Strong anion-anion hydrogen bond in the ionic liquid 1-ethyl-3-methylimidazolium hydrogen sulfate

被引:20
|
作者
Ribeiro, Mauro C. C. [1 ]
机构
[1] Univ Sao Paulo, Inst Quim, Dept Quim Fundamental, Lab Espectroscopia Mol, Av Prof Linea Prestes 748, BR-05508000 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
PHASE-TRANSITIONS; CRYSTAL-STRUCTURE; INFRARED-SPECTRA; AQUEOUS-SOLUTION; RAMAN; CATION; WATER; DISSOCIATION; FREQUENCIES; ABSORPTION;
D O I
10.1016/j.molliq.2020.113178
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 discusses the remarkable differences in the mid- and far-infrared regions of the spectrum of the ionic liquid 1-ethyl-3-methylimidazolium hydrogen sulfate, [C(2)C(1)im][HSO4], in comparison to ionic liquids based on other anions. The infrared spectrum unveils the occurrence of anion-anion hydrogen bond in [C(2)C(1)im][HSO4]. The band related to the anion O-H stretching mode,.(OH), covers a large frequency range (2000-3400 cm(-1)) and exhibits the spectral pattern of strongly hydrogen bonded systems. The far-infrared (FIR) spectrumof [C(2)C(1)im][HSO4] also exhibits the signature of the anion-anion interaction, that is, the stretching mode of the hydrogen bond,.(O.O), at similar to 170 cm(-1). Hydrogen bond between [HSO4](-) anions also occurs in ionic liquids containing imidazolium cation with longer alkyl chain ([C(4)C(1)im]+) or tetraalkylammonium cation. The vibrational frequencies of nu(OH) and nu(O center dot center dot center dot O) modes satisfy empirical correlations that characterize the anionanion interaction in [C(2)C(1)Im][HSO4] as a strong hydrogen bond. (C) 2020 Elsevier B.V. All rights reserved.
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页数:7
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