Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
27551 | Journal of Photochemistry and Photobiology A: Chemistry | 2011 | 6 Pages |
A new pyrazole-based fluorescent sensor, 5-amino-3-(5-phenyl-1H-pyrrol-2-yl)-1H-pyrazole-4-carboxamide (compound 1), was studied for fluoride anion (F−) detection in organic or water-containing solution. This compound displayed both changes in UV–vis absorption and fluorescence emission spectra upon addition of F−. With increasing of F−, blue emission intensity increases drastically and reaches saturation with 607-fold enhancement at 424 nm. The results indicate that compound 1 has highly selectivity for fluoride detection over other anions, such as Cl−, Br−, I−, HSO4−, H2PO4− and AcO− in DMSO or aqueous DMSO solutions. 1H NMR titration and other experiments confirm that the sensing process is mainly from the deprotonation of the pyrazole–NH in compound 1.