Dual optical detection of a novel selective mercury sensor based on 7-nitrobenzo-2-oxa-1,3-diazolyl subunits

A novel macromolecule based on 2-[3-(2-aminoethylthio)propylthio]ethanamine covalently bound to two 7-nitrobenzo-2-oxa-1,3-diazolyl moieties was prepared as a fluoroionophore and a chromophore for the selective optical detection of Hg2+. The sensor was prepared in two steps and its fluoroionophoric...

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Main Authors: Wanichacheva N., Siriprumpoonthum M., Kamkaew A., Grudpan K.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-61349160485&partnerID=40&md5=a7098bee42609479177ba1c543f30327
http://cmuir.cmu.ac.th/handle/6653943832/5907
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spelling th-cmuir.6653943832-59072014-08-30T03:23:36Z Dual optical detection of a novel selective mercury sensor based on 7-nitrobenzo-2-oxa-1,3-diazolyl subunits Wanichacheva N. Siriprumpoonthum M. Kamkaew A. Grudpan K. A novel macromolecule based on 2-[3-(2-aminoethylthio)propylthio]ethanamine covalently bound to two 7-nitrobenzo-2-oxa-1,3-diazolyl moieties was prepared as a fluoroionophore and a chromophore for the selective optical detection of Hg2+. The sensor was prepared in two steps and its fluoroionophoric and chromophoric properties toward various transition metal, alkali, and alkali earth cations were investigated. Compound 4 selectively binds Hg2+, and the binding is indicated by both fluorescence quenching and a chromogenic change which can be detected by the naked eye. In an 80:20 acetonitrile/water solvent mixture, 4 acts as an ON-OFF fluorescence switch upon Hg2+ binding, exhibiting efficient quenching and a detection limit of 10-7 M or 20 ppb. © 2009 Elsevier Ltd. All rights reserved. 2014-08-30T03:23:36Z 2014-08-30T03:23:36Z 2009 Article 00404039 10.1016/j.tetlet.2009.01.118 TELEA http://www.scopus.com/inward/record.url?eid=2-s2.0-61349160485&partnerID=40&md5=a7098bee42609479177ba1c543f30327 http://cmuir.cmu.ac.th/handle/6653943832/5907 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description A novel macromolecule based on 2-[3-(2-aminoethylthio)propylthio]ethanamine covalently bound to two 7-nitrobenzo-2-oxa-1,3-diazolyl moieties was prepared as a fluoroionophore and a chromophore for the selective optical detection of Hg2+. The sensor was prepared in two steps and its fluoroionophoric and chromophoric properties toward various transition metal, alkali, and alkali earth cations were investigated. Compound 4 selectively binds Hg2+, and the binding is indicated by both fluorescence quenching and a chromogenic change which can be detected by the naked eye. In an 80:20 acetonitrile/water solvent mixture, 4 acts as an ON-OFF fluorescence switch upon Hg2+ binding, exhibiting efficient quenching and a detection limit of 10-7 M or 20 ppb. © 2009 Elsevier Ltd. All rights reserved.
format Article
author Wanichacheva N.
Siriprumpoonthum M.
Kamkaew A.
Grudpan K.
spellingShingle Wanichacheva N.
Siriprumpoonthum M.
Kamkaew A.
Grudpan K.
Dual optical detection of a novel selective mercury sensor based on 7-nitrobenzo-2-oxa-1,3-diazolyl subunits
author_facet Wanichacheva N.
Siriprumpoonthum M.
Kamkaew A.
Grudpan K.
author_sort Wanichacheva N.
title Dual optical detection of a novel selective mercury sensor based on 7-nitrobenzo-2-oxa-1,3-diazolyl subunits
title_short Dual optical detection of a novel selective mercury sensor based on 7-nitrobenzo-2-oxa-1,3-diazolyl subunits
title_full Dual optical detection of a novel selective mercury sensor based on 7-nitrobenzo-2-oxa-1,3-diazolyl subunits
title_fullStr Dual optical detection of a novel selective mercury sensor based on 7-nitrobenzo-2-oxa-1,3-diazolyl subunits
title_full_unstemmed Dual optical detection of a novel selective mercury sensor based on 7-nitrobenzo-2-oxa-1,3-diazolyl subunits
title_sort dual optical detection of a novel selective mercury sensor based on 7-nitrobenzo-2-oxa-1,3-diazolyl subunits
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-61349160485&partnerID=40&md5=a7098bee42609479177ba1c543f30327
http://cmuir.cmu.ac.th/handle/6653943832/5907
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