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Atomistic Insight into Tetraalkylphosphonium-Bis(oxalato)borate Ionic Liquid/Water Mixtures. I. Local Microscopic Structure
Stockholm University, Sweden.
Stockholm University, Sweden.
KTH Royal Institute of Technology, Sweden; Ghent University, Belgium.
Luleå University of Technology, Sweden; Warwick University, UK.
Vise andre og tillknytning
2015 (engelsk)Inngår i: Journal of Physical Chemistry B, ISSN 1520-6106, E-ISSN 1520-5207, Vol. 119, nr 16, s. 5251-5264Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Atomistic simulations have been performed to investigate the microscopic structural organization of aqueous solutions of trihexyltetradecylphosphonium bis(oxalato)borate ([P6,6,6,14][BOB]) ionic liquid (IL). The evolution of the microscopic liquid structure and the local ionic organization of IL/water mixtures as a function of the water concentration is visualized and systematically analyzed via radial and spatial distribution functions, coordination numbers, hydrogen bond network, and water clustering analysis. The microscopic liquid structure in neat IL is characterized by a connected apolar network composed of the alkyl chains of [P6,6,6,14] cations and isolated polar domains consisting of the central segments of [P6,6,6,14] cations and [BOB] anions, and the corresponding local ionic environment is described by direct contact ion pairs. In IL/water mixtures with lower water mole fractions, the added water molecules are dispersed and embedded in cavities between neighboring ionic species and the local ionic structure is characterized by solvent-shared ion pairs through cation-water-anion triple complexes. With a gradual increase in the water concentration in IL/water mixtures, the added water molecules tend to aggregate and form small clusters, intermediate chain-like structures, large aggregates, and eventually a water network in water concentrated simulation systems. A further progressive dilution of IL/water mixtures leads to the formation of self-organized micelle-like aggregates characterized by a hydrophobic core and hydrophilic shell consisting of the central polar segments in [P6,6,6,14] cations and [BOB] anions in a highly branched water network. The striking structural evolution of the [P6,6,6,14][BOB] IL/water mixtures is rationalized by the competition between favorable hydrogen bonded interactions and strong electrostatic interactions between the polar segments in ionic species and the dispersion interactions between the hydrophobic alkyl chains in [P6,6,6,14] cations.

sted, utgiver, år, opplag, sider
2015. Vol. 119, nr 16, s. 5251-5264
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URN: urn:nbn:se:ri:diva-27040DOI: 10.1021/acs.jpcb.5b00667Scopus ID: 2-s2.0-84928485335OAI: oai:DiVA.org:ri-27040DiVA, id: diva2:1054044
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A3495

Tilgjengelig fra: 2016-12-08 Laget: 2016-12-08 Sist oppdatert: 2020-02-03bibliografisk kontrollert

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