Affiliation:
1. University of Chinese Academy of Sciences Beijing 100049 P. R. China)
2. CAS Key Laboratory of Green Process and Engineering State Key Laboratory of Multiphase Complex Systems Beijing Key Laboratory of Ionic Liquids Clean Process Institute of Process Engineering Chinese Academy of Sciences Beijing 100190 P. R. China
3. Advanced Energy Science and Technology Guangdong Laboratory Huizhou Guangdong 516003 P. R. China
Abstract
AbstractThe synthesis of cyclic carbonate from CO2 and epoxide is one of the valid routes in line with atomic economy to achieve CO2 conversion. Combining the advantages of high activity and easy separation for heterogeneous catalytic reaction system, a series of heterogeneous catalysts poly(ionic liquid)s with high ionic density (HDPILs) were designed and synthesized. Looser structures and high ionic density were obtained by using muti‐center ionic liquids with different number of substituents as cross‐linking agents. Ply[PhSVIM]Br, the copolymerized HDPILs with six substituents on the benzene ring was optimal. The catalyst exhibited excellent catalytic performance for CO2 cycloaddition with 98 % conversion and 99 % selectivity under optimal conditions. These HDPILs have comparable catalytic activity to homogeneous catalysts and convenient product separability. Particularly, combining XPS and DFT, a structural performance relationship was revealed, the multi‐center ionic liquids used instead of the traditional crosslinking agent as the polymeric backbone can contribute to the reduction of the anion and cation binding energy (BE) and freeing of Br−, which leads to efficient catalytic activity. This study provides a novel strategy for developing a highly efficient catalysts for CO2 conversion to high value products.
Funder
National Natural Science Foundation of China
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Cited by
4 articles.
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