| Literature DB >> 25668691 |
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.Entities:
Keywords: Chemosensor; Cyanide; Fluorescent “turn-on”; High sensitivity; Specific selectivity
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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