化学
催化作用
组合化学
有机化学
纳米技术
材料科学
作者
Shibo Xu,Yicong Li,Tianhao Yu,Jinyu Guo,Cao Yun,ZhongXiang Zhang,Chao Liu,Jingjing Wu,Fanhong Wu
标识
DOI:10.1002/ejoc.202500194
摘要
A green light‐driven, organophosphine‐catalyzed iododifluoroalkylation of alkynes using iododifluoroketones has been developed, eliminating the need for additional metal catalysts and bases. This protocol enables the efficient and sustainable synthesis of CF2‐derived alkenyl iodides under mild conditions, demonstrating excellent tolerance to iododifluoroketones, iododifluoroesters, and perfluoroalkyl iodides. Preliminary mechanistic studies suggest that the catalytic phosphine functions not only as a Lewis base, forming a charge‐transfer complex with difluoroalkyl iodides through halogen‐bonding interactions to generate Rf radicals, but also as a halogen transfer shuttle catalyst to facilitate the catalytic cycle.
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