%0 Journal Article %1 :/content/aip/journal/jcp/136/7/10.1063/1.3685100 %A Yasaka, Yoshiro %A Klein, Michael L. %A Nakahara, Masaru %A Matubayasi, Nobuyuki %D 2012 %J The Journal of Chemical Physics %K imported %N 7 %R http://dx.doi.org/10.1063/1.3685100 %T Rotational dynamics of benzene and water in an ionic liquid explored via molecular dynamics simulations and NMR T1 measurements %U http://scitation.aip.org/content/aip/journal/jcp/136/7/10.1063/1.3685100 %V 136 %X The rotational dynamics of benzene and water in the ionic liquid (IL) 1-butyl-3-methylimidazolium chloride are studied using molecular dynamics (MD) simulation and NMRT 1 measurements. MD trajectories based on an effective potential are used to calculate the 2H NMRrelaxation time,T 1 via Fourier transform of the relevant rotational time correlation function,C 2R(t). To compensate for the lack of polarization in the standard fixed-charge modeling of the IL, an effective ionic charge, which is smaller than the elementary charge is employed. The simulation results are in closest agreement with NMR experiments with respect to the temperature and Larmor frequency dependencies of T 1 when an effective charge of ±0.5e is used for the anion and the cation, respectively. The computed C 2R(t) of both solutes shows a bi-modal nature, comprised of an initial non-diffusive ps relaxation plus a long-time ns tail extending to the diffusive regime. Due to the latter component, the solute dynamics is not under the motional narrowing condition with respect to the prevalent Larmor frequency. It is shown that the diffusive tail of the C 2R(t) is most important to understand frequency and temperature dependencies of T 1 in ILs. On the other hand, the effect of the initial ps relaxation is an increase of T 1 by a constant factor. This is equivalent to an “effective” reduction of the quadrupolar coupling constant (QCC). Thus, in the NMRT 1 analysis, the rotational time correlation function can be modeled analytically in the form of aexp (−t/τ) (Lipari-Szabo model), where the constant a, the Lipari-Szabo factor, contains the integrated contribution of the short-time relaxation and τ represents the relaxation time of the exponential (diffusive) tail. The Debye model is a special case of the Lipari-Szabo model with a = 1, and turns out to be inappropriate to represent benzene and water dynamics in ILs since a is as small as 0.1. The use of the Debye model would result in an underestimation of the QCC by a factor of 2–3 as a compensation for the neglect of the Lipari-Szabo factor.

@article{:/content/aip/journal/jcp/136/7/10.1063/1.3685100, abstract = {The rotational dynamics of benzene and water in the ionic liquid (IL) 1-butyl-3-methylimidazolium chloride are studied using molecular dynamics (MD) simulation and NMRT 1 measurements. MD trajectories based on an effective potential are used to calculate the 2H NMRrelaxation time,T 1 via Fourier transform of the relevant rotational time correlation function,C 2R(t). To compensate for the lack of polarization in the standard fixed-charge modeling of the IL, an effective ionic charge, which is smaller than the elementary charge is employed. The simulation results are in closest agreement with NMR experiments with respect to the temperature and Larmor frequency dependencies of T 1 when an effective charge of ±0.5e is used for the anion and the cation, respectively. The computed C 2R(t) of both solutes shows a bi-modal nature, comprised of an initial non-diffusive ps relaxation plus a long-time ns tail extending to the diffusive regime. Due to the latter component, the solute dynamics is not under the motional narrowing condition with respect to the prevalent Larmor frequency. It is shown that the diffusive tail of the C 2R(t) is most important to understand frequency and temperature dependencies of T 1 in ILs. On the other hand, the effect of the initial ps relaxation is an increase of T 1 by a constant factor. This is equivalent to an “effective” reduction of the quadrupolar coupling constant (QCC). Thus, in the NMRT 1 analysis, the rotational time correlation function can be modeled analytically in the form of aexp (−t/τ) (Lipari-Szabo model), where the constant a, the Lipari-Szabo factor, contains the integrated contribution of the short-time relaxation and τ represents the relaxation time of the exponential (diffusive) tail. The Debye model is a special case of the Lipari-Szabo model with a = 1, and turns out to be inappropriate to represent benzene and water dynamics in ILs since a is as small as 0.1. The use of the Debye model would result in an underestimation of the QCC by a factor of 2–3 as a compensation for the neglect of the Lipari-Szabo factor.}, added-at = {2016-05-13T18:52:29.000+0200}, author = {Yasaka, Yoshiro and Klein, Michael L. and Nakahara, Masaru and Matubayasi, Nobuyuki}, biburl = {https://www.bibsonomy.org/bibtex/2d8d990e3dfdbe094953954ce5caba856/templehpc}, description = {Rotational dynamics of benzene and water in an ionic liquid explored via molecular dynamics simulations and NMR T1 measurements}, doi = {http://dx.doi.org/10.1063/1.3685100}, eid = {074508}, interhash = {7b0fbfd7ec311fbc1f8b790682751182}, intrahash = {d8d990e3dfdbe094953954ce5caba856}, journal = {The Journal of Chemical Physics}, keywords = {imported}, number = 7, timestamp = {2016-05-13T18:52:29.000+0200}, title = {Rotational dynamics of benzene and water in an ionic liquid explored via molecular dynamics simulations and NMR T1 measurements}, url = {http://scitation.aip.org/content/aip/journal/jcp/136/7/10.1063/1.3685100}, volume = 136, year = 2012 }