par Keymeulen, Flore ;De Bernardin, Paolo ;Giannicchi, Ilaria;Galantini, L.;Bartik, Kristin ;Dalla Cort, Antonella
Référence Organic & biomolecular chemistry, 13, page (2437-2443)
Publication Publié, 2015-01
Référence Organic & biomolecular chemistry, 13, page (2437-2443)
Publication Publié, 2015-01
Article révisé par les pairs
Résumé : | The use of micelles to transpose lipophilic receptors, such as uranyl-salophen complexes, into an aqueous environment is a valuable and versatile tool. Receptor 1 incorporated into CTABr micelles forms a supramolecular system that exhibits excellent binding properties towards fluoride in water, despite the competition of the aqueous medium. To fully evaluate the potential of micellar nanodevices, we extended our previous study to other types of surfactants and to a uranyl-salophen receptor with a more extended aromatic surface. Paramagnetic relaxation enhancement experiments were used to obtain information on the location of the two receptors within the micelles and complementary information was obtained from dynamic light scattering experiments. With these data it is possible to account for the key factors necessary to obtain an efficient supramolecular device for anion binding in water. |