Abstract
A new method of synthesis of poly(ester carbonate)s, based on the reaction of dihydroxy compounds with diphenyl dicarbonates containing ester groups was presented. The monomers utilized were diphenyl dicarbonates of cis/trans-1,4-cyclohexane dicarboxylate and of terephthalate units with butanediol or bisphenol A. The process consisted of a precondensation step under a stream of dry argon at atmospheric pressure with the elimination of phenol, followed by a melt polycondensation step at 225 or 250 degrees C under vacuum. The prepared polymers consisted of linear chains containing partial random sequence distribution of monomer residues in the backbone. The inherent viscosities of polymers were from 0.23 to 0.48 dL/g and their T-g values were in the range -9 to 134 degrees C. This method may open door to novel polycarbonates containing other organic functional groups. (c) 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014, 131, 39904.