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    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 327 (1985), S. 399-410 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photoinduced Electron Transfer between Arenediazonium Cations and AnionsAnions X⊖ can act as donors in electron transfer reactions to photoexcited arenediazonium ions. The yield of the arene formed in this reaction increases with decreasing electrochemical oxidation potential EoxD of X⊖ (X⊖ = BPh4⊖, Br⊖, HOOC—COO⊖, Cl⊖, BF4⊖). The oxidized donor X· (Cl·, ·COO⊖) and aryl radicals Ar· benig intermediates of the reductive dediazoniation of ArN2⊖ can be detected by spin trapping with nitrosodurene (ND) and phenyl-tert-butylnitrone (PBN). A solvent effect in the electron transfer reaction is interpreted in terms of ion pairing, where the electron transfer is favored by preorientation and a short distance between the electron donor and the acceptor previous to excitation of ArN2⊖ by light.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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