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Therrien, Bruno
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Therrien, Bruno
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bruno.therrien@unine.ch
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Voici les éléments 1 - 10 sur 42
- PublicationAccès libreHydrogen-bonded metalla-assemblies(2018)
Les métallo-assemblages d’arene ruthenium ont montré un grand prometteur biologique. Inspirés par la combinaison de la liaison hydrogène et de la complexation des métaux du groupe de Mendoza, nous avons récemment préparé une série des métallo-assemblages. Par conséquent, pour étudier plus en profondeur les métallo-assemblages liés par des liaisons hydrogènes, nous avons utilisé le système mélamine/barbiturique rosette avec complexes de type tabouret de piano ou métallo-clips dinucléaires. L'introduction d'un groupe pyridyle sur le fragment acide barbiturique ou le fragment mélamine permet la coordination des métaux à la périphérie de la rosette.
Des nouveaux métallo-assemblages rosettes ont été préparés et caractérisés. Des métallo-assemblages rosette trinucléaires neutres et cationiques ont été synthétisés, ainsi que des métallo-assemblages rosette hétéro-hexanucléaires. La coordination de métallo-clips dinucléaires a produit des métallo-assemblages hexanucléaires cationiques. Globalement, les assemblages rosette avec des complexes de type tabouret de piano offrent des grandes opportunités dans le domaine de la chimie supramoléculaire., Hydrogen bonds are the most utilized non-covalent interactions in biological systems, due to their directionality, stability, reversibility and diversity. The weak strength of hydrogen-bond can be modified by combining several hydrogen bonds in the same unit, like in the melamine∙cyanuric/barbituric acid rosette-type system.
Arene ruthenium metalla-assemblies have showed a great biological potential. Inspired by the combination of hydrogen bonding and metal complexation from the group of de Mendoza, we have recently prepared a series of hydrogen-bonded metalla-assemblies. Therefore, to further investigate hydrogen-bonded metalla-assemblies, we used the melamine/barbituric rosette-type system with piano-stool complexes or dinuclear metalla-clips. The introduction of a pyridyl group on the barbituric acid moiety or the melamine moiety allows coordination of metals at the periphery of the rosette.
New rosette-type metalla-assemblies have been prepared and characterized. Neutral and cationic trinuclear rosette-type metalla-assemblies have been synthesized, as well as hetero-hexanuclear rosette-type metalla-assemblies. Coordination of dinuclear metalla-clips has produced cationic hexanuclear metalla-assemblies. Overall, rosette-type assemblies with piano-stool complexes offer great opportunities in the field of supramolecular chemistry. - PublicationAccès libreSynthesis, characterization and exploration of the catalytic, supramolecular and biological applications of dinuclear complexes(2013)
- PublicationAccès libreThiolato-Bridged Arene–Ruthenium Complexes: Synthesis, Molecular Structure, Reactivity, and Anticancer Activity of the Dinuclear Complexes [(arene)2Ru2 (SR)2Cl2](2012)
; ; - PublicationAccès libreStudy of complexes of platinum group metals containing nitrogen bases derived from pyridine aldehydes: Interesting molecular structures with unpredicted bonding modes of the ligands(2011)
; Rao, Kollipara MohanA series of mono-cationic dinuclear half sandwich ruthenium, rhodium and iridium metal complexes have been synthesized using ((pyridin-2-yl)methylimino)nicotinamide (L1) and ((picolinamido)phenyl)picolinamide (L2) ligands: [(η6-arene)2Ru2 (μ-L1)Cl3]+ (arene = C6H6, 1; p-iPrC6H4Me, 2; C6Me6, 3), [(η5-C5Me5)2M2(μ-L1)Cl3] + (M = Rh, 4; Ir, 5), and [(η6-arene)2Ru2(μ-L2)(μ-Cl)]+ (arene = C6H6, 6; p-iPrC6H4Me, 7; C6Me6, 8), [(η5-C5Me5)2M2(μ-L2)Cl2]+ (M = Rh, 9; Ir, 10). All the complexes have been isolated as their hexafluorophosphate salts and fully characterized by use of a combination of NMR and IR spectroscopy. The solid state structure of three representatives 4, 6 and 9 has been determined by X-ray crystallographic studies. Interestingly, in the molecular structure of 4, the first metal is bonded to two nitrogen atoms whereas the second metal center is coordinated to only one nitrogen atom with two terminal chloride ligands. Fascinatingly in the case of the complexes with the symmetrical ligand L2, both ruthenium centers having η6-arene groups are bonded to nitrogen atoms with a bridging chloride atom between the two metal centers, whereas the metals with η5-Cp∗ groups are bonded to the ligand N,O and N,N fashion. - PublicationAccès libreRu2(CO)4(OOCR)2L2 sawhorse-type complexes containing axial 5-(4-pyridyl)-10,15,20-triphenylporphyrin ligands(2011)
; The thermal reaction of Ru3(CO)12 with various carboxylic acids (benzoic, 4-hydroxyphenylacetic, ferrocenic, stearic, oleic, 4-(octadecyloxy)benzoic) in refluxing tetrahydrofuran, followed by addition of 5-(4-pyridyl)-10,15,20-triphenylporphyrin (L), gives the dinuclear complexes Ru2(CO)4(OOCR)2L2 (1: R = –C6H5, 2: R = –CH2-p-C6H4OH, 3: R = –C5H4FeC5H5, 4: R = –(CH2)16CH3, 5: R = –(CH2)7CHdouble bond; length as m-dashCH(CH2)7CH3, 6: R = –p-C6H4O(CH2)17CH3). Complexes 1–6 were characterised by IR, NMR, and ESI-MS as well as by elemental analysis. The UV–Vis spectra show the Soret band centred at 417 nm and the Q bands at 515, 550, 590 and 645 nm, respectively. - PublicationAccès libreArene ruthenium bis-saccharinato complexes: Synthesis, molecular structure and catalytic oxidation properties in aqueous solutionArene ruthenium complexes [(η6-arene)Ru(sacc)2(OH2)] (arene = para-cymeme, benzene) containing an aqua and two saccharinato ligands have been synthesized from [(η6-arene)RuCl2]2 and sodium saccharinate in a water-ethanol mixture (1:1). The aqua complex [(η6-MeC6H4Pri)Ru(sacc)2(OH2)] reacts with acetonitrile to give the acetonitrile complex [(η6-MeC6H4Pri)Ru(sacc)2(NCMe)]. The corresponding benzene derivative [(η6-C6H6)Ru(sacc)2(NCMe)] was obtained from [(η6-C6H6)RuCl2]2 and saccNa in an acetonitrile-methanol mixture (1:1). All new complexes show a piano-stool geometry with two mono-hapto nitrogen-bonded saccharinato ligands in addition to a H2O or MeCN ligand. All complexes of the type [(η6-arene)Ru(sacc)2(OH2)] and [(η6-arene)Ru(sacc)2(NCMe)] were found to catalyze the oxidation of secondary alcohols with tert-butyl hydroperoxide (ButOOH) to give the corresponding ketones in aqueous solution.
- PublicationAccès libreHalf sandwich platinum group metal complexes containing tetradentate N-donor ligand bearing two pyrazolyl-pyridine units linked by an aromatic spacer(2010)
; Rao, Kollipara MohanReaction of the bis-bidentate ligand, 1,3-bis((3-(pyridin-2-yl)-1H-pyrazol-1-yl)methyl)benzene (NN∩NN), containing two chelating pyrazolyl-pyridine units connected by an aromatic spacer with platinum group metal complexes results in a series of cationic binuclear complexes, [(η6-arene)2Ru2(NN∩NN)Cl2]2+ (arene = C6H6, 1; p-iPrC6H4Me, 2; C6Me6, 3), [(η5-C5Me5)2M2(NN∩NN)Cl2]2+ (M = Rh, 4; Ir, 5), [(η5-C5H5)2M2(NN∩NN)(PPh3)2]2+ (M = Ru, 6; Os, 7), [(η5-C5Me5)2Ru2(NN∩NN)(PPh3)2]2+ (8) and [(η5-C9H7)2Ru2(NN∩NN)(PPh3)2]2+ (9). All these complexes have been isolated as their hexafluorophosphate salts and fully characterized by use of a combination of NMR spectroscopy, IR spectroscopy and mass spectrometry. The solid state structures of three complexes, [2][PF6]2, [4][PF6]2 and [6][PF6]2, has been determined by X-ray crystallographic studies. - PublicationAccès libreAnticancer activity of new organo-ruthenium, rhodium and iridium complexes containing the 2-(pyridine-2-yl)thiazole N,N-chelating ligand(Elsevier, 2010)
; ; - PublicationAccès librePermanent Encapsulation or Host–Guest Behavior of Aromatic Molecules in Hexanuclear Arene Ruthenium Prisms(2010)
; ; Cationic arene ruthenium metallaprisms of the general formula [Ru6(p-cymene)6(tpt)2(OO∩OO)3]6+ {tpt = 2,4,6-tris(4-pyridyl)-1,3,5-triazine; OO∩OO = 9,10-dioxo-9,10-dihydroanthracene-1,4-diolato [1]6+, 6,11-dioxo-6,11-dihydronaphthacene-5,12-diolato [2]6+} have been obtained from the corresponding dinuclear arene ruthenium complexes [Ru2(p-cymene)2(OO∩OO)Cl2] by reaction with tpt and silver trifluoromethanesulfonate. Aromatic molecules (phenanthrene, pyrene, triphenylene, coronene) present during the synthesis of these metallaprisms are permanently encapsulated to give carceplex systems. All empty cages ([1]6+ and [2]6+) and carceplex systems ([guest⊂1]6+ and [guest⊂2]6+) were isolated in good yield as trifluoromethanesulfonate salts and characterized by NMR, UV, and IR spectroscopy. The host–guest properties of [1]6+ and [2]6+ were studied in solution in the presence of small aromatic molecules (phenanthrene andpyrene). The stability constant of association (Ka) wasestimated by NMR spectroscopy for the following host–guest systems: [phenanthrene⊂1]6+, [pyrene⊂1]6+ and [phenanthrene⊂2]6+, [pyrene⊂2]6+. All Ka values were found to be larger than 2.0 × 104M–1 for these host–guest systems ([D3]acetonitrile, 21 °C). - PublicationAccès libreMono and dinuclear half-sandwich platinum group metal complexes bearing pyrazolyl-pyrimidine ligands: Syntheses and structural studies(2010)
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