Department of Chemistry, The University of Manchester, Manchester, UK.
Angew Chem Int Ed Engl. 2023 Jul 17;62(29):e202303104. doi: 10.1002/anie.202303104. Epub 2023 May 3.
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.
电子给体-受体(EDA)复合物的光激活已成为生成自由基的一种可持续、选择性和通用的策略。然而,EDA 络合对供体和受体组件施加了电子约束,这可能会限制使用该方法生成的自由基的范围。利用𬭸盐的新型 EDA 络合策略允许从天然官能团生成自由基。例如,通过芳环的活化形成的芳基𬭸盐由于其缺电子性质可以作为 EDA 络合物中的受体组件。这种“𬭸标签”方法放宽了对母体底物的电子约束,并极大地扩展了可以使用 EDA 络合生成的自由基的范围。在这篇综述中,将介绍这些𬭸盐的新应用,并强调通过这种创新可以获得的化学空间区域。