Thèse de doctorat : Université de Neuchâtel, 2018.
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...
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In: JBIC Journal of Biological Inorganic Chemistry, 2009, vol. 14, no. 5, p. 693-701
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In: JBIC Journal of Biological Inorganic Chemistry, 2012, vol. 17, no. 6, p. 951-960
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In: JBIC Journal of Biological Inorganic Chemistry, 2009, vol. 14, no. 1, p. 101-109
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Thèse de doctorat : Université de Neuchâtel, 2013.
The work presented in this thesis involves the synthesis and characterization of dinuclear ruthenium, rhodium and iridium complexes. The catalytic, supramolecular and biological applications of these dinuclear complexes will be discussed. In the first part, the synthesis of sawhorse-type diruthenium tetracarbonyl complexes and their catalytic applications in the supercritical carbon dioxide...
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In: European Journal of Inorganic Chemistry, 2012, vol. 2012, no. 9, p. 1531-1535
Treatment of an arene–ruthenium dichloride dimer with thiols RSH to lead to cationic trithiolato complexes of the type [(arene) 2Ru2(SR)3]+ was shown to proceed through the neutral thiolato complexes [(arene)2Ru2(SR)2Cl2], which have been isolated and characterized for arene =...
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In: Inorganica Chimica Acta, 2011, vol. 371, no. 1, p. 59-62
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 =...
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In: European Journal of Inorganic Chemistry, 2012, vol. 2012, no. 4, p. 727-732
Superparamagnetic core-shell-type Fe3O4/Ru nanoparticles (particle size ca. 15 nm) synthesized by co-precipitation, adsorption and reduction methods were found to selectively hydrogenate the carbon-oxygen double bond in trans-4-phenyl-3-penten-2-one (conversion 100 %, selectivity > 90 %) with a catalytic turnover of 900 under mild reaction conditions (30 °C, 15 bar...
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In: Journal of Organometallic Chemistry, 2011, vol. 696, no. 21, p. 3285–3291
Arene 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...
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In: Journal of Organometallic Chemistry, 2010, vol. 695, no. 3, p. 409-414
A series of neutral, anionic and cationic arene ruthenium complexes containing the trichlorostannyl ligand have been synthesised from SnCl2 and the corresponding arene ruthenium dichloride dimers [(η6-arene)Ru(μ2-Cl)Cl]2 (arene = C6H6, PriC6H4Me). While the reaction with triphenylphosphine...
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