Coordination abilities of Good's buffer ionic liquids toward europium(III) ion in aqueous solution

resumo

Good's buffer ionic liquids (GB-ILs) are new class of ILs with self-buffering capacity at the physiological pH range for biological research. GB-ILs are formed by the combination of Good's buffers as anions and various organic bases as counter ions. In this work, the complexation of europium(III) ion with tricine and tricine-based GB-ILs, tetramethylammonium tricinate, tetraethylammonium tricinate, tetrabutylammonium tricinate, cholinium tricinate, and 1-ethyl-3-methylimidazolium tricinate in aqueous solution were determined potentiometrically at T = 298.2 K and ionic strength I = 0.1 mol.dm (3) NaNO3. The protonation constants of the studied ligands (L) and their overall stability constants (lg beta) with Eu(III) were determined. The best model that fit the potentiometric data was consisted of six main species, EuL2+, EuL2+, EuL3, EuH-1L+, EuH-2L2- , and EuH-3L33-. The lg beta(Eu(tricine)), lg beta(Eu(tricine)2), and lg beta(Eu(tricine)3) are 5.75, 9.51, and 12.79, respectively. The overall stability constants (lgb) of tricine-based GB-ILs were found to be greater than those of tricine. The species distribution diagrams of these complexes were calculated and discussed in terms of percent Eu(III) and pH. We present a density functional theory (DFT) study to understand tricine chelating to Eu(III). (C) 2015 Elsevier Ltd. All rights reserved.

palavras-chave

RARE-EARTH IONS; STABILITY-CONSTANTS; AMINO-ACIDS; EQUILIBRIUM-CONSTANTS; BIOLOGICAL-RESEARCH; COMPLEX-FORMATION; GLASS-ELECTRODE; CATION-EXCHANGE; METAL-COMPLEXES; EXTRACTION

categoria

Thermodynamics; Chemistry

autores

Taha, M; Khan, I; Coutinho, JAP

nossos autores

agradecimentos

This work was financed by national funding from Fundacao para a Ciencia e a Tecnologia (FCT, Portugal), European Union, QREN, FEDER and COMPETE for funding the CICECO (project PEst-C/CTM/LA0011/2013), QOPNA (project PEst-C/QUI/UI0062/2013) and LSRE/LCM (project PEst-C/EQB/LA0020/2013). M. Taha and I. Khan acknowledge FCT for the postdoctoral Grants SFRH/BPD/78441/2011 and SFRH/BPD/76850/2011, respectively.

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