High Efficiency Organic Lewis Pair Catalyst for Ring-Opening Polymerization of Epoxides with Chemoselectivity

Ring-opening polymerization (ROP) is a versatile approach to well-defined polymers. Achieving both high efficiency and precise control remains a major challenge. We herein report room-temperature living ROP of epoxides catalyzed by combined organobase and triethylborane (Et3B) with water or alcohols as initiators. Extremely high catalytic efficiency (turnover frequency up to 6000 h(-1)) is exhibited despite the relatively mild Lewis basicity and acidity, and the catalyst loading can be minimized to 44 ppm. Poly(ethylene oxide) products are noncytotoxic toward a variety of cell lines even without purification. Poly(propylene oxide) with molar mass as high as 210 kg mol(-1) and low dispersity (D-M < 1.1) can be achieved owing to the absence of detrimental transfer reactions. The chemoselectivity allows the catalyst to be readily applied to living ROP of glycidyl ethers, tailored synthesis of diverse functional/block/nonlinear (co)polyether structures, and one-pot one-catalyst synthesis of polyether-based polyurethane. Our study reveals the effective cooperation modes of the Lewis pair and hydroxyl, including the reversible formation of three-component initiation/propagation center with appropriate basicity, activation of epoxide by uncomplexed Et3B, and fast activity exchange between dormant and active hydroxy species.