Hydroxy-Rich Covalent Organic Framework for the Efficient Catalysis of the Cycloaddition of CO2

被引:10
作者
Pang, Yiying [1 ]
Wang, Bowei [1 ,3 ,4 ]
Gu, Xiaoyi [1 ]
Shen, Huawei [2 ]
Yan, Xilong [1 ,3 ,4 ]
Li, Yang [1 ,4 ]
Chen, Ligong [1 ,3 ,4 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300350, Peoples R China
[2] Shaoxing Xingxin New Mat Co Ltd, Shaoxing 312300, Zhejiang, Peoples R China
[3] Tianjin Univ, Inst Shaoxing, Tianjin 312300, Zhejiang, Peoples R China
[4] Tianjin Engn Res Ctr Funct Fine Chem, Tianjin 300350, Peoples R China
基金
中国国家自然科学基金;
关键词
CYCLIC CARBONATE SYNTHESIS; FIXATION; DIOXIDE; CAPTURE; ADSORPTION; TEMPERATURE; COMPOSITE; EPOXIDES; SITES;
D O I
10.1021/acs.langmuir.3c01719
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The cycloaddition of CO2 with epoxides to cyclic carbonates is one of the most promising and green pathways for CO2 utilization, and the development of highly efficient catalysts remains a challenge. In this work, a novel hydroxy-rich covalent organic framework (TFPB-DHBD-COF) was synthesized, and it served as an efficient heterogeneous catalyst for the reaction of CO2 with 1,2-epoxybutane under mild conditions, providing the desired products in 90% conversion. The abundant hydroxy groups in the pore channels of TFPB-DHBD-COF could not only activate epoxides and CO2 via hydrogen bonding but also obviously enhance its stability through intramolecular five-membered ring hydrogen bonding. Thus, this COF also exhibited outstanding stability and tolerance for diverse substrates. Undoubtedly, this work has enriched the application of tailored COFs in the activation and utilization of CO2.
引用
收藏
页码:16721 / 16730
页数:10
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