Interaction of water diluted in 1-butyl-3-methyl imidazolium ionic liquids by vibrational spectroscopy modeling

被引:49
作者
Danten, Y. [1 ]
Cabaco, M. I. [2 ,3 ]
Besnard, M. [1 ]
机构
[1] Univ Bordeaux, Inst Mol Sci, CNRS, UMR 5255, F-33405 Talence, France
[2] Univ Tecn Lisboa, Dept Fis, Inst Super Tecn, P-1049001 Lisbon, Portugal
[3] Ctr Fis Atom UL, P-1694003 Lisbon, Portugal
关键词
Ionic liquids; Vibrational spectroscopy; DFT calculations; Hydrogen-bonded complexes of water in ionic liquids; Cooperative phenomena; MOLECULAR-DYNAMICS SIMULATION; REFINED FORCE-FIELD; N-BODY CLUSTERS; PHASE-BEHAVIOR; DIELECTRIC-SPECTROSCOPY; PHYSICAL-CHEMISTRY; SCALING FACTORS; MIXTURES; FREQUENCIES; ANIONS;
D O I
10.1016/j.molliq.2009.07.001
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This work is aimed at providing physical insights about the interactions of water dissolved in imidazolium ionic liquids (ILs) involving different anions using both DFT calculations and vibrational spectroscopic measurements (IR absorption and Raman scattering) in the region of the 1)0,, stretching vibrations of water (3400-3800 cm(-1)). More precisely, we have investigated interactions of water with a series of cation-anion couples involving the 1-butyl-3-methyl imidazolium cation with fluorinated anions (namely, hexafluorophosphate (PFG-) and tetrafluoroborate (BF4-)) and anions with sulfonyl groups (i.e. the tri-fluoro-methane-sulfonate (CF3SO3-) and bis-(tri-fluoro-methane-sulfonyl) imide (CF3SO2)(2)N- anions). The local organisation in these water/ILs solutions have been assessed from structures of a single water molecule interacting with a cation-anion pair dimer determined at the DFT-B3LYP/6-31 + G** level. The predicted structures show that the water molecule preferentially interacts with two distinct anions by forming associations of type (A center dot center dot center dot H-O-H center dot center dot center dot A). The interaction energy has been evaluated and decomposed as a sum of different many-body (2 up to 5 bodies) interaction terms. We emphasize the role of the non additive interaction forces and especially the role of the 3-body contribution processes in the structural organisation. We show that the doubly hydrogen-bonded nature of the interactions of water leads to well-defined spectral features (i.e. shifts, IR and Raman intensities) associated with the symmetric 1)1 and the anti-symmetric 1,3 stretching modes of water and in particular the separation A1)13 between these two vibrational transitions and IR absorption intensity ratio estimates R =11)3/112, consistent with the previous spectroscopic observations as well as with those reported here. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 66
页数:10
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