Ionic and radical pathways in the photolysis of 1-(4-chloromethylphenyl)propene
Abstract
The direct photolysis of 1-(4-chloromethylphenyl)propene (5) in t-butyl alcohol affords products derived from both homolytic and heterolytic carbon–chlorine bond fission, whereas triplet sensitized irradiation of (5) results only in cis–trans isomerization.
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