Experimental and theoretical studies on solvation in aqueous solutions of ionic liquids carrying different side chains: the -butyl-group the methoxyethyl group

We used solvatochromic compounds to probe solvation in mixtures of water, W, and four ionic liquids (ILs), 1-R-3-methylimidazoliumX, where R = n -butyl or methoxyethyl and X = acetate and chloride; these are denoted as (C 4 MeImAc), (C 3 OMeImAc), (C 4 MeImCl), and (C 3 OMeImCl). Our aim was to inve...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:RSC advances 2017-03, Vol.7 (26), p.15952-15963
Hauptverfasser: de Jesus, Jéssica C, Pires, Paulo A. R, Mustafa, Rizwana, Riaz, Naheed, El Seoud, Omar A
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:We used solvatochromic compounds to probe solvation in mixtures of water, W, and four ionic liquids (ILs), 1-R-3-methylimidazoliumX, where R = n -butyl or methoxyethyl and X = acetate and chloride; these are denoted as (C 4 MeImAc), (C 3 OMeImAc), (C 4 MeImCl), and (C 3 OMeImCl). Our aim was to investigate the effects on solvation when an ether linkage is substituted for a -CH 2 - group in the IL side chain. We used the solvatochromic probes 2,6-dichloro-4-(2,4,6-triphenylpyridinium-1-yl)phenolate (WB) and 5-nitroindoline, 1-methyl-5-nitroindoline to determine the solvent polarity, E T (WB), and Lewis basicity, SB, respectively. From UV-Vis spectral data, we calculated E T (WB) as a function of the water mole fraction ( χ W ) at different temperatures; from 15 to 60 °C for WB in IL-acetate-W; 25 °C for SB and WB in IL-chloride-W. For all IL-W mixtures, the dependence of E T (WB) on χ W is non-linear and, surprisingly, shows negligible dependence on the nature of the side chain. Values of the SB of IL-W were higher for C 4 MeImX-W than for C 3 OMeImX. A rationale for these results is the deactivation of the ether oxygen due to the formation of intramolecular hydrogen bonds with the hydrogens of the imidazolium ring. Our hypothesis is confirmed by quantum chemistry and molecular dynamics calculations (energy of the conformers and radial distribution functions), density, and 1 H NMR data (chemical shifts, line widths). We attributed the non-linear dependence of the solvatochromic parameters on χ W to preferential solvation of the dyes. We treated E T (WB) data with a model that includes the formation of the complex solvent IL-W. Equilibrium constants for solvent exchange in the solvation layer of WB were calculated; their values showed that IL-W is the most efficient solvent species present. We used solvatochromic compounds to probe solvation in mixtures of water, W, and four ionic liquids (ILs), 1-R-3-methylimidazoliumX, where R = n -butyl or methoxyethyl and X = acetate and chloride.
ISSN:2046-2069
DOI:10.1039/c7ra00273d