Hydroxyl-anchored covalent organic crown-based polymers for CO2 fixation into cyclic carbonates under mild conditions

Covalent organic polymers (COPs) are a kind of promising material for carbon dioxide (CO2) reutilization. Herein, a series of covalent organic crown-based polymers (COCP-H, COCP-OH, COCP-CH3, COCP-Bu, COCP-NH2) were designed and synthesized. These synthesized COCPs were characterized by FT-IR, SEM, BET and C-13 CP MAS NMR. Notably, the novel COCP-OH catalyst with hydroxyl and crown ether groups on the framework simultaneously was particularly effective in cycloaddition reactions, giving a cyclic carbonate yield of 94.8% after 24 h at 70 degrees C with 1 bar of CO2, using 0.0735 mmol of KI and 71 mg of COCP-OH. It is worth considering that there is a synergetic effect between the hydroxyl group and KI activated by the crown ether fragment, which plays a crucial role in accelerating the reaction rate. The coordinated interaction of crown ether with KI was also confirmed by X-ray photoelectron spectroscopy (XPS). Thus, this study provides a new approach to fabricate multifunctional COP materials for the coupling reaction of CO2 under mild conditions.

Automated summary

The study synthesized a series of covalent organic crown-based polymers and found that one of them, COCP-OH, with hydroxyl and crown ether groups, exhibited high catalytic efficiency in cycloaddition reactions, providing a new approach for CO2 coupling reactions.