Thiophene aldehyde-diamino uracil Schiff base: A novel fluorescent probe for detection and quantification of cupric, silver and ferric ions

Abstract

A new Schiff base from the condensation of 5,6-diamino-1,3-dimethyluracil with 5-methylthiophene-2-carboxaldehyde was synthesized. The compound was characterized by spectral data (UV-Vis, IR, 1H NMR, fluorescence, MS). Ethanolic solutions of the Schiff base exhibit a strong fluorescence emission at 385 nm (λex = 341 nm), and have been employed as a turn-off fluorescent probe for selective detection of Ag+, Cu2+ and Fe3+ ions in presence of other cations such as Na+, K+, Ca2+ and Mg2+ ions abundant in natural water. The interaction between the tested compound and copper, silver or iron ions is associated with a significant fluorescence decrease, showing detection limits of 2.1-14.2 ppb. Under optimal conditions, the developed sensor was successfully employed to determine Ag+, Cu2+ and Fe3+ ions in real samples and proved to be selective and sensitive. © 2015 Published by Elsevier B.V.

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5,6-diamino-1,3-dimethyluracil, Ag+/cu2+/fe3+ ions, Fluorescence probe, Methyl-2-thiophenecarboxaldehyde, Schiff base, Water pollution, Aldehydes, Cations, Copper, Diamines, Fluorescent dyes, Iron, Limit of detection, Models, molecular, Schiff bases, Silver, Spectrometry, fluorescence, Thiophenes, Water, Water pollution, chemical, Fluorescence, Functional groups, Iron compounds, Metal ions, Probes, Aldehyde, Cation, Diamine, Fluorescent dye, Thiophene derivative, Detection and quantifications, Fluorescence emission, Fluorescence probes, Fluorescent probes, Schiff-base, Selective detection, Analysis, Chemical structure, Chemistry, Procedures, Spectrofluorometry, Validation study, Ions

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