非晶态阿斯匹林醌从整齐的机械化学:衍射纳米晶域和快速再结晶暴露于溶剂蒸汽†‡

Silvina Pagola, James Howard, Johannes Merkelbach and Danny Stam
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摘要

阿斯匹林醌是通过液体辅助研磨机械化学方法制备成结晶固体,或通过纯研磨或纯球磨制备成非晶相(由x射线粉末衍射确定)。我们以前的工作证明,使用傅里叶变换红外光谱,机械化学反应发生在机械处理干净的混合物。本文报道了微晶电子衍射(microED)在人工研磨合成的非晶粉末中,在大多数非衍射颗粒中发现了两个微米级的衍射颗粒。值得注意的是,其中一个的显微ed数据得出了已知的阿斯匹林醌的晶格参数。此外,这种所谓的“x射线无定形”相在暴露于N,N-二甲基甲酰胺或己烷蒸气时(以较低的速率)迅速再结晶;但在封闭容器的环境条件下,它可以保持20个月以上的无定形状态。两种再结晶材料的晶格参数和结晶度在实验误差范围内是相同的。然而,从N,N-二甲基甲酰胺蒸气中再结晶的材料比从己烷中回收的类似相中观察到的x射线粉末衍射峰略强,分辨率更高。正如预期的那样,Williamson-Hall图显示前一种固体的平均晶域尺寸更大。这些结果说明了利用微能电显微镜研究非晶相的结构特征,以及溶剂蒸气在促进非晶相再结晶中的一般作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Amorphous quininium aspirinate from neat mechanochemistry: diffracting nanocrystalline domains and quick recrystallization upon exposure to solvent vapours†‡

Amorphous quininium aspirinate from neat mechanochemistry: diffracting nanocrystalline domains and quick recrystallization upon exposure to solvent vapours†‡

Quininium aspirinate is mechanochemically prepared as a crystalline solid by liquid-assisted grinding, or as an amorphous phase (as determined by X-ray powder diffraction), by neat grinding or neat ball milling. Our previous work demonstrated using FT-IR spectroscopy that a mechanochemical reaction had occurred in the mechanically treated neat mixtures. Herein is reported that microcrystal electron diffraction (microED) afforded the discovery of two diffracting micron-size particles in the amorphous powder synthesized by manual grinding, among a majority of non-diffracting particles. Remarkably, microED data of one of them led to the known lattice parameters of quininium aspirinate. Furthermore, this so-called ‘X-ray amorphous’ phase quickly recrystallizes upon exposure to vapors of N,N-dimethylformamide, or hexane vapours (at a lower rate); but it remains amorphous for longer than 20 months when stored at ambient conditions in a closed container. The lattice parameters and the degrees of crystallinity of both recrystallized materials are identical within the experimental error. However, slightly more intense and better-resolved X-ray powder diffraction peaks are observed in the material recrystallized from N,N-dimethylformamide vapours than in the analogous phase recovered from hexane. As expected, Williamson–Hall graphs lead to a larger average crystalline domain size for the former solid. These results illustrate the use of microED for the investigation of structural features in amorphous phases, and the generic role of the solvent vapours in promoting their recrystallization.

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