Impact of Size and Electronegativity of Halide Anions on Hydrogen Bonds and Properties of 1-Ethyl-3-methylimidazolium-Based Ionic Liquids
Publication type: Journal Article
Publication date: 2019-05-14
scimago Q2
wos Q2
SJR: 0.634
CiteScore: 4.8
Impact factor: 2.8
ISSN: 10895639, 15205215
PubMed ID:
31088056
Physical and Theoretical Chemistry
Abstract
The effect of the anion size and electronegativity of halide-based anions (Cl-, Br-, I-, and BF4-) on the interionic interaction in 1-ethyl-3-methylimidazolium-based ionic liquids (ILs) C2mim X (X = Cl, Br, I, and BF4) is studied by a combined approach of experiments (Raman, IR, UV-vis spectroscopy) and quantum chemical calculations. The fingerprint region of the Raman spectra of these C2mim X ion-pairs provides evidence of the presence of the conformational isomerism in the alkyl chain of the C2mim+ cation. The Raman and IR bands of the imidazolium C2-H stretch vibration for C2mim X (X = Cl, Br, I, and BF4) were noticeably blue-shifted with the systematic change in size of anions and the electronegativity. The observed blue shift in the C2-H stretch vibration follows the order C2mim BF4 > C2mim I > C2mim Br > C2mim Cl, which essentially indicates the strong hydrogen bonding in the C2mim Cl ion-pair. DFT calculations predict at least four configurations for the cation-anion interaction. On the basis of relative optimized energies and basis-set-superposition-error (BSSE) corrected binding energies for all ion-pair configurations, the most active site for the anion interaction was found at the C2H position of the cation. Besides information about the C2H position, our DFT results give insights into the anion interaction with the ethyl and methyl chain of the cation, which was also confirmed experimentally [ Chem. Commun. 2015 , 51 , 3193 ]. The anion interaction at the C2H site of the cation favors a planar geometry in C2mim X for X = Cl, Br, and I; however, for BF4, the system prefers a nonplanar geometry where the anion is located over the imidazolium ring. TD-DFT results were used to analyze the observed UV-vis absorption spectra in a more adequate way giving insights into the electronic structure of the ILs. Overall, a reasonable correlation between the observed and the DFT-predicted results is established.
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Sanchora P. et al. Impact of Size and Electronegativity of Halide Anions on Hydrogen Bonds and Properties of 1-Ethyl-3-methylimidazolium-Based Ionic Liquids // Journal of Physical Chemistry A. 2019. Vol. 123. No. 23. pp. 4948-4963.
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Sanchora P., Pandey D. K., Rana D., Materny A., Singh D. Impact of Size and Electronegativity of Halide Anions on Hydrogen Bonds and Properties of 1-Ethyl-3-methylimidazolium-Based Ionic Liquids // Journal of Physical Chemistry A. 2019. Vol. 123. No. 23. pp. 4948-4963.
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TY - JOUR
DO - 10.1021/acs.jpca.9b04116
UR - https://doi.org/10.1021/acs.jpca.9b04116
TI - Impact of Size and Electronegativity of Halide Anions on Hydrogen Bonds and Properties of 1-Ethyl-3-methylimidazolium-Based Ionic Liquids
T2 - Journal of Physical Chemistry A
AU - Sanchora, Paridhi
AU - Pandey, Deepak K
AU - Rana, Debkumar
AU - Materny, Arnulf
AU - Singh, Dheeraj
PY - 2019
DA - 2019/05/14
PB - American Chemical Society (ACS)
SP - 4948-4963
IS - 23
VL - 123
PMID - 31088056
SN - 1089-5639
SN - 1520-5215
ER -
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@article{2019_Sanchora,
author = {Paridhi Sanchora and Deepak K Pandey and Debkumar Rana and Arnulf Materny and Dheeraj Singh},
title = {Impact of Size and Electronegativity of Halide Anions on Hydrogen Bonds and Properties of 1-Ethyl-3-methylimidazolium-Based Ionic Liquids},
journal = {Journal of Physical Chemistry A},
year = {2019},
volume = {123},
publisher = {American Chemical Society (ACS)},
month = {may},
url = {https://doi.org/10.1021/acs.jpca.9b04116},
number = {23},
pages = {4948--4963},
doi = {10.1021/acs.jpca.9b04116}
}
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Sanchora, Paridhi, et al. “Impact of Size and Electronegativity of Halide Anions on Hydrogen Bonds and Properties of 1-Ethyl-3-methylimidazolium-Based Ionic Liquids.” Journal of Physical Chemistry A, vol. 123, no. 23, May. 2019, pp. 4948-4963. https://doi.org/10.1021/acs.jpca.9b04116.