Porous sulfonyl binuclear carbonate poly(ionic liquid)s for one-pot fixation of diluted CO2 into dimethyl carbonate

The direct utilization of diluted CO2 skips the additional enrichment and purification operations required for high-purity CO2, making it shine in the green catalytic process. However, achieving diluted CO2 cycloaddition coupling transesterification with epoxide and methanol over poly(ionic liquids) catalyst and understanding the relevant mechanism at the molecular level are still challenging. Here, a novel porous sulfonyl binuclear carbonate poly(ionic liquid)s (SC-PILs) were successfully prepared by the integration of acidic monomers pre-polymerization with basic anions post-etching, regulating the chemical property of free anions and increasing the specific surface area of copolymerized materials. Relying on the synergy of the built abundant pores and the exposed basic anions, SC-PILs could one-pot efficiently catalyze the cycloaddition coupling transesterification reaction of the simulated flue gas (15% CO2 + 85% N2) without any co-catalyst, and dimethyl carbonate (DMC) with the yield of 80% was obtained. Theoretical studies deeply understood the activation difference of binuclear CO32− anion on CO2 compared with mononuclear CH3COO− anion and the ring-opening mechanism of [CO32−+CO2] adduct on epoxides, providing a better choice for high-value utilization of diluted CO2 from flue gas. [Display omitted] •A novel porous sulfonyl binuclear carbonate poly(ionic liquid)s (SC-PILs) are successfully prepared.•SC-PILs provide the built abundant pores and the exposed binuclear carbonate basic anions.•SC-PILs can one-pot efficiently catalyze the cycloaddition coupling transesterification of the simulated flue gas.•The activation difference of binuclear CO32− anion and the ring-opening mechanism of [CO32−+CO2] are explored.