铜
反向
电合成
催化作用
苯甲醛
联轴节(管道)
产量(工程)
箔法
纳米材料基催化剂
材料科学
羟胺
无机化学
多相催化
纳米技术
化学工程
工作(物理)
电化学
化学
电解
偶联反应
甲烷氧化偶联
作者
Yandong Wu,Jiawang Chen,Ta Thi Thuy Nga,Yanzhi Xu,Mengyi Qiu,Dongdong Wang,Ruiqi Wang,Chao Xie,Wenjie Wu,Qinghua Liu,Chung‐Li Dong,Shuangyin Wang,Yuqin Zou
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-10-17
卷期号:64 (51): e202517830-e202517830
被引量:4
标识
DOI:10.1002/anie.202517830
摘要
Abstract Exposed coordinatively unsaturated sites (CUS) with the reducing geometrical sizes of catalysts commonly offers significant advantages in heterogeneous electrocatalytic processes. However, this empirical rule might be unsuitable for the innovative electrocatalytic C–N coupling reaction, as one of the parallel reactions. In this study, we observe an inverse size‐effect in the electrocatalytic synthesis of benzaldehyde oximes (BAO) from nitrates and benzaldehyde. Cu nanocatalysts with more exposed CUS thermodynamically favor the over‐reduction of coupling intermediates, i.e., adsrobed hydroxylamine (*NH 2 OH) and benzaldehyde (*Ph‐CHO), leading to a low BAO yield. Notably, Cu foil with few CUS enables the enrichment of *NH 2 OH and *Ph‐CHO, achieving a BAO yield of 91%. Moreover, this electrosynthesis strategy on Cu foil demonstrates versatility and broad applicability for producing various oximes. This work highlights the significant potential of inverse size effects in guiding the design of catalysts for electrocatalytic C–N coupling reactions.
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