The use of chiral surfactants results in a powerful tool to form chiral assemblies of (L)proline-functionalized porphyrin derivatives in EtOH/H2O exploiting hydrophobic effect. The formation of chiral heteroaggregated species strictly depends both on the configuration of the chiral center of the surfactant and on its concentration, opening the possibility to tune the supramolecular asymmetry of the final structures.
The aggregation of amphiphilic (L)-proline-porphyrin derivatives in ethanol-water mixtures promoted by chiral anionic surfactants
Ceccacci F;Mancini G;
2017
Abstract
The use of chiral surfactants results in a powerful tool to form chiral assemblies of (L)proline-functionalized porphyrin derivatives in EtOH/H2O exploiting hydrophobic effect. The formation of chiral heteroaggregated species strictly depends both on the configuration of the chiral center of the surfactant and on its concentration, opening the possibility to tune the supramolecular asymmetry of the final structures.File in questo prodotto:
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