首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Bifunctional MOF heterogeneous catalysts based on the synergy of dual functional sites for efficient conversion of CO2 under mild and co-catalyst free conditions
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Bifunctional MOF heterogeneous catalysts based on the synergy of dual functional sites for efficient conversion of CO2 under mild and co-catalyst free conditions

机译:基于双功能位点协同作用的双功能MOF非均相催化剂,可在温和无助催化剂条件下有效转化CO2

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摘要

We reported herein a strategy for combining CUS-based MOF (CUS = coordinatively unsaturated metal sites) with ionic liquid (IL) functional sites to form bifunctional heterogeneous catalysts with extra high activity for CO2 fixation. Based on this strategy, two quaternary ammonium salt and quaternary phosphorus salt ionic liquid functionalized CUS-containing MOF heterogeneous catalysts, MIL-101-N-(n-Bu)(3)Br and MIL-101-P(n-Bu)(3)Br, have been prepared for the first time by a post-synthesis modification method. Due to the synergetic role of dual functional sites including Lewis acid sites in the MOF framwork and Br- ions in the IL functional sites, MIL-101-N(n-Bu)(3)Br and MIL-101-P(n-Bu)(3)Br exhibit high catalytic activity for the cycloaddition of CO2 and epoxide under mild and co-catalyst free conditions, which significantly outperforms other benchmark MOF catalysts. Moreover, such bifunctional catalysts can be easily recovered and recycled several times without leaching and loss of activity. Our work thus paves a way for the development of IL functionalized MOFs as heterogeneous catalysts for CO2 fixation.
机译:我们在本文中报道了将基于CUS的MOF(CUS =配位不饱和金属位点)与离子液体(IL)功能位点结合以形成具有更高活性的CO2固定双功能多相催化剂的策略。基于此策略,两种季铵盐和季磷盐离子液体官能化的含CUS的MOF多相催化剂MIL-101-N-(n-Bu)(3)Br和MIL-101-P(n-Bu)( 3)Br,是通过后合成修饰方法首次制备的。由于双功能位点(包括MOF框架中的Lewis酸位点和IL功能位点中的Br-)具有协同作用,MIL-101-N(n-Bu)(3)Br和MIL-101-P(n- Bu)(3)Br在温和和无助催化剂的条件下,对CO2和环氧化物的环加成反应具有很高的催化活性,这明显优于其他基准MOF催化剂。而且,这样的双官能催化剂可以容易地回收和再循环几次,而不会浸出和失去活性。因此,我们的工作为开发IL功能化的MOF作为固定CO2的非均相催化剂铺平了道路。

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