硫
接受者
化学
电子受体
激进的
芳基
光化学
电子供体
基质(水族馆)
组合化学
有机化学
盐(化学)
催化作用
物理
烷基
海洋学
地质学
凝聚态物理
作者
Leendert van Dalsen,Rachel E Brown,James A. Rossi‐Ashton,David J. Procter
标识
DOI:10.1002/ange.202303104
摘要
Abstract The photoactivation of electron donor‐acceptor complexes has emerged as a sustainable, selective and versatile strategy for the generation of radical species. Electron donor‐acceptor (EDA) complexation, however, imposes electronic constraints on the donor and acceptor components and this can limit the range of radicals that can be generated using the approach. New EDA complexation strategies exploiting sulfonium salts allow radicals to be generated from native functionality. For example, aryl sulfonium salts, formed by the activation of arenes, can serve as the acceptor components in EDA complexes due to their electron‐deficient nature. This “sulfonium tag” approach relaxes the electronic constraints on the parent substrate and dramatically expands the range of radicals that can be generated using EDA complexation. In this review, these new applications of sulfonium salts will be introduced and the areas of chemical space rendered accessible through this innovation will be highlighted.
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