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

Huan Qi, Rui Xie, Guan‐Wen Yang, Yao‐Yao Zhang, Cheng‐Kai Xu, Yuhui Wang, Guang‐Peng Wu

2022Macromolecules31 citationsDOI

Abstract

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···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.

Topics & Concepts

ChemistryBifunctionalCatalysisPolymerizationPhosphoniumLewis acids and basesBoraneSteric effectsReactivity (psychology)Frustrated Lewis pairPolymer chemistryRing-opening polymerizationOrganic chemistryPolymerPathologyAlternative medicineMedicineCarbon dioxide utilization in catalysisOrganoboron and organosilicon chemistrybiodegradable polymer synthesis and properties