Construction of silsesquioxane and phosphinum‐based ionic porous hypercrosslinked polymers for efficient heterogeneous catalytic CO<sub>2</sub> cycloaddition
He Huang, Chaoran Meng, Zixuan Xu, Shijie Wang, Yanan Chang, Shuo Wang, Juan Chen, Zhouyang Long, Guojian Chen
Abstract
Abstract In this work, we reported a facile one‐pot route to construct polyhedral oligomeric silsesquioxane (POSS) and phosphonium‐based ionic porous hypercrosslinked polymers (denoted as P‐iPHCPs) with multiple catalytic active sites, which could be regarded as efficient heterogeneous catalysts for the conversion of carbon dioxide (CO 2 ) to highly value‐added cyclic carbonates. The targeted polymers P‐iPHCPs were prepared from a rigid building block octavinylsilsesquioxane (VPOSS) and a low‐cost commercially available organic ionic salt methyltriphenylphosphonium bromide ([Ph 3 PMe]Br) by the AlCl 3 ‐catalyzed Friedel‐Crafts reaction. The series of polymers P‐iPHCPs that synthesized by different molar ratios of VPOSS to [Ph 3 PMe]Br possess hierarchical micro/mesoporous structures with high surface areas ranging from 376 to 429 m 2 g −1 and behave the flower‐like nano‐morphology. Especially, the desired multiple active sites involved the mixed anions including free Cl − , Br − anions and the in‐situ formed metal‐halogen complex anion [AlCl 3 Br] − within phosphonium segments, and the enriched POSS‐derived SiOH hydrogen bond donor (HBD) groups that derived from the breakage of POSS cages during the synthetic process. The typical polymer P‐iPHCP‐14 has the aforementioned nucleophilic‐electrophilic multiple catalytic active sites, which was regarded as an efficient recyclable heterogeneous catalyst for synergistic catalytic conversion of CO 2 with various epoxides into cyclic carbonates under mild conditions.