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Title: Ion-pairing dynamics of Li{sup +} and SCN{sup -} in dimethylformamide solution: Chemical exchange two-dimensional infrared spectroscopy

Abstract

Ultrafast two-dimensional infrared (2DIR) spectroscopy has been proven to be an exceptionally useful method to study chemical exchange processes between different vibrational chromophores under thermal equilibria. Here, we present experimental results on the thermal equilibrium ion pairing dynamics of Li{sup +} and SCN{sup -} ions in N,N-dimethylformamide. Li{sup +} and SCN{sup -} ions can form a contact ion pair (CIP). Varying the relative concentration of Li{sup +} in solution, we could control the equilibrium CIP and free SCN{sup -} concentrations. Since the CN stretch frequency of Li-SCN CIP is blue-shifted by about 16 cm{sup -1} from that of free SCN{sup -} ion, the CN stretch IR spectrum is a doublet. The temperature-dependent IR absorption spectra reveal that the CIP formation is an endothermic (0.57 kJ/mol) process and the CIP state has larger entropy by 3.12 J/(K mol) than the free ion states. Since the two ionic configurations are spectrally distinguishable, this salt solution is ideally suited for nonlinear IR spectroscopic investigations to study ion pair association and dissociation dynamics. Using polarization-controlled IR pump-probe methods, we first measured the lifetimes and orientational relaxation times of these two forms of ionic configurations. The vibrational population relaxation times of both the free ionmore » and CIP are about 32 ps. However, the orientational relaxation time of the CIP, which is {approx}47 ps, is significantly longer than that of the free SCN{sup -}, which is {approx}7.7 ps. This clearly indicates that the effective moment of inertia of the CIP is much larger than that of the free SCN{sup -}. Then, using chemical exchange 2DIR spectroscopy and analyzing the diagonal peak and cross-peak amplitude changes with increasing the waiting time, we determined the contact ion pair association and dissociation time constants that are found to be 165 and 190 ps, respectively. The results presented and discussed in this paper are believed to be important, not only because the ion-pairing dynamics is one of the most fundamental physical chemistry problems but also because such molecular ion-ion interactions are of critical importance in understanding Hofmeister effects on protein stability.« less

Authors:
; ; ; ;  [1]; ;  [1]
  1. Department of Chemistry, Research Institute for Natural Sciences, Korea University, Seoul 136-701 (Korea, Republic of)
Publication Date:
OSTI Identifier:
21560016
Resource Type:
Journal Article
Journal Name:
Journal of Chemical Physics
Additional Journal Information:
Journal Volume: 134; Journal Issue: 6; Other Information: DOI: 10.1063/1.3552961; (c) 2011 American Institute of Physics; Journal ID: ISSN 0021-9606
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; 74 ATOMIC AND MOLECULAR PHYSICS; ABSORPTION SPECTRA; ABSORPTION SPECTROSCOPY; ANIONS; CARBON NITRIDES; CATIONS; DISSOCIATION; INFRARED SPECTRA; ION EXCHANGE; ION PAIRS; ION-MOLECULE COLLISIONS; LITHIUM; LITHIUM IONS; MOLECULAR IONS; PROTEINS; SOLUTIONS; SPECTRAL SHIFT; THERMAL EQUILIBRIUM; THIOCYANATES; TWO-DIMENSIONAL CALCULATIONS; VIBRATIONAL STATES; ALKALI METALS; ANTITHYROID DRUGS; CARBON COMPOUNDS; CARBONIC ACID DERIVATIVES; CHARGED PARTICLES; COLLISIONS; DISPERSIONS; DRUGS; ELEMENTS; ENERGY LEVELS; EQUILIBRIUM; EXCITED STATES; HOMOGENEOUS MIXTURES; ION COLLISIONS; IONS; METALS; MIXTURES; MOLECULE COLLISIONS; NITRIDES; NITROGEN COMPOUNDS; ORGANIC COMPOUNDS; ORGANIC SULFUR COMPOUNDS; PNICTIDES; SPECTRA; SPECTROSCOPY

Citation Formats

Lee, Kyung-Koo, Park, Kwang-Hee, Kwon, Donghyun, Choi, Jun-Ho, Son, Hyewon, Park, Sungnam, Cho, Minhaeng, and Multidimensional Spectroscopy Laboratory, Korea Basic Science Institute, Seoul 136-713. Ion-pairing dynamics of Li{sup +} and SCN{sup -} in dimethylformamide solution: Chemical exchange two-dimensional infrared spectroscopy. United States: N. p., 2011. Web. doi:10.1063/1.3552961.
Lee, Kyung-Koo, Park, Kwang-Hee, Kwon, Donghyun, Choi, Jun-Ho, Son, Hyewon, Park, Sungnam, Cho, Minhaeng, & Multidimensional Spectroscopy Laboratory, Korea Basic Science Institute, Seoul 136-713. Ion-pairing dynamics of Li{sup +} and SCN{sup -} in dimethylformamide solution: Chemical exchange two-dimensional infrared spectroscopy. United States. https://doi.org/10.1063/1.3552961
Lee, Kyung-Koo, Park, Kwang-Hee, Kwon, Donghyun, Choi, Jun-Ho, Son, Hyewon, Park, Sungnam, Cho, Minhaeng, and Multidimensional Spectroscopy Laboratory, Korea Basic Science Institute, Seoul 136-713. 2011. "Ion-pairing dynamics of Li{sup +} and SCN{sup -} in dimethylformamide solution: Chemical exchange two-dimensional infrared spectroscopy". United States. https://doi.org/10.1063/1.3552961.
@article{osti_21560016,
title = {Ion-pairing dynamics of Li{sup +} and SCN{sup -} in dimethylformamide solution: Chemical exchange two-dimensional infrared spectroscopy},
author = {Lee, Kyung-Koo and Park, Kwang-Hee and Kwon, Donghyun and Choi, Jun-Ho and Son, Hyewon and Park, Sungnam and Cho, Minhaeng and Multidimensional Spectroscopy Laboratory, Korea Basic Science Institute, Seoul 136-713},
abstractNote = {Ultrafast two-dimensional infrared (2DIR) spectroscopy has been proven to be an exceptionally useful method to study chemical exchange processes between different vibrational chromophores under thermal equilibria. Here, we present experimental results on the thermal equilibrium ion pairing dynamics of Li{sup +} and SCN{sup -} ions in N,N-dimethylformamide. Li{sup +} and SCN{sup -} ions can form a contact ion pair (CIP). Varying the relative concentration of Li{sup +} in solution, we could control the equilibrium CIP and free SCN{sup -} concentrations. Since the CN stretch frequency of Li-SCN CIP is blue-shifted by about 16 cm{sup -1} from that of free SCN{sup -} ion, the CN stretch IR spectrum is a doublet. The temperature-dependent IR absorption spectra reveal that the CIP formation is an endothermic (0.57 kJ/mol) process and the CIP state has larger entropy by 3.12 J/(K mol) than the free ion states. Since the two ionic configurations are spectrally distinguishable, this salt solution is ideally suited for nonlinear IR spectroscopic investigations to study ion pair association and dissociation dynamics. Using polarization-controlled IR pump-probe methods, we first measured the lifetimes and orientational relaxation times of these two forms of ionic configurations. The vibrational population relaxation times of both the free ion and CIP are about 32 ps. However, the orientational relaxation time of the CIP, which is {approx}47 ps, is significantly longer than that of the free SCN{sup -}, which is {approx}7.7 ps. This clearly indicates that the effective moment of inertia of the CIP is much larger than that of the free SCN{sup -}. Then, using chemical exchange 2DIR spectroscopy and analyzing the diagonal peak and cross-peak amplitude changes with increasing the waiting time, we determined the contact ion pair association and dissociation time constants that are found to be 165 and 190 ps, respectively. The results presented and discussed in this paper are believed to be important, not only because the ion-pairing dynamics is one of the most fundamental physical chemistry problems but also because such molecular ion-ion interactions are of critical importance in understanding Hofmeister effects on protein stability.},
doi = {10.1063/1.3552961},
url = {https://www.osti.gov/biblio/21560016}, journal = {Journal of Chemical Physics},
issn = {0021-9606},
number = 6,
volume = 134,
place = {United States},
year = {Mon Feb 14 00:00:00 EST 2011},
month = {Mon Feb 14 00:00:00 EST 2011}
}