Abstract
An asymmetric hydrazide, (12E, 13E)-2-((naphthalen-1-yl) methylene)-1-(1-(2-hydroxynaphthalen-6-yl) ethylidene) hydrazine (abbreviated as AH) is synthesized and characterized by standard techniques and crystal structure of AH has been obtained. The naked eye detection of F− in aqueous acetonitrile (acetonitrile: water=7:3/v:v) by AH has been investigated by UV–Visible titration and in presence of other anions, the limit of detection being 1.31×10−6(M). The mechanism of F− sensing has been explored by 1H NMR titration. AH undergoes hydrogen bonding with F− followed by deprotonation. The practical utility of AH has been explored by successful test kit response and color change in toothpaste solution.
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More From: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
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