Issue 11, 1991

Photolysis of dioxiranes in the presence of a nitroxide radical scavenger: the intermediacy of radical anion and diyl species in the production and trapping of methyl and trifluoromethyl radicals

Abstract

Electron transfer between dioxiranes 1 and nitroxide 2 affords the dioxirane radical anion–oxoammonium cation pair, which generates methyl radicals that are trapped by the nitroxide.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 771-773

Photolysis of dioxiranes in the presence of a nitroxide radical scavenger: the intermediacy of radical anion and diyl species in the production and trapping of methyl and trifluoromethyl radicals

W. Adam, S. E. Bottle and R. Mello, J. Chem. Soc., Chem. Commun., 1991, 771 DOI: 10.1039/C39910000771

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