Direct arylation reaction of heteroarenes mediated by photoinduced electron transfer

IF 3.261 Journal of Photochemistry and Photobiology Pub Date : 2023-08-01 Epub Date: 2023-05-25 DOI:10.1016/j.jpap.2023.100183
Eiji Yamaguchi, Oe Karin, Akichika Itoh
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引用次数: 0

Abstract

Electron donor–acceptor (EDA) complexes are interesting chemical species that function as molecular complexes. In this context, chemists have actively studies the use of halogen bonding as a noncovalent interaction in photochemistry. This study focused on developing a direct arylation reaction using aryl radicals generated by photoinduced electron transfer (PET) through halogen-bonding interactions. The study also involves optimizing reaction conditions for a photo induced direct arylation reaction using phenols as halogen bonding acceptor and plausible reaction mechanism. Our results demonstrated that this method provides a facile and efficient approach for synthesizing complex biaryls containing heteroarens using readily available heteroarenes.

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光诱导电子转移介导的杂芳烃直接芳基化反应
电子供体-受体(EDA)复合物是一种具有分子复合物功能的化学物质。在此背景下,化学家们积极研究利用卤素键作为光化学中的非共价相互作用。本研究的重点是利用光诱导电子转移(PET)通过卤素键相互作用产生的芳基自由基进行直接芳基化反应。本研究还优化了以苯酚为卤素键受体的光诱导直接芳基化反应的反应条件和反应机理。结果表明,该方法是一种简便、有效的合成含杂环芳烃的复合双芳基化合物的方法。
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