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Hg2+-selective chemosensor derived from 8-hydroxyquinoline having benzothiazole function in aqueous environment

Authors
Youk, Jin-SooKim, Young HeeKim, Eun-JinYoun, Na JinChang, Suk-Kyu
Issue Date
Jun-2004
Publisher
KOREAN CHEMICAL SOC
Keywords
8-hydroxyquinoline; benzothiazole; Hg2+ -selectivity; fluoroionophore
Citation
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.25, no.6, pp 869 - 872
Pages
4
Journal Title
BULLETIN OF THE KOREAN CHEMICAL SOCIETY
Volume
25
Number
6
Start Page
869
End Page
872
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24828
DOI
10.5012/bkcs.2004.25.6.869
ISSN
0253-2964
1229-5949
Abstract
Newly synthesized 8-hydroxyquinoline based benzothiazole derivative 2 showed a distinctive Hg2+-selectivity over other transition metal ions in aqueous solution. The fluorescence emission at 455 nm of 2 was completely quenched upon interaction with Hg2+ ions in dioxane-H2O system (9 : 1, v/v). The selectivity was decreased in the order of Hg2+ much greater than Cu2+ > Cd2+ > Pb2+ approximate to Zn2+ approximate to Ni2+, and Hg2+ concentration dependent fluorescence quenching profile was observed in the presence of common interfering metal ions as background. The fluorescence behavior of 2 suggests that the prepared compound could be used as a fluorescent signaling subunit for the construction of new Hg2+-sensitive ON-OFF type supramolecular switching systems.
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