Rational Optimization of Bifunctional Organoboron Catalysts for Versatile Polyethers via Ring-Opening Polymerization of Epoxides

Quaternary ammonium and phosphonium borane bifunctional catalysts have shown high catalytic performance in ring-opening polymerization (ROP) of epoxides to produce polyether. Herein, we systematically investigate a series of well-defined organoboron catalysts by varying the electronic and steric properties of the Lewis acidic boron (B) centers, manipulating the steric hindrance on the ammonium cation (N+), adjusting the distance between B and N+, and regulating the nucleic B number of the catalysts. The investigation on the dinuclear catalysts indicated that the reactivity of a given catalyst could be speculated by its B- N-B angle and the B center dot center dot center dot B distance. We found that the increase of Lewis acidity and the number of B centers of the organoboron catalysts are useful for a high catalytic activity for ROP of epoxides. The Lewis acidity of the B centers was determined using the acceptor numbers, showing an order of borinane (23.4) > BBN (21.7) > BCy2 (18.8) > Bpin (15.5). Moreover, we demonstrated the production of various telechelic polyols in the presence of different chain transfer agents using the organoboron catalysts. The produced telechelic samples have a well-defined terminal functionality with controllable molecular weight. Lastly, these organoboron catalysts were utilized to produce block copolymers, allyl-terminated macromonomers, and random copolymers.

Automated summary

This study systematically investigates the catalytic performance of a series of well-defined organoboron catalysts in ring-opening polymerization (ROP) of epoxides. It is found that the increase of Lewis acidity and the number of B centers of the catalysts contribute to a high catalytic activity. Additionally, the catalysts are capable of producing telechelic polyols with controllable molecular weight in the presence of different chain transfer agents.