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微晶体固体的动态核极化 NMR 光谱学。

Dynamic nuclear polarization NMR spectroscopy of microcrystalline solids.

机构信息

Centre de RMN a Tres Hauts Champs, Université de Lyon (CNRS/ENS Lyon/UCB Lyon 1), 69100 Villeurbanne, France.

出版信息

J Am Chem Soc. 2012 Oct 10;134(40):16899-908. doi: 10.1021/ja308135r. Epub 2012 Sep 25.

Abstract

Dynamic nuclear polarization (DNP) solid-state NMR has been applied to powdered microcrystalline solids to obtain sensitivity enhancements on the order of 100. Glucose, sulfathiazole, and paracetamol were impregnated with bis-nitroxide biradical (bis-cyclohexyl-TEMPO-bisketal, bCTbK) solutions of organic solvents. The organic solvents were carefully chosen to be nonsolvents for the compounds, so that DNP-enhanced solid-state NMR spectra of the unaltered solids could be acquired. A theoretical model is presented that illustrates that for externally doped organic solids characterized by long spin-lattice relaxation times (T(1)((1)H) > 200 s), (1)H-(1)H spin diffusion can relay enhanced polarization over micrometer length scales yielding substantial DNP enhancements (ε). ε on the order of 60 are obtained for microcrystalline glucose and sulfathiazole at 9.4 T and with temperatures of ca. 105 K. The large gain in sensitivity enables the rapid acquisition of (13)C-(13)C correlation spectra at natural isotopic abundance. It is anticipated that this will be a general method for enhancing the sensitivity of solid-state NMR experiments of organic solids.

摘要

动态核极化(DNP)固态 NMR 已应用于粉末微晶固体,以获得约 100 倍的灵敏度增强。将葡萄糖、磺胺噻唑和扑热息痛用双氮氧自由基双自由基(双环己基-TEMPO-双酮,bCTbK)的有机溶剂溶液浸渍。仔细选择有机溶剂,使其成为化合物的非溶剂,以便获得未改变的固体的 DNP 增强固态 NMR 谱。提出了一个理论模型,该模型表明,对于具有长自旋晶格弛豫时间(T1((1)H) > 200 s)的外部掺杂有机固体,(1)H-(1)H 自旋扩散可以在微米长度尺度上传递增强的极化,从而产生实质性的 DNP 增强(ε)。在 9.4 T 和约 105 K 的温度下,获得了微晶葡萄糖和磺胺噻唑的约 60 的 ε 值。灵敏度的大幅提高使得能够以天然同位素丰度快速获得(13)C-(13)C 相关谱。预计这将是增强有机固体固态 NMR 实验灵敏度的一般方法。

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