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Mechanism of benzophenone ketyl radical formation in acid alcohols studied by pulse-radiolysis and rigid-matrix techniques. [Gamma rays]

Journal Article · · J. Phys. Chem.; (United States)
DOI:https://doi.org/10.1021/j100457a018· OSTI ID:6873484
 [1]; ; ; ;
  1. Inst. of Physical and Chemical Research, Saitama, Japan
The mechanism of the benzophenone ketyl radical formation in acid methanol, ethanol, and 2-propanol was studied by using pulse-radiolysis and rigid-matrix techniques. When a 0.1 M ethanol solution of benzophenone containing hydrogen chloride (1.2 M) was irradiated at 77 K by ..gamma.. rays from /sup 60/Co, the absorption spectrum of the trapped intermediates was ascribed solely to benzophenone ketyl radicals. The pulse-radiolysis study of the solution at 100 K revealed that the ketyl radicals are produced by protonation of presolvated benzophenone anion radicals. At 153 K, the ketyl radicals were observed to be produced also by hydrogen-atom transfer from CH/sub 3/CHOH and CH/sub 3/CH(OH)CH/sub 3/ to benzophenone; the temperature dependence of the transfer rate constant was studied.
OSTI ID:
6873484
Journal Information:
J. Phys. Chem.; (United States), Journal Name: J. Phys. Chem.; (United States) Vol. 84:20; ISSN JPCHA
Country of Publication:
United States
Language:
English