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Arene-perfluoroarene interactions in crystal engineering 8. Structures of 1:1 complexes of hexafluorobenzene with fused-ring polyaromatic hydrocarbons

机译:晶体工程中的芳烃-全氟芳烃相互作用8.六氟苯与稠环多芳烃的1:1配合物的结构

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A series of 1:1 complexes of hexafluorobenzene (HFB) with naphthalene, anthracene, phenanthrene, pyrene and triphenylene were prepared and their X-ray crystal structures determined at low temperatures. Each structure contains infinite mixed stacks of alternating nearly-parallel molecules of HFB and arene, which display various 'slip' distortions and form different 3-dimensional motifs. The naphthalene, anthracene and pyrene complexes show polymorphism. Crystal packing of HFB complexes is compared with that of corresponding octafluoronaphthalene complexes. Ab initio DFT calculations on the infinite lattices give lattice parameters and 'slip' parameters in close agreement with the experimental crystal structures, while showing that intermolecular cohesion is predominantly of electrostatic, rather than van der Waals, origin.
机译:制备了一系列六氟苯(HFB)与萘,蒽,菲,pyr和联苯的1:1配合物,并在低温下确定了它们的X射线晶体结构。每个结构包含HFB和芳烃交替交替的近乎平行分子的无限混合堆栈,这些分子显示出各种“滑移”变形并形成不同的3维图案。萘,蒽和pyr配合物显示出多态性。将HFB配合物的晶体堆积与相应的八氟萘配合物的晶体堆积进行比较。在无限晶格上进行从头算DFT计算得出的晶格参数和“滑移”参数与实验晶体结构非常吻合,同时表明分子间内聚力主要是静电产生的,而不是范德华力。

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