Prisner Thomas, Denysenkov Vasyl, Sezer Deniz
Institute of Physical and Theoretical Chemistry and Center of Biomolecular Magnetic Resonance, Goethe University Frankfurt, Germany.
Institute of Physical and Theoretical Chemistry and Center of Biomolecular Magnetic Resonance, Goethe University Frankfurt, Germany.
J Magn Reson. 2016 Mar;264:68-77. doi: 10.1016/j.jmr.2015.11.004.
Dynamic nuclear polarization (DNP) at high magnetic fields has recently become one of the major research areas in magnetic resonance spectroscopy and imaging. Whereas much work has been devoted to experiments where the polarization transfer from the electron spin to the nuclear spin is performed in the solid state, only a few examples exist of experiments where the polarization transfer is performed in the liquid state. Here we describe such experiments at a magnetic field of 9.2 T, corresponding to a nuclear Larmor frequency of 400 MHz for proton spins and an excitation frequency of 263 GHz for the electron spins. The technical requirements to perform such experiments are discussed in the context of the double resonance structures that we have implemented. The experimental steps that allowed access to the enhancement factors for proton spins of several organic solvents with nitroxide radicals as polarizing agents are described. A computational scheme for calculating the coupling factors from molecular dynamics (MD) simulations is outlined and used to highlight the limitations of the classical models based on translational and rotational motion that are typically employed to quantify the observed coupling factors. The ability of MD simulations to predict enhancements for a variety of radicals and solvent molecules at any magnetic field strength should prove useful in optimizing experimental conditions for DNP in the liquid state.
高磁场下的动态核极化(DNP)最近已成为磁共振波谱学和成像领域的主要研究方向之一。尽管已有大量工作致力于在固态中进行从电子自旋到核自旋的极化转移实验,但在液态中进行极化转移的实验却为数不多。在此,我们描述了在9.2 T磁场下进行的此类实验,该磁场对应于质子自旋的核拉莫尔频率为400 MHz,电子自旋的激发频率为263 GHz。我们在已实现的双共振结构背景下讨论了进行此类实验的技术要求。描述了获取以氮氧化物自由基为极化剂的几种有机溶剂质子自旋增强因子的实验步骤。概述了一种用于从分子动力学(MD)模拟计算耦合因子的计算方案,并用于突出基于通常用于量化观测到的耦合因子的平移和旋转运动的经典模型的局限性。MD模拟在任何磁场强度下预测各种自由基和溶剂分子增强效果的能力,应有助于优化液态DNP的实验条件。