151. Cationic polymerization of glycidyl phenyl ether by benzylammonium salts
- Author
-
Takeshi Endo and S. Nakano
- Subjects
chemistry.chemical_classification ,Polymers and Plastics ,Bulk polymerization ,Organic Chemistry ,Cationic polymerization ,Ether ,Polymer ,Ring-opening polymerization ,chemistry.chemical_compound ,chemistry ,Polymer chemistry ,Materials Chemistry ,Benzyl group ,Reactivity (chemistry) ,Ionic polymerization - Abstract
Novel cationic initiators, p-substituted benzylanilinium SbF 6 - salts (1), were synthesized from the corresponding benzylchloride and N,N-dimethylaniline, where Cl - was exchanged with SbF 6 - . Their catalytic activities in the cationic polymerization of glycidyl phenyl ether (GPE) were examined and compared to that of benzylpyridinium SbF 6 - salts (2), latent thermal initiators previously reported by Endo et al. It was found that 1 acted as a latent thermal initiator in the cationic polymerization of glycidyl phenyl ether (GPE) above 80°C for 10 min. Furthermore, 1 showed higher activity than 2 having the same p-substituents, except for a p-Cl group in the cationic polymerization of GPE. Both the GPE polymer structure and the benzyl group reactivity in 1 or 2 indicate that 1 generates benzyl cations that are active species for the cationic polymerization of GPE, and that in cationic polymerization using 2, side reactions generating active species other than benzyl cations occur
- Published
- 1995