Autor(es): Baptista, Rosa Maria Ferreira ; Santos, Daniela ; Cunha, N. F. ; Castro, Maria Cidália Rodrigues ; Rodrigues, Pedro António Veiga ; Machado, A. V. ; Belsley, M. ; de Matos Gomes, Etelvina
Data: 2025
Identificador Persistente: https://hdl.handle.net/1822/95121
Origem: RepositóriUM - Universidade do Minho
Assunto(s): benzothiazole; diphenylalanine dipeptides; optical properties; self-assembling
This work explores the self-assembly and optical properties of a novel chiral, aromatic-rich Boc-Phe-Phe dipeptide derivative functionalized with a benzothiazole bicyclic ring that forms supramolecular structures. Leveraging the well-known self-assembling capabilities of diphenylalanine dipeptides, this modified derivative introduces a heterocyclic benzothiazole unit that significantly enhances the fluorescence of the resulting nanostructures. The derivative’s rich aromatic character drives the formation of supramolecular structures through self-organization mechanisms influenced by quantum confinement. By adjusting the solvent system, the nanostructures exhibit tunable morphologies, ranging from nanospheres to nanobelts. The nonlinear optical properties of these self-assembled structures were studied and an estimated (Formula presented.) of ~0.9 pm/V was obtained, which is comparable to that reported for the highly aromatic triphenylalanine peptide.
