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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 108 (1986), S. 3762-3770 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 118 (1985), S. 1183-1192 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Sterically Hindered Free Radicals, XIII Wittig's Radical 4-Benzoyltriphenylmethyl and Analogous Mono-4-substituted Trityl RadicalsThe mono-4-R-triphenylmethyl radicals 1, 8b - f, R = tBu, CF3, COMe, COPh, CN, Me, or their quinonoid dimers 4, 9b - f are prepared, most of them for the first time. The degree of dissociation of the latter at 25°C is surprisingly high (≦ 33%, 0.01 M), donors and acceptors being effective here likewise. ESR data are given and discussed.
    Notes: Die mono-4-R-Triphenylmethyl-Radikale 1, 8b - f, R = tBu, CF3, COMe, COPh, CN, Me, bzw. deren chinoide Dimere 4, 9b - f werden dargestellt, überwiegend erstmalig. Die letzteren dissoziieren bei 25°C überraschend stark (≦ 33%, 0.01 M), wobei Donoren gleichsinnig wirken wie Akzeptoren. ESR-Daten werden angegeben und diskutiert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Sterically Hindered Free Radicals, XII. The Radical tert-Butyldiphenylmethyl, Its Dimer, and Their Autoxidation. A ReinvestigationThe radical Ph2C.  -  tBu (1) dimerizes giving reversibly the quinonoid derivative 3, and not the ethane-like 2 as reported in the literature. In equilibrium there are less radicals 1 than in the case of triphenylmethyl, ΔHdiss = 18.5 ± 2 kcal/mol for 3. Both the radical 1 and its dimer 3 are rapidly oxidized by oxygen. 1 gives the dialkyl peroxide 6 which fragmentates already at 20°C mainly to benzophenone and tBu., 3 leads to the ketone 7, probably via the hydroperoxide 10. 3 rearranges catalysed by acid and by base as well via a 1,5-hydrogen migration forming the benzenoid derivative 4. Preparative and ESR details are given.
    Notes: Das Radikal Ph2C.  -  tBu (1) dimerisiert reversibel zum chinoiden Derivat 3 und nicht zum ethan-artigen 2, wie in der Literature berichtet. Im Gleichgewicht liegt weniger Radikal 1 vor als im Fall von Triphenylmethyl, ΔHDiss = 18.5 ± 2 kcal/mol für 3. Sowohl das Radikal 1 wie sein Dimeres 3 werden durch Sauerstoff rasch oxidiert. 1 gibt das Dialkylperoxid 6, das schon bei 20°C fragmentiert, hauptsächlich zu Benzophenon und tBu., 3 führt zum Keton 7, wahrscheinlich über das Hydroperoxid 10. 3 lagert sich, sowohl säure- wie basenkatalysiert, unter 1,5-H-Verschiebung um in das benzoide Derivat 4. Einzelheiten zu den Darstellungen sowie zur ESR-Spektroskopie werden angegeben.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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