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在无微波的魔角旋转条件下,对氮氧化物掺杂样品进行固态核磁共振时核自旋极化的扰动。

Perturbation of nuclear spin polarizations in solid state NMR of nitroxide-doped samples by magic-angle spinning without microwaves.

作者信息

Thurber Kent R, Tycko Robert

机构信息

Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-0520, USA.

出版信息

J Chem Phys. 2014 May 14;140(18):184201. doi: 10.1063/1.4874341.

Abstract

We report solid state (13)C and (1)H nuclear magnetic resonance (NMR) experiments with magic-angle spinning (MAS) on frozen solutions containing nitroxide-based paramagnetic dopants that indicate significant perturbations of nuclear spin polarizations without microwave irradiation. At temperatures near 25 K, (1)H and cross-polarized (13)C NMR signals from (15)N,(13)C-labeled L-alanine in trinitroxide-doped glycerol/water are reduced by factors as large as six compared to signals from samples without nitroxide doping. Without MAS or at temperatures near 100 K, differences between signals with and without nitroxide doping are much smaller. We attribute most of the reduction of NMR signals under MAS near 25 K to nuclear spin depolarization through the cross-effect dynamic nuclear polarization mechanism, in which three-spin flips drive nuclear polarizations toward equilibrium with spin polarization differences between electron pairs. When T1e is sufficiently long relative to the MAS rotation period, the distribution of electron spin polarization across the nitroxide electron paramagnetic resonance lineshape can be very different from the corresponding distribution in a static sample at thermal equilibrium, leading to the observed effects. We describe three-spin and 3000-spin calculations that qualitatively reproduce the experimental observations.

摘要

我们报道了在含有基于氮氧化物的顺磁性掺杂剂的冷冻溶液上进行的带有魔角旋转(MAS)的固态(13)C和(1)H核磁共振(NMR)实验,这些实验表明在没有微波辐射的情况下核自旋极化存在显著扰动。在接近25 K的温度下,与未掺杂氮氧化物的样品的信号相比,三硝基氧化物掺杂的甘油/水中(15)N、(13)C标记的L-丙氨酸的(1)H和交叉极化(13)C NMR信号降低了多达六倍。在没有MAS或接近100 K的温度下,有和没有氮氧化物掺杂的信号之间的差异要小得多。我们将在接近25 K的MAS下NMR信号的大部分降低归因于通过交叉效应动态核极化机制的核自旋去极化,其中三自旋翻转驱动核极化趋向于与电子对之间的自旋极化差异达到平衡。当T1e相对于MAS旋转周期足够长时,氮氧化物电子顺磁共振线形上的电子自旋极化分布可能与热平衡下静态样品中的相应分布非常不同,从而导致观察到的效应。我们描述了定性再现实验观察结果的三自旋和3000自旋计算。

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