[Fe2L3]4+ cylinders derived from bis(bidentate) 2-pyridyl-1,2,3- triazole "click" ligands: Synthesis, structures and exploration of biological activity

63Citations
Citations of this article
53Readers
Mendeley users who have this article in their library.

Abstract

A series of metallosupramolecular [Fe2L3](BF 4)4 "click" cylinders have been synthesized in excellent yields (90%-95%) from [Fe(H2O6](BFe 4)2 and bis(bidentate) pyridyl-1,2,3-triazole ligands. All complexes were characterized by elemental analysis, IR, UV-vis, 1H-, 13C- and DOSY-NMR spectroscopies and, in four cases, the structures confirmed by X-ray crystallography. Molecular modeling indicated that some of these "click" complexes were of similar size and shape to related biologically active pyridylimine-based iron(II) helicates and suggested that the "click" complexes may bind both duplex and triplex DNA. Cell-based agarose diffusion assays showed that the metallosupramolecular [Fe 2L3](BF4)4 "click" cylinders display no antifungal activity against S. cerevisiae. This observed lack of antifungal activity appears to be due to the poor stability of the "click" complexes in DMSO and biological media. © 2013 by the authors.

Cite

CITATION STYLE

APA

Vellas, S. K., Lewis, J. E. M., Shankar, M., Sagatova, A., Tyndall, J. D. A., Monk, B. C., … Crowley, J. D. (2013). [Fe2L3]4+ cylinders derived from bis(bidentate) 2-pyridyl-1,2,3- triazole “click” ligands: Synthesis, structures and exploration of biological activity. Molecules, 18(6), 6383–6407. https://doi.org/10.3390/molecules18066383

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free