荧光团
荧光
分子内力
化学
检出限
光化学
光诱导电子转移
电子转移
选择性
Mercury(编程语言)
猝灭(荧光)
计算机科学
立体化学
色谱法
生物化学
量子力学
物理
催化作用
程序设计语言
作者
Xiang Cheng,Shuai Huang,Lei Qian,Fei Chen,Fan Zheng,Shibo Zhong,Xueyan Huang,Bin Feng,Xueping Feng,Wenbin Zeng
标识
DOI:10.1016/j.cclet.2021.10.024
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.
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