Low-Cost Polymer-Supported Quaternary Ammonium Salts as High-Efficiency Catalysts for Cycloaddition of CO2 to Epoxides

Polystyrene grafted with quaternary ammonium salts were obtained by direct quaternarization of chloromethylated polystyrene with N , N -dimethylethylamine, N , N -dimethylglycine (denoted as PS-QNS and PS-CQNS, respectively). These two polymer-supported ionic liquids were found to show high catalyti...

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Published inCatalysis letters Vol. 142; no. 11; pp. 1376 - 1381
Main Authors Zhang, Yuan-Yuan, Chen, Lang, Yin, Shuang-Feng, Luo, Sheng-Lian, Au, Chak-Tong
Format Journal Article
LanguageEnglish
Published Boston Springer US 01.11.2012
Springer Nature
Springer
Springer Nature B.V
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Summary:Polystyrene grafted with quaternary ammonium salts were obtained by direct quaternarization of chloromethylated polystyrene with N , N -dimethylethylamine, N , N -dimethylglycine (denoted as PS-QNS and PS-CQNS, respectively). These two polymer-supported ionic liquids were found to show high catalytic efficiency towards the cycloaddition of CO 2 to epoxides. The effects of catalyst amount, reaction temperature, initial CO 2 pressure, and reaction time on the yield of cyclic carbonates were investigated systematically. Under the optimal reaction conditions (150 °C, initial CO 2 pressure 2.0 MPa and 5 h), propylene carbonate yield and selectivity in the cycloaddition of CO 2 to propylene oxide over PS-CQNS were 96.2 and 99.3 % whereas those over PS-QNS were 97.9 and 99.5 %, respectively. It was observed that the reusability of PS-QNS was excellent. From the viewpoint of industrial application, PS-QNS is attractive in terms of catalytic efficiency, cost and simplicity in preparation. Graphical Abstract Polystyrene bearing quaternary ammonium salt ionic liquids (denoted as PS-QNS and PS-CQNS) were fabricated and evaluated for solventless synthesis of cyclic carbonates from CO 2 and epoxides. The catalysts are low in cost and simple to prepare, and show good activity, selectivity, stability and reusability towards the cycloaddition reaction.
ISSN:1011-372X
1572-879X
DOI:10.1007/s10562-012-0909-y