Zn-based ionic liquids as highly efficient catalysts for chemical fixation of carbon dioxide to epoxides

被引:50
|
作者
Liu, Mengshuai [2 ]
Wang, Fangxiao [2 ]
Shi, Lei [2 ]
Liang, Lin [3 ]
Sun, Jianmin [1 ,2 ]
机构
[1] Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150080, Peoples R China
[2] Harbin Inst Technol, Acad Fundamental & Interdisciplinary Sci, Harbin 150080, Peoples R China
[3] Harbin Inst Technol, Sch Life Sci & Technol, Harbin 150080, Peoples R China
来源
RSC ADVANCES | 2015年 / 5卷 / 19期
基金
中国国家自然科学基金;
关键词
CYCLIC CARBONATES; ORGANIC CARBONATES; COUPLING REACTION; SALEN-COMPLEX; CO2; CYCLOADDITION; OXIDE; ORGANOCATALYST; CONVERSION; STYRENE;
D O I
10.1039/c4ra14111c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The novel Zn-based task-specific ionic liquids (Zn-TSILs) catalysts were developed for the coupling of carbon dioxide and epoxides to form cyclic carbonates under mild reaction conditions without using additional organic solvents and cocatalysts. Due to the synergistic effects of the cation and anion in this catalytic system, excellent yields and selectivities to cyclic carbonates were achieved with high TOF values up to 794 h(-1). Among the catalysts investigated, OH-containing Zn-TSILs showed better activity than COOH-containing Zn-TSILs, and [(CH2CH2OH)Bim]ZnBr3 was found to be the best. Additionally, the influences of CO2 pressure and catalyst concentration were also investigated over [(CH2CH2OH)Bim]ZnBr3. In addition, the rate constants as well as the activation energies for the cycloaddition reaction catalyzed by Zn-TSIL and TSIL were comparatively determined. The activation energy was calculated to be 34.1 kJ mol(-1) for bare TSIL catalyst, whereas the Zn-TSIL reduced the activation energy value by 14.7 kJ mol(-1). Moreover, the Zn-TSIL was easily recyclable without significant loss of activity, representing the exceptionally promising candidate for the effective fixation of CO2 to epoxides.
引用
收藏
页码:14277 / 14284
页数:8
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