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原位光谱研究苄醇的氧化脱氢和歧化反应。

In situ spectroscopic investigation of oxidative dehydrogenation and disproportionation of benzyl alcohol.

机构信息

Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Cardiff, CF10 3AT, UK.

出版信息

Phys Chem Chem Phys. 2013 Aug 7;15(29):12147-55. doi: 10.1039/c3cp50710f. Epub 2013 May 15.

Abstract

In the solvent free oxidation of benzyl alcohol, using supported gold-palladium nanoalloys, toluene is often one of major by-products and it is formed by the disproportionation of benzyl alcohol. Gold-palladium catalysts on acidic supports promote both the disproportionation of benzyl alcohol and oxidative dehydrogenation to form benzaldehyde. Basic supports completely switch off disproportionation and the gold-palladium nanoparticles catalyse the oxidative dehydrogenation reaction exclusively. In an attempt to provide further details on the course of these reactions, we have utilized in situ ATR-IR, in situ DRIFT and inelastic neutron scattering spectroscopic methods, and in this article we present the results of these in situ spectroscopic studies.

摘要

在无溶剂条件下,使用负载型金钯纳米合金氧化苄醇时,甲苯通常是主要的副产物之一,它是由苄醇的歧化反应生成的。酸性载体上的金钯催化剂同时促进苄醇的歧化和氧化脱氢生成苯甲醛。碱性载体完全阻止了歧化反应,金钯纳米粒子则专一催化氧化脱氢反应。为了进一步了解这些反应的过程,我们采用了原位衰减全反射红外光谱(ATR-IR)、原位漫反射红外光谱(DRIFT)和非弹性中子散射光谱学方法,本文介绍了这些原位光谱研究的结果。

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