环己酮
化学
肟
环己酮肟
羟胺
电化学
组合化学
催化作用
有机化学
电极
物理化学
作者
Yujia Yuan,Lisong Chen,Zhipeng Wan,Kai Shi,Xue Teng,Hao Xu,Peng Wu,Jianlin Shi
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-05-24
卷期号:10 (21)
标识
DOI:10.1126/sciadv.ado1755
摘要
State-of-the-art technology for cyclohexanone oxime production typically demands elevated temperature and pressure, along with the utilization of expensive hydroxylamine sulfate or oxidants. Here, we propose an electrochemistry-assisted cascade strategy for the efficient cyclohexanone ammoximation under ambient conditions by using in situ cathode-generated green oxidants of reactive oxygen species (ROS) such as OOH* and H 2 O 2 . This electrochemical reaction can take place at the cathode, achieving over 95% yield, 99% selectivity of cyclohexanone oxime, and an electron-to-oxime (ETO) efficiency of 96%. Mechanistic analysis reveals that, in addition to the direct ammoximation by in situ–generated OOH* by electrocatalytic ORR, Ti-MOR also play a major role in capturing OOH* directly and converting the in situ–generated H 2 O 2 to OOH*, thus accelerating the ORR-coupled cascade production of cyclohexanone oxime. This work paves a mild, economical, and sustainable energy-efficient electrocatalytic route for the oxime production using oxygen, ammonium bicarbonate, and cyclohexanone.
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