脂质过氧化
化学
共轭体系
光化学
活性氧
猝灭(荧光)
光动力疗法
取代基
荧光
激进的
分子
紧身衣
组合化学
生物物理学
抗氧化剂
有机化学
生物化学
物理
量子力学
聚合物
生物
作者
Jianqing Li,Zeyan Zhuang,Jingjing Guo,Xiaobin Dong,Junyi Gong,Ben Zhong Tang,Zujin Zhao
标识
DOI:10.1002/advs.202305516
摘要
Abstract Photocyclization is demonstrated as a powerful tool for building complicated polycyclic molecules. And efficient photocyclization is competent as an artful strategy to develop photo‐responsive smart materials. Herein, an efficient free radical‐mediated photocyclization for triphenylphosphindole oxide (TPPIO) derivatives to generate tribenzophosphindole oxide (TBPIO) derivatives at ambient condition is reported. The reaction mechanism and substituent effect on photocyclization efficiency are thoroughly investigated. Additionally, photophysical and photochemical properties of TPPIO and TBPIO derivatives are measured for comparison and deeply deciphered by theoretical calculation. TPPIO derivatives own typical aggregation‐induced emission feature but barely generate reactive oxygen species (ROS), while TBPIO derivatives experience aggregation‐caused quenching but show efficient Type I ROS generation capacity. Further, in vitro experiments demonstrate that this photo‐conversion can efficiently occur in situ in living cells to activate photodynamic therapy (PDT) effect to trigger lipid peroxidation with selective fluorescence “light up” in lipid droplet area under continuous irradiation. This work extends the optoelectronically and biologically interesting phosphindole oxide‐containing π‐conjugated systems through an efficient synthetic strategy, provides in‐depth mechanistic descriptions in the aspects of reaction and property, and further presents their great potentials for photoactivated and self‐reported PDT.
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