Suppr超能文献

糠醛和 5-(羟甲基)糠醛的还原升级的催化转移加氢/氢解反应。

Catalytic transfer hydrogenation/hydrogenolysis for reductive upgrading of furfural and 5-(hydroxymethyl)furfural.

机构信息

Institute for Chemical and Bioengineering, ETH Zürich, Wolfgang-Pauli-Strasse 10, 8093 Zürich (Switzerland), Fax: (+41) 44-633-42-58.

出版信息

ChemSusChem. 2014 Jan;7(1):268-75. doi: 10.1002/cssc.201300774. Epub 2013 Nov 13.

Abstract

The sequential transfer hydrogenation/hydrogenolysis of furfural and 5-hydroxymethylfurfural to 2-methylfuran and 2,5-dimethylfuran was studied over in situ reduced, Fe2 O3 -supported Cu, Ni, and Pd catalysts, with 2-propanol as hydrogen donor. The remarkable activity of Pd/Fe2 O3 in both transfer hydrogenation/hydrogenolysis is attributed to a strong metal-support interaction. Selectivity towards hydrogenation, hydrogenolysis, decarbonylation, and ring-hydrogenation products is shown to strongly depend on the Pd loading. A significant enhancement in yield to 62%, of 2-methylfuran and 2-methyltetrahydrofuran was observed under continuous flow conditions.

摘要

糠醛和 5-羟甲基糠醛经串联转移加氢/氢解反应生成 2-甲基呋喃和 2,5-二甲基呋喃,在原位还原的 Fe2 O3 负载 Cu、Ni 和 Pd 催化剂上,以 2-丙醇作为氢供体进行了研究。Pd/Fe2 O3 在转移加氢/氢解中均表现出显著的活性,这归因于较强的金属-载体相互作用。加氢、氢解、脱羰和环加氢产物的选择性强烈依赖于 Pd 的负载量。在连续流动条件下,观察到 2-甲基呋喃和 2-甲基四氢呋喃的产率显著提高到 62%。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验