Manganese(II) and Zinc(II) metal complexes of novel bidentate formamide-based Schiff base ligand: synthesis, structural characterization, antioxidant, antibacterial, and in-silico molecular docking study

A new bidentate Schiff base ligand (C H Cl N ), condensation product of ethylene diamine and 4-chloro N-phenyl formamide, and its metal complexes [M(C H Cl N ) (OAc) ] (where M = Mn(II) and Zn(II)) were synthesized and characterized using various analytical and spectral techniques, including high-re...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Frontiers in chemistry 2024-07, Vol.12, p.1414646
Hauptverfasser: Juyal, Vijay Kumar, Thakuri, Shweta Chand, Panwar, Mohit, Rashmi, Prakash, Om, Perveen, Kahkashan, Bukhari, Najat A, Nand, Viveka
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:A new bidentate Schiff base ligand (C H Cl N ), condensation product of ethylene diamine and 4-chloro N-phenyl formamide, and its metal complexes [M(C H Cl N ) (OAc) ] (where M = Mn(II) and Zn(II)) were synthesized and characterized using various analytical and spectral techniques, including high-resolution mass spectrometry (HRMS), elemental analysis, ultraviolet-visible (UV-vis), Fourier-transform infrared (FTIR) spectroscopy, AAS, molar conductance, H NMR, and powder XRD. All the compounds were non-electrolytes and nanocrystalline. The synthesized compounds were assessed for antioxidant potential by DPPH radical scavenging and FRAP assay, with BHT serving as the positive control. Inhibitory concentration at 50% inhibition (IC ) values were calculated and used for comparative analysis. Furthermore, the prepared compounds were screened for antibacterial activity against two Gram-negative bacteria ( and ) and two Gram-positive bacteria ( and ) using disk-diffusion methods, with amikacin employed as the standard reference. The comparison of inhibition zones revealed that the complexes showed better antibacterial activity than the ligand. To gain insights into the molecular interactions underlying the antibacterial activity, the ligand and complexes were analyzed for their binding affinity with tyrosyl-tRNA synthetase (PDB ID: 1JIL) and cell membrane protein OmpF complex (PDB ID: 4KR4). These analyses revealed robust interactions, validating the observed antibacterial effects against the tested bacterial strains.
ISSN:2296-2646
2296-2646
DOI:10.3389/fchem.2024.1414646