Abstract
Development of efficient, cheap and recyclable catalysts for a reaction under green reaction conditions is still a very attractive topic. In this work, the cycloaddition reactions of CO2 with various epoxides to form five-membered cyclic carbonates catalyzed by chitosan functionalized 1-ethyl-3-methyl imidazolium halides (CS-EMImX, X = Cl, Br) without additional solvent and metal co-catalyst were achieved in high yield and selectivity. The catalyst could be easily recovered and reused five times with high catalytic activity and selectivity. Besides, a possible catalytic cycle for the hydrogen bond assisted ring-opening of epoxide and activation of CO2 induced by the nucleophilic tertiary nitrogen of the chitosan was also proposed. The process represents a simple, ecologically safe and cost-effective route to synthesize cyclic carbonates with high product yield, as well as easy catalyst recycling.
| Original language | English |
|---|---|
| Pages (from-to) | 654-660 |
| Number of pages | 7 |
| Journal | Green Chemistry |
| Volume | 14 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 3 Jan 2012 |
| Externally published | Yes |
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