均分解
催化作用
芳基
卤化物
光化学
亲核细胞
基质(水族馆)
偶联反应
联轴节(管道)
金属
化学
组合化学
卤代芳基
材料科学
过渡金属
化学反应
均相催化
反应条件
反应中间体
反应机理
化学合成
还原消去
作者
Geyang Song,Jiameng Song,Qi Li,Xiaoli Shi,Xinyi Liu,Deng Pan,Tengfei Kang,Jianyang Dong,Gang Li,Huaming Sun,Juan Fan,Chao Wang,Dong Xue
标识
DOI:10.1038/s41467-026-70925-y
摘要
Abstract Photoinduced transition metal catalysis offers innovative strategies for fostering novel chemical reactions and improving established ones. In this work, we present a highly efficient, photoinduced Mn(II)-bipyridine catalyzed C–N, C-O and C-S coupling reaction between aryl halides—particularly less reactive aryl chlorides—and nucleophiles containing nitrogen, oxygen, and sulfur. This protocol does not need an external photocatalyst, as the single Mn(II)–bipyridine complex simultaneously serves as both the light-harvester and the metal catalyst. This method exhibits excellent substrate scope, covering eight different nitrogen sources for C-N coupling, as well as C-O coupling with alcohols, C-S coupling with thiophenols, encompassing more than 150 examples, with yields reaching up to 94%. Mechanistic studies suggest that this reaction may be initiated and sustained by the Mn(I) species through the photoinduced homolysis of the catalyst precursor bipyridine-Mn(II)(OAc) 2 , likely proceeding via a Mn(I)/Mn(III) catalytic cycle.
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