Abstract
A highly efficient method for the synthesis of cyclic carbonates from carbon dioxide and epoxides in the presence of polymer-supported quaternary onium salts (PS-Q+X-) and aqueous solution of metal salts under mild conditions, is described. In comparison with conventional homogeneous catalysts, immobilized tributylmethylammonium chloride (PS-TBMAC) is a recyclable, effective catalyst for the studied reaction. The presence of an aqueous solution of zinc iodide as a co-catalyst enhances significantly the catalytic activity of PS-TBMAC. Using this two-component catalyst system (polymer-supported quaternary onium salts and aqueous solution of metal salts), the reaction of CO2 with selected epoxides can be conducted with high product yield (71-91%) and selectivity (97-99%) under mild reaction conditions (temperature 110 °C and initial CO2 pressure 0.9 MPa). Propylene carbonate was obtained in the best yield (91%). In addition, the advantages of this method include a short reaction time, solvent-free conditions, and an easy separation of catalyst system.
| Original language | English |
|---|---|
| Pages (from-to) | 266-274 |
| Number of pages | 9 |
| Journal | Applied Catalysis A: General |
| Volume | 482 |
| DOIs | |
| Publication status | Published - 22 Jul 2014 |
Keywords
- Carbon dioxide
- Cyclic alkylene carbonates
- Epoxides
- Metal salts
- Polymer-supported quaternary onium salts
ASJC Scopus subject areas
- Catalysis
- Process Chemistry and Technology
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