Advanced search
Start date
Betweenand
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

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

Full text
Author(s):
de Jesus, Jessica C. ; Pires, Paulo A. R. ; Mustafa, Rizwana ; Riaz, Naheed ; El Seoud, Omar A.
Total Authors: 5
Document type: Journal article
Source: RSC ADVANCES; v. 7, n. 26, p. 15952-15963, 2017.
Web of Science Citations: 7
Abstract

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 -CH2-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, ET(WB), and Lewis basicity, SB, respectively. From UV-Vis spectral data, we calculated ET(WB) as a function of the water mole fraction (cW) at different temperatures; from 15 to 60 degrees C for WB in IL-acetate-W; 25 degrees C for SB and WB in IL-chloride- W. For all IL-W mixtures, the dependence of ET(WB) on cW 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 H-1 NMR data (chemical shifts, line widths). We attributed the non-linear dependence of the solvatochromic parameters on cW to preferential solvation of the dyes. We treated ET(WB) data with a model that includes the formation of the complex solvent ILW. 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. (AU)

FAPESP's process: 14/22136-4 - Use of green solvents and their mixtures for optimizing chemical processes
Grantee:Omar Abou El Seoud
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 16/13932-7 - Solvation in ionic liquids-molecular solvents binary mixtures: effects of the mixture composition and temperature, and applicability on cellulose dissolution
Grantee:Jessica Carol de Jesus
Support Opportunities: Scholarships in Brazil - Scientific Initiation