| Literature DB >> 25652555 |
Hui Wang1, Steven P Kelley, Jimmy W Brantley, Gregory Chatel, Julia Shamshina, Jorge F B Pereira, Varun Debbeti, Allan S Myerson, Robin D Rogers.
Abstract
Liquid multi-ion systems made by combining two or more salts can exhibit charge ordering and interactions not found in the parent salts, leading to new sets of properties. This is investigated herein by examining a liquid comprised of a single cation, 1-ethyl-3-methylimidazolium ([C2mim](+)), and two anions with different properties, acetate ([OAc](-)) and bis(trifluoromethylsulfonyl)imide ([NTf2](-)). NMR and IR spectroscopy indicate that the electrostatic interactions are quite different from those in either [C2mim][OAc] or [C2mim][NTf2]. This is attributed to the ability of [OAc](-) to form complexes with the [C2mim](+) ions at greater than 1:1 stoichiometries by drawing [C2mim](+) ions away from the less basic [NTf2](-) ions. Solubility studies with molecular solvents (ethyl acetate, water) and pharmaceuticals (ibuprofen, diphenhydramine) show nonlinear trends as a function of ion content, which suggests that solubility can be tuned through changes in the ionic compositions.Entities:
Keywords: IR spectroscopy; NMR spectroscopy; concentration effects; ionic liquids; solvent effects
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Year: 2015 PMID: 25652555 DOI: 10.1002/cphc.201402894
Source DB: PubMed Journal: Chemphyschem ISSN: 1439-4235 Impact factor: 3.102