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Discovery of New Metastable Polymorphs in a Family of Urea Co-Crystals by Solid-State Mechanochemistry

机译:通过固态力学化学发现尿素共晶体家族中新的亚稳态多晶型物

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Members of a homologous family of 1:2 cocrystals comprising even-chain alpha,omega-dihydroxyalkanes and urea have been reported previously to fall into three well-defined structure types, although surprisingly polymorphism was not observed for any member of this series. Here we report the discovery of the first examples of polymorphism within this family of materials, specifically for 1,6-dihydroxyhexane-(urea)(2) and 1,8-dihydroxyoctane-(urea)(2). The new polymorphs have been prepared by mechanochemical milling, and the crystal structures have been determined directly from powder X-ray diffraction data. On the basis of periodic density functional theory calculations, the new polymorphs are assigned as metastable with respect to the polymorphs reported previously. Under ambient conditions, the new polymorph of 1,6-dihydroxyhexane(urea)(2) transforms to the previously known polymorph over a matter of days. However, the new polymorph of 1,8dihydroxyoctane-(urea)(2) has significantly greater kinetic stability, which can be rationalized on the basis of the specific structural reorganization required to transform to the previously known polymorph.
机译:先前已经报道了由偶数链的α,ω-二羟基烷烃和尿素组成的1∶2共晶体的同源家族的成员落入三种明确定义的结构类型,尽管令人惊讶地未观察到该系列任何成员的多态性。在这里,我们报告了该材料家族中多态性的第一个实例的发现,特别是针对1,6-二羟基己烷-(脲)(2)和1,8-二羟基辛烷-(脲)(2)。通过机械化学研磨制备了新的多晶型物,并且直接从粉末X射线衍射数据确定了晶体结构。根据周期性密度泛函理论计算,相对于先前报道的多晶型,将新的多晶型指定为亚稳态。在环境条件下,新的1,6-二羟基己烷(脲)(2)的多晶型物会在几天内转化为以前已知的多晶型物。但是,新的1,8-二羟基辛烷-(脲)(2)的多晶型物具有更大的动力学稳定性,可以根据转化为先前已知的多晶型物所需的特定结构重组来合理化。

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