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Updated: May 29, 2025

Atomic Scale Structural Studies of Macromolecular Assemblies by Solid-state Nuclear Magnetic Resonance Spectroscopy
Published on: September 17, 2017
Nuclear Magnetic Resonance and Computational Studies of Sodium Ions in an Ionic Liquid/Water Mixture
Katarzyna Dziubinska-Kühn1, Renaud B Jolivet1, Christopher A Rumble2
1Maastricht Centre for Systems Biology, Maastricht University, Paul-Henri Spaaklaan 1, 6229 EN Maastricht, Netherlands.
Abstract:
We report a computational protocol for simulating electric field gradient dynamics around Na+ cations in mixtures of 1-ethyl-3-methylimidazolium tetrafluoroborate ([Im21][BF4]) and water validated by comparison to measurements of nuclear magnetic resonance (NMR) T1 relaxation times. Our protocol combines classical molecular dynamics simulations of a scaled charge model of [Im21][BF4] and TIP4Pew water to generate the electric field gradient (EFG) correlation function, CEFG(t), with quantum chemical calculations for determining the EFG variance . Although we demonstrate that the Sternheimer approximation is as valid in these mixtures as it is in neat water, we do not recommend using the Sternheimer approximation as it underestimates by ∼10% compared to a set of computationally efficient density functional theory calculations. Our protocol is capable of reproducing both the composition- and temperature-dependence of T1 over the full range of experimentally accessible [Im21][BF4]/water compositions and a temperature range of 285-350 K. We also show that scaling the [Im21][BF4] charges does not simply speed up the dynamics of the solvent, but has effects on the shape of CEFG(t). Following validation of our protocol, we analyze the shape and relaxation times of CEFG(t) to show that the mechanism by with T1 changes is different when the composition of the mixture varies compared to changes in temperature. As composition changes, the balance between inertial and diffusive relaxation alters, whereas temperature only affects the time scale of the diffusion portion of the relaxation. We also show that solvation shell of Na+ in these mixtures is significantly more labile than in neat [Im21][BF4] and that water and BF4- anions compete to be in the Na+ solvation shell. This validated computational protocol opens the door to more detailed interpretation of NMR T1 relaxation experiments of monatomic ions in complex liquid environments.
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