Data di Pubblicazione:
2019
Abstract:
In this work we have studied the complexation of curcumin (HCur, 1,7-bis-(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione) with Al(III) and Fe(III) at 37 °C and in 0.16 M NaCl. The protonation constant of curcumin was also determined to evaluate the competition of the ligand for the metal cations and H+. Speciation profiles obtained by potentiometric titrations show that in aqueous solution a complexation occurs at 1:1 ligand-to-cations ratio. With the aim to define the coordination sites of curcumin with these metal ions a mass spectrometry and UV–Vis spectroscopy characterization was carried out. It was found that aluminum binds to the keto-enol moiety of curcumin, while iron binds to the guaiacol (2-methoxyphenol) one. This unexpected experimental evidence was supported by a thorough computational study.
Tipologia CRIS:
14.a.1 Articolo su rivista
Keywords:
Aluminum curcumin complexes; Coordination sites; DFT; Iron curcumin complexes; Stability constants
Elenco autori:
Beneduci, A.; Corrente, G. A.; Marino, T.; Aiello, D.; Bartella, L.; Di Donna, L.; Napoli, A.; Russo, N.; Romeo, I.; Furia, E.
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