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Organic core–shell-shaped microanoparticles from twisted macrocycles in Schiff base reaction

机译:Schiff碱反应中扭曲的大环有机核-壳形的微米/纳米颗粒

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Functional self-assemblies derived from noncovalent interactions such as lipid vesicles and DNA chiral double helices are a typical feature of natural life activity. Because of this phenomenon, a self-assembly approach for various functional organic particles is a desirable objective in supramolecular chemistry. Here, we report the discovery of enantiomeric conformers from a twisted macrocyclic host ( MH ), which was obtained from an achiral precursor by Schiff base reaction. Further studies suggest that a series of unexpected and stable core–shell-based organic microanospheres can be directly precipitated from a simple reaction solution with high yield. A single-crystal X-ray diffraction analysis of MH revealed that the unusual C–H?π interaction triggered self-assembly of the enantiomeric forms in the solid state plays an important role in the formation of the core–shell-shaped organic particles.
机译:源自非共价相互作用的功能性自组装,例如脂质小泡和DNA手性双螺旋,是自然生命活动的典型特征。由于这种现象,在超分子化学中,用于各种功能有机颗粒的自组装方法是理想的目标。在这里,我们报告从扭曲的大环宿主(MH)的对映体构象体的发现,它是通过席夫碱反应从非手性前体获得的。进一步的研究表明,可以从简单的反应溶液中以高收率直接沉淀出一系列意想不到且稳定的基于核壳的有机微/纳米球。 MH的单晶X射线衍射分析表明,异常的C–H?π相互作用触发了固态对映体形式的自组装,在核-壳形有机颗粒的形成中起着重要作用。

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