Solid-State 1H Spin Polarimetry by 13CH3 Nuclear Magnetic Resonance

Q3 Physics and Astronomy
S. Elliott, Quentin Stern, S. Jannin
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引用次数: 5

Abstract

Abstract. Dissolution-dynamic nuclear polarization is emerging as a promising means to prepare proton polarizations approaching unity. At present, 1H polarization quantification remains fastidious due to the requirement of measuring thermal equilibrium signals. Lineshape polarimetry of solid-state nuclear magnetic resonance spectra is used to determine a number of useful properties regarding the spin system under investigation. In the case of highly polarized nuclear spins, such as those prepared under the conditions of dissolution-dynamic nuclear polarization experiments, the absolute polarization of a particular isotopic species within the sample can be directly inferred from the characteristics of the corresponding resonance lineshape. In situations where direct measurements of polarization are complicated by deleterious phenomena, indirect estimates of polarization using coupled heteronuclear spins prove informative. We present a simple analysis of the 13C spectral lineshape asymmetry of [2-13C]sodium acetate based on relative peak intensities, which can be used to indirectly evaluate the proton polarization of the methyl group moiety, and very likely the entire sample in the case of rapid and homogeneous 1H-1H spin diffusion. 1H polarizations greater than ~10–25 % (depending on the sign of the microwave irradiation) were found to be linearly proportional to the 13C peak asymmetry, which responds differently to positive or negative microwave irradiation. These results suggest that, as a dopant, [2-13C]sodium acetate could be used to indirectly gauge 1H polarizations in standard sample formulations, which is potentially advantageous for: samples polarized in commercial dissolution-dynamic nuclear polarization devices that lack 1H radiofrequency hardware, measurements which are deleteriously influenced by radiation damping or complicated by the presence of large background signals, and situations where the acquisition of a thermal equilibrium spectrum is not feasible.
13CH3核磁共振固态1H自旋极化测定
摘要溶解-动态核极化是制备质子接近统一极化的一种很有前途的方法。目前,由于需要测量热平衡信号,对1H偏振的量化仍然比较挑剔。固体核磁共振谱的线形偏振法用于确定所研究的自旋系统的一些有用性质。在高极化核自旋的情况下,例如在溶解-动态核极化实验条件下制备的核自旋,样品内特定同位素的绝对极化可以直接从相应的共振线形特征中推断出来。在极化的直接测量因有害现象而变得复杂的情况下,利用耦合的异核自旋间接估计极化是有用的。我们基于相对峰强度对[2-13C]乙酸钠的13C谱线形状不对称性进行了简单分析,可以用来间接评估甲基部分的质子极化,并且很可能在快速均匀的1H-1H自旋扩散的情况下评估整个样品。1H极化大于~10 - 25%(取决于微波辐照的标志)与13C峰不对称成线性正比,其对正、负微波辐照的响应不同。这些结果表明,作为掺杂剂,[2-13C]乙酸钠可用于间接测量标准样品配方中的1H极化,这可能有利于:在商用溶解动态核极化装置中极化的样品缺乏1H射频硬件,测量受到辐射阻尼的有害影响或由于大背景信号的存在而变得复杂,以及获取热平衡谱不可行的情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.50
自引率
0.00%
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0
审稿时长
14 weeks
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