Cationic ring-opening polymerization of 2-substituted-2-oxazolines initiated by carbon black surface

Summary Carbon blacks were found capable of initiating the ringopening polymerization of 2-substituted-2-oxazolines at relativery high temperatures. The activation energy of the polymerization of 2-methyl-2-oxazoline was estimated to be 13.4 kcal/mol. Carbon black lost the initiating activity of the polymerization upon the blocking of carboxyl groups on the surface by the treatment with potassium hydroxide or diazomethane. Therefore, it was concluded that carboxyl groups on carbon black play an important role in the initiation of the polymerization. Furthermore, it was found that during the polymerization, poly(N-acylethyleneimine) was grafted onto carbon black by the termination of growing polymer chain with the surface.