Nitrogen-rich covalent organic polymers and potassium iodide for efficient chemical fixation of CO2 into epoxides under mild conditions

Resource utilization of carbon dioxide (CO2) to add value to the chemicals used in the preparation of cyclic carbonates has gained significant interest in sustainable chemistry and environmental preservation. Herein, new nitrogen-rich urea covalent organic polymers (NUP-1, NUP-2, NUP-3) with multiple urea groups simultaneously acting as acidic nodes were designed and synthesized in a simple method. These synthesized NUPs were characterized using FT-IR spectroscopy, C-13 CP MAS NMR, SEM, PXRD, TGA, XPS spectroscopy, CO2 adsorption and nitrogen adsorption-desorption. The novel NUP-3 catalyst was particularly effective in the cycloaddition reactions having obtained a 93% yield of cyclic carbonate after 24 h at 90 degrees C with 0.1 MPa of pressure, using 1.0 mol% of KI and 70 mg of NUP-3. The results showed that the functionalized NUP-3 used as a catalyst for the cycloaddition reaction of CO2 and epoxide with an alkali-metal salt, exhibited good activity under mild conditions. In addition, a mechanistic insight into the effects of urea groups on the activation of both epoxide and CO2 was gained using DFT calculations.

Automated summary

Resource utilization of CO2 to add value to chemicals in the preparation of cyclic carbonates has gained interest, with nitrogen-rich urea covalent organic polymers being designed as effective catalysts for cycloaddition reactions under mild conditions. The results showed promising yield of cyclic carbonates and a mechanistic insight into the activation of epoxide and CO2 using DFT calculations.