Abstract
Schiff bases are regarded as “privileged ligands” due to their capability to form complexes with a wide range of transition metal ions yielding stable and intensely colored metal complexes. In this study, equimolar amounts of 4-methyl-5-imidazolecarboxaldehyde and thiosemicarbazide were combined and the Schiff base 4-methyl-5-imidazolecarboxaldehyde thiosemicarbazone was prepared as a new bidentate complexing agent. The synthesized ligand was reacted with palladium (II) and platinum (II) ions yielding air-stable complexes. For characterization purpose, mass spectra and x-ray analysis of the ligand and infrared spectra, electronic spectra, thermal analysis, proton nuclear magnetic resonance and 13-carbon nuclear magnetic resonance spectra studies were carried out on the obtained ligand and its complexes. The characterization data showed that the ligand acts as a bidentate coordinate to the metal ions through azomethine nitrogen and sulfur atom. An in vitro antimicrobial investigation was also carried out for the free ligand and its metal complexes against four bacteria; Bacillus cereus, Staphylococcus aureus (Gram-positive), Escherichia coli and Salmonella typhimurium (Gram-negative) and one Fungi; Candida albicans. The results showed that the antimicrobial activity of the prepared complexes showed higher activity than the free ligand.
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