碳酸盐
磺酰
离子液体
酯交换
环加成
碳酸二甲酯
环氧丙烷
化学
聚合
单体
环氧化物
无机化学
高分子化学
有机化学
催化作用
共聚物
烷基
聚合物
环氧乙烷
作者
Jing Ding,Peiru Wang,Yuting He,Linyan Cheng,Xue Li,Cheng Fang,Hongping Li,Hui Wan,Guofeng Guan
标识
DOI:10.1016/j.apcatb.2022.122278
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI