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- W2040850855 abstract "The electron transfer photooxygenations of aromatic compounds were carried out with trityl salts. Under these superoxide-free reaction conditions, only anthracene and 1,1-diarylethylenes were photooxygenated, stilbenes isomerized, and quantitatively recovered were naphthalene, phenanthrene, alkylnaphthalenes, tetraphenylethylene and 1,1,4,4-tetraaryl-1,3-butadienes. The reactivities of their radical cations toward triplet oxygenation were discussed on the basis of the quantum yield measurements and product analyses." @default.
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- W2040850855 title "Chemical Behavior of Aromatic Radical Cations under Superoxide-Free Electron Transfer Photooxygenation Conditions" @default.
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