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Stable radicals during photodecarbonylations of trityl-alkyl ketones enable solid state reactions through primary and secondary radical centers
Authors:Kuzmanich Gregory  Natarajan Arunkumar  Shi Yanhui  Patrick Brian O  Scheffer John R  Garcia-Garibay Miguel A
Affiliation:Department of Chemistry and Biochemistry, University of California, Los Angeles, 90095-1559, USA.
Abstract:The solid state photoexcitation of several triphenylmethyl-alkyl ketones resulted in the loss of CO and the exclusive formation of radical-radical combination products. Differences in reactivity suggest a stepwise mechanism with the unprecedented formation of primary and secondary radicals in some of the radical pair intermediates in the solid state.
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