| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5219040 | Tetrahedron | 2012 | 5 Pages |
Abstract
A tetrathiafulvalene donor has been annulated to 2,3-di(1H-2-pyrrolyl)quinoxaline affording a new chemosensor 1, which shows a unique optical selectivity and reactivity for the fluoride ion over other anions in CH2Cl2 leading to a colorimetric response. Electrochemical polymerization of 1 occurred in the presence of fluoride.
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