费斯特共振能量转移
化学
超分子化学
光化学
紧身衣
荧光
蒽
纳米技术
能量转移
组合化学
分子
化学物理
有机化学
量子力学
物理
材料科学
作者
Peipei Jia,Lin Xu,Yi‐Xiong Hu,Weijian Li,Xu-Qing Wang,Qing‐Hui Ling,Xueliang Shi,Guang‐Qiang Yin,Xiaopeng Li,Haitao Sun,Yanrong Jiang,Hai‐Bo Yang
摘要
During the past few decades, fabrication of multistep fluorescence-resonance energy transfer (FRET) systems has become one of the most attractive topics within supramolecular chemistry, chemical biology, and materials science. However, it is challenging to efficiently prepare multistep FRET systems with precise control of the distances between locations and the numbers of fluorophores. Herein we present the successful fabrication of a two-step FRET system bearing specific numbers of anthracene, coumarin, and BODIPY moieties at precise distances and locations through an efficient and controllable orthogonal self-assembly approach based on metal–ligand coordination and host–guest interactions. Notably, the photosensitization efficiency and photooxidation activity of the two-step FRET system gradually increased with the number of energy transfer steps. For example, the two-step FRET system exhibited 1.5-fold higher 1O2 generation efficiency and 1.2-fold higher photooxidation activity than that of its corresponding one-step FRET system. This research not only provides the first successful example of the efficient preparation of multistep FRET systems through orthogonal self-assembly involving coordination and host–guest interactions but also pushes multistep FRET systems toward the application of photosensitized oxidation of a sulfur mustard simulant.
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