Abstract
A novel [FEII2L3]4+ metallo-organic helicate results from subcomponent self-assembly of a C3-symmetric triamine (4,4',4"-(1,3,5-triazine-2,4,6-triyl) trianiline), octahedral iron(II) and 2-formyl pyridine in CH3CN solution. The constitution of this supramolecular helicate was confirmed by ESI-MS and 1H NMR spectra. Different planar aromatic guests were selected to investigate host-guest interactions by shifts of 1H NMR signals. The results show that electron-rich aromatic molecules with matched size and symmetry, such as pyrene, are subject to be bound with the outstretched arms of the helicate ligand via aromatic π-πinteractions.
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CITATION STYLE
Jiang, P., Wua, W. Y., Tanga, T. H., Chen, Z. F., Fang, Y. C., & Wan, R. (2019). 1H NMR study of the host-guest chemistry in a supramolecular helicate FEII2L3 solutio. Quimica Nova, 42(4), 412–417. https://doi.org/10.21577/0100-4042.20170355
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