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Synthesis of thionaphthalimides and their dual Hg2+-selective signaling by desulfurization of thioimides

Authors
Moon, Jung OkChoi, Myung GilSun, TaihaoChoe, Jong-InChang, Suk-Kyu
Issue Date
Jan-2013
Publisher
ELSEVIER SCI LTD
Keywords
Hg2+ ion; Colorimetry; Fluorogenic signaling; Desulfurization; Thionaphthalimide; Ratiometry
Citation
DYES AND PIGMENTS, v.96, no.1, pp 170 - 175
Pages
6
Journal Title
DYES AND PIGMENTS
Volume
96
Number
1
Start Page
170
End Page
175
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/14965
DOI
10.1016/j.dyepig.2012.08.007
ISSN
0143-7208
Abstract
A series of new thionaphthalimide derivatives were prepared, and their Hg2+-selective signaling behavior was investigated in aqueous acetonitrile solution. A monothionaphthalimide (anti) exhibited pronounced Hg2+-selective chromogenic signaling behavior through a solution color change from red to yellow, which was easily detectable by eye. It (anti) also showed prominent off-on type Hg2+-selective fluorescent signaling behavior. The signaling is due to the Hg2+-assisted desulfurization of the thioimide to its imide structure. The presence of other common metal ions did not interfere with the Hg2+-signaling of the monothionaphthalimide (anti). The detection limit of monothionaphthalimide (anti) for the determination of Hg2+ ions in 30% aqueous acetonitrile was estimated to be 2.7 mu M. (C) 2012 Elsevier Ltd. All rights reserved.
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