Abstract
The Arrhenius activation energies (EA) have been determined for the near diffusion-controlled bimolecular termination reactions of some semiquinone radicals in a series of solvents. It was often found that EA was less than the activation energy of diffusion (ED) is the solvent. An explanation has been proposed in terms of the rate of encounters between the radicals and the rate at which the radicals react during an encounter.
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Schedule a callMore From: Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases
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