Spectral studies, crystal structures, DNA binding, and anticancer potentials of Pd(II) complexes with iminophosphine ligands: Experimental and computational methods
Journal Publication ResearchOnline@JCUAbstract
Herein, we studied the synthesis and the biological properties of palladium(II) complexes derived from iminophosphine ligands DPPB-3-hydroxybenzohydrazone (DPPB-HBH), DPPB-4-phenylthiosemicarbazone (DPPB-PTSC), and DPPB-thiosemicarbazone (DPPB-TSC) (DPPB = 2-(diphenylphosphino)benzaldehyde) using theoretical and experimental methods. The molecular structures of [PdCl(DPPB-HBH)]Cl, [Pd(DPPB-HBH)(2)] Cl-2 center dot 2CH(3)CN, [PdCl(DPPB-PTSC)], and [PdCl(DPPB-TSC)] were characterized by various spectroscopic tech-niques and X-ray crystallographic for [PdCl(DPPB-HBH)]Cl, [Pd(DPPB-HBH)(2)]Cl-2 center dot 2CH(3)CN, and [PdCl(DPPB-PTSC)], confirming the distorted square-planar geometry for the palladium atoms. Complexes with the general formula [PdCl(Ligand)(x)] (x = 1) were employed to evaluate biological activities such as cytotoxicity against the MDA-MB-231 breast cancer cells and DNA binding ability. The results revealed the high cytotoxicity of the palladium complexes compared to the reference drug cisplatin (IC50 = 24.59 mu g/mL), as well as their moderate binding ability to DNA through electrostatic interactions and groove binding. It was also found that [PdCl(DPPB-HBH)]Cl has the highest activity among others (IC50 = 9.3 mu g/mL). Their interaction mode with DNA was investigated using molecular docking and NCI calculations, which showed complete agreement with the experimental results. Furthermore, quantum chemistry calculations were used to analyze the structure-activity relationship and introduce reactive sites, which determined the cause of the difference in the reactivity of the samples.
Journal
Inorganica Chimica Acta
Publication Name
N/A
Volume
547
ISBN/ISSN
1873-3255
Edition
N/A
Issue
N/A
Pages Count
16
Location
N/A
Publisher
Elsevier
Publisher Url
N/A
Publisher Location
N/A
Publish Date
N/A
Url
N/A
Date
N/A
EISSN
N/A
DOI
10.1016/j.ica.2022.121368