Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 32-37 |
| Number of pages | 6 |
| Journal | Frontiers of Environmental Science and Engineering in China |
| Volume | 3 |
| Issue number | 1 |
| Early online date | 21 Nov 2008 |
| DOIs | |
| Publication status | Published - Mar 2009 |
User-Defined Keywords
- Carbon dioxide
- Cationic organobismuth complex
- Coupling
- Cyclic carbonate
- Terminal epoxide
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