The role of substituents of chlorostannoxanes on the reactivity of the catalysts during the synthesis of cyclic carbonates using epoxides and carbon dioxide

被引:7
作者
Pulla, Sharon
Ramidi, Punnamchandar
Jarvis, Benjamin L.
Munshi, Pradip [2 ]
Griffin, William O.
Darsey, Jerry A.
Dallas, Jerry L. [3 ]
Pokala, Vedavalli [4 ]
Ghosh, Anindya [1 ]
机构
[1] Univ Arkansas, Dept Chem, Little Rock, AR 72204 USA
[2] Rubamin Labs Ltd, Vadodara, Gujarat, India
[3] Univ Calif Davis, Nucl Magnet Resonance Facil, Davis, CA 95616 USA
[4] Univ Pacific, Sch Pharm, Hillsboro, OR USA
关键词
carbon dioxide; chlorostannoxanes; cyclic carbonates; epoxides; substituents; mechanistic study; PROPYLENE CARBONATE; SALEN COMPLEXES; ETHYLENE CARBONATE; DIMETHYL CARBONATE; CYCLOHEXENE OXIDE; CO2; COPOLYMERIZATION; TRANSESTERIFICATION; POLYMERIZATION; POLYURETHANES;
D O I
10.1002/ghg.43
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
We report a study on the effect of substituents on the activity of chlorostannoxane catalysts in coupling epoxides and carbon dioxide for cyclic carbonate synthesis. All butyl-substituted (1a) chlorostannoxane was found to yield cyclic carbonates in high turnover number (TON 2340) at 300 psi CO2, 130 degrees C in 2 h. All the reactions were performed under solvent-free conditions in the presence of a Lewis base which acts as a co-catalyst. The activity was found to change with change in the substituents on the catalysts. The effect of change in substituents was studied with respect to variation in essential parameters, such as time, temperature, pressure, and difference in catalyst to co-catalyst ratio. (c) 2012 Society of Chemical Industry and John Wiley & Sons, Ltd
引用
收藏
页码:66 / 74
页数:9
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