Synthesis of Polyester Having Pendent Hydroxyl Groups via Regioselective Dehydration Polycondensations of Dicarboxylic Acids and Diols by Low Temperature Polycondensation

摘要

In this article, we describe the one-step synthesis of polyesters having pendent hydroxyl groups by Lewis acid-catalyzed, regioselective, dehydration polycondensations of diols (glycerol and sorbitol) and dicarboxylic acids [tartaric acid (TA) and malic acid (MA)] containing pendent hydroxyl groups, using low temperature polycondensation technique. Direct polycondensations of TA or MA and 1,9-non-anediol catalyzed by scandium trifluoromethanesulfonate [Sc(OTf)(3)] successfully yielded linear polyesters having hydroxyl functionality (M-n = ca. 1.0 X 10(4)). To demonstrate the reactivity of the pendent hydroxyl group, a glycosidation was performed. Poly(nonamethylene L-malate) showed significant higher biodegradability, compared with poly(nonamethylene L-tartrate) or poly(nonamethylene succinate). Stable poly(nonamethylene L-tartrate) emulsion could be prepared using poly(vinyl alcohol) as the surfactant, although emulsions consisting of poly(nonamethylene succinate) were unstable and phase-separated within a few days. Furthermore, direct polycondensations of TA and diethylene glycol (DEG) or triethylene glycol (TEG) successfully produced water-soluble polyesters having hydroxyl groups. This new polycondensation system may be extremely effective not only for advanced material design using functional monomers but also for effective utilization of biomass resources as chemical substances.