共 65 条
A solid Zn complex catalyst for efficient transformation of CO2 to cyclic carbonates at mild conditions
被引:12
作者:

Ge, Yuansheng
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China Univ Geosci Wuhan, Fac Mat Sci & Chem, Sustainable Energy Lab, 388 Lumo Rd, Wuhan 430074, Peoples R China China Univ Geosci Wuhan, Fac Mat Sci & Chem, Sustainable Energy Lab, 388 Lumo Rd, Wuhan 430074, Peoples R China

Liu, Wei
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China Univ Geosci Wuhan, Fac Mat Sci & Chem, Sustainable Energy Lab, 388 Lumo Rd, Wuhan 430074, Peoples R China China Univ Geosci Wuhan, Fac Mat Sci & Chem, Sustainable Energy Lab, 388 Lumo Rd, Wuhan 430074, Peoples R China

Zou, Yizhen
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China Univ Geosci Wuhan, Fac Mat Sci & Chem, Sustainable Energy Lab, 388 Lumo Rd, Wuhan 430074, Peoples R China China Univ Geosci Wuhan, Fac Mat Sci & Chem, Sustainable Energy Lab, 388 Lumo Rd, Wuhan 430074, Peoples R China

Cheng, Guoe
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China Univ Geosci Wuhan, Fac Mat Sci & Chem, Sustainable Energy Lab, 388 Lumo Rd, Wuhan 430074, Peoples R China China Univ Geosci Wuhan, Fac Mat Sci & Chem, Sustainable Energy Lab, 388 Lumo Rd, Wuhan 430074, Peoples R China

Ke, Hanzhong
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China Univ Geosci Wuhan, Fac Mat Sci & Chem, Sustainable Energy Lab, 388 Lumo Rd, Wuhan 430074, Peoples R China China Univ Geosci Wuhan, Fac Mat Sci & Chem, Sustainable Energy Lab, 388 Lumo Rd, Wuhan 430074, Peoples R China
机构:
[1] China Univ Geosci Wuhan, Fac Mat Sci & Chem, Sustainable Energy Lab, 388 Lumo Rd, Wuhan 430074, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
Zinc complex;
o-hydroxy benzyl-amine;
CO2;
conversion;
Cyclic carbonate;
Heterogeneous catalyst;
POROUS ORGANIC POLYMERS;
AMBIENT CONDITIONS;
HIGHLY EFFICIENT;
EPOXIDES;
DIOXIDE;
METAL;
CONVERSION;
CYCLOADDITION;
PORPHYRIN;
ORGANOCATALYSTS;
D O I:
10.1016/j.tet.2022.132857
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
A solid Zn Complex (Zn(HBA)(2)) with o-Hydroxybenzyl-Amine, which can be easily prepared by a one-step synthesis method, was exploited for the CO2 transformation to cyclic carbonates. The results demonstrated that Zn(HBA)(2) is a high-efficiency catalyst in the coupling reaction between CO2 and epoxides under solvent-free conditions. Under mild conditions (80 degrees C, atmospheric CO2), epoxides with different substituents have been successfully transformed into the relevant cyclic carbonates with high yields and selectivity (>99%). The turnover frequency (TOF) was reached to 21,667 h(-1) for the coupling of CO2 and epichlorohydrin (ECH) into chloropropene carbonate (CPC) under 120 degrees C and a 1.8 MPa of CO2 pressure within 3 h. This catalyst is capable of recovering and reusing by simple filtration. The catalytic mechanism of Zn(HBA)(2) for the cycloaddition reaction was proposed. (C) 2022 Elsevier Ltd. All rights reserved.
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