Novel Hydroxyl-Functional Aliphatic CO2-Based Polycarbonates: Synthesis and Properties

A series of novel functional polycarbonates, specifically poly(solketal glycidyl ether carbonate-<i>co</i>-propylene carbonate)s with varying compositions, were synthesized through the ring-opening copolymerization of solketal glycidyl ether, propylene oxide, and carbon dioxide. The reaction was catalyzed by rac-(salcy)Co^IIIX complexes with bis(triphenylphosphine)iminium salts as co-catalysts, achieving high selectivity. The resulting terpolymers exhibited number-average molecular weights ranging from 2 × 10⁴ to 1 × 10⁵ and a narrow, bimodal molecular weight distribution, with dispersities of 1.02-1.07 for each mode. Interestingly, the addition of a small amount of water to the reaction mixture yielded a terpolymer with a unimodal molecular weight distribution and a dispersity of 1.11. Subsequent acidic hydrolysis of the solketal protective groups produced poly(glyceryl glycerol carbonate-<i>co</i>-propylene carbonate). All terpolymers were amorphous, with T<i>_g</i> near or below room temperature. The hydroxyl-functional polycarbonates underwent cyclodepolymerization under milder conditions compared to polycarbonates with protected hydroxyl groups.