Literature DB >> 25668691

Fluorescent "turn-on" detecting CN(-) by nucleophilic addition induced Schiff-base hydrolysis.

Qi Lin1, Yi Cai2, Qiao Li2, Bing-Bing Shi2, Hong Yao2, You-Ming Zhang2, Tai-Bao Wei3.   

Abstract

A new chemosensor Sz based on Schiff-base group as recognition site and naphthalene as the fluorescence signal group was designed and synthesised. It could fluorescent "turn-on" detect cyanide (CN(-)) via a novel mechanism of nucleophilic addition induced Schiff-base hydrolysis. Adding the CN(-) into the solution of Sz could induce Sz to emit blue fluorescence at 435 nm instantly. Moreover, Sz could also colorimetric detect CN(-). Upon the addition of CN(-), the Sz showed dramatic color change from yellow to colorless. These sensing procedures could not be interfered by other coexistent competitive anions such as F(-), AcO(-), H2PO4(-) and SCN(-). In addition, Sz showed high sensitivity for CN(-), the detection limits is 3.42×10(-8) M of CN(-), which is far lower than the WHO guideline of CN(-) in drinking water (less than 1.9×10(-6) M). The CN(-) test strips based on Sz could act as a convenient CN(-) test kits.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Chemosensor; Cyanide; Fluorescent “turn-on”; High sensitivity; Specific selectivity

Mesh:

Substances:

Year:  2015        PMID: 25668691     DOI: 10.1016/j.saa.2015.01.042

Source DB:  PubMed          Journal:  Spectrochim Acta A Mol Biomol Spectrosc        ISSN: 1386-1425            Impact factor:   4.098


  2 in total

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Journal:  Sensors (Basel)       Date:  2016-05-19       Impact factor: 3.576

2.  The Synthesis and Anion Recognition Property of Symmetrical Chemosensors Involving Thiourea Groups: Theory and Experiments.

Authors:  Xuefang Shang; Zhenhua Yang; Jiajia Fu; Peipei Zhao; Xiufang Xu
Journal:  Sensors (Basel)       Date:  2015-11-06       Impact factor: 3.576

  2 in total

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