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Achieving chiral resolution in self-assembled supramolecular structures through kinetic pathways

机译:通过动力学途径实现自组装超分子结构的手性拆分

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Chiral phase transitions were studied in a self-assembled 2,6-dibromoanthraquinones supramolecular system prepared on Au(111) using scanning tunneling microscopy. As the molecules were deposited at about 150K, they formed heterochiral chevron structures (a racemate) consisting of two alternating prochiral molecular rows. When the as-deposited sample was warmed to 300K followed by cooling to 80K, phase-separated homochiral structures (a conglomerate), as well as the chevron structures, were observed. We propose molecular models for the structures that are in good agreement with abinitio studies and can be explained by hydrogen bonds and halogen bonds. We found that heterochiral chevron structures were more stable than homochiral structures due to two additional halogen bonds per molecule. We considered kinetic pathways for the phase transitions that were made possible via a disordered liquid phase entropically stabilized at 300K. We show how chiral resolution can be achieved by exploiting kinetic paths allowed in supramolecular systems.
机译:在Au(111)上制备的自组装2,6-二溴蒽醌超分子体系中,使用扫描隧道显微镜研究了手性相变。当分子以约150K沉积时,它们形成了由两个交替的前手性分子行组成的异手性V形结构(外消旋体)。将沉积后的样品加热至300K,然后冷却至80K,观察到相分离的同手性结构(团聚体)以及人字形结构。我们提出了与脱氧核糖核酸研究非常吻合的结构分子模型,可以用氢键和卤素键来解释。我们发现,由于每个分子有两个额外的卤素键,所以杂手性V形结构比同手性结构更稳定。我们考虑了通过熵稳定在300K的无序液相使相变的动力学途径成为可能。我们展示了如何通过利用超分子系统中允许的动力学路径来实现手性拆分。

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