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首页> 外文期刊>Angewandte Chemie >Concentrating Immiscible Molecules at Solid@MOF Interfacial Nanocavities to Drive an Inert Gas-Liquid Reaction at Ambient Conditions
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Concentrating Immiscible Molecules at Solid@MOF Interfacial Nanocavities to Drive an Inert Gas-Liquid Reaction at Ambient Conditions

机译:在固体@ MOF界面纳米覆盖物中浓缩不混溶的分子,在环境条件下驱动惰性气液反应

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Gas-liquid reactions form the basis of our everyday lives, yet they still suffer poor reaction efficiency and are difficult to monitor insitu, especially at ambient conditions. Now, an inert gas-liquid reaction between aniline and CO2 is driven at 1atm and 298K by selectively concentrating these immiscible reactants at the interface between metal-organic framework and solid nanoparticles (solid@MOF). Real-time reaction SERS monitoring and simulations affirm the formation of phenylcarbamic acid, which was previously undetectable because they are unstable for post-reaction treatments. The solid@MOF ensemble gives rise to a more than 28-fold improvement to reaction efficiency as compared to ZIF-only and solid-only platforms, emphasizing that the interfacial nanocavities in solid@MOF are the key to enhance the gas-liquid reaction. Our strategy can be integrated with other functional materials, thus opening up new opportunities for ambient-operated gas-liquid applications.
机译:气液反应形成我们日常生活的基础,但它们仍然遭受较差的反应效率,并且难以监测Insitu,特别是在环境条件下。 现在,通过在金属 - 有机骨架和固体纳米颗粒之间的界面处选择这些不混溶的反应物,在1ATM和298K处在1ATM和298K处被驱动苯胺和CO 2之间的惰性气液反应。 实时反应SERS监测和仿真肯定了苯基氨基甲酸的形成,其预先不可检测,因为它们对后反应后处理不稳定。 与ZIF-ONLE和仅实体平台相比,固体@ MOF合奏会产生超过28倍的反应效率的改善,强调固体@ MOF的界面纳米盖是增强气液反应的关键。 我们的策略可以与其他功能材料集成,从而开辟了环境运行的气液应用的新机会。

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