Absolute rate constants of the vinyl benzoate polymerization have been measured by use of the intermittent illumination method in various aromatic solvents and ethyl acetate at 30°C. The determination of absolute rate constants showed that effects of solvent on the polymerization rate of vinyl benzoate were mainly ascribed to the variation of k p values with solvents rather than that of k t values. The k p values for solvents used increased in the order: benzonitrile < ethyl benzoate < anisole < chlorobenzene < benzene < fluorobenzene < ethyl acetate. There was an eightfold difference between the largest and the smallest values The large variation among k p values was explained neither by the copolymerization through solvents nor the chain transfer to solvents, but by a reversible complex formation between the propagating radical and aromatic solvents. This explanation was supported by a correlation between k p values and calculated delocalization stabilizations for the complexes.
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Kamachi et al. (1978) studied this question.
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