Optimal sensitivity for 1H detected relayed DNP of organic solids at fast MAS

IF 2 3区 化学 Q3 BIOCHEMICAL RESEARCH METHODS
Saumya Badoni, Pierrick Berruyer, Lyndon Emsley
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Abstract

Dynamic nuclear polarization (DNP) combined with high magnetic fields and fast magic angle spinning (MAS) has opened up a new avenue for the application of exceptionally sensitive 1H NMR detection schemes to study protonated solids. Recently, it has been shown that DNP experiments at fast MAS rates lead to slower spin diffusion and hence reduced DNP enhancements for impregnated materials. However, DNP enhancements alone do not determine the overall sensitivity of a NMR experiment. Here we measure the overall sensitivity of one-dimensional 1H detected relayed DNP experiments as a function of the MAS rate in the 20–60 kHz regime using 0.7 mm diameter rotors at 21.2 T. Although faster MAS rates are detrimental for the DNP enhancement on the target material, due to slower spin diffusion, we find that with increasing spinning rates the gain in sensitivity due to 1H line-narrowing and the folding-in of sideband intensity compensates a large part of the loss of overall hyperpolarization. We find that sensitivity depends on the atomic site in the molecule, and is maximised at between 40 and 50 kHz MAS for the sample of L-histidine.HCl·H2O studied here. There is a 10–20 % difference in sensitivity between the optimum MAS rate and the fastest rate currently accessible (60 kHz).

Abstract Image

快速 MAS 条件下有机固体 1H 检测中继 DNP 的最佳灵敏度
动态核极化(DNP)与高磁场和快速魔角旋转(MAS)相结合,为应用异常灵敏的 1H NMR 检测方案研究质子化固体开辟了一条新途径。最近的研究表明,在快速 MAS 速率下进行 DNP 实验会导致自旋扩散速度减慢,从而降低浸渍材料的 DNP 增强。然而,DNP 增强本身并不能决定 NMR 实验的整体灵敏度。虽然由于自旋扩散较慢,较快的 MAS 速率不利于目标材料上的 DNP 增强,但我们发现,随着旋转速率的增加,1H 线窄和边带强度折叠所带来的灵敏度增益弥补了整体超极化的大部分损失。我们发现灵敏度取决于分子中的原子位点,在本文研究的 L-histidine.HCl-H2O 样品中,灵敏度在 40 至 50 kHz MAS 之间达到最大。最佳 MAS 速率与目前可用的最快速率(60 kHz)之间的灵敏度相差 10-20%。
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来源期刊
CiteScore
3.80
自引率
13.60%
发文量
150
审稿时长
69 days
期刊介绍: The Journal of Magnetic Resonance presents original technical and scientific papers in all aspects of magnetic resonance, including nuclear magnetic resonance spectroscopy (NMR) of solids and liquids, electron spin/paramagnetic resonance (EPR), in vivo magnetic resonance imaging (MRI) and spectroscopy (MRS), nuclear quadrupole resonance (NQR) and magnetic resonance phenomena at nearly zero fields or in combination with optics. The Journal''s main aims include deepening the physical principles underlying all these spectroscopies, publishing significant theoretical and experimental results leading to spectral and spatial progress in these areas, and opening new MR-based applications in chemistry, biology and medicine. The Journal also seeks descriptions of novel apparatuses, new experimental protocols, and new procedures of data analysis and interpretation - including computational and quantum-mechanical methods - capable of advancing MR spectroscopy and imaging.
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