Abstract
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 micro/nanospheres 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.
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CITATION STYLE
Chen, H., Huang, C., Ding, Y., Zhang, Q. L., Zhu, B. X., & Ni, X. L. (2019). Organic core-shell-shaped micro/nanoparticles from twisted macrocycles in Schiff base reaction. Chemical Science, 10(2), 490–496. https://doi.org/10.1039/c8sc03824d
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