The exquisite integration of ESIPT, PET and AIE for constructing fluorescent probe for Hg(II) detection and poisoning

被引:35
作者
Cheng, Xiang [1 ,2 ,3 ]
Huang, Shuai [1 ,2 ,3 ]
Lei, Qian [1 ,2 ,3 ]
Chen, Fei [1 ,2 ,3 ]
Zheng, Fan [1 ,2 ,3 ]
Zhong, Shibo [1 ,2 ,3 ]
Huang, Xueyan [1 ,2 ,3 ]
Feng, Bin [1 ,2 ,3 ]
Feng, Xueping [4 ]
Zeng, Wenbin [1 ,2 ,3 ]
机构
[1] Cent South Univ, Xiangya Sch Pharmaceut Sci, Changsha 410013, Peoples R China
[2] Cent South Univ, Mol Imaging Res Ctr, Changsha 410013, Peoples R China
[3] Cent South Univ, Hunan Key Lab Diagnost & Therapeut Drug Res Chron, Changsha 410013, Peoples R China
[4] Cent South Univ, Xiangya Hosp, Changsha 410013, Peoples R China
基金
中国国家自然科学基金;
关键词
Aggregation-induced emission; Excited state intramolecular proton transfer; Photoinduced electron transfer; Mercury ions; Fluorescent imaging; MERCURY POLLUTION; HG2+;
D O I
10.1016/j.cclet.2021.10.024
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Excessive mercury ions (Hg2+) in the environment can accumulate in human body along with the food chain to cause serious physiological reactions. The fluorescence probes were considered as convenient tool with great potential for Hg2+ detection. Most existing probes suffer from aggregation-induced quenching (ACQ) effects and insufficient sensitivity. Herein, a novel type of fluorophore was developed by combining the aggregation-induced emission (AIE) and excited state intramolecular proton transfer (ESIPT) characteristics. Subsequently, a phenyl thioformate group with photoinduced electron transfer (PET) effect was connected to give an efficient "turn-on" probe (HTM), which exhibited good selectivity toward Hg2+, short response time (30 min), coupled with extremely low detection limit (LOD = 1.68 nmol/L). In addition, HTM was used successfully in real samples, cells and drug evaluation, underlying the superiority of HTM to detect Hg2+ in practical applications. (C) 2021 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页码:1861 / 1864
页数:4
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