Fluorescence in complexes based on quinolines-derivatives: a search for better fluorescent probes.
Autor: | Mecca CZP; Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Laboratório de Química de Calixarenos, Espectroscopia Molecular e Catálise, Universidade Federal de São Paulo, Rua Prof. Arthur Riedel, 275, CEP 09972-270, Diadema, SP, Brazil., Fonseca FLA; Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Laboratório de Química de Calixarenos, Espectroscopia Molecular e Catálise, Universidade Federal de São Paulo, Rua Prof. Arthur Riedel, 275, CEP 09972-270, Diadema, SP, Brazil; Fundação do ABC, Faculdade de Medicina, Av. Príncipe de Gales, 821, CEP 09060-650, Santo André, SP, Brazil., Bagatin IA; Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Laboratório de Química de Calixarenos, Espectroscopia Molecular e Catálise, Universidade Federal de São Paulo, Rua Prof. Arthur Riedel, 275, CEP 09972-270, Diadema, SP, Brazil. Electronic address: ibagatin@unifesp.br. |
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Jazyk: | angličtina |
Zdroj: | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy [Spectrochim Acta A Mol Biomol Spectrosc] 2016 Nov 05; Vol. 168, pp. 104-110. Date of Electronic Publication: 2016 Jun 04. |
DOI: | 10.1016/j.saa.2016.06.006 |
Abstrakt: | Quinoline-derived fluorescent complexes were designed; synthesized by the reaction of 5-nitro-8-hydroxyquinoline and 5-chloro-8-hydroxyquinoline with Al(3+), Mg(2+), Zn(2+), and Cd(2+) salts (1-8); and characterized. The (1)H NMR spectra of complexes 1 and 5, containing Al(3+), were consistent with an octahedral structure having approximate D3 symmetry, and the results supported the favored facial isomer (fac). Data for complexes 2-4 and 6-8 supported the formation of tetrahedral structures. Intense luminescence was detected for complexes 5-8, even with the naked eye, as indicated by quantum yield values of 0.087, 0.094, 0.051, and 0.021, respectively. Furthermore, in contrast to 5-nitro-8-hydroxyquinoline, the 5-chloro-8-hydroxyquinoline ligand exhibited bands at different energies depending on the coordinated metal, which supported its potential application in ionic and biological probes, as well as in cell imaging. (Copyright © 2016 Elsevier B.V. All rights reserved.) |
Databáze: | MEDLINE |
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