摘要
Bifunctional Zn-salen complexes with multiple hydrogen bonding donors and protic ammonium bromides were developed as efficient catalysts for the formation of 4-phenyl-1,3-dioxolan-2-one from styrene oxide and CO 2 . Owing to synergistic effects of multiple sites on epoxide activation (Lewis acidic zinc, phenolic hydroxyl group and protonated tertiary ammonium able to activate epoxide and bromide anion acting as a nucleophile), the easily-synthesized Zn-salen complexes showed outstanding performance at mild reaction conditions (CO 2 0.1 MPa, 100 °C) using only 0.3 mol% catalyst amount. Besides, this protocol is applicable to a variety of epoxides including internal epoxide, giving the corresponding cyclic carbonates in good to excellent yields. Notably, 200 mmol-scale experiment was successfully conducted and TON of 49288 ± 13 and TOF of 39473 ± 8 h −1 were achieved.
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