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首页> 外文期刊>Journal of magnetic resonance >Liquid state DNP at high magnetic fields: Instrumentation, experimental results and atomistic modelling by molecular dynamics simulations
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Liquid state DNP at high magnetic fields: Instrumentation, experimental results and atomistic modelling by molecular dynamics simulations

机译:高磁场下的液态DNP:分子动力学模拟的仪器,实验结果和原子建模

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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. (C) 2015 Elsevier Inc. All rights reserved.
机译: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领域之一。尽管已经有许多工作致力于在固态下进行从电子自旋到核自旋的极化转移的实验,但是仅存在几个在液态下进行极化转移的实验的例子。在这里,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400 MHz核拉莫尔频率和电子自旋的263 GHz激发频率。在我们已经实现的双共振结构的背景下讨论了进行此类实验的技术要求。描述了一些实验步骤,这些步骤允许获得几种有机溶剂的质子自旋的增强因子,其中氮氧化物自由基作为偏振剂。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,该方案用于突出基于平移和旋转运动的经典模型的局限性,通常将其用于量化观察到的耦合因子。 MD仿真能够预测在任何磁场强度下各种自由基和溶剂分子的增强的能力,应被证明可用于优化液态DNP的实验条件。 (C)2015 Elsevier Inc.保留所有权利。

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