Publication: (Pyrazolyl)pyridine ruthenium(III) complexes: Synthesis, kinetics of substitution reactions with thiourea and biological studies
dc.contributor.author | Omondi, Reinner O. | |
dc.contributor.author | Ojwach, Stephen O. | |
dc.contributor.author | Jaganyi, Deogratius. | |
dc.contributor.author | Fatokun, Amos A. | |
dc.contributor.author | Jaganyi, Deogratius | |
dc.date.accessioned | 2024-06-26T06:46:53Z | |
dc.date.available | 2024-06-26T06:46:53Z | |
dc.date.issued | 2024-08-01 | |
dc.description.abstract | Reactions of 2-bromo-6-(3,5-dimethyl-1H-pyrazol-1-yl)pyridine (L1), 2,6-di (1H-pyrazol-1-yl) pyridine (L2) and 2,6-bis(3,5-dimethyl-1H-pyrazol-1-yl)pyridine (L3) with RuCl3·3H2O led to the formation of their respective metal complexes [RuCl3(L1)] (1), [RuCl3(L2)] (2) and [RuCl3(L3)] (3). Solid state structure of complex 3 established the formation of a six-coordinate mononuclear compound in which L3 is tridentately bound. The order of reactivity of the studied complexes with thiourea (TU) nucleophile is in the form 1 > 2 > 3, in line with density functional theory (DFT) studies. The complexes displayed minimal cytotoxic activity against the HeLa cell line, consistent with molecular docking experiments which showed weaker DNA binding affinities. | |
dc.identifier.uri | https://doi.org/10.1016/j.inoche.2018.06.006 | |
dc.identifier.uri | https://erepository.mku.ac.ke/handle/123456789/5935 | |
dc.language.iso | en | |
dc.publisher | Inorganic Chemistry Communications | |
dc.title | (Pyrazolyl)pyridine ruthenium(III) complexes: Synthesis, kinetics of substitution reactions with thiourea and biological studies | |
dc.type | Article | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | 796ae3c9-5bd6-4962-be3f-97e396eacbc6 | |
relation.isAuthorOfPublication.latestForDiscovery | 796ae3c9-5bd6-4962-be3f-97e396eacbc6 |
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