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1.

図書

図書
editor: H. Fischer ; authors: J.A. Howard
出版情報: Berlin ; Tokyo : Springer, c1997  xiii, 434 p. ; 28 cm
シリーズ名: Landolt-Börnstein Zahlenwerte und Funktionen aus Naturwissenschaften und Technik, Neue Serie / Gesamtherausgabe, K.-H. Hellwege ; New Series, Group 2 . Molecules and radicals ; v. 18 . Radical reaction rates in liquids ; subv. D2
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Introduction
Magnetic properties of nuclei
Spinning nuclei in magnetic field
Theory of nuclear resonance
Chemical shift; Coupling Constant
Organization of Data
Data for Boron-11 NMR
Data for Phosphorus-31 NMR
Introduction
Magnetic properties of nuclei
Spinning nuclei in magnetic field
2.

図書

図書
J.A. Howard, J.C. Scaiano ; Herausgeber, H. Fischer
出版情報: Berlin ; Tokyo : Springer, 1984  xi, 431 p. ; 28 cm
シリーズ名: Landolt-Börnstein Zahlenwerte und Funktionen aus Naturwissenschaften und Technik, Neue Serie / Gesamtherausgabe, K.-H. Hellwege ; Gruppe 2 . Atom- und Molekularphysik ; Bd. 13 . Kinetische Konstanten von Radikalreaktionen in Flüssigkeiten ; Teilband d
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Introductory material
General introduction / H. Fischer
Carbon-centered radicals / 4:
Rate constants of displacement reactions with molecules in solutions / M. Bonifacic ; K.-D. Asmus4.1:
Introduction / 4.1.0:
Absolute rate constants / 4.1.1:
Aliphatic radicals and radicals derived from other non-aromatic compounds / 4.1.1.1:
Aromatic radicals and radicals derived from compounds containing aromatic and heterocyclic constituents / 4.1.1.2:
Radicals with undefined stoichiometry and structure / 4.1.1.3:
Relative rate constants / 4.1.2:
Graphical data / 4.1.2.1:
Isotope effects / 4.1.3:
Rate constants of electron transfer reactions with molecules in solutions / 4.1.3.1:
Reactions in aqueous solutions / 4.2.0:
Reactions in nonaqueous solutions / 4.2.1.1:
Errata / 4.2.2.1:
Index of substances (See Vol.13E)
Introductory material
General introduction / H. Fischer
Carbon-centered radicals / 4:
3.

図書

図書
editor, H. Fischer ; authors, J.A. Howard ... [et al.]
出版情報: Berlin : Springer, c2004  xi, 535 p. ; 28 cm
シリーズ名: Landolt-Börnstein Zahlenwerte und Funktionen aus Naturwissenschaften und Technik, Neue Serie / Gesamtherausgabe, K.-H. Hellwege ; group 2 . Molecules and radicals ; v. 26 . Magnetic properties of free radicals ; subv. C
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Molecules and Radicals / Landolt-BörnsteinGroup II:
Magnetic Properties of Free Radicals / Volume 26:
Nitrogen and Oxygen Centered Radicals / Subvolume C:
Title Pages, Contributors, Preface, Table of Contents
Title Pages
Contributors
Preface
Table of Contents
General introduction / H. FischerI:
Definition and substances / A:
Magnetic properties / B:
Arrangements of the tables / C:
Monographs, reviews and important conference proceedings / D:
Data / II:
Nitrogen-centered monoradicals, biradicals and high-spin nitrenes / F.A. Neugebauer9:
Introduction / 9.1:
General remarks / 9.1.1:
Arrangement of tables / 9.1.2:
Abbreviations / 9.1.3:
Aminyl radicals of type R&sbond;N&sbond;R (R &dbond; H, C) / 9.2:
Acyclic aminyl radicals / 9.2.1:
Alkylaminyl radicals / 9.2.1.1:
Vinylaminyl radicals / 9.2.1.2:
Arylaminyls / 9.2.1.3:
Aminyl radicals with heterocyclic substituent / 9.2.1.4:
Cyano- and acylaminyl radicals / 9.2.1.5:
Cyclic aminyl radicals / 9.2.2:
Monocyclic aminyl radicals / 9.2.2.1:
Aminyl radicals from four-membered rings / 9.2.2.1.1:
Aminyl radicals from five-membered rings / 9.2.2.1.2:
Aminyl radicals from six-membered rings / 9.2.2.1.3:
Fused polycyclic aminyl radicals / 9.2.2.2:
Based on five-membered rings / 9.2.2.2.1:
Based on six-membered rings / 9.2.2.2.2:
Based on seven-membered rings / 9.2.2.2.3:
Germylaminyl radicals of type R&sbond;N&sbond;GeR3 / 9.3:
Hydrazyl and hydrazonyl radicals: R1&sbond;N&sbond;NR2R3, R1&sbond;N&sbond;N&dbond;CR2R3 / 9.4:
Acyclic hydrazyl radicals / 9.4.1:
Leading atom of R1, R2, and R3: Hydrogen or carbon / 9.4.1.1:
Alkylhydrazyl radicals / 9.4.1.1.1:
Arylhydrazyl radicals / 9.4.1.1.2:
Cyano- and acylhydrazyl radicals / 9.4.1.1.3:
Leading atom of R1 : Other than hydrogen or carbon / 9.4.1.2:
Leading atom of R2: Other than hydrogen or carbon / 9.4.1.3:
Leading atom of R1 and R2: Other than hydrogen or carbon / 9.4.1.4:
Cyclic hydrazyl radicals / 9.4.2:
Monocyclic hydrazyl radicals / 9.4.2.1:
Hydrazyl radicals from three-membered rings / 9.4.2.1.1:
Hydrazyl radicals from five-membered rings / 9.4.2.1.2:
Hydrazyl radicals from six-membered rings / 9.4.2.1.3:
Fused polycyclic hydrazyl radicals / 9.4.2.2:
Acyclic and cyclic hydrazonyl radicals / 9.4.3:
Acyclic hydrazonyl radicals / 9.4.3.1:
Cyclic hydrazonyl radicals / 9.4.3.2:
Oxyaminyl radicals: &sbond;N&sbond;O&sbond; / 9.5:
Acyclic oxyaminyl radicals: R1&sbond;N&sbond;O&sbond;R2 / 9.5.1:
Leading atom of R1 and R2: Carbon / 9.5.1.1:
Leading atom of R2: Other than carbon / 9.5.1.2:
Leading atom of R1: Other than carbon / 9.5.1.3:
Cyclic oxyaminyl radicals / 9.5.2:
Thioaminyl radicals: &sbond;N&sbond;S&sbond;, &sbond;N&sbond;S(&dbond;O)&sbond;, &sbond;N&sbond;SO2&sbond; / 9.6:
Acyclic thioaminyl radicals / 9.6.1:
Sulfenamidyl radicals: R1&sbond;N&sbond;S&sbond;R2 / 9.6.1.1:
Sulfinamidyl radicals: R1&sbond;N&sbond;S(&dbond;O)&sbond;R2 / 9.6.1.1.1:
Sulfonamidyl radicals: R1&sbond;N&sbond;SO2&sbond;R2 / 9.6.1.3:
Cyclic thioaminyl radicals / 9.6.2:
Monocyclic thioaminyl radicals / 9.6.2.1:
Thioaminyl radicals from five-membered rings / 9.6.2.1.1:
Thioaminyl radicals from six-membered rings / 9.6.2.1.2:
Thioaminyl radicals from eight-membered rings / 9.6.2.1.3:
Fused polycyclic thioaminyl radicals / 9.6.2.2:
Bridged thioaminyl radicals / 9.6.2.3:
Selenoaminyl radicals: &sbond;N&sbond;Se&sbond; / 9.7:
Iminyl radicals: >C&dbond;N / 9.8:
Iminyl radicals of type RCH&dbond;N / 9.8.1:
Iminyl radicals of type R1R2C&dbond;N / 9.8.2:
Diazenyl radicals: R&sbond;N•+&dbond;N / 9.9:
Iminoxyl radicals: >C&dbond;N&sbond;O / 9.10:
Acyclic iminoxyl radicals / 9.10.1:
Iminoxyl radicals of type RCH&dbond;N&sbond;O, leading atom of R: Carbon / 9.10.1.1:
Iminoxyl radicals of type R1R2C&dbond;N&sbond;O / 9.10.1.2:
Leading atom of R1 and R2: Other than carbon / 9.10.1.2.1:
Cyclic iminoxyl radicals / 9.10.2:
Monocyclic iminoxyl radicals / 9.10.2.1:
Fused polycyclic iminoxyl radicals / 9.10.2.2:
Bridged iminoxyl radicals / 9.10.2.3:
Nitrogen-centered biradicals / 9.11:
Aminyl biradicals / 9.11.1:
Hydrazyl biradicals / 9.11.2:
Acyclic hydrazyl biradicals / 9.11.2.1:
Cyclic hydrazyl biradicals / 9.11.2.2:
Thioaminyl biradicals / 9.11.3:
Acyclic thioaminyl biradicals / 9.11.3.1:
Cyclic thioaminyl biradicals / 9.11.3.2:
Cyclic selenoaminyl biradical / 9.11.4:
Biradicals with different kinds of radical centers / 9.11.5:
Type R1N.....CR2R3 / 9.11.5.1:
Type R1N.....N(O)R2 / 9.11.5.2:
Type R1N.....O / 9.11.5.3:
High-spin mono- and polynitrenes / 9.12:
Mononitrenes / 9.12.1:
Alkyl nitrenes / 9.12.1.1:
Cyano nitrene / 9.12.1.2:
Carbonyl nitrene / 9.12.1.3:
Aryl nitrenes / 9.12.1.4:
Heterocyclic nitrenes / 9.12.1.5:
Boryl nitrene / 9.12.1.6:
Phosphoryl nitrene / 9.12.1.7:
Sulfonyl nitrenes / 9.12.1.8:
Silyl nitrenes / 9.12.1.9:
Stannyl nitrene / 9.12.1.10:
Mononitrenes and additional radicals (S = 3/2, S = 2) / 9.12.2:
Nitrene and benzyl / 9.12.2.1:
Nitrene and aminyl / 9.12.2.2:
Nitrene and hydrazyl / 9.12.2.3:
Nitrene and nitroxyde / 9.12.2.4:
Nitrene, alkyl and aminyl / 9.12.2.5:
Nitrene and carbine / 9.12.2.6:
Quinonoidal dinitrenes (iminyl biradicals) / 9.12.3:
Dinitrenes (S = 2) / 9.12.4:
Arylene dinitrenes / 9.12.4.1:
Bis(arylnitrenes) linked by >C&dbond;CH2 or >C&dbond;O / 9.12.4.2:
Bis(arylnitrenes) linked by &sbond;HC&dbond;CH&sbond;, &sbond;[C&tbond;C]n&sbond;, &sbond;(1,3-C6H4)&sbond;,.or &sbond;C&tbond;C&sbond;(1,3-C6H4)&sbond;C&tbond;C&sbond; / 9.12.4.3:
Bis(arylnitrenes) linked by carbocyclic or heterocyclic bridges / 9.12.4.4:
Bis(arylnitrenes) linked by &sbond;CONH&sbond; / 9.12.4.5:
Bis(arylnitrenes) linked by hetero atoms: O, S, Si / 9.12.4.6:
Heterocyclic dinitrenes / 9.12.4.7:
Polynitrenes (S ≥ 3) / 9.12.5:
References for 9 / 9.13:
Review articles / 9.13.1:
References for 9.2-9.12 / 9.13.2:
Oxy- and peroxyalkyl radicals / J.A. Howard10:
Carbonyloxy radicals / 10.1:
Sulfinyl radicals / 10.3:
Alkylperoxy radicals / 10.4:
Alkenylperoxy radicals / 10.5:
Substituted alkylperoxy radicals / 10.6:
Aromatic peroxy radicals / 10.7:
Thiylperoxy radicals / 10.8:
Sulphonylperoxyl radicals / 10.9:
Peroxyl radicals from biological molecules / 10.10:
Polymer peroxyl radical / 10.11:
Metal centered peroxyl radical / 10.12:
References for 10 / 10.13:
Aroxyl radicals / R. Mecke ; H.H. Jäger ; M. Jäger11:
Arrangement of the tables / 11.1:
Carbocycles / 11.1.3:
Monocyclic compounds / 11.2.1:
Phenoxyls / 11.2.1.1:
Phenoxyl / 11.2.1.1.1:
Monosubstituted phenoxyls / 11.2.1.1.2:
Tyrosyl / 11.2.1.1.2.1:
Tyrosine derived radicals / 11.2.1.1.2.2:
Tyrosine radicals in biological systems / 11.2.1.1.2.3:
Disubstituted phenoxyls / 11.2.1.1.3:
Trisubstituted phenoxyls / 11.2.1.1.4:
2,3,4-trisubstituted phenoxyls / 11.2.1.1.4.1:
2,3,5-trisubstituted phenoxyls / 11.2.1.1.4.2:
2,3,6-trisubstituted phenoxyls / 11.2.1.1.4.3:
2,4,5-trisubstituted phenoxyls / 11.2.1.1.4.4:
2,4,6-trisubstituted phenoxyls (1/6) / 11.2.1.1.4.5:
2,4,6-trisubstituted phenoxyls (2/6)
2,4,6-trisubstituted phenoxyls (3/6)
2,4,6-trisubstituted phenoxyls (4/6)
2,4,6-trisubstituted phenoxyls (5/6)
2,4,6-trisubstituted phenoxyls (6/6)
3,4,5-trisubstituted phenoxyls / 11.2.1.1.4.6:
Tetrasubstituted phenoxyls / 11.2.1.1.5:
Pentasubstituted phenoxyls / 11.2.1.1.6:
Condensed ring systems / 11.2.2:
Systems with condensed non-aromatic rings / 11.2.2.1:
Naphthoxyls / 11.2.2.2:
Anthroxyls / 11.2.2.3:
Polycondensed systems / 11.2.2.4:
Heterocycles / 11.3:
N-heterocycles / 11.3.1:
O-heterocycles / 11.3.2:
5-membered heterocyclic systems / 11.3.2.1:
6-membered heterocyclic systems / 11.3.2.2:
Condensed dioxol systems / 11.3.2.3:
S-heterocycles / 11.3.3:
Cations / 11.4:
Bi- and polyradicals / 11.5:
References for 11 / 11.6:
General symbols and abbreviations / III:
Symbols
Substances or part of substances
Molecules and Radicals / Landolt-BörnsteinGroup II:
Magnetic Properties of Free Radicals / Volume 26:
Nitrogen and Oxygen Centered Radicals / Subvolume C:
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