| Abstract: | Novel vinyl monomers containing 1,4,5,6-tetrahydropyrimidine were prepared by the reaction of N-substituted-1,3-diaminopropane with N,N-dimethyl-formamide dimethylacetal, which gave 1-alkyl or aryl substituted 1,4,5,6-tetrahydropyrimidines, Alkylation of the tetrahydropyrimidine derivatives by chloromethylstyrene produces the N-methyl-N′-vinyl benzyl-1,4,5,6-tetrahydropyrimidinium chloride in high yields. These monomers were readily polymerized in dimethylformamide by AIBN at 80°C. Homopolymers and soluble linear copolymers were prepared and copolymerization parameters were rationalized. Further, insoluble terpolymers prepared from these monomers, styrene and divinylbenzene were tested for the sorption of the weakly acidic gases gave excellent results. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35 : 2411–2420, 1997 |
