SYNTHESIS AND ACTIVITY OF ARYL BENZYL METHYL SULFONIUM SALTS AS CATIONIC INITIATORS - EFFECT OF SUBSTITUENT ON ARYL GROUP

Benzyl o-, m-, and p-substituted phenyl methyl sulfonium salts (2b-2g) were synthesized and their activities as cationic initiators were evaluated in the bulk polymerization of phenyl glycidyl ether (PGE). Especially, their activities were estimated with respect to the effect of substituents on the aryl group. In the polymerizations of PGE with a series of benzyl p-substituted phenyl methyl sulfonium salts, the order of their activities was found to be 2c (CH3OCOO) > 2b (CH3COO) > 2d (CH3O) almost-equal-to 2a (HO). In particular, 2c was the most active initiator of all, capable of initiating the polymerization of PGE even at room temperature. In the polymerizations with 2a, 2e (m-Cl), 2f (o-CH3), and 2g (m-CH3), the activity of 2e was the highest of all while those of 2a, 2f, and 2g were almost the same. These results strongly suggested that the electron-withdrawing group placed on the aryl group undoubtedly enhanced the activity of the sulfonium salts as the cationic initiators.