Abstract
A series of functionalized ionic liquids (ILs) immobilized on B-doped mesoporous SiO2 catalysts were fabricated for effectively converting CO2 into cyclic carbonates under metal-absent and cocatalyst-free conditions. Functionalized imidazolium ILs were in-situ synthesized by Debus-Rdziszewski imidazole reaction. Among the prepared catalysts, 5B−SiO2−NH2−3−I catalyst owing to the synergistic effects of nucleophile, Lewis acid-base and hydroxyl hydrogen bond donors in the catalyst, presented the better catalytic activity for propylene epoxide to the product of propylene carbonate with 99% yield and selectivity at 110 °C and 2 MPa CO2. The catalyst also displayed moderate yield for various mono-substituent epoxides. Besides, the gradual decline in the product yield during consecutive runs could be easily refreshed by aqueous acidic solution washing.
| Original language | English |
|---|---|
| Article number | e202200234 |
| Journal | Asian Journal of Organic Chemistry |
| Volume | 11 |
| Issue number | 8 |
| DOIs | |
| State | Published - Aug 2022 |
| Externally published | Yes |
Keywords
- CO cycloaddition
- Heterogeneous catalysis
- cocatalyst-free
- cyclic carbonate synthesis
- metal-free
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