催化作用
化学
亲核细胞
光催化
分子内力
组合化学
光催化
过渡金属
表面改性
光化学
反应条件
金属
有机化学
协同催化
反应中间体
氯化物
氧化还原
均相催化
反应中间体
激进的
反应机理
亲核加成
作者
Naoki Oku,Keito Fuke,Rikako Masui,Ken Yamazaki,Yasunori Matsui,Hiroshi Ikeda,Tomoya Miura
标识
DOI:10.1038/s41467-026-69807-0
摘要
Photoredox catalysis enables the generation of radical intermediates under mild conditions, yet photoredox catalysts have heavily relied on precious transition metal complexes. Therefore, the development of photocatalysts based on earth-abundant metals is increasingly demanded. Here, we report a highly photooxidative capability of a heteroleptic copper(II) complex for promoting anti-Markovnikov hydration of alkenes. The copper(II) complex containing bathophenanthroline and 3,4-dimethoxybenzenethiolate ligands is generated in situ from copper(II) chloride dihydrate. Upon visible-light irradiation, the copper(II) complex is photoexcited and exhibits an excited-state lifetime sufficiently long to oxidize various alkenes, including aliphatic substrates. Consequently, anti-Markovnikov hydration can be achieved under mild conditions, and the late-stage functionalization of natural products and pharmaceutical derivatives is also feasible. The developed catalytic system can be extended for photooxidative reactions of alkenes, such as intramolecular cyclization reactions and anti-Markovnikov addition of nucleophiles other than water.
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