Solvation Mechanism of Task-Specific Ionic Liquids in Water: A Combined Investigation Using Classical Molecular Dynamics and Density Functional Theory

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• 作者：Surya V. J. Yuvaraj ; Ravil K. Zhdanov ; Rodion V. Belosludov ; Vladimir R. Belosludov ; Oleg S. Subbotin ; Kiyoshi Kanie ; Kenji Funaki ; Atsushi Muramatsu ; Takashi Nakamura ; Yoshiyuki Kawazoe
• 刊名：Journal of Physical Chemistry B
• 出版年：2015
• 出版时间：October 8, 2015
• 年：2015
• 卷：119
• 期：40
• 页码：12894-12904
• 全文大小：765K
• ISSN：1520-5207

文摘

The solvation behavior of task-specific ionic liquids (TSILs) containing a common, L-histidine derived imidazolium cation [C₂₀H₂₈N₃O₃]⁺ and different anions, bromide-[Br]^{鈭?/sup> and bis(trifluoromethylsulfonyl)amide-[NTF₂]鈭?/sup>, in water is examined, computationally. These amino acid functionalized ionic liquids (ILs) are taken into account because of their ability to react with rare earth metal salts. It has been noted that the TSIL with [Br]鈭?/sup> is more soluble than its counterpart TSIL with [NTF₂]鈭?/sup>, experimentally. In this theoretical work, the combined classical molecular dynamics (CMD) and density functional theory (DFT) calculations are performed to study the behavior of the bulk phase of these two TSILs in the vicinity of water (H₂O) molecules with different concentrations. Initially, all the constructed systems are equilibrated using the CMD method. The final structures of the equilibrated systems are extracted for DFT calculations. Under CMD operation, the radial distribution function (RDF) plots and viscosity of TSILs are analyzed to understand the effect of water on TSILs. In the DFT regime, binding energy per H₂O, charge transfer, charge density mapping, and electronic density of states (EDOS) analyses are done. The CMD results along with the DFT results are consolidated to support the hydrophilic and hydrophobic nature of the TSILs. Interestingly, we have found a strong correlation between the viscosity and the EDOS results that leads to an understanding of the hydration properties of the TSILs.}