首页> 外文期刊>Acta crystallographica. Section C, Structural chemistry. >Solid-state NMR meets electron diffraction: determination of crystalline polymorphs of small organic microcrystalline samples
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Solid-state NMR meets electron diffraction: determination of crystalline polymorphs of small organic microcrystalline samples

机译:固态NMR符合电子衍射:小有机微晶样品的结晶多晶型物的测定

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A combination of solid-state NMR (ssNMR) and electron diffraction (ED) has been used to determine the crystalline polymorphs in small-organic micro-crystalline molecules. Although ~13C cross-polarization magic angle spinning (CPMAS) is a widely used method for determining crystalline polymorphs, even in a mixture, it sometimes fails if the molecular conformations are similar. On the other hand, ED can, in principle, differentiate crystalline forms with different lattice parameters, even when they have very similar molecular conformations. However, its application is usually limited to inorganic molecules only. This is because the ED measurements of organic molecules are very challenging due to degradation of the sample by electron irradiation. We overcame these difficulties by the use of ~1H double-quantum/single-quantum correlation experiments at very fast magic angle spinning, together with ED observations under mild electron irradiation. The experiments were demonstrated on l-histidine samples in L-histidine-HCl·H_2O, orthorhombic l-histidine and monoclinic l-histidine.
机译:固态NMR(SSNMR)和电子衍射(ED)的组合已被用于确定小型有机微晶分子中的结晶多晶型物。虽然〜13C交叉偏振魔角纺丝(CPAMS)是一种广泛使用的方法,用于确定结晶多晶型物,即使在混合物中,如果分子构象相似,它有时会出现故障。另一方面,即使当它们具有非常相似的分子构象时,ED可以用不同的晶格参数区分结晶形式。然而,其应用通常仅限于无机分子。这是因为由于样品通过电子照射降解了有机分子的ED测量非常具有挑战性。我们通过在非常快的魔法角度旋转的情况下使用〜1h双量子/单量子相关实验来克服这些困难,以及在轻度电子照射下的ED观察结果。在L-组氨酸-HCl·H_2O,正晶型L-组氨酸和单斜晶L-组氨酸中对L-组氨酸样品进行了实验。

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