Abstract
Abstract The rate constants for the radical addition of a trifluoromethyl radical to aryl-substituted vinyl triflates have been determined by applying competition kinetics at a single concentration point. The rate constants range from 4.1× 106 to 5.6× 106 M−1 s−1 and depend on the electronic properties of the benzene rings on the aryl-substituted vinyl triflates.
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