Organische Kation-Radikale und Polyradikale ; Substanzenverzeichnis für die Bände II/1 und II/9 = Organic cation radicals and polyradicals ; Index of substances for volumes II/1 and II/9
معرفی کتاب «Organische Kation-Radikale und Polyradikale ; Substanzenverzeichnis für die Bände II/1 und II/9 = Organic cation radicals and polyradicals ; Index of substances for volumes II/1 and II/9» نوشتهٔ H. Fischer (auth.), H. Fischer, K.-H. Hellwege (eds.)، منتشرشده توسط نشر Springer-Verlag Berlin Heidelberg در سال 1980. این کتاب در فرمت pdf، زبان انگلیسی ارائه شده است.
empirical parameters, PN nuclear magneton see vol. II/9 a, section 1.1.4 g g-tensor a, b, c, d [MHz] magnetic hyperfine coupling gis isotropic part of g (g-factor) constants in Mega-Hertz gNA nuclear g-factor of nucleus 1 see vol. II/9 a, section 1.1.4 2 spin-Hamilton operator ais CmTl isotropic part of a in milli-Tesla external magnetic field vector a, CmTl hyperfine coupling tensor of :o i nuclear spin operator of nucleus A nucleus I in milli-Tesla effective electron spin operator &I Bohr magneton TCKI temperature in Kelvin Fischer The aromatic hydrocarbon cations to which EPR and ENDOR have been applied during the period from 1963 to 1976 are divided into the following groups: Cation radicals from benzene and its alkyl derivatives (l&1.1), from polyphenyl and its alkyl derivatives (18.1.2), from naphthalene and its alkyl derivatives (18.1.3) from anthraceneand its alkyl derivatives (18.1.4) from further condensed aromatics and their derivatives (18.1.5), from non-alternant hydrocarbons and miscellaneous compounds (18.1.6) from halogen derivatives of polyphenyls (18.2.1) and from halogen derivatives of naphthalenes (18.2.2). In each subdivision, the derivatives are ordered according to increasing order of alkyl groups or number of alkyl carbon atoms. In the case of polynuclear condensed aromatic hydrocarbons the compounds are listed according to increasing number of C-atoms of the gross formula, when equal numbers of benzene nuclei are involved. Data of dimer cation radicals follow directly the respective monomer cations. Cyclophanes, related ring compounds and tetraphenylet'hylene are regarded as derivatives of corresponding simpler bridged hydrocarbons. Some publications from 1977 are also cited. General introduction....Pages 1-4 18.0 Introduction....Pages 5-5 18.1 Cation radicals from aromatic hydrocarbon compounds and their alkyl derivatives....Pages 6-19 18.2 Cation radicals from halogenated aromatic hydrocarbons....Pages 19-20 18.3 References for 18.1 and 18.2....Pages 21-21 19.0 Introduction....Pages 22-24 19.1 Alkyl and H-substituted amines....Pages 25-28 19.2.1 Monoaryl amines....Pages 28-39 19.2.2 Diaryl amines....Pages 40-47 19.2.3 Triaryl amines....Pages 47-52 19.2.4 Phenylene diamines....Pages 52-59 19.3.1 Aminoolefines and -diimides....Pages 60-67 Part 1....Pages 68-78 Part 2....Pages 79-88 19.3.3 Other hydrazaaromatics....Pages 89-93 19.4.1 Alkyl and H-substituted hydrazines....Pages 93-105 19.4.2 Aryl hydrazines....Pages 105-115 19.5 [N-O] compounds....Pages 116-118 19.6 Miscellaneous/uncertain structure....Pages 119-119 19.7 References for 19....Pages 120-123 20.0 Introduction....Pages 124-124 20.1.1 (OH)n-compounds and their alkyl derivatives....Pages 125-128 20.1.2 (OH)n(OR)m-compounds and their alkyl derivatives....Pages 128-128 20.1.3 (OR)n-compounds....Pages 129-137 20.1.4 Diphenyl ether....Pages 137-137 20.1.5 Diphenyl sulfide with O-containing substituents....Pages 138-139 20.1.7 (SR)n-compounds and alkyl-substituted diphenyl sulfide....Pages 140-141 20.2 Heterocyclic compounds containing O and/or S atoms as ring members....Pages 142-146 20.3 References for 20.1 and 20.2....Pages 147-147 21.0 Introduction....Pages 148-150 21.1 Carbon-centered polyradicals....Pages 151-160 21.2 Oxygen-centered polyradicals....Pages 160-171 21.3.1 Hydrazyl biradicals....Pages 172-177 21.3.2 Verdazyl biradicals....Pages 177-185 21.3.3 Tetrazodinyl biradicals....Pages 185-185 21.3.4 Triradicals....Pages 186-187 21.3.5 Tetraradicals....Pages 187-187 21.4 References for 21.1 - 21.3....Pages 188-189 22.0 Introduction....Pages 190-190 22.1.1 Bis(dialkyl nitroxides)....Pages 191-191 22.1.3 Bicyclic bis(dialkyl nitroxides)....Pages 192-192 22.1.4.2 Bis(pyrrolidinyl-1-oxyls)....Pages 193-202 22.1.4.3 Bis(pyrrol-inyl-1-oxyls)....Pages 202-212 22.1.4.5 Bis(imidazolinyl-1-oxyl-3-oxides)....Pages 212-213 22.1.4.6 Bis(oxazolidinyl-1-oxyls)....Pages 213-220 22.1.4.7 (Pyrrolinyl-1-oxyl)-(piperidinyl-1-oxyl)....Pages 220-222 22.1.4.8 (Imidazolinyl-1-oxyl)-(piperidinyl-1-oxyl)....Pages 222-223 22.1.4.9 (Oxazolidinyl-1-oxyl)-(piperidinyl-1-oxyl)....Pages 223-225 22.1.4.10 (Pyrrolinyl-1-oxyl)-(diazacycloheptyl-1-oxyl)....Pages 226-226 22.1.4.11.2 X = 1 atom....Pages 227-229 22.1.4.11.3 X = 2 atoms....Pages 229-231 22.1.4.11.4 X = 3 atoms....Pages 232-245 22.1.4.11.5 X = 4 atoms....Pages 246-248 22.1.4.11.6 X = 5 atoms....Pages 249-250 22.1.4.11.7 X = 6 atoms....Pages 250-254 22.1.4.11.8 X = 7 atoms....Pages 255-260 22.1.4.11.9 X = 8 atoms....Pages 260-263 22.1.4.11.10 X = 9 atoms....Pages 264-267 22.1.4.11.11 X = 10 atoms....Pages 268-270 22.1.4.11.12 X = 11 atoms....Pages 271-273 22.1.4.11.13 X = 12 atoms....Pages 274-277 22.1.4.11.14 X = 13 atoms....Pages 277-277 22.1.4.11.15 X = 14 atoms....Pages 278-278 22.1.4.11.17 X = 16 atoms....Pages 279-279 22.1.4.11.19 X = 18 atoms....Pages 280-281 22.1.4.11.20 X > 20 atoms....Pages 282-284 22.1.5 Bis(alkyl aryl nitroxides)....Pages 284-286 22.1.6 Bis(imidazolinyl-1-oxyls)....Pages 287-289 22.1.7 (Imidazolinyl-oxyl)-(imidazolinyl-oxyl-oxides)....Pages 289-290 22.1.8 Bis(imidazolinyl-oxyl-oxides)....Pages 291-293 22.1.9 Bis(acyl nitroxides)....Pages 308-308 22.2 Trisnitroxides....Pages 293-298 22.3 Tetrakisnitroxides....Pages 299-303 22.4 Pentakis(piperidinyl-1-oxyls)....Pages 303-304 22.5 Hexakis(piperidinyl-1-oxyls)....Pages 305-307 22.6 Phenoxyl nitroxide....Pages 308-308 22.7 References for 22.1 - 22.6....Pages 309-312 Introduction....Pages 313-316 Ag - C6....Pages 317-329 C7 - C11....Pages 329-341 C12 - C18....Pages 341-355 C19 - Zn....Pages 355-368 Radicals derived from high polymers and biological compounds....Pages 369-369
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