Landolt-Börnstein: Numerical Data and Functional Relationships in Science and Technology – New Series / Molecules and Radicals Part 1

R.F.C. Claridge, Robert D. Farley, Sylvain Marque, Christopher Charles Rowlands, Paul Tordo9783540432746, 3540432744

Volume II/26 supplements the previous compilations II/l, II/9 and II/17 of the magnetic properties of free radicals. Due to the still rapid growth of the field and the necessary inclusion of new subjects the volume is divided into subvolumes which will appear in fast succession. Together with the earlier publications volume II/26 offers an up-to-date and comprehensive survey and collection of structures and data on the important chemical intermediates, namely radicals, polyradicals and related species such as carbenes. As before the species have been grouped according to chemical aspects. For each group of substances the literature has been compiled and extracted by experts in the fields. For the reader’s convenience an index of substances follows in the last subvolume.

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Table of contents :
cover-large.JPG……Page 1
front-matter.pdf……Page 2
B Magnetic properties……Page 12
PREVIOUS DOCUMENT……Page 0
C Arrangements of the tables……Page 14
D Monographs, reviews and important conference proceedings……Page 16
A Symbols……Page 18
B Abbreviations……Page 19
C Substances or part of substances……Page 21
13.1.2 Formulae and structure……Page 23
13.1.4 Remarks……Page 24
13.2 Phosphinyl radicals X2P• and related species……Page 25
13.7.2 References for 13.2……Page 42
13.3 Phosphonyl (X2P•=O) and thiophosphonyl (X2P•=S) radicals……Page 43
13.7.2 References for 13.3……Page 53
13.4 Phosphoranyl radicals X4P•, including related species……Page 54
13.7.2 References for 13.4……Page 89
13.5 Phosphoniumyl cation radicals X3P•+, phosphine dimer cation radicals X3P•P+X3, phosphate anion radicals, and related species……Page 91
13.7.2 References for 13.5……Page 109
13.6 Miscellaneous……Page 110
13.7.2 References for 13.6……Page 136
14.1 Introduction……Page 137
14.2.1 Thiyl radicals of the type RS•, R-S•R, R-S•-R2……Page 138
14.10 References for 14.2.1……Page 142
14.2.2 Sulfinyl radicals of the type R-S•=O……Page 143
14.10 References for 14.2.2……Page 145
14.2.3 Sulfonyl radicals of the type RS•O2……Page 146
14.10 References for 14.2.3……Page 148
14.2.4 Sulfuranyl radicals of the type X-S•-R2, X2–S•-R, S•X3, S•X4……Page 149
14.10 References for 14.2.4……Page 150
14.10 References for 14.2.5……Page 151
14.2.6.1 Cation radicals of the type R2S•+, RPS•+ (incl. Se, Te)……Page 152
14.2.6.2 Cation radicals of the type RS-SR•+……Page 154
14.2.6.3 Cation radicals of the type R2S-O•+, R2S-O2•+, and R-S•+-N-R……Page 157
14.10 References for 14.2.6……Page 159
14.2.7.1 Anion radicals of the type R=S•–, RSH2•–, R3S•– (incl. Se, Te)……Page 160
14.2.7.2 Anion radicals of the type RS-SR•–……Page 169
14.2.7.3 Anion radicals of the type RS-X•–, RS-O•–, RS-O2•– (incl. Se, Te)……Page 174
14.10 References for 14.2.7……Page 175
14.3.1 Silyl radicals X3Si•……Page 176
14.10 References for 14.3.1……Page 189
14.3.2 Silyl radicals from polysilanes……Page 190
14.10 References for 14.3.2……Page 192
14.3.3 Silicon-centered anion radicals……Page 193
14.10 References for 14.3.3……Page 194
14.10 References for 14.3.4……Page 195
14.3.5 Silicon-centered cation radicals……Page 196
14.10 References for 14.3.5……Page 206
14.4.1 Germyl radicals X3Ge•……Page 207
14.10 References for 14.4.1……Page 209
14.10 References for 14.4.2……Page 210
14.10 References for 14.4.3……Page 211
14.5.1 Stannyl radicals X3Sn•……Page 212
14.10 References for 14.5.1……Page 213
14.5.2 Tin-centered anion radicals……Page 214
14.10 References for 14.5.2……Page 215
14.5.3 Tin-centered cation radicals……Page 216
14.10 References for 14.5.3……Page 217
14.6.1 Boryl radicals X3B•……Page 218
14.10 References for 14.6.1……Page 223
14.10 References for 14.6.2……Page 224
14.10 References for 14.6.3……Page 225
14.7.1 Aluminum-centered neutral radicals……Page 226
14.10 References for 14.7.1……Page 234
14.10 References for 14.7.2……Page 235
14.10 References for 14.8.1……Page 236
14.8.2 Gallium-centered radical anions……Page 237
14.10 References for 14.8.2……Page 238
14.9.1 Cation radicals……Page 239
14.10 References for 14.9……Page 243
15.1.1 General remarks……Page 244
15.1.4 Reviews and books……Page 245
15.2.1 Hydrocarbon radical anions……Page 246
15.8 References for 15.2.1……Page 292
15.2.2.1 Substituted radical anions……Page 293
15.2.2.2 Perfluoro and perchloro substituted radical anions……Page 308
15.2.2.3 Substituted fluorenones……Page 310
15.8 References for 15.2.2……Page 318
15.3.1.1.1 Arylfurans……Page 319
15.3.1.1.2 Nitrofurans……Page 320
15.3.1.1.3 Arylbenzylfurans……Page 322
15.3.1.2 Bromonitrodioxanes……Page 323
15.3.1.3 Oxoporphycenes……Page 325
15.8 References for 15.3.1……Page 326
15.3.2.1 Halegenoimidazoles……Page 327
15.3.2.2 Pyrazines and pyrazinophanes……Page 328
15.3.2.3 Phenanthroline and phenanthroline based platinum complexes……Page 330
15.3.2.4.1 Bipyridyls……Page 331
15.3.2.4.2 Dipyridylacetylenes……Page 332
15.3.2.5 Porphycenes……Page 333
15.3.2.6 Pyrimidines……Page 337
15.3.2.8 Boron substituted nitrogen containing heterocycles……Page 338
15.3.2.9 Indolines……Page 344
15.8 References for 15.3.2……Page 347
15.3.3.1 Thiophenes and polythiophenes……Page 348
15.3.3.2      Dicyanomethylidenethiopyrans……Page 349
15.3.3.3 Weitz type S-donors……Page 351
15.8 References for 15.3.3……Page 353
15.3.4 Phosphorus containing heterocycles……Page 354
15.8 References for 15.3.4……Page 355
15.8 References for 15.3.5……Page 356
15.8 References for 15.3.6……Page 357
15.4 Anion radicals from nitro compounds……Page 358
15.8 References for 15.4……Page 374
15.5.1.1 Arylesters……Page 375
15.5.1.2 Thioesters……Page 385
15.5.1.3 Oxocarbothioate and dithioate esters……Page 387
15.8 References for 15.5.1……Page 392
15.5.2.1 Aliphatic aldehydes and ketones……Page 393
15.5.2.2 Furyl and thienyl aldehydes and ketones……Page 396
15.5.2.3 Tropones……Page 408
15.5.2.4 Benzene dicarbaldehydes……Page 409
15.5.2.5 Thiopyrane-2-thiones……Page 410
15.5.2.6 Silanones……Page 411
15.8 References for 15.5.2……Page 414
15.5.3.1 Ethanediones……Page 415
15.5.3.2 Cyclobutanediones……Page 416
15.5.3.3 But-2-ene-1,4-diones……Page 418
15.5.3.4 Thiadiazoloquinoxalinediones……Page 420
15.5.3.5 Hypericin……Page 422
15.5.3.7 Diones derived from carbohydrates……Page 423
15.8 References for 15.5.3……Page 425
15.8 References for 15.5.4……Page 426
15.6.1.1 Open chain azoalkenes……Page 427
15.6.1.2 Cyclic azoalkenes……Page 429
15.6.1.3 Azopolycycloalkenes……Page 439
15.8 References for 15.6.1……Page 440
15.6.2.1 Benzo[c]cinnolines……Page 441
15.6.2.2 Azobenzene derivatives……Page 443
15.8 References for 15.6.2……Page 444
15.6.3 Arylazophosphonates……Page 445
15.8 References for 15.6.3……Page 446
15.6.4 Bidiazines……Page 447
15.8 References for 15.6.4……Page 450
15.6.5 Tetrazines……Page 451
15.8 References for 15.6.5……Page 452
15.7.1.1 Diphenylsulphides and sulphones……Page 453
15.7.1.2 Aliphatic disulphides……Page 454
15.8 References for 15.7.1……Page 456
15.7.2.1 Imines……Page 457
15.7.2.2 Imides……Page 464
15.8 References for 15.7.2……Page 465
15.7.3 Fullerenes……Page 466
15.8 References for 15.7.3……Page 468
15.7.4 Tetracyanoquinodimethanes……Page 469
15.8 References for 15.7.4……Page 470
15.8 References for 15.7.5……Page 471
15.7.6 Phosphaalkenes……Page 472
15.8 References for 15.7.6……Page 475
15.8 References for 15.7.7……Page 476