One-step synthesis of nitrogen-rich organic polymers for efficient catalysis of CO2 cycloaddition

被引:13
作者
Chen, Zewen [1 ]
Zhi, Yunfei [1 ]
Li, Wenlong [1 ]
Li, Shuangjiang [1 ]
Liu, Yi [1 ]
Tang, Xiaoning [1 ,2 ]
Hu, Tianding [1 ]
Shi, Lan [1 ]
Shan, Shaoyun [1 ]
机构
[1] Kunming Univ Sci & Technol, Sch Chem Engn, Kunming 650500, Yunnan, Peoples R China
[2] Kunming Univ Sci & Technol, Sch Met & Energy Engn, Kunming 650500, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
Carbon dioxide; Organic polymers; Nitrogen-rich; Hydrogen bond donors; Cyclic carbonate; COVALENT TRIAZINE FRAMEWORKS; CARBON-DIOXIDE; CYCLIC CARBONATES; CHEMICAL FIXATION; HIGHLY EFFICIENT; IONIC LIQUIDS; MICROPOROUS POLYAMINALS; FACILE SYNTHESIS; ADSORPTION; EPOXIDES;
D O I
10.1007/s11356-023-26728-5
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Nitrogen-rich organic polymer poly(chloride triazole) (PCTs) was synthesized by a one-step method as metal-halogen-free heterogeneous catalyst for the solvent-free CO2 cycloaddition. PCTs had abundant nitrogen sites and hydrogen bond donors, exhibited great activity for the cycloaddition of CO2 and epichlorohydrin, and achieved 99.6% yield of chloropropene carbonate under the conditions of 110 celcius, 6 h, and 0.5 MPa CO2. The activation of epoxides and CO2 by hydrogen bond donor and nitrogen sites was further explained by density functional theory (DFT) calculations. In summary, this study showed that nitrogen-rich organic polymer is a versatile platform for CO2 cycloaddition, and this paper provides a reference for the design of CO2 cycloaddition catalysts.
引用
收藏
页码:67290 / 67302
页数:13
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