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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 63 (1980), S. 456-466 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Study of the Photochemical Behaviour of Some Diaryl-1,3-triazenesThe photolysis of Diaryl-1,3-triazenes gives products whose structures are consistent with a cage recombination process of homolytically formed radicals and subsequent abstraction of hydrogen from the solvent molecules by arylamino radicals. In aromatic solvents, a free-radical chain process leads to the formation of products resulting from the homolytic substitution on the solvent. Quenching experiments show that singlet and triplet excited states are reactive but that intersystem crossing efficiency is low.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
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