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  • Substituent effects  (1)
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    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1851-1859 
    ISSN: 0009-2940
    Keywords: Carbonyl oxides ; Quinone oxides ; Dioxiranes ; Substituent effects ; Matrix isolation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Triplet 4-oxocyclohexadienylidenes 6, matrix-isolated in Ar/ 2% O2 at 10 K, react with triplet O2 on annealing the matrix. Primary reaction products are quinone oxides 4, which have been characterized by IR and UV/Vis spectrometry. They are very photolabile; long-wavelength irradiation converts them into spiro-dioxiranes 5, which in turn yield lactones 10 upon irradiation with visible light. Experimental data have been obtained for quinone oxides 4a-g; additionally, ground-state properties and UV/Vis absorptions of quinone oxides 4a,b and 4e-1 have been calculated by the MINDO-3/UHF and CNDO/S methods. Since the theoretical and experimental maxima of the π → π* transitions are in good agreement, we conclude that our semiempirical calculations give an adequate picture of quinone oxides 4 which may best be described as dipolar diradicals.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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