Spectroscopic and TDDFT studies of N-phenyl-N′-(3-triazolyl)thiourea) compounds with transition metal ions

Abstract

Reaction of N-phenyl-N′-(3-triazolyl)thiourea) (H3L) with M(ClO4)2 (M = Co(II) (1), Ni(II) (2) and Cu(II) (3)) afforded [M(H2L)2] complexes, which were characterized experimentally and theoretically using different analytical, and spectral tools. The susceptibility of Staphylococcus aureus and Escherichia coli bacteria towards H3L and its complexes was evaluated. The thiourea ligand coordinates to the 3d-metal ions via C–S−, and triazole nitrogen yielding coordination compounds between the tetrahedral, and square-planar geometries (“flattened” tetrahedron, D2d symmetry). Full geometry optimization, vibrational analyses, and natural bond orbital analyses of the proposed conformations of 1–3 were executed at B3LYP/def2-SVP to gain some knowledge about the local minima structures, natural charge of the coordinated metal ion, electronic configuration as well as the hybridization of M–L bonds. The electronic structures of the local minimum structures of 1–3 were investigated by time-dependent density functional theory calculations. Coordination of the thiourea ligand to Co(II) and Cu(II) ions did alter the toxicity against the tested microbes, while chelation of Ni(II) ion gave rise to inactive species.

Keywords

• Antibacterial activity
• NBO
• TDDFT
• Thiourea ligands
• Triazole