A colorimetric and turn-on fluorescent chemosensor for selectively sensing Hg2+ and its resultant complex for fast detection of I- over S2-

被引:28
|
作者
Huang, Ximing [1 ]
Lu, Zhengliang [1 ]
Wang, Zhuo [2 ,3 ]
Fan, Chunhua [1 ]
Fan, Wenlong [1 ]
Shi, Xiaomin [1 ]
Zhang, Haitao [1 ]
Pei, Meishan [1 ]
机构
[1] Univ Jinan, Shandong Univ, Sch Chem & Chem Engn, Key Lab Chem Sensing & Anal, Jinan 250022, Peoples R China
[2] Beijing Univ Chem Technol, Coll Sci, Beijing 100029, Peoples R China
[3] Hunan Univ, State Key Lab Chem Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Colorimetric; Chemosensor; Mercury; Iodide; Sulphide; Fluorescence; HYDROGEN-SULFIDE; AQUEOUS-SOLUTION; SENSITIVE DETECTION; INORGANIC MERCURY; PROBE; IODIDE; SENSOR; FRET; BODIPY; ANION;
D O I
10.1016/j.dyepig.2016.01.008
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A novel bipyridine-functionalized turn-on fluorescent chemosensor was successfully synthesized and fully characterized by H-1 NMR, C-13 NMR and MS, UV-vis and fluorescence spectroscopies. The sensor specifically binds to Hg2+ over other competing ions with a significant fluorescence enhancement as well as a visual colour change under physiological conditions. The detection limit of Hg2+ was as low as 32 nM, confirming very high sensitivity toward Hg2+. Moreover, the fluorescence intensity and colour change of the sensor-Hg2+ was quenched by I- or S2- and was proportional to their concentrations with a detection limit of 0.37 mu M and 0.43 mu M, respectively. The reaction of I- grabbing Hg2+ from the sensor-Hg2+ finished in 10 s due to a stronger binding force, much faster than that of S2-, which allowed fast detection of I- over S2- even in a competent environment. In addition, the sensor was successfully used for the highly sensitive detection of Hg2+ in living cells. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:33 / 40
页数:8
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