Thermal oxidation of tetracyclones (2,3,4,5-tetraarylcyclopentadienones)
作者:Thies Thiemann、Jesus Iniesta、David J. Walton
DOI:10.3184/030823408x310792
日期:2008.3
Tetracyclones are transformed to a mixture of diacylstilbenes and α-pyrones, when they are heated in diphenylether saturated with oxygen.
当四旋风在氧饱和的二苯醚中加热时,它们会转化为二酰基二苯乙烯和 α-吡喃酮的混合物。
Oxidation of aromatic compounds: XVII. Oxidative cross-dimerization of diarylacetylenes in the system CF3CO2H-CH2Cl2-PbO2. Characteristic of cation-radicals of diarylacetylenes by cyclic voltammetry and ESR spectroscopy
作者:A. V. Vasil’ev、A. P. Rudenko
DOI:10.1134/s1070428010090034
日期:2010.9
The oxidation of mixtures of diarylacetylene ArCa parts per thousand CAr and Ar'Ca parts per thousand CAr' in a system CF3CO2H-CH2Cl2-PbO2 (0A degrees C, 1.5 h) results in products of cross-dimerization, (Z)-1,2,3,4-tetraarylbut-2-ene-1,4-diones Ar(ArCO) C=C(COAr')Ar'. The routes of transformation of intermediate cation-radicals of diarylacetylenes [ArCa parts per thousand CAr](+center dot) into the final products of oxidative dimerization are elucidated. By cyclic voltammetry and ESR spectroscopy the high reactivity of the diarylacetylene cation-radicals is demonstrated, the character of their singly occupied molecular orbitals (a(2) or b(1)) has been revealed by ESR method.
Vasil'ev; Rudenko, Russian Journal of Organic Chemistry, 1997, vol. 33, # 11, p. 1555 - 1584