RESUMEN
A new multifunctional and highly selective chemosensor for Co(2+) and Cu(2+) was designed and synthesized. could simultaneously detect both Co(2+) and Cu(2+) by changing its color from pale yellow to pink and to orange in a near-perfect aqueous solution. The binding modes of to Co(2+) and Cu(2+) were determined to be a 2 : 1 complexation stoichiometry through Job's plot, ESI-mass spectrometry analysis and (1)H NMR titration. The detection limits (1.5 and 2.1 µM) of for Co(2+) and Cu(2+) were lower than the DEP guidelines (1.7 µM for Co(2+)) and the WHO guidelines (31.5 µM for Cu(2+)) for drinking water. The chemosensor could be used to quantify Co(2+) and Cu(2+) in water samples. Moreover, could be used as a practical, visible colorimetric test kit for both Co(2+) and Cu(2+). The sensing mechanisms of Co(2+) and Cu(2+) by were supported by theoretical calculations.
Asunto(s)
Compuestos Cromogénicos/química , Cobalto/análisis , Cobre/análisis , Agua Potable/análisis , Ftalazinas/química , Cationes Bivalentes/análisis , Colorimetría/métodos , Límite de Detección , Modelos Moleculares , Bases de Schiff/química , Espectrofotometría Ultravioleta/métodosRESUMEN
A simple and easily synthesized colorimetric and fluorescent receptor 1, based on 4-diethylaminosalicylaldehyde moieties as a binding and signaling unit, has been synthesized and characterized. The receptor 1 has a selective colorimetric sensing ability for copper (II) ion by changing color from colorless to yellow in aqueous solution, and could be utilized to monitor Cu(II) over a wide pH range of 4-11. In addition, the detection limit (12µM) of 1 for Cu(2+) is much lower than that (30µM) recommended by WHO in drinking water, and its copper complex could be reversible simply through treatment with a proper reagent such as EDTA. Moreover, receptor 1 exhibited both a color change from colorless to yellow and fluorescence enhancement with a red shift upon addition to F(-) in DMSO. The recognition mechanism was attributed to the intermolecular proton transfer between the hydroxyl group of the receptor and the fluoride.
RESUMEN
A new simple 'naked eye' chemosensor 1 (sodium (E)-2-((2-(3-hydroxy-2-naphthoyl)hydrazono)methyl)benzoate) has been synthesized for detection of CN- in a mixture of DMF/H2O (9:1). The sensor 1 comprises of a naphthoic hydrazide as efficient hydrogen bonding donor group and a benzoic acid as the moiety with the water solubility. The receptor 1 showed high selectivity toward cyanide ions in a 1:1 stoichiometric manner, which induces a fast color change from colorless to yellow for CN- over other anions. Therefore, receptor 1 could be useful for cyanide detection in aqueous environment, displaying a high distinguishable selectivity from hydrogen bonded anions and being clearly visible to the naked eye.
Asunto(s)
Ácidos Carboxílicos/química , Colorimetría/métodos , Cianuros/química , Aniones , Cianuros/síntesis química , Soluciones , Espectrometría de Masa por Ionización de Electrospray , Espectrofotometría UltravioletaRESUMEN
A multifunctional fluorescent and colorimetric receptor 1 ((E)-N'-((8-hydroxy-1,2,3,5,6,7-hexahydropyrido[3,2,1-ij]quinolin-9-yl)methylene)benzohydrazide) for the detection of both Al(3+) and CN(-) in aqueous solution has been developed. Receptor 1 exhibited an excellent selective fluorescence response toward Al(3+). The sensitivity of the fluorescent based assay (0.193 µM) for Al(3+) is far below the limit in the World Health Organization (WHO) guidelines for drinking water (7.41 µM). In addition, receptor 1 showed an excellent detection ability in a wide pH range of 4-10 and also in living cells. Moreover, receptor 1 showed a highly selective colorimetric response to CN(-) by changing its color from colorless to yellow immediately without any interference from other anions.