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Crystal engineering of homochiral molecular organization of naproxen in cocrystals and their thermal phase transformation studies

机译:萘普生同晶体手性分子组织的晶体工程及其热相变研究

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Since the racemic naproxen does not have the desired crystal structure essential to induce preferential enrichment, we used crystal engineering principle to produce the required homochiral R- and S-chains in the solid state. The cocrystal structures of racemic and S-naproxen (NPX) with bipyridine (BPY) and piperazine (PIZ) were determined, which consist of homochiral 1D naproxen chains that are associated by weak non-covalent interactions. Thermal studies of both racemic and S-naproxen-bipyridine cocrystals indicated a monotropic polymorphic transformation upon heating and the new crystalline phase was characterized by DSC, PXRD, hot-stage microscopy, and FT-IR spectroscopy.
机译:由于外消旋萘普生不具有诱导优先富集所必需的所需晶体结构,因此我们使用晶体工程原理生产了固态所需的手性R和S链。确定了消旋和S-萘普生(NPX)与联吡啶(BPY)和哌嗪(PIZ)的共晶体结构,该结构由纯手性1D萘普生链组成,这些链通过弱的非共价相互作用而缔合。外消旋和S-萘普生联吡啶的共晶体的热学研究表明,加热后会发生单向多晶型转变,并且通过DSC,PXRD,热台显微镜和FT-IR光谱对新的结晶相进行表征。

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