Phosphorus-Centered Radicals, Radicals Centered on Other Heteroatoms, Organic Radical Ions: Landolt-Börnstein: Numerical Data and Functional Relationships in Science and Technology - New Series, cartea 26E2
Autor Alwyn G. Daviesen Limba Engleză Hardback – 23 mar 2009
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Specificații
ISBN-13: 9783540876397
ISBN-10: 3540876391
Pagini: 445
Ilustrații: IX, 445 p.
Dimensiuni: 193 x 270 mm
Ediția:2009
Editura: Springer Berlin, Heidelberg
Colecția Springer
Seriile Landolt-Börnstein: Numerical Data and Functional Relationships in Science and Technology - New Series, Molecules and Radicals
Locul publicării:Berlin, Heidelberg, Germany
ISBN-10: 3540876391
Pagini: 445
Ilustrații: IX, 445 p.
Dimensiuni: 193 x 270 mm
Ediția:2009
Editura: Springer Berlin, Heidelberg
Colecția Springer
Seriile Landolt-Börnstein: Numerical Data and Functional Relationships in Science and Technology - New Series, Molecules and Radicals
Locul publicării:Berlin, Heidelberg, Germany
Public țintă
ResearchCuprins
I General introduction.- III General symbols and abbreviations.- 16.1 Introduction.- 16.2.1.1 Monosubstituted 1,2-benzosemiquinones.- 16.2.1.2 3,4-Disubstituted 1,2-benzosemiquinones.- 16.2.1.3 3,5-Disubstituted 1,2-benzosemiquinones.- 16.2.1.4 3,6-Disubstituted 1,2-benzosemiquinones.- 16.2.1.5 4,5-Disubstituted 1,2-benzosemiquinones.- 16.2.1.6 Trisubstituted 1,2-benzosemiquinones.- 16.2.1.7 Tetrasubstituted 1,2-benzosemiquinones.- 16.2.1.8 Imino-1,2-benzosemiquinones.- 16.2.2.1 Unsubstituted 1,4-benzosemiquinones.- 16.2.2.2 Monosubstituted 1,4-benzosemiquinones.- 16.2.2.3 Disubstituted 1,4-benzosemiquinones.- 16.2.2.4 Trisubstituted 1,4-benzosemiquinones.- 16.2.2.5 Tetrasubstituted 1,4-benzosemiquinones.- 16.3 1,4-Naphthosemiquinones.- 16.4 9,10-Phenanthrosemiquinones.- 16.5 9,10-Anthrosemiquinones.- 16.6 Other semiquinones.- 17.1 Introduction.- 17.2 Radical cations of alkanes.- 17.3.1 Radical cations of cyclohexanes.- 17.3.2 Radical cations of other cycloalkanes.- 17.4.1 Radical cations of acyclic monoenes.- 17.4.2 Radical cations of acyclic di- and higher-enes.- 17.4.3 Radical cations of cyclic monoenes.- 17.4.4 Radical cations of cyclic di- and higher-enes.- 17.5 Radical cations of alkynes.- 17.6.1 Benzene hydrocarbons.- 17.6.2 Radical cations of bi-, tri-, and tetra-phenylenes.- 17.6.3 Radical cations of biphenyls and higher biaryls.- 17.6.4 Radical cations of azulenes.- 17.6.5 Radical cations of polycyclic aromatic hydrocarbons.- 17.7 Radical cations of cyclophanes.- 17.8.1 Radical cations of aliphatic alcohols and ethers.- 17.8.2 Radical cations of furans.- 17.8.3 Radical cations of carbonyl compounds.- 17.8.4 Radical cations of phenols and aromatic ethers.- 17.9.1 Radical cations of aliphatic amines and derivatives.- 17.9.2 Radical cations of imines.- 17.9.3 Radical cations of diazo compounds.- 17.9.4 Radical cations of azo compounds.- 17.9.5 Radical cations of hydrazines.- 17.9.6 Radical cations of aromatic amines.- 17.9.7 Radical cations of nitroso and related compounds.- 17.9.8 Radical cations of pyrroles.- 17.9.9 Heteroaromatic compounds containing 1 or 2 nitrogen atoms.- 17.9.10 Heteroaromatic compounds containing 3 or 4 nitrogen atoms.- 17.9.11 Radical cations of heteroaromatic compounds containing both nitrogen and sulphur.- 17.10.1 Radical cation of sulfides.- 17.10.2 Radical cations of thiophenes.- 17.10.3 Radical cations of thiofulvalenes.- 17.10.4 Radical cations of aromatic and heterocyclic sulphur compounds.- 17.10.5 Radical cations of other compounds of sulfur, selenium, and tellurium.- 17.11.1 Radical cations of alkyl halides.- 17.11.2 Radical cations of aryl fluorides.- 17.12 Radical cations of compounds of phosphorus.- 17.13.1 Radical cations of organosilanes.- 17.13.2 Radical cations of organomercury compounds.- 17.13.3 Radical cations of other organometallic compounds.
Caracteristici
Includes supplementary material: sn.pub/extras