New sensing mechanisms for design of fluorescent chemosensors emerging in recent years

费斯特共振能量转移 荧光 分子内力 化学 准分子 光化学 超分子化学 纳米技术 分子 材料科学 立体化学 有机化学 量子力学 物理
作者
Jiasheng Wu,Weimin Liu,Jiechao Ge,Hongyan Zhang,Pengfei Wang
出处
期刊:Chemical Society Reviews [Royal Society of Chemistry]
卷期号:40 (7): 3483-3483 被引量:1740
标识
DOI:10.1039/c0cs00224k
摘要

During the past decade, fluorescent chemosensors have become an important research field of supramolecular chemistry and have attracted great attention because of their simplicity, high selectivity and sensitivity in fluorescent assays. In the design of new fluorescent chemosensors, exploration of new sensing mechanisms between recognition and signal reporting units is of continuing interest. Based on different photophysical processes, conventional sensing mechanisms including photo-induced electron transfer (PET), intramolecular charge transfer (ICT), metal-ligand charge transfer (MLCT), twisted intramolecular charge transfer (TICT), electronic energy transfer (EET), fluorescence resonance energy transfer (FRET), and excimer/exciplex formation have been investigated and reviewed extensively in the literature. This tutorial review will mainly focus on new fluorescent sensing mechanisms that have emerged in the past five years, such as aggregation-induced emission (AIE) and C=N isomerization, which can be ascribed to fluorescence changes via conformational restriction. In addition, excited-state intramolecular proton transfer (ESIPT) has not been well reviewed yet, although a number of chemosensors based on the ESIPT mechanism have been reported. Thus, ESIPT-based chemosensors have been also summarized in this review.
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