Abstract

Novel titanium (IV), vanadyl (II), nickel (II), copper (II), cobalt (II), mercury (II) and silver (I) coordination compounds were established from a ligand created from a diazotization coupling process between 1-(4-aminophenyl)ethanone and barbituric acid. Analytical, spectroscopic, and thermal approaches were used to detect the best structural geometry of the compounds. The coordination compounds were constructed with (1M:2L) stoichiometry. With the exception of titanium (IV), vanadyl (II), and silver (I), all chelated compounds were non-electrolytes. Except for the vanadyl complex, which possessed square pyramidal geometry, and the silver one with tetrahedral geometry, the chelates of titanium (IV), copper (II), nickel (II), mercury (II) and cobalt (II) possessed an octahedral one. The ligand functioned as an ON-neutral bidentate moiety. The thermal manner of all compounds was studied by thermogravimetric analysis (TGA). According to XRD and TEM analysis, all compounds were nanosized. Theoretical calculations were performed to gain more information about the structure of the ligand and Ag chelate by DFT/B3LYP/LanL2DZ. The ligand and some of its chelates were explored as antibacterial, antifungal, and antitumor agents. According to the findings, the (H2L) activity was enhanced by complexation. The antitumor activity of the Ag(I) chelate was dramatically higher than that of the ligand and other chelates, with an IC50 of 11.5 gmL-1. For antimicrobial, Cu(II) chelate outperformed other complexes and the control drug against A. brasiliensis, B. cereus and P. vulgaris.

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