苯甲醇
苯甲醛
催化作用
光催化
产量(工程)
化学
量子产额
转移加氢
选择性
光化学
有机合成
组合化学
材料科学
有机化学
物理
量子力学
钌
冶金
荧光
作者
Jiahao Li,Shu‐Lin Meng,Xinling Zhang,Yulin Yin,Chen‐Ho Tung,Li‐Zhu Wu
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-06-06
卷期号:64 (32): e202508442-e202508442
被引量:1
标识
DOI:10.1002/anie.202508442
摘要
Abstract Inspired by the secondary coordination sphere of nitrite reductase, we report herein the first photocatalytic benzaldoxime synthesis from NO x − ( x = 2, 3) and benzyl alcohol. Different from introducing co‐catalysts, the integration of glutathione (GSH) relay with CdS quantum dots (QDs) can effectively mediate hole transfer and facilitate selective benzyl alcohol oxidation to benzaldehyde. At the same time, GSH assists continuous proton transfer to promote selective NO x − reduction and form NH 2 OH in situ. As a result, the synergic C–N coupling delivers a series of benzyl oximes from NO x − and benzyl alcohols with excellent yield and selectivity. Benzaldoxime synthesis proceeds at a rate of 18.7 mmol g cat −1 h −1 and TON of 52,875, accomplishing 90.6% benzyl alcohol conversion and 72.3% benzaldoxime yield, which is comparable to the best records for electrocatalytic benzaldoxime synthesis. The excellent long‐term recyclability and scaled reaction to produce 0.58 g benzaldoxime with a yield of 41% demonstrate efficient, atom‐economic, and step‐economic photocatalytic oxime synthesis via selective C–N coupling from abundant resources.
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