RESUMEN
An easily synthesized fluorescent probe for detecting copper in aqueous samples, with a short response time and at neutral pH, has been investigated. Through the chelation of Cu2+ ions or by binding to CuO nanoparticles, the fluorescence emission of the 2-(aminomethyl)aniline derivative H2L is quenched by over 50%. Spectroscopic determination of the association constants of H2L with some metal ions showed that the ligand has a higher affinity toward Cu2+ than toward other d-block metal ions. The comparative bonding ability of the aniline-based fluorescent probe in d-block metal complexes was studied in solution by a combination of UV-Vis, 1H NMR and mass spectrometry analyses. Besides these, the bonding behavior has been investigated in the solid state by X-ray diffraction, FT-IR spectroscopy and elemental analysis. The crystal structures of Pd2(L)2 and Co(L)(HL)(H2O) were elucidated.
RESUMEN
The noticeable enhancement in fluorescence emission of O2N2-donor naphthodiaza-crown macrocyclic ligand (L) in the presence of Hg2+ was observed in which the fluorescence quantum yield of free ligand L as well as L/Hg2+ complex were found to be as 0.29 and 0.49, respectively. The observed ultra-low limit of detection (LOD) for Hg2+ by L was determined as low as 1.0 × 10-11 M in water. A 1:1 stoichiometry was also established for L/Hg2+ together with a binding constant K BH = 66,543 by employing fluorescence spectrophotometry. The competition experiments on L/Hg2+ demonstrated highly selective detection of Hg2+ in the presence of the library cations. A two path mechanism for detection of metal ion in terms of coordination of metal ion to L and/or the formation of counter ion was proposed by using of 1H NMR and fluorescence spectroscopy. Graphical Abstract pH dependence mechanism of interaction between Hg2+ and macrocyclic ligand L.