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首页> 外文期刊>Angewandte Chemie >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:支持离子液相中的双金属纳米颗粒作为芳族基材选择性加氢氧基的多官能催化剂

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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:嵌入在酸性负载的离子液相(Feru @ Silp + IL-SO3H)中嵌入的双金属铁钌纳米颗粒充当多官能催化剂,用于芳族底物中的羰基的选择性加氢氧基。 催化剂材料从分子组分系统地组装,以将允许允许氢解的酸和金属位点组合,而无需氢化芳环。 所得材料具有高活性和稳定性,C = O基团的催化加氢氧基在各种取代的芳族酮中的CH2单元中,因此提供了一种有效和良性替代传统的Clemmenenen和Wolff-Kishner减少,这需要化学计量试剂 。 Feru @ Silp + IL-SO3H材料的分子设计为多官能催化系统(MM @ Silp + IL-Func)打开了一般的方法。

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