| People | Locations | Statistics |
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| Naji, M. |
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| Motta, Antonella |
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| Aletan, Dirar |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Taccardi, Nicola |
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| Kononenko, Denys |
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| Petrov, R. H. | Madrid |
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| Alshaaer, Mazen | Brussels |
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| Bih, L. |
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| Casati, R. |
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| Muller, Hermance |
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| Kočí, Jan | Prague |
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| Šuljagić, Marija |
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| Kalteremidou, Kalliopi-Artemi | Brussels |
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| Azam, Siraj |
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| Ospanova, Alyiya |
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| Blanpain, Bart |
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| Ali, M. A. |
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| Popa, V. |
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| Rančić, M. |
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| Ollier, Nadège |
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| Azevedo, Nuno Monteiro |
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| Landes, Michael |
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| Rignanese, Gian-Marco |
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Roller, Alexander
University of Vienna
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (16/16 displayed)
- 2024Fungal Carbon: A Cost-Effective Tunable Network Template for Creating Supercapacitorscitations
- 2023Latonduine-1-Amino-Hydantoin Hybrid, Triazole-Fused Latonduine Schiff Bases and Their Metal Complexes: Synthesis, X-ray and Electron Diffraction, Molecular Docking Studies and Antiproliferative Activitycitations
- 2023Solid-state 13C NMR, X-ray diffraction and structural study of methyl 4-O-methyl β-D-glucopyranosides with all eight possible methyl-substitution patternscitations
- 2023A Novel Molecular Assembly of a Cobalt-Sulfate Coordination Polymer and Melaminecitations
- 2021Defect {((WO7)-O-VI)W-4(VI)} and Full {((WO7)-O-VI)W-5(VI)} Pentagonal Units as Synthons for the Generation of Nanosized Main Group V Heteropolyoxotungstatescitations
- 2020Naphthoquinones of natural origin: Aqueous chemistry and coordination to half-sandwich organometallic cationscitations
- 2020Cation-Directed Synthetic Strategy Using 4f Tungstoantimonates as Nonlacunary Precursors for the Generation of 3d-4f Clusterscitations
- 2019Synthesis, crystal structure and characterization of two new Cr(III)-substituted polyoxotungstates: [Cr((OCH2)3CCH2OH)2W6O18]3- and [H3Cr2W10O38(H2O)2]7-citations
- 2018Complexes of pyridoxal thiosemicarbazones formed with vanadium(IV/V) and copper(II)citations
- 2018Iron(II) and copper(II) paratungstates B: a single-crystal X-ray diffraction studycitations
- 2017Introducing the 4-Phenyl-1,2,3-Triazole Moiety as a Versatile Scaffold for the Development of Cytotoxic Ruthenium(II) and Osmium(II) Arene Cyclometalatescitations
- 2017Comparative equilibrium and structural studies of new pentamethylcyclopentadienyl rhodium complexes bearing (O, N) donor bidentate ligandscitations
- 2016Synthesis, characterisation and cytotoxic activity of organoruthenium(II)-halido complexes with 1H-benzimidazole-2-carboxylic acidcitations
- 2015Tris-Functionalized Hybrid Anderson Polyoxometalates: Synthesis, Characterization, Hydrolytic Stability and Inversion of Protein Surface Chargecitations
- 2014Antitumor pentamethylcyclopentadienyl rhodium complexes of maltol and allomaltolcitations
- 2011Ruthenium- and Osmium-Arene Complexes of 2-Substituted Indolo[3,2-c]quinolines: Synthesis, Structure, Spectroscopic Properties, and Antiproliferative Activitycitations
Places of action
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article
Synthesis, characterisation and cytotoxic activity of organoruthenium(II)-halido complexes with 1H-benzimidazole-2-carboxylic acid
Abstract
<p>Three new ruthenium(II)-arene halido complexes of general formula [(η<sup>6</sup>-p-cymene)RuX(L)] (C1-C3) were synthesised by reaction of [(η<sup>6</sup>-p-cymene)RuX<sub>2</sub>]<sub>2</sub> (X<sup>-</sup> = Cl<sup>-</sup>, Br<sup>-</sup>, I<sup>-</sup>) with 1H-benzimidazole-2-carboxylic acid (HL) in ethanol. The complexes were characterised by elemental analysis, mass spectrometry, IR,<sup>1</sup>H and<sup>13</sup>C NMR spectroscopy. The 1H-benzimidazole-2-carboxylate was found to act as a bidentate N,O-chelating ligand. Single-crystal X-ray diffraction analysis confirmed the "piano-stool" geometry of C3. The cytotoxic activity of the ligand precursor and ruthenium complexes was tested in human cancer cell lines: cervical carcinoma (HeLa), breast carcinoma (MDA-MB-231), myelogenous leukemia (K562) as well as in one normal human fetal lung fibroblast cell line (MRC-5), by MTT assay. The results show that ruthenium(II)-arene complexes possess enhanced cytotoxicity when compared to that of HL. The latter was devoid of activity in the range of concentrations up to 300 μM. Complex C3, carrying an iodido leaving ligand, exhibited moderate, but selective cytotoxicity toward HeLa, MDA-MB-231 and K562 cell lines, with IC<sub>50</sub> values: 73.7, 60.9 and 53.9 μM, respectively, being less toxic against MRC-5 cells (IC<sub>50</sub> = 175.9 μM). Complexes C1 and C2 showed moderate to low cytotoxicity in HeLa and K562 cells.</p>