首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >Bimetallic Nanoparticles in Supported Ionic Liquid Phases as Multifunctional Catalysts for the Selective Hydrodeoxygenation of Aromatic Substrates
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Bimetallic Nanoparticles in Supported Ionic Liquid Phases as Multifunctional Catalysts for the Selective Hydrodeoxygenation of Aromatic Substrates

机译:负载离子液体中的双金属纳米颗粒作为芳香族底物选择性加氢脱氧的多功能催化剂

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摘要

Bimetallic iron–ruthenium nanoparticles embedded in an acidic supported ionic liquid phase (FeRu@SILP+IL‐SO3H) act as multifunctional catalysts for the selective hydrodeoxygenation of carbonyl groups in aromatic substrates. The catalyst material is assembled systematically from molecular components to combine the acid and metal sites that allow hydrogenolysis of the C=O bonds without hydrogenation of the aromatic ring. The resulting materials possess high activity and stability for the catalytic hydrodeoxygenation of C=O groups to CH2 units in a variety of substituted aromatic ketones and, hence, provide an effective and benign alternative to traditional Clemmensen and Wolff–Kishner reductions, which require stoichiometric reagents. The molecular design of the FeRu@SILP+IL‐SO3H materials opens a general approach to multifunctional catalytic systems (MM′@SILP+IL‐func).
机译:嵌入酸性支持的离子液相(FeRu @ SILP + IL-SO3H)中的双金属铁-钌纳米粒子充当多功能催化剂,用于芳香族基质中羰基的选择性加氢脱氧。催化剂材料由分子组分系统地组装,以结合酸和金属位点,从而允许C = O键的氢解而无需芳族环的氢化。所得材料具有高活性和稳定性,可在多种取代的芳族酮中将C = O基团催化加氢脱氧成CH2单元,因此,它是传统的Clemmensen和Wolff-Kishner还原反应的有效且良性的替代方法,后者需要化学计量试剂。 FeRu @ SILP + IL-SO3H材料的分子设计为多功能催化系统(MM'@ SILP + IL-func)开辟了一条通用途径。

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