| Literature DB >> 28836050 |
Weerachai Nasomphan1, Pramuan Tangboriboonrat1, Srung Smanmoo2.
Abstract
A new "turn-on" fluorescent chemosensor based on dansyl derivative was prepared for Cu2+ ion sensing. Hydroxyl, imine and azomethine groups in Schiff base derived compound 1 were deliberately introduced for facilitating the binding of Cu2+ ion. Of screen metal ions, compound 1 showed a high degree of selectivity toward Cu2+ ion. Other interfering metal ions did not affect the fluorescence intensity of compound 1, except Hg2+ and Fe3+ ions exhibited a significant degree of fluorescence quenching. Upon binding of Cu2+ ion, compound 1 displayed a chelation enhanced fluorescence (CHEF) resulting in increasing of the fluorescence intensity. The molecular optimized geometry indicated the binding ratio between compound 1 and Cu2+ ion at 1:1 with the binding constant of 1.68 × 10- 7 M- 1. The optimized condition for sensing ability of compound 1 with a detection limit of 5 × 10- 7 M was found at the physiological pH 7.2 with the excitation wavelength of 366 nm. Due to no cytotoxicity and good photophysical properties, compound 1 was extended its application for the detection of Cu2+ ion in Vero cells. Compound 1 could be potentially used as an intracellular fluorescent chemosensor for tracking Cu2+ ion. Graphical Abstract.Entities:
Keywords: Cell imaging; Copper (II) ion; Dansyl derivative; Schiff base; Turn-on fluorescence
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Year: 2017 PMID: 28836050 DOI: 10.1007/s10895-017-2161-8
Source DB: PubMed Journal: J Fluoresc ISSN: 1053-0509 Impact factor: 2.217