1. Effects of changing ions on the crystal design, non-covalent interactions, antimicrobial activity, and molecular docking of Cu(II) complexes with a pyridoxal-hydrazone ligand.
- Author
-
Gatto, Claudia C., Dias, Lucas M., Paiva, Clarisse A., Silva, Izabel C. R. da, Freire, Daniel O., Tormena, Renata P. I., Nascimento, Érica C. M., Martins, Joao B. L., Dong, Wen-Kui, and Badea, Mihaela
- Subjects
- *
CRYSTAL structure , *ANTI-infective agents , *MOLECULAR docking , *HYDRAZONES , *COPPER ions - Abstract
The present work reports the influence of the presence of different ions (Cl-, Br-, NO3-, or SO42-) on the formation and proprieties of Cu(II) complexes with pyridoxal-benzoylhydrazone (PLBHZ). Four new complexes were successfully synthesized, [CuCl2(PLBHZ)] (1), [CuBr2(PLBHZ)] (2), [CuCl(PLBHZ)H2O]-NO3-H2O (3), and [CuSO4(PLBHZ)H2O]-3H2O (4), and characterized by spectroscopic and physicochemical methods. A single-crystal X-ray study reveals the Schiff base coordinated to the metal center tridentate by the ONS-donor system, resulting in distorted square pyramidal coordination geometries. Noncovalent interactions were investigated by 3D Hirshfeld surface analysis by the dnorm function, 2D fingerprint plots, and full interaction maps. The ion exchange is important in forming three-dimensional networks with π···π stacking interactions and intermolecular hydrogen bonds. The in vitro biological activity of the free ligand and metal complexes was evaluated against Gram-positive and Gramnegative bacterial strains and the free pyridoxal-hydrazone ligand showed higher activity than their Cu(II) complexes. Molecular docking was used to predict the inhibitory activity of the ligand and complexes against Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli bacteria. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF