联苯
苯
催化作用
氢化物
化学
光化学
亲核细胞
联轴节(管道)
铕
偶联反应
药物化学
催化循环
二苯并噻吩
无机化学
材料科学
作者
Yongli Cai,Shixiong Zhang,Yanbo Deng,Li Rao,Jianping Guo,Ping Chen
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-10-18
卷期号:64 (50): e202517421-e202517421
被引量:1
标识
DOI:10.1002/anie.202517421
摘要
Abstract Catalytic coupling of benzene to biphenyl through direct C─H bond activation and C─C bond construction represents an ideal, atom‐economical strategy, offering a streamlined alternative to classical multi‐step functionalization approaches, and thus has been a long‐sought after goal. Herein, we report that such a pathway can be realized over a sub‐nanostructured europium hydride (Eu–H) catalyst under mild condition. The Eu–H catalyst achieved a biphenyl production of 53.7 mmol g Eu −1 with a turnover number (TON) of 16.3 over 144 h at 150 °C. Mechanistic studies suggest that hydride species (H − ) in Eu–H preferentially deprotonate benzene to form a [C 6 H 5 –Eu] intermediate, which subsequently undergoes nucleophilic attack on another benzene molecule, resulting in biphenyl formation and regeneration of the Eu–H species to complete the catalytic cycle. This work not only provides a strategy for benzene coupling to biphenyl but also demonstrates the promising role of hydrides in transforming arenes into value‐added molecules.
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