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Hg2+-selective fluoroionophore of p-tert-butylcalix[4]arene-diaza-crown ether having pyrenylacetamide subunits

Authors
Kim, Ju HeeHwang, Ah-RanChang, Suk-Kyu
Issue Date
Oct-2004
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
calix-aza-crown ether; fluoroionophore; pyrene; Hg2+ selectivity; ON-OFF type switching
Citation
TETRAHEDRON LETTERS, v.45, no.41, pp 7557 - 7561
Pages
5
Journal Title
TETRAHEDRON LETTERS
Volume
45
Number
41
Start Page
7557
End Page
7561
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24752
DOI
10.1016/j.tetlet.2004.08.125
ISSN
0040-4039
Abstract
A new ionophore having two pyrenylacetamide moieties based on the p-tert-butylcalix[4]arene-diaza-crown ether has been prepared and its fluoroionophoric properties were investigated. Bis(pyrenyl) derivative was found to exhibit selective ON-OFF type sensing behaviour toward Hg2+ ions over other representative transition and heavy metal ions. The fluorescence quenching efficiency of larger than 20-fold was observed with 100equiv of Hg2+ ions and the association constant was found to be 4.5 x 10(4) M-1 in methanol. The ionophore also exhibited a very efficient quenching of excimer fluorescence selectively upon treatment with Hg2+ ions in 50% aqueous methanol solution. The observed Hg2+ -selective ON-OFF type fluorescence behaviour could be utilized as efficient sensing and switching devices for the design of other supramolecular systems. (C) 2004 Elsevier Ltd. All rights reserved.
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