Synthesis, structural elucidation and antiradical activity of a copper (II) naringenin complex

CELIZ, GUSTAVO; MOLINA, JOSÉ; CELIZ, GUSTAVO; MOLINA, JOSÉ; SUAREZ, SEBASTIÁN A.; BRONDINO, CARLOS D.; SUAREZ, SEBASTIÁN A.; BRONDINO, CARLOS D.; ARIAS, ANALÍA; DOCTOROVICH, FABIO; ARIAS, ANALÍA; DOCTOROVICH, FABIO

BIOMETALS

SPRINGER

Lugar: Berlin; Año: 2019 vol. 32 p. 595 - 610

0966-0844

Coupling the extraction and derivatization of flavonoids to the Citrus processing industry is attractive from both the environmental and economicpoints of view. In the present work, the flavonoid naringin, obtained by ??green?? extraction with a water:ethanol mixture from waste grapefruit industry, was hydrolyzed to obtain naringenin. This flavonoid was used to synthesize the complex trans-di(aqua)bis(7-hydroxy-2-(4-hydroxyphenyl)-4-oxo-5-chromanolato)copper (II). This compound was characterized by spectroscopic techniques (UV/Vis, IR, Raman,NMR and EPR), and by thermal analysis (TG andDSC). Then, a monocrystal of the complex obtained by dissolution and recrystallization in DMF was analyzed by single crystal X-ray diffraction. This is the first report of the crystal structure of a Citrus flavonoid complex. Additionally, its antiradical activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH) was determined and compared with that for naringenin,demonstrating that coordination to copper enhances the antiradicalar activity of naringenin. According to the Mulliken population analysis conducted, by copper favors the delocalization and stabilization of the produced radical, since it acts as an electronic density acceptor.