| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275654 | Tetrahedron Letters | 2009 | 5 Pages |
Abstract
New fluorescent chemosensor 1 with two amidoanthraquinone groups (1-AAQs) at the lower rim of p-tert-butylcalix[4]arene has been synthesized. The significant changes of absorption and fluorescence bands show that chemosensor 1 is selective toward fluoride ion (Fâ) over other anions such as Clâ, Brâ, Iâ, CH3COOâ, H2PO4-, HSO4-, and OHâ. The ESIPT process of 1 is inhibited by the fluoride-induced H-bonding followed by deprotonation of NH of the 1-AAQ.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Hyo Sung Jung, Hyun Jung Kim, Jacques Vicens, Jong Seung Kim,