环氧化物
催化作用
环加成
路易斯酸
亲核细胞
化学
部分
离子液体
环氧丙烷
协同催化
溴化物
组合化学
有机化学
共聚物
聚合物
环氧乙烷
作者
Moliang Zou,Weili Dai,Mao Pei,Bing Li,Jie Mao,Shuqu Zhang,Lixia Yang,Shenglian Luo,Xubiao Luo,Jian‐Ping Zou
标识
DOI:10.1016/j.micromeso.2020.110750
摘要
The rational integration of multiple functional components into a suitable matrix material is a promising strategy for constructing efficient catalysts for specific applications. Herein, a novel Zn-containing imidazolium bromide was facilely anchored onto MIL-101(Cr) (MIL-101(Cr)-(AIm)2ZnBr2) via a coordination bond between the amino group in ionic liquid (IL) moiety and unsaturated Cr3+ center in MOF framework, which catalyzed the efficient synthesis of cyclic carbonates through the cycloaddition of CO2 and epoxides. The as-prepared MIL-101(Cr)-(AIm)2ZnBr2 groups the essential factors that facilitate the superb cycloaddition efficiency, involving: (1) Cr (III) and Zn (II) working as Lewis acid sites for polarizing epoxide; (2) amino groups and ternary N species as Lewis basic sites for activating CO2; (3) Br− anion as nucleophile to accelerate the opening of epoxy ring. Combining the high surface area (1146 m2/g) and numerous open pores, a high up to 97.3% of propylene carbonate yield and 100% of selectivity are achieved. Additionally, benefited from its good chemical stability, the catalyst maintains its high activity even after five successive runs. This work proposes a new strategy for constructing multifunctional catalyst for CO2 conversion by highlighting the synergistic effect enabled by one host.
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