化学
钯
反应性(心理学)
还原消去
协调球
烷基
氧化加成
外层电子转移
立体化学
计算化学
分子
有机化学
离子
催化作用
医学
替代医学
病理
作者
Haobin Li,Rui Feng,Guo Wang,Yimeng Wang,W.‐C. LIU,Shuai Guo
摘要
Despite recent advancements in synthetic methods for palladium-catalyzed C-F couplings, the mechanistic understanding─particularly concerning high-valent palladium species─remains underexplored. In contrast to the commonly proposed inner-sphere mechanism, which involves C-F reductive elimination at a palladium(IV) center, the outer-sphere pathway is poorly understood, and little experimental evidence has been provided using well-defined, isolable high-valent Pd systems. In this study, we present the design and synthesis of a series of isolable and characterizable palladium(IV) alkyl systems. Their reactivity in C-F bond formation has been investigated and systematically compared. Through the isolation of intermediates, reactivity comparisons, kinetic studies, and DFT calculations, this work presents, for the first time, isolable palladium(IV) model systems that enable the direct observation of C-F bond formation via an outer-sphere pathway.
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