Abstract
We report the synthesis of a novel, water-soluble aryl-extended calix[4]pyrrole receptor. The water-solubilising groups are placed at the lower rim of the receptor, leaving the binding pocket unperturbed and open for modification. Binding studies were performed with a series of pyridine N-oxides. These studies revealed the ability of the receptor to bind neutral and charged N-oxides in basified water with stability constants higher than 104 M-1.
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CITATION STYLE
Hernández-Alonso, D., Zankowski, S., Adriaenssens, L., & Ballester, P. (2015). Water-soluble aryl-extended calix[4]pyrroles with unperturbed aromatic cavities: synthesis and binding studies. Organic and Biomolecular Chemistry, 13(4), 1022–1029. https://doi.org/10.1039/c4ob02108h
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