| Literature DB >> 26573285 |
Aasif Helal1, Hong-Seok Kim2, Zain H Yamani3, M Nasiruzzaman Shaikh3.
Abstract
A new highly selective, chromogenic, and fluorogenic Cu(2+) chemosensor, fluorescein-N-methylimidazole conjugate 1, and another fluorescein-N-imidazole conjugate 2 were synthesized and investigated by UV-visible and fluorescence spectroscopy. The sensing of Cu(2+) quenches the emission band of 1 at λmax = 525 nm, with an association constant (K a = 1.0 x 10(7) M(-1)) and a stoichiometry of 1:1 in a buffered H2O: MeOH solution (4:1, pH = 7.4). The Cu(2+) detection limit for chemosensor 1 is 37 nM. The presence of the N-methyl group in 1 increased the Cu(2+) binding selectivity, resulting in a stronger binding constant and a broader pH working range (pH 5-10) in comparison to 2. The fluorescence in 1 and 2 is caused by electron transfer phenomenon from the imidazole nitrogen to fluorescein, which is readily inhibited by Cu(2+) binding.Entities:
Keywords: Copper ion-selective; Fluorescein-N-methylimidazole electron transfer; Fluorescent chemosensor
Year: 2015 PMID: 26573285 DOI: 10.1007/s10895-015-1713-z
Source DB: PubMed Journal: J Fluoresc ISSN: 1053-0509 Impact factor: 2.217