This communication describes a convenient route to optically active propylene carbonate by a catalytic kinetic resolution process resulting from the coupling reaction of CO2 and racemic epoxides using simple chiral SalenCo(III)/quaternary ammonium halide catalyst systems.

Vitrimers endow cross-linked polymers with malleability and reprocessability via exchange reactions. However, designing of reprocessable, shape-memory polymer materials with high strength via a catalyst-free method remains a challenge under mild conditions. Here, we propose a facile strategy to address this dilemma by introducing the exchangeable imine bond and N-coordinated boroxine into a polybutadiene (PB)-based network. Specifically, PB grafted with 2-aminoethanethiol is reacted with the formyl group of phenylboronic acid and dehydrated to form a dual-dynamic covalently cross-linked network at room temperature. The dynamic network draws on the advantage of imine (toughness) and N-coordinated boroxine (strength), making the PB-based materials exhibit favorable malleability, mechanical property, reprocessability, and thermal-induced shape-memory behavior. We can obtain customized high mechanical properties by tuning the cross-linking density, and the tensile strength reaches a high value (12.35 MPa) without fillers or any other additives. Meanwhile, the unique network framework makes the material recycle over several times without sacrificing its property. This work presents a facile and effective approach to achieve a multifunctional polymer with customized attributes. Besides, this strategy can recycle end-of-life rubber to alleviate environmental pollution and provide inspiration for fabricating targeted materials by uniting the dynamic covalent or noncovalent bonds.