化学
检出限
荧光
荧光团
硫化氢
葡萄酒
分析物
选择性
转身(生物化学)
聚集诱导发射
组合化学
色谱法
生物化学
催化作用
硫黄
有机化学
物理
食品科学
量子力学
作者
Yanan Meng,Xinya Yao,Keli Zhong,Yang Li,Lijun Tang
标识
DOI:10.1002/ejoc.202300022
摘要
Abstract Hydrogen sulfide (H 2 S), as one of the important endogenous biological regulators, plays a critical role in mediating a wide range of physiological processes. The development of rapid, sensitive, and reliable detection techniques for H 2 S would be highly appealing. In this paper, a new type of AIE‐based fluorescence turn‐on probe TPA‐M for the detection of H 2 S has been constructed, involved the rapid release of AIE‐based fluorophore TPA‐CHO with a remarkable fluorescence turn‐on phenomenon in THF/H 2 O (2/8, v/v, HEPES=20 μM, pH=7.3) medium, exhibiting the attractive advantages such as high sensitivity with the detection limit as low as 1.92×10 −3 ppm, excellent selectivity over other anion analytes and biothiols, significant anti‐interference ability and fast response time (within 10 min). What's more, the practical application evaluation indicated that the probe TPA‐M could be efficiently employed in imaging exogenously added H 2 S in living MCF‐7 cells and detecting H 2 S in actual water and wine samples.
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