Suppr超能文献

C Pd 封装在金属-有机骨架 UiO-67 中,具有高催化活性,可用于串联加氢反应。

High Catalytic Activity of C Pd Encapsulated in Metal-Organic Framework UiO-67, for Tandem Hydrogenation Reaction.

机构信息

Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, Guangdong, 515063, China.

出版信息

Chemistry. 2018 Dec 20;24(72):19141-19145. doi: 10.1002/chem.201803900. Epub 2018 Nov 21.

Abstract

Metal nanoparticles (NPs) stabilized by MOFs are very promising for catalysis, whereas introduction of C into MOFs has been very rarely used, and there was no report for their cooperative catalysis in organic syntheses. In this work, C @UiO-67 was synthesized by a one-pot method, so that C is uniformly distributed on UiO-67 in molecular form. Pd NPs coordinating with C have been successfully embedded into the framework. The obtained multifunctional C Pd @UiO-67 catalyst exhibits remarkable synergistic catalytic activity in cascade reactions under mild conditions, where UiO-67 affords Lewis acidity and C Pd offers higher hydrogenation activity relative to solely Pd NPs.

摘要

金属纳米粒子(NPs)被 MOFs 稳定后在催化方面非常有前景,然而,将 C 引入 MOFs 中很少被使用,并且在有机合成中也没有关于它们协同催化的报道。在这项工作中,通过一锅法合成了 C@UiO-67,使得 C 以分子形式均匀分布在 UiO-67 上。与 C 配位的 Pd NPs 已成功嵌入到骨架中。所得到的多功能 C@Pd@UiO-67 催化剂在温和条件下的级联反应中表现出显著的协同催化活性,其中 UiO-67 提供路易斯酸度,而 C@Pd 相对于单独的 Pd NPs 提供更高的加氢活性。

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