCOL.4.452 R~c,H;N,O~~

[Ru(~H3),(NH2CH2C02Et)]3+, 4,310 RuC,H,SNsSZ [RU(NH~)~{HS(CH~),SH}]~+, 4,308 RuC4H25N602

[R~I(NH,)~{OC(OE~)CH,NH,}]~+, 4,310 RuC4IzN202 [Ru(CN),I,(C0)z]2-.4,283

[Ru(OH)(NO~)~(0N=~CONHCONH~O)(~O)]-. 4, RuC4120, Ru12(CO)+,4.432:6.267 RuC4N202S2 {Ru(NCS)*(C1O),],,.4, 326

464

RuC,O,,

[R~O~(C~O,),IZ-, 4,429 RuC5H,C1204 RuCk,(CO),(EtOH). 4.443 RuC,H,,CI2O4 Ru(aca~)Cl~(OH~)~. 4.424 RuC~H~~CI~OSZ [RuC13(CO)(SMe,),]-,4,432 RGHi,N, [Ru(NH,),(py)]*-,4,294,295 KuC,H,,N,O,S ‘, 4,307 [Ku(SO,)(NHz)&y)] RuCjHl9N90 [Ru(NH,),(hypoxan t hinr)]3’, 4,296 RuCjH~oCIN,$s [RuCl(H2NCSNHz)5]z+. 4,437 RuCSH20N6 [Ru(?lH3),(py)j2’,1,336.404; 4,293,294,300; 6,652 [Ru(NH,),(py)P-, 1,333,336,349,365; 4,289,296. 297,6,632 [Ru(NH3)&y)l4-, 1,297

[RuCL,(MeSCH,CH,SMe)]-,4,433 RuC,HizCIqNO,Sz RuCl,(NO)(DMSO),, 4,439 RuC,HizCl,O,Sz [RuCI,(DMSO)J, 4,439 RuC4H13C13N3 RuCl,(dien), 2,47 RuCaHi4N6 [Ru(NH3),{HN=CMeC(Me)=NH)12+.

4.303

RuC,H 16CIzN4 RuCl,(en),, 1,301; 4,322 Wh; 4,32>325 [RuCl,(en),]+,1,300, RuC4H 1sNH [Ru(N2)~(en)2]2’4,323 ,

RUGHI& [Ru(N,)(N,)(cn),]+, 2,231;4,323

RUC4Hi6Ni o RU(N~),(~~)~, 4,394 [Ru(N,)~(en)~l+, 4,323 RuC4HI8C1N40 [R~Cl(en),(0H~)]~+, 4,323 RUC4HisN6 [Ru(NH,),{ N=C(Me)C(Me)=N}]**. 6.458

296,317 [ R u ( N H , ) , ( ~ ; ~ = C H C H = N C ~ = ~4,295,296 ~~~~+,

[Ru(NHT)~(~-PYNH~)]~’ ,4, 293,294 RuC,H,,N,OS [Ru (NSC(NH&}(en j2(OHz)]1+, 4,323 RuC,H,,N,O [R~(NH,),(1-inerhyIcytosine)l~~, 4,296 R~CgH26N50 [RU(OH)(NH~M~),]~’, 4,323 RuC5N60 [Ru(CN),(NO)]*-. 4,281,282,362 RuCgN6OS5 [RU(NCS)~(NO)]~-, 4,362 RUC,I\j602

[Ru(CN)s(NO,)Jq .4,281,282 RuC~HN~ [RuH(CN)# .4.281 RuChH2N6 [RuH,(CN)J-,4.282 RUC,H,O,S, RU(S~CSM~)~(C~)~, 4,435 RUC&O,

547

Cumulative Formula Index

Ru(S,CNMe,)z(NOz)(NO). 4, 362 RUC6Hi6N404 IRu(C,O,)(en),l ’ ,4,321,429 R L ~ , H , ~ C I N ~~O [ R u C ~ ( N H ~ ) ~ ( ~ - ~ ~4.296 CONH~)]~RuCfiHIRClzN4 [RuCI,{(HzNCH2CHzNHCH2)z)]+,1,300; 4,323 RUC~H~~CI~O~SS RuC13(DMS0)3,2,641: 4,439 [RuCI~(DMSO)~]-, 4.438 RUC6H181N60 [RUI(NH~)~(~-P~CONH~)]’~. 4.304 RUCsH,sNaO [Ru(NH~),(~-~~CONH,)]~+, 4.296 ’

~

RUC<(DMSO),(OH,), 4,438 RuC6H20NSSe IRu(SePh)(NH3),lZ+,4,440

RuCsHz2%

RuC,N,OZS, [RU(NCS)~(CO),]~-, 4,365 RuC6N6 [Ru(CN)4(NC)zIS-. 4,281 [Ru(CN),(NC)],-, 4,281 [RU(CN)6j3-. 1,405; 2 , 9 ; 4,284,476; 6,534 [Ru(CN),]*-, 1,405; 2 , 9 ; 4,281,283,362.476.526 RuC,N,O [Ru(CN),(CNO)]*-, 4,284 RuC6N60J [Ru(CN),(CNO),(O)]’-, 4,284 RuC&Or, [Ru(CNO),]‘ , 2 , 13 RUCgN& [Ru(NCS),(SCNjl3-, 4,365 [Ru(NCS),J3-, 4.365 [RU(SCN)6]‘-. 4.365 RuC606S6 R~(SzCz02)3.4,336 RUc601z [Ru(Cz0,)31Z-, 4,429 [R~(Cz04)3]~-, 4,324,327,429,476 KuC7t t,ClZ {RuC12(nbd)),. 4.347 RuC,H,B r 0,Si RuBr(SiMc,)(CO),, 4,285 RuC~H~O~P Ru(CO),{P(OMe),), 4,371

[Ru(NH3),(2-pyCoMe)lZ+,4,311 RuC,H,nCI,N, .

_

__

I

[Ru(H~NCH~CH~NHCH~)~CH~}C~~]-, 1,300 ,4,295 4,323

[RU(NH~-)~(~-~~CONH,)(OH,)]~+, 4,293, 304, 309 [Ru(NH3),(4-pyCON H,)( OK,)]’+. 4,308

RuC,H2,N6 [Ru(NH,),(NCPh)lZ+, 6,458 [ R u ( N H ~ ) ~ ( N C P ~ 4,302,6,449,450,452 )]~+, RuC,H2,N50 [RU(NH,),(~-P~CHM~OH)]”, 4,311 RuC~H~~N~ [ R u ( N H ~ ) ~ ( ~ - ~ ~ C H = C H1,L369 )]~+. RuC8H4CiN,O9

RuC6HZ1N7

[Ru(NH3),{ HN=cCH=CHC(=NH)CH=cH}]z+, 4, 303 RUC~HZIN~O [Ru(NH3)5(4-pyCONHz)]’+, 4.293 [Ru(NH~)~(~-~~CONH~)]~+, 1,367: 4.296,297 RuC6HzlN,0 [R~(NH~),(7-methylhypoxanthine)]~-, 4,296 RuCsHz4N6 [Ru(en),]’+, 4,321-323 IRu(en),l”+, 4,321,322,324: 6.652

[RuCi<enH)(en)z]2+.4.324 [RuCl(enH)(en),13+. 4.324 RuC6HzsNs [Ru(NH3),(EtC=CEt)lZf. 4.292

R~k<(Cb),(py),4,326 RuCSKN~OIO

RU(OH)(ON=~CONHCONH~O)~(NO). 4.464 RuCSHBCI,O [RuCl,(nbd)(CO)]-, 4,345 RuCsH,,C1,N, RuCI,(NCMe),. 4,365 RuCsH,zN202S4 Ku(S~CKMM~,),(CO),, 4,435 RuC8Hl8Cl3S3

RuC13{S(CH2CHzCHZSMe)z}, 4,433 RuCJT1,Cl,N,O2 [Ru(caffeine)(NH,),Cl,]+, 4,937 RuC8H2,,3r3NOSz RuBr,(SEt,),(NO), 4,362 RUCSH~~CIZN~S~ RuC1z(MeC(S)NHz}4,2,647 RuCsHzoNs

[RU(~’H,),(~;~=CHCH=NCH=~H)~~*+. 4.295

RuCsH2&0

[RU(CNCH,P~)(NH,)~(OH~~]~+, 4,291 RuC8HZ1NS [RU(~=CWCH=NHCH=C:H)(NH,),(F;I=CHCH= RGGCH)]~+, 4,295 RuCfiHZzN, [Ru(CNCHzPh)(NH?)S]”, 4,291 [Ru( CNCHzPh)(NH3),]3+, 4,291

R U C ~ H ~ ~ B ~ ~ O ~ S ~ Cumulative Formula Index

548

4. [Ru{ (02CCH2)2NCH2CH,N(CH2COJ2}(N2)1z-~, RUC~H,~B~~O~S~ 467 RuBr,(DMSO),, 4,437,439 RuC~H,~CIZO~S, RuC~~H~~CINZO~ [RuCl{(02CCH2)2NCHzCH2N(CH&OzH)RuCl,(DMSO),, 4,350,353.437-439.463 RUC~KZ~CI~S~ CHzCO2}]-. 4.467 R u C I ~ ( S M ~4,432 ~)~, RuCIOHT~NZO~ [Ru(OH) { (02CCH2)zNCHzCHzN(CH,C02)2)1" 4, RuCSHZJZO~S~ 466 Ru12(DMS0),,4,437 RuC1oHi4C1NOSa RuCaHzsNs [ R U ( ~ O ~ ) ( N H ~ N H4,364 ~)~]~+, RuCI(McCSCHCSMe),(NOj, 4,362,436 RuCloH14CtNOS RuCgH4N7 Ru(acac),(CI)(NO). 4.362. 464 [Ru(CNj,(~=C€ICII=NCt1=~ HI]'-, 4,282 RuC~H~N~O~ [Ru(C,O,),(NO)(PY)I-, 4.429 RuCsHjN7 [RU(CN),(HN=CHCH=NCH=CH)J~-. 4.326 [RuCIz{02CCH2N(CH2COZH)CH2CH2N(CH*COzH)RuC9HSO3S CH,CO,)l-, 4,467 {Ru(SPh)(CO)3},, 4,431 RuC9HiOO3S (R~S(CO)~(C~HIO)},, 4,430 RuC~H~~C~N~S~ RuC1(S2CNMez),(q2-SCNMez), 4,434 RuCgHlsCIN3Ss RuCI(S,CNMez),, 4,434 RuC9H181N3S, Ru(S2CNMe2)3T,1, 82 RUC9HiaItN3& Ru(S,CNMe&I,, 4,434 RUC~HIBW~S~ Ru(S2CNMeJ3, 4,362,433 RUCgH1&0Se6 Ru(Se,CNMe,),(NO), 4,440 Ru(edta), I, 488 Ru&HZ~CIOZP~ RuCl(Me)(CO),(PMe,),, 4, 386 RuCloHzoCIzS? RuC12(1,4.8,1I-tetraihiacyclotetradecane),4,477 RuC~HZIN~ [RU(NH~)~(~Y)(~~=CHCH=NCH=CH)~~~. 4,295 RuCioH20C1,Sa RuCI,( 1.4 ,S,11-tetrathiai~clotetradecane), 4.477 RuCgH24CIzN4 [RuC1,(H,N(CH,)JNH(CHz),NH(CH,),NH,) I+, 2,56 RUC10H20Nb [Ru(bipy)(KH,),1", 1.336; 4,297 RuC IOH3C105S5 [Ru(b~py)(NH,)~]~--, I. 336; 4, 297 [Ru(DMSO),CI]~+, 4,439 RuClOH1N8O9 RuCioH2~Ns [Ru(ON=&ONHCON H?O)2(\3eCN)( N O ) ]+ ,4,4h5 [RU(NH3)4tPS)2Pi, 4,295 RUC~J-ISCIZN~OZ [Ru(NH3),(p!)2j3', 4,295 Ru(O),Cl,(bipy), 4,352,422 RGoH22Ns [Ru(en),(d~irnidazole)]~+, 4,322 RuClOHsC13NZ RuCl,(bipy), 4, 347 RuCIOHZIC[ZN~ Ru(l,4,8,1 l-tetraazacyclotetradecane)C12,1,301 RuCIOHsC14NZ [Ru(1,4,8.11-tetraazacyclotetradecane)Clz]' 1.300; 1. RuC14(bipy), 4,357 474 [RuCl,(bipy)]-, 4,353,357 [RuCI4(bipy)l2-, 4,353 RUCinHz5N206S3 Ru(Gly-Gly)(DMSO),, 4,466 RUC~OHRNZO~ RuC ,0H30C10SS5 RuOJbipy), 4,352 [RuCI(OSM~~)~~SO M~~)~] ' ,4,438 RuCloHlo RuCp,, 1,337 RuC1uH;oF 1u N 5p, Ru(PF,NMe,),, 4,366 ~uCl"HIoC~2N2Oz RuC~OH~~N~O~P RuOzClz(py)z, 4,327 RttCjoH,oU12N~Sz Ru(NH&{P(OEt);;l(fi;r=CHCH=NCH=CH),4.391 RUC1IHloC13N20 {R~CM~-PYSH)Z},, 4,431 [RuC13(CO)(py)J. 4.326 RuCinH,,Cl,N,O RuCl,(biG)(OH,), 4,353 RUCI~H~~C~~P RuC,oHloC13N RuC13(3-Me-1-Ph-phosphole), 4,418 R~CI,~HC(N%HM. 4,357 RUCiiHi2Nz09 [Ru{(02CCHz)2NCH2CHZN(CHzCOz)z}(C0)]2-, 4. 466 RUC~~H,~CI~NO RuCI~(CO)(CO~)(NCMC), 4,365 RuC1111IyCIINS, RuCl,(EtSCH&H2SEtj(py), 4,432 RUC~~H~~N~OS~ Ru(SZCNEt,),(CO), 4,435 RUCILH~~CI~NSO~S~ RuCl,(adenine)(DMSO),, 4,439 RuC~IHZ~C~~S~

-.

549

Cumulative Formula index

RuCl,{MeC(CH,SEt),}. 4,133 RuCI~HJW~Z [RU(ON=C-O)~]-. 4,464,465 RuCizH6NioOi3 Ru(ON=&2ONHCONHtO),(NOj, 4,465

[Ru(phen)(NH,),]2t, 4.297 RuC1zHziNxOz 4, 31 I IRu(NH3).,( 10-n~ethylisnalloxazine)~~t,

R;c~~H~~c~~os~

RuCIz(CO){MeC'(CTI,SFt),) 4,133 RuC,,H,aC170Sa RU&(CO){MeC(CH,SEt),). 4.433 RuCizHz.J'Js02 [Ru(NH~),(~-~~CONH~)~]~+, 4,295 [ R U ( N H ~ ) , ( ~ - ~ ~ C O Y4,297 H~)~]~+, RuCizHz,PzS, Ru(S,PMe,),(cod). 4.405 RuCizH,oCl&, RuC13(SEt2),, 2,552; 4. 432 KuCI~H~~P~S~ R~(Szt'Etz),, 4,436

[Ru(CNCHZPh)(NH,),(4-pyCONH2), 4,291 RUC14H2&;8

i,HzoN,

550

Cumulative Formula Index RG~HzINO~ Ru(acac)z{0NCH(COMe),).4,362 RUCisHzi06 Ru(acac),, 1,65; 4,423; 6,267,269 [Ru(acac),]-, 4,424 RUCisHziS6 Ru(MeCSCHCSMeL. 4,362,436

RUC~~H~~CIZN? RuCl,(nbd){ HNTH&J2, 4,324 RUCi7H46P4 R U { ( C H ~ ) ~ C M ~ ~ } (4,388 PM~~)~, RuC~~HI~CI~N~O RuCl,(CO)(py)(phen), 4,345 RUC18H14N204

Ru(salen)(CO),, 4,463 RuC, ,H, ,GIN,

[RuC1(2,2'-b1pyrazine)~(NCMc)]+. 4.335 [R~(~~d)(NCMe),(Me0H)]~~,4,365 R'JCI~~ON$~ Ru(S,CNEt,),, 4,433 [ R U ( S ~ C N E ~ ~4,434 )~]+, RuCISH30N3Se6 Ru(Se,CNEt2),, 4,440 RUCijH30N4OS6 Ru(SZCNEt,),(NO), 2, 103;4,362,434 R U GcH,aNo, -I

I ,

[Ru(CNBU')~(NH~NH~)~]~+, 4,364 RGsH4zOzP4 Ru(ql-OAc)(Me)(PMe,),, 4,386,402 RuCisHasClOisP, [RuCI{P(OMe)3}5]+,4,376 RuCi,H&isPs RuMe{P(OMe),},{ P(O)(OMe)>},4,366,386 Ru{P(OMe),},, 4,366,371 RuC15H,,N5S,o Rut(StCNEt,)s, 4,434 RuCisN7 [Ru(NH3)s(Nz)12+,4,300 RuCi6HioCIzNzOz RuCl,(CO)z(NCPh),, 4,365 RUC16HliCI2N3O RuCI,(CO)(terpy), 4,356,392 R~CI~HIZCIZNS RuCI,(2,2'-bipyra~ine)~, 4.335 RuC1,H141z0zSeZ Rulz(CO)z(PhSeCH2CH2SePh),4.440 R~CihHi.iN40~ Ru(ONO)(salen)(NO), 4,463 RUCi6H16NZ06

R ~ ( O A ~ ) ~ ( C O ) ~ (4,326 PY),, R~CI,HI~N~OZ

RUCisHisFiJ'S Ru(PF1)4(PPh,),4,367 RUCiaH,,N606 Fe{ON(NO)Ph),. 2.510 RuC18HlsObSe3 Ru(OzSePh),. 4.440 RuCISHI~S~ Ru(SPh),, 4,431 R G s H i sOzS4 Ru(2.3,8,9-dibenzo-l,4,7.lO-tetrathiacyclodecane)(CO),. 4.436 KUC~~H~~CIN~ RuHCl(cod)(py)z,4,326 RUC18132604 Ru(acac)2(cod), 4,124 RuCixHnO& Ru(EtOSCHCSMe),, 4,436 RuC~~H~~CINZO~P [RuCI(NH=NPh)(CO)z(PButPr,)l+, 4,395 RUCi8H3003

[Ru(q6-Me,C6H,){Me2C(OH)CHzCOMe}(Me,CO)12'. 2,366 I

_

RUC~~H,;N~S

[Ru(MeCN),( SEt,)( cod)12+,4,432 R~CiaH34Ni&4& [R~(adenine),(DMSO)~]~+, 4,438 RuCisH35CIN RuHCI{HN~Hz)5},(.od), 4,457 RuC18H38P4

RuH(~'-Ph)(Ph~PCHzPPh~)~, 4,453 RuC, ,kt,O,P [Ru(oH,),(p(c6H,,),}]+, 4,463 RuC19H,4C12N02P RuCI,(C0)2(2-~yPPh2),4,409;5 , 1107

[RU(CO),(NCM~)~(~~)~]~+, 4,326,345 RuC16HisIzNz0z

R U I ~ ( C ~ ) ~ ( ~ - H ~ 4.381 NC~H~M~)~, RUCi6HzJ" [ R U ( ~ O ~ ) ( N C M ~ 4,365 ),]~+, RUCi6HxN6 [RU(CNCH~P~)~(NH,),]~+, 4,291 RuC,,H,,O,Si, Ru( SiMe,)(CO), { C,H,( SiMe,)) 2. 15, RUClbH2704P Ru(C0).,(PBut3), 4,371 RuC1&13;CiZN4 RuCl,iPr'N=CHCH=NPri)7.2. 210 R U C ~ ~ H ~ ~ N ~ P ~ R ~ H , ( C N B U ' ) ~ ( P M4,452 ~~)~, RUCi6H4zP4 RuEtz(MezPCHzCHzPMe2)z, 4 386 RUCI~H~~P~S~ Ru{(CHz)zSiMez)(PMe3)4, 4,388 RUC16H47CIPs [RuCI(CH2PMe,)(PMe,)4]i ,4,376.386 R ~ C I ~ ~ ~ I S P S [RuMe{P(OMe),),]++4,376,386 R G iClJ'J,Oz RuCl,(CO),(terpy), 4,356 RuCI~H~~C~J'JZ RuCl,(nbd)(bipy), 4,347 RG7Hzz04 Ru(acac)z(nbd), 4,424 -'

I -

,

Ru(CO),(4-MeOC6H4N=CHCH=NC6H4OAMe-4),4, 364 RuC19H,9C130P RuCl,(PPh,)(MeOH). 6 , 258 RuCl9HzzCI2N2 RuC1z(nbd)(H2NPh)z.4,324 RUCI~HZ,CI~OP~ RuCI,( CO)(PMe,Ph),( C,H,), 4,390 RUC,~H~~CI~OS~ RuCI3(SPhPr'),(MeOH). 4,432 RuC H 2 0 P 4 *,H,I(PMe,I,, 4,389 _ _ .. . Ru(8-quinolinolate),(CO),, 4,465 R~CZOHISI~OZP [RuI,(CO),(PPh,)]-. 4,383 RUCzoH16CIN,S [R~Cl(bipy)~S]-, 4,348,349 RuC,,Hi,CIN,O [RuCl(NO)(bipy),]+. 4.348,349 [R~CI(N0)(bipy),]~-, 2,109;4,34&350,354,357 RUC~~H,~CIN~O~ RuCI(NO,)(bipy),. 4,348,349 [R~Cl(NO,)(bipy)~]+, 4,348 RUC,,Hi6CIN,O, [R~Cl(NO,)(bipy)~]',4,348

551

Cumulative Formula Index

RUC22H16N6

[RuC1(NH,)(py)4]+,4,326 R~CzoHzdN402 ~Ru(p~),(OHz)z]~+, 4,327 R~CzoH24N408

[Ru{ 02CCHZN(CH2COzH)CH2CHZN(CHzCO~H)CH,COz)(py)z, 4,467 RuCzoH24~601, [Ru((02CCHJzNCH~C:HzN(CH~COz)z}~(N2)]4 .4,

467 RuCZ~I.IZSCI~~P~ RuCl(COMe)(CO),(PMe,Ph),, 4,386 RUCZIIH~K~J'JSI RuCI3(SPhPr'),(MeCN),4,432 RUCzoH26N6 [Ru(NH,)z(p~),l~+, 4,294 RuC20H280ZP2

[RU(O H ~ H C H = C H N = C~ = N C H =

CHCH=N)z(fi;=CHN=CHCH=cH)]+,4,

RuMez(CO)z(PMeZPh)z, 4,386,388 RUC,OH;~CI~NP~S RuC1,(NS)(PEtzPh)z.2,121 RUC~~H~~CI~I~~OP RuCI2(CO)(py),(PButZMe), 4,392 RUCZOH~ONSSB [ R U ~ N ( S ~ C N E4,435 ~~)~~+, RuC~OHJZCIZNZ RuC12(cod) {H2N(CHJSMe},, 4,324 RuCwHdL [R U ( C Y B U ' ) ~ ( N H ~ N H ~4,364 )~]~+, RuCzoH4sOzPzSiz R U ( S ~ M ~ , ) , ( C O ) ~ ( P4,286 E~~)~, RuCzoH&IP2 RuHCI(depe),, 6,303 R~CziHizN3S6 Ru(benzothiazole-2-thioIate),,4,431 RuC2~1Ii~ClzOzPS RuCIz(CO)z(CS)(PPh3),4,383 RuC21H15C1603PSi2 Ru( SiCl,),(CO),(PPh,), 4,285 RGiHt,WSz Ru(S,CO)(CO),(PPh,), 4,406 RuCalHl6ClN40 [R~Cl(CO)(bipy)2] I , 4,346; 6,269,499 KuCZ1H16N403

Ru(CO;)(bipy),, 4,323,350,351,353 RuCZ1Hl7N40 [R~H(CO)(bipy)~l+, 4,346,459; 6.499 RuCz1HL7O3P RuI.I,(CO)dPPh,), 4,452 RUC,,H~,N,'O~ [Ru(CO)(bipy)2(OHz)]z+,4,346 RuCzI H,qF607PSi -'

~u(PhzPCH,SiMez~H)(CO)z(02CCF3)2. 4, 286 RuCa,H2,CI3N3O3 RuCI,(?,h-lutidine N-oxide12,2.496 RUC21H2'803P2 RuMc(COMe)(CO)z(PMezPh)z,4,386 RuC,iH,&PA Ru(S2P!vlvlez)z(CO)(PMezPh)z,4,405 RuCZ~H~,CIOP~ RuHC1(CO)(PBu'zEt)z,4,457 RUCZIHSINI [ R ~ ( C N B L I ' ) ~ ( N H ~ N M4,364 ~~)~J~+, RUCZZHISO~P Ru(CO)d(PPh,), 4,368,370,371,452 RuCZ~H,~CI,N~OZ RuCIz(CO)2(bipy),,4,357 RUCZZH16N402 [Ru(C0)2(bipy)zJz+, 4,34h RuC2,HiP&, Ru(CzO,)(bipy),, 4,345,353 RG2Hic.Nb Ru(CN),(bipy),. 4,282,345

Cumulative Formula Index

RUCZZHI~N~

552

[Ru(2,2’-bipyra~ine)~]~+. 4,334,335,347; 6,510 [Ru(2,2’-bipyrazine),13+.4,334 [R~(2,2’-bipyrirnidine)~]Z+, 6,5 10

IRu(CN),(biPy),l+, 4,284 R~CdfihN& Ru(NCS),(bipy),, 4,350 Ru(SCN)z(bipy),, 4,284 RUC~~H~~CI~O~P

RuC~~(CO)~(~-CH~=CHC~H~PP~~). 4. 390 RuCzzH1yC1N5 RuCl(bipy),(NCMe), 4,349 [RuCl(bipy),(NCMe)]+, 4,34Y. 353 RG~Hi9N303 Ru(salen)(CO)(py), 4,463 [Ru(salen)(CO)(py) I+,4,463 RuC22HiJJ6O [R~(No)(bipy)~(NCMe)]~’ ,4.348 [Ru(NO)( bipy),( NCMe)13”,4 348 RG~HIYNLI Ru(N3)(bipy),(NCMe) ,4,350 RG&zoN404 R ~ ( C Z O ~ ) ( P4,327 Y)~, RUC~H~ON~S~ Ru(NCS)z(py)s, 4,327 RuCZ~H~~CIN~OS [RuCI(hipy),(DMSO)]+, 4,3513 RuC,~H,~N~O~ R(OMe)2(bipy)z,4,351 RuCmHz4Ns fRu(bipy),(cn)12’ ,4,351 KUC22H24N6 [Ru(bipy)2(en)]2+,4,322 R~CZ.ZH-I,,N~ [Ru(bipy)(en)(~y)~I*+, 4.322 RLIC~~HZ~CIZO~PS~ RuC12(DMS0)2(PPh3),4,408 RUC~ZHZEQ~PZ

Ru(PhN=NPh)2(CO),, 4,468 RUC~~H~~F~NO~P~

RUC22H40N402SR

RUc25H19NS0Z

RLI(T~~-O~CCF~)~(PF~NMC~)(PP~~), 4,402 RUC,~H~,N~ [Ru(bipy),(McCN),J”, 4,334,348,361; 6,29 RuC24H2nNbOS [ R U ( N C S ) ( ~ ~ ~ ~ ) ~ (’ D ,4,350 MF)] RUC24H26N102 [ R ~ ( b i p y ) ~ ( D M E )4,351; l ~ + , 6 , 532 RUC24H2bN104

Ru(OAc)z(py),. 4.426 R~CuH28402 [R~(bipy)~(EtOH),]~+, 4.353 RUC~~H~~NZO~P~ Ru(N03)z(PMe2Ph)3,4, 401 RUC~~H~~C~~NZP~ RUCI,(NH~NH,)(PM~,P~)~, 4,391 RuC,,H~,N~O, 4: 426 Ru(OAC)~(BU‘NC)~, RuCdLPA 4,405 Ru(S2PEt2)z(PMezPh)2, RuC24HS4N401SP2

Ru(NO)(NO,),( OP(ORu),}2, 6,942 KuCz4H,~Cl,01,P4 RuCl,{P(O€t),},: 4,378 RuCzSH,9Cli\ls [RuCl(bipy)(terpy)]+. 4$356, 357 RuCZSHIJ’JSO Ru(COMe)z(C0)2(PMezPh)2+ 4.386 [Ru(0)(terpy)(bipy)]z+,4, 357 RuC~~H~~CIP~ RUCZsHi9N60 R U ( ~ - ~ ~ ) ( C I ) ( M ~ ~ P C H 4,386 ~ C H ~ P M ~ ~ ] ~ . [Ru(NO)(terpy)(bipy)13+, 4, 356 [Ru(CO)z(S,CNEt,),]+, 2.586 Ru‘%HJ‘J, [Ru(bipy)(TMEDA),]”, 4,322

[Ru(NO,)(terpy)(bipv)J+,4,356 RuC,,I-I,,N,O, [Ru(N03)(tcrpy)(bipv)12’ ,4, 356 RUC~~H~~N~O RUCZZH40P4 RuH(2-np)(Ph,PCH,IJP‘h,)z, 4,453 [Ru(OH)(terpV)(b;py)12+, 4,357 RUC~~H~~CIO~P~ RUC,~H~~CIN, RuHC1(CO)Z(PBu‘Pr,)z,4,457 [RuCl(bipy),(py)]*. 1 , 336; 4, 348,350, 357; 6.30 RuC~~H,,CI~O~P [RuCl(bipy),(py)lz+,1 , 336; 4,357 R u C ~ ~ ( C O ) ~ ( ~ - C H ~ = C H C4.~390 H ~ P P ~ ~ ) > RuCZ5H2,N50 R~Cz3H1703P [R~O(bipy)~(py)]~’, 1,332,334; 4, 351,352 R U ( C O ) ~ ( ~ - H ~ C = C H C ~4.372 H~PP~~)~ [Ru(rerpy)(bipy)(OH2)l2+,4,356,357 R~C23HiyClN40 [Ru(terpy)(bipy)(OH,)P+, 4,357 ~RuCl(bipy),(OCMe,)]-, 4,357 RuC~SH~IN~O RUC~~H,~CI,O,PS [Ru(NO)(b~py),(py)13‘,4,349,350 RuClz(C0)3(Ph,PCH2CHzSI’h) 4: 409 RUC25H21N602 RuC,~H~,CIN~O [R~(NOz)(bipy),(py)]+,4,348,349 [R~Cl(bipy)~(OCMe~)]+. 4, 34Y 360 RuCa5HaIN603 RuCzdmNzOz [Ru(N03)(bi~v)z(~y)j*. 4,349 Ru(salen)(nbd), 4,463 RuCzsHz2N,O RuC2,H24C1,05PSiz [R~(OH)(bipy)~(py)]~’~ 4,351 Ru(SiC13)z(CO)z(PPh3){P(OMe)3). 4,286 RUCxHz2N6 [R~(terpy)(bipy)(NH,)]~~, 4,356 R~CZ&IO~P~S, [Ru(S2CH)(PMeZPh),{P(OMe),} J’. 4,406 [Ru(terpy)(bipy)(NH3)l3-, 4,297 RUC~~H~OCINOPZ RuC25Hz3ClNS RuHCI(CO)(CNMe)(PBut2Et), , 4, 457 [RuCl(bipy)(py)31Tl4.348 RUC21H12F903S6 RuC25HZ3N50 RU{SCH=CHCH=CC(S)=CHCOCF~}~, 2, 65 2 [Ru(bipy),(py)(0H2)]2+, 1,334; 4,35@352 RuC,,H, ,CI,N, [RU(~~PY)~(PY)(O -4,351 H~)I~. RuCl,(phen),, 4,353 RUC25H24N6 RUC24H1605P [R.(biPY)a(PY)(NH3)1’t, 4,349 Ru(hfacac),(CO)(PPh,). 2.375 RuC~,H,,N,OPS, Ru(SzCNMe2),(CO)(PPh,), 4,405 RuC2sH.&lN023 RuCI(NO,)(CO)(PM~~P~)~, 4,401 [RU(2~2’-bipyra~ine)~]+, 4,334 RuC~~H~~CIZOP~ I

553

Curnulutive Formula Index

RuC1z(CO)(PMezPh)3,4.381 RUC~SH~~CIZO~P~S RuC~,(CS~{P(OMe),Phl.,, 4.383 .~ RUC~~H;~NO~P; ~~

RuMe(COMe)(CO)(CNBu')(PMe,Ph),,4, 387 RuC2&,N, [ R ~ H ( C N B U ~ ) ,4,458 ~+. RuCz,HsoNsS,o [Ru(S,CNE~,),]+~ 4: 1055

RGOR16Nfl

Ru(CO)~(PBU'~),, 4,371 RUCZSH&IZI\TI

R~C1~{2-(2'-pyridyl)quinoline}~, 4,353 RUC~~HZ~CIZN~O~ RuClz{PhCOC(Ph)=NOH} { PhCOC(Ph)=NO) 464

. 4.

RUCZ6H12N20i0

Ru,(CO),(X-quinolinolate),, 4.46s RuCz6H,,F,,PS, [Ru{S,Cz(CF,)z),(PPh,)I-, 4,406 RuCxHid40, [Ru(CO),(phen),lZ', 4, 345 RUCZ~HI~N~ Ru(CN),(phen),, 4,282 RUCZ~HISN~~ZS~

Ru(benzothiaz0le-2-thiolate),(py)~(CO)~,4,431 RuCXHI~F~N~O~S

[R~(O,SCF~)(terpy)(bip!;)]+~ 4.357 [Ru(O3SCF3)(terpy)(bipy)I2+.4,357 RUCz6HzoN6

[Ru(bipy),(N=~CH=CHCH=CH~=N),4,335 RuC~~H,OO~P,S~ Ru(SZPPh2)2(C0)?,4,436 RUCL6Hz1ClN502 [Ru(bipy),(4-pyCOzH)CI]+. 6.70 [RuCI{ N( O)C,H40H}(bipy)2]+. 4.349 R~Cz.&ziN703 [Ru(N0,)(4-pyCONHz)(bipy),l+. 4,348 RUC~~HZ~C~~N~O~ RuC12(HON=CPhN=NPh)2>4.364 RUCz6HnNh [ Ru(bipy),{ (NH)zC6H4}]'+,4>335 RUCz6HzzN8 Ru(bipy)z(r;iCH=NCH=~H~z,4,359 RUC~~H~~CINO~P RuCl(r11-C3Hs)(CO),(PPh,)(~'~MeCH=CN), 4, 390

[Ru(terpy)(bip)i)(NCMe,)li ' , 2 , 127; 4, 356 RUC~SH~~~LPZ RuH2(CO)z(dppe),4,452 R~CzsH2sCl3S4 RuC13(PhSCHzCH2SPh),, 4,432 C2 8 28 6 [Ru(terpy)(bipy)(NHZPr1)]*+, 4,356 RUC~~H~~CIN,P, [RuCl(phen)(PMe,Ph),]+, 4,392 RUC~~H~~CI~N~P~ RuCl,(phen)(PMe,Ph),, 4,392 RuC,,H,,CIOP KuCI(Me)(cod){ PPh2(C,II,0Mc-2)1., 4,4U9

[ R u ( ~ o d ) ( p y ) ~ ]4,326; ~ * , 6,269 RUC~~H~~CINOP~

RuC1(Ph)(C0)(CNBut)(PMe,Ph),,4. 38.1

RUC26H24N6

[ R ~ ( p h e n ) ~ ( e n 4) ?] 322 ~~ RuCZ,H26CIlzNOPz RuCIIz(NO)(PMePhz)2,4.394 RuCz6Hz6C1NOP2 RuCI(NO)(PMePh&. 4. 394 RUC~~HZ~C~~NOP~ RuC13(NO)(PMePh2)2.4. 393 RUC26HzsN40z [ R ~ ( b i p y ) , ( O C M e ~ ) 4.351,359 ~]~+~ RUCZ~H~~CIZNZP~ RuC12(bipy)(PMe2Ph)2. 4.392 RuC,,H3003P2 RuPh(COMe)(CO)2(PMezPh),.4,386 RuC,,H,,CI,OP, RuCIz(EtOH)(PMe2Ph);,4. 399 I

[Ru(nbd)(bipy),l2-, 4, 347 RUCZ~HMN~

[Ru(bipy),(2-pyC(Me)=NH)]*+, 4.336 [Ru(bipy)2(py)(MeCN)]2+,4.352; 6,29 RuC,,Hw.N, ., [Ru(bipy),(2-pyCHMeNH2)Iz ' ,4,336 RuCZ~HZ~P~ [ R U I ~ ( P ~ ~ P C H Z C H ~ C H ~ P4.459 P~,)Z]+. RuC,,H,,N,O,

{P(OMe)3)3]+.4,385 RuC30Hi5Br3F903S3 Ru { 3-BrC6H,C(S)=CHCOCF3}?. 2.652 RUC30Hi5CljF903S3 Ru{~-CIC~H~C(S)=CHCOCF,),, 2,652 RUC30HI8F903S3 Ru{PhC(S)=CHCOCF3),, 2,652 RuC3oH,zN, [ R ~ ( t e r p y ) ~4,354 ]~~, [ R u ( t e r ~ y ) ~ ]4,350 ~-, RGOH22NR [ R u ( p h e n ) , ( d ~ i m i d a ~ o l ~4,322 )]~~, RGoHzJN~ Ru(bipy), 4,327 [R+pj),j-, 4,327 [Ru(bipy),]+, 1,404,4,327,332,1002: 6,25.499,509, 526,531 [Ru(bipy)#+, 1,64,335,336,348,349.351. 355.357, 394,396,400,404,409,490,495.539: 4.289, 290,327,328,332-335,345,347,350, 351.784. 1001.5,836; 6, 15, 16,23,25.26,29. 31.400. 198,499,500,501,502,505,506.507.508.509,

510,513,515,517,519,520,521.523.525,526, 527,528,529,530,531,552 [ K ~ ( h i p y ) ~ 1,332,73h,348.349.351,356.3Y6,404. ]~+, 49(1; 4,372,335,350. 1001; 6,16,25,31.499, 509,515,516,517.519,523,524,52h. 530. 531 RuC30H26F303PZ

Ru(0,CCF3)(CO){Ph2P(CHz),PPh2) 6.235 I

RUC~OHZ~N~ I R u ( b i p ~ ) ~ ~ p y4,348 )~l+~

RuC3O H 2 8 6

5 54

Cumulative Forrnulu h d e x RuClz(py)x(PPh,), 4, 391 RUC33H30N302P

[Ru(te~py)(OH,)~(PPh~)]~+, 4,356 RuG~H~~C~~PZ RuCl,(PMePh,),(nbd), 4,390 RUC33H45P4SZ [Ru(S2CHPMe2Ph)(PMezPh),]+, 4,406 [Ru(S2CH)(PMe2Ph),]+, 4,406 RuC,&LOP, [ R u H ( M ~ O H ) ( P M ~ , P ~,4,399,458 )~J RIICJ&L WJ [Ru(MczC0)3(PMezPh),d'+, 4,39Y RUC34H24N6

[ R ~ ( b i p y ) ( p h e n ) ~ ]4.335,345 ~-. RUCWHZGN~ [Ru(phen),(p>),l2'. 4347,348,353 RUC~~HZ~CI~NZPZ R~C12(2-~yPPh2)z, 4.409 RuC34HzsN202P RuCl(salen)(PPh,). 4.397 RUC34H3oN6 [Ru(bipv),(4-HzC=CHpy)Zlz+, 6,30 [Ru(CNCH,Ph),(bipy),j'+, 4,351 Ru{ C(Me)=NBu'}(C0Me)(CO)(CNBu')(PMc2Ph),, RUC34H3aN602 4,388 [Ru{N(0)C,H,Mtt},(bipy)2]2+, 4,349 RuCdhCIP, [KuCI{PhP(CM2CH2PPh2)2}] I , 4, 380 RuC~~H~~OPI Ku(CO)(dppm)(cod), 4,372 RuCl,(acac)(dppe), 4,417 KuC~~H~~CINZP~ [RuC1{2-(PhlPCH,CH2)py},]+, 4,408 RGiH3iNq Ru{HC(~~N=CHCH=~H)~}(~-~~CH=CH,)~]~+,~, RuC~~H~~CIZNZPZ 357 RuCIz{2-(Ph2PCH,CH,)py),, 4,408 R~C31H4jClzOP3 RuC~~H~~CIN~P~ RuCIZ(CO)(PEt,Ph),, 4,381 [RuCI(bipy)(PMe,Ph),]+. 4,392 RuC3,H,,BrOP3 RuC~~H~~NOP~ R u H B c ( C O ) ( P F ~ ~ P6~, )303 ~, RuP~(COP~)(CNBU')(PM~,P~)~. 4,387 RuC~ZH~CCINB RuC~~H~~CIP~ Ru(phthalocyanine)CI, 2,867; 4,474.175 RuC1(Ph2PCH2CH2CH2PMez)2r 4,376 R u C d inNs RUC~&L,OJ', Ru(phtha1ocvaninc). 2,867; 4,174

[Ru(bi~y)~(phen)]'+, 4,335,345 RUC32Hd6 ~ R u ( b i p y ) ( ~ h e n ) ( p y ) ~4,348 l~+, RuC32H28C1N204P R u C ~ ( ~ - H O C ~ H ~ C H = N O2-HOC6H4CH=NO)H)( (PPh,), 4, 398 RuC32HzsNz02S4 IRu{SZCN(CHZP~)~}Z(CO)~]+. 4.135

[Ru(NfI,N€IMe),{P( OMe)2Ph}4]z+,4,391 RUC~SH~SCI~N~P [RuC12(PhCN)(bipy)(PPh3)]+,4,417 RUC35H30NSPS2 R ~ ( N C S ) Z ( P Y ) ~ ( P4,392 P~~), RGsH~JOZPZ Ru(COj,(dppm)(cod), 4, 372 R U C ~ S H ~ ~ [Rh(nhd)(dpph)]' , 6 >241 R U C ~ ~ ( ~ - M ~ O C , H ~ N = C H C : H = N C ~ H ~ ORUC35H31N90 M~-~}~,~, 364 Ru(phthalocyanine)(CO)(NCMe), 4,475 RuCJ I,,CIN,O, [RhCl(2,6-lutidine N-oxidc),] 2c,2,496 388 RuC3,H490zP,S RLIC~,H,ON~O,P,S, RU(SOCP~)~(~~)(PM~,P~),. 4.407 [Ru(SOCOEt)(PMe,Ph),]+, 4,407 RGzHwP4 RGJhoNOzP4 [ R U H ~ ( P M ~ , P ~4,462 )~]+, [ R U ( O ~ C N M ~ ~ ) ( P M ~4.404 ~P~)~]-, RUC&i6NsO R~C3sH5W"Sz Ru(phthalocyanine)(CO), 2. 867; 4. 474 IRu(S*CNMe,l(PMe,Ph),If, 4,405 R u C ~ ~ H ~ ~ F ~ ~ ~ - S ~ R;C~~H~ONIO Ru{ 3-MeC6H4C(S)=CHC0CF,),. 2.652 { Ru(phthalocyanine)(&=CHCH=NCH=eH)} RU{~-M~C,H,C(S)=CHCOCF~]~~ 2.652 474 RG~H~sN,O [Ru{2-OC6H4)benzimidazole)(b~py)2] ' 4,354 RuC,,H,,CI,N,P RuCl,~PPh3)~terpy), 4,356. 392 RuC~~H~SN~ [R~(bipy),(4-Me-4'-H~C=CHbipy)~~', 6,30 RUC~~H~~CIZN~P ~

~

4.

555

Cumulative Formula Index

..

.. .

RuC38H30CIZOP2Se

.

[Ru(bipy),{ bipy-4,4'-(C02NHC12Hzs)z}]2+7 6,506 RuCd&iCI,P, RuC1, { PhP[ CH,CH,CH,P(C+.H, 1)2]z}, 4,380 RuC36H72PZ

RUH6{P(C6H11)3)zI4,463

Ru(NO)(NO~),{(BUO),PO}~, 1 541 RuC~~H~SN~O~P~ WC0)3(PhJ'py),, 5, 1107 RUC~~H&IOP~ ~ucl(C6H,~Phz)(CO)(PPh3), 4,389 RUC~~H~~B~NO~P~ RuBr(C0) (NO) (PPh3)2,4,368 RUC~~H~~CINO~P~ RuCI(CO)(NO)(PPh,),, 4,368 RuC~,H~,CI~OP, RuC13(CO)(PPh3)2,4,383 RUC~~H~~CI~P~S [RuCI,(CS)(PPh,),]-, 4,383 RuC37H30N203P2

Ru(C0)3(PhzPpy)2.4,370 RuC~~HIONLW'~ R u ( N O ~ ) ~ ( C O ) ( P P ~4,401 ~)Z, RuC37H31BrOP1 R u H B ~ ( C O ) ( P P ~ ,2,204 )~, RuC3,H3,CIOP2 RuHCI(CO)(PPh3)?, 2,204 RUC~~H~INOJ'Z RuH( NO,)( CO)(PPh3)2,4,401 RuC37H3,C120P2S RuCl,(OH,)(CS)(PPh,)2,4, 383, 399 R~C~TH&W&'~ RuClz(OH,)(CO)(PPh3),, 4,399 RuC3,H3d&OP, RuCI,(PPh,),(MeOH), 4,377 RUC37H37C120P3

RuCI~(CO){PhP(CHzCH2CHzPPh,)2},4,383 RuG~H~s~OP~

RUH~(CO)(P~P(CH~CH~CHZPP~~)~}, 4.451 RG7H3903Pz [RuH(H ,O)~(M~O H )(PP~,)~]+, 4,399,459 RuC37H44BrN40 Ru(octaethylporphyrin)(Br)(CO), 4,471 RG7H44N40 Ru(octaethylporphyrin)(CO), 4,469,471,472 [Ru(octaethylporphyrin)(CO)] +,4,471 RUC37H47N502 Ru(octaethylporphyrin)(OMe)(NO), 4,473 RuC?~H,~CI,OP~ RuCI~(CO){PHP{CH~CH~CH~P(C~H~ 1 ) 2 } 2 } , 4.383 RuC,,H~~CI,OP, R ~ C I I ( C O ) { P ( C ~ H ~4,381 ~)~}~. RuC3,H6,C10P, R ~ H C I ( C O ) ( P ( C ~ H I Y4,457 )~}~. RuC~,H~~C~O~P,S R~~TC~(CO){P(C~H~,),}~(SOZ), 4,408,457 RGaH2iN90 Ru(phthalocyanine)(py)(CO), 2,867; 4,475 RuC38H2802P2

RuH,(CO),(S-Ph-dibenzoph~sphole)~.4,452 RuC~~H~~CIN~O~PZS> [RUCI(N~S~)(CO)~(PP~,),~', 2, 120; 4.398 KuC,@,,CI,OPS RuCI,(CO)(CS)(PPh,), 4.383 RuC3,H3,C120P2S R u C ~ ~ ( C O ) ( C S ) ( P P4,383 ~~)~, RUC~~H,~C~,OP~S~

R I I C ~ ~ H ~ ~ C I ~ O P ~ S ~ Cuinulative Formula Index

556

Ru(octaethylporphyrin)(CO),, 4,469 RuC,,H,,N, [Ru~o~~acthylporphynn)( CN )*I-, 4,473 RGBH,J'J@, Ru(octaethylporphyrin)(02)(NCMe), 4,473 RuC~SH~~C~ZP~ RuCI,(PPh3)(ButPCH=CMeCMe=~H),,2, 1042

RuCI,(CS)( MeOH)(PPh3)1 , 4,383 399 RuC3xH34CI,02P, RuCl,(CO)(MeOH)(PPh,), .4,399 RuCl,{ PPhz(C6H40Me-2)}2,4,408 [RuC1,{PPh,(C,H40Me-2)},]+, 4.418 R u C ~ ~ P Z R U H ? ( M ~ C N ) ( P P4,452 ~~)~, RUC3sH36N604 [R~(bipy),{bipy-4,4'-(CO~Pr')~)]~+. 6.531 RuC3&3@zP3 Ru(C0)z{PhP(CHzCH2CH2PPh2)2). 1.372 [Ru(CO),{PhP(CH,CHzCH,PPh2)2)]2-, 4,383 RUC~SH~SFCN" RuH~(PF~)(PF~NMc~)(PP~~)~. 4.451 RuC3sH3803P4S2 Ru(S,PMez){(Ph,PO),H,J, 4,405

RUC~,,H,,NOP~S, Ru(CN)(q2-CS2Me)(CO)(PPh,),, 4,283,406 KuC4nH??O,P,S, .. _ _ . Ru(co),{c(s)5Me}(rrh3)~,2,581 [Ru(T)~-CS,MC)( CO)z( PPh3)J , 4,406 RuC,,,H3,CIzO,P2 RuCl,(CO),{ PPh,(C,H,OMe-2) } ,, 4,409 +

Cumulative Formula Index

557

RuCl(C0Et)(CO)(PPh3)z 4.387 RUC~OH~~C~ZN~PZ RuClz(MeCN)2(PPh3)2,4,396 RuC4oH3604Pz Ru(+OAc),(PPh;),, 4,402:6.234,258 RuC4oH37ClZNOP2S RuCl,(CS)(PPh3)2(DMF), 4.399 RuC4oH37ClzNOzPz RuCl,(CO)(DMF)(YPh,),, 4.383.399 RuCl,(HONCMeCOMe)(PPh,),, 4,397 R~C40H38ClzNzOzPz R U C I ~ ( H ~ D M G ) ( ? P4,347 ~~)~, RuC~~H~~CIZPZS~ {RuClz(Ph2PCH2CHZSPh)2),,,4+409 R~C~VH~SNZOPZ ~

[Ru(OH,)(M~CN)~(PP~,),]~ ' .4,397

RuC~OH~~CIO~P~S [RuCl(CS){P(OMe)Ph,},]+, 4,383 RuC~OH~~C~O~P~ (RuCl(CO){P(OMe)Ph,)3]+. 4,382 RuC~OH~~CIZOP~ RuCl,(CO)(PMePh,),, 4,390 RuC~OH~~CI~O~P~ RuClz(CO){P(OMe)Phz}3~ 4.381 RuCwHwN207P~ Ru(NO,),(CO)(PMePh,),, 4.401 RuC40H40C12NZPZ RuClz{PPh2(C6H4NMc2)}2, 4,408 RuC~~I~~~C-IZOP~ RuCl,{ 1,2-(MePhP),C,H,} (2(MePhP)C,H,P(O)MePh}, 4,380 RuC~OH~IOP~ RuHz(CO)(PMePhz)3,4,451 RuGoH~zP~S~ Ru(SZPMez)Z(PPh3)2r 4,405 R~C4oH4704P4 [RUH(CO){P(OM~)~) {PhP(C'H,CH,CHzPPhz)z}]+l 4,

460 RuC,oH,,ClN,P, [RuCl(3,4,7,t;-Me,pliei~)(Ph.se,Phj,li. 4.302 RUC~OHS~NOPS [ R U ( N O ~ ) ( P M ~ ~ P4.301 ~)~]+, RuC40H56P5 [RuH(PMe,Ph),]', 4,458 RUC~OH~Z~~'~ RuHZ{P(OEt)zPh},, 4,451 RuC~OH~OCIF~N~~P [RuCl(MefiCH,CH,NMet= ~NMeCHzCH,P1'Mel,(PF,j]-, 4,385 RUC~IH~OF~~PZSZ Ru{S,C,(CF,)z}(CO)(PPh,),, 4:406 RUC41H30F605P2

6,235 Ru(O,CCF~),(CO)(PP~,)~~ RuC,,H,,CIN, [RuCl(terpy)(pyCH=CHPh)3j-; 4,356 RuC4,H3,N3OP [Ru(q-CH,Ph)(Co)(PPh,)(terpy)]+, 4:356,392 RUC~IH~~OPZ Ru(CO)(2-HzGCHC6H4PPhz)2 4.372 RuC41H&IOPz

Ru(2-CHMeC6H4PPh,)CI(C0)(2-CHz= C H C ~ H ~ P P ~4,390 I~), RUC41H&13NPZ RuCl,(PPh3)z(py), 4,416 RuC~~H~~NZOPZS~

RuC,,H,,NP,Si,

[ R U H ( C ~ ) ( M ~ C N ) ~ ( P P4,459 ~~),~+, RUC~~H~~C~~OP~S~

RuClZ(CO)(PhzPCH,CH,SPh)2, 4,410 RLIC~IH~~C~~NO~PZ

RUCI~(CO)(ACNM~~)(PP~~)~, 4,399 RuC~,H~~NP~

RuH(q-C3H5)(MeCN)(PPh3),, 4,457 RuC~IHWOPZ RuH(CO)(PPh3)z(THF), 4,39Y RuC1,kI&rNj Ru(nctaethylporphyrin)(Br)(py), 4,472 R G I H ~ J ~ Ru(octaethylporphyrin)(CO)(TNF), 4,470 RuC42H20C12NP2S R~CI~(CS)(PY)(PP~,),, 4,392 RuC~~HZ~FPO~S~

Ru{~-C~~H~C(S)=CHCOCF~}~, 2,652 RUCaHx.Nio Ru(phthalocyanine)(py),, 2,867; 4,475 RUC~~H~OC~~~ZPZ RUC12(C6CI402)(PPh,)2,4,400 RuC&,oS6 R U ( S ~ C ~4,436 P~~)~~ RUC~~FT~~F~O~PZ RuH(hfacac)(CO)(PPhJz, 2,375;4,300 RG2H&W22

RUC~~(CO)?(~-CH?=CHC~H~PP~~)~, 4,390

R U C ~ ~ H ~ ~ O ~ P ~

Ru(C0)2(2-H12C=CHC6H4PPh,)2, 4,372 R U ( C ~ ) ~ ( Z - P ~ ~ P C ~ H ~ C H = C H C H M ~4, C,H~PP~~-~) 372 RuC~~H~~CI~N~P~ [RuCI2(N,Ph)(PPh3),]+,2,134 RuC~~H~~CI~N~P~ RuC13(N2Ph)(PPh3)z, 2,134,139 RUC~ZH~~N~PZS~ Ru(NCS)2(Md2N)2(PPh3)z,4,397 RUC42bN6

[R~(4,7-Me,phcn),]~+, 6,506 KUC:42H37C103P2 RuCl(acac)(CO)(?Ph,),, 4,400 RuC~~H~,NC)~P~ Ru(acac)(CO)(NO,)(PPh,),, 2,375; 4,400 RuC4,H,,C1,O2P2S2

RuCI2(CO)z(Ph2PCHzCHzSPh)z,4,409 RuC~~H~&J'Z RuH(acac)(CO)(PPh,),, 2,375;4,400 R~C~ZH~FJ'~ R u H ( P P ~ ~ ) ~ ( ~ -4,457 C~H~), RuC~ZH~~C~~O~P~S RuCl,(CO)(SO,)(triphos), 4,382 RuCdLoCLF4P4

(RuC12(PF?CH2CH=CH2)2(PPh3)2},,~ 4.378

RUC~~H~~NP~

KuH(~~~-C~H~)(M~.CN)(PP~~),, 4,457 KuCq,H&lP, [RuCl{(Ph,PCHzCH,PPhCH,)z}l+, 4,377 RuC~IH~~C~~NP~ RuC12(N(CHzCH2PPhz)3}, 4,380 RG~H~ZNJ'~

R~(N~)~{N(CHZCHZPP~Z)~}, 4,394 RuC~~H~ZO~P~

[RU(~~-OAC)(CO)(PM~P~~)~, 4,403

RuC42H43C12NOPZ RuCl2(HON=CMeBu')(PPh,),, KUC,,H,,Cl,N,O,P,

4,397

RuClz(HON=CMc2)2(PPh3)2, 4,397 RuC~~H~J'~ RuH2(PMePh2)4,4,451 RuC*2H,,P3 RuH(yC3HS)(PMePh2),,4,457 RuC4,HJ9NPZSi2 RuH{N(SiMe3),}(PPh3),, 4,457

Cumulutive Formula Index

RGZH49N50

RuC4ZH49N50 Ru(octaethy1porphyrin) (CO)(py). I , 495 ; 4 47 1-473 [Ru(~ctaethylporphyrin)(CO)(py)]~+ 4,171 RGzH49NsS Ru(octaethylporphyrin)(CS) (py). 4, -173 RUC4zH4d6 Ru(octaethylporphyrin)(CN)(py). . . .. 4,473 RuC4;HS5F3OZP5 [R U ( ~ ~ - O ~ C C F ~ ) ( P M +, ~ 4.403 ,P~)~]

558

RUC~(;~~CH,CH~)(CO)(PP~~)~, 4,389 RUC~~H~ZNZOJ'Z

Ru(OAc),(CNMe),(PPh,),.4, 384

RUC~~H~~BTN~OP~

RuBr(CO)(PPh,),(CH,=C(Me)NC(H)NPr'}, 2,204 RuC44H,,ClN>OP,

RuCl{CH2~C(Mc)NCHNPr}(CO)(PPh,),, 4,395 RuCA,Hd,NOP,S,

RUHCI(PPI&(P~'N=CHCH=NP~~), 2,210 RuC44H48C10P4S [RuCl(DMSO) { (PhzPCHzCHzPPhCHz)z}]+, 4,377 RuCS~H~~NZPZ RuHZ(PPh,)z(Pr'N=CHCH=NPr'), 2,210 RUC~~H~~OZP~S~~ R U ( S I M ~ ~ ) ~ ( C O ) ~4,286 (PP~~)~. RuC~~H,&IOP,S~ [RuC1(MeOH)(SZCPEtPhz)(PEtPh,),~+, 4,407 RuC',,H,,N,O Ru(octaethylporphyrin)( N,Ph)( EtOH), 2, 836 RuC4sH28ClN40 Ru(tetraphenylporphyrin)Cl(CO), 4,469

[Ru( b$y),(py)(OPPh3)]2', 4,352 RuC~~H~~C~~NZOP~ { RUCIZ(NNC~H~OMC-~)(PP~~)~}~, 4.395 Ru(te trap henylporphyrin)(CO) ,4,472 RuC~~H~~C~~NZPZ R U C I ~ ( N ~ C ~ H ~ M ~ - 2, ~ )136; ( P4,394 P~~)~, RUGSH~SN~OI~S~ R~{(4-0~SC~H,),porphyrin)}(CO)]~-, 4,472 RdkH3sClzPz RuC45H37C1N9P3 R~Cl,(P Ph~)~(nbd), 4,390 R u H C._ ~ ~ ( ~ - P,V4.409 )~P)~. RuC~~H~~C~OZP~ RLIC~~H~,CIO~P~ IR~Cl(CO)~(triphos)]+, 4,383 r\uCI(2-MeCdC,H4)(CO)(PPh,)2, 4,389 RuC~~H~~CIO~PZ RuC1(COChH,Me-4KCO)(PPh,),, 4,387 RuCI(Me02CCH2CHC02Me)(CO)(PPh,),, 4,384 Ruc43w39CIP2 RuHCl(PPh,),(nbd), 4,457 R~C43H3902P3 Ru(CO),(triphos). 4,372 RuC~~H~ONOPZS~ [RU(S,CNE~Z)(CO)(CS)(PP~,),I',4,406 RuC~~H~SC~ZP~SZ IiuClz(SzCPEtPhz)(PEtPh2)z, 4.407 RuC43H47OP3 RuHz(CO)(PEtPh,),, 4,451 RUC43H5zN6 Ru(octaethylporphyrin)(NCMe)(py), 4.472 [Ru(octaethylporphyrin)(NCMe)(py)l+.4.472 RuC44HClNZOPz RuC~(CO)(PP~~)~{CH~=C(M~)NC(H)NP~'}, 2,204 RuC~~H~OCLOJ'~ RU~~-~~C~CI~)(C~)Z(PP~,),. 4.401 Ru(CO),(CNC6H4Me-4)(PPh,),,4,371 [ R U ( ~ - ~ Z C ~ C ~ ~ ) ( C ~ ) Z4,418 (PP~~)~] RLICLAH~~NOIP? RGaH3oFizPzS4 Ru(CO3)(CO)(CNC6H4Me-4)(PPh?)2, 4,371.384.4U2 Ru { S&( CF3)z)2( PPh3)z. 4,406 RUC~~H~&INO~PZ R~Cd330zP3 RuCI(CO)~(CONHC~H~M~-~)(PP~~)~, 4,391 Ru(CO)Z{P~P(C~H~PP~~-Z)~}. 4,372 RuC~~H~~C~~NOPZ RuC~JLC~ZN~P~ [R~Cl,(bipy)(PPh~)~]+. 4,417 RUC~Z(CO)(CNC~H~CI-~)(PP~~)~ 4.384 RuC~~H~~CIO~PZ RuC~~H~~NZPZ RuH( C6H4PPhz)(bipy)(PPh3),4,455 RuCl(q2-OZCPh)(CO)(PPh3),, 4,387,403 RUC~~H~~FINZOZP~ R~C~~H~SNZPZS~ R~(2-pyS)z(PPhi)z,4.431 [RuI(NzHC~H~F-~)(CO)~(PP~~)~]-. 4,364 KUC~~H~OC~ZN~P~ RuC44H35N202P2 [Ru(CO)~(N~P~)(PP~,)~]+. 2. 131 RuCIZ(py)Z(PPh3)2,4,391 RUC~~H~~CIN~OZPZ RUC~~H~ONZPZ RuH,(bipy)(PPh,),. 4.452 [RuCl( NH=NPh)( CO),( PPh3)J -.4.395 RuC4.+LoNJ'z RUC44H36N202PZ RuH(NNPh)(C0),(PPh3),, 4. 395 [R~(bipy)~(dppc)l~-, 4,351 RuC4,H4,CIZNOPz RuC~~H~~F~OSPZ Ru( OzCCF3)(acac)(CO)(PPh3),. 4.400 RUCI,(CO)(HCNM~C,H~M~-~)(PP~~)~, 4,384 _ r l -

+.

RUC46H4404P~ R u ( a c a ~ ) ~ ( P P h4,400 ~)~, RuC46Hs4N6 Ru(octaethylporphyrin)(py),, 2.836; 4.471-473 [Ru(octaethylporphyrin)(pp),]+. 4.471 RG7H34N40z Ru(tetraphenylporphyrin)(CO)(EtOH), 2,836; 4,469 . . RUC~,H~~NO~P~

RUC~OH~~N~OF~

kuH(PhN=NCH=NNPh)(CO)(PPh,),,

4,396

RuC,,H,,CI,P,

Ru(CO)(OAC)(HC=NC~H,MC-~)(PP~,)~, 4,384 RuC~,H~,CINO,P~ RuCI(CO)(0Ac) (HCNHC6H4Me-4)(PPh3)Z,4,384 RuC,,Ha,NO,P, -. -_

[Ru(CO)(OA~)(HCNHC,H4Me-4)~PPh3)2j ’ ,4,384

RUC47H43NP2

RuH(~~-C~H~P~)(MCCN)(PP~~)~, 4,457

RuCanHd,~ Ru(phthalocyanine)(CNCH2Ph)z, 4,475 RuC~~H~~C~ZNZP~ RuCl,(phen)(PPh&, 4,392 RUC~SH~~N~OZ {Ru(tetraphenylporphyrin)(OEt)(HOEt), 4,473 R~C48H4oN402 Ru(tetraphenylporphyrin)(HOEt),. 4,473 RuC~~H~INSP~ RuH(N,)(PhNNNPh)(PPh,),, 4,458 RUC~.SH~A”OZPZ Ru(G-methyl-2-pyridinolate)20,, 2, 7YS; 4,466 RuC12(PHPh2)4,4,378 RuC4,Hi4N03P2

Ru(CO)(OAc)(HCNMeC6H4Me-4)(PPh,),,4,384 RuCaRHaXIPa RuHCi(PHPhJ4, 4. 452 R~C~~H~SOZP~S~ Ru(SOCPh)z(dppe) (PMe,Ph). 4, 408 RuC48H46P4 RuH,(PHPhz)4,4,451 R~C~~H~RCIZNZO~I

Ru(CO)(S,CNEt2)(HC=NC6H4Me-4)(PPh;),.4, 384 RuCi,,H&1204P2

RUCI~~PP~~(C~H~COCHCOBU‘-~)}~H~, 4,109 RuC~H~OP~ I ) , 4,457 RuH(PPhj)2(PhCH=CHz)( 1-3-q-C6H1 RuC~~H~~CIY~P~ 4,356,392 [R~Cl(PPh,)~(terpy)]+, RuC~~H~~CIOP~ [RtiCI(CO)(dpprn),]+, 4,383 RUC~~H~~N~OP, RuH(~-McC,H~NNNC,H,MC-~)(CO)(PI’~,),. 1.205: 4.395 K u C 1H,,O ~ P4 [RuH(CO)(dppm),]+, 4,383 RuC5,H37C1NOP2 R U C I ( C U ) ( ~ - M ~ C , H , N C C , H , M ~ - ~ ) (4.383 PP~~~~. RuC~ZH~JNZO~P~ Ru(salen)(PPh,),, 4,397 RUCS~H~SW’~ [Ru(CH~)(CO)(dppm),]+,4,383 [ R u H ( C O ) d d p ~ m ) ~4,383 l+, RGtHdJ20P2

RuH(4-MeC,H4NCHNC,H,Me-4)(CO)(PPh,),, 2.204; 4.395

RuC5,HJLNOP4 RuC~Z(~-MCC~H~CN)?(P~~PCHZCO,E~),, 4,397

RUC48H48N20ZPS

Ru{(OCMeCHCMeNCH,),}(PPh,),, 4,398 RUcd4e.N~ [ R ~ ( M e ~ p h e n ) ~1,351 ]~-, RUC~BH~BNGO~

[Ru(h’O)(dppe),] ’ , 2 , 103, 105; 4, 370 RuCwHaaPi

gh(dGpej2[, 6,276

uH(C6H4 PhCHLCH2PPhz)(dppe),4,456 RuC&SOP~ Ru(4-MeOC6H4N=CHCH=NC6H40Me-4),, 2, 210; RuHz(dppe),. 4,451,461 4,364 R G z Hs I Pa [ R U ( ~ - M ~ O C ~ H ~ N + Z H C H = N C ~ H ~ O M ~ - ~ [RuH,(dppe),l+, )~]~~,~, 4,462 364 RUC~~H~~CIO~P~ [RuC1{P(OMe)PhJ4]+, 4,376,410 RuC,,HwN,OJ’,

Ru(4-MeC6H4NCONC6H4Me-4)(CO),(PPh,),. 4, 396 [RuMe(C0) (CNBu‘)(triphos)]’ 4, 382 RuCanH=,OxPaS? -- ... [Ru(S2CHPMelPh){P(OMe)Ph,),l +,4,406 R~C~BH~PS [Ru(PhC=C)(PMe,Ph),l’, 4,376 RuCasHd,OsP,

Ru’(CO)(~-OC~H,NO)(2-OC6H4NOz)(PPh,),, 4,398 RuC~~H&J~PZ Ru{MeO,CCH=CC( COzMe)=CHC(COZMe)=CH} (CO)(PPhs)z, 4.404 RUCS~H~&~~N~O~PZ

R~C1,(4-pyC0Me),(PPh,)~. 4,392 RuCSOH~OCI~N~P~ RuCI,(CNPh),(PPh,),. 4,384 R~CsoH400zPzS2 Ru(SOCPh)z(PPha)Z,4,407

RuCI,(HONCPhCPhOH)( PPh,),. 4.397 RuGoHaNz04P~

Ru(~-OC~H~CH=NOH)~(PP~~)Z, 4, 398

R u C ~ ~ H ~ ~ K ~ ~ ~ P ~ S ~ Ku{(4-MeC,I-r,SO,N),C~}(CO),(PPh,),. 2. 285 RuCS,H,,N,O,P, Ru{(2-OC6H4CH=NCH,),CH2}(PPhS)?, 4, 398 R~CS~~ROP, Ru(CO)(dppe)l, 4,372 RuC&&P, [RuH(CO)(dppe)]+,4,383 RuCdhoN606 [R~{bipy-4,4’-(CO~Pr~)~}~]~+, 6,s 10 RuC~.,H~~N~ Ru(tetraphenylporphyrin)(py)2, 4, 472 [Ru(tetraphenylporphyrin)(py),l+, 4,472 R~Cd43P3 RuH,(S-Ph-dibenzoDhosohole),. 4.462

RUCS~H~SCI~P~

Cumulative Formula Index

560

R~CjqH45C13P3 RuC13(PPh3)3,4,416 RGJLH45C12P3 RuClZ(PPhq)?,1,45

RuHCI(CO)(PPh,)3, 4,377,456,459,463; 6,232,233, 235. 303.304 RuC~,H~~CIP,S RuHCI(CS)(PPh3),. 4.383,456 RUC&L@P~ R u H , ( C O ) ( P P ~ ~4.451; ) ~ . 6,235,258,304 RuC~~H~~OZP, RuH(O,CH)(PPh,),, 4,455

RuCsj,H,,CIO,P,S? RuHC1(3-HO?SChH,PPhZ)3,6,734 RUC5dH46CIP3 RuHCI(PPh3),, 4,452,453,462.163: 6. 232,233,235, 303,304 RUC~~H,~NOP, RuH(NO)(PPh,),, 2, 103, 105: 4.370: 6.235,258

Ru(CN)2{P(CsH+PPh2-2)3}, 4,282 RuC5&4N,OP2

RuCI2(PPhq)q, 4,287,356,364.377.101.116, 235,258,269,293,299,303, 306. 357 RuC~~H~~CI~NP~

463; 6,

RuCI,(NPPh3)(PPh3)2,4,419

Ru(~-~,H&=NC(P~)=NNP~}(CO)(PP~~),, 4,396

.. .~

RuC:I,(DMSO)~F(OPhj3}3,4,408

(Ph2PCH2CH2CH2PPh2), 4.456 RUC54H550P1 fRuH(EtOH)(dppe)J I , 4,399.459 RuCJ IS,HrN4P Ru(octocthy1porphyrin)Hi-(PPli,). 4,473 RuCs4HS9N4P Ru(octaethylporphyriti)(PPh,). 4. 473

RuHCI(PPh,),, 4,399 RuC~~H~~CI~OP~ RuC12(CO)(PPh3)3,4,381 R~C55H&1d'&

RuCl,(SzCPPhg)(PPh~)2,4,111 RuC,,H,,NO,P, [ Ru(CO)(N@)(PPh,),]+ .4,370 RuCSSH~SOP~

kuH(C,H,PPh,)(CO)(PPh3)2.4.456 RuC H OTP, a ( O P h ) , ) (CO)(PPh,){ P(OPh),), 4,456

RuH(02CC&C0zH)(PPh3)3,4,455 RuCS7HS2NO2P3 RuH(O,CNMe,)(PPh,),, 4,404,455 RUC57H5" [KuH(ChBut)(dppej2]' 4,459 RuC,,II,,N,P, Ru(2-p!/NPh),(PPh,),, 4,3Y2 RuCS8H,lNO,P3 [Ru(OAc)(MeCN)(PPh,),] + ,4,397 RuC~LZNZP~ [RuH(MeCh'),(PFh,),]+. 4,459 RUC58H55P3 RuH,(PPh&(THF), 4,451

561

Cumulative Formula index

RIIF~P

hC8*H7&IOjP6S RuC1(O2SOZ)(NO)(triphos),,2,425 R ~ C ~ ~ H ~ S C ~ Z P ~ RuClz(triphos),, 4, 380 RUC92H66N803

{Ru(tetraphenylporphyrin)(OEt)}zO: 4>473 RUC~~H~ZIG~P~ Ru(tetraphenylporphyrin)(dppm),, 4.473 RuC13 RuCl,? 4,308,444,463 [RuC131-. 4.441 KUC13cht.121 C1306P2 R u C I ; ( ~ ~ ~ ) ( P ( O M ~ )4,416 3),, RuCIJO RuCI,(NO), 4.327, 362 RUTI302

[RuO,CI,]-. 4,422 RuCI, RuC1,. 4.446 [RUCI,]~-,4.441 RuC1,K [RuNCl,]-. 1 , 44; 4,364 RuC1,O [RuOCII]* ,4,43S KUC1,OZ [ R u ~ ~ C ~ , 4,450 I~-, RuCI+S (RuCI,S),,, 4, 430

RuCI, 377

[RuCl,]*-. 4, 435

Ru C1,N 0

[RxCl,(NU)J-; 4,357,363 ~RuCls(NO)]z-:2,103,114; 4,298,348,362-364; 6,809

Ruck, [RuCl,jZ-. 4.289,327,447; 6,823 [ R u C & ] ~2,696: -~ 4,444; 6,298,823 RuCoC3H,,N, ,04S [CO(NH3)5(&-HA C:1 I=NCH=C'H jRtl(YH,),(SOI)]Z' , 4,696

RuCoC:?If35N,,C)2

~CO(NII?)~(OCCH~~~-~)RU(NH~)~(~I~C~)J~'~1.733 RuCOC,~H,&'

1I

[C~(~~~,(NH,)(CL-NC)R~(CN),I ,4,283 RuC7,HwCIO 12P4 ~ u C l { 2 - C 6 H 4 0 ~ ( O P h{P(OPh),},, )z} 4,389 RuC7zH6nClzP4 RuCIz(PPh3)4,2.696: 4,367,377; 6,303 RuCwH,,ClPn RuHCliPPh,),, 2,696

R u H Z ( P P ~ ~2,204,210. )~, 1026;4,45U, 462,463; 6,233, 234,235,258,293.303 RuCnHc,,P4 [RuH3(PPhi)4IT, 4,463 RGZH~IP~ [KuH(PPh3)4] ' , 4,458 RuGzH~~N~Pz Ru(octaethylporph)rin)(PPh3),, 4,373 [Ru(octaethylporphyrin)(PPh,),l- , 1,495 RuC7zHssNe (Ru(octaethylporphyr1n))z. 2. 836 RUC~~H~OOP~ Ru(CO)(PPh3)4,4. 372

R U ( ~ ~ I M ~ C N ) ( 4,367 PP~~)~, RuCxoH~eN4P2 Ru(tctraphenylporphyrin)(PPh,),, 4,473 RuCsoHsoO84 {RuH(OH)(PPh,),(THF)]z. 4, 399

RuCOC.,,,H~ tNi-10 [Co(YH3),( HzO){ NCC(CHzCHz)3CCN}Ru(NH3)5]5+, 4.679 RuCOCi6HIICi04P

RuCoHCI(&-PPhZ)(CO)4,4,373 RUCOC1sH16~1204 CO{L-OzCCH(NH2)CH2&CHNHCH=~),( pNC)RU(CN)~]"-,4,283 RUCOC~~H~~O~P RuCo(p-PPh,)(CO),, 4,373 RLICOC~~H~~OJ'~ nuCo~y-PPhZ)(~O)(.(PPh3), 4,373 RUCOCS;H?OO~P~ RuCo(p-PPh,)(CO)s( PPh,), 4,373 RuCrHz5Pi506 [Ru(NH,),JOH,)( p-NH)Cr(OHz)5]5', 4,299 RuF~O~P RuO4PF3?4 ?420 RuF,O RuOF,. 4,449 RuF, RuFS, 2.680 RUF6 R u F ~4:, 449 [RuF,]-, 4,448 [RuF6I2-, 4.447,448 [RuF,]; . 1,398; 4,444 RUF,D4P, R U O ~ ( P F ~4,) 420 ~, RuF7P

RuF~P

Cumulative Formula Index

562

RuH,N,O, (RuF4(PF3)),,,4,447 [R;(NO;)(NO,)(NO)(OH,),]',4, 361 RuF, RuH6S6 RuFs, 4,450 [Ru(SH),I3-. 4.430 RuFI~P~ RuH,CI,O, [Ru(PF,),]*-, 4,366,451 RUCI,(OH~),~ 4.442 RuFI~Ps [RuCI,(OH,),]+, 4, 446 R U ( P F ~ )1,41; ~ , 4,366,371 RuH9Cl3N3 RuFeC8Hl8CI5O,P2 RuCI,(NH,),, 4.308 RuCl(FeCl,)(CO),(PMe,),, 4,387 RuH,,CIO, RuFeC9H,9Ni2 I F ~ ( C N ) , ( ~ - ~ ; ~ ~ C H C : H = N C H ~ ~ ~ H ) K ,4, U ( N H , ) ~[RuCI(OH,),] ] ' .4,442 [RuCI(OH,),]~+,4, 446 317 RuHloNO, RuFeC,,H,,N, [Ru(NU)(OF12)5]3f, 4,362 [RU(I\'H~)~(FCCN)]~+, 4,317 Ru€lloN205 RuFeCl3HI6N, [Ru(NH3)5(FcCH=CHCN)]2'. 4, 3 17 [Ru(N2)(0H2)jlZ-, 4.421 RuFe2CsHi8CIsO2P2 RuH,,~~ [Ru(OH)(OH2),]'-, 4,421 Ru(FeCl,),(CO),(PMe,),. 4. 382 RuHI,BrN50 RuFe,C6N6 [RuBr(NO)(NH,),j2+, 4,298 Fe4[Ru(CN),], 4,281 RuH12Br2N4 RuGeC,H9O4 [RuBr,(NH,),]+. 4,309 [ R u ( G ~ M ~ , ) ( C O ) ~4,287 ]-, RuHI,CIN4O2S RuGe,C,CI,O, Ru(GeCI,),(CO),, 4,287 [RuCI(NH,),(SO,)]+, 2,634,635; 4,292,296,306,307. 316,320 RuGeaCl8, Ru(GeMe,),(CO),, 4,287 RuH12CIN50 JRuC1(NO)(?rH3),12 .4.29X RuGe,Ci,HIs06 Rul-I,,Cl2N, RU&kMe~),(Co)6,4,287 [RuCI,(NH;),] ' 1.300; 4,292,295,299,307-309 RuG~,C~,H~~O,P, Ru(NH,)~CI,,1.301,483 Ru(GeMe,),(C0)2(PPh,)L,4.287 RuHC14N02 RuHiJ'J402 [RuCI,(OH)(NO)]*-, 4,363 [Ru(O)2(NH3),I2-, 4, 305 RuHC15 RuHizNs [RuHCl5I3-,2,696 [ R u ( N H ~ ) ~ ( N ~4,300 )~]~-, RuH, .N.O RuHC150 (RuCL5(OH)12-,4,353 Ru H F 2P4 [Ru(H,O),)~'. 1.371; 4,325,327,420,421.442 [RuH(PF,),]-. 4, 451, 461 RUHN5010 [Ku(H,0)s13+. 4.420.421 [ R u ( H , O ) ~ ] ~4.421 +. [RU(OH)(NO)(NO,),1'-, I , 103. 798: 4,361: 6,941 RuH,Br,O RuH~>CIN~~ [RuCl(OH)(NH,),]', 4,309 [RuBr,(OH,)lZ-, 4,445 RuH,C14NOS RuHI1N,O, [Ru(OH)(NO)(NH,),]*~,2, 110; 4,298,548 [Ru(NS)CI~(H,O)] , 2 , 120 KuH~CI~O~ RuH~~CIN~O [RuCI(NH3),(0H2)]*+,1,309 [RUCI,(OH)~]~ -,4,448 RuH2C1,0 RUHI~CIN~O~S~ [RuCI,(H,O)]-, 6,298 RuCl(HS03),(NHj),. 2,634 [RUCI~(H,O)]~-. 4,289,299,308,321.515.446 RuHi4N402 Ru(NH~),(OH),.4,298 RuHzF12P4 RuH,(PF3)4,4, 451 4.305 [KU(NI~,),(OI~*)~]~-. KUFI~~N~O~S RuHZNjOi4 [Ru(NH,),(OH,)(SO~)]", 4, 307 IRu(NO)(NO,),(H,O)I-, 6,942 RuH30F RLIH~~N~O~S Ru(SO,)(NH,),(OH,), 4,295, 304, 307, 316 [RuO,(OH),]-, 4,422 [ R u O ~ ( O H ) , ],4,422 ~ RUH~~N~O~SZ RuH,C13N03 Ru(HSOj)2(NH;)&. 4.306 R U C I ~ ( N O ) ( O I I4, ~ )362,363 ~, KuH1,N,O, [ R u ( N O ) ( € I ~ ~ ) ( ~ I2,~ 110,4,298 ),~~+, RuH4CI40, RUH14N6O [RuCI4(H,0),]-, 4,445,446: 6.298 [RU(NH~>,(N~)(OH,)]~*, 4,299, 300 RuHJ'LOii Ru(NO,)(NO~),(NO)(OH,)~. 4.361 [Ru(NO)(NH,)(NH,),]*+,4,298 RuHI5BrN5 RuHJ'hOi, R~(NO)(N03)3(H20)2,4.361; 6.912 [ R U B ~ ( N H , ) ~ ]4.~298 -, RuHlSCIN5 RuH,NO [R~(NH~)(0H,)]~+,4,299 [RuCI(NH~)~]+ 1.377.505; 4,305,308 RuH, [RuCI(NH3)i]2+.1,366.367,406,4, 280,289-292.294, [RuH,I4-, 4,460 298,299. 302,304-306,308,309,312,317 RuH,Cl,O, RuCI,(OH)~(OH~ 4,448 )~, RuH6C1303 RuCI,(OH,),, 4,445 [ K U ( N ~ I ~ ) ~ ( S2,~634; ~ ) ]4,~ 306,307 +. [R~CL;(OH2)3]-,4,442 R~Hi5N503S

.

563

Cumulative Formula Index

RU(SO,)(NH~)~ 306 ,~, R~HisNs03S2 [ R u ( S ~ O ~ ) ( N H ~ )4.307. ~ ] ' , 318 RuHisN6O [RU(NO)(NH,),]~+, 2, 111: 4.297-299,301,302,317 RuHisN602 [Ru(NOz)(NH3)s]",4,298; 6.776 RuH i SN7 Ru(NH,),(N,), 4, 299 [Ru(NH3),(Nz)] ' ,4,299 [RU(NH,)~(N,)]~', 2, 115; 4. 289,295,29&301,306, 317,318,321 [RU(NH~)~(NZ)]'+, 1,301 RuH1,N70 4. 299,301 [RU(NI.T~)~(N~O)]~+'. RUHisN8 [ R u ( N ~ ) ( N H ~ ) 4,299> ~ ] ~ + . 303.317 RuHi6N4Oz [ R U ( N H , ) ~ ( O H ~ )4,296.297, ~]~+, 310 [Ru(NH,),(OH,),]~+, 4,297.305, 310 RuH16N50 [Ru(OH)(NH3)s]Zf.4. 2901301,305,306,309; 6,435

Ru04 Ru04. 4,352, 360,423 [RuO,]-, I , 336; 4,422 [RUO+]'-, 1.336; 4,421-423 [RuO4I3-. 4,421 R~oinS4 R ~ ( S 2 0 j ) z4,430 ~ RuOsC8BrCI3O8Si Os(CO).,BrRu(SiCI3)(C0),, 4,285 Os(CO),{RuBr(SiC13)(CO)3}.4,285 RuOsCZ4HJ6C12Ni0

RUH16N6

R u P W &i,O, Ru(PbMe,),(CO),, 4, 289 RuPdC36H2BC12N202P2 RuPdCl2(COj2(Ph2Ppy),,5, 1107 RuPtC,,H,gN,

[ Ru(NH3),(NH)13'+,4. 303 RuHI+N,O,S [Ru(NH,)s(NHSO,)J' 4.303 RuH,,N,O [Ru(NH3),(OH2)lZ+, 1,360. 366, 370,488; 2,634,747; 4,290,291,293,294.297,299,301,304-308,312, 317,318 [Ru(NH,)S(OHz)]"', 4,297.304.305 RuH~~NSS [RU(NH,),(SH,)]~+,2,517: 4.307 [RU(NH~)S(SHZ)]~+ 4,307 RUHi7N6 [Ru(NHZ)(NH~)~]*+, 4.290 RuHi7NeO3S [Ru(NH3),(NH,SU,)]"+. 4,3113 RuHisN6 [RU(NH,)G]~', 1,336,348.350, 351,356,365,370,372, 485; 2,27; 4,289,290.294,296,298,299,301, 304-306,308,319 [Ru(NH,),13', I , 336,348. 350.351,446; 2,27, 115; 4, 289,290,297-299.302.303,308,311.317; 6,28, 99, 190,458,471 [ R u ( N H ~ ) ~ 4.290 ]~+, [ R u ( N H ~ ) ~ ]4,290 ~'-, RuH3oNinO [ { R U ( N H ~ ) ~ } ~ 4O ]318 ~+. RuH3nNi~ [ { R U ( N H ~ ) ~ I ~ ( N4,299 ~)I'+: RuH~C~H~CI~NO~ RuCI(HgCI)(CO)3py,4.280 RLIH~C,~H>~CIU~P~ [Ru(HgCl)(C0)3(PPh3)2]', 4,280 R~H~CAOH~OF.~~~', [Ru(HgCF3j(CO),(PPh.q)?]* 4.280 RuHgC4nHd602P2 Ru(HgCF,)(CF,)(cO)z(PPh,),. 4.280 RuIzNO RuIZ(NO), 4,326 RuLi2C47H6002P4 RuHMe(PPh3),(LiMeOEt2jZ5 4.454 RuMnCS4H4006P2 RuMn(~-PPhz)(CO)e(PPh;)Z.4.373 RuMnCS5H44C10sP4 RuMnCI(CL-dppm),(CL-CO),(CO),4, 373 RuMoC~oHiqN4S4 MoS4Ru(bipy),, 3, 1422; 4.352 RuN,O,o Ru(NO)(NO3)3.6,938 RuN7Oi7 [Ru(NO)(NO)(NO,),]~-.1,531 I

I

RuSn2C4Clh04

[OsRu(N=CHCH=NCH=~H)(bipy),C1,12', 4, 537 RuOsC,, kLJ,oOz [OsRu(fi=CHCH=NCH=~C02)(bipy),la+. 4.537 RuOSC~~H~~N~~

[OsRu(2,2'-bipyrimidine)(bi~y)~]~+, 4,537 RUOSC73&&~~OP,

Ru(CO)(PPh~)~(~-C1)~0~Cl(PPh~)~,4,411 RUOSC,~H~~N~

OsRu(octaethylporphyrin),, 4,618 RuOsHz,N,,O

[RU(NH~)~(H~O)(~-N~)OS(NH~)S]~+, 4,318,556

[R~(CN)(bipy),(p-CN)Pt(dien)]~+, 4,283 RuP~,C~~H~,CI~,N~ Ru(CN),( bipy)?{PtCI2(C2H4)},,4,283 R~PtzC3oH4zNi2 [Pt(dien)(NC){Ru(bipy),(CN)Pt(dien)}I4+, 4,283 RUPf&6H6nOi6P4 { P(OPh)3}4,4,374 Ru€'t,(CO)4 RuRhCS1H44C10P4 RuRhCI(p-CO)(dppm)2,4,373 RuRhC,,&CI,P, RhCl(PPh,)z(~-CI),RuC1(PPh,),, 4, 1076 RuSbC,H904 Ru(CO),(SbMe,), 2, 1038 RuS~C,~H,,O~ Ru(,CO)d(ShPh,),2, 1038; 4,371 RuSbC36H30C13NOP RuCl,(NO)(PPh,)(SbPh3), 4,393 RUS b2C36H&L,NO RuC13(NO)(SbPh3)Z, 4,394 RuS~~CS~H~~CI~ {RuCl,(SbPh3),},, 4,379 RuS~~C~SH~SCIZO RuCl,(CO)(SbPh,),, 4,383 RuS b4C72H6nBr2 RuBr2(SbPh3)4,4, 379 RuS~C~~H~~CI~N~ [R~(bipy),{4-Me-4'-(Cl~SiCH~CH~)bipy}]~+, 6.25 RUS~C~CISOZ IRuCl2(SnCI,),(CO),lZ-, 4,288 RuSnC4C1,0, RuCl(SnCl3)(C0)4,4,288 RuSnC7H9C10J RuCI(SnMe,)(CO),, 4,288 RuSnC14H3,C130,S3 [Ru(SnC13)(CO),(SEtz)3]+,4,289,432 RuSnC2,H&I3NP

(-)-RU(S~C~~)M~(C~H~)(P~ 2,19 ~PNH~HM~P~) RuSnC39H30140,P2 [RuI(CO)3(PPh3)21Sn13, 4, 289 RuSnC40H36C1402P2 RuCI(SnCI3)(CO)(PPhJ2(OCMe2), 4.288 RUS~C~~H~~CI~N~P~ RuCl(SnCl,)(CNEt),(PPh3),, 4,289, 384 RuSnCJBH45C13P4 RuH(SnC13)(PHPh2)4,4,289,452 RUSnzC~C1604

Cumulative Formula Index

RuSn,C,C1,04

564

Ru(SnCI,),(CO),, 4,288 RuSnzCsHz4C~604S4 Ru(SnCI3),(DMSOj4,4, 289 RuS&,oHisO4 R U ( S ~ M ~ ~ ) , ( C4,O288 )~, RuSnzC12HZOC16N4 R U ( S ~ C I ~ ) ~ ( C N4,289 E~)~, RuSnZCl9NO [RUC~~(S~CI~)~(N 4,288 O)]~-, RuSn4CIl4 [RuCI,(S~CI,),]~-,4,288 RuSn5C1FlS [RuCI(SnF3)s]4...,4, 288 RUSllsCIi6 [RuCI(SnC13),j4-,4,288 RuSn6Cl18 [RU(snc13)6]4-,4,288 RuSn6Fls [RII(S~F&]~-, 4,288 RUzASzC63H63C16 [RuClz{ As(C6H4Me-4)3)(pCl),RuCI { As( C6H4Me-4)3},]z--.4,415 RUZAS3C63H63C16

[Ru,Cl,{ As(C6H4Me-4),)3]'- 4,415 Ru~As~C~JLSCL RuZClS(PhZAsCH,CH2As~h~)~, 4.41 5 RuzAs~C&SZI~NZO~ { Ru12(N0)(AsMePh,),j,, 4, 374 RU~AS~C~~IX~~CI~O~ ~

-

{RuC12(CO)(PhzAsCHzCHzAsPhz)}z, 4.413 R ~ z A ~ ~ C ~ H ~ O C I ~ ~ Z [{RuCIz(AsPh3)z}z(i-Oz)12+, 4,401 RUZAS~C~ZHSOC~S R~2ClS(AsPh3)4,4,379 RUZAS~C~OSH~OC~~~Z [ ( R u C I * ( A S P ~ ~ ) ~ } ~ ( 4.416 ~-O~)~~+. R@ I o C ~ ~ H W C W Z P ~ S R U C I ~ ( P P ~ ~ ) ~ ( ~ -(N2BloH,SMe2)(PPh,)z, CI)~RU 4,412 Ru2Br, [Ru&,]~-, 4,445 Ru2BrI00 [Ru~OB~~ 4,448 ~]~-, RuzCzC1,NOz [ , R U ~ N C ~ ~ ( C O4,364 )~]~-,

.

__

[(R~Cl(en),~~(u-oH)]~', 4, 325 Ru2C8H35N1304S

[{Ru(YH,),(~~'=CHCH=NCH=~H)}~(NH~)(SO,)]"'. 4,320

[{Ru(NH3)s}2(4.J'-bipy)]4+, 1,516; 4,313 [{R~(NH~)~]~(4..l'-bip!i)l5 ' , 1, 333, 359,362 ~RUCl~(CO)2}z, 4,442 RUZC~H~ENIO~~SZ [ { Ru(NH3j4(S04)} z(fi=CHCH=NCH=kH)lZ', 316

~U2C1UH40NIi 4,

R;1C1ZH3BN14

565

Cumulative Formula Index

RUZC32H6008P2

KU2C12H40N15

[{Ru(NH3 4(fl=CHCH=NCH=cH)},(NH3). (Hi=CHCH=NCH==&Hl1"+. 4.320

Ru2(0iCCF3)2(p-02CCF3)Z( p-OH,)(cod), 4,425 Ru2c24H;lCINll [Ru( NH3)5 (fi=CHCH=NCH=~H)RuCI(bipy),j3*, 1. 361

Ru,O(OAc),(CO)(PPh,), 4,428 RUzCzsH386 {RuH NN=CHCH= H)(cod)},(m= b H ) , 461 RuG~H~N~S~O Ru,(S2CNEt,)s, 4,434

COC 7-s

RuzCI~~e~CH2CH2NMeC'= NMeCH,CH,NMej,(PPh,),,

4,413

567

Cumulative Formula Index

RUZC~ZHSSC~ZNS~ {Ru(octaethylporphyrin)C1),0,4,473 RuzC7zHstJs {Ru(octaethylporphyrin)),, 2.843; 4,474 R~zC7zH9oN803 {Ru(octaethylporphynn)(OH)},O, 4,473

RUZC~~H~OC~~~P~ [ R U ~ C I ~ ( C O ) ( P P ~ ,4,415 )~]+. RuZC~~H~OCI~P~S

Ru(CS)(PP~~)~(~-CI)~RUCI(PP~~)~, 4,392 R u & I ~ ( C S ) ( P P ~4,~ )383 ~, RUZC~~H~OC~~P~S~ {R~ClZ(CS)(PPh3)z)2,4.383, 411.413 RUzC74H69C1306P6 Ru{P(OMe)Phz}z{HOPPh2}(v-CI),Ru{(PhZPO),Hz}, 4,411 R~2C74H94Ns03 {Ru(octaethylporphyrin)(OMe)}zO,2, 836 RuzC7JLCLNzP4 {RuCI,(MeCN)(PPh,),),, 4.396 Ru~C~~H~~CI~NOPQ RuzCl4(AcNMez)(PPh&, 4. 377 RUZC~H~ON~P~S~ {Ru(NCS)dPPh,),},, 4.418

,

Cumulative Formula Itidex Ru2PtC34H240sP2 Ru,Pt(CO)a(dppe), 4,374 RU2SbC6Cl706 {RuCI,(CO)~}~(S~C 4,443 I~), Ru2SnCSCl6O5 Ru,Cl,(CO),(SnCI,), 2.684; 4,288 R U ~ S ~ C ~ ~ H ~ ~ C I ~ O ~ P ~ Ru(SnCl,)(CO)(PPh,)(p-CI)3Ru(CO)(PPh3)z.4, 288 Ru2Sn2Cl,Hl ,Os {Ru(p-SnMe,)(CO),),, 4,288 Ru,Sn,CIl,N20, 4.O288 [ R U Z C ~ ~ ( S ~ C I ~ ) ~ -, (N )L]~ '

RU2Sn4C16H300b

568

569

Cumulative Formula Index

Ru,C,,H,,N,O,"

SbAS,Hg,Ci&Ii,Fi, Hg,(A~F6)2(SbPh3), 5 , 1058 S bAs,NiC,,H,,CI

[Ni{Sb(C6H4AsMez-2)3}Cl]+, 5,6h S~AS~N~C~~H~~NS

[Ni{Sb(C6H4AsMe,-2),)(NCS))'.5.66 SbAuC 18Hi5Cl AuC1(SbPh3), 5,870 SbBr3C15PS SbCI5(Br,PS), 2,642 SbBr6 [SbBr,] ,3,271 [SbBr613-, 1,73 SbCC1,N [SbCl,(CN)]-, 3,277 SbCH, (SbMe),, 3,262 SbCzCIaNz SbCl,(NC)z, 3,277 SbCzHsCI3 SbC1,Mez. 3,257 SbC3C14N303 SbC14(NC0)3,3,277 SbCjFs Sb(CF&, 3,258 SbC,H,IN SbI(NPr), 3,261 ShCSH&I [SbMe,CI]+, 3,257 SbC3H9C104 SbMe,(OClO,), 3,264 SbCqH9CIZ SbCI2Me3,3,257 SbC3N3 Sb(CN)3, 3,271 SbC4H6CI [SbCl(CH=CH2)2]+, 3,257 SbC4H&lOSZ SbCI{(SCH2CH,)ZO}, 3,265,266 SbCsH1302 SbMe(OEt),, 3,269 SbCsHi3Sz SbMe(SEt),, 3,269 SbCSHI4O [SbMe3(CH2CH20H)]+,3,279 SbC,HI, SbMe,, 1,41 SbC6HS (SbPh),, 3,262 SbC6H51N SbI(NPh), 3,261 SbC6H9C12 SbC12(CH=CHz)s, 3,257 SbCGH903S3 Sb(AcS)3,2,645 SbC,H&l,O (SbMe3C1),0, 3,264 SbC6HlSNSi SbMe2(NMe(SiMe3)}, 3,260 SbCf.HI8N3 Sh(NMe,),, 3,259,271

SbC6H180PS SbMe,(OP(S)Me,), 3,2S8 SbC,H,,O,P,S, Sb((MeO),PS2}3. 2.643; 3,268 SbC&,z [Sb(C,O,),]?-, 1 , 82; 3,268 SbCsH2zN2SiZ Sb{NEt(SiMe2)}2,3,260 SbC&f1503S6 Sb(S,COEt),. 1. 3 7 , 8 2 3 , 2 6 6 SbC,H,,N,Si, SbMe{NMe(SIMe3))2,3,260 SbC9HZ7Si3 Sh(SiMe3)3.3.259 ShC,oIli,N,Ofi [Sb(cdta)]-, 2,783 SbC,oHz,N SbBu',(NMe,). 3,260 SbCiZHioF SbPhZF, 3,258 SbCIzHi2Cl3N [SbCl3(PhzNHZ)]+, 3.272 SbCizHuS3 Sb(SBu'),, 3. 265 SbCizH3J'J& Sb{NMc(SiMc,)},, 3,260 SbCIjHIOClxNL SbCI3Ph(N2CPh),3,264 SbC:ISH,,N,Sh Sh(S2CNETz),7 3, 266 SbCi7Hi7C120z Sb(acac)PhzC12,2,383 SbCisCId3 Sb(SC6C15)3,3,265 SbCi8Hi&l,PS Sb(Ph3PS)CIs. 2.642 SbCiaHi5S SbSPh,. 3.266

Sb(NPr2)3.3.2M1 SbCisH4206P& Sb(S,P(OPr'),),. I , 81,82; 3,268 SbC20H,,N,02 Sb(NCO)2Ph3. 3.260 SbCmHwS SbSPhz(C6H3Mez-2.6),3.266 SbCziH1503S3 Sb(SOCPh)3,3,267 SbCziH17Nz03Sz Sb(S2COEt)(8-quinolinr,latc),,3,267 SbC*IIE,N S Sb{S&N-H,)3},, 3,265

570

571 Sb(OH)Ph4,3,258 SbCz4H44PSiZ Sb(PC6HzBut3){CH(SiMe3)~~, 3-26] SbC3oH z3 Sb(C,H,C,H,)Ph,, 1.46 SbC3oHzs SbPhs, 1,39,40; 3, 258 SbC35H35 Sb(C6H4Me)s,I , 41) S~C~F,HJ'& Sb(SzPPhz)3,L S 2 ; 3.267 SbC3,HXN

Sb(octaethylporphyrin)CI, 2.822 SbC36H46N40z [Sb(octaethylporphynn)(OH),] . .2,822 SbC44HZsClN4 Sb(tetrapheny1porphyrin)Cl. 2,822 SbC44H3oN40z [Sb(tetraphenylp~rphyrIn)(OH)~]+ .2. 822 SbClO SbOCI, 3,264,271 SbC13Fz SbC13F2,3,274 SbC14 [SbCl4]-, 3,274 SbCl4F SbCI4F,3,274 SbC14N6 SbCI4(Nj)Z, 3,276 SbCIS SbCIs, 3,271,272,276.278 [SbClsl2-, 3,271,274 SbC1SOS8 SbCI,(S,O), 2,636; 3,276

SbCI,(SeOCl,), 3,276 SbClJ SbCIs.IC13,2,678 SbClxOP SbCI,(OPCI,), 2 , SO0 SbC18PS SbClS(C13PS), 2,642 SbCrC3H904 Cr04(SbMe3),3, 942 SbCrCloHl6CI4P [CrC14(2-MezPC6H4SbRez)]-,3,853 SbCWs4H4sI2 CuzIz(SbPh3)3,5 , 537 SbF [SbF12+,3,272 SbFO SbOF, 3,264 SbF0,P

[Sh$(PO,)]-, 3,271 SbFz [SbFz]+,3,272 SbF, SbFS,2,678,680; 3,271,272.940 [SbFSl2-,1,50 SbF, [SbF6]-, 3,271,276,314 SbFeC7H904 Fe(CO),(SbMe,), 2, 1038 SbFeC44HZBF6N4 Fe(tetraphenylporphyrinate)(FSbF,), 3, 271 SbGe3C1,H4, Sb(GeEt,),, 3, 25Y SbH2F4O2 [SbF,(OH)Z]-, 3,265 SbHz05P SbO(HzP04),3,263

SbH404 [Sb(OH),]-. 6,854 SbH606 [Sb(OH)rj-, 2,296; 3,265 [Sb(OH),IZ-. 6,854 SbH9Si3 Sb(SiH,),. 3.258,259 S ~ H G ~ H I ~ C ~ ~ HgCI,(SbPh,Me). 5 , 1084 SbHgCi,HisI,S EKg(Ph3SbS)Il. 2,644 SbHgC20HIsN2SZ Hg(SCN),(SbPh,), 5. 1084 SbHg, &h Hg, gSbF,j, 5 . 1049 SbMo6HzOz4 [ S ~ M O ~ H ~ O3, ~ ,1044 ]~-, Sb NbCl NbSbCllo,3.591 SbNbF,, NbFS.SbF5.2.678 SbNIC72H6o Ni(SbPh3)4,5 , 9 SbNiSr06 SrNiSbO6, 5,297 Sb06 [SbO,]"-, 3,265 SbOsC22HIj04 OsjCO),(SbPh,), 2, 1038 SbPb3CiaH4s Sb(PbEt,)j, 3,259 SbRhCzlH21Clz RhCI,CSb(C6f-14Me-2)3},4, 933 SbRhSnCs4H4SCls RhClz(SnC13)(ShPh,),, 4, 1032 SbRuC,H9U4 Ru(CO),(SbMt+), 2, 1038 SbRuC22H150J Ru(CO)d(SbPhS),2, 1038; 4.371 OP SbRuC36H30CI,N RuCI,( NO)( PPh,)(SbPh,), 4,393 SbK~~C6Cl706 (RuC1z(C0)3}f(SbC13),4,443 SbS2

[SbSJ. 6,853 SbS3 ISbSq13-, 6,853 -_

sbs,

lSbS4l3-, 2,519 ISbS,l'-. 6.853

Cumulative Formula lrzdex [Sbz(C4Hz06)z12-r3,278 Sb C H CI m 6 H 4 ) C l ,3,258 sb,c;&,oCl6 (SbCI,)Z(PhPh), 3,270 SbzCizHiiC16N (SbC13)2(Ph2NH),3,272 SbzCizHm (SbCMe=CHCH=CMc),. 3,261 SbzC&,o (SbPhz)2,3,261,263 Sb2C36H30N60 {SbPh,(N,))zO, 3,260 Sb2C49H4003 (Ph,Sb)*CO>, 2,447 SbiCdFii Cd(SbF6)2,2,501 SbZClZF9 [SbzClzFgl-, 3,274 SbZClsNs (SbCI,N,)z, 3,271 Sb2CrF15 CrF,Sb2Fll, 3,933 [CrF4Sb2Fll]-, 3,933 Sb2CrOZF15 (CrF4SbzFl,)O2,3,933 SbzCUC36H3oISz Cu(Ph3SbS)zI,2,644 SbzF4

[Sb2F4]2*,3,271,272 SWii ISb2Fl11-. 3,271,275 Sb;Fe&;H3007

Fe(CO)4(p-SbPh,)Fe(CO)3Ph(SbPh3)2.1038

572

573

Cumulative Formula Index

{RhCI3(Ph2SbCHzSbPhz)3}z-4, I025 ScAg,ZnF7 Ag,ScZnF,, 1, 111 S~A~~C~SH~ZCI~OI, SC(CIO& { PhzAs(O)CH,CH,As( O)Phz}3,3, 1065 SCB~CBHZSOZ Sc(BH4)3(THF)Z,3. 1064 ScBr, IScBr,13 , 3 , 1067 ScC3H3Cj, Sc(OH)(02CC:H2C02),2.444

[
S~~~-~-~,~-BU'~C,H~M~),(THF), 3, 1065 SCC~~HB~OJ'

Sc(4-0-3.5-Bu1~C6HzMc)3(OPPh3), 3, 1065 ScCla [SCCl4]-, 3. 1oh7 SCCI, 3, 1067 IScC1,12-, -_ SCCI, [ S C C I ~ 3, ] ~1067 ~, SCCSCI, C~SCCI,,3. 1067 ScF, [ScF,]-. 3, 1067 ScF, [ScFJ-, 3, 1067 ScH4C1402 [ScCI,(H,O)z]-, 3,1064 [ScCl,( H,O)z]Zf,3, 1067 COC 1-s.

Cum dative Formula Index HgC12(.H2NCSeNHJ,5, 1074 SeHgC,,,H &I2P HgClz(ScPFh3).5 , 1074 SeHgO, HeScO,. 5.1067 SeHiO, HgSeO,, 5 , 1067. I069 SeHn204 -~ Hg2Se04.5.1050 Sel, ISeIf,l2-. 3.303 ~

~ScCI(H,0)5]2’, 3, 1064 ScHioOs [Sc(OI?),( Hz0)2l3-, 3, 1064 SCH~ZCI~N~ SCC~~(NH>)Q, 3, 1060 SCHI zOa [SC(H,O)~]?+, 3, 1064 SCHi309 [ S C ( O H ) S ( H , ~ ) .,+3], ~106.1 ScHI5Br3N5 SCB~~(NH 3, ~1060 )~, ScH&LNj [SCCI(NH,),]~+,3, 1060 SCH~~CI~NS S C C I ~ ( N H ~3,) 1060 ~, ScMn2H4 Mn,ScH,, 4,60 ScNCOtC

[Sc(rz’b3)5]2 , 3 , 1064

sCogs2

[Sc(SO,),]-, 3, 1064

Cu(cn),(SeCKj,, 5.734741 SezCu205 Cu2(Se,05),S1 649 Se2HgC2H8C1,N4 HgC12(HZNCSeII;H2)2. 5,1074 Se2HgC4H8C12 HgC12($eCH2CH2SeCHz~H,), 5,1074 Se&gC4HloC12 HgCl,(MeSeCH,CH,SeMe), 5, 1074 Sc2HgC24H,,Cl?P2 HgClZ(SePBu3)z.5, 1073 Se2HgzG4H,,I4P2 Hg,14(SePRu3)2,5, 1073 Se211g,C12 Hg3Se2Cl2,5,1071 SezHgP,

Hg3Se2F,,5.1071 Se,CuIn,Br CuIn,SqBr, 1, 111 S&gC& [Hg(SeCN),] -,5, 1064 Sed [Se4I2-,3, .c6 Se4CDN3 [Se(SeCN),] ‘ 3,305 ScdHg [HgSe,16-, j?1071 Se41IgC4N, [I-lg(ScCN)a]z-.5,1064 Se4HgSrC4N4 SrHg(SeCN),. 5 , 1064 Se4HgzC48H40C1208 Hg,(SePh2)4(C104)z,5 , 1053 Se4Hg3C72H6oy60184 {Hg(N0,)2)3(SePPh5)4.5 , 1073 Se5CloHzoNz Se(Se,CNEt,),, 1.60 SebCOHgCbNb [CoHg(SeCN),I2-, 5 . 1064 Se611g2P2 Hg,PzSc,, 5,1071 SiAs2RhC5,H3,CI, RhHC1(SiC13)rAsPh3i,,4, 1020 SiAs2RhC4,H4,Ch& RhHCl{si(oEt),}(A~Ph~)~, 4, 1020 SiCH2 Si(H)=CH, 3,190 SiCH3F4 [SiMeF,]-, 3- 200 SiCzH6 SiH(Me)=CH,, 3. 190 SiC,H,F, [SiMc,F,] 3.200 SiCzHpN SiH3(NMe,), 3,216 SiC,H, Si(hk)FCH,. 3.188-190 SiC,H,, Si(Me)>=CHMe. 3.188 ~

sc,c42 Sc,CI,,, 1,27; 3, 1068 S e G N 8, [Se(SC?N)3]+,3, 305 SeC4HI6Cl2N4 [SeClz(en),]2+,3,304 SeCioH~ocWz [ S ~ C M P Y ) ~3,304 I+, SeCloH16N,0zS4 Se(S,~NCH2CH20CH2~Hz)2. 1. hO SeCloH20NzS4 Se(S,CNEt,),, 1, 60 sea, [SeC16]’-, 3,303 SeF, [SeF,]-, 3,301,302,319 Sekti [SeF,]’ ,3,302 [SeFJ-, 6,854 SeHz03 SeO(OH),, 6,360 SeHgCH4CI2N,

-.

~~

575

Cumulative Formuh Index

SiC4H,,Nz SiMe3(HC=N2), 3, 188 SiC4HI3N SiHMe2(NMez), 3, 216 Sics& $ifH)=CHCH=CHCH=CH.

SiM&(MeNNNMe), 2, 196 SiC6H5F5 [SiPhF5IZ-,3,200 SiC6HfJ Si(Me)=CHCH=CHCH=CH. SiC7H9F3NZ SiF3{N(Me)CH2py-2},3, 199 SiC8H6F4oZ SiF3(CH2O2CC6H4F-4)3.199 SiCsHzoOz SiBu'z(OH)z, 3,206 SiC8HZ0O4 Si(OEt)4,2,337 SiC8HZ4N4 Si(NMe,),, 2, 162 SiC,,H,F,N, SiF,(bipy), 3,200 Sic H 6' -),Ph, 3.214

SiC46H34N402 Si(tetraphenylp~rphyrin)(OMe)~, 2, 822 SiCoC7H904 Co(SiMe,)(CO),, 4,657 SiCOC6&203P3 CoH,(Si( OEt),) (PPh3),, 4,655 SiF5 [SiF,]-, 3,200 SiF6 [SiFJ-, 3,200; 6; 847 SiFeF, FeSiFb, 4, 1236 SiFe2CZOHlsCI2 {FeCp(C,H,)},SiCI,, 6,19 SiCrdO, [GaSiOJ, 3,135 SiH204 [Si04H,12-, 6, 852 SiH3F4N SiF4(NH3), 3, 200 SiH3F4NP2 (SiH,)N(PF,),, 3,215 SiH,04 [SiOaM3] ,6,852 Si If,O, SiO,H,: 6,852 SiHg,H,F6OZ HgaSiF,(HzO),, 5,1050 SiInC,H,,O InMe,(OSiMe,), 3, 161 SIIIIC~H,BN~ InMe,(N,SiMe,), 3, 159 SiIrC16H32C1 IrHzCl(C,Mej)(SiEt,), 4, 1166 SiIrC35H350P2 ~r(CO)(PPh,CH2CHzSiMe2)(PPh,), 4,1164 SiMoW, ,O,, [SiMoW1104j4-, 3,1036 SiMt>12042 6, 529 [S~M(I,,O,~]~-, SiNhC10H29N3 Nb(NMez),(CH,SiMe3), 3,653 SiNbC,,H,,O, Nb(CH2SiMe3)(q2-C02)(q5-CpMe)2, 3,666 Si04 [SiO4I2-, 3,203 [SiO4I4-: 3,203; 6,832,845,855 SiPtCloH,&103 PtCI(CH,=CHOSiMe,)(acac), 5,404 SiPtC14H3412P2 PtHT2(SiH2C=CH)(PEt3),, 5,357

3,190

3.190

s i C m - 2 ) 2 F , 3,214

[SiPhZF4l2-,3,200 SiCl2Hl4C1NZ0$i(OCH2CHz3H)MeCI( 8-quinolinolate), 3,212 SiCI2H3,C1N3 2. 162 Si(NHBu'12CI, ,SlC1;H2106 [Si(a~ac)~]+, 1, 195; 2.379 SiC,,H,,NOz $i(OCH2CH2NHCH2CH20)Ph2. 3.212 Si(ONPhCOPh)Me>.2.507 SiCi6H36P4 Si(PBu'),, 3,216 SiC18H5CI8O4 $ifOCACI,O-2LPh. 3.214 SiC18HIzClO4 $i(OC6H4d-2)z(C6H4C1-2). 3.213 SiC2oHz8P2 SiPhz(PHut)z,3, 216 SiCziHis06 [Si(tr~polonate)~]+. 2,397 I-

s i C i - 2 ) 2 ( c , , , H 7 - 1 ) ,3,214 SiC~6H1704 Si(02C10H6-2,3)2Ph, 3.214 SiC32H16CIZNe Si(phtha10cyanine)CI~~ 2.869 SiC3zHi6FzN8 Si(phthalocyanine)F,, Z1 864 SiC32H18N80~ Si(phthaIocyanine)(OH),. 2.864 SiC33H16N90 Si(phthalocyanine)(NCO). 2 . 864 SiC36Hio8Ni806P6 [si(hmpt)6l4+,3: 199 S~C~SHSON~O~ Si(octaethy1porphyrin)( OMe), . 2,822 S~C~ZHW.N&, [Si{O(2-MeC6H4)NCOPh},]+. 2. 507 SiC4SH3306 [Si(PhCOCHCOPh),]+. 2.379

SiRhC37H34C13P2

~

~

SiPtCz5H26ClP PtCI(SiMePhnp)(PMc,Ph), 5,420 SiPtC29H35CIP2 PtC1(SiMePhZ)(PMe2Ph)2,5,420 SiPtC34H35F3P1 PtH(Si(C6H4F-4),}(PMe,Ph),, 5,357 SiPtC;6H,oP2 P ~ H ( S ~ H S ) ( P ( C ~ I 5,358 ~II)~)~, SiPtC H P P t € ? ; e H 2 ) 3 } ( P P h 3 ) 2 , 5,357 SiPtC4,Hs,N2P3S Pt { Bu'N=P(S)NBu'(SiMe,)) (Ph3P)2.5,443 SiPtCs3H46P2 PtH(SiMePhnp)(PPh,),, 5,420 SiPtC54H46P2 PtH(SiPh,)(PPh,),, 5,357 SiPt2C54H82PZ .Pt2(p-SiMe2)(pC=CPh)(CECPh) (P( C6H1 ) 3 } 21 5,4I6 SiRhC,,H,,CI,P, RhHC1(SiC13)(PPh3)2,4, 1020 SiRhC3,H3,C13P, RhHCI( SiC1,Me) (PPh3),, 4, 1020

,

SiRhC3BH37CIZP2

Cumulative Formula Index

SiRhC311H37C12P2 RhHCI(SiCIMez)(PPh,)2. ~, . ,~ 4, 1020 S ~ R ~ C ~ ~ H ~ ~ C ~ P , RhHCI(SiMe3)(PPh3),, 4, 1020 SIRhC,qH,iO,Pz RhH, { Si(OMe),} (PPh3)2,4, 1018 SiRhC40H43P2 RhH2(SiHEtZ)(PPh3),,4, 1018 SiRhC42H46CI03P2 RhHCI{Si(OEt),}(PPh,),, 4.1070 SiRhC42H46C1P2 RhHCI(SiEt,)(PPh,), , 4 , 1020 SiRhCs,H4,C1P, RhHC1(SiPh3)(PPh3)2.4, 1020 S~RUC,,HZ&I,NG [R~(bipy)~{4-Me-4'-(CI~SiCH,CH,lbipy} 1' -,6 , 2 5 SiS, [Sisal4-, 3,205 SiTi5c50H,608 Ti,(OPh),(SiMe,), 3,335 SiW12040

6,496 [SiW,20,0J2~, SiZrC6Hl8Cl4N2 ZrC1,{(NMez)2SiMe2},3, 372 Si,AIC7H21ClN3 hlCI.({NMc(SiMe,)},NMc], 3,109 Si2AlCrCZsH4,NOsP C r ( C O ) 5 ( ~ - P P h Z ) A I ( C H z S i M e ~ ) ~3, ( ~112 ~~e3). Si2AL&H18Br4O2 {AlBr2(OSiMe3)),, 3,114 Si,B3HfCloH,oNPz Hf(BH4)3{N(SiMe2CHZPMe2)2) 3.384,433 Si,C,H,CI, ~iCI,CH,SiCl,~H,,3,206 SiZC4H12 SirMe,)=SiMe,. 3. 184 Si,C;H,;S, $iMe,SSiMe,$, 3,206

Si,C*H,A

[SiMe,(MeNNNMe)l,, 2 , 1Y6 SilClaH2s Si(Pr')2=SiPr'z, 3, 190 SiZC16H36 Si(Bu'),=SiBu',, 3, 190

Si,CrCAt,H,,NO; CrO(NBu*)(OSiMe,),, 3, 945 Si2CrC14H36N20z C ~ ( N B L I ' ) ~ ( O S ~ M3,~ ,945 )~, Si~CTC36H3004 Cr02(OSiPh3),, 3,941 Si3Cr2C16H30N4 {CrCp(NH)(NSiMe,)},, 3.945 Si2CuC,H,, [Cu{C(SiMe,),}]-. 5,550 Si2CuC7HI9Br [CuBr{CH(SiMe,),}l-, 5 : 550 Si,CuOlo [ C U S ~ ~ ,O5 7~1~6 ] ~ Si2GaCBHZ2 GaCl(CH2SiMe3),, 3, 139 Si2Ga2C8H26C1N2 ~

~

-~

,

576

{GaClMe(NHSiMc,)},, 3,131 Si2Ga20R [Ga,Si,0,J2-. 3,135 Si2Ga20g [Ga2Si209]4-l3. 135 Si2H4 Si(H,)=SiH,, 3, 184 Si2H6F2NP (SiITj)2N[PF2)c3,215 Si,Ilf2CloH28C~,NP1 [HfCll (N(SiMe2CH2PMe2)*}HICI,l,,,3,384 Si,InC,H,,O, [InMc,(OSiMc,),j.". 3, 101 Si2IrCZ2Hli IrH2(C,Me5)(SiEt3),, 4, 1 166 Si21rC31H3,1NP2 Irl(Me){N(Sin,lz,CHPPh*~2}, 4, 1161 -~ Si21rC32H40ClPZ hC1(PPh2CH2CH23ible,),, 4, 1164 Si,Mo,C,,H4,0,P2 Mo~(OAc)~(CH~SiMe2),(PMe3),, 3, 1303 SizMozC 18H4604P2 MO~(OAC)~(CH~S~M~~)~(PM~~),, 3,1307 SizOs [Si,0,l2-, 6, 856 Si,O, [Si2O6J4'.. 6,856 Si207 [Si201]3-: 3.203 [Si20,]6-1 6.855 Si2PtC30H36C1NP2 PtC1{N(SiMe2CH2PPh2)2},5,453 Si,PtC30H37C1zNP2

PtCI2(HN(SiMe,CH,PPh2),},5,453 S~ZP~C&,~C~,P, Pt(SiMeCI,),(PPh,),. 5 : 419 Si2PrC,0H,,0P2 PtH(Me,SiOSiMe,Hj(BPhl)z, 5,357 Si,PrC,,H4,Y2 ~t.(SiMePh~)l(PMe,Pli),, 5,420 Si2PtCJaHg2P2 Pt (CH2SiMe3ja(PPh3j,, 5 , 393 Si,PtC,6H,,P2 5,420 Pt{ 1,2-(Me2Si)2C6H4)(PPh3)2, Si2RhCs3H4,i%P3 Rh(N(SiMe2CH2PPh2),)(PMe,), 4,1041 Si2RhC4ZH48NP1 Rh{N(SiMe3)2}(PPh3)2.4,907 Si,RhC48H5,YP3 Rh{N(SiMe,CH2PPhz)2}(PPh3), 4, 1041 Si,SnC,,H,, Sn(Me,SiC,H,),I 3: 219 Si2TiCa0HJ202 ?'i(OPh)2(Me3SiCH2)Z,3, 335 Si2CJC,,i I&I,C12 3. 1147 -U(OSiMeEi2)2C121,. SilZrCbH,&I,NIO ZrCIZ((KMeSih~e,),O~, 3,378 Si2ZrC7H2&12NZ ZrC12{(NMeSi!vle2)zCH2}I 3,378 Si2ZrC7H21C12N, ZrCl~((NM~Sih;Ie,),NMe},3,378 Si2ZrC20H18N4 Zr{(NBur)2SiMez},.3.378 Si3A1C9Hz7 AI(SiMe3),, 3. 107 Si3A1C9H2,03 AI(OSiMe,),, 3. 114 Si,AIC,,H,,O, AI(OSiPh&, 3, 114 S~~CI~HI~PJ (SiMel)3P2(PBuL)2,3,216 Si,Ci,Hx

577

Cumulative Formula Index

Si6UCX8H55N3

Si(Me),=C(SiMe,)( SiMeBuXz) + 3, 189, 190 Si3C38H3&02 Si4PdTeZC26H60N2S2 Si(phthalocyanine)(OSiMe&. 2.864 Pd(SCN), { Te(CH2CH2CH2SiMe3)2}2. 5 , 1 144 Si3C39H39N Si4PtC84H70P2 (SiMePh,),N, 3,216 Pt{ (SiPh,),SiPh2}(PPh3),, 5,420 Si3GaC9HZ7 Si4SnC14H38 Ga(SiMe3),, 3, 129 Sn{CH(SiMe3)2}Z,3,216 Si3GaC9HZ7O3 Si,TaC,H,,CI,N, Ga(OSiMe,),, 3, 134 TaC13(N(SiMcZ)2),,3,610 Si3H9N Si4Tel0 (SiH3)3N, 3,21S iSiilt,,,]4-; 3,205 Si3HfC,H2,CI2N2 Si,TiC, P,,O, HfCl2{(NSiMe3),SiMe2). 3.378 Ti(O-SiMe,),, 3.335 Si31nC9H27 Si4ZrC1ZH36C12N2 I I I ( S ~ M ~3,~ 158 )~, ZrC12{N(Sihle3)2)2.3, 377 Si31rC13H391NOP2 Si4ZrCl2H3,N, IrHI{SiH,N(SiH,),~(CO)(PEt,),, 4, 1126 Zr(MeNSiMe,SiMe,NMe),, 3,378 Si31rC1;H3910P3 Si4ZrC12H36N402 IrHI{SiH,P(SiH3),}(CO)(PEt3),,4, 1126 Zr{(MeKSiMe2)20}2,3,378 SiJr2C26H6912N02P4 Si4ZrC,zH,604
Cumulative Farmulu Index Si6ZrC16H48N4 Zr((NSiMe3)2SiMe2}2,3,378 S~~ZTC~~HS~C~N~ ZrCl{N(SiMe,),},, 3,377 Si&C72H6009 ~ Z ~ { ( O S I P ~ , ) , O3,418 ),~~~,

S~BMOZC~~H~SN~ M O ~ { S ~ ( S ~ M ~ ~ ) , ) ~ (3,N 13 M14 ~,)~, SisNb,C2,H7,CI,N4 NbZC14(N(SiM~3)2}4, 3,652 Si,Zr,C,6H,8N40 (ZrMe{N(SiMe,)2}2}20,3,386 SmBr, SmBr,, 3,1110 SrnCaH,,N06 ~Sm{Et02CCHzN(CHzC02)2}]-, 6,122 S ~ C I ~ H ~ O ~ ~ P ~ S S [Sml(EtO)zPS2)41-. 2,644 SmC,JL&O 1 6 Srn(N03)3(H20)(2-methoxy-l.3-xylyl- 18-crown-6), 3, 1093 SmCixIiziN,Os [Sm(NO,)(OH)(H,O)( N=CH(2,6-p4.)CH= NCHZCH,N=CH(2,&py)CH=NCH,C kit}]+, 3,1096 SrnCiaHdb06 [ S I ~ ( ~ - ~ ~ C O N H N H ~ )3.~ ( 1090 H~O)~]~+. SmCzoH,4C1301a Srn(C104),(dibenzo-18-crown-6) 3. 1092 SmC21H17010 Srn(2-0,CC6H,0H),(H,0), 2,181 SrnC24H16N709 Sm(NO3)4phen)~,3,1109 SrnC14H5ZN50 J', Srn(NO,),{ OPPr',(CH,CONEt,)) 3. 1084 SrnC36H45N40 Srn(octaethylporphyrin)(OH).2.822 1

SmC36H66P3S6

Srn~S2P(C6Hll),13, 3,1087 SmC6zH650,PzS4 [Sm{S2P(OEt),),(OPPh,),]', 1.78 SmC62H6@7P5S4 [Srn {S,P(OEt),} ,( OPPh3)3]+.3. 1083 SmC72H6oC1304P4 SmC13(0PPh3),, 3, 1082 SmCI, SmCl,, 3, 1110 SrnC130,z Sm(C104),, 3, 1 I I I Sml, SmI,,3, 1110 SmN4OI2 [Sm(N03)4]-, 3, 1076 SmNsOls @I(NO,),]~-, 3, 1076

SmZrF, SrnZrF,, 3,428

578

SnAuC36HJOC13P2 Au(SnCI3)(PPh3),. 5.904 SnAuC54H45C13Pj Au(SnCl,)(PPh,),. 5,904 SnAu,BaS, Au,BaSnS,, 5. 873 SnBC3H9F4 SnMe,BF,, 5.689 SIlRC3f 112 [BH,SnhIe,l-, 3,91 SnBCI, [BCI,SnCI,] . 3 . 9 3 SnB20C14H3604

Sn(acac),(9-( 1 ,2-B&Hl1j2, 2,392 SnBzoHgCwH360,

S~(~C~C)~{Y-(~.~-B~~C~H,,}H~{Y-( 1,2-BlOC2HI1)}.2. 392 SnBr, [SnBr,]-, 3, 195 SnBr6 [SnBr,]'-, 3, 200 SnCH3CI4 [SnMeCI,]-. 3.200 StlCH,N,Oy SnMe(NO,);, X,82,3,212 SnCH,O, [Sn(OH),(C03)] .6,HS4 SnCH4CI,N,S SnC12{SC(NH2)2). 3, 194 SnC2H,0, Sn(O,CH),. 3.222 SGH6 [SnMe,],. 1. 126 SnC2H6C13 [SnMe,Cl,]-, 3,320 SnC2H6C14 [SnMe2CI4I2 .3.200 SnC2H6F206S2 SnMe2(OSOIF)Z.3,211 SnC,H,N,O, SnMez(N03),, l,jY,3.212 SnC2H60, Sn(OMe),. 3.220 SnC,H,Br, [SnMe,BrJ. 3.199 SnC3H9CI2 [SnMe,CI,]-. 3.200 SnC,H9N0, SnMe,(NO,). 3,210 SnC3H,N, SnMe,N,. 3,210 SnC3H9N302S, SnMe,(NSN=S=NSO,), 3,210 SnC,I 1 ,,,O SnMe,(OH). 3,210 SnC,H6C14N, SnCI,(MeCN),, 3.200 SnC4H6O2S4 Sn(S2COMe),. 3.221 SnC4H,CI30, SnCI3(CH2CH2CO,Evie),3, 198 SnC,H8C1,0z S n C I , ( ~ C H , C H , ~ C H , ~ H ,3, ) , 194

sn& ;: H.),

3.220 SnC,H,NS SnMe,(h'CS). 3,210 SnC4H12N2 Sn(NMe,),, 3,220 S~C~HIJ'JZOZ SnMe,(N(Me)NO,}, 3,210 SnC,H,,O SnMe,(OMe), 3,208.210

579

Cumulative Formula Index

SnC4Hl,0zS SnMe,(O,SMe), 3,210 SnC4H120ZSe SnMe3(03SeMe),3,210 SnC4Hlz04 Sn(OMe),, 2,346 snCsi-15 [SnCp]+,3,217 SnCqH,C1 SnCpCl, 3,218,219 SnCSH9F3O2 SnMel(02CCF3), 3,210 SnC,H9N3 SnMc3{N(CN),}, 3,210 SnC5HllN204 SnMe(H2NCH2C02)2,2: 735 ~,

~

SnC,H,;N SnMe,(N=H,), 3,217 SnC,H,,N02 s~M&(o,CCH,NH~). 3. 210 SnC,H,,N SnMe,(NMe,), 2, 180 SnC6H6N2S2 SnMe2(S2CZ(CN),},2.605 SnCbHgF6N SnMe,{N=C(CF,),) 2, 279 SnC6H10Br202S4 Sn(SzCOEt)zBrz,1,57 SnC4HloCI,0,S4 Sn(SZCOEt),Cl,, 1 , 5 7 S ~ C ~ H ~ Z O , SnMe,(ONHCOMe),. 2,508; 3,211,212 SnC4H14S SnPr',S, 3,213 SnC,HI8CIZOZSZ SnMe,CI,(DMSO)Z, 3,200 SnC6H18ClaNL02 SnCI,(Mc,NO),, 2.497 SnC6HlsP2S4 Sn(S,PMe,),Mc,, 1.59 SnC,Hl3NO2 SnMe,(f4COCHzCHz~O),3,210 SnC7HI5NO3 Sn{OCHZCH,),N}Me, 3,212 SnC8H9CI3O2 Sn(CH=CH,),(O,CCCl,), 3.210 SnCsHlZ08 Sn(OAc),, 1,94: 3.212 SnC8HI4C1N SnMe,Cl(py), 3, 199 SnC8HlsNZ04 Sn(ONMeCOMe),Me,, 2,508 S~C~HI~NZS, SnMe,(SzCNMeZ),. 1. 59: 3.215 SnCsHi8Oz Sn(OBu')2, 3,220 SnC8H19C10 SnBu',(OH)CI, 3,207 SnC8HzOI2P~S4 Sn(SZPEt2)212,1, 57 SnC8HzONzO4 SnMe,(ONMeCOMe),.3,212 SnC8Hd4 Sn(NMe,),, 2, 172, 177. 178 SnC9H,,01P SnMe3{OzP(OH)Ph}. 3.210 SnC,H,,NO SnMe,(ON=C,H,,). 3,208,210 SnC9HZ1NO4S Sn{(OCH,CH,),N} Me( DMSO) 3 . 2 12 SnC10H2F1204 '

SnC,,H,,P,

Sn(hfacac)2, 2,392 SnCloH8F,KZ SnF,(bipy). 3.203 SnCioHio SnCp,, 2. 17; 3.217-219 SnC,oH,oI,",02 SnI,(p!;ridine N-oxide),, 2,496 SnCIoH14C1204 Sn(acac),C12. 6, 121 [ S n C l , ( a c a ~ ) ~ ]2,376 ~+. SnCloH,,N,09 [Sn(H,0)(edta)12-, 2,783 SnCl,,H14U, Sn(acac),, 2,378,391 SnCmH,, [Sn(C,Me,)j+, 3,217,218 .SnC,,H,,NO, Sn(ONHCOPh)Me,, 2,507 SnC1oHzo~,OzS, Sn(S2COEt2)212,I , 57 SnC10H2,N2Si SnN(Bu')Si;Ve2~Bu',3,220 SnC~llH,,CI,N2 SnMeCI3(py),, 3,200 SnC11Hd02 SnMe,(phthalide), 3,210 SnC, 1HI SnEt,(tropolonate), 2,372 SnCl1H1,IO, SnMeI(acac)2, 2,392 SnC, 1Hzz02S SnBu2(0,CCHZCH2S),6,123 SnCizHizO SnCp(C5H4COMe),3,218 SnCl,Hz0O4 Sn(acac),Me2, 1.58; 2,372,381; 3,212 SnC.l,H,,104Sfi Sn(S,COEt(Z(SCSOEt),, 1.57 SnC12H3102 [SnBu,(OH,),]+. 2, 297 SnC, 2H36NzSi4 Sn{N(SiMe,),},: 3.220 SnC13H300 SnBu,(OMe), 3,208 SnCl4H,Cl30, Sn(2-hydroxyanthraquinon-I-olate)C13, 6,86 SnCl4H,,ClS4 $ I I ( S C ~ H $ - ~ - M ~ - ~3,214 )~CI, [SnC1(S2C,H3Me)J, 2,605 SnC14H12C13N SnC13{C,H4{C(=NH)C6H,Me-4}-2), 3. 198 SnC,,IJ,,0,S2 SnBu,(O,OCH,CH,SH),, 6,123 SnCI4H3& Sn{CH(SiMe,),},, 2, 17 SnC ,5HgClj04 SnCI3(2-methoxyanthraquinon-1-olate),6.55 SnCl5Hz0N [Sn(C,Me,)(py)l+, 3,218 SnClSHJ9N6O2P2 [SnMe,(hmpt),]+. 3, 199 SnC16~12C~404 SnC14(1.2-dirnethoxyanthraquinone). 6,55 SnCl 6Hl,N,03 SnPhz{H,NCHzCONHCH,CO,}, 2,763 SnC 6Hl,N02 Sn(ONPhCOPh)Me,. 2, SO7 S~CI~I'I~~N~S~ SnMe(S2CNEt2),, 3,215 SnC,,H,,O, Sn(OBu'),. 2,346, 349 SnC16H36PZ SnBu',(PBu')2, 3,216

Cumulative Formula Index SnC17H,6C120 SnMe,Cl,{PhC=C(Ph)CO}, S IIC~,H,~ CIN~ [SnMe,(terpy)CI]+, 3, 199 SnC,.H,,CI

3.199

SnC1BH28Nfi60S3 [Sn(NO3)Ph,(DMSO)3]'. 1.77 SnC,*H, ,NO Sn@h3(NCO), 3,210 SnC19H15NS SnPhdNCS), 3,210 SnCzoHl8CINO3 SnCIIONPhCOPhMOMelPh. 2.508 SnCZ0&02 SnPh,(OAc), 3,210 SnC2,Hlf104 Sn(PhCOCHCOMc),, 2,372 SnC20H23N2 [Sn(C,Mc,)(hipy)j+, 3,218 SnC2&o Sn(C,Me&, 3,218 SnC,H3,O4PZS4 SnPhz{SzP(OEt)2}z,3,215 SnC20H35N3 Sn(C6H,,),(flN=CHN=cH), 3,210 SnCzoH40N4Ss Sn(S2CNEt2),(SCSNEt2)2, 1,57 SnC,iH&106 Sn(02C7H5)3C1,1,82 snC21II18s6 [Sn(S2C6H3M~)3]-, 2,605 SnCZZHl8C12Nz SnPh,C!,(hipy), 3,200 S~CIZH~~O~PS~ S ~ P I I ~ { ( E ~ O ) ~ 2,644 PS~}, SnC22H~504P SnPh,{OzP(OEt)2}, 3,209 SnCZZH30N~S4 Sn(S,CNEt2)zPh2, 1,57 SnCZ3Hl9NS SnPh,(Spy-4), 3,213 SnC23H2402 Sn(CH,Ph),(OAc), 3,210 SnCZ4HlsFN02 SnPh3(0CsH3F-2-NO-4), 3.210 SnCdL004PS4 Sn{S2P(OPh)z}2,3,222 SnCa4H2&IOP SnMelCI(Ph3PCHCOMe). 3, 200 SnC,,H,,S2 Sn(SC6H3Pr',-2,6),, 3,220 SnC24H3804PZS4 SnPhz{SzP(OPri)z}z,3,215 SnC2,HZ0CINO2 SnCl(ONPhCOPh)Ph,, 2,508 , \

I

580

Sn(ONPhCOPh)Ph,, 2.508 S~C~ZHI~CI&. Sn(phthalocyanine)CI,, 2,863,864 SnC32H16N8 Sn(phtha1ocyanine). 2.863,864 SnC3zH 18N80z Sn(phthalocyanine)( OH),, 2,864 SnC32Hz5C1N204 SnCIIONPhCOPhLPh. 2,508 SllC33H2602 SnPh,(PhCOCHCOPh), 2,373

(Sn(phtha1ocyanine)O } n, 6, 151 SnC36H30C14P2S2 S I I ( P ~ ~ P S ) ~ 2.6Ltl CI,~ SnC36H3002Si2 Sn(OSiPh3),. 3- 220 SnC36H44C1ZN4 Sn(octaethyIporphyrin)CI,, 2,853 SnC3hH44N4 Sn(octacthvlporphvrin), 2,822 SnC36H46C12N4 Snloctaethylchlorin)CI,, 2,853 S~C~~'H~~CIZN Sn(octdethylisobacteriochIorin)Cl,, 2,853

Sn(ONPhCOPh),Ph,, 2,508 SnC44H28C12N4 Sn(tetraphenyIporphyrin)CI,, 2, 822, 853 SnC44Hz8N4 Sn(tetrapheny1porphyrin). 2, 822 SnC44H30C12N, Sn(tetraphenyIchtorin)CIZ. 2,853 SnC44H32ClzN1 Sn[tetraphenylisobact~riochlorin)CI,,2, 853 SnCcwH,ZN i t , Sn(phthalocqanine),, 2,863-865 SnCdL Sn(C5Ph5),, 3.217,218 SnCI, (SnC13]-, 3.195 SnCI, [SnC14]z-,3.195 SnCI4N206 [SnCl.,(N0,),12-, 3,8 . SnCI, [SnCI,]-. 3.200 SnCI, [SnC16]2 , 1. 16,3,200: 6,292 SnCIBOP [SnClS(0PCl1)] 3.200 SnClloOzPz SnC14(0PC13)z,2, 498 SnCoCu2CloH140, CoCu,Sn(yAcO),CpMe, 1, 122 SnCo3Cl,Br0,, {Co(CO],},SnBr. 2, 19 SnCrCl8HZ3NOS Cr(CO)s(SnBu',py), 2,17, 19 SnCrC19H380SSi4 Cr(CO)j(Sn{CH(SiMe,)*}*}r 2, 17, 19 SnCrC,,H&, CrO,(OSnPh&. 3.942 SnF, [SnF3J ,3.195: 6. 12 SnF6 [SnF6l2-, 1.538: 3.200; 6, 12,854

-.

581

C'umulutive Formulu Index

SnFeC'121136CI,0,,P, Fe(StiCl,)CI{ P( O M S ) ~ }4.~ .1233 SnFeCI4HloO4 Fe(CO),(SnCpA 2, 17 SnFeC14Hi408 Fe(CO),{Sn(acac),], 2. 18 SnFeC15H45C1301jP5 Fe(SnC13){P(OMe),)5, 4, 1233 SnFeCzoH,,C13NO~P Fe(SnCI,)(CO),(NO)(PPh3). 4.I189 SnFeC2,H2,,OZS2 Ph?Sn(CS,)Fe(CO),Cp. 2, 5x3 StlFczCi,CI,04 {FeCp(CO),}2SnC12,2 , 19 SnFe,C,,H,O, {FeCp(CO)2},SnMe2, 2 , 19 SnGaC6Hls [GaMe,SnMe,]-. 3.129 SnGa,Cl, Sn(GaCl,)2, 3, 139 SnHO, [SnO(OH)]-, 2,296.3.201 SnH,O, [Sn(OH),]-, 3,204; 6.12 SnH,06 [Sn(C)t1),]2 , 2 , 341:3,204; 6, 4,12 SnHgC61118 H.g(SnMe,),, 5, 1085 SnHgMn2Cs3H,sN40, Sn(tetraphenylporphyrin)Mn(CO),HgMn(CO),, 2,843 SnI, [SnI,]-, 3, 195 SnInC12H30 [InMe,(SnMe,)]'-, 3, 158 SnInC18HISC1,N2 InC1,(SnPh3), 3,158 SnInCi8HI5CI, [InC13(SnPh3)]-, 3, 158 SnlnC36H39N2 1n(C,H4CH,NMU,-2),[SnPh,j, 3, 158 snIl-c2,w2,0,P Ir(CO),(SnMe,)(PPh,), 4. 1103 SnhC36H31C14P2 IrHC1(SnC13)(PPh3)2,4, 1103 SnIrC36H3ZC140P2 IrH2(SnC13)(CO)(PPh,)2. 4 . 1103 SnIrC3,H30C130P2 IrCl(SnCl,)(CO)(PPh,),. 4. 1103 SnIrC37H30C150PZ IrCI(SnCI,)(CO)(PPh,)2. 1. 1128 SnJrC37H31C140P2 IrlTCl(SnCI3)(CO)(PPh3),. 4. 1103. 1127 SnIrC37H3zCI,C)P, IrHZ(SnC13)(CC))(PPh,),, 1.1127 SnIrC,J I,,Cl,0P2 IrCI(SnCl,)Me(Co)(rrh;)2.4;112.8 SnIrC;9H3,LLP Ir(CO),(SnPh3)(PPh3): 4, I103 SnIrC39H34C130P2 Ir(SnC13)(C,H,)(CO)(PPh3)2. 4. 1103 SnhC54H46C14P3 IrHCI(SnCl,)(PPh,),. 4. 1127 SnIr2C42H30C1206P2 {Ir(C0)3(PPh3)}2(SnC12)z 4. 1103 SIlIr2C44H3606P2 {Ir(CO),(PPh3)),(SnMeZ).4, 1103 SnMnC,H,O, Mn(CO),(SnMe,),2, 19 SnMnCisH.,70z Mn(C0)2(C5H4Mc)(SnCp,), 2. 17 SnMnCZ3Hl5O4S2 (OC),Mn(CS,)SnPh,, 2. 58.3 SnMn3Ci,C10,,

SnRuC,VH,U1403P,

(Mn(CO),),SnCI, 2, 19 SnMoC2H604 SnMe,(MoO,). 3. 1376 S~MOCJO&C~~N~ [Mo(S~C~,)(CNBU')~]+, 2, 19 SnMoC30H54C13N6 [.Mo(CNBU)~(S~CI,)]+, 1,73 SnN,012 Sn(SO,)+?1,94; 3,212 Sn(O,YO),, 2,418 SnNbC29H2s0 NbCp2(CO)(SnPh3), 2, 19 SnNiC4C1404S4 [Ni!S~c'za,)2(Sncl,)]~-,5, 182 SnNiC60H5,NP3

[N~~SI~P~~){N(CH,CH,PP~~)~}]+, 5,139 S nNiH, .CI,O,

SnOsCI, [ O S ( S ~ C I ~ ) C,I4~, ]527 ~ SnOs,C,,H,,O,S,I' Os;H(S)(SCH,~(CO),(PMe,Ph)(SnMe,), 2, 19 SnOs3Cz4H4L~010S14 Os,(SnHz)(CO)i,{CH(StMe~)2}~, 2, 19 SnPtC31H32C1402PZ PtCl(SnCl,)(dtop), 6,266 SnPtC36H30C1,P2 PtCl(SnCI,)(PPh,),, 6,248 SnPtC36H31C13P, PtH(SnC13)(PPh3)Z.5,358,371; 6,248,263 SnPrC3-H30C130P, pt~l(SnC13)(CO)(pph3)2, 5,371 SnPtC,,H,,CI,OP, PtH(SnCl,)(CO)(PPh3),, 6,263 SnPtC,,H,,ClP, PtMe(SnMe,CI)(PPh,),. 2, 180 SnPtC40H37C130P2 P~(SIICI,)(COP~)(PP~,)~, 6,264 SnPtC42H35C13PZ Pt(SnC13)Ph(PPh3)z,5,400 SnPtC42H39F6NP2 Pt(SnMe,){ NC(CF,),} (PPh,),. 2, 126 SnPtC5,H,5C1P2 PtCI(SnPh;)(PPh3),, 5,420 SnPtCS6H4,P2SZ Pt { MeSC(S)SnPh,} (PPh3)2,5,487 SnKeCZ3Hj,UjS2 (OC)4Re(CSz)SnPh3,2,583 SnReCt4H,,0;S2 (OC),Ke (CSJSnPh,. 2,553 SnRe2ClsHlhNxO6 { Re(CO),) ,Sn(phthalocyanine), 2. Xh8 SnRe2C50H28N,06 Sn(tetraphenylporphyrtn){Re(CO)3}2, 2,844 SnRhClBH,,Fl2P, Rh(PF3)?SnPh3,4,904 SnRhSbCj,H&l, RhCl2(SnCI3)(SbPh3),,4, 1032 SnRuC4C1404 RuCl(SnCI,)(CO),, 4,288 SnRuC,H,ClO, RuCI(SnMc,)(CO),, 4,288 SnRuCI4H3&l3O2S3 [Ku(SnCI3)(CO),(SEt,),]+, 4,289,432 Sn KUC;,!J,,CI~NP (- )-Ru( SnCl3)Me(C6H6)(PhzPNHCHMePh). 2. 19 S~RUC~~H~~I,O~P~

S ~ R U C ~ ~ H ~ ~ I ~ O ~ PCumulutive ~ Formula Index [RuI(CO)3(PPh3)z]Sn13,4,289 SnRuC40H36C1402P2

RuCI(SnCl,)(CO)(PPh3),(OCMe,).4.288 SnRuC42H40C14N2P2

RuC1(SnCI3)(CNEt),(PPh3),4.289. 384 SnRuC4*H4,CI3P4 RuH(SnCI,)(PHPh,),, 4,289,452 SnRu2C5Clb05 Ru,C13(CO)5(SnCI,), 2,684; 4.288 SnRu2C56H,,C1,0,P,

-

Ru(SnC13)(CO)(PPh,)(p-Cl)3Ru(CO)(PPh3)2, 4,288 S ~ R U ~ C ~ ~ C I , ~ ~ ~ Ru3(CO),,SnCI,, 4,288 SnS, [SnS3I2-, 3,205; 6,853 S~TCC,,H,,C~~N~O, TC(DMG)~(S~CI,)(OH), 6,974,978 SnWCsHllCI 0 S W C O ) ,{ CH,C(CH ) H2}(SnMeC13),3.1007 Sn WC3,H W(CHC6H4Me-4)(SnPh,)( CO),Cp, 2,19 Sn2B,Co,C3,H2,C12N1201~ [Sn,Co,Cl,(CO),,][Co{HB(~N=CHCH=~H),],, 2, 19 Sn2C7Hl& (SnMe,N=),C, 3,210 Sn,C,H&O, SnMe,(NCO).SnMe,(OH), 3, 210 Sn2CsHz4N4 {Sn(NMez)(p-NMe2))2,2,170 S~ZC~HZOO~ (SnMe302C),CH2,3,210 Sn2C14H3,N3Si Sn,(SiMe,)(NBu'),, 3,221 Sn2Ci6H36S2 (SnBu',S),, 3,213 SnzCi6H36Scz (SnBu',Se),, 3,213 S n K 16H3hTe2 (SnBu',Te),, 3,213 Sn2CdW4 (SnEt,),(PBu'),, 3,216 Sn2C2d%W16 Sn2(02CC6H4N02-2)40,3,222 SnzC36H300 (SnPh,),O, 3,206 SnzC36H30S (SnPh3),S, 3,213 Sn~C36H3oSe (SnPh3),Se, 3,213 Sn2CIF3 SnZF3CI,3,195 Sn2C02C6H1202 {CoCp(CO)(SnMe,)},, 2. 19 Sn,CrC, H IsOsTe Cr(CO),{Te(SnMe3)2), 2, 670 Sn2F31 Sn,F,I, 3, 195 Sn2FS [Sn,F5]-, 3, 195 Sn2FezC12HlzOs {Fe(C0)4(SnMe,)},, 2, 19 Sn2FeK28Hzo08 {Fe(CO),(SnCpz)l2, 2, 19 Sndh Sn(H,)=SnH,, 3,217 SnJ-LO, [{Sn(OH),~,OIZ-,3,204 Sn2HfC13H26 Hf(PhMe)(SnMe,),, 2, 16 Sn2Hg2Br5 [Hg,(SnBr,)(SnBr,)]+, 5 , 1058 SnzHg,BrSCI04

Hg,BrCIO4~2SnBr,, 2 , 4 Sn,IrBr,, [1rBr4(SnBr3)J. 4-1127 SnZMn4C20H2020 {Mn(CO),},Sn2H,, 2, 19 SnZMoCll0 [ M o C I ~ ( S ~ C I , ) ~3, ] ~1342 -. SnZNiC4CI8O4S4 [Ni(S2Cz02SnC14)2]2-5 , 182 Sn,0sS4 Sn,(O,S,),, 2,431 Sn20sC8H2UClhNJS4 OS(MCC(S)NF~~)~~S~UI,),, 2,647 Sn,OsCI,NO [Os(NO)C13(SnC13)2]Z-.4,548 [ O S ( N O ) C I ~ ( S ~ C I ~4,) ~549 ]~+ Sn2PtC12H3,Cl6P, [PtH(SnC13)2(PEt3)2]-I5,371 Sn,PtC&3&1606P2 Pt(SnC13)2{p(oph)3},, 2, 19 S~~P~C~,&OCI~P~ [Pt(SnC13)Z(PPh3)21, 5.421 Sn,PtC5,H,J', PtH,(SnPh,),(PMe,Ph)2, 5,358 Sn2PtC56H5808P2 Pt{Sn(xac),Jz(PPh&, 2, 18; 5 , 421 Sn2PtC1,, [PtC12(SnC1,)2]2-,5,121 Sn,Pt,C,H,,CI, Pt3Sll2Cl,j(COd): 5.421 Sn2RuCZC1,0, [RuCI2(SnCl3),(C0),]~~, 4,288 Sn2RUC4C1604 Ru(SnCI,),(CO),. 4.258 Sn2RuCsHZ4Cl6O4S4 Ru(SnCl,),(DMSO),, 4,289 Sn,RuCl,,Hl,O, Ru(SnMe,),(CO),, 4,288 Sn,RuC,IH,OCI,N, Ru(SnCI,),(CNEt),, 4:289 Sn,RuCI,NO [RuC1,(SnC13),(iYO)]2-. 4,288 Sn2RuzC12H1208 {Ru(p-SnMe,)(CO),),, 4,288 Sn2RuZCll2N2O2 [RU2CI6(SnCI,),(E*IO)2]~-,4,288 Sn2S3 Sn2S3,3,202 Sn2S5 [Sn2S,]2-. 3,205 SnZVC41H3005 [V(C0)5(SnPh,),]-, 3,457 Sn2W4S16 [Sn2(WS&I4 2. Shb S~~WLSC~~HIO~~OPZ [W,,P,(SnPh),O,dls-. 3, 1049 Sn3BiC,H,, Bi(SnMe,),, 3.281 Sn3BiClsH45 Bi(SnEt3)3, 3; 281 Sn3BiC,4H45 Bi(SnPh&. 3.281 Sn3BrF, Sn3F5Br,3, 195 Sn3C6H1808P2 (SnMe2)3(P04)2,3,211 Sn,C,H,,S, Sn3S,Me,, 1, I42 Sn3C9H27N ( S I I M ~ ~ )3.215 ~N, Sn3C16H36NZ02 Sn3(OBu'),(NBu1),, 3.221 Sn3Cl6Hd~

582

583

Cumulative Formula Index

Snp(NBu')2(HNBu')z, 3, 221

[Cr(CO)4(SnPh3)3]-. 2. 16, 19 Sn3Fs Sn,F,, 3, 195

1

{Fe(Cb)4}2SnMc}2Sn,2. 19 Sn 3 H z03 [Sn30(OH)z]r'.3,202 Sn,H,O,S Sn30(OH)2(S04), 2.303 Sn304 Sn304,3,202 Sn3PtCsHl2CI9 [Pt(SnCl,),(cod)]-. 2.20 Sn3PtzC66HnO& {Pt(PPh3)}z{Sn(acac),)3. 2. 18; 5,421 Sn3ShC,,H4, Sb(SnPh3)3, 3,259 SnlZrCS8H55N 2r(NEtZ)(SnPh3),, 2. 180: 3.370 Sn3ZrC61H51NO Zr{ NPhC(O)H} (SnPh?)?. 3. 37U Sn4 [Sn4I2-, 3,46 Sn,C711,,N5Si Sn4(SiMez)(NMe)5,3,221 Sn4ClzHz4N40~S4 [(SnMe2(NCS)}zO]2,3,208 Sn4Ci6Fz401s 3. 222 {SnZ(02CCF3)40)z, Sn4Ci6H36N4 S ~ I ~ ( N B U3,' ) 221 ~, Sn4CZ4HZOP4 {PhSnPj4, 1, 153: 3,216 Sn4C4~H4,Q40~ {(SnPhzCI),O},. 3, 207 Sn4C48H4zC1Z04 {SnPh,CIOSnPh,(OH)),, 3,207 Sn4C54H45N03 Sn(N03)(SnPh3)3,1.37 Sn4PtC7,HssOzP PtH{ Sn(C6H4Me-3),}3 { Sn(c6H4Me-4),}(OMe),(PEt,). 5.358 Sn4PtHC116 [PtH(SnCI4),l3-, 5,487 Sn4RhZCIl4 ({RhCI(SnC13),}214-,4,906

SrC , , ~ , , ~ , O , S ,

[Pr(SnCl,),]3-, 5,421 Sn,RuCIF 15 [RuC1(SnF3),j4-. 4 288 Sn5RuCl16 [ Ru CI ( S ~ C I ~ ) , ] 4, ~ -288 , Sn6C4Hiz08 Sn6(u3-0)4(u3-0Me)4r 1, 139, 160; 3. 220 S ~ ~ C I ~ I ~ P , (SnMe,),P,. 3,216 Sn6C4aHlosNlzOn [{ S n B ~ ~ ~ N ~ 1 0 ) ~ S t3,208 iBu~],, Sn,CI,,O,, 1S ~ ~ O ~ C I ~ ( ~ C ~ O ~ )2,426 (~ZCIO~)~}~, Sn,OsCII8 [Os(SnC1,)J4 ,4,527 Sn,KuClIB [Ru(SnCf&P-, 4,288 Sn6RuFI8 [Ru(SnF3),I4-, 4,288 Sn7ZrzClzoHloo {Zr(SnPh3)3}2SnPh2,3,370 SnBMo2C26H78N4 Moz{Sn~SnMe3),},(NMe2),,3,1310, 1314 Sn8Pt3CIz0 [Pt3SnaClzo14,5.421 SnxTl [T1Sn8]'-, 1 , 165; 3, 168 3, 168 [TISII~]~-. Sn, [ S I I ~ ]$~4 6~ , Sn9PtC36H30P2 [PtSn9(PPh3),]", 5,421

%,TI [T1Sn9I3-. 3. 168 Sn,oOS2* [Snlo04S2~l",1,167 Sn21H4C1d10 Sn2,C!1,(OH)406, 3, 195 SIC4H,06 Sr( D,CCti(OH)C't l(OH)C'OI}, 2,479

SrC44H,2Rr101 SrBr2(HOCH2CHZO11)z.3 , 1 4 SrC6H,,CI2Ol1 SrCl,(epiinositol)(H,0),, 3,25 SrC8H12N60,I 1. 130 Sr(H20)4(C4H2N304)2r SrCloHllNzOs [Sr(edta)12-. 2.784 SrC10H13~ZOs [Sr(Hedta)]-, 2,784 SrC I 1H14N20, [Sr(tmta)l2-, 2,784 SrC,,H ,5N208 [Sr(Htmtd)] ,2,784 SrC12H,6N20S

{Sb(SnMe,),},. 3.261 Sn4ZrC7zH60 Zr(SnPh3)4, 3, 370 SnSCloH30Pz (SnMe2),Pz, 3, 216 SnA [SnSF9]+,3,195 Sn,OSBr,6 [0s(SnBr3),BrI4-, 4, 527 Sn,OsCIIS [ O S ( S ~ C I ~ ) , ]4.527 ~-. Sn~OsCll6 [OS(S~CI~),CI]~-. 4.527 [ O S ( S ~ C ~ ~ ) , C I4.527 ]~-. SnsPtC1,, [Pt(SnCI3),]-, 2, 19

[Sr(tela)J2-, 2,784 SrClZH17N208 [Sr(Hteta)]-. 2,784 SrCllH30?140

Sr(N03)2(h(CHzCH20H)3}2, 3.23 S~CizH1sC~2Niz

SrCll(en)6, 3, 11 SrC,,&N;O,

~Sr{~=CH(2,5-furyl)CH=CN(CH,CH20),-

CH,CH,NH,O)P+. 3.44 -,, SrC,,H&1301s Sr (il'-ace tobenzo- 18-crowti-h)(CI04)*, 3,42 SrCr4HZ6N2O7SZ Sr(~CS),{HO(CH,CH,O),tr}, 3. 17 I

_

Cumulative Formula Index Sr(NCS)z{HO(CHzCH20),H) 3, 17

[Sr(H20)8J2C. 1.84 SrHgC4H,N403S, Sr[Hg(SCN),]. 2.297 SrHgSe4C4N, SrHg(SeCN),, 5. 1064 SrNiN6OlZ [SrNi(N0z),]2-. 5,701 SrNiSbO, SrNiSbO,, 5.297 Sr,FcO, Sr,FeO,, 4.266 sr3OZ4% [SF~(SO,),]", 3 , 1076

5 84

T TaAIC1SH4804P4

Ta{HZAI(OCHzCHzOMe)z)(dmpe)z, 3,679 TaAlCz4Hs6Qs TaAl(OPr’),, 2, 344 TaAsCiRHl,C~, TaCI,(AsPh,), 3, M)O TaAszCloHi6C14 TaCl,(diars), 3, 642 T ~ A s ~ C ~ ~ H ~ ~ B ~ ~ [TaBr,(diars),]+. 1, 88; 3. 594,599 TaAs4C20H3ZC14 TaCl,(diars), 3, 644 [TaC14(diars)z]t, 1,W; 3.599 ‘I‘aAuC,,H,,O6P Au{Ta(CO),}(PPh,), 5,904 TaBC12H,9C1N6 TaClMe3{(pyrazotyl),BH},3,622 TaBCI3Hz5CIN4 Ta{H,B(&N=CMeCH&Me),} Me,CI, 2,248 TaB2Ci4HzzNs Ta { H,B( fiN=CHCH=cH),) ,Me,, 2,248 TaBrN TaNBr, 3,654 TaBrO, TaOBr,, 3,626 TaBr30 TaOBr,, 3,626 TaBr,N [TaBr,NI2-, 3,620 TaBr, TaBr5, 3,589,590 TaBr6 [TaBr,]-, 3,594 TaCzF,Oz [TaF,(O,CCF,)]-, 3.607 TaC,H3ClsN TaCI,(MeCN), 3,597 TaC,H6Br,S TaBr,(Me,S), 1,287 TaC3HZCISN2 TaCI5(NCCH,CN), 3,597 TaC3H6F15P5 Ta(PF3),(q3-allyl),3,683 TaC,H,Br,N,O TaOBr,{CBr(NMe)}(MeNC). 3,624 TaC4H6C1,N20 TaOCI,(MeCN),, 3,635 TaC4Hs14N0 TaI,(OEt)(MeCN). 3.606 TaC4HI2Br4 TaBr,(SMe,),. 3,643 TaC4N40S4 [TaO(NCS).,-, 3,635 TaC,H,,F,O,PS TaF,{OP(OEt),SMe), 3.595 TaC5H1SC1204SZ TaOCI,(OMe)(DMSO),, 3.633 TaC~H1505 Ta(OMe),, ,- 2,339; 3, Nl3 TaC505 [Ta(C0),l3-, 3,684

TaC,H,,Cl,O, TaCl,(OCH,CH,OMe),, 3,606 TaC6Hl9CI1N3 TaC13(NMe2)Z(NHMez), 3,609 T ac6N6s6 [Ta(NCS),]-, 3,624 TaC,N&e6 [Ta(NCSe)J, 3,624 TaC,O, [Ta(co)6]-, 3,684 TaC7H5CI5NS TaSCl,(PhNCCI,), 3,596,626,635 TaC,H7F4N0, [Ta(O,)F,(Z-Mcpy N-oxide)]-, 2,319 TaC,H, ,N2 Ta(NMe&Me3, 3,610 TaCBH5Cl2N5S5 [TaS(NCS)4(PhNCC12)]-,3,626 TaCBH,CIz03 TaCI,(CO),(Cp), 3,666 TaCBH,03 ITa(CO)dCp)lZ-, 3,685 TaC8H603 [TaH(CO),(Cp)l-, 3,685 T aC H I N0 TaT,(OPh)(MeCN), 3,603 TaCsHi2Br5N4 TaBrz{ CBr(NMe)},( MeNC) ,3,624 TaC,H,,Cl TaCIMe,(Cp), 3,612 TaCaHI6Cl3OJ TaCl,(OMe),(acac), 3,607 TaCsN&1303 TaOC13(1)CH2CH20CHz~HHZ)Z, 3,641 TaCs016 ]Ta(Cz04)4]5-,3,666 TaCPH,O, Ta(CO),(Cp), 3.682 TaC9H,,C1 TaCp(CHMe,)CI, 2,703 TaC H N m M e ) M e , ( C p ) . 3,612 TaCaH,,04 Ta(OMe),(Cp), 3,616 TaC9HlBCI2N30, TaCI,{NMeC(O)Me},, 3,623 TaC9HZ7Cl3P3 TaC13(PMe3),,3,656 TaC9HZ7C1,P3 TaCI,(PMe,),, 3,644 TaC9H2J3P3 TaI,(PMe,),, 3,656 TaCloHBCI3N20 TaOCi,(bipy), 3,629 TaC,J-IaClsN2 TaCl,(bipy), 3,597 TaCioHi,CI,N2 TaCl,(py),. 3,594,641 TaCloH,,C1,O4 TaCI,(O,CBu’),, 3,606 TaCI~H27N4

585

Curnularive Formula Index Ta(NBu')(NMe,),, 2, 165, 166; 3,613.617 TaC, Ta(NMe2)5,2, 166,168, 179;3,609.611 TaC12H8N208 [ T a ( 0 z ) z ~ 2 - ~ ~ C O 6.329 z)z1~, TaCizH16Sz Ta(SMe),(Cp),, 3,652 TaCiZH2& Ta(NPh)(NMe,),, 2, 166 TaC,,HZ,CI,O, TaCI4(18-crown-6),3,641 1 aC12H24N4S8 [ T A ( S ~ C N M ~I , , )1,94,3,608 ~] T~C,ZH,&IO~P, TaCI(CO),(PMe,),, 3,680 TaCl,H2,F50P TaFs(OPBu3),3,595 TaC12H2,CIP,

TaC1(PMe3)2(H2C=CH2)(HzC=CHCH,). TaCizH30C14P~ TaC1,(PEt3),, 3,642,644 TaC12H3&I~P4 TaCl,(dmpe),, 3,677 'TaC12(R.le2PCH2CH2PMe2),, 2, 1013 TaC12H32C14P4 Ta(MezPCH2Cl-lzPMez)zC1J.1,89; 3.642. 644 [T~(Mc~PC'H~CH,PMC,)~CL~] ' ,1,89 TaCl,H,,N4 Ta(NMe&(Bu'), 2, 178 TaC12H34CW4 TaH2Clp(dmpe),, 3,679 TaC72H34C~~P4 TaH,C12(Me2PCH2CH2PMe2)z. 2.692 TaCizH36C1zP4 TaC12(PMe3)4,3,678 T~CIZH,~C~~N~~~PZ TaOC13(€lMPA)2,3,629 TaC, ,H3,P4 TaH,(dmpe),, 3,654 TLICI~H,~P~ TaH,(Mc,PCH,CH,PMc,),, 2,091 696,702 'l'aC11H3&IPj TaH2Cl(PMe3)4,3, 660 TaC12H,&12P4 2, 1013,3.679 TaH2C12(PMe3)4, TaCi3H14C1~N~ Ta(bipy)CI,Me,, 1,77; 3,598 TaCi3HnO6 Tz~(OEt)~(acac), 3,604 TaC13HdsO6 3, 611 Ta(NMe2)2(02CNMe2)3, TdC14H26N Ta(CH2NMe)(q5-CsMrs)Me,. 2. 184 TaCLQH3ZC10LP4 TaCI(CO),(dmpe),, 3, 679, 681 T~Cj4H3j02P4 TaH(CO)2(dmpe)2,3,681 TaC,,H,,CIP4 TaCI(PMe3),(H,C=CH2), 3, 682 TaCISHI C1402 Ta(PhCOCHCOPh)CI,, 2,377 TaCl,H3,N Ta(qS-C5Me,)Me,(NMe,), 2, 184 TaC15H30N3S7 TaS(S,CNEt2)3, 1,82; 2,524 TaC1SH30N50SS5 Ta(OSCNMe,)s, 3,610 TaCisH30N~0~~ Ta(O,CNMe,),, 3, h l l "I'aCI,H350S Ta(OP&, 2,347 TaC15H4J'5 Ta(PMe3)3(rpCHzPMe,)(rl-CHPMe,) 3.461

3,683

TaCl6HZ8CI,NOP Ta(NPh)Cl,(PEt,)(THF), 3,616 T~CI~HUPZ Ta(C5Me,)(PMe3),H4,2,692 TaCl6Hd, Ti(CHMe&EEt)(NEr,),, 2, 183; 3,612 TaCi7HZ7NP TaH,(NBu')(Cp)(PPhMe,), 3,616 TaC17H3&INP, Ta(NPh)CI(PMe,)3(W2CH2), 3,665 TaC,,H,,O, Ta(OMc)(OBu'),, 2,339 TaC 18H12S6 [Ta(S,CdL),l-, 1,63 TaCiSH isC1sKP [TaCl,(NPPh,)] . 2 , 123 TaC18H43N30 TaO(NPr',),, 3,616 TaC18H4z06 [Ta(OPr'),]-. 2,344 TaC19HISC14N [TaCl,(py)(PhC=CPh)]-, 3,661 TaC2uH,505 Ta(OBu'),, 3,600 TaCZoHSoN5 Ta(NEtz)s, 2 , 172; 3, 009,611 TaCZZHZ5C1302P TaC,,H2,C1302P, 3,607 TaC2,H4,,CIP4 TaCI(dmpc)2(q4-C, 3,683 TaC24H20104 TaI(OPh),, 3,603 TaC24H2307 (Ta(0PPhz0),(0H),},, 6,1014 TaCZ4HS4F4P3 [TaF4(PBu3),]+,3, 594

TaCZ6HZ4ClZP TaCl,(dppe). 3.600 TaC28H2008 [Ta(tropolonatc),]+, 2, 397 TaC,8H,,Rr,NP2 [TaBr,{CBr(NMc))(dppe)]' ,3,624 1aCz8HQ2Cl3O2 Ta(OC61l,B~'~-2,6),Cl,,2, 338 TaC3011,4N6 Ta(bipy),, 3,683 TaGoHZsO5 Ta(OPh),, 2.340; 3,603 TaC30H4702 Ta(OC6H,Bu',-2,6),(=CH,)Me, 2, 358 TaC3iH29C14PI TaCl,(dppe)(Cp). 3.594 TaC3iH5,02 Ta(OC6H3B~IZ-2,h),Me,. 2,358 TaC3,1 l,,BrlNt, Ta(phrhalo~aninc)Br,,2,861,865 TaC32H70N208

{Ta(OBut),('l'HF)),I~-~\I,), 3, 618 TZIC~~H;OC~~N~P, [TaCI4(NPPh3)J, 2,124 TaC36H3004P TaO(OPPh,),. 3.639

Ta(PhCOCHCOPh),, 2,377; 3,650 TaCIF, ['raF,Ci] --, 3,594 TaCI,F4 [TaF4Cl2]-,3,594 TaCl,S, Ta(S,)CI,, 3,646 TdCl3F3

587

Cumulative Formula Index

[TaF3C13] ,3,594 TaCI4F2 [TaFzCI4]-,3,594 TaC1, TaCI,, 3,589,590,626 TaCl,N, [TaC1,N3]-, 3,619 TaCISN4S4 TaCI5(S4N4),3,599 TaCI,O [TaOClslZ-,3,627

Cr02F,.TaF5, 3,940 TaFO, TaO,F, 3,625 TaF30i [Ta(Oz)zF3]2-,3,637 TaF,O, [Ta(02)2F4]3-,3,636 TaF, TaF,, 2,680; 3,589,590 T~F,O, [Ta(0,)F,12-, 1,76; 2.319; 3, 637 TaFh [TaF,] , 1, 151; 3,592; 6,813 [TaF612-, 1,498 TaF, [TaF7l2-, 3,591; 6.813 TaF8 [TaFsl3-, 1,84; 3,591 TaHZCI2O3 [TaO,CI,(HZO)]-, 3,628 TaI,O TaO12,3,646 TaI, TaI,. 3.640 TaI, Tal,, 3,589,591 TaNhC10H30010 NhTa(OMe)lo, 3,601 TaOCI, TdOC13, 3,626 Ta0,P TaOPO,, 3.639 Taps6 Tap&, 3,639 TaS3 TaS3, 3,654 TaS,Tl, Tl3TaS4,2,521 TaSe,TI, TI,'TaSe,, 2,521 TaSi4C8H,,Cl3NZ TaC13{N(SiMe2),},,3,610 TaWF,, [TaWFlol-. 3,593 TaZnC20H;l TaH(Cp),Zn(Cp),. 3,639 Ta2BrloN [TazBrloN]3-, 3,620 T~~C~HSC~& Ta2C16,(SMe2)3, 3,658 Ta2C8H1ZC16N4 {TaCI3(MeNC)1,(NCMeCMeN) 2, 168 TanCaHznC16N.

Ta2fG4Hd4

[TaCl,(NMe2)2(HNMe,)]20, 3,627

~T~Clz~(~s-C5Me4Et)}2{(p-H)(p-CHO)}, 3,654 T~zCZ~H~~CISN~ Ta2Cls(H2NNPh,),, 3,610 TaZC,,€I,,C1,N4 Ta2C1,(4-picoline),, 3, 657 Ta2C24H42C12N201 l'aC1,(OPr')4(4-picoline)2,3,664 NC24H60C16%

{TdC1,(NBu')(NHBut)(NH,Bu')}2,3,614

T~CZ~HSOC~~SLI

Ta2Cl,(S(CH2),CH2}4(p-C1)2(y-Bu'C=CBu'), 3.661 T~zC,O H ,~CIZN ZO ~ Ta,C1,(OPr')6(4-picoline)2, 3,649 TaZC32H7BN2P4 { Ta( CHCMe,)(CH2CMe3)(PMe3),},(~-N2), 3 , 6 17 Ta2C&d&N2P2 {TaCI,(NPPh,)},, 2,124; 3,619 Ta2CQ4H76C1408 {TaC1,(ButCOCHCOBu'),)2,3,650

Ta2CIBN6 {TaCl,(N,)),, 2,229; 3,619 TazCl90 [TazC190]-,3,628 TalCIl0O [Ta,C1,00]2-, 3,627 Ta2F805 [Ta20(02)2Fs]*-,2.319 Ta2FI00 {Ta2OF,,l2-, 3,626 Ta2020S5

Taz(S04)5.3,638

Ta,FO,

Cumulative Formulu Index

588

['l'hF,j3-. 3,1115 TbH,2C130,8 Tb(C104)3(H,0),. 3. 1074 TbHisOg [Tb(H20),I3-. 3. 1075 TbN309 Tb(N0,)3,3, 1108 TbN40iz [Tb(NO,),]-. 3.1076 TbZMozO, Tb,(MoO,),, 3, 1376 Th201,SA TbZ(SO&. 1.261

TcAs4CzoH,,C1, [Tc(diars),CI41'. 1.89; 6,978

TcBr40 [TcOBrJ, 6, 982 TcCH307Pz [Tc(O3PCH,PO,)(OH)1-, 6,978,987

T&,H~o,s~ [TcO{SCH,C(O)S},J-. 6. 976,978.982 TcC,H,OS, [TcO(SCH2CH2SL] ,6,978,98&982,984 TCC~H~O~S [Tc(O)($CI I,Cf 2, 805 TCC~H~O~SZ ITcO(SCH2CH,0)21-, 6,978,979,982

[ T ~ 0 , ( e n ) ~ ]6.978,980.982 +. TcC4N402 [TCO~(CN),]~-? 6.979.981,982 TcCI~O~S~

[TcO(C,O,S,),]-. 6,981 ?cC,H?N,02 17'cO[OMe)(C'h),12-, 6,981, 982 TcCsNjO rTcO(CN)51z-.6.981.982 T~'c,H~N,O& Ta6CIl5,1,27; 3,670,671

[Tb{(EtO),PS2}4]-, 2,644 TbC24Hd80s [Tb(DMF),I3+, 1,286; 3, 1086 TbC33H5706 Tb(Bu'COCHCOBu'),, I , 408; 3.1078 TbC36H45N40 Tb(octaethylporphyrin)(OH), 2, Q2 TbC4833N9 [ T h ( t e r ~ y ) ~ ]3, ~ +1071 +,

nc1,

TbCl,, 3, 11 13 TbC13012 Tb(C104)3,3, 1108 TbF7

[TcO(SCH2CONCH2CH2NCOCH2S)].-, 6,978,979. 982

Tc0,ibipyjCi. 6,977 TCCI~H~CI~N~O TcO(bipy)CI,, 6,978 TcCioHioNioz [TcOApy),l+, 6,982 TcC,oHl,NIO, [l'cO(edta)l-, 6,978,982 [TcO(cdta)\'-. 6.978 TcC, ,H I ,N,O,S, TcO{SCMeJCH(NHJ)C02}{SCMe2CH(NH2)COIH). 6,978.979.982 TcCloHzoC1zN;S; TcClz(NS)(S2CK*;EtJZ.2, 120

TCCIOH~ON& TcN(S,CNEt2)2, 6,975,978. 979. 982 T~CioHxN402 [Tc02(1,5,8,12-tetraazacyclotetradecane)]+, 6,978, 980,982 TcC~~H~ON~O~ TcO(H,O){ MeCOCHC( Me)=NCH2CH2N= CMeCHCOMe).6.978,982

T~O{2-(2-Oc6H,CH=N)C6H+O}Cl,6,978,979,982 TcCI~H&',O~ TcO{N(0)=CMeCHMeNCH,CMe2CHzNCHMeCMe=N(OH)), 6,996 TCC~~HI~CINZO~ TcO(salen)Cl, 6,978.982 TcCISHYSN~S~

TcC140 . [TcOCI,]-, 6,981.982 TcC16 [TcC1612-,6,982 TCFS TcF,, 2,680

Tc(DMG),(SnCI,)(OH), 6.974.978

TcUYO, LO,(NO,)(TcO,), 6,945 TcZrKi;OI3 Zr(NO,),(TcO,). 6, 945 TC&Hi?03Ss

{TCO(SCH~CH~S)Z)TCO(SCH~CH~S), 6,980 TC~CSH~~CIZO~ Tc,(OAc)jCI,, 3, 1230 Tc2CsOs Tcz(CO)s, 1,289 TC?CIZHI?F;~O~+

~Tc(~O){N(CI~,00z)3)12, 6,974,980 Tc,CZ,H&;40.,, [ T C ( ~ - O ? ( O ~ C N ( C C ) ~ H ) C ~ ~ ~ C : H Z N1 2( ~6 ~ . ~~.I)C:O~) 980 TCi~zo~~,N,C)& {TcO(S,CNEt2),},(~-0), 6,975,980 TC2Cd32yq06 {TcO{ (2-0C6H,CH=NCHz)>CH,} 1I ( p-0) 6.978980: 982 TczCls [ T C ~ C I ~ 3,1230 ]~-, Tc,UNO,~ '-JO@O,)(TcO,)2, 6,945 Tc,CJO ,(, UO,(TcO,),, 6 , 945 Tc2YCls Y[l'C,CI,I. 2, 306 TeBr,Cl, TeCI,Br2, 3,302 Te Br ,C1, [TeCI,Br,]". 3.302 TeBr, TeBr,. 3,302 TeBrj [Te3r5]-. 3: 301 TeBr, [l'eBr612 1 . 7 3 ; 3,302 TeCX [NCTcl-. 2: 225 TeC,,H,CI, TeC.I,(CH,),, 1.44 TeC,N,S, Te(SCN)2, 3,303 TeC,H602S4 Te(S,COMe),, 1,60 TeC4H1,O4P2S, Te{(MeO),PS2),, 2, 644 TeC4H16NsSI [Te{(H2N),CS}4]2+,1,60; 2,639 TcC~H~F~N TeF,pyl 3,301 l'~C,H,C1202 te(Cf fzCOCIi2CO~H2)C12, 2,370 'l'eC;EIhU2 ~f'e(CH2CUCH,COC'H,),2,370 TeC,H1,0,S, Tc(S,COEt),, I , 60 TeC8Hl,N4S2 [TePh(HzNCSNH2),]+,3,305 TeC8HI6F3O4 [TeF,(dCH,CH,OCH,~H,),]+, 3,304 TeC,Hl,03S6 [Te(S,COEt),]-, 3,305 TeC OH,OBrICllh' TeC12Br2(py)2,3: 302 TcC~~H.~,CI,N,O, [TeCL,(py N-oxide),] ' ,3,304 'TeCyoHi6N2O2S4 'l-e(S2~NCH,CF~,0C€~,~H,),, I , 60 TeClU€IzoN2S4 Tc(S,CNEtf)2, 6, 121 TeCIoH24ClaN4S2

,

Cumulative Formula Index TeCI,(Me,NCSNMe,),, 3,307 TeC,,H1403 TeO(C6H40Me-4),, 6,361 TeCI4H~4O4 TeOz(C6H40Me-4),,6,361 Te‘&Hi,c1zOz TeC1dCH2COPh),, . - 6,120, 122 TeC20H3‘ZN404Ss Te(S2CflCH2CH,0CH,~HH,),, 3,307 TeC,nH40N4SR

TePh4,1,44 TeG6H2J%~S~ Te{SC(=NNHPh)N=N~Ph),, 1,546 TeC48HliN2P4S4 Te{(SPPhz)ZN)z,1,60 TeCI3 [TeC13]+,3,301 TeCI4 TeCL 3,302,304

[TeCl6l2-, 1,73; 3,303 TeCu106 CU~(T~O 5,651 ~), TeFzOz [TeOZFzj2-,3,302 TeF, TeF,, 3,302,304 TeF, [TeF,]-, 1,50; 3,301,304,319 TeF6 TeF,, 3,304 [TeF,]’-, 3,302 TeF, [TeF7l3-,3,303 TeF8 [TeF,Iz-, 3,299 TeHgC4HloC12 WgC1,(TeEt2), 5 , 1074 TeHgGAoIz HgI,(TePhz), 5, 1074 TeHgOB HgTe03, 5,1068 TeHg2Hz06 HgzHzTe06,5,1068 TeHg30, Hg,Te06, 5, 1068 TeI, TeI,, 3,302 TeMo60z4 [Mo6TeOZ4I6-,1, 161 Te06 [Te0616-,2,413

4+,

3. 305

[Pd(TeO6),l8-, 5, 1124 Te,PdSi4C&60N2S2

Pd(SCN)2{Te(CHZCH2CH2SiMe3)2}2. 5,1144 Te2PtCBH20C12 PtCI,(TeEt,),, 5,476 Te2PtCz8HzsClz

PtC12{Te(CH2Ph)2}2, 5,476 Te3Cl13 [Te3CI13]-,2.685 Te3HgClsH15 [Hg(TePh),]-. 5.1074 Te4C116 {TeC14}4,2,685 Te4FZo04Xe Xe(OTeF,),, 3,320 Tc4FZO0 ,Xe XeO(O?’eF5)4,3, 320 Te4h {TeJ4}4.2.685 Te,,F,,O,Xt Xe(OTeF,),, 3,320 ThBZC24H24Br2N16 ThBr,{(pyrazol-l-yl),B),, 3, 1143 T~B~CZ~H~~C~NI~ ThCI{(pyrazol-l-yl),BH},, 3,1142 ThB5C30H40N20 [Th{(pyrazol-l-yI),BH,},]-, 3, 1142 ThBr, ThBr,, 3,1173 ThCZH3ClZNO ThOCIJMeCN), 3.1143

ThO(NCS),, 3, 1142 ThCZO6 Th(CU3)2,3,1155 ThC3F3OS [Th(CO,),F,]”-. 3. 1156 ThCsO, [Th(C0)3]2-,3,1156 ThC4H408 Th(OzCII)4, 3.1154 ThCJ16C14N2 ThCI,(MeCN),, 3, 1143 ThC4HsO I IS Th{O(CH,CO,),~(SO,)(H,O),, 3, 1144 ThC4N& ‘I’h(NCS)4,3, I142 ThC4Os Th(CzO4)z, 6,923 ThCsOi5 [Th(C0,),16-, 1,99; 3, 1156; 6,854,912 ThC,H,CGO; ThClZ(lr2-O2C6H4), 3, 1150 ThChHiN501, Th(N03),(pyridine-.l-carboxylic acid), 3, 1155 ThC6H18C1403S3 ThCI,(DMSO),, 3,1170 T~C~HIVN,OI,S~ Th(N03)4(DMSO)3,3, 1170 ThC6Hi8NK’iJ’z [Th(NO,j,(Me,PO),]-, 3, 1132, 1168 ThC,N,Se6 [Th(NCSe)6IZ-.3.1142 ThCTH3N04 Th(pyridine-2,6-dicarboxylate), 3, 1155 ThCSHzFizO, Th(O,CCF,),(OH2). 2,306 ThCsHsNsOiz Th(N03)4(pyrazine)2,3, 1140 ThGHiA Th(OAC),, 3, 1’1.54 ThCsWZoCl,N4 ThCl,(piperazine),, 3, 1141 ThCBHt4P4Sa Th(SZPMeJ4.1,94; 3, 1173 ThCsN& [Th(NCS),I4-, 2,236; 3,1142

590

ThC,,H*,Br404

Cumulative Formula Index ThCwH,&id',

Th{OP(0)(OCHzCHEtBu)2}4, 6,798,916,917 ThCsoHin02oP5 Th{HOP(O)(OCH,CHEtBu),) { OP(0)( O C H ~ C H E ~ B U6.918 )~}~, ThC96H206014P+, T~{HOP(O)(OCH~CHE~BU)~}~{ OP(0)(OCH2CHEtBu)2)j.6,917 ThC&,o,NOd'6 Th(N03) { HOP(O)(OCH~CHE~BU)~),( OP(0)(OCH2CHEtBu)2)3.6.917 'rhC12sH2~0d'~ Th{HOP(O)(OCHzCHEtBu)2}4{OP(0)(OCH2CHEtBu)2}4.6.916 l'hC14 ThCI,, 3, 1173 ThC16N202 ThC14(NOC1)2,3, 1165 ThCrH407 Th(OH),(Cr04)(H20),3,1146 ThF2 [ThF21Zf,6 , 8 5 2 ThF8 [ThEa]'-. 3.1174 ThHzN2OS Th(OH),(NO,),, 6,914 ThH1N4013 Th(NO2)4(H&). 6.916 Th H20,S Th(OH),(SO,), 3, 1146; 6,914 ThH20,P2 Th(HPO4)2,6.852 ThH3012P3 [Th(HP0,),I2-. 6.852 ThH6N4015 Th(N03)4(H20)3.1,99; 3,1132, 1146 ThH6023Ss [ T ~ ( S O , ) , ( H Z ~ ) 6,915 ,~~-, ThHioN,O,, Th(N03)3(OH2)5,2,30h ThHIZBr4N4 ThBr4(NH,),, 3. 1137 ThH1312N5

ThI2(NH2)2(NH3)3.3,1137 ThHI4I3N5 Th13(NH2)(NH3)ar3, 1137 ThI, ThI,, 3, 1173 ThM03012 [ T h ( h 4 0 0 ~ ) ~ 3, ] ~ 1376 -, ThMo,2UH60,5 [(UMoi2O,2){~(OH),)l4-,3, 1047 ThN4012 Th(N0,),.3, 1151:6.798,810, Y17, Y18,923 ThN5015 [Th(NO,),]-, 3, 1152; 6,916 ThN6018 [Th(N03),12-. 3, 1132,1152;6,916,918 [Th(NO3),I3-. 1. 101 Th0,Te ThO(TeO,), 3, I153 Th06S Th(O,)(SO,). 3. 11-16 Tho& Th(SOJ)2,3,1152 ThO,Se, 'Th(SeO,),, 3.1153 ThOi2P4 Th(PO&. 3. 1152 T h o 12s3 [Th(S04)3]2-,6.915 ThOi& [Th(S04)4]". 3,1152; 6,915

592

593

Cumulative Formuh Index

Th2{HOP(0)(OCH,CHEtBu)2}4{OP(O)(OCH2CHEtBu)z)S. 6.916 ThzHzN602o T ~ ~ ( P - O H ) ~ ( N6O ~)~, . 914

ThZS5

Th,S,. - - . 3.. 1171 Th,Se, ThzSes, 3, 1173 Th,HsOs [Th3(OH)s]7t, 6,914 ThOi6P4 Th3(P04)4,6,914 Th4HsOs [Th4(OH),]8+, 6,914 Th4HizOiz [Th4(OH)i214+,6. 887 Th6H15015 [Th6(OH),s]’+. 6.887.914 Th6N4032 Th6(02)1o(N03)4, 3. 1146 TWiz Th&, 3, 1135 Th7Se12 Th7Se12,3,1135 TiA1C14H21CI TiCp,(p-CI)(p-CH2)AlMe3. 5.385 TiA1203 TiAI2O3,3,331 T~ASC,~H~,C~~ TiCI4(AsPh3),3,347 TiAs2ClOHl6C1, TiCl,(diars), 3,349 TiAs,C,oHlsC130 TiCl,(diars)(H20), 3,349 ‘riAS2C36H3oCl.q TiCI4(AsPh3)2,3, 347 T~AS,C~~H~~CI~ TiC1,{MeC(CHZAsMe2),), 3,344 T ~ A S ~ C ~ ~ H ~ ~ C I ~ T ~ C I , ( M ~ C ( C H , A S P ~ 3.338 ~)~},

1, 88; 3,348,356,357 TiCl,(diar~)~, T~AS,C~~H~J~ Ti14(diars)2,3. 349 TiAs4CZ8H36Ci4 3,349 TiC14(1r8-(MeZAs)ZC,I,Hh}Zr TiBC&i,oC13N6 Ti { HB(&N=CHCH=CH), )C13,2.248 TiBCl 3H18C12N6o Ti{HB(RN=CHCH=C € I ) , JCI,(THF) ,2,248 TiBCl4HlsCIN6 Ti{HB(&N=CHCH&H),}Cp,CI, 2.248

TiC4HI2CI3S2

TiBC,6H18N4 Ti (H2B(&N=CHCH=cH),}Cp2, 2,248 TiBC22HzzNB Ti {B(hN=CHCH=cH),}Cp,, 2.248 T I B L H , .Br,N, T~Br3(Br2Bz(N~e2),}, 3, 357 TiB3HI z Ti(BH,),. 3.348 Ti BrzCI, [TiC1,Br,13 ,3.331,355 TiBr, T13r4. 3, 329 TiBr, [ T I B ~ , ] ~3. - , 358 [TiBr6lJ-. 3. 331 TiCC1,F303S TICI~(SO~CF,). 3.335 TiCH3CI3 TiC1,Me. 3.343 TiCH3C130 TiCI,(OMe), 3,343 TiCH4F5N20 [TiF,(MeOH)]-, 3,354 ‘TiC2C12FGOhS2 TiC12(S03CE3)L.3,335 TiCzH6Cl20 TiC12(OMe)2,3,343 TiCzH6C1J TiC13(NMe2),3,329,356 TiC2H6Fs0 [TiF,(EtOH)]-, 3,354 TiCzH6F50S [TiF,(DMSO)]-, 3,354 TiC3E7F5K0 [TiFj(DMF)]-, 3,354 TiC,H,CI,N TiCI,(NMe3), 3, 356,357 TiC3H,&i3N4 Ti{(H2NCH2)3NICl,,2, 5’1 TiC3Y3 Ti(CN),, 3,352 TiC41-14C12F60, TiCI2(OCH2CF3),, 3,335 TiC,H6BrCI,Nz [TiCl,Br(MeCN),]-, 3,355 TiC4H6C12Y2 TiClz(MeCX),, 3, 328 TiC4H6CI,Nz TiC14(MeCh’)2,3,355,356 [TiCl,(MeCN),]-, 3,331 ‘liC4H60,I [Ti(C,O,),(H,O),j , 1, 7 8 ; 3, 332 TiC,H7Ci3N2O2 TiCI,(HDMG), 3,345 TiC,H7Cl30 TiC13(OCH2CHzCH=CH2), 3,337 TiC,H7N06 TiO{HN(CH2C0,),}(HzO), 3.342 TiC4H8Br3O2 TiBr3((kH2CH20CH2cH2),3,174 TiCIHBCI,O TiCI,(THF), 3,332 TiC4H,CI4N2OZ TiClJFIJXvfG). 3,345

TiCI,(OBu). 3,334 TiC,H,&1202 TiCI,(OEt),, 2, 337; 3. 334 TiC4H12C1,S2

TiC,H, zC13S2

Cumulative Formula index

TiCl,(SMe,),, 3, 356 TiC,H,,O, Ti(OMe),, 2,349; 3,333 TiC4HIZS4 Ti(SMe),, 3,338 TiC4H16CI,04 [Ti(MeOH),Cl,l+, 3,331 TiC,N,S2 ~Ti(SzCz(CN)2}]z-~ 3,339 TiC,N4 [Ti(CN),I2-, 3,352 [Ti(CN)4J4-,3,352 TiCQOY [Ti(C,O&] ,3,33O, 331 Tic409 TiO(C,O,),, 3,336 TiC,H5F5N [TiF,(py)l-, 3,354 TiC5H5Se, TiCpSe,, 2,667 TiC5H7C103 TiOCl(acac), 3,336 TiC,H7CI3O2 TiCl,(acac), 3,336 TiCsH702 Ti(acac), 6,203 TiC,H,F,N, [TiF5(3-pyCN)]-, 3,354 [l'iF5(4-pyCN]--,3,354 TiC6H6ClF903 TiCl(OCH,CF,),, 3,335 TiC,H,Cl,N, TiCI,(MeCN),, 3,331,355,356 TiC6Hl,04 Ti{O(CH2)30}2,3,337 TiC,H,,ClN,O, TiCI(OPri),(N3), 3,329 TiC,H,,CI,O, TiC13{O(CH2CH2C)Me)2}7 3,332 TiC6HI4N6O2 Ti(OPr')2(N3)2,3, 320 TiC61I 15C13P TiCI,(PEt,), 3.347 TiC6H18Br3N2 Ti3r3(NMe3),, 3,328 TiC6Hl8CI2N,O TiOCl,(NMe,),, 3, 329 TiC6H18C13N2 TiC13(NMe3)2,3,328,356,357 Tic6H2,N6 [Ti(en),l3+, 3, 328 TiCbH24N;Z06 [Ti(fl,NCONHZ)J3+,3,330,331 TiC,N, [Ti(CN),I3.-, 3, 331,352 TiC,,N,S, [Ti(NCS),]'-, 3,331 TiC60,, [Ti(Cz04)3]z-,3,336 TiCIH,F2N06 [TiF~(0,){2,6-py(C02),)12, 2,319: 3,351 TiC7H5N06 Ti0 { 2,6-py(C02),}( H 2 0 ) ,3.342 TiC,H,N,O, TiCp(NCO)*, 2,227 TiC7H7N08 Ti(02)(H20)2{2,~-py(COz)2), 2,319: 3. 351; 6 , 321 TiC,H,,CI,N, TiCpCI,(NHNMe,), 2, 151 TiC,H 1304 Ti(OMe),(acac), 3, 336 TiC,H,9C13P2 TiCI,Me(Me2PCH,CH2PMez). 2.699 _

1

594

TiC7N7 [Ti(CN),j4-, 3,352 TiC8HI2I3N4 Ti13(MeCN),. 3,328 TiC8Hl4CI2N, TiCpC12(qz-Me,NNMe).2. 145 TiC8H16Cl302 TiCI,(THF),, 3,332 TiC,H, ,CI,O, 'l'iC14(THF)2.3, 3% ~I'iCRHIXCl3O2 TiCMOBuL. 3.348 TiC,H,,CI,N;P, T i C l , ( B u ' ~ C I ) ,3,349 TiC,H,,O, Ti(OEt),, 2,346.347, 349; 3.334 TiCsH,,C13P2 TiCl3Et(MezPCH2CH,PMe2),2,699 TiCsHzlN2Sz Ti(NMe,)2(SEt)2, 3.338 TiC8H23N3S Ti(NMe2),[SEt). 3. 338

Ti(MeNNNMe)4, 2 , 196 TiCONB [Ti(CN)H15-q 3. 352 TiC9H6C13N0 TiC13(8-quinolinolatc),3,345 TiC9H7C14N0 TiCI,(S-quinolinol), 3,345 TiC9H&IN&. TiCI(S2CNMe2),.3%338 TiC9HI8Cl3O3 TiCI3(0CMe2),. 3.331 TiC,I-I,,C103 TiCl(OPr'),. 3,329 TiClOHRCl4N2 TiCl,(bipy), 3, 356 [TiCl,(bipy)) ,3,328 71iC10H814N2 lIX4(bipy)]' 3,328 TiCloH ,oC:I,N2 TiCl,(py),, 3,328 TiCIOHIOC14N2 TiC14pyz,3,356 TiCl~HloN6 TiCp2(N3),? 2.228 TiCloHl0S, TiCp,S,. 2,545,607 TiC1oHloSe, TiCp,Ses, 2,607.666 T~GoHIz [TiH,CpJ, 2,705 TiCIOHI2N2O9 3,343 [Ti0 ((02CCH2)2NCH2CH2N(CH2C02)2}]2-, TiC,OHI,N,O,O [Ti(02){(02CCH,)2NCH2CH2N(CH2COz)z}]23,343 TiC10HlzS2 TiCp,(SH)2, 2 , 518 TiC,oH,4C1,04 TiCl,(acac),, 3.336 TG0HI4O2 [TiCp,(OH,),J2+. 2.297 TiC,oHi&6 TiO(acac),. 6. 1011 TiC10H,yFh04 Ti(OPr'),(OCI I 2 C F 3 ) 2 . 3,335 TiCIOH20C14NI TiCI,(ButN=CHCH=NBu'), 2,209 TiC,oH20Cls0, {TiCI4(MeOCH2CH2CH=CH2))2,3.337 ~

~

Cumulative Formula Index

595 TiCdb004 Ti(OCHCH2)2(0Pri)2, 3,334 TIC, IHIOCI&” TiCpClz(NZPh),2, 132, 135. I36 TiCllH12CIZNZ TiCpCI2(HzNNPh),2,151 Ticl 1H23F304 Ti(OPr’)3(0CH2CF3),3,335 TiCl1Hz3N3 T ~ C P ( N M ~ ,2, ) ~180 , TiC12H&I&”Oz ,TIC13(4-pyCNN-oxide),, 3. 174 TiC12H8C14N2 TiCI4(phen),3.356 TiC12HloC1202 TiCIz(OPh),, 3,334 TiC12H10N202 TiCp,(NCO),, 2,228 TiCI2HloN,S, TiCp,(NCS),, 2,228 TiClzHl4CIzNz0 TiOCI2(2-Mepy),, 3,329 TiC1zH14Nz06 Ti(NCO)z(acac),, 3, 336 TiCitH16 TiMe2(n-Cp),, 2, 115 TiC12H&W3 TiC13(THF)3,3,332,356 TiC12H&14N4 TiCI4(Me2C=NN=CMeZ),, 3,329 TiClzHzs04 Ti(OPr’),, 3,334; 6, 344, 346 TiC12H30C13N4 3.328 TiC13{N(CH2CH2NMe2)3} TiC12H30C13P2 TiCI3(PEt3),,3, 347 TiC12H36C13N602P2 TiCI,(HMPA),, 3, 335 TiC12H3604Si4 Ti(OSiMe3)4,3, 335 TiC12.~H~2.5C12NZ.50 TiOCl2(py),.,, 3,329 TiCl&b30~ {Ti(OPh),Me},,, 3, 335 T~CI~HIOF~S~ TiCp2{S2C,(CF3),}.2,607 TiC14H10F6Se2 TiCp,{Se,C,(CF3),}, 2.609 TiC14H44 T ~ C ~ ~ ( S Z C Z2,609 HZ)~, TiC14H190 TiHCp,(THF), 2,705 TiC14H36Nz04 Ti(OPr’),(en), 3,334 TiC15H11C13N3 TiCl,(tcrpy), 3, 328 TiCl5HI5Br3N3 TiBr3py3,3,355 TiClSHl5Cl3N3 TiCMpy),, 3,331 TiC15H1s13N3 TiIdpy)~,3,328 TiC,5H,,C106 TiCl(acac),, 2, 376 TiC,,H,,O, Ti(acac),, 1,251 [Ti(acac),]+, 2,376; 6. 121 [Ti(aca~),]~’-, 3, 336 TiCl6HI4Cl2N2O2 TiCl,(salen), 3, 340-342 TiCl6Hl5CINZ TiCp,CI(N,Ph), 2, 130 TiC16H&13N& I

TiClp(salenH,), 2, 733 TiCd~fiO& TiCp,{S2C2(C02Me),}, 2,607,609 TiCi6H1604Se2 TiCp,{Se,C,(C02Me),}, 2,607,609 TiCi6H1806 337 Ti(1, ~ - O Z C ~ H ~ ) ( C S 3, H~ O~)~, TiC16H2,NSi2 TiCp,{CH2SiMe2N(SiMe3)},2, 184 TiC,6HzsNzSiz TiCp,{NN(SiMe3)2}, 2, 148 TiC16HisPz TiCp,(PMe3),, 3.346 TiClhH360 TiMe3(0CBu13),2,342 TiC16H3604 T~(OBU‘)~, 2,338, 340,346,349 Ti(OBu)4, 3,348; 6,346 TiC1,HlsCl2O2 TiCp(OPh)2C12,3,334 TiC18H,,Q,N,0Z TiC1,(8-quinolinolate),, 3, 345 TiG8Hl,N2O3 TiO(8-q~inolintilate)~, 1,528 TiC18H 2 0 6 ITi(02C6H4)3]2-,2,398 TiC,,H,,CI,N,O, TiCI,(S-quinolinol),, 3,345 TiC18H15Br4P TiBr4(PPh3),3,347 TiCI8Hl5Br4PS Ti(Ph3PS)Br4,2,642 TiClaHl jC14PS Ti(Ph3PS)CI4,2,642 TiCl8HzoO4S2 Ti(CsH4Me)2{S2C2(C02Me)2}, 2,609 TiC 1BH26Nj07P T~(OT)(~-~YCO~),(HMPA), 2,319; 3.345; 6,329,331 TiC18Hd’~ Ti(C5H4Me)2(Me2PCH2CH2PMe,), 3,346 Tic I 8 H d h 8 ’ 3 ‘I’i{OzP(QPf)~}~, 3,332 TiC18H53CIN3Si6 TiCI{N(SiMe,),},, 3,329 TiCI8Hj4N3Si6 Ti{N(SiMe3)2}3,3,328 TiCi0H14C12N202 TiClz{1.2-(2-OC6H4CH=N)zC6H4},3, 341 TiC,,H,,CI,N, [TiCl,(bi~y)~]+, 3,328 T~CZOHI~IZNJ [TiI,(bipy)Z]’, 3,328 TiC20H,7C12N20t TiCl,{2-{ 2-(2-0C,H4CH=N)C6H4NHCH2} C&140W), 3,341 TiCzoH24C13N,0, TiCl,(salenH,)(THF), 3. 341 TiC20H30S3 Ti(CjMej)ZS312,541 TiC20H3202Si2 Ti(UPh)z(Me,SiCH,),, 3,335 TiC2,H4&04S4 Ti(SCONEt2)4,3, 339 TiC,~H,,N,S, ~. Ti(S,CNEt,),, 1.94; 3, 338 TiC,nHnaNn Ti(NPr&(NMe,), 2, 164 TiC21H15CIC)6 Ti(tropolonate),CI, 3,338 TiC,,H,,CIN,O, TiCl(salen)(py), 3, 342 TiCz3HZoCl2NP TiCpC12(NPPh3),2,123 ~

TiC36Hq4N402 'ri(O,)(octaethylpoI.phq.rinj, 2,317,319,320, X23; 3, 350,351; 6.329 TiC3,H4,N,0 TiO(dimethyloctaeth!;lporphyrin), 3, 350 TiCaH6303 T~(OC,H,BU'~-Z.~)~. 2,346 TiC4,H2@Br2N4 Ti(0,)(TCNE)(2-pyC02)2(HMPA)I 3,345 TiBr,(tetraphcn!;Iporphyrin), 3.352 TiC24H30N204 TiC44H2RFNI [Ti(d e n )(THF),]*+, 3, 34.2 TiF(trtraphenylpurphyrin), 2.823: 3.329,349 TiC24H44IZPZ TiC44H28FN101 3,346 TilZ{P(CbH11)2}2. TiF(O,j(tetraphenylporphyrin), 3, 330, 349 TiC,,H,,13P, 'I'iC,4H2,F,N, Ti13{P(C6Hll)2}2, 3, 346 TiF,(tetraphsnylporphyrin), 2,823; 3,330.349 TiC1,H+,P2 [Ti~:,(tetraphenr:lporphprin)j , 3, 330, 349 Ti{p(c6Hii)z}z33,346 TiC,4H2,1i,0 TiCL6H20C1ZNZ04 TiO(tetraphenldporphyrin), 2,823; 3,350 TiCIZ(ONPhCOPh),,2,506 .. . TiC44H28N40Z TiC26H24C14P2 Ti(O,)(tetraphenylporphyrin), 2, 320.612; 3,330.349, TiCl,(diphos), 3,349 352: 6.321 TiCz6Hs6017P4 TiC,,H,,N,O Ti(OCH,0,){OP(0)(OH)OP(O)(OBu~OC8Hl,}2, 6, Ti(OMe)(tetraphenylporphyrin), 3,349 1012 TiC,,H,,FN, TiC2,H,,C1N30, TiF(tctraphcnylporphyrin)(McNCH=NCH=tH), 3 , TiC1(S-quinolinolate)3,3,338, 345 349 TiC28H200S 7'i(2-OC6H4CHC)),,3,345 TiC3&IZ6P TiHCp,(PPh,), 2,705

TiC23H,,@3 TiC:p(OPh)3,3,334 TGHI6LN4 [TiI,(phen),]+, 3, 328 TiC,,H,,O, Ti(OPh),, 2, 342; 3.334 TiC&26N,07P

T~(hlezNCH,Ph),(BufCOCHCOBu') 3.332 TiC&,,1\T6 Ti(hipy),, 3,327 [Ti(bipy),]-, 3,327 [Ti(bipy),], ,3,327 TiCwH,6NzOfi T i ( O P r ' ) 2 { O C ~ 1 2 C H 2 N ( C H , ~ ~6~, I012 ~~~)~),, TiC32H,,CIN, TiCl(phthalocyanine), 2, 865; 3, 352 TGJbCLN, TiCl,(phthalocyanine), 2,865; 3,352 TiC32H16Ns0 TiO(phthalocyanine), 2,865; 3 %352 TiC32Hl&-Oz Ti(phthalocyanine)(OH),. 2. 865 TiC32H22N206 Ti(8-q~inolinolate),(2-OC~H,CHO)~. 3. 345 TiC~H4806 Ti(acac),(2,6-Pri,Ph0),, 2,379

(OCH2CHEtBu),}2, 6, 1012 TiC36Hzd404 Ti(S-quinolinolate),, 3, 345 TiC36H3DBr4PZ TiBr4(PPh3)*,3,347 TiC36H30C14P2Sz Ti(Ph,PS),Cl,, 2,642 TiC36H~N404 Ti(OC6H4CH=NEt)4, 3.340 TiC36Hd4o5 TiO(meso-porphyrinMe, ester). 3, 349 liC36H44F2N4 Ti(octaethylpclrphyrin)F,, 2. X23 ITi(oclaethylporphyrin)F,1 , 2, 823 TICW,HUN~ Ti(octaethylporphyrin), 2,325 TIC,,H,,N,O TiO(octaethy1porphyrin). 2,325,823: 3.350

Ti(0Pr') { OP(0)(OCsHI7),}3 , 6, 1012 TiC57H9,010S3 Ti(OPri){OS(0)ZC6HIC12HZs}3, 6, 1012 TiCs7Hl120, Ti(OPri)~OzCCHMe(CH,),4Me}3, 6, 1012 TiCsoH,,,O,oPz [Ti(OC,H, ,),~OP(OC,,H,,),},~2~, 6, 1012

TiCI,O TiOCI,, 3,329 TiC13 TiCI,, 3,331,335, -348,356,357 TiCI?F?PS? TiCI;(SiPF,). 3,338 TiCl3NZ TiC1(N2):3.329 TiCI,N, TiC13(N3),2.228 TiCI4 TiCI,, 1,406; 3.32&326,329,333,335,348,356-358 [TiCIJ. 3. 171 TiQh ~I'iC14(n'3)I]~-, 2.128: 3,325, TiU5 [TiCI5] ,3.355.356

TiCI,(PCI,), 3, 355 TiClIoOzPz TiCL4(0PC1,)z,2 . 500 TiCIIJOZPZ TiC13(OPC13j(~~-CI)~TiCl~(OPCl~). 2 . 498 TiF4 TiF,, 3, 329 TiFj [TiF,1-, 3,354 TiF, [TiF,],. ,3,351; 6- 101I [TIF6I3-.3, 174.33 I TiFeH,

597

Cumulative Formula Index

Ti,ReC 36H54Ci,N,O,

FeTiH,, 2,693 TiHz TiH,, 3,353 TiHzBr,O [TiBr,(H,O)]-, 3,357 TiH2F50 [TiF,(H,O)]-, 3,354 TiH2N2 [Ti(NH)J, 3,352 TiH3C14P TiCI4(PH3),3,347 TiH404 Ti(OH).,, 1,538 TiHhC130, TiCI,(H,O),, 3,330 '~'IH~C~~PZ TiCI4(PH3),,3, 347 TiHsCI,04 [TiCI,(H,O),]', 3,330 TiH, ,C10, [Tkl(H~O),]Z+, 3, 330 TiH1106 [Ti(OH)(H,0),]2-, 3,352 TiH,,O, [TcHiO)6]3-', 1,24Y,271. 284: 3.330,331 7'iHfCsH24C1,N, HfCI4(Ti(NMcZ),),3, 372 TiHg,FJz Hg,I,TiF,, 5 , 1062 TiI, TiL, 3,325,347 TiI, [Ti161Z-,3, 357 TiMoC,aH,aNa06 Mo(CO);{C(NMe2)OTi(NMe,),), 2, 182 TiN,O,, Ti(N03)4r1,94; 2,414: 3,336 TiO,S, [Ti(SO,),]-, 3,331 Tip Tip, 3, 347 TIP, TIP,, 3,347 Ti2C24H72C16N1Z06P4 TiReC,6H,,C~,N,0P, {TiC!,(HMPA),},(~-O,), 3,335 TiC14(THF){(N,)ReCI(PMe,Ph)4}, 3. 329; 4,133, TiZC34H30C12NZ TiReZC36H54C17NZOZP4 (TiCp,CI) ,(NCPhCPhN), 2,127 TizOC1,(EtzO){(Nz)ReC1(PMe,Ph)4}, 4, 133 TizC,4H30C14N, TiRezC64HssClsN4Ps {TiCpC12(NNPhz)}2, 2, 150 TiC14{(Nz)ReCI(PMeZPh)4}2, 3,329; 4.133 TizC,oH&L08 TiVCzOH30N4014 {Ti(OPh),C1(THF),),H, 3,335 TiV{(0,CCH2)2NCH2CH2(CH~CH20H)CH~COz}z, 3, Ti2Cs4H122012 486 [{Ti{ 3,5-di-r-butylcatecholate(2 -)} { 3,5-di-t2,398 butylcatechnlate(1-)}},I2-, T~VCZOH,,CI~NA V{(MeCOCHCMe=NCH,)ICl(p-O)TiClz(T~IF)2, 3, T&I, 567 [TiaCI,]-, 3,356 TiVC,,H,,Cl4O5 Ti,ClaN, 3, VCl{(MeCOCHCMe=NCH,)2}O{TiC13(THF)z}, j{Tk&)}2]2-, 2,228 484 Ti2CI9 TiZrC8HZ4Cl4N4 [Ti,Cl,]-, 2,684; 3.355 ZrCl,{Ti(NMe,),), 3,372 [Ti2CLJ-, 3, 355 TiZA~2C10H16F8 (TiF&(diars), 3,349 [Ti2C1,0]2-,2,683; 3,355 Ti2A~6C78H72C18 Ti,CI,,O,P, (TiC14)Z(PhZAsCHzCHzAsPhz)a. 3,347 {T~C14(OPC13))z, 2,500 Ti2BCZH6C1,N Ti,F, 3, 356 [Ti2F9] ,3,329 'I'i2CI6(Me2NBC1), Ti2RC3,H3,N8 Ti2FIl [Ti,{B(AN=CHCH=kH)4}Cp4]L, 2,248 [TizF,l]3-, 3,354 TizB4C3~H36N404 TiiHI6Ol3 3,340 {Ti[{2-OC6H4CHZN(B~T,)CH,),I},, ICTI(0,~(H,0)4J,012+, 3,343 Ti,C,HbNOll Ti,MnC20H,0C14 (TiCp2Cl)2MnC12, 2,678 [Ti20(0,)2{N(CHzC0,)3~~~-. 2, 319 Ti2ReC36HS4ClfN202 Ti2C6012 COC 7--7

I

Ti2ReC36H54C17N202

Cumulative Formula Index

{ReCI(Nz)(PPhMe,)4)(Ti,CI,O)(Et,O), 3. 329

TizZnCZoHZoC14 (TiCp,Cl)zZnClz,2,678 Ti2ZnC26H& Zn(SCH2CH2S)3(TiCpz),. 5.976 Ti3B~C8HZ4Br14N4 [(TiBr4)3{(Me,N)zBBr}z]. 3. 357 Ti3C36H3106 {Ti(OPh),},H, 3,335 Ti3C36H81C1909 {TiC13(0Bu)3}3r 3,334 Ti,PrC,4H,,CI,,P, Pt(TiCl,.PPh,),, 3,347. 356 Ti4Cl,H4801, {Ti(OMe),},, 1,149; 3,333 Ti4G4HZ4N4028 [ITiO[N(CH,C0,)31~41q~, 3,342 Ti4Cz8Hn016 Ti4(OMe)4(OEt)lZ, 3,333 Ti4C32H32C14 {TiCl(cot)},, 2,685 Ti4C3,HsoO1, {Ti(OEt),},, 1, 149, 161; 2,348; 3,333 TiSC48H40C1208

Ti,(OPh)8CI,, 3,335 Ti,C,,H,,O,Si TiS(OPh),(SiMe,), 3,335 Ti5C1I, [Ti5Clll]-, 3,357 TiSCll9 [TI5CIl9]-,3, 357 Ti5PtC54H45C120P3 ,, 3,347 (TiCI4),Pt(TiCl4.PPh3) Ti6C30H3008

T&Cp,Os, 1, 141, 160; 2,304 T~~C~ZHSUOXJ Ti604(OEt)lh. 3, 334 ~~.LJLoOR {1'1:(OPh)4}2,3,335 Ti7C36H90024 Ti,06(0Et)l~.1. 161 Ti+&H950~ Ti705(OEt),,, 1, 161 Ti7C40H100044 Ti7024(OEt)20, 2, 350 TIAIH, TlAlH,, 3, 170 TIAIZHSCI 'I'ICI(AIH4)2,3,175 TIAIIH~~ TI(AIkI4)3,3, 17.5 TlBH4 TIBH,, 3,170 TIBIH&I TICI(BH4)2,3,175 TIBr TIBr, 3,170 TIBrCI, [TICI,Br]-, 3,174 TIBr, TIBr,, 3, 174 TIBr, [TlBr4]-, 3, 171, 175 TlBr, [TIBr,12-, 3, 175 ?'1Br6 [TIBr6I3 , 3 , 171, 175

TICHO, TI(O,CH), 3, 169 TlCN TlCN, 3,167

TICNO TICNO. 3. 168 TICNS TICNS, 3, 168 TlCNSe TICNSe. 3. 168 TIC,H3Br2O2 T1(OAc)Br2.3, 169 TICZH302 TI(OAc), 3. 169 TIC,H,O TlOEt. 3, 168 TIC2Yz TI(CNI,. 3. 171 TIC4H604 T1(OAc17. ,- 3. 171 T1C4H802 [T1(6CHzCHzOCH,~H,)]+, 3,171 TIC,H,,O TlMe;(OEt), 3,169 TIC,H,,CIN&, TIC1(H2NCSNH&, 3,170 TIC,H,6FNsS4 TIF(lI,NCSNH,),, 3, 170 T~C~HI~NS%% TIN0,(H2NCSNHz),, 3, 170 TIC,H,8NBO4PSq TlH2PO4(H2NCSNH,),,3,170 T1C4N4 [TI(CN),]-, 3, 171 T1C408 ['Wc,o,),]-, 3,173 T1C5HF60, Tl(hfacac), 2.372,375; 3,169 TIC5HF70, Tl(acac), 3, 169 TIC5H7O2 Tl(acac), 2,376, 391 TICSHIINQ [TIMe2{(H,?ICH2),N}]', 2,51 TIC,H,O TlOPh, 2,345: 3.169 TIC6HSOSS T10,SOPh. 3.169 T1C6H706 Tl(ascorbate), 3, 169 T1C6H,0, TI(OAc),. 2,206; 3, 173 TIC6H24CI:N6 T1CI3(en),, 3. 172 TIC6N6S6 [TI(S2C==NCN)q13-. 3, 174 TIC7HSOSZ TISZCOPh. 3. 169 TlC7H14NS2 TI(S,CNPr,), 3, 16Y TIC8BrN4S4 [ Tl{S,C,( CN),) ,Br] 2 - , 3, 174 T1CaHizOs [TI(OAc),]-, 3, 171 T1C8N4S4 [TI{ %C,(CN)z } a ] -,3,174 TIC9W6N0 Tl(oxinate). 3. 169 TIC,HI,NS, TI(S2CNBu,).3.169 TICIOHIOC~~~Z TICl3(py),,3. 172 'I'IC11H16N02 TIMe2{i-PhCIIzCI1(NH,)CO,}, 2,745 T~CIIHZINB~~S~

598

599

Cumulative Formula Index

TI(O2CPh)(H2NCSNH2j4. 3.17U TIC1ZHsC13N2 TlCl,(phen), 3, 172 T1Ci2N6S6 [TI{S2C2(CN)2}3]3-, 2,605: 3, 174 TICi3HsNsS3 TI(NCS),(bipy), 3, 172 TG,H& 3. 174 [T1(3,4-S2C6H7Me)2]-.

TIOH, 3.168 T1H09S2 [Tl(OH)(SOa)z]-. 3, 171 Tl&B r 3 0 2 [TIBr3(OH)2]2-,3, 172 TlH204P TIHIPOI, 3. 169 TIH, [TIH4]-, 3, 175

T1C1SH11C12N3

T1H6N101L

[TICl2(terpy)]+,3, 172 TICISHIICW~ T1C13(terpy),3, 172 TICiPiiOz TI(PhCOCHCOPh), 3,169 TIC1sHisC13N30 TlCl3(phen)(DMF),3,172 TICisHi4CLNz TICI4(quinoline),,3, 172 TICzoHi6N4 [Tl(bi~y)~l+, 3,168 TICLZHZ~O~ Tl(C6H5)3(l,4-dioxane). 2,206

Tl(KO3)f(H20)~, 1, Y7,2,306 TIH,Br,O, [TIBrz(OH,),] ' , 3 , 172 'l'lH1206 [TI(OFT2)6]'+,3, 172

TlC22H3006

[TIMe2(dibenzo-l8-crown-6)j-. 3.175 T~C~~HI~C~ZN~ Tl(phen)2C12,3, 172 T~CZ,HI,N~O~ T1(8-quinolinolate),, I , 528 TlC36H30N9 TI(PhNNNPh)3,2,206 TGsH47N407 Tl(octaethy1porphyrin)(OAc), 2,821 T~C~OH~ONS~S [Tl(py N-oxide),l3*, 3, 174 TGsH3iN4 Tl(tetrapheny1porphyrin)Me. 2.821 'rIC64Hi36016P4 TI{ OP(O)(OCHiCI 1EtHu),},{HOP(O)(OCH2CHEtBu),), 6.798 TIC1 IICl, 3, 170 TIC10 TIOCI, 3, 173 TICI3 TIC13,3,174 T1Cl3Ol2 T1(CI04)3,3, 173 TICI, [TiC14]-, 3, 174 TICIS [T1C15I2-, 3, 175 TIC16 [TICl6l3-,1,524; 3, 171, 175 TICIhOhP3 T1(02PC12)3,3, 173 TIF TIF, 3,170 TlFO TIOF, 3,173 TIF, [?'IF2]-, 3,170 TIF3 TIF,. 3.174 [TIF;]'-. 3, 170 TIF4 [TIF4]-,3,174 [T1F4l3 , 3 , 170 TIGa,H 12 TI(Ga114)3,3, 175 TIH TIH, 3,170 TlHO

TI1 TII, 3,170 Tl13 TU3,3, 170 TIN TIN. 3,168 TINO, TIY03, 3, 169 TIN300 TI(NO,),,3, 173 TIN4012 [Tl(NOd41-, 3,173 TIOH TIOH. 3,168 TI02 I O 2 , 3,168 T104P TlP04, 3, 173 T1PbsBr904 TIPb8O4Br,, 1, 163: 2,304 TIPdCioH&io Pdll(OAc),. 3, 173 T1S TIS, 3,171 TIS2 (TISZ),,,3, 171 TIS, [TIS.J-. 3. 171, 174 TlSe TlSe, 3,171 TISn, [TISngl3-.1 , 165 TI,C03 T12C03,3, 169 Tl,C,Ni,S2 Ti2{S2C==C(CN)2),3,170 T~KBH~~NIC,O~S~ Tl,SO,(H,NCSKHH,),, 3, 170 T~ZC~H~~NI~O~S~ TI~CO~(H~NCSNH 3,170 ~)S, TKd'hSh [T1,{S2G=C(CN)2}3]4-, 3, 170 T12C36H44N4

Tl,(octaethylporphyrin), 2,821 T12C44H28N4 Tl,(tetraphenylporphyrin), 2,821 nc13 T12C13,3. 171 T12C19 [TlzC1913-, 3, 175 TI~CUO& T12{Cu(S0,),], 2 , 638 Tl2F2 TIIF>,3. 170 1 3 9

[T12F,11-, 3, 174 TI,HO,P

TI,HO,P

Cumulutive Formula Index

T120, 3, 168 TI203 TI2O3,3, 172 T1203S T1$03,3,169 Tl204S TlzS04, 3, 169,171

08Sz. Tl,(SO,),, 3, 173

TI2

TLGHi,O, {Tl(OMe)),. 1.139.153; 2,348; 3, 168 TLO? TI4O3,3, 171 TL~IzY, T1,P,0,2, 3 , 169

'rI4s3

'1'I4S3. 3. 171 TI,Tr,

TlzS, 3, 169 7185

TIZSs, 3,171 TI2Se TI,Se, 3,169 T12Se3 TI,Se,, 3, 174 TlzTe TI,Te, 3,169

'l'12Tc3,3, 171, 174 TI,CBN,S,

Tl,Te,. 3. 171 TI,O,,Te TI6TeO1,. 3. 173 TWn [TI,F,,]*-. 3. 171 TI706 T16TI0,, 3,169 TIP32 [Tl,F,,]S 3, 174 TmC,,l I,,TSSO8 [Tm(DMF),I3-, 1,2X6,3, 1080 'l'rnC36H4FN40 Tm(oc~aethylporphyritl)(C)II ) , 2, 822 Tm2012S3 Trn,(S04)3. 1.261

600

U ucos

UB3C;,H4;P4

U(BH4)3(Me2PCH2CH2PMe2)2. 2,1041

U(BH,),, 3,1132, 1135, 1175 UBrO, U02Br, 3,1185 UBr, UBr,, 3,1135, UBr4CI0 UOCIBr,, 3, 1211 UBr102 [U0,Rr,]2-, 3, 1212 UBI, UBr,, 3,1185 UBr, [UBr,12-, 3, 1175 ~ U B I ~ ]3,1136 ~-, UCC13N03 [UOzC13(NCO)]2-,3, 1191 UCF305 [UOZF3(C0,)l3-, 3, 1201 UCH,CI,NO, UCl,[MeNO,), 3, 1159 UCH3N30Io U0,(N03),(McNOz).3. 1202 UCH406 UO,(OH)(O,CH)(H,O). 3,1198 UCH,.CLN. Udi(CNj(NH3),, 3,1136. 1137

UOz(CO;), 3, 1201; 6,852,890,896,898 UCzH206 UO,(O,CH),. 3,1198 UCZH3ClzF3N UCI2F3(MeCN),3, 1179 UCZH3C12N02 U02C12(MeCN). 3.1191 UC2H3C13N UClJvieCN), 3, 1133 UC,Hd& 1102(02rH)z(H,O), 3, 1198 uc,114010 [ u O d C O ~ ) d H ~ O ~ 6,888 ~lz-, UCzHiNO [U[SO,),(AcNH2')1'-, 3, 1161 UC2Hs06 [UOI(OAC)(OH)~]-,3, llY8 [ U 02(OH),( OAc)] -,3, 1193 UCZHSOTP UOz(HP03)(HCHO)2, 3,1196 UC7HhC12?4,0,, U02( C104)2(MeN02)2.3, 1202 UC2H6C1?03 UOIClz(EtOH), 3, 1193 uc,116CI,o, UOCt,(EtOH), 3,1180 UC2H,F,O,S UU,F,(DMSO). 3,1208 UCZH,J302 U(OMe)2F3,3, 1181 UCzH6N20, UO3(HCOYH,)Z,2,491 UC,H,O, U02(C,O,)(HzO),, 3,1192,1201 UC2HsCI4Nz UCI4(en). 3. 1138 UC2HaFjN4Sz UF5(H2NC(S)NH2}?,3,1184 UCzHBN,O*S UO.(S04)(H2NCONHZ)z, 3, 1205 UCZHgK;,ObP UOz(IIPO,)(en), 3, 1189 UCzHgOTPS U02(HP0,)(DMSO)(H20),3, 1208 UCZN202S2 U02(NCS)2,3.1191

uc,yv,o,

[CO~(CN)2(N03)2]2p,3,1187 UCZO, UO(Cz0,). . ~ 3,1156 . UC206 UO2(CzO4), 6,919,928 UCA [UO-z(CO&]' .6,H4X, 852,897

uc,o*s [ild3(czo4)(so3)]2-, 2,638

UC.,O,, [UOz(Oz)(C,O3)2]", 3, 1201; 6,897 UC,CI90 UCl,(Cl&=CClCOClj, 3,1183

601

Cumulative Formula Index

[UOz(CO3),]'-. 6, 902 [UOz(C0,)3]4--,3,1201;6,798,805.821.822,848.854, 888,889,890,896,897.898.909. 912,924; 6,893 UC,O,, [U0i(CO3),]", 6, 852 UGHOii 3, 1193. 1201 [UOz(C,04)z(OH)]3~, UCIH~N~O, IU02(NC0)4(Hz0)]2-,3, 1191 I;C.H,O, U(O,CH),, 3, 1154 UC,H,O I , , [UOz(6ZCH)4]'-,3, llY8 UC,H,NO, UO,{HN(CHzCOz)z} 3,1200 UCJLOh UO,(OAc),, 3, 1198 UCaHLO, UO;{(CH,CO,),}(H,O), 3,12u1 UC&08 UO,(HOCH,COz),, 3,1203 UO,(O,CCH=CHCO2)(H,0'12, 3. 1201 I

U(NCS),(H,O),, 3, 1142 UC&O, UO2(OAc)2(H,O),6,890

UCSHlSN6O5 [UO~(OAC)(HZNCONH~)~]+. 3. I205

602

[U(NCS)*14 , I , 24, 84.86; 3, 1132. 1139, 1142 UC8016 [U(C,O4),l4-, 1,99;3, 1157

U{OCH(CF,)Z}(TMEDA), 3, 1137 UGH,,CI,P, UCL(PMe3)3, 3,1144 UCioHzF120G UO,(hfacac)z, 2,384,385 UC14(HMPA)z, 3, 1132, 1165 UCl,jbipy), 3, 1179 UCioHsN3Os UOz(N03)(bipy), 3,1190 'JCioHioClzNz03 UOzClz(bipy)(H20).3,1190 UCioHioClsNz UC~S(PY),,3, 1179 UCioHioN~0s UO,(NO~)(py)z,3, 1189 UCioH IZNzO i o [UO2(cdta)]'-. 3.1213 UCioH14NzO10 UO,(H,edta), 3, 1212 UCioHi406 UOz(acac),, 6, 910 UCioHi& UOz(acac)z(H,O), 3,1193 UC10H20NZ06 UOz(EtzNCOz),,3, 1201 UCioHzsClOs U(OEt),Cl, 3,1194 UCioHzsOs U(OEt),, 2,340; 3, 1181 UCioHz6ClzO2Si2 U(OSiMeEt2),C12, 3, 1147 UC10H3007SS [UO,(DMSO)s~z~, 1,74; 3, 1208 UCloH3007Se5 [U02(OSeMe2)5]2-,2,493 UCIZHLIC~ZN~O, UO,Cl,(phen), 3, 1190 UCizH8C1sNz UCl,(phenazine), 3, 1179 UC1ZH~ClsNzO [UOCl,(phenazine)]z-. 3,1179 UC1zHloBrC1zOz U(OPh)zClzBr, 3, 1181 UCi2HioC12N406 [U0zC1z{ON(NO)Ph)2]2,2.512 U G zHioC1zOz U(OPh),C12. 3,1147 UCl2HY0Cl5Se2 UCl,(Ph,Se,), 3,1185 UC~ZHI~C~ST~Z UCI5(Ph2'I'e2),3,1185 UCi2Hl0NO4 U02(tropolonate)(py), 2,397 UCizHioN406 UOz{ON(NO)Ph},, 2.512 UCizHi2NzOs UO,(OH)(OAc)(bipy). 3, 11W UCizHi4FdJ7S U0z(CF,COCHCOMc)2(DMSO), 2,384 UCiZHZ4C1306 UC13(18-crown-h),3, 1136 [UCI3(18-crown-6)]' , 3 , 1178 UCI~HZ,N~OSSZ [UOz(OEt)(EtzNCOS)2]--. 3. 1209 UC12H27N2012P

UC12H36N406

[U02(Me,NO),]2+, 2.497 UCdioN4O9 [UO,(CO,){ON(NO)Ph},]z-, 2,512 UCi3HiiF120ioP UOz(hfacac),{(MeO)3PO}, 3,1207; 6,910 UCi;Hi@6 U(OEt)3(2-OC,H4C02), 3, 1183 UCi3H29N303S4 U02(Et2NCS2),(Me3NO),3, 1206 UC~~H~YV~O~ U(pyridine-2,6-dicarboxylarr)2,3,115S UC,dW,Oic [U0z(2,6-pyridincdicarboxylate)z]2,3, I199 ~~C14H1@Ft207

UO,(hfdCX),(THF)> 2,384,385; 3,1195 UCi,HioOs U02(tropolonate),, 3, 1195 UC,,Hl,N;Os UO,(OH)(OAc)(phen), 3, 1190 UCi,Hi,ND,

Cumulative Formula Index

604

U(OCH,CF,),(NEt),, 3, 1179 UCI~HZBFMNZOS U(OCH2CF3)5(Me3N)2r 3,1179

UC16H40N4 U(NEt,)4,2,164,174,180; 3,1141

[U(D&lF),P-. 3, 1162 UC24H60C13K404

[UCI,(EtCONEt,),] ' .3, I164 UC24bZN 1 2 0 h P 4 [UOz(HMPA)41Z-,3.1207

UC25H16N9S5

[U(NCS),(bipy)l]-, 3. 1139 UCzHz5N5Oz [ U O ~ ( P Y ) ~ ]3.~ -1189 . UCZ5HS0N05 U(OBu'),(py). 3. 1179 UCZ~HI~N~OZS, U02(NCS)2(phen)z,3,1190 UC&24CI,Pz UCl,(dppe), 3. 1144 UC26H2505 U(OPh),(OEt), 2,310;3, 1181 UC26H4,Pl UH(r15-C,Me,),(Me,PCH,CE I,PMeZ), 2, 104 1 U C Z ~ H ~ ~ N ~ O ~ UOZ(8-quinolinolate),(quinoline), 3, 1190 UCnHi9N305 U0z(8-quinolinolate)2(8-hydroxyquinoline),3, 1213

UCz7Hz7ClNOS U(OPh),Cl(DMF), 3,1183 UCzsHzoClOs U(tr~polonate)~Cl, 3, 1182 UCzsHznO, U(tropolonate)4,3, 1149 UCz~H3sF6OioPSz

UO,(SCH=CHCH=CCOCHCOCF~)~{ OP(OBU)~},

6,910 UCmHwN2 U(q5-C5Me5)Z(NEt2)2,I , 181 UCzsH6oC13N404 [UC13(EtCONEtz),]', 3, 1132 UC28H7ZN1601ZS4 U(NCS),(HMPA),, 1,87; 3. 116 UC30H3604Pz U(OPh)4(MezPCHzCHzPMe2).2.1041 UC3oHsoNzOz U(qS-CSMeS)2(qZ-C0KEt2)z, 2. 181 UGzHie.NsOz UO,(phthalocyanine). 3, 1214

UC64H32N16

U(phthalocyanine),, 2,865; 3, 1178 UC64H1380184 UOz{ HOP(O)(OCHzCHEtBu)z}z{OP(O)-

(OCH~CHEtBu)~}~,6,796,904,909 UC66Hd1206 [U(antipyrine),13*, 3.1134 UC120lO UO~(C10~)~,3,1193 UCI? LJC1,. 3, 1132,1135 UC14 UCI,, 3.1134,1173 [UCI,j-, 3. 1136 UC1402 [U02C14]2-, 1,549,3,1211 UCI, UCl,, 3,1185 UC1,O [uOcl5]-, 3,1211 [UOClS]'-, 3,1179 UCISOl [uozc15]3-. 3,1212

uc1,

UO,(N~,)~{~OP(O)(,~CH,CHE~BLI)~}~, 6,906 UC3ZH740L8P4

UO~{HOP(O)(OBU),),(OP(O)(OBU)~}~, 6,405,907 uc34~2Sc1Z04

UOZC1Z{(PhCH=CH)2CO}2,3,1195 UCwHzsOio U(tropolonate),, 3, 1182 [U(tropolonate),]-~.3: 1150 UC~sH36NsOsSz UOz(NCS),(antipyrine),. 3. 1205 U C ~ SH~SNSO, [U02(2,6-lutidine~V-oxide),]~'~, 2,497 UGsH,sOs U(OCEt3)5,3, 1181 UC36H30Br40ZP, UBr,(Ph3PO)Z, 3, 1165 U'&H,OCIZF,OZPZ UC12F3(Ph3PO)Z,3,1184 UC36H30C1402P2 UC14(Ph3P0)2,3, 1132, 1165 UC&3oFsOzPz UFS(Ph3P0)2,3, 1184 UC36H3006 [U(OPh),]-, 3, 1181 UC36H3007Pz UO(O,),(OPPh3),.6,329 UC36Hsz04P4 U(MeZPCHzCHzPMcz)z(0Ph)4, 1,89; 3,1144 UC391.151N903 [U(4-dimethylaminoantipyrint.!3]3+I3, 1134 U'&1~buN9 UO,(superphthalocyanine), 2 . 889,6, 194

U0,{HOP(0)(OCH,CHEt13u)2) { OP(0)(OCHZCHEtBu),),, 6.907 UCe.nH44Os U(PhCOCHCOPh)j, 1,94

UCI6, 3, 1211 [uc16] ,3, 1186 [Uc1,]2-, 3,1132 UCI& [uOzC16]'-, 3. 1212 UCI7 [UCl,]*-, 3,1186

uc1,os

UCI,(SOC12), 3, 1184 UClS [UClSl3-, 3,1186 UCrC,H,,N,O, UOZ(CrO,)(AcNHz)z,3, 1204 UEr2MoI2HZ0Os2 I(UMo,20,,)IEr(OH,)s},lz , 3 , 1047

u v207s,

UO(SO,F),, 3, 11.52 UF30sS2 UO*(SO3F)Z, 3, 1196 UF,O UOF,, 3,1211 UF40iS4 U(S03F),. 3,1152 UFS UF,, 3,1185 [UF,]-, 3,1132,1173 [UF5]2-.3. 7136 UFjO [UOFSJ-. 3, 1211 L!F,O, [UO,F,]?-, 1,74,3,1211 UF6 uF6.3, 1210 [UF,]--,j, 1186 [UF,],-. 3,1174 [UF6I3-. 3,1136 'Cj'F,O,sS6 [U(FO,)J, 3,1152 UF7 [UF,]-, 3, 1211 [UF,t2-. 3,1186 [UF7J3-. 3. 1132,1174 UFB [UF,]2-, 3,1211 [UF,]>-, 3. 1186 [UFSl4-. 3, 1174

U F9

[UF,13-, 3,121 1 UGe2W22078

Cumulative Formula Index [U(GeW 1039)z]1z-,3, 1048 UHZCIZN U(NH2)C12,3,1135

uo. [U02P207J2-, 3, 1196 UOqTe?

[UO;(H2P02),]-, 3,1196 UH709P UOI(HPO~)(H~O),, 3, 1193 UHnO,$e UOz(SeO4)(H20j,, 3, 1197 UHsOiSz U(S04)z(Hz0)4,3, 1144 UHgC13N3 UC13(NH3)3,3, 1132 UHi& [UOz(Hz0)5]”, 1,74; 2,306; 6,890 UHlzBr4N4 UBrdNH,),, 3, 1137 UH&N, UCl4(NH3),, 3,1137 ’

[WO,(P0,)l4-, 3, 1196 UOS

606

UZC14H14N2018 { U02(2,6-pyridincdicarboxylatc :V-oxidc)(H20)Z}z.3, 1200 UzCisHzoOis Uz(OCHzCH2COz)j, 3,1183 UzCi6H3oNzOi4 {U02(OAc)z(AcNMe2)},. 3. 1204 U~CZOH~SCISNS~~ (UC1,)2(AcNMe2)s,3. 1162 UZCZ~H~ON~~I~ {UOz(2-HOC,H,CO,)(NO,)(4dimcthylaminopyridine)}2, 3, 1203 UZC3ZH80N8 (U(NEt,),),, 2, 174; 3, I132

U2{PhCH(0)C02}5.3. 1183 UZC44H42014P2 {U0,(OAc)2(Ph3PO)}2,3. 1207

399

VR S ~ C ~ ~ I ~ ~ O S ~ VO(S,AsMe2),, 3,527 VAsIClIHZ4Cl4 VCI,( 1 , ~ - ( E ~ ~ A s ) ~ C ~3,498 HA}, VAS,C&~~CI~ VCL(diars),, 3,498 VAS~C~~H~,O~ [VO(OAsPh3),12+, 3,522 \’AUC&1@6P V(C0)6(AuPPh3),1,73; 5,904 vA~3C&&d’3 {Au(PPhq))o,V(CO),, 5,904.905

VBr2.3.467 VBr20 VOBr,, 3,530 V B r, [VBr,]-, 3,467 V€3ri0 [VOBrJ. 3, 530 V3r40 IVOBr4l2 , 3 , 5 3 0 VRr,

[Vt3r512-. 2, 297; 3.4X3 VBr,O [VOBr# , 3,530 VCCL+NS VCk2(NCS),3,475 \.’CH,CI,N VC13(NMe), 2, 167 VCH3C150 IVCI,(OMe)]*-, 3,502 VCH,,NO;S [v(HzO),(NCS)]+, 3,465 VCNS [V(YCS)]”. 3,475

vco;

VCO,. 3,467 VC2ClN2S2 VCI(NCS)Z, 3,475 VCzF3Os [VU(C204)F3I3-. 3,518 VCZHzFzO, [VO(C204)F2(H,0)I2-, 3,s18 VCZH2N3S2 V(NCS),(NH2), 3,474 VCzHz04 V0(02CCH20), 3,520 VCzH205 VO(O,CH),, 3,513,514

[VO(C201)F(H,0)2]-, 3,517,5,18 VCzHSF2N02

VOF,(McCN)(H,O). 3.496 VC2H5N06S V(AcNH,)O(SO,). 1. 120 VC‘,H,CI,O, [VOCI,(EtOH)]-. 3- 502 VCZH~F~NZO~ VOF2(HCONH,),.3.523 VCZH60PS2 VO(S2PMe2). 3.527 VC2H7C14N VCl4(NHMez), 3,490 VC2HSClzPU’Z VC12(NHMe),. 3,490.191 VC,H,Cl,O, VCl,(McOH)?, 3.466 VCZHSF2N40SZ VOF2(H2NCSNL12)2,3.S2c) VC2HsFzN,% VOF2(H2NCONH2),,3.523 VCzHioNO6 [VO(Gly-O)(H,0)3] ‘.3.546 VGHi2N07 [VO(Gly-O)(H20j4]+.3.546 VC2Hi3N07 [VO(O,CCH,NH,)(H,O),] *+ , 3,546 VC2NZ [V(CN),]’ , 3 , 4 5 7 VC:,O, V(C,U,). 3.467 [v(C,o,)]-,3,472 [V(G04)1+, 3, -180 VCZOS VO(C,O,), 3,518 VC3H2N205S VO(NCCH,CN)(SO,), 3.496 VC3H2Os V0(02CCH2C02).3.518 VC3H306 V(02CH),, 3,480 VC,H,N,OS, VO(NCS)2(H2NCSNH>),3,495 VC3H404 VO{02CCH(0)Me). 3.520 VC3HsNOIS V{SCH,CH(NH,)CO,). 6,496 .~ VC,HsO,[VO{O,CCH(OH)hle)]’. 3,520 VCqHnNOjS [VO{0,CCH(NH,)CH2SH}(H20)]+, 3,546 VC3H9C1,N VC13(NMe3),3.474 VC3H9Cl4N VC14(NMe3),3,490 VC3H9FZN03 VOF,(H,O)(DMF). 3,523 VC3H90133 V(MeSO,),, 3,479 VC3N30S3 [VO(NCS),]-, 3,495 VC3N3S3 V(NCS)3, 3.475

608

609 [VO(NCS)4]a-, 2,220

vC:,CI,Os

vo(o*cccI,),,3.514

VC,K6O2 [V(NO),(CN),IZ-,3,459

VC4HzC1405 VO(O,CCHCl,'),, 3.514 VC,H;N~O~S, [VO(NCS),(H,O)]' -.3,495 VC,H,Oi VO(O,CCH=CHCO~). 3.518 VC4H201o [VO(C,O,),(H,O)]- .3.517 [VO(C,0,)z(HZ@)]2 .3.518 VC,t14C:12C),

vc.40,

~, ~

[V(C,O,~zO,]3-1,57 VC,H,C12N,0 VOCl,(purine), 3,568 3

VCSHSCl2h V(py)C'I,, 3. 404

vO(ozccH,cl),, 3,514

VC5HjC'12N50

VC,H,CI,S VCl,(thiophene), 3,529 VC4H405 VO(OzCCH,CHZCO,),3,518 VC4H40A 3,520 [V0(O2CCH20)?l2-.

VOCl,(adenine), 3,568 VCSHjClZNjO2 VOCl,(guanme),3,568 VCSH6O: VO{O2C(CH~)~COZ}, 3,518 VCGHRNOoP [i'6{0,P(0)CH,N(CH,C0,),}(H20)]2-, 3,551

vc,-h-o,

Vjn'O)(CO),, 1.290 VC5N,0

VO(OAc),, 1.271:3.514,515 VC,H,FN,O, [VO(GIV-O),F]-. 3.546 . VC,H,OS, [VO(SCH,CH&]'-. 3.528,524 ~

~ C < (M e C O C N )z3,490 ,

VC,H,N,O,

VO(Gly-O)2(H,O). 3.546 VC4H1003PSZ VO{S,P(OEt),}. 3.527 VC,HIZCI,NZ VC1,(Me,N)2, 3.491 VC4HiZCl,OS2 VOClZ(SMe2),.3.529 VC,H,,CI,03S, VOCl*(DMSO),.3. 522 VCIHIZCI& VC13(Shle2)2, 3,481 VC4H,,NzOS2 VO(SCH2CH2NH212, 3.554

VC,H,,OP,S,

VO(S2PMe,)2.3.527 VGHit04 V(OMe),, 2, 347; 3.502 VC~HI~NZO~ [ V O ( O ~ C C H ~ N H ~ ) ( G 1 ~ - O ~ ( H3,546 ~O),~t,

VC,H,,CI,N,O VOCI,(NHMe,)?. 3.490 VC,HiJ'JIoO, VO{H2NC(=NH)NC(=YH)NH,)2(HZO),

VC,H*oC12N,O 3.490 VOCI~(NH,MC)A, VC,N,OS, [VO(S,CCN),1'-, 3,528 VC4N4

[V(CN)4J2-, 3,462 VC,N,OS, [VO(NCS),]-.3.495

VC6H1003S4 3,497

VO(S,COEt),, 3,528

61 0

Cumulative Formula Index

VC6H;,N8O, VO{MeNHCONC(=NH)NH,}?. 3.497 VChHiiC12Nq06 VCI,(HOzCCH,NH2)3, 3,484 VC6Hi6N 2 0 6 [V0(0zCCHMeNH3)2(H20)]-,3,546 V C di 6 ~ 1 0 0 VO(MeNHC(=NH)NC(=NH)Ntf,),. 3,497 VCtjH18C12N20 VOCl2(Me3N),, 3,490

vc,ni,c1,0,s3

VOC11(DMSC))3,3,522 VC6H18C13N2 VC13(NMe3),, I , 45; 3,474 VC6H21C13N3Si3 VCI,(Me6cyclotrisilazane), 3. 476 VC6H2,C130P2 VC13(Me2PCH2CH2PMe2) (THF). 3, 476 VGHd, [V(en),12+. 3,463 [V(en)$+, 3,474 [V(en),I4+', 3,491 T7C6H24N1206 [V(H2NCONH,),13', 3,480 VC6H24O6 [V(MeOl 1)6]2' ,3,46h VC&dJ,N, V(MeNH,),,Cl,, 3,463 VC6N& [V(S2CCN)3]2-, 3,528 VC6N6 [V(CN)6I4-, 3,462,474 VCd6S6 [V(NCS)6]3p, 3, 475 [V(NCS),]", 3,464

vc6x6!k6

[V(NCSC),]'-, 3,476 VChN,O IV(NO)(CN),l"-, 3,459

V(NO)(MeCN)4C12,3, 459 VCsHiSs V(S2CMe)4,3.524 VC~HI~O~S~ VO(S2COPr')2.3.528 VCsHi40s V0(0*CPr)2,3.513 VCsH16Br203 VOBr2(THF)*.3,497 V C ~ H I ~ N ~ ~ & VO{Me02CCH(NH2)CW2S}2,3,547 VC:,H17c!*N20, VC12{U,CCH(NH,)CH(OH)Me}(HO,CCH(NH,)CH(OH)Mc) ,3,484 VC,HI,CI,O, VCIZ(OBu)Z, 3,502 VCsHisN502PS2 VO(NCS),(HMPA). 3.495 VCsH&IZOS2 VOC12(SEt2),, 3,529 VCSH20C13S2 VCI3(SEt2),, 2.553; 3.481 VC&J% V(Me2N),, 3,491

, . . ~.

.

VC~H;,NO,S, VO(S,COPr'){HNTH,),}. 3,528 VGHmN6 [ V ( ~ n ) ~ 3,474 l~+, VCloC24CIZN,US2 VOCl2(Me,NCSNMe,),, 3,529 VCioH2FnOs VO(hfacac),, 2.388 VCloHsBr2N20 VOBr,(bipy): 3.493 VC1oHsCIzN20 VOCl,(bipy). 3,493 VCioHsC14N2 VCl,(bipy), 3,493 VCioHsF605 VO(MeCOCHCOCF,),. 3,505 VCloH8N203S2 VO(Z-pyS N-oxide),. 3.554 VC.i,,H,N,O,S VO(SO,)(bipy), 3,493 VCioHio VCp2, I , 155 VCloHloBr2Nz0 VOBr,(py),,3.493 VCioHioC1zNz V(PY),ClZ, 3.464 VClOHloCl6Si2 VCp2(SiCI3),. 2: 16 VCioHioF2N20 VOFz(py)z, 3.493 VClOHI,NO,

V0(2-OC,H,CH=YCHMeC0,)(OH2),3,543

vc

12C1205 VO(MeCOCCICOMe),, 3,507 VCIOHl,N,~, VO( 2-pyCH,N(CH,CO,),} (HZO), 3,548 VCioHizN208

611

Cumulative Formula index

[V(edta)]-, 3,485 VCioHi3N~08 [V(Hedta)]-, 3,548 VCioHi3Nz09 [VO(Hedta)]-, 3,548 VCioHi4Nz08 [V{O2CCH(NH2)CH2CHZCO2}JI 3,484 VCioHi404 V(acac)z, 3,470 VCioHi,Os VO(acac)2, I , 47; 2,372,379.495; 3,471,504,505,507, 509,535; 6,341,346.1013 VCioHisN20s [VO{(OZCCH2)2NCH,CH2N(CHzCH20H)CHzC02}] .3,486

VO(NCS),(py),, 3,493,495 VCi2HIoN405 VO{ON(NO)Ph},, 2,511 VCiaHioOPSz VO(S>PPhz), 3,527 VCi zHizFeN20, VO{ {F3CCOCHC(Me)=NCHz}2}, 3.535 VCizHi2N20S2

V${(MeCOCHC(Me)=NCHzj2},3,524

VO(02CCHMeNHCHMeC02H)2,3,549 VCi,HzzN4OS4 VO(S2CfiCH2CH2NMeCH2cH2)2,3,525

Cumulative Formula Index

VC13H36N03Si3

612

VO(O,CCH=CHCO,l(phen), .. , 3,555 vc,6Hi,,k,03sz V O ( ~ ~ C ( S ) N H C ( O ) ~ , ~3,554 Z)~, VC,,H,nN,O< -” -” . V0(2-benz~midazoIe~arboxylate)~, 3,493 vCi6HizN~o~ V0(8-quinolinolate)(OzCC,H4NHz-2), 3,557 VCi6HizN406 V0(2-benzimidazolecarboxylate),(Hz0), 3,493 VC 16H14CIzN20, VCl,(salen), 3,535 VC~~HMNZO~S VS(sa1en). 3.571 VC16Hi,N,03 VO(salen), 3,534 VCi6Hi,Oj VO(O,CCH,Ph),. 3,514 VCi6Hi&z03 V0(2-OC,H,CH=NMe)z. 3,537 VC16Hi6Nz05 V0(2-OC6H4CMe=NOH),, 3,553 VCI~HI~NZO, V0(3-Me0-2-OC6H3CH=NOH)z. 3,553 VCifiHzJ’J-iO, V O { ~ , ~ - ( ( M C C O ) ~ C H ~ N } &3,553 ,H~}, vci 8 2 1N o s VO(acac)2(J-pyMe), 3.507 VCI6Ib 4 N 2 0 , VO{(MeCOCHCOCHzCHMeNCH,),), 3,561,562 VCi+,H,,CIN,O, 3,482,567 VCl{(MeCOCHCMe=NCH2)z}(THF), VCi6HzsN& VCp2{NN(SiMe3)2),2,144, 148 VC~~H~~CINOS [VCI(NO)(THF),]+, 3,458 VCI~H~~NZO~ -I

522

~VO(benzimidazole)z(H20)]z~, 3,493 VCIJHI~C~PNS V{H~C(~~N=CHCH=~H)~}~CI,. 3,463 VCi4Hi7NzOzSz VO(S,COPr’)(py),, 3,528 VCiJiisNioOs [VO{2.6-py(CONHNHz),}2]‘+,3, 494 VCi4Hzz07 VO(acac)2(dCHZCHzOCH2CHz).3.507 VCi4fLsNzOS4 VO(S2CNPr’,),, 3, $25 vciJH34c1203P2 VOC12(OPMePr’2)z,3,522 VCi5H~Fia06 V(hfacac)?, 3,479 VCISHIONZOS VO(OzCCH,COz)(phen), 3,493,555 VC15~12F9°6 V(MeCOCHCOCF1)3,3,479

V0(2-SC6H,NH,),(py), 3,554 VC17H1 N,O,S VO(~CH=CHCH=CCH=NCHzC~lzS03)(py),,3, 543 VCi,Hz6NzO, VOI(MeCOCHCOCH2CHMeNCHz)zCHz}, 3,561 VC17H;6N303S V{(MeC0CHCMe=KCH2),}(NCS)(THF), 3,484

Cumulative Formula Index

613

VC,,HI,N,Q

VCZOH~ONSS V(SzCNEtz)4,3,526 VCZiH19ClN302 VCl(salen)(py). 3, 483 VCziHid'hO3 VO(salen)(py), 3,483 VC,,Hl,NO, VO(acac),(4-pqPh), 3,507 VCZIH2BCW6 [VC12(NNhfePh)(HZNNMePh)z]+,2,101,146,148 VCzZH,,F~NzO, VO(MeCOCHCOCF,),(phen), 3,509 VC22H20NZ09SZ VO(S2CNEtPh),, 3,525 VCisHzoNzO3 V0(2-OC,H,CH=NEt),.

V0(4-OzNC,H4CSCHCOzEt)z,3,554

3,537

VCzzHzoN6Sz V ( ~ J ' ) ~ ( N C S3.464 )~. VCZZHZZNLO~ Vo(acdc),(phen). 3,509 VC,,H .N,O

VO&CMeCHCMeNC,H,NCMeCHCMeNt,H,), 3, 5 60

VC,,H,zN,S

VS(hCMeCHCMeNC6H,NCMeCHCMeN&H4) 3, 560 L'CzzHzz W z VOIPhCSCHC0,EtL. 3.554 ~" , vczzH2~c1zw4 [VCl2(&=CMeCH2CMe= NC6H,NCMeCHCMeNc6H4]+,3,560 VCz2~zsNz03 VO(~-OC~H~CH=NBU 3,537 )~, VC22H31N203S V{(MeCOCHCMe=NCH,),}(SPh)(THF),3.484 VC,,H,IN@, V((McCOCHCMe=NCH,),)(oPh)(THF). 3,484 VCZzH32ClN8 [V{H,C(~N=CMeCH=~Me),),C11', 3,463 VCZZH30, VO{8C=C(CHO)CMezCHzCMe,~Hz}2, 3,510 VCsHi7N83 V0(8-quinol1nolate)~(py), 3,551,552 VC=Hi6CiN40 [VOCl(phen)$, 3,492 VCZ~HI~C~ZN~ VCl,(phen),, 3,493 VCZ4Hl6CI2N5O V(NO)(phen),C12, 3,459 VC24Hlb"l

[V(phen),]", 3,475 VG~HI&O [VO(phen),lZ+,3,492 VC~~HI~NL~SS VO(S04)(phen)2,3,492 VCz4H17N40 [V(OH)(phen),P+, 3,475 COC 7-u

vC,,H,,NO,P, V(NO)(CO),(dppc). 3,458

VC31H35C1N504 VCI{3.5-pyJCONH(CH,),N=CHC6H,O-2}~~, 3.483 VC~ZHI~NBO VO(phtha1ocyanine). 2. 861,865; 3,559;6,1014

VS(octaeth?llporphyrin), 3,558

VC3,H,,N,Se VSe(octacthylporphyrin), 3.559 VC42H30S6

615

Cumulative Formudu lpldex

V(SzCzPh*)3, 1,63; 3,161 [V(SzCzPhz)3]-, 3,461 [V(SzC2Phz)3]Z-~, 3. 461 VC4zH6006 [V(1,2-02-3,5-B~’2C6H2)3]-. 3.503 VC44HzsN40 VO(tetrapheny1porphyrin). 3.557 VC~~H~RN~S VS(tetrapheny1porphyrin). 3.558

VO{HOP(0)(OCH,CHEtBu)2}2{OP(O)(OCH2CHEtBu)l}2. 6.796,902 VC~H~OC~ZNOSP, V(NO)(OPPh3)4CI,. 3, 159 VC~ZH~OO& VIOSiPh,),, 3,502

VCUC,,H,~N,O, Cu(V0) ( (2-0-3-OzCC6H3CH=NCH2)z}(MeOH),3, 565 VCGSHI~NZO~ CUVO{(~-O-~-O~CC~H~CH=NCHZ)Z}, 5,662 VFZ VF2. 3.167

vFzo

VOF,, 3.529 VF, [\’F3]-. 3.467 VF30 VOF,, 2 , 681 [VOFJ. 3. 52’). 530 VFd VF,, 2, 681 V-FdO [V0F,l2-. 3.529 VF, VFS.2.680 [VF,]”. 3. 482 VF,O [VOF5IZ , 1, 50 [VOF,]”, 3,529 VF, . [VF,]-. I, 21 [VF6lZ-,1,21; 3,531 [VF,13-, 1,21;3,4X2 vF,oP4s, VO(SZPFz)I, 3,528 L’F186 [V(PF;)J. 3.460 VFezC14S4 [(FeCk2),(VS4)]3-. 2,565 VHFIRP~ VH(PF3)6.3.460 VHO [V(OFf)]z I , 2,296 I

\‘I I O *

VCI,(S2N3), 3, 555 VCLO VOCI,, 3,490,493,502.509 VCl*OS V(C104)2,3, 470

vc13

VCI;, 3,471, 490 [vCl3]-, 3,467 VCI3O [vOcl3]-, 3,530 VCI, V U 4, I , 271 ; 3,490,493 [VC14] , I , 251,252; 3.482 VCI,O [VOCl,]’-. 3,489.493, 530 VCI, [VCI,]-, 1. 40, 3. 531 [VCl,]’-, 3,482 VC1,O [VOC15]3-,3, 530 VC16 [VC16]2-,1,271; 3.531 [VC1,I3-. 1,252; 2,297 VCtlCIOHI4NZOQ C u ( M e 2 N C 1 ~ 2 C H ? h M e 2 ) ( C 2 0 ~ ~ V O3,565 (~~04), VCLIC~~H~~CI~N~O~ { 2-OC,~r4Cr-r=N(cFl,),N=CHC,H,o-2} (VO)CUCI~ 3,565 VCuC, 6H1,CI,N,O, VO(salcn)CI,CuCI. 5.572 VCuC16H2ZNZ05

Cu(VO){(MeCOCHCOCHCMeYCH2),)},3,562

VH, Cl ZNZ

[ v o ( u r i ) ] + .3.5(10 VH04 [VHO,]’-, 3,1026 [VO4HIZ-,6,851 VH0,P VO(HP0,). 3. 512 VH2C12K VCl2(KH2).3,474 VH2Cij0 [VC1,(H,O)]+, 3,478 VHPA [VOF,(H,O)]”-, 3, .529 VH202 V(OH)2. 3.470.471 VH204 [VH,O,]-, 3. 1026; 6,851 VH205P [VO(H2P04)Ji,3,512 VHz09P2 [VO(HP0,)2]Z-. 3, 512 VH3F4K VF4(NH;) . 3,490 VH3NC1, [V(NH3)C1s]2-, 2,27 VHJO, [V0(0z)2(NH3)]-,1, hl,2,319 VH303 V(0Hj3. 3,470 VH304 [VO(OH),] ,3,500, 1028 V04H,,6,851 VH3W’z [VOX(HPO,),]-, 3,512 VH4C12N2

VHdClZN2

Cumulative Formula Index

616

V(NH2)zC12,3,491 VH4CIzOz V(H;0j2C12, 3,466 VLFOF [VO(Pz0,)2]6~. 3.512 VPdCi4Hz409Pz

VO(acac){{OP(OMe)z},PdCp},3,567

vs4

[VS4I3-, 2,521 VSC, [VSe,]3 ,2,521 VSII~C:~,H~~O~ [V(CO)5(SnPh,),]-, 3,4.57 VTiC20H30N40,4 TiV { (02CCH2),NCH2CH2(CHzCH,OH)CH,CO,},

I

3.

486 VTiCZoH34C13N205 V { (MeCOCHCMe=NCH,),CI( v-O)TiCl2(THF),. 3,

567 VTiC20H34C1405 3. VC!{ (MeCUCHCMe=NCH,),}O{TiC13(THF)2}.

484

[V(H2O)6IZ+,1,284,336,367,369,371,378; 3,465,

VzB&,,H,,CIJ’4 { V( y-Cl)(p-Me,PCH,PMez)BI-l,),. 3,465 VZBZCSOHS~CW~ {V(v-a)(p-dppm)(BE+))2,3,465 V,B,ZnZC52%P4 VZZnZH4(BH4)2(PMePH2)4, 3,460

466.469.548

VI,, 3,467

VI3 [VI,]-, 3,467 VM~ZCI~HZ~C~ZNOS

VO(NCO)MgzC12(THF)3,3,471 VN., [V(N,)]”, 3,476 VNv VW,),, 3,476 VNii V(N2)6, 3,459 VNi, [V(N3)6]”-. 3,476 VNiC16H,zNz0s

NI(VO){(M~COCHCOCHCM~NCH,)~},~.~~~ VNiC26H24N205 Ni(VO){(PhCOCHCOCHCMeNCH,),r. 3,561 VNizC18H34013P4 VO{{OP(OMe)z}zNiCp}z},3.547

vo

[VOIZ-, 2,296,301,961 [VO]3’,2,296 VOS, [V0S3l3-, 2,521 VOSe3 [VOSe3I3-, 2,521

voz

VOz, 3,1028 [VO,]’, 2,296,301; 3,1026,1027 VOSZ [V0,Sz]3-, 2,521 V02Se, [VOzSeZ]3-,2,521

vo3

IVOJ, 2.296;3,1027

vo,

[VO4I3-, 2,413; 3,1026 V0,S VSO,, 3,470

vo5s

{ VO { O2CCH(0H)Me},},, 3,520 VzCizH3iN607S {VO( 1,4,7-triazacyclononane)),(y-OH)(y-SO4), 3,492 V&zH3&604 OH 492 )~, (VO(1 , ~ , 7 - t r i a z a ~ v c l o n o n a n e ) } ~ ( ~ -3,

617

Cumulative Formula Index

V3C24H24F18016

483

ku5"(04V),0,: 2,430 V,F,O, [Vz02F7]3-,3,529 V2H07

V30(02CCF3)6(THF)3, 1, 145 V~C~IHS~CLZN~O

V~(~-NP~)~CI~(NBLI')~(P~NCONHBU'), 1 144 V3C46H38016 V,O,(OzCPh)G(THF), 3,480,515 V3C12HioO17 (V0)3(citrato)2,3,522 V3HOIO [V3HOlo]4-,3, 1026 V3H201o

[V3M2C)1013-,3, 1025, 1027 L'iMoi0040 [ V , M O ~ ~ O ~3,, 1041 ]~~, V308

[V,Os]-, 3, 1027 [V30,]*-, 3, 1028 v309

IV30,]",

3, 1025, 1027

v3010

[V3010]5-,3, 1026 V3024P6 [(Vo)3(P*o7)3lG-, 3.512 V3W15062P2

[v'vvv*w15062 P~~~0-, 3. 1u5 I V4C32HSOO1h {V(OEt),},, 2.348

V,HOl, [V411012]3 , 3 , I027 1'4HO 13 [V1H013]5-, 3,1026 V4H2013 [V4H2OI3l4-.3,1026 V,HioOi4 [(VO)4(OH)lo]2-,3, 500,512 V409 [V,o,]*-, 3,500 v401, [v40,,14-,3,1026 v4013

[V,O,,lh-, 3, 1026 v4W8040P

[w*v4040P]'-. 3, 1036, 1049 V4W9040 [(V)W9V3040]6-.3, 1037

WAgCNS, [AgCN(WS,)]’-.

2, 566

WBr,O WORr,. 3,976 WBr4S WSBr,, 3,979,980 WBr, WBr,. 3.984 WBrjO (WOBr51Z-.3.985 WBr, WBr,. 3.974 [WBr6I2-. 1.122; 3,989 WCH,Cl, WMrCI,. 3. 975 WCH3Cl5S WCI,(SMe), 3,975 WC‘,(119N WCl,(NC,CI,). 3. 980

[ w o ( o H j z ( N c s ) 2 ] - , 3,988 WC2H,Br,h’ \I’Br,(MeCN),. 3, 989 WC,H,CI,N WCI,(MeCN), 3,989 WCIHIFJN2 W(NH)F,(McCN), 2, 167 WC,H,CI,O

[~i‘CI,(OEt)~”. 3, 984 WC~H6Br~0, [WBr,(OhIe),]-, 3, 984 WC,H6Cl30, WCl,(OMe)2, 3,984 WGHIOF~OL WOF,(OEt,). 3, 980 WC2NCI, WCI,(?rC,Cl,), 3,981 Mic207

WBC54H50BrClN2P3

WHClBr(PMcZPh),{NN(H)BPh,), 3, 1013 WBrz WBr,, 3,998 WBr2CI2N2O2 [W(N0)2C12Br2]Z-.3. 1011 WBrZNZO, {W(NO),Br,},, 3, 1014 WBrzO WOBr,, 3,990 WBrzOz W02Br2,3,976 WBr,N WNBr,, 3,980 WBi-30 WOBr,, 3,985 WBrJSe WSeBr,, 3, Y86 WBr, WBr,, 3,988

[WO,(C,0,)]2 ,3.978 WC:3t4GC1302Se

WSeCl3(C‘H20C2H40),3,980 WCAF3Od’ [WO,F,(OPMe,)]-, 3,978 WC3N30’S3 [W02(NCS)3]2-. 3.988 WC,Br210, [W(C0),IBr2]-. 3, 1006 WC4Br,04 W(C0),Br2, 3, 1005 WC,Br304 [W(CO),Br,]-. 3, 1005, 1007 WCACIK 0 5 W(CO),(NO)CI, 3, 1014 wc4C1,2Kz WCt,( NCCCI3)(NCCI2CCl3),2, 265 WCdHN,O: [W(O)(OH)(CN),]”- ,3,998 WC1HK402S4 [WO(OH)(NCS),12-, 3,988

619

Cumulative Formula Index WC4HzN40z [W(O)(OHz)(CN)4]' ,3,998 WC4H40S4 WO(NCS)4,3,976 WC4H6Br3N20 WOBr,(MeCN),, 3,985 WC~H~CIZNZOZ WO,CI,(MeCN),, 3,978 WC,H,CI3NzO WOC13(MeCN),, 3,985 WC~H~OCI~O~S WOSC12(MeOC~-IZC~120Me), 3, Y80 WCdH10C13S3 WSC1,(MeSCH2CH,SMe), 3,985,986 WCHi(FsN WF,(NEt,), 3,975 WGHizC1z04 WCl2(0Me),, 3,975 WGHmN303 WO,(dien), 3,978 WCaN4OS4 [WO(NCS)4]'-, 3,988 WC&'& [WO,(CN),]'-, 3,998 WC,HO,S [W(CO),(SH)]-, 2,517,645 WCSHZOSS w(CO),(sH,), 2,516 WCS% WHZCp, 2,695 WCSH7C1204 [WOZ(acac)CI,]-, 2,377; 3,978 WC5N50SS fWO(NCS)5]z-, 3,988 w c 6 h N 07 {WO(02)2(2-pyC02)1-,6,329 WC&ISC&N WC14(NPh), 2,167 WC,H,CI,N [W(NPh)CI,]-, 3,981 WC6HI1Cl4NS WCI,{SCFJ2S(CH2)2CH2}(MeCN). 3. 989

W(0MeL. 2.349: , 3.975 . WC6HzoN;07P WO(Oz)2(HMPA)(H,O), 6,329,332 WCANO, [W(CO),(NCO)]-, 2,237 WC6Nb [W(CN),]", 3,998 WCAN.3, W(NCS),, 3,975 [W(NCS),]-, 3,988 [W(NCS),]'-, 3,989 WC606

W(CO),, 2,199,237 WC7HN7

[W(CN),HI4 3,998 WCTHN7O [W(CN),(OH)IJ-. 2.297 WC7HzN70 [W(CN),(OH,)]3-. 2.297 WC7H3NOS W(MeCN)(CO),. I. 500 WC7H,0,S [W(CO),(AcS)j-. 2.615 wc7H&b W(CO),(OAc), 2,438 WC7HSNUSS W{Mec(S)NH,}(CO)5, 2,647 WC,H,O,S W(CO),(DMSO). 2,490

[W(CN),15-, 3.998 WC8H&IO3 wCIcp(cO)3. 2.204 WC8H.503 WIICp(C0)3,2,690 WCSH~NZO~ [W(MeNC(H)NMeCO)(CO),]-, 2,203 WC,H,N,% WCp(CO)L(N2Me).2, 134,136, 140 WCgHgO,P W(CO),(PMe,). 2.1039 WC~HizN602 [W(NO)2(MeCN),]z'. 3.1014 WCSH16C1305 WOCI3(C4H,0,)2.3.985 WCBHI~I~ZPZ [W(CO),(Me2PCHzCH,PMez)I]',3,1007 WC&zoF&" WF,(NEt2)2.3.975 WC8N8 [W(CN),l3-, 1,336; 3,997 [W(CN),p-, 1,84.334,4@6;3,997 ~

620

WHZCp,, 2,697,7U7. 71 I WCinHizOzS4 W(S2C2Me2)z(CO)2.2,615 WCioHi4Nz06 W(NO),(acac),, 3, 1011 WCinHi406 WO,(acac),, 3,978 WCinHzoN2OzS4 WOz(S2CNEtZ)z. 3, 978 WCIUHZON~OZS~ W(NO)z(S,CNEt2)2,3, 1014 WCl1HZsCl20P W(O)(CHBu')CI,(PGt,). 3.981' WC12FlsSe, W{Se,C2(C'F,),},, 3,983 WCizHinCWzO2 WOC14{PhNN(O)Ph}. 3.980 WCl2Hl4Br4NZ [WBr,(Mepy),]-, 3.998 WCizHisNz04S W(CO),(Bu'NSNBu'). 2. 191 WClZHl*S, W(S,C,Me,),, 2,615; 3. 983 [ W ( S Z C Z M ~ Z ) ~3,983 ]*-, wc 12~LOS12 W(S,CSGt),, 1 , 9 4 WC12H24N4S8 W(S2CNMe,),, 3,975.997 WCizHz7N% W=N(OBu'),, 2 , 358 {WN(OBU')~},,3, 982 WCIZHZ~NO~ W(OBu'),(NO), 2. 356 WC12H3oC130P2 WOC13(PEt3)2, 3,985 WCizH36CINzP4 WCI(N,)(PMe,),, 3, 1011 WC12H36N4P4 W(N1)Z(IJMe3)4r3, 1011 WC,,H,,N, W(NMez)6,2, 163, 168, 173, 178, 179, 181; 3,975,981 WCl,H,8C1zP4 WH2CIz(PMe3)4,3, 1015

wc 22J%

IN04

Cumulative Formula Index

622

WC34H36PZS4 W(SzCzMe2),(diphos), 3. 983 WC35H34NOP W(CO)(PPh3)(N=CBu1Ph)Cp, 2,280 WC35H63N7 [W(CNBu),]+. 1.72 [W(BufNC),12+, 3,1005,1006 WC36H283P WCp(CO),(PCPh=CPhCPh=CPh), 2, 1043 WC36H30Ci204P

'

WCI202(QPPh,),. 3,981 WC3J~,&12C)4P2 wo2ci,(oPPh3jz, 2.500;3, Y78 WC383oCLN% WCI,(NO)(OPPh,)?, 3, 1014 WC~JJ~OCLPZ WC14(PPh3)2,3,989 WC~~H~OF~N~PZ WF4(NPPh3)2,2. 124 WC36H3006 W(OPh)6,2,338,347; 3,975 [W(OPh),]-, 2. 349 WC36H36BrC1N2P3 [WCIBr(PMe,Ph)3(NzH3)j+, 3, 1013 [WHCIBr(PMe,Ph),( N Nil2)]+. 3, 1013 WC3GH44CiN40 WO(octaethy1porphyrin)Cl. 2.826 WC16H62P3 WHh(PPr'2Ph)312,700; 3, 1015 WC36HB8012P4 WH4(P(OPr')3}4,3. 1015 WC37H47N402 WO(octaethylporphyrin)( OMe), 3,986 WC38H23CWZOJ'

W(C0),(5.7-dichlor0-8-quinolinolate)~(PPh~),3, 1005, 1008

WC38H30Br20zP2 W(CO),(PPh,),Br,. WC,sHd,02

3, 1005

W(NBu')(NHBut)2(0CPh2CPh,0). 2, 183 WCRYH~OB~~WZ W(C0)3(PPh3)aBr2.3, 1005 WC3,H,,C~,OP* W(C0)3(PPh3)2CI,,3, I005 WC39H6803P2 W(+-Hz)(CO)3 { P(C6Hi 1 )3}2.2,690 WC4oH64P4 WH,(PEt,Ph),, 2.703 WC42H49y402 WO(octaethylporphyrin)( OPh), 3,986 W C ~ ~ H ~ I F ~ O ~ P ~ WH,(02CC.F,),(PMePh2)3, 3, 1015 WC44H20Nl

4O14

W(phthalocyanine){ OC6H2(N0,)3}2, 2,866 WC45H31NJ02 WO(tetraphcnylporphyrin)(OMe), 3, 986 WC52H4aC1NOP4 WCI(NO)(diphos),, 3 . 1012, 1014 WC52H4aC10P4 [WOCl(diphos),]-. 3, 989 WCdL&W'4 WCl,jdppe),, 1.398 [WC12(dppe)2]-l 1,498 WCszHdJ4P4 W (N) (K31(diph os)z . 3,997 W(N,),(diphos),. 2+147; 3, 1011 WCS2H,,CIN?P, WCl(diphos),(N?H), 3. 10'12 WC52H49NZP4 [ W H ( N ~ ) 2 ( d ~ p ~ ~ ~3,s )1012 ~]2+, WC52H19N4P1 [WH(N2),(diphos)1+. 3, 1015 WCSZHjOBrN2P4

623

Cumulative Formula Index

WF4

WC13F3 WC13F3, 3,975 WC13N WNC13. 3,980 WC13N0 W(NO)Cl3, 3, 1014 WCI3O WOCI,. 3,985 WCI,S WSC13.3.986 WC17Se WSeCI,. 3.986 WCI, WC14.3,988 WCldFS [WSFCI4]-, 3, Y7Y WC52H57P4 WC14N [WH,(PMePh,),]+, 3,1015 [WNC14]-, 3.980 WC53H48BrC12N2P4 WC14Nz02 [WBr(diphos),(NN=CCI,)]'. 2, 146; 3, 1013 [W(NO)2C14]Z-,3, 1014 WC53H48BrF3N2P4 WBr(diphos),(N=NCF,). 3, 1014 WCI4O WOCI,, 3,976 WC53HSoBrN2P4 WCI4O2 [WBr(diphosf2(N2CH2)] . 3 . 1013 [wo*c14]2-, 3.978 WCS3HS1BrN2P4 WCI4S WBr(diphos)*(N,Me). 2. 130. 140; 3, IO13 WSCI,, 1 . 4 4 : 3,979,980 WCS3H52BrN2P4 WCI4Sc WBr(diphos),(N,HMc), 3, 11113 WSCCI,. 3,980 WCS3HSzNOP4 WClj W (N H)(OMe)( dip ho%),,3,997 WCIS. 3.984 WCdLaOzP4 WCl5HI5CI3N4 [W(CO)2(diphos)z]', 3, io05 WNCMpy),, 3,981 W C ~ ~ H S ~ C ~ ~ N ~ O P ~ WCISK WCl,(diphos),(N,HAc), 3, 1013 [WNClJ, 3.981 WCS4Hs3BrN2P4 WC1,O WBr(N,Et)(dppe),. 2. 133 [woCl5]2-, 3,985 WCS5Hs6BrN4P4 WCI,S [WBr(diphos)2{NN=C(NHMe)2)]+, 3, 1013 [WSCIJ, 1,50;3,980 WC56HS7BrN20ZP4 WCI6 [WB~(~~~~OS)~(NN=CH(CH~)~OH)OH]' ,3, 1013 WCl,,, 2, 697: 3,974 W C ~ M WH4(PEtPh2),, 3, 10[5 [WCIJ, 3. 984 [Wcl6]2-, 3, 989 WCWH~~N~OZP~S WC1,,N04P, [W(02SC6H4Me-4)INNH2)(dppe)2]*.2, 147 { WKCI;(OPCI,)),, 3,981 WC~~HSSC~~N~P~ WCoC,,H4405P* WCI2(NNPhz)(PPhj)3,2. I37

[WBr(NNH~)(dppe),l', 2, 146 WCSZHSOC~NJ'~ [WCI(NNH,)(dppe),]' 2.116.147 WCSZH~OC~ZP~ WH2C12(diphos)2,3, 1012,1015 WC&SOFNZP~ [WF(NNH2)(diphos)2] 6.719 WCS~HSONJ'~ W ( N ~ ) ~ ( P M C P ~ ~ ) ~3. ( ~101 ~ 1P ~ O S ) . WC,ZHSZP, WH,(diphos),, 2, 702,3, 1012. 1015 WC~ZHS~P~ [WkIs(dppe)2]' , 2 , 7 0 2 W C ~ ~ H ~ A P ~ WH,(PMePh,),, 3, 1015

'.

+

[Co(Ph2PCH2PPhzPPPPPPh2CH,PPh2)W(C0),]+. 2, WSF,CI, 3,979 WC1F4S [WSF,CI]-, 3,979 WCIO, [ w o 3 c I ] - , 3,978 WC12F2S WSF2C12,3,979 WC12F,S [WSF3C12]-, 3,979 WC12F4 WCIZF4,3,975 WClzN202 [W(NO),C12},j, 3 , 1014 WCI2OS W0SCl2, 3,979 WCI2O2 WOZCI,, 3,976 WC1,SSe WSSeCI,, 3,979 WC12S* WS,CI,, 3.977,97!4

wc13

WCI?, 3, 1011 WC1,FS WSFCI,, 3, 979

1058 WCrCl3HaN2O7 W C p ( C O ) , ( Y m r ( C O ) s , 2, 136 W C U C ~ ~ H ~ ~ O ~ P ~ CuW(CO)3(PPh3)ZCp,5,572 wcus, ICu(WS,)]-. 2,565,566 WCUK54H45P3S4 Cu2(WS4)(PPh,),, 2,560 W CUIWC++H&P,S3 ( C U , W S ~ ) ( P P ~ ~ 2,566 )~O. WC U ~ C ~ ~ H ~ ~ C I O P ~ S ~ {CU(PP~~)},CIS,(WO),5,572 ( C U ~ W S ~ C I ) ( P P ~2,566 ~)~O, WCU~C~~H~~CIP~S~ (Cu3WS3CI)(PPh3),S, 2,566 WCU3Cl3S4 [WS4(CuCl)3]2-, 2,566; 5,572 WCu3Q, Cu3W06,5 . 651 W FO, [WO,F]-. 3,978 WF203 [WO,FJ-. 3.978 WF3O3 [WO;F3]3-, 3.978 WF4

Cumulative Formula Index

WF4 wF4,3,988 WF,O WOF,,

3,976

W40,

[WO(O,)F,]’-, 2,319; 3,977,980 WF,S WSF,, 3,979 WF, WF5, 2,680; 3,984 wFsN3 WFSNn, 3,975 WFSS IWSF5]-, 3,979 WF6 WF6, 3,974 [WF6]-, 1,498 [WF6]’-, 1,498 WF6N3 [WF6N3]-, 3,976 WF,OXe WOF4XeF,, 3,976

624

WMoCsHIdOe MoW(OAc),,3. 1307 WMoCmH36Os MOW(O,CBU‘)~, 3,999,1232 [MoW(O2CBut),]+, 3,1009 WM0Cz4HzjN404 MoW(&=CMeCH=CHCH=cO)d, WMoHC1, [MoWC18H13-,3,1316 WMoHCI, [MoWCI,H]3 .3,999 WNiS, [Ni(WS,)j2-. 6.112

W0Cl2 WOCI,, 3,990 WOF2 WF20,3,990 WOSSe, [WOSSe2]z-. 2,521 WOS,Se [WOS,Se]*-, 2,521

wos3

WF, [WFxlz-. 3,976; 6,854 [WFJ-, 3, Y84 WF,&Te WFAOTeF,), 3, 97s WF,O,Te, WF4(OTeFs),, 3,975 WFeBriOS, [FeBr2(WOS4)IZ-,2,566,570 \NFeCI7H& [Fe(SPh),(WS4)lz-, 2,565 WFeCZ9HZ2O5P W(CO),(PhPCHCHPh)FeCp,, 2.1055 WFeC29Hi805Pz ~, ~

WCp(C0),(2,4,6-Me3C6H2PCH=PC6H2Me32,4,6)Fe(CO)?, 2, 10.55 WFcClNiSj [FeCl(N3)(WS4)12-.2,565

WFeCl,S, [FcC12(WS4)]2-,2,563,565,574.575 WFeS4 [Fe(WS4)]-, 2,564 WFe2CI4S4 [(FeC1Z)2(WS4)]z-1 2,565 WGeCI3H8Br4N2O3 3, 1007 W(CO)?{bipy)(GeBr,)Br. .. WHS, [WS,(SH)]-, 2,519 WHTFqO, IW62F3(HzO)1-,3,978 WH2S4 WSZ(SH)z, 2,518,519 W1ZOZ WO&, 3,976 WI3 W13, 3,998 wI4 WI4,3,988 WIG4Hd403 In(octaethylporphyrin)WCp(CO), ,2.843 WIG6H4J’Z

(WOS,]2-, 2.521: 3,982 wosc, ,t,521,561 [WOSe,],

wo,s,

[wo,s,]~-,

2.521; 3.982

WO,Se, [W02Se,]z-, 2. 521; 3,982 W03S [W03S]” ,2.521 W0,Se [Wo,SeIZ-. 2,521 WO, [WO,l2-. 3,973.978,1033, 1034,1259; 4,825; 6,805, 1016

wos [WO,]“-. 2,296 WPbCZaHZs04 2, 16 (WHCpz),Pb(OAc),, WP~~C~TH~~CIO~P~ Pd2WCp(CO)2CL(dppm)2.5, 1110 WRhC4JLzPz Rh(PPh3),(p-H),WCp,, 4, 1076 [WCpz(~~-H)zRh(PPh3)z]+, 2,692 WSSe, [WSSe3I2-, 2,521

ws,

[WS4]’-, I , 172; 2. 521,545,562; 3,982 WSe, [WSe,12-. 2.521: 3,982 WSnC,H,,CI 0 3 S 1 W(CO),{-H,}(SnMcClz), 3,1007 WSnGJLO, W(CHC6H4Mc-4)(SnPh3)(C0)2Cp, 2, 19

[IrH(PPh3)2(~-H)2(q-o:l-S-q-C5H4WCp]*, 4, 1152 wIrc54H4006p3

I r W (pPPh2)(CO),(PPh,), W I ~ 6 ( r HI s05P4

,4,1163

IrWH(C0)5(pPPh2)2(PPh3)2, 4 , 1163 WLi,C8H2, Li,w( Me),, 3, 976 WMn2C4O,, MnZ(CZ04)2W03, 4, 50

3,1009,1307

[AU,(WOS,)~]~-, 2,566,568

625

Cumulative Formula Index { W(Co),},(PcH=CMeCMe=tH), 2, 1042 WZCI~H~OIOP j , 2, 1042.1050 W(C0 ),),(P=CHCMe=CMecH,

WSC14{p-$CH2S(CHz)z~H2) WSCI4. 3.980

WZC14(p-OEt)z(p*-Me2COCOMe2), 3.992

Wz(fi=CMeCH=CHCH=eO)4, 3,1008.1010 WzCz4HzsNs W,($!=CMeCH=CHCH=CNH),, 3,1008. 1010 W2CLka06 W,(OPr'),(~-C,H4)(r12-C,H2),2,357 WzC24Hs406 W2(OB~t)6. 2.346,358,359; 3,982, 1001 W2C24H66Sk W,(CH,SiMe,),, 3, 1000 WzCz&4O, W2(0Bu1)6(U-CO),2, 355 WZ~26HUZO4 W2(CH2Ph)2(OPr1)4,2,359 W2C26H50

{WH4(CjMe4B~')}2, 2,692 W2C26H5606

W~(OBU')~(U-C~HZ), 2,357 WzCz6H7,N,Sis W,{ Si(SiMe3)3)2( NMe, j4, 3, 1002 - ._ __ . W2C14(MezPCH2CH2PMe2)2, 3, 1009. 1010

1010

, 1003 1003

(WOF4)2XeF2,3.976 W2FeC6Hl4N,O2Ss [Fe(DMF)2(WS4)2]Z-.2.566, 575 W2FeC1,H80,,,P2 F ~ P C H = C H C HH)~,{w(co) , W ~ F ~ H ~ O ~ S ~ [Fe(H,0),(WS,)2]z-, 2, S W , 566 W,FeNOS, [FC(NO)(WS,)~]~-: 2,575 WzFeS8 [Fe(WS4j2I2-.2.564,574;3,982 [Fe(WS4),13-. 2,564- 566: 575; 3,982 WPe2C2JLN404 W2{CpFe(CO),)2(NMez)4,3,1002 W2Fe2S1o [Fe2S2(WS,),I4--, 2.566.569 W2Fe3Slo [Fe,S2(WS4),]4-I 2,566 [W2Fc7CZ4H60S20 [W2Fe,S8(SEt),J4-., 1, l6S I

W2H4013

W,(p-CO), { p-(3,5-xylyl)NC(H)N (xyly 1-3.5)},{3,5~ylyl)NC(H)N(~ylyl-3,5)} { (3.5-

xylyl)NC(H)Nxylyl-3.5)(CH2)}. 2. 199 W2C72H88N803 [WO(octaethylporphyrin)),O, 3,986 WzCsJ%JJsO3 (WO(tctraphcnylporphyrinj}20, 2,826 WzCd2Ss fCd(WS,),12-, 2,575

w;cl,‘O,s,

w c l , ( o ) ( ~ - s ) , w c l , ( o ) , 3,987 W,Cln [WiCla]4-, 3, 1009, 1010 W2C18Se3 I(WC14)2(pz-Se)(p~,~2-Sez)lz-. 2, 667 [W2C18Se3]z-,3,987 W2CI9 [W2Cl9]*-, 3,999 [W2C19]3-,2,684; 3,999, 1010, 1242 W2CIIO

W2Cl]0,3,9R4,987 W2ClloN [W,NCI1,,I2-, 3, 980 w2cl,oo I(WCl,)2012’, I, 272; 3,990 w,c002s, [Co(WOS3),]’-, 2,572,575 [c0(w0s3),]”, 2,575

w2coo4s4

ICO(WOzSJz]”, 2,572,575,575 ~Co(w02s2)2]3-, 2,575

w,coss

[CO(WS~)J-, 2,525 IcO(ws4),12-, 2,564,566,572.575; 3, 982

[w(oz),(~)~w(o)io,)~(H2O)z]’-. 3, 977 WHgS, [Hg(WS,),IZ-, 2, 566.575 W2Ni02S6 [Ni(WOS3),I2.. 2,575 W2Ni04S4 [Ni(W0,S2)2j2-,2.570,575 WzNiSs [Ni(WS4)z]2-?2.564,566,570,571,575 w 202s1u [W202S,(S4jz]z-.2.546 w70,

627

Cumulative Formula Index

W8bOn

W3C29H6609

W,(p,-CMe)(OPr'),, 2,358 W~C~OH~OO!~ W30(0Pr')lo. 2, 176 W~C~OH~INOIO W?(NH)(OPr'),o, 2, 176

~w;C19]3-, 3,998 W3Cr3C6SHl190Z8 W,{ OCH2Bu'}OJCr3(02CBu')12,3.994

~WO~WS4)2(H,0)]z,2,562.565 W30SB [W3OSSIz,2,563; 3,997

W6Cll*,3. 1011 WbCllB {W6Cl12}C16.1, 160 W6H0,, [W60200H]5-. 6.496 w61,Z

WJ,,, 3. l u l l

W6MIlOzl [MnW,Oz2]*-, 3, 1044 W6NiH602, INiW,H60,4]4-. 3, 1044 WBNiOZ4 [NiW602,]8-. 3, 1044 W6019 [W6019]'-. 3, 1033, 1035 [W,01913-. 3. 1051, 1052 W6PtH3OZ4 3, 1044 [PtW6H3024]5-. W,PtO, {PtW60,4]8-, 3, 1044 WfOZ4

3, 1033, 1034, 1044 1W/3024]6-.

[Nb,W4019]4-, 1, 162; 3.1047 W4Nb2ReC30,, [ReNb2W4019(C0)3]3-. I, 162; 3, 1047 W4Nb2RhCioHisOw [Rh(CSMeS)(Nb,W,019)]z~. 3. 1017 WJWR~~C~~H~OOI~ [{Rh(nbd)}s(Nb2W4C)19)213-,3, 1047 WAO.,.[W40,,]8-, I, 149; 3, 1033, 1034. 1258

-

w4019

[W40i9]2 , 3 , 1258 W's," [W~Sl0l2-,2,520

[WxVJ040P]7-,3. 1036, 1049 WSVjO4O [VsW8040]7-,3, 1041 W9AsO33 [ A S W ~ O ~ 3,1042 ~]~-, W9C03H90,0Si [W9Si{C~(OH2)}3037]1n-. 3, 1049 W9Nb3RhCSHl2O4,,Si [Rh(cod)(SiWgNb3O4,)l6-,3,1047 W9Nb3RhC10H15040Si [ Rh(CsMe,)(SIW9Nh30,0)]5-, 3, 1047 WO ,P , [W;034P]7--. 3,1039, 1049 W,O& [W,034Si]'L'-, 3, 1038, 1049

W9SbO3i [SbW,O3,j9-,

3,1042

w 9v 4 0 0 4

Cumulative Formula Index

[CeWl~036]8-,3, 1046 W oMo2040Si 3,1036 w10032

[W1,032l4-, 3,1033,1034,1258 [wln032]5-,3,1051 W10036P [W1003,P17-, 3, 1039 w10036si

[Wlo036Si]8-,3, 1038 wlov2o~op [WloV2040P]5-,3, 1036 WiiBC0Hz04o [ B W ~ ~ C O ( O H ~ ) O3,1048 ~~]~-, WllB039 [BW1103919-, 3,1048 W;,BOio [BW12040]5-. 3,1048 W,..,BeCoH2O4, [BeW IC6(OH2)03,]6-~,3,1037 [BeW-, Co (OHZ)O,,] 7--,3, 1037 W,_ ,BeMnH,Oao _ [BeW,lMn(OH,)0~,]7-, 3, 1048 W ,,CoFeH204, [ C Q W ~ ~ F ~ ( O H ~ ) O3,~1048 ,]~-, W11QH4O40 [W11(H~)CO( OH2)039] '-, 3. 1048 WiiC0zHz040 [ C O W ~ ~ C O ( O H ~ ) O3.1037 ~~]~-. WiiMnH~044P [PMnWl1039(OH2)]5-,4,47 WI 1M0040Si [ M O W ~ ~ O ~ ~3,S1038, ~ ] ~1041 -, WllNiHZ040Si [Wl,SiNi(OH2)039]6 , 3 , 1048 ~

w 11039p

[wl10,,P]7-, 3, 1030 Wl1O3& [W11039Si]8-,3, 1038 W Re04,P [RePWl1040]4 , 4 , 192 WllSiMo040 [ S ~ M O W ~ ~ O3,1036 ~]~-, WizA104o

[W,z(OMe)P039]Z-,2, 350 W12Q040 I , ]336; I C O W ~ ~ O ~, O ~ 3, 1037; 4,827 [ C O W ~ ? O ~ 1,336; ~ ] ~ - ,3,1042,1052 W12CU04rr

[CuW,,04,]"-, 3, 1042 [ C U W ~ , O ~ ~3,] 1050 ~-, W, .GeOln [GeWly040]4-, 3, 1038 WizH04o [W12(H)040]7-.3, 1033,1034 WIZH2040 [W12(HZ)040l6-. 3, 1033, 1034,1037. 1050, 1258;6,806 [ W I ~ ( H Z ) O ~ 3, ~ ]1052 ~-, W12H2042

W~OAS&OI~O [ K A s ~ W ~ ~3,~1042 ~ ~ ~ ] ~ ~ - . w48°1S4p8

[W4,5O184Paj4'-, 3,1039, 1040

628

XcF [XcF] ', 3,313.314 XeFz XeF,, 3,312,314,316 XeF,NNO,S, [Xe{N(SO,F),}]', 3, 319 XeF203S XeF(OS0,F). 3.320 XeF, [XeFql', 1,45: 3.312-311

X~F~NO,S,

XeF{N(SO,F),}. 3.319 XeF, XeF,, 1,53: 3,312.314.317 XcF4N208S4 Xe{N(S02F)2}1,3,319 XCF:,

[XeE5]+,1 , SO: 3.312.31s XeF, XeF,, 1,37; 3,312,315 XeF7 [XeF,]-, 3,312.315.316 XeF,

629

YC4H408 [Y(O,CH),]-, 3, 1076 YC8HB016 [Y(02CH),]5-, 3,1076 YCisH,iO6 Y(acac),, 2,373 YC1SHZ4N306S3 [Y(NCS),(18-crown-6)], 3, 1092 YC1BH4ZN3 Y(NPr*-J3. 3, 1072 YCzoH4F2408 [Y(hfacac),]-, 2,373,381; 3, 1081 YC20H16F1208

[Y(CF3COCHCOMe)41 . - ,2,381 YC3&Oh YrPhCOCHCOMeL. 2.373

Yb(l15-C~MeS)CI(MelPCH2PMe2). 2, 1041

Yb{ N(SiMe&}2(Me2PCH2PMe2), 2, 1041 YbCiaH4zN3 Yb(NPr',),. 3. 1072 YbC18H52N2P2Si4 Yb{N(SiMe3)2},(MezPCH,CH2PMez), 2, 184 YbC,,H,,NO, Yh(acac),(MeCOCH=C(NH,)Me}, 1,81; 2,723 YbC20H40N1S8 [Yb(SzCNEtz),]-. 3,1087 YbCziH~N3012 [Yb{2,6-(OzC)2~y},]~3 , 1090 YbCZ5H32N07

Yh(acac),(PhCOCH=CMeNH,).2,723 YbCz5H,,CIPz Yb(CsMes)2C1(R.lezPCH2PMeZ), 3, 1073 YbCzdLJ'z Yb(C5Mes),(Me,PCH,PMe2), 3,1073 YbC32H1,ClNa Yb(phthalocyanine)Cl, 2.861 YbC3;H5706 Yb(Bu'C0CHCOBu'L. ,". 3.. 1079 YbC3kH45N40 Yh(octaethyiporphyin)(OH), 2,822 YbC,,B,,,N,P,Si, Yb{N(SiMe,),),( PBu,),, 3, 1111 YbC72H60N3024P6 ~ b - 7

ry,1.13-.

3.1100

(Yb(H20)2(edta)]--,2,783 ~C12H24N2012 [Yb(N03)2(18-crown-6)]+,3,1094 YbC,,H,,NP2Si2

Yb{N(SiMe3)Z}(MeZPCHzCH2PMe,). 3. 1I 1 1 YbCI5HZ106 Yb(acac),, 2,373; 3, 1077 YbCisHn07 Yb(acac)3(H20), 1,81 Y~CI~HZ~C~PZ

Yb{N{OzP(OPh)z),},. 3, 1084 YbF4 [YbF4]-, 3,1099 YbH707 [Yb(OH),I4-, 3,1076 YbHis09 [Yb(H20)9]3', 3, 1074 YbNsOis [Yb(N0,)s]2-. 3, 1086 YbNaC,8H54N3Si6 NaYb{N(SiMe,),),, 3-I l l 1 YbNaCzoH5,NzO2Si, NaYh{N(SiMe,)2}l(~Et2)z, 3, 1111 YbZFe3~51H60011 {Yb(C,Mes),}zFer~CO)iz 3. 1112 Yb10izS3 Ybz(S0~)3,1,261

630

ZnAg,ScF, Ag,ScZnF,, 1, 1 1 1 ZnAIF, [ZnA1F,14-, 3,121 ZnAS4CizH3604 [Zn(OAsMe,)4]Z+,2,199 ZnAs4CZOH3~04 [Zn(diars dioxide),]*+.5 , 966 ZnB3HI2 [Zn(BH4)J, 5,931 ZnB4Hl, [Zn(BH,),I2-, 5, Y3l ZnBa,H,,O,,P, Ba2Zn(P309)2(H20)ln. 5,962 ZnBr, [ZnBrJ, 5,985 ZnBr, [ZnBr4I2-,5,929,983.98s ZnC2H302 [Zn(OAc)]+,5,683 ZnC2H30,P Zn(03PCH2CHO),5,963 ZnC,H,N,S, Zn(S2CNH2),, 6,532 ZnC2H6C102 [ZnCl(OMe),]-. 5.1305 ZnC2H60 ZnMe(OMe), 5,965 ZnC,H,O& Zn(O,SMe),, 5,961 ZnC2H7CI2NOP ZnCI,{OP(Mc)CH,NH,}. 5.966 ZnC2H8Br2O2 ZnBr,(MeOH),, 5,983 ZnC2H8CI,0, ZnC1,(MeOH)2, .~ 5 . 983 ZnCZN, ZdCNL. ,- 1.187 ZnCzb4 Zn(C,O,), 5,971.972 ZnC& [Zn(CS,),]z-, 5.977 ZnC3H204 Zn{(O2C),CH2). 5,972 ZnC,H,04 Zn(02CCH2C0,11).5, Y72 ZnC3H612NS2 [ZnI,(S,CNMe,)]-, 5,979 ZnC3H8CIN3S Zn(en)(NCS)Cl, 5,934 ZnC3HizN603Ss Zn(tu),(S,O,), 2, -131 ZnC4Hz05 Zn(O,CCOCH,CO,). 6. 455.456,473 ZnC4H,04S Zn{(O,CCH,),S), 5.977 ZnC,H,N,S, Zn(S,CNHCH,CH,NHCS,), 6 . 1026 ZnC4H604 Zn(OAc),, 2.437: 5.92A,969.99R ZnC4H7N203

[Zn(HLNCH2CONHC‘IIZC:o,)1+.2,7(91 2nC,H8K40, [ZII{(C‘C)NH~),)~]~+, 5,945 ZnC4H8N6S4 Zn{(H2N)ZCS},(NCS)Z,2,639 ZnC4Hlo ZnEt,. 2,215 ZnC,H, oCl,N20z ZnCI,(HCONHMe),, 2,492 ZnC4HLo08 Zn(O,CCH,OH)(H,O),, 2,472 ~nC4H,*O13 [Zn(C20,),(H,C))SI2-, 5, 971 ZnC,Hl lNIO,P, Zn(O,PCH,CH,NH,),, 5,963 ZnC4H,,N,O,S, Zn(S~NHCH2CH2fiHH)2(SZ03), 5,978 ZnCaH1~04 [Zn(OMe),I2 , 5,965 ZnC,H, qOd [Zn(O.Me),(MeOH)]-, 5,965 ZnC4H,,N202 [Zn(H2NCH2CH20H),]*+, 5,935 ZnC4HI6N4 [Zn(en),]*-. 5,929,932,935 LnC4HI6N5O2 Z ~ i ( e n ) ~ ( h C 5,934 )~), [Zn(en),(NO,)]*. 5,962

ZnC,K4 [Zn(CN),]*-, 1,538: 2,10. 12; 5,928- 930,6. 13. 822 ZnC,N,O, [Zn(CNO),]’-, 2, 13; 5,986 ZnC,Y,S, [Zn(CNS),12-. 1,548 [Zn(II;CS),]2-. 5,984,985 ZnC,O* [Zn(C204)2]2-.5,971 ZnC,H,ClS ZnC[(2-pyS), 5, Y74 ZnCSHaClZN, ZnCl,lpurinc), 5,957 ZnC,H,N, [Zn(adenine)l‘, 5, 956 ZnC5HI4N2 ZnH(MeNCH,CH2NMe2),5. Y34 ZnC,H, jC12N3 ZII{€~~N CH ~CH ~N H (CH~),”~}CI~, 2,50 ZnC5H20C105 [ZnCl(MeOH),]+, 5,983 ZflCsO5

Zn(CsOs), 2,455 ZnC6H4N,01 Zn(O,CCH,CN),, 5,971 ZnC6H,CI2N3 Zn(C6HjN3)CI2,5,950 ZnC,H +,O Zn(2-pyCH=NO), 6,472 ZnChH,NO, [zn{N(CH*C02)3}]-,2,789 ZnC6H,N, Z~(&CH=NCH=~H),.5,949

631

Crarnulutive Formula Index

ZnCbH6N,

znC&I\'6 [Zn(NCH)6]z+,5,932 ZnC6H,N& Zn(HNN=CHN=CH),(SCN),, 5,95 1 ZnC6H7CI,N5 ZnC1,19-methvladenine), 5 . 957

znc,w,,,o,

Zn(O,CCII(OtI)Me},, 5, 970,972 ZnC6HIiNLOh Zn{ HOCH2CH(NH2)C02},,2.745

632

[zn{r;r=CHNHCH=~CH,CFr(N~1COCH2CH2NH2)C02}]+. 2,760 ZnC&isN3S6 [Zn(S2CNMe2)3]-,5,979 ZnC9H2& [Zn(fiHCH2CH,NHCH2CH2NHCH2CH2NHCH2CH$H2)]'+. 2,912 ZnCloH2F1204 Zn(hfacac),, 5,967

,~

ZOCJIIZNZSA

Zn(S2CNMe2)z, 5,979; 6 , 1026 ZnC,H~,CINO ZnCI(OCHLCHlNEt2),5,965 ZnC6H14N306 Zn{H,N(CH2CONH)2CH,C02}(H20)2.2.763 ZnC,.H,,O, Zn(O;CCH20Me)2(0H2)2,5,705 Zn{S-O,CCH( OH)Me}{ R-O,CCH(OH)hle] (H,O),, 2,373 ZK6f[ I ~ C ~ ~ N I ZnCl,(TMEI)A), 5, 935 ZnC6HlRN4 [Zn((H,NCH,CH2NHCHz)L}]2' .5.937 ZnC6HizNZOn [Zn(H3rZCH2CHzCO?H)2(H,0)~]2+. 2.745 ZnC6kI,,N, [Zn(en),12-, 5,020,932 ZnC7KlIN ZnHEtpy, 2,216 ZnC7H18N,S [Zn(tren)(NCS)]+,2,235 Z~C~H~O, ZII(O,CCH=CHCO,H)~,5,072

NH2CH2C02}]+, 2,76U 7.nr,H,20,, Zn!~S)-0,CCH2CH(OH)C02}(H20~,. 2.476 z"cBH14N:406 Zn{L-HZNCOCH2CH(NH,)C02}2.2.745 ZnC,H,,CI,N2O2

ZnCs?i& [Zn(NHCHzCH2NHCH2CH,NHCF12C H ~ N H C H ~ H 2. ~ )912 ~~+.

ZnC9HI2N2S

[Zn{2-pyt(Me)NHCHlCH2S}]2+. 5 . 95 1 ZnC9HI3N208 [Zn{N(CH2C02)3)(H2NCH,C0,Me)]-. 6,418 ZnCdi3N403

' , 5.958 [Z~i(b~py)lz ZnCloHsN20?S2 Zn(2-S-py N-oxide)2. 6. 1026 ZnCloHBN2S2 Z n ( 2 - p ~ S )5.913 ~. ZnCloHloC12N2 Zn(py)zC12.5,929,952 Z~CIOHIOF~K~O~SZ Zn(py),(SO,F),. 5,964 ZnCloHIOIIN202 ZnI,(py A-oxide),. 2, -196; 5.965 Z n C J Il,& Zn(N,)zpy,, 2,235 ZnCioI I1,N,D, [Zn(edta)]*-,2.781; 5.996 ZnCI0H1,N2O8S2 Zn(3-pyS03)d0H5L 5,705 ZnCl0HI3N20~ [Zn(Hedta)]-, 2,784 ZnCIoHl,N,O ZnC1,(3-pyCONEt2). 5.952 ZnCloH14N404 Zn( OAc) ,(H&CH=NCH=C H),, 5,949 ZnCloH14NiO4 [Zn{&=CHh'HCH=CCH,CH(NHCOCH,NHCOCH,NH2)COz)J', 2,761 ZnC,,,IlI4O4 Zn(acac),, 2.372; 5,967 7,nCloH,,N204 Zn{0,CCH(NH,)CH,CHzC02H]2, 5,939 ZnCloH16N20it1S2 Zn(3-pyS03),(H,0),. 5.955 ZnCioH1604 [Zn(MeCOCH,COMe)2]2-, 2,402 ZnC10H18C12Ns04 5 Zn(H,NNH&NC( Me)=CHC( O)=~}2(H20)2CIz, 951 ZnCloH1805 [Zn(MeCOCH2COMe),(H,0)]z+, 2,402

ZnCloHZ4N4 [Zn(AHCH CH NHCH2CH2NHCH2CH2e H 2 ) ] Z + 2,912 , ZnC10H3812N@2 ZnI,(PriCOCH=CMeNHPri)2, 2,723 ZnCIIk2N204 Zn{HOCH2t=CHli=CMeC(0)=cCH2N= CMeCO,} . 1 .370 ZnCi,H,,N2Os [Zn(tmta)la-, 2,784 ZnCl ,HI5NO2S4 Zn(S,COEt)2(pq). 5.977 ZnCl 1 H i 5 N 2 0 ~ [Zn(Htmta)]-. 2,784 ZnCiiH1604P {Zn(PhMePO2)(dCH2CH2OCHZ~H2)},,, 5,959 Z~CIIH~~N,

633

Cumulative Formula Index

[Zn(f4HCH2CH2NHCH2CHCH,NHCHzCH2CHZNHCH~CHzEH2)]2i, 2,912 ZnC,,H,Cl,N, Zn(C6H4N3j2C12r 5,950 ZnC12HsN2 [Zn(phen)12+,5,958 ZnC&8N206 Zn(2-pyCO, N-oxideI2, 5.965 ZnCI2{(2-pyCH=N),), 5,953 ZnC12HloCI& ZnCl,(bcnzotriazole),. 2.78 ZnCl,Hl,,N40, (PY)~Z~(CNO),, 2,13 ZnC12Hlo02 Zn(OPh)z, 2,340 ZnG2HloOsS2 Zn(03SOPh)z,5,998 Zn(4-pyCOz N-oxide)2(H20)2.5. 965 ZnC12H14C12NZ Zn(PhNHz)zC12,5,933 ZnCIZH1406S2 Zn(02SPh)2(Hz0)z.5,964 Z~CIZHI~N~~S [Zn{ (OzCCH2)2NCITZCIT,N(Cl12CH2C02)2}]Z-, 2, 787 ZnClzHlhN8 [Zn(Hf4CH=NCH=GH),I2-, 5,948,949 ZnC12Hl6N8Os [Zn(teta)]'-, 2, 784 Z~CIZHI~NIOO~ Zn(H~CH=NCH=~H),(NO,),, 5,949 ZnC1~Hl7N2Os IZn(Hteta)l-, 2,784 ZrklzHlSN404 Zn(OZCEt),(H&CH=N CH=C H)z, 5,949 ZnClzHzsN,

ZnC ,7H,,N84S2

[Zn(Hdtpa)lZ-,2,788 ZnC14H20NZ0s [Zn{( 02CCHzCH2)2NCHzCHzN(CH,CH2COI)Z:12, 2.787 ZnC,,H,,N,O, [Zn(2~~yCH,CONH,)z(HzO)~]z+, 5, 954 ZnC,,H,,N& Zn( (S=CMeC:I I=CMcNCHICH,),}, 5,977 ZnC,,H,2Ni,04 Ln(OAc),(EtfiCH=NCH=&i),, 5,949 [Zn-(dl~en){(2-py),NH}]z', 5,955 ZnC14H?20ZSZ Zn(EtOC(Me)=CC(S)Me},, 5.968 ZnC1,H7?YV, ZnEtc-p;CHEtNBu'), 2,216 ZnEt,(2-pyCH=NBut), 2,216 ZnCllH24Nz06 Zn{ DL-0,CCH(NHAc)CHMez}2,5,939 ZnCl4H3& ZnEt(ErHu'NC:H=(:I

INRu'), 2, 215

ZnC14H32Y\1, [Zn{rC'(klc)CH2CH2N(Mc)CH2CH2CHzN(Mc)CH,CH,~'(M~)CH,CH,~H,} ]2+,2 . 9 I? ZnC 14H33h 8, [Zn(C201)(HN(CHzCHLCH2NHJ)z)2]2 ' .5.93h [Zn{H2N(CH2)3NH(CI12)3Nl Iz)2(Cz04)]2'. 2 , 4 7 ZnC15HIIF6N~OZ fZn(hfa~ac)(py)~]+, 5,967 ZnCl5Hl5Y5O3 Zn(py)3(N03)z,5, 929 ZfiCISHIBNS03 [Zn(AckY=CHCH=cH),1Zf, 5,951 ZnCI5H,O6 [Zn(acacH)3\zt,5,967

[Zn($lHCH2CH2CHZNHCH2CH2CH2NHCH,CH2CHzNHCH2CHTH2)]2I , 2.912 ZnClzHzsPzSa Zn(S2PPrz)z,5, 981) ZnC12H3012N4 Zn{N(CH2CH2NMe2)3}12. 5,938 ZnCl~H3zN40 [Zn{N(CHzCH2NMe2)3}(HzO)]2-, 5,937 Z~CI~H~ZN~O~ Zn(TMEDA)2(N02)2,5:962 ZnC12H34N6 2 ] 2 + , 2,47 [Zn{H2N(CH2)3NH(CH2)3VH2} ZnC12H3606S6 [Zn(DMSO),]*', 5.959. 966

, CH2NHz)CO2), 2,?60 Zn{h=CHNHCH= CHzCH(NH2)COh'HCH O ~2,760 )~, - ~ C-,ZnC16H24W4 [Zn(HSe=NCH=CHflMe)4]2+. 5,974 ZnC16HdzNz02 ZnI,(MeCOCH=CMeNHPr'),, 2,723 ~

ZnCI4HiZN2O4 Zn(4-OzCC6H4NH,),, 5.939 ZnCI4Hl4Cl2N, Zn(4-pyCH=CW2),CI,, 5,W3 ZnC14H140s Zn(2-OzCC,H40H),(H,O), - 2 . 4 8 1 ZnC14H~6CIZN402 Z ~ ( ~ - ~ ~ N H A C5.945 )~CI,, ZnC14HlsN30

Z~I{SP(S)(OBU),}~. 6, 1024 ZnC16H3h08P2 Zn{OP(0)(OBu)z}2,6, 1024 ZnCl7HI,YO4S2

Zn(O,SPh),(py), 5,964 ZnC,,H,,N,Si, -_ Zn{(NSiMe3-)2},(py),5,933 ZnCisHizNzOi Zn(S-quinolinolate),, 1,528,529.545: 5.953 ZnCIBHl5I3P [Zn13(PPh3)]-,5,579 ZnClBH16Br2N2O2 Zn(PhCOCHCH,NH),Br,, 5,951 ZnCi~Hi6N-t [Zn(8-arninoquinolinc),12+, 5,953 .I

I

Z.nC,hH,,N,OP [Zn{OP{CH,C=NC(Me)=CMeNH}

3)

I?+, 6,601

Zn { 2-(OCH2)C6H4C(Me)=NMe}2 , 5.942 ZnC20H24NsS4 [ZII(S=~N=CIICH=CII~~ 5.975

ZnC2,HI6F6O4S2 Zn(J-MeOC6H4C(s)=CHCOCF,}~.2.652 ZnC22Hl,N204S2 Zn(02SPh)2(bipy),5.964 ZnC22Hd2O4 Zn(acac),(phen), 5,967 ZnCZZHZ4N205 Cd(acac)2(phen)(H20),5,967

[Zn(phen)2(H20),]2+, 5.9% ZnC&I& [Zn(SPh),12-, I , 171: 2.526

ZnC2,1 124C12Ns Zn(2-ClC6H,NHNNMe)z(bipy), 5,948 ZnC24H28N408 5, 966 [Zn(2-pyCH20H~'V-oxide),]~-, ZnC24H72C12K12012P4 Zn(C104)2(HMPA),. 2, 500 ZnC24H72N1204P4 [Zn(HMPA)4]2C? I? 286 ZnC25H,oS5 (ZnMe),(SBu')S, 5. 973 ZflC26H1,F,O,& Zn{PhC(S)=CHC,OCF,},, 2.651 ZnCZhHI9N4O1 [Zn(phen),(OAc)J+,S.hh9,704,706 ZnC26H2sNzS4 Zn(5-BuS-8-quinoIinothiolate),, 5,973 ZnC2sHI406 Zn(anthraquinon-I-olate),, 6.86 ZnC3oH22OzS2 Zn{PhC(S)=CHCOPh},, 2,65 1 ZnC30Hz4N6 [Zn(bipy)#+, 5,958 ZnC3,,H2,C12N, Zn{(2-py),NH)3C129 5,955 %nC&HzaNzS? Zn{S2CN(CH2Ph)2)2. 6 . 58 ZGnH3oN,O, [Zn(py N-oxide),lz-, 5.704,965 ZnCxzHi 2NsO I S 4 [Zn{(03S)4phthalocyanine}]4 ,6,513 ZnC32H,,CINa Zn(chlorophthalocyanine), 2, 868 Z~C~ZHI~N~ Zn(phthalocyanine), 2- 861,863,868; 5,995; 6,511 [Zn(phthalocyanine)]"-. 2. 870 ZnC32H26N40JS2 Zn(02SPh)2(bipy),. 5 , 554 7.nC34H35N5 Zn(sapphyrin), 2,889 ZnCdhN4 Zn(tetr;ibenzoporpbyrin) 6 , 195 ZI~C~~H~~CI~OZP~ ZnCI,(OPPh3)2,5.966 ZnC3JL4N4 Zn(octacthylporphyrin), 2.842: 5,993 ZnC3&6C120P2 Z~CI,{P(C~H,I),}{OP(C,HI,)~}, 5,959 ZnC36Hm04 Zn { 02C(CH&,Me} 2I 5.998 ZnC3sHzd, Zn(phthalocyanine)(H,NC6tl, ]), 2,868

Zn(te;raphenylporphy.rin). 2,842; 5,995; 6,511,526, 528.617 ZnC44H3nN4 Zn(tetraphenplchlorin), 2 , 853 ZnC44H32N4 Zn(tetraphenylisobacteriochlorin),2, 853 ZnC44H32Ns012S4 [Zn{(4-0,SC,H4),porphyrin}j4-, 6 . 5 1 1 Z~C~~H~GNB [Zn{tetra(h'-methylpyridin~um)porphyrin)]~+. 6,511, 515,522.529 ZnC4,11,,€I, Zn(tctrnpyridylporphprin)(py), 2, 842,852 ZnC45H30CIN4 Zn(h'-methyltrtraphenylporphyrin)CI, 2, 849

ZnEt(N-methyltetraphenylporphyrin),2, 849

635

Cumulative Formula Index

ZnC48HJ'Js Zn(naphthalocyanine), 5 993 ZnC49H35N5 Zn(tetraphenylchlorin)(py), 2.852, 85.1

ZriC104S [ZnSO,CI]-, 5,964 ZnClzOs Zn(C104),, 5,961 ZnCI, [ZnCI,]-, 5,983,984.985 ZnCI4 [ZnC14]Z-,5,705,929,981.983,984,985,986; 6,851, 1024 C~{zn(NC$)~)(en),, 5,9SR ZnF, [ZnF,]-, 5,983 ZnF4 IZnF,12-, 5,986; 6.854 Z~HFOZnF(0HI. 5,928 ZnHzC14 ' ZnH2CI4,5,984 ZnH,CI,N [Zk$NH3)],, 1,126 ZnH3OSP Zn(O,POH)(OH,), 2.428 ZnHS? [Zn(fiS)3] ,6,853 ZnH,C104 Zn(O,C~j(OH,),, 2,126 ZnH4Mo06 Zn(O,MoO)(OH,)Z, 2.429 ZnH4N20, 5, 961 Zn(N03)2(HZ0)2. ZnH404 IZn(OH)41Z-.5.931. 960; 6,5, 12, 14 Zn'H404P2'.. Zn(02PH2),, 2,425 ZnH504 IZn(OH),(H,O)]-, 5.960 ZnHsOs 5S Zn(03S)(OH& S ? 2.428 ZnH,CIZNZ Z ~ ( N H , ) ~ C I5.932 ,. ZnH,N. ZniN3)2(NH,)2,2.235 ZnH604 Zn(OH),(H,O),, 5,960 ZnHaN4 [Zn(NH2)4]2-,5,932 ZnHsNlo Zn(N2H4)2(N3)2r 5.932 ZnH9CIN3 [Zn(NH3)3C1]+,5.932 ZnH9N303S, Zn(NH3)3(S20.7).5.977 ZnH12N4 IZn(NH,I,12'. 2,27,28; 5.930.932; 6 , 13

Zn2CJL

ZnHgC,,H,N,S, Zn(phen)Wg(SCN),, 5, 1064 ZnHgCasH16NsS4 Zn(phen),Hg(SCN),, 5, 1064 ZnHgK4H8N404 H ~ Z Z ~ ( C N ) ~ ( H5,961 ~O)~, &I4 [ZnI4I2-, 5,986 ZnKC2H7 KZnMe,H, 5,931 ZnK2H4 KJnH,, 5,931 Zn L1H3 LZnII,. 5,931 ZnLi,H, Li,ZnH,, 5. 931 ZnMgH4 MgZnH, ,5,93 1 ZnMoC, ,H,,CIO, M O C ~ ( C O ) , Z ~ C ~ ( O5,988 E~)~, Z~MO~CI~HIOO~ {MoCp(CO),),Zn, 5,988 ZnMo202S6 [Zn(MoOS,),12-, 2,575; 5,964 ZnMo,S, [Z~(MOS,),]~ ,2,570,571,575 ZnNjOIz [ZII(NO,),]~-,5,962 ZnN, Zn(N,)2, 5,932 ZnN12 [Zn(Nd412-, 5,932 ZnNbCISH,, NbH2(Cp),Zn(Cp), 3,639 ZnNiC&?& Zn(NH,),Ni(CN),, 5,932 Znh'iC404S4 ZnNi(S,C,O,),, 5,182 Z~NIC,,,H,,N,O,S~ NiZn(NCS),(THF),, 5,988 ZnNiC, ;H3,N30, YiZn { (PhCOCHCOCHCHMeNCH,),)(py) 5.968 ZnO&

Zrk'bH,-2160,, Zn{Pb(I03)6}(H20)6. 5,961 ZnRe2C38H16Ns06

(Re(CO),}2Zn(phthalocyanine), 2,868 ZnRe2C5,HzRN4O6 Zn(tctraphenylporphyrin){Re(CO),},, 2,844 ZnSI2 [ Z ~ ( % ) Z ] 2,542 ~-,

ZnTaCzuH21 TaH(Cp),Zn(Cp),, 3,639 ZnTi2CIOHZUCl4 (TiCp,CI),ZnCl,, 2,678 ZnTi2C26H32S6 ZI-I(SCH~CH~S)~(T 5,976 ~C~~)~, ZnWO, [ZnWO6I4-,5,704 ZnWSe, [Zn(WSe4)l2-.3,982 ZnW,O,S6 [Zn(WOS3),]2-, 2,575 ZnW& [Zn(WS4),]2-, 2,566,570,575 Z~ZBZVZCSZH~'~

V2Zn2H4(BH4)2(PMePhz)J.3r460

Zn2C2H6C140, [Zn2C14(0Me)2]2-, 5.965 ZniCsHzi

zn2ca21

Cumulative Formula Index

636

,.

Zn2(acac)(OzCCC13),,2,380 ZnZC12H26C14N2SZ {ZnCl2(S~HCH2CH2NHMeCH2~H2)},, 5,975 ZnZCl5H&IS, Zn,CI(2-pyS),, 5,974 Zn,C16H,2N806 [Zn2{&=CHNHCH=CCH2CH(NH2)COWHCHzCO,)z]'+, 2,760 Zn2C,,,IL,,N,Ol~ (Zn(py N-oxide),(O,NO)z},, 5,668,671 Zn,G,H,fF12 ZnZ(C6H4N3)4r 5,950 ZnZC24H50N4

Zn,Et,{Bu'N=CHCH(NBu')CH(NBu')CH=NBu')

2.202

480

,

2.215

ZrAs2C8H,,CI3F4 Z rC I3 { FZ ~ C (A ~ M e , )= C (A s ~ ~ e , )~3,366,370 F, } ,

ZrBr4{MeAs(CH,CH,CH,AsMe,),), 3,383 ZrAs4C20H32C14 ZrCl,(diars),, 3. 383 ZrBC9HloCI,N6 ZrCI, (HB ($iN=CHCH=cH) \ .3.38 I

ZrBCl,H,,CI,N,O

ZrC1,(OBu')(HB(~N=CMeCH=~Me)3}, 2,248: 38 1

ZTBC,,H~~N~O Zr{HB(&IV=CMeCH=f%e),} (OBu')Me2, 2,248 ZrBC23H39CIZN60 ZrCI,(OBu') {BuBfiN=CMeCH=cMe),}, 3,381 ZrB,C24HZ4CI,N,6 ZrCl,{B(flN=CHCH=~H),)2, 3,382 ZrB4C48H48N32 Zr { B(fiN=CHC,H=CH),},, 3,382 ZrBr, ZrBr,. 3.422 ZrBr6 [ZrBr6IZ-,3. 430.431 ZrCCI,NO ZrCI,(NCO), 3.379 ZrCCI,NSe ZrCl,(h'CSe). 3. 381 ZrCH4C14N,S ZrC14(H2NCSNH2),3.121 ZrCH,CI,N,O ZrCl4(H2NNHC0NH2),3,438 ZrCH5CI,N3S ZrCI,(H2NNHCSNH2).3,438 ZtC2CI3N2O2P ZrCl,{P(NCC))2).3.383 ZrC2CI3N2P ZrCI,((PCN),}. . . 3.383 ZrC2C:14N202 ZrCI4(NCO),, 3, 381 [ZrC14(NCO),]a-, 3.379

3.

637

Cumulative Formula Index

ZrC2C14N,Se ZrCI,{Se(CN),}, 3,381 ZrC,CI& ZrCI4(NCCI),, 3. 381 ZrC,F,d6 [Zr(C03)2F4]4-,3, 410 ZrC2H3CI5N [ZrCI,(MeCN)]-, 3.432 ZrC,H,O, [&(OH)3(C204)] , 3. 412 ZrC,H,O, Zr(02)(C204)(HzO)2, 3,388 ZrC,HSC1,O [ZrCi,(OEt)l2-, 3,392.131 ZrC2H6C1,0 ZrC1,(Me20), 3,401 ZrC2H6CI40, [ZrC14(OMe)z]2-,3,392 ZrC2H6C15N [ZrC15(NHEt)lZ-,3,372 ZrC2H,C1,N,O, ZrCI,(H,NCONH,),, 3.382 ZrC2H9CI3N2 Zr(NHMe)CI,, 2. 163 ZrC2Hl,,017S~ [ Zr(C,O4)(S~),),(H,o).]t -.3.408 ZrC,HO,, [ZrOH(C0,),]3-, 6,1013 ZrC3H2N3OLS3 [ZrO(NCS)3(H20)1-, 3,287 ZrC&C140 ZrCl,(Me,CO), 3.404 ZrC3H7CI30 ZrCI,(OPr'), 3, 391 ZrC3HI3Cl2N3 ZrCI,(NHMe),(NH,Me). 3,372 ZrC4CI4N4S2 ZrCI,{S(CN),},, 3,381 ZrC14F12012S4 Zr(03SCF3),, 3,418 ZrC4HbBr4NL ZrBr,(MeCN),, 3,382 ZrC4HACl4N2 ZrCI,(McCN),, 3,382 ZrC4H6F20&2 Zr(OAc),(S03F),, 3.408 ZTC&j05 ZrO(OAc),, 3,287 ZrC4H606 [ZrOz(OAc)Z]2~. 6 , 1013 ZrC411h07 Zr(OII)~(02C'CH=CHC0,1-1). 3,410 ZrC,HnCI,O, Zki(%cdEr), 3,404 ZrCI4( CH,CH,OCH, H2), 3 , 4U4 ~

Zr(SCH2CH2S),, 3,418 ZrC4HI2Cl2N2O2 ZrC12(0CH2CH2NH2)2. 3,437 ZrC4HIZCI2N4O5 ZrOC12(HCONH2)4,2.492: 3, 416 ZrC4HI2Cl4N4O4 ZrCl4(HCONH2),, 3,414 ZrC4Hl2Cl4O2 ZrCI,(Me,O),, 3,103 ZrC,HI,Cl4S~ ZrCI4(SMe2),,3,418 ZrC4H1204

Zr(OMe),, 3, 389

ZrGHllN505

ZrC4N404 Zr(OCN),, 3 179 ZrC,O, [ZrO(C204)2]2-. 3,412 ZrC4OI2 [Zr(CO,),]"-, 3,410 ZrC5H,Cl4NO2 ZrC14(NCCH2C02Et),3,405 ZrC5H,C1,02 ZrClJaLac), 3,392 ZrC5Hl,F4N,0 ZrF,{(Me,N):CO}, 3,382 ZrC';N, [Zr(CNj5]j-,364 ZrC6H4C14N4 ZrCI,(NCCH,CN),, 3,382 ZrC6H,CI30 ZrCI,(OPh). 3.392 ZrC6H,CI3h',O ZrCI3(4-pyCONNH2),3,437 ZrC6HH,0,, [ZrOH(OCH2C02)3]3-, 6,1013 ZrCbHxCI4N2 ZrCI,{NC(CH,),CN}, 3,382 ZrC611nCI,N,02 Zkl;(KCCHiCONH2)2, 3,416 ZrCBH,F09S Zr(OAc),(SO,F), 3,408 ZrC,H ,CI4N2 ZrCI,(Et2NCH2CN), 3,371,382 ZrC6H,zC1402 ZrCIJ(Me,CO)z. 3,404 ZrCaHIZCI40, ZrCI,(HCO,Et),, 3,404 ZrC,H,,O, ZrO(O,CEt),(H,O), 3,410 ZrC,H, ,Br4N,02 ZrRr,(DMF),, 3,416 ZrC6H,,C10, ZrOCl(OPr'),. 3, 391 ZrC,H,,CI,N,O, ZrOC12(DMF)2,2,492; 3,416 ZTC~H~JC~~O~ ZrC12(OPr')2.3,391 ZrC6Hd&,o Zr(NO,j,(DMF),, 3,374 ZrC6HljC14N ZrCI,(NEt,), 3,371 ZrC6H&I4N2 ZrCI,(TMEDA), 3,372 LrC6HI8Cl2N20Si2 ZrCI,{(NMeSiMe,),O), 3,378 ZI+C~H~~CI,N~ Z T C I ~ ( N M3, ~ ~371 )~, ZrC,,H&I4KzSi ZrCI,( (NMe,),SiMe,}, 3,372 ZrC6N606 [Zr(NC0)6]2-', 3,379 ZrC6N,S6 [Zr(NCS),12-. 3, 380 Z.rC6K6Se6 [Zr(YCSe),]'-, 3, 380 ZTC6012 lZr(C204)312-,3,411 ZrC60lh [WCO3MC2O4)I6-, 3,410 ZrC,H,CI,N ZrCI3(2,4-Me,py). 3,369 ZrC1,(3,S-Me2py), 3,369 ZrC,H,CI,N ZrC1,(Z16-Me,py). 3,372 ZrC7H,,N5O5 Zr(OH),{ ~ . ~ - P ~ ( C O N N H(H,O). , ) ~ ) 3,440

ZrC7HzoClzNzSiz

Cumulative Formula lndex

ZrC,H,,Cl,NZSi, ZrClz{(NMeSiMe,),CH,}. 3,378 ZrC7H21C12N3Si2 ZrCl,{(NMeSiMe,),NMe}l 3,378

Zr(O,CCl,),, 3, 410 ZrCBH8C1,N, ZrCl,(fi=CHCH=NCH=cH),. 3.373 ZrC8H*CI,S2 ZrCl,($CH=CHCH=CH),, 3.421 ZrCRHI,On Zi( OAc), ,3,409 ZrC,H,,CI,O, ZrCln(THF)2,3,403,404 ZrC,H~&O,ZTC~HI~C~~S~ ZrC14{wHz)4}z, 3,418

638

ZrCl,Hl,CI ZrClMe(n-Cp),. 2. 115 ZrClZHRCI2N2O2 ZrO(phen h:-ouide)Cl2.3,439 ZrCI2H8ClZO5Se2 Zr0(OZSeC6H4C1-4)2. 3.418 ZrCl2H8Cl4NZ ZrCl,(phen), 3,374 ZrCI2H8NzO9Sez ZrO(O,SeC,,H,NO,-3),, 3,387,418 ZrClzHg05 [Zr(0H)(1.2-O2ChH4)J, 3,403 ZrC1,HloC1202 ZiCI,(OPh),, 3. 392 ZI C12HlONZOZ ZrCp,(NC0)2. 2.228 ZrCl2Hl2CI2&O4 Zr(3-NCacac),Cl2.3, 400 ZrCl2HI2N8 Zr(fiCH=NCH=cH),. 3.377 ZrC12H16 ZrMe,(x-Cp),, 2. 115 Z~CI~H&ZN&

ZrF2{S2CN(CH2CH2)2NC(S)SH)2, 3,419

ZrCIZHZOQi Zr(02CEt)4.3,WY ZrClZH20012 Zr{OZCCH(OH)Me)4,3,413 ZrC8H2&1$4 ZrCL(MeSCH,CH,SMe),, 3.418 ZrCRH,,Cl,N,Si, Zk<{(NSikle,),SiMe,}, 3,378 ZrCBHZ4N4 Zr(NMe,),, 2,163,179; 3,375.376 ZrCBH24N1~ Zr(MeNNNMe),, 2,196 ZrC8016 [Zr(C2O4),l4 , I , 94; 3,411 ZrC,H7F4N0 ZrF,(&quinolinol), 3,438 ZrCPqC14N,0, ZrCl,(MeCOCN),, 3,405 ZrC,H,,CI03 ZrCl(OPr'),, 3,391 ZrC9019 [Zr(COB)(Cz04)4]6-,3,410 ZrCloH8C1,N,03 ZrOCl,(bipy N,N-dioxide), 3,287 ZrCloHsC14N2 ZrCl,(bipy), 3,374 Z~CJLOC~~NZ Z r C l d p h , 3,366 ZrCloH10C14NZ ZrCl4(pyIz,3,372 ZrCloHll [ZrHCpJ+, 2,703 ZrCIOHllCl~N~ [ZrCI,(MeCN)(pyrazine),]+. 3.374 ZrCloHI4C~~04 Zr(acac),Cl,, 3,400 ZGoH14NzOio Z r ( a c a ~ ) ~ ( N O2,372; ~ ) ~ , 3, 397,400,401 Z~CIOHI~C~~NZ ZrCl4{NC(CHz),CN},3,382 Z~C10H16NZ010 Zr(H,O),(edta), 2,783; 3.385:336.437 ZrC,oH.,aC1206 Zr{MeCH(O)COzEt},CI2, 3.414 ZrCloH20C14N4 ZrCI,(Et,NCN),, 3,382 ZGo020 [Zr(C204)516-.3,411 '

Zr(SOCNMe,),, 3,420 ZrClzHZ4N40s Zr(O,CNMe,),. 3.410 ZrC,;Hi804 Zr(OPr7,. 2. 347: 3. 38LL391.397.402 ZrC,;H,,ki,N~ ZrC1,{N(CHzCH2SMc2)3},3,372 ZrClZH300d [Zr(OEt),]"., 2 , 344 ~,

ZrC12H32C14P4 ZrC14(drnpe),,3. 383 ZrClZH&I2N,Si4 ZrC12{N(SiMe3)2}2. 3.377 ZTC~~H,~N,O~S~, Zr{ (MeNSiMez),O) 2 , 3,378 ZrC,,H,,N,Si, Zr(MeNSiMe,SiMe,NMe),, 3,378 ZTCi~H3604Si4 Zr(OSiMe,),. 3,391 ZrC12H3607SG [ZrO(DMSO)bj2+.3, 416 ZrCI3H9Cl4N ZrCI,(S ,h-benzoquinoline),3,372 ZrC13H3,,04 Zr(OMc)(OBu')3. 3.389 ZrC14H806 Zr(2-OC,H4C0,),, 3,413 ZrCIaHIoC120a Zr(2-OC6H4CHO)zC12, 3, 402 ZrC14H1~C1402 ZrC1,4(PhCH0)2. 3.404 ZrCl4HI4Cl2N4O2 ZrC12(PhCONNH,)2.3, 437 Z~CI~HI~FAOZ ZrF4(PhCOKHNH2),, 3,438 Z~C14H18N3010 [Zr{{(O2CCHJ2NCH2CH2),NCH,CO,}]-, 3.436 ZrC14Hl9N301I, Zr(Hdtpa), 2,788 ZrC14H23N3S6

ZrCp(SzCNMez)3.3.419 ZrC14Hz4N203S2

639

Cumulutive Fnrmiila Index

ZrO(NCS)2(Me2CHCH2COMej2.6 . 813 ZrC14H2805 Zr(acac)(OPr'),, 3, SUI ZrCI4H4,,N4Si4 Zr{(MeNSiMeZ),CH2},.3.378 ZrCl4H4,N6Si4 Zr{(MeNSiMe,),NMe),. 3.378 ZrC15HllF402 [Zr(PhCOCHCOPhjFJ. 3.392 ZrCl5Hl5CI3N3 ZrCMpy)3,3, 369 ZrCi5HI5Cl4N3 ZrC14(py),, 3,372 ZrC,,H ,,CIO, Zr(acac),CpCI, 2,383 Zr(acac),CI, 1, 82: 2.373.377,383; 3,399,400 ZrCi5HziIO6 ZrI(acac),, 2,375; 3. 397.. 399 z~c,,H,,NO, Zr(acac),(N03), 2,372; 3, 397.400 ZrClJL605 Zr(OPr'),(HOPr'), 2, 352 ZrC,6HRC14N4 ZrC1,(1,2-(NC)2~6H4j213. 382 ZrClnI-II ,Oh Zr{PhCH(0)CC)Z}2,3. 413 ZTC~~H~~C~~N~SZ ZrCI,(PhCH=NNHCSNH,). 3,437 ZrC16Hl,CI04 Zr(acac),CIPh, 3,401 ZrCl6HZ7NSiZ ZrCp,(CH2SiMe,N(SiMe3)}, 2, 184 ZrCi6HzsNs0& Zr(NCS)4(DMF)4,3, 380

ZrCi6H36N2014P?

Zr(NO,),{ OP(O)(OBu),) :. 6.944 ZrC,,H,,N8S4 Zr{NMeC(S)NMez}4. ~, 3.749

zrc1&3604

ZrfOBu'L. 2.339. 310.346

ZrC,,H,,CIO,

Zr{PhCH(O)COZMe),CI2,3,414 ZrCl8HZUCIINIO4 ZrCl,(MeCONHNHCOPh)2, 3.436 ZrClBH28OIo Zr(MeCOCHCO,Me),(OPr'), 3,402 ZrC,,H,,CI,NP,Si, ZrCI,j~(SilLle,dH,PPr',),}, 2. 1040 ZrC18H44N4 Z.r(N€t2),(NPri2),3, 375 Zi-C.~,BI~l,4C'1N3Si6 ZrC1{N(SiMe3),}3.3,377 ZrC, .H,,,O,

z;{P~CH(OH!CO,I,{PI,CH(O)CO~)(OP~'),

3.413 Z.rC,,H,F,,O, Z.r(hfacac),, 3,398 ZTC2&F1806 Zr(hfacac),Cp. 2. 383 ZrCZOH16Br3N4 ZrBr,(bipy),, 3, 366 ZrC2,HJ4N4 ZrF4(bipg),. 3.374 ZrC,oH16Fi20s Zr(CF,COCHCOMe),, 2,381; 3,398,399 ZrC24H16Y10S [ZrO(hipy N,,V-d-dio~ide)~]2 ' , 3, 287 ZrC,,HI6N,O8 Zr(OkClI=CHCI I=CHC:O),, 3. 418 ZrC,,H1 J,O, Zr(CF,COC,HCOMe),Cp, 2,384 ZrC,,H,,O,S, Zr(MeC(S)CHCOMe},, 3,439 ZrC*oHzsOs Zr(acac),. 1.32,94; 2,372,373,377.381 : 3.397. 398, 409; 6, 1013 ZrC20H40N404S4 Zr(SOCNEt2j4,3, 420 ZGoH40N4Ss Zr(S,CNEt,),. 3,419 Zr(S1CNhkPr)4, 3,419 Zrb'dOH4401 Zr(OCMe,Et),, 3 , 3x9 2.rCZOH4505 ( Z ~ ( O B U ' ) ~2,344; ]-, 3,392 ZrC20H48N4Si2 Zr{(NBuL),SiMe,},, 3, 378 ZrC20H,6C1,N2P4Si4 ZrC12{N(SiMe,CH2PMez)~}z, 3,383 ZrCZ,HIsS6 [Zr(l,2-S2C6H3Me-4)J-,3,421 ZrCZlHZ7Cl4N3O3 ZrC1,(2,6-Me2py N-oxide),, 3,414 ZrCZ2H60PZSil Zr(MeZPCHZC€-I,PMe,)(CH,SiMe,),, 2. 1040 Z r C , , ~l(lN403 ~ [ZrU(phcn N-uxide),]z+, 3,439 ZG,HI~N& Z r ( b i ~ y ) ~ ( N C s1,89; ) ~ , 2.228; 3 , 380 ZrC24H16N8Se4 Zr(YCSe),(bipy),. 3, 380 ZrC24H1604 Zr(2.2'-O2biphenyI),, 3,403 ZrC24HzoC1204P2 ZrC12{OP(0)Ph2}2,3,418 ZG,H*ON,O* Zr{OY(NO)Ph},, 2,512; 3,417 ZrC2,HZnO4 Zr(OPh),, 2, 340: 3, 392 ZrC,,H,,S4 Zr(SPh),, 3,418 ZrC24€T20Se4 Zr(SePh),. 3.421 ZrCz4H,,C10, Zr{ (?)-PhCH(OH)CO,},CI, 3,413

ZrC24H24Ns

zz14(dppej, 3,383 ZrC26H54C1Z02 ZrC12(OCBu'3)2,3,392 ZrC26HS4C1302 [Zr(OCBut3)2C11]-,2,339 Z~CZBH2008 Zr(tropolonate),, 3,402 Zr(2-OC6H4CHO),,3,402: 435 Zcz8&6N4Ss Z T ( S ~ C N P 3,419 ~~)~,

Cumulative Formula Index ZrC45H33C106 Zr(PhCOCHCOPh),CI, 3,400 ZrC4sH3306 [Zr(PhCOCHCOPh),]', 3,400 ZrC46H36N40s Zr { 3,4-(2-OC6H4CH=N)2C6H3c02Et}2 , 3,435 Z1'C46H5&404 Zr(octaethylporphyrin)(acac),, 3,440 ZrC4,HS6N4O3 Zr(octaethylporphyrin)(acac)(OPh), 3,440 ZrC48H4008P4 Zr{OP(O)Ph,},, 3,418 ZrG2H40N40~ Zr(ONPhCOPh),, 3,417 ZrCs4H42N404 Zr(tetraphenylporphyrin)(acac)2, 2,824 Z~CSSH~ON~O~ Zr(tetraphenylporphyrin)(acac)(OPh), 2,824 ZfC56H48N12 Zr(&NPhCH=CHflPh),, 3,378 ZrC60H4408 Zr(PhCOCHCOPh),, 3,397,398 ZrC66H7zNiz06 3,416 [Zr(antip~rine)~]~+, ZrC-nH6009S16 [Zr{(OSiPhz),O)J-, 3,418 ZrCd2F8 CdZZrFs,3,428 ZrC120 ZrOCl,, 2, 300; 3,384,386 ZrC13N, ZrCI,(N,), 3,379 ZrC1, ZrC14,3,371,422 ZrCl& [ZrC14(N3)2]2-, 3,379 ZrC140 [ZrOC1,I2-, 3,386 ZrC1401s Zr(CIO,),, 3,384,4U8 ZrC1, [ZrCIS1-,3,432

Zi(chlorophthalocyanine)C12,2,865; 3.440 ZrC32&012 Zr(3-MeO-2-OC6H,CHO),,3,402 Zr(2-OC6H4C02Me),,3,414 Zr{(+)-PhCH(OH)CO,},, 3,413 ZrOCl(02PCl,)(POC13),3,407 ZrC32H74N~O~~P4 Z r ( N 0 3 ) ~ ~ H O P ( O ~ ( O ~ u ) ~ } z ~ O P O6,944 ( O ~ ~ ~ ,ZrC170P ),, ZrC14(POC13), 3,414 ._ ZrC33H36N604 z~cI,o~P, [ZrO(antipyrine),12+,3,416 ZrCI3(O2PCl2)(POCl3), 3,407 ZrC36H21C1N804 ZrCllnOzPz Zr(chlorophthalocyanin)(OAc),. 3 440 ZrC14(PQCl&, 3,414 ZrC36%,N4O, Zr(8-quinolinolate),, 3,437 ZTC~IZHZ~N~O~S~ Zr(SOCNMe2),,3,420 ZrCd24N~ ZrCI1202S2 Zr(phen),, 3,366 {ZrC1,(SOC12))2,3,414 ZrC36%0N202 ZrCrF6 Zr(2-OC6H4CH=NEt),, 3,438 CrZrF,, 3,757 ZrC&4.&04 ZrCuF, Zr(NPhCONMe2)4,3,439 CuZrF,, 3,427 ZrCu2Fs CuzZrF8,3,428 ZrFzO Zr(acac)2(PhCOCHCOPh)2,3,398 ZrOF,, 3,287 ZrC40H50N404 ZrF,02 Zr(octaethylporphyrin)(OAc),, 2. 824; 3,439 Zr(O,)F,, 3,388 Ze42H63C103 ZrF,O,S, ZrCI(OC6H3ButZ-2,6)3,3,392 Z;O(Sb3F)z, 3,408 ZrC44H28C12N4 ZrLO Zr(tetraphenylporphyrin)CI,, 3,440 [ZrOF,]-, 3,287 ZrC44H32NloOSe4 ZrF4 Zr(NCSe),(phen),(THF), 3,380 ZrF4, 3,422 ZK44H760s Z~(BU'COCHCOBU')~, 3,398 ZrF4012S4

640

Cumulative Formula Index

641 Zr(S03F)4,3,408 ZrF, [ZrF,]-, 3,425427,429 [ZrF,lz-, 3,370,423

[ZrF,]'-, 3,423-429;6, 854,927 ZrF, [ZrF713-,3,423-427,429 Zrk, [ZrF8I4-,1,84,86; 3,423,424,426,428,429 ZrF12 .[ZrZFlZI4,3,427 ZrFeClzHllC14N ZrCI4{(NCCHZC5H,)FeCp}, 3,382 ZrHF,OZ [ZrF,(OOH)l2-, 3,388 ZrHF6Oz [ZrF6(OOH)]3-,3,388 ZrHN3010 Zr(OH)(NO,),, 6,943 ZrH2F40 ZrF4(Hz0),3,422 ZrH2N208 Zr(OH)2(N03)2,6,943 ZrHzO6S Zr(OH),(S04), 3,407 ZrH209S2 Zr(S04)dHd% 3,407 ZrH4F4Nz ZrF4(N2H4),3,374 ZrHSCi3Nz ZrC13(NHz)(NH,),3,371 ZrH6FaOs '

Zr,ClloO

Zr2CllOO

Cumulative Formula Index

642

{ Z ~ C ~ , ~ ~ - C I ) ( I L - C H , ) R ~ ( P P ~ ~4,414 )~}~(~-CI)~, Zr2Sn7C120H100 {Zr(SnPh,),),SnPh,. 3.370 Zr3CsH2008 Zr304(OEt)3,3,390 Zr3C30H3003

Zrab IZr2F1214-,3,424,427, 428. 430

Zr3(p-0)3Cp,.1. 111:3, 386 Zr3H404 [Zr3(OH)4]8-,6,812 Zr4F1003 Zr4F,003r3,287 Zr4 F 1,< [ Z T ~ F ,, ~ 3 ,]423. ~ 427 Zr4Fz1 [Zr4F2115-, 3,123.424.426 Zr4F2, [Zr4F2,l8--,3, 427 Zr4H3?Oz0 [Zr,(OH)8(HLO)1214+, 3,385 Z~~H~IIOU [Zr,(OH)8(Hz0),6]8+.3,384- 385; 6, 943 Zr,Cl,, Zr,CI,2, I , 27 Zr&, [Zr6F3,I7-.3.423.424.426. 1174 ZrhI ZrJ,,. I. 27. 171 Zr13C36H108044 Zrl3O8(OMe),,. 2. 350; 3.390