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 / Stefanelli, M; Coticone, R; Sbardella, P; Ceccacci, F; Mancini, G; Mandoj, F; Paolesse, R; Venanzi, M; Monti, D. - In: JOURNAL OF PORPHYRINS AND PHTHALOCYANINES. - ISSN 1088-4246. - 21:4-6(2017), pp. 391-397. [10.1142/S1088424617500377]

The aggregation of amphiphilic (L)-proline-porphyrin derivatives in ethanol-water mixtures promoted by chiral anionic surfactants

Monti D
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.
2017
chiral surfactants; porphyrins; self-assembly
01 Pubblicazione su rivista::01d Recensione
The aggregation of amphiphilic (L)-proline-porphyrin derivatives in ethanol-water mixtures promoted by chiral anionic surfactants / Stefanelli, M; Coticone, R; Sbardella, P; Ceccacci, F; Mancini, G; Mandoj, F; Paolesse, R; Venanzi, M; Monti, D. - In: JOURNAL OF PORPHYRINS AND PHTHALOCYANINES. - ISSN 1088-4246. - 21:4-6(2017), pp. 391-397. [10.1142/S1088424617500377]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1468825
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