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Synthesis of Three Ru(II) Polypyridyl Complexes of 2-(4-(Pyrrolidine-1-yl)phenyl)-1H-imidazo[4,5-f][1,10]phenanthroline: Characterisation, DNA Binding, Antimicrobial and Cytotoxicity Studies
Corresponding Author(s) : Markandeya Namani
Asian Journal of Chemistry,
Vol. 38 No. 7 (2026): Vol. 38, No 7 (2026)
Abstract
Three Ru(II) complexes having general formula, [Ru(A)2PPIP](ClO4)2·2H2O, where PPIP = 2-(4-(pyrrolidine-1-yl)phenyl)-1H-imidazo[4,5-f]-[1,10]phenanthroline and A = phen = 1,10 phenanthroline (1), bpy = bipyridine (2), dmb = 4,4'-dimethyl 2,2'-bipyridine (3) were synthesised. In order to conduct the structural investigation of these complexes, various techniques such as 1H NMR, 13C NMR, FT-IR, ESI mass and UV-visible were utilised. The Ru(II) complexes were confirmed to have an octahedral geometry based on the spectroscopic and analytical results. Their interaction with DNA was systematically investigated using UV-Vis absorption, fluorescence quenching and viscosity measurements, all of which consistently indicated an intercalative binding mode. The agreement among these techniques strengthens the proposed DNA-binding mechanism. Furthermore, DNA cleavage studies revealed that all the three Ru(II) complexes effectively converted supercoiled DNA (Form I) into nicked circular DNA (Form II), demonstrating their significant DNA-cleaving capability. In vitro biological evaluations against both Gram-positive and Gram-negative microbial strains revealed that the Ru(II) complexes exhibited superior antimicrobial activity compared with the PPIP ligand. Cytotoxicity studies further demonstrated that the Ru(II) complexes were more potent than the free ligand, while showing enhanced activity relative to the reference standards. In addition, molecular modelling investigations were performed to elucidate their geometric and electronic characteristics. The electrostatic potential surface contours for the complexes were also analysed to obtain the insights into the charge distribution and their nucleophilic level of sensitivity.
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J. Parekh, P. Inamdhar, R. Nair, S. Baluja and S. Chanda, J. Serb. Chem. Soc., 70, 1155 (2005); https://doi.org/10.2298/JSC0510155P