Hydroxyl-functionalized ionic liquid-modified covalent organic frameworks for efficient CO2 cycloaddition conversion

被引:5
作者
Wang, Lipeng [1 ]
Yin, Meilin [1 ]
Li, Rui [1 ]
Tang, Shaokun [1 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Minist Educ, Tianjin 300354, Peoples R China
来源
MOLECULAR CATALYSIS | 2024年 / 564卷
关键词
Covalent organic frameworks; Hydroxyl-functionalized ionic liquids; Chemical grafting; CO; 2; conversion; Cycloaddition; ENHANCED CATALYTIC-ACTIVITY; HYDROGEN-BOND DONOR; CYCLIC CARBONATES; EPOXIDES; SALT; ACID;
D O I
10.1016/j.mcat.2024.114331
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Converting CO2 into high-value chemicals is an essential way to mitigate greenhouse impact and realize sustainable utilization of resources. In this work, the COF materials named X-QCOF (X = OH, OCH3) were synthesized by a three-component Povarov reaction, followed by chemical grafting of hydroxyl-functionalized ionic liquid into the COFs neutral backbone via quaternization to obtain the hybrid materials IL-X-QCOF (X = OH, OCH3). The resultant IL-X-QCOF can efficiently catalyze the cycloaddition reaction of CO2 and epoxides in the absence of metals, additives and solvents. Among them, IL-OH-QCOF exhibits a yield of 97.2% of cyclochloroallyl carbonate with a high turnover frequency (TOF) value of 217.7. The inherent high specific surface area of the COF-based materials promotes mass transfer efficiency, and meanwhile the abundant hydroxyl groups and bromine anions occurring in the backbone create excellent catalytic effect. Attributed to the chemical grafting approach, the product yield keeps over 90% when IL-OH-QCOF is reused for 6 cycles.
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页数:10
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