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有机合成中的光致配体到金属电荷转移(LMCT):反应模式与研究进展

Photoinduced ligand-to-metal charge transfer (LMCT) in organic synthesis: reaction modes and research advances.

作者信息

Yang Yingying, Huang Xinxiang, Jin Yi

机构信息

Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, Yunnan Provincial Center for Research & Development of Natural Products, School of Pharmacy, Yunnan University, Kunming, 650091, P. R. China.

出版信息

Chem Commun (Camb). 2025 Jan 28;61(10):1944-1961. doi: 10.1039/d4cc06099g.

Abstract

In recent years, visible light-induced ligand-to-metal charge transfer (LMCT) has emerged as an attractive approach for synthesizing a range of functionalized molecules. Compared to conventional photoredox reactions, photoinduced LMCT activation does not depend on redox potential and offers diverse reaction pathways, making it particularly suitable for the activation of inert bonds and the functional modification of complex organic molecules. This review highlights the indispensable role of photoinduced LMCT in synthetic chemistry, with a focus on recent advancements in LMCT-mediated hydrogen atom transfer (HAT), C-C bond cleavage, decarboxylative transformations, and radical ligand transfer (RLT) reactions.

摘要

近年来,可见光诱导的配体到金属的电荷转移(LMCT)已成为合成一系列功能化分子的一种有吸引力的方法。与传统的光氧化还原反应相比,光诱导的LMCT活化不依赖于氧化还原电位,并提供多种反应途径,使其特别适用于惰性键的活化和复杂有机分子的功能修饰。本综述强调了光诱导LMCT在合成化学中不可或缺的作用,重点关注LMCT介导的氢原子转移(HAT)、C-C键裂解、脱羧转化和自由基配体转移(RLT)反应的最新进展。

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