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Triazolium-promoted highly selective fluorescence "turn-on" detection of fluoride ions

Authors
Cho, JiheeKim, IllanMoon, Jong HunSingh, HardevJung, Hyo SungKim, Jong SeungLee, Jin YongKim, Sanghee
Issue Date
9월-2016
Publisher
ELSEVIER SCI LTD
Keywords
Fluoride detection; 1,2,3-triazolium; Fluorescent probe; Pyrene; DFT calculation
Citation
DYES AND PIGMENTS, v.132, pp.248 - 254
Indexed
SCIE
SCOPUS
Journal Title
DYES AND PIGMENTS
Volume
132
Start Page
248
End Page
254
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/87621
DOI
10.1016/j.dyepig.2016.05.005
ISSN
0143-7208
Abstract
Through copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, new pyrene-appended triazole- and triazolium-based fluorescent probes have been synthesized and their binding capabilities for anion recognition were investigated. The probes showed different fluorescence behavior in response to fluoride (F-) ions. The probe bearing a triazolium moiety, displayed a high selectivity towards F- ions via C-H center dot center dot center dot F- hydrogen bonding interaction and de-protonation that was accompanied by fluorescence "turn-on". Further, the experimental observations were well supported by H-1 NMR spectroscopy and density functional theory (DFT) calculations. (C) 2016 Elsevier Ltd. All rights reserved.
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