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  • 1
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 2219-2230 
    ISSN: 1434-193X
    Schlagwort(e): Retrodisproportionation ; Arenes ; EPR spectroscopy ; Thermochemistry ; Coal liquefaction ; Catalysis ; Hydrogen transfer ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The transfer of hydrogen from excess 9,10-dihydroanthracene (DHA) to acceptors such as α-methylstyrene is catalyzed, i.e. occurs at temperatures in the range 200-260 °C instead of 280-320 °C, when hydrocarbons with weaker C-H bonds than DHA, e.g. 6H-benzo[cd]pyrene (4), 7H-dibenzo[a,kl]anthracene (5), 4-methyl-7H-benzo[de]naphthacene (6) or 8H-dibenzo[b,fg]pyrene (7), are added to the reaction mixture. The reactions are initiated by bimolecular H-atom transfer from 4-7 to the acceptor (retrodisproportionation) and proceed by nonchain radical mechanisms. This is supported by isotopic labelling and kinetic isotope effects, substituent and solvent effects, EPR spectroscopy of intermediate radicals, and by a comparison of the thermochemical and kinetic characteristics of these reactions.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 0570-0833
    Schlagwort(e): arenes ; coal liquefaction ; hydrogenations ; radical reactions ; reaction mechanisms ; Arenes ; Coal liquefaction ; Hydrogenation ; Radical reactions ; Reaction mechanisms ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Uncatalyzed transfer hydrogenations are H2-transfer reactions in which donors that contain weakly bound hydrogen atoms undergo an H-atom transfer (retrodisproportionation) onto an acceptor containing unsaturated bonds such as C=C, C=O, C=N, N=N, N=O. Transfer hydrogenolyses are reactions in which σ bonds are cleaved upon additon of H2. These hydrogenations are terminated by H, transfer; they do not follow a radical-chain mechanism. The initial steps of both types of reactions, H-atom transfer, complement the bimolecular formation of 1,4-diradicals from alkenes or heteroalkenes within the scope of bimolecular radical formation (Molecule-Induced Radical Formation, MIRF). The title reactions play an important role in coal liquefaction, aromatization reactions with nitroarenes or quinones, and possibly biochemical dehydrogenations. This review focuses on mechanistic studies, structure-reactivity relationships, and current applications of these reactions.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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