TY - JOUR
T1 - Cationic organobismuth complex as an effective catalyst for conversion of CO2 into cyclic carbonates
AU - Zhang, Xiaowen
AU - Dai, Weili
AU - Yin, Shuangfeng
AU - Luo, Shenglian
AU - Au, Chak-Tong
N1 - Funding Information:
Acknowledgements This work was supported by the National Natural Science Foundation of China (Grant No. 20507005) and Outstanding Young Research Award of National Natural Science Foundation of China (Grant No. E50725825). Prof. Yin also shows sincere thanks to Dr. Shimada of National Institute of Advanced Industrial Science and Technology (AIST, Japan) for his kind help on organobismuth chemistry.
PY - 2009/3
Y1 - 2009/3
N2 - In order to achieve high-efficiency conversion of CO2 into valuable chemicals, and to exploit new applications of organobismuth compounds, cationic organobismuth complex with 5,6,7,12-tetrahydrodibenz[c,f][1,5] azabismocine framework was examined for the first time for the coupling of CO2 into cyclic carbonates, using terminal epoxides as substrates and tetrabutylammonium halide as co-catalyst in a solvent-free environment under mild conditions. It is shown that the catalyst exhibited high activity and selectivity for the coupling reaction of CO2 with a wide range of terminal epoxide. The selectivity of propylene carbonates could reach 100%, and the maximum turnover frequency was up to 10740 h-1 at 120°C and 3 MPa CO2 pressure when tetrabutylammonium iodide was used as co-catalyst. Moreover, the catalyst is environment friendly, resistant to air and water, and can be readily reused and recycled without any loss of activity, demonstrating a potential in industrial application.
AB - In order to achieve high-efficiency conversion of CO2 into valuable chemicals, and to exploit new applications of organobismuth compounds, cationic organobismuth complex with 5,6,7,12-tetrahydrodibenz[c,f][1,5] azabismocine framework was examined for the first time for the coupling of CO2 into cyclic carbonates, using terminal epoxides as substrates and tetrabutylammonium halide as co-catalyst in a solvent-free environment under mild conditions. It is shown that the catalyst exhibited high activity and selectivity for the coupling reaction of CO2 with a wide range of terminal epoxide. The selectivity of propylene carbonates could reach 100%, and the maximum turnover frequency was up to 10740 h-1 at 120°C and 3 MPa CO2 pressure when tetrabutylammonium iodide was used as co-catalyst. Moreover, the catalyst is environment friendly, resistant to air and water, and can be readily reused and recycled without any loss of activity, demonstrating a potential in industrial application.
KW - Carbon dioxide
KW - Cationic organobismuth complex
KW - Coupling
KW - Cyclic carbonate
KW - Terminal epoxide
UR - http://www.scopus.com/inward/record.url?scp=62249198979&partnerID=8YFLogxK
U2 - 10.1007/s11783-008-0068-y
DO - 10.1007/s11783-008-0068-y
M3 - Journal article
AN - SCOPUS:62249198979
SN - 1673-7415
VL - 3
SP - 32
EP - 37
JO - Frontiers of Environmental Science and Engineering in China
JF - Frontiers of Environmental Science and Engineering in China
IS - 1
ER -