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使用纳米结构镍核壳催化剂对烯烃进行环境氢化和氘化反应。

Ambient Hydrogenation and Deuteration of Alkenes Using a Nanostructured Ni-Core-Shell Catalyst.

作者信息

Gao Jie, Ma Rui, Feng Lu, Liu Yuefeng, Jackstell Ralf, Jagadeesh Rajenahally V, Beller Matthias

机构信息

Leibniz Leibniz-Institut für Katalyse e.V., Albert-Einstein-Strasse 29a, 18059, Rostock, Germany.

Dalian National Laboratory for Clean Energy (DNL), Dalian Institute of Chemical Physics, Chinese Academy of Science, 457 Zhongshan Road, 116023, Dalian, China.

出版信息

Angew Chem Int Ed Engl. 2021 Aug 16;60(34):18591-18598. doi: 10.1002/anie.202105492. Epub 2021 Jun 24.

Abstract

A general protocol for the selective hydrogenation and deuteration of a variety of alkenes is presented. Key to success for these reactions is the use of a specific nickel-graphitic shell-based core-shell-structured catalyst, which is conveniently prepared by impregnation and subsequent calcination of nickel nitrate on carbon at 450 °C under argon. Applying this nanostructured catalyst, both terminal and internal alkenes, which are of industrial and commercial importance, were selectively hydrogenated and deuterated at ambient conditions (room temperature, using 1 bar hydrogen or 1 bar deuterium), giving access to the corresponding alkanes and deuterium-labeled alkanes in good to excellent yields. The synthetic utility and practicability of this Ni-based hydrogenation protocol is demonstrated by gram-scale reactions as well as efficient catalyst recycling experiments.

摘要

本文介绍了一种用于多种烯烃选择性氢化和氘化的通用方案。这些反应成功的关键是使用一种特定的基于镍-石墨壳的核壳结构催化剂,该催化剂可通过在氩气气氛下于450°C将硝酸镍浸渍在碳上并随后煅烧方便地制备。应用这种纳米结构催化剂,工业和商业上重要的末端烯烃和内烯烃在环境条件下(室温,使用1巴氢气或1巴氘气)均能被选择性氢化和氘化,以良好至优异的产率得到相应的烷烃和氘标记的烷烃。通过克级反应以及高效的催化剂循环实验证明了这种基于镍的氢化方案的合成实用性和实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10dd/8453733/41748e4c5c68/ANIE-60-18591-g006.jpg

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