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首页> 外文期刊>ACS catalysis >MOF-Based Catalysts for Selective Hydrogenolysis of Carbon Oxygen Ether Bonds
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MOF-Based Catalysts for Selective Hydrogenolysis of Carbon Oxygen Ether Bonds

机译:基于MOF的碳氧醚键选择性加氢水解催化剂

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摘要

We demonstrate that metal organic frameworks (MOFs) can catalyze hydrogenolysis of aryl ether bonds under mild conditions. Mg-IRMOF-74(I) and Mg-IRMOF-74(II) are stable under reducing conditions and can cleave phenyl ethers containing beta-O-4, alpha-O-4, and 4-O-5 linkages to the corresponding hydrocarbons and phenols. Reaction occurs at 10 bar H-2 and 120 degrees C without added base. DFT-optimized structures and charge transfer analysis suggest that the MOF orients the substrate near Mg2+ ions on the pore walls. Ti and Ni doping further increase conversions to as high as 82% with 96% selectivity for hydrogenolysis versus ring hydrogenation. Repeated cycling induces no loss of activity, making this a promising route for mild aryl-ether bond scission.
机译:我们证明金属有机框架(MOFs)可以在温和的条件下催化芳基醚键的氢解。 Mg-IRMOF-74(I)和Mg-IRMOF-74(II)在还原条件下稳定,并且可以将含有β-O-4,α-O-4和4-O-5键的苯基醚裂解为相应的碳氢化合物和酚。在不添加碱的情况下,反应在10 bar H-2和120摄氏度下发生。 DFT优化的结构和电荷转移分析表明,MOF将基质定向在孔壁上Mg2 +离子附近。钛和镍的掺杂进一步提高了转化率,使氢解相对于环氢化的转化率高达82%,选择性为96%。重复循环不会引起活性损失,这使其成为轻度芳基-醚键断裂的有前途的途径。

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