New Procedure To Calculate All Equilibrium Constants in Flavylium Compounds: Application to the Copigmentation of Anthocyanins

• Tipo: Artigo em Revista Científica Internacional
• Data: 2019

Autores

Mendoza, J (Autor) Outra; Basilio, N (Autor) Outra; Victor de Freitas (Autor) FCUP; Pina, F (Autor) Outra

Revista

Título: ACS Omega

Vol. 4

Editora: American Chemical Society

Indexação

ISI Web of Knowledge - 34 Citações

Scopus - 35 Citações

Outras Informações

ID Authenticus: P-00R-0ZV

DOI: 10.1021/acsomega.9b01066

Abstract (EN): A new experimental procedure to calculate all equilibrium constants of the multistate of species of anthocyanins and related compounds, including those in basic medium, is reported. The procedure is based on a series of pH jumps monitored by stopped flow from an extended pH range of solutions at pseudo-equilibrium (when there is no significant formation of trans-chalcones) or at equilibrium to pH = 1.0. The experimental procedure is described for the anthocyanin model compound 4'-hydroxyflavylium, which exhibits a peculiar behavior in moderately acidic medium, because the quinoidal base, hemiketal, and cis-chalcone have similar mole fractions at pseudo-equilibrium, permitting good discrimination among these species. The experimental procedure can be extended to the copigmentation phenomenon and allow the calculation of the 1:1 copigmentation constants of the flavylium cation, quinoidal base, hemiketal, and cis- and trans-chalcones (this last from the equilibrium) and their respective ionized forms. The method was applied to calculate the copigmentation constants of the model compound 4'-hydroxyflavylium as well as malvidin-3-glucoside with caffeine. In the last compound, the strongest interaction takes place with the quinoidal base (K = 303 M-1) and flavylium cation (K = 134 M-1) and, to a lesser extent, with the ionized quinoidal base (K = 43 M-1) and cis-chalcone (K = 17 M-1). The caffeine interaction with the hemiketal and the other ionized species is negligible.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 13