| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5224654 | Tetrahedron | 2008 | 6 Pages |
Abstract
Novel fluorogenic 1,3-alt thiacalix[4](N-phenylazacrown-5)ether ionophore has been synthesized by conjugation of the N-phenyl group with borondipyrromethene (BODIPY) fluorophore moiety. The ionophore exhibits pronounced off-on type fluorescent responses to some transition metal ions, in particular to Cu2+. In a PVC membrane electrode, distinct Ag+ selectivity was observed in potentiometric transduction.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Viktor Csokai, Mihály Kádár, Diem Lan Ha Mai, OlÃvia Varga, Klára Tóth, Miklós Kubinyi, Alajos Grün, István Bitter,
ether-BODIPY ionophore Synthesis, optical and electroanalytical characterizations of a thiacalix[4](N-phenylazacrown-5)ether-BODIPY ionophore](/preview/png/5224654.png)