Synthesis, structural studies and biological activity of new Cu(II) complexes with acetyl derivatives of 7-hydroxy-4-methylcoumarin

J Inorg Biochem. 2015 Apr:145:94-100. doi: 10.1016/j.jinorgbio.2015.01.006. Epub 2015 Jan 23.

Abstract

The new Cu(II) complexes with 6-acetyl-7-hydroxy-4-methylcoumarin (HL1) and 8-acetyl-7-hydroxy-4-methylcoumarin (HL2) have been obtained by the electrochemical method. The density functional theory calculations and X-ray absorption spectroscopy techniques have been used to geometrically describe a series of new compounds. The studies have been focused on the coordination mode of the hydroxy ligands to the metallic centre. The complexes, Cu(HL1)2 and Cu(HL2)2⋅0.5H2O, have flat square geometry with oxygen atoms in the first coordination sphere. Two bidentate anionic coumarins are bonded to the metal cation via the acetyl and deprotonated hydroxyl O atoms. Biological activity, including microbiological and cytotoxic, has been evaluated and found to be enhanced in comparison with the parent ligands. Moreover, the Cu(II) complex with 8-acetyl-7-hydroxy-4-methylcoumarin shows similar antifungal activity as commercially used fluconazole.

Keywords: 7-hydroxycoumarin; Coumarin derivative; Cu(II) complex; DFT; Electrochemical synthesis; XAFS.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Anti-Infective Agents / pharmacology
  • Cell Line, Tumor
  • Copper / chemistry*
  • Drug Screening Assays, Antitumor
  • Humans
  • Hymecromone / chemical synthesis
  • Hymecromone / chemistry*
  • Hymecromone / pharmacology*
  • Male
  • Mice
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Spectroscopy, Fourier Transform Infrared
  • X-Ray Absorption Spectroscopy

Substances

  • Anti-Infective Agents
  • Hymecromone
  • Copper