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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 80 (1968), S. 69-77 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Photolyse von Jodaromaten sind Biphenyl- und Phenanthren-Derivate sowie Elementorgano-Verbindungen zugänglich. Ringschlußreaktionen ermöglichen die Umwandlung von o-Terphenyl in Triphenylen und von Benzaniliden in Phenanthridone. Bei der Photolyse von 1,2-Dijodbenzol in Lösung wurde Dehydrobenzol nachgewiesen. Zahlreiche freie Radikale sind durch die Photolyse substituierter aromatischer oder verwandter Jodverbindungen wie CH3J, JCN, JCH2COOH, RC ≡ CJ zugänglich. Auch aromatische Bromverbindungen lassen sich leicht photolysieren. Photochemisch ausgelöste Reaktionen gestatten den Austausch von Jod gegen 131J, H, D, Cl oder Br.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 7 (1968), S. 36-44 
    ISSN: 0570-0833
    Keywords: Photolysis ; Iodoaromatic compounds ; Dehydrobenzene ; Free radicals ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Under appropriate conditions, the photolysis of iodoaromatic compounds yields derivatives of biphenyl and phenanthrene, as well as organometallic compounds. Ring closures of o-terphenyls to triphenylenes and of benzanilides to phenanthridones are described. The formation of dehydrobenzene (benzyne) on photolysis of 1,2-diiodobenzene in solution has been established. The photolysis of various substituted iodoaromatic compounds or of substances such as CH3I, ICN, ICH3, COOH, or RC≡CI, provides a general method for the generation of a large variety of free radicals in solution. The potential uses of photochemically initiated exchanges of iodine in ArI for 131I, Li, D, Cl, or Br are noted.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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