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Süss-Fink, Georg
Nom
Süss-Fink, Georg
Affiliation principale
Fonction
Professeur ordinaire
Email
georg.suess-fink@unine.ch
Identifiants
Résultat de la recherche
Voici les éléments 1 - 9 sur 9
- PublicationAccès libreRhodium-Catalysed Carbonylation of Methanol Using a New Multifunctional Ligand - Isolation and Structural Characterisation of the Macrocycle [Rh2I6(CO)2(C6H4N3CH2CO2C4H2SCO2CH2C6H4N3)]2(2001)
;Thomas, Christophe M. ;Neels, Antonia; The new multifunctional ligand thiophene-2,5-bis(carboxylatomethylenebenzotriazole) (1) reacts with [RhCl(CO)2]2 to give the rhodium complex [RhCl(CO)(1)]2 (2), which was found to catalyse efficiently the iodide-mediated carbonylation of methanol. The macrocyclic carbonyliodorhodium complex [Rh2I6(CO)2(1)]2 (3) was isolated from the catalytic mixture and structurally characterised. - PublicationAccès libreNucleophilic addition reactions on the electron-deficient cluster dication [H4Ru4(C6H6)4]2+ : synthesis and structural characterisation of the water-soluble cluster cations [H3Ru4(C6H6)4 (CO)]+ and [H3Ru4(C6H6)4 (OH)]2(2001)
;Chérioux, Frédéric ;Maisse-François, Aline ;Neels, Antonia; The electron-deficient (58e) cluster cation [H4Ru4(C6H6)4]2+1 was found to react in aqueous solution with simple nucleophiles to give electron-precise (60e) clusters. With carbon monoxide, the cluster cation [H3Ru4(C6H6)4(CO)]+3 is formed. The reaction with water needs NaN3 as catalyst and yields the cluster dication [H3Ru4(C6H6)4 (OH)]2+4a; the reaction with alcohols leads to the analogous clusters [H3Ru4(C6H6)4 (OR)]2+ (R = Me: 4b, R = Et: 4c, R = PhCH2: 4d, R = Ph: 4e, R = 4-EtC6H4: 4f). The single-crystal X-ray structure analyses of the chloride salts of 3 and 4a reveal a tetrahedral Ru4 metal core. Each ruthenium atom is coordinated by a η6-benzene ligand, while the carbonyl or hydroxo ligands are found as µ3 capping ligands over a triangular face of the Ru4 tetrahedron. - PublicationAccès libreCluster build-up in aqueous solution: synthesis, structure, protonation and catalytic properties of the trinuclear cation [(η6-C6H6)(η6-C6Me6)2Ru3(μ2-H)3(μ3-O)]+(1999-08-27)
;Faure, Matthieu ;Jahncke, Manfred ;Neels, Antonia ;Stœckli-Evans, HelenThe trinuclear oxo-capped cluster cation [(η6-C6H6)(η6-C6Me6)2Ru3 (μ2-H)3(μ3-O)]+ (2) was synthesised by reacting [(η6-C6Me6)Ru(H2O)3]2+ with [(η6-C6Me6)2Ru2(μ2-H)3]+ in aqueous solution. The single-crystal X-ray structure analysis of the tetrafluoroborate salt shows the cation to contain a H2O molecule hydrogen-bonded to the μ3-oxo ligand. Acidification experiments show two protonation steps occuring at this H2O molecule and the oxo cap of the triruthenium cluster. The cluster cation 2 catalyses the hydrogenation of aromatic compounds in aqueous solution under biphasic conditions. - PublicationAccès libreOxidative functionalisation of alkanes: synthesis, molecular structure and catalytic implications of anionic vanadium(V) oxo and peroxo complexes containing bidentate N,O ligands(1999)
; ;Stanislas, Sandrine ;Shulpin, Georgiy B. ;Nizova, Galina V.; ;Neels, Antonia; Claude, SaturninA mixture of [NBu4][VO3] and pyrazine-2-carboxylic acid (Hpca) in acetonitrile catalysed smoothly the reaction of alkanes RH (R = CH3 or C6H11) with molecular oxygen (from air) and hydrogen peroxide to give the corresponding alkyl hydroperoxide ROOH as the primary product. The oxo and peroxo anions [VO2(pca)2]– and [VO(O2)(pca)2]–, isolated as the tetrabutylammonium or ammonium salts from acetonitrile solution and fully characterised by single crystal structure analyses, are assumed to be involved in the catalytic process. A screening of different N,O ligands showed Hpca to be the best co-catalyst, while anthranilic acid (Hana) proved to be almost inactive. The isolation and crystal structure analysis of the analogous oxo compound [NBu4][VO2(ana)2] showed a fundamental difference in the co-ordination of the bidentate N,O ligands which might explain the different catalytic activities: while in [VO2(pca)2]– the two pca ligands are bonded through a nitrogen and an oxygen atom (N,O co-ordination), in [VO2(ana)2]– the two ana ligands are co-ordinated via two oxygen atoms of the carboxylato group (O,O co-ordination). - PublicationAccès libreTri- and Tetranuclear Mixed-Metal Clusters Containing Alkyne Ligands : Synthesis and Structure of [Ru3Ir(CO)11(RCCR’)]-, [Ru2Ir(CO)9(RCCR’)]-, and [HRu2Ir(CO)9(RCCR’)](1999)
;Ferrand, Vincent; ;Neels, AntoniaThe tetrahedral cluster anion [Ru3Ir(CO)13]- (1) reacts with internal alkynes RCCR to afford the alkyne derivatives [Ru3Ir(CO)11(RCCR)]- (2: R = R’ = Ph; 3: R = R’ = Et; 4: R = Ph; R’ = Me; 5: R = R’ = Me) which have a butterfly arrangement of the Ru3Ir skeleton in which the alkyne is coordinated in a μ4-η2 fashion. Under CO pressure they undergo fragmentation to give the trinuclear cluster anions [Ru2Ir(CO)9 (RCCR)]- (6: R = R’ = Ph; 7: R = R’ = Et; 8: R’ = Ph; R’ = Me; 9: R = R’ = Me), in which the alkyne ligand is coordinated in a μ3-η2 parallel fashion. Protonation of these trinuclear anions leads to the formation of the corresponding neutral hydrido clusters [HRu2Ir(CO)9 (RCCR)] (10: R = R’ = Ph; 11: R = R’ = Et; 12: R = Ph; R’ = Me; 13: R = R’ = Me). The protonation of the butterfly anions 2 and 3, however, gives rise to the formation of the neutral tetrahedral clusters [HRu3Ir(CO)11(RCCR)] (14: R = R’ = Ph and 15: R = R’ = Et), respectively. The analogous clusters [HRu3Ir(CO)11(PhCCCH3)] (16) and [HRu3Ir(CO)11(CH3CCCH3)] (17) are only accessible from the reaction of the neutral cluster [HRu3Ir(CO)13] with the corresponding alkynes. The complexes 2, 4, 5, 6, 10, 12 and 15 are characterised by X-ray structure analysis. - PublicationAccès libreTriruthenium–iridium clusters containing alkyne ligands : synthesis, structure, and catalytic implications of [(µ-H)IrRu3(CO)11(µ3-η2-PhC≡CPh)] and [IrRu3(CO)10(µ4-η2-PhC≡CPh)(µ-η2-PhC=CHPh)](1998)
;Ferrand, Vincent; ;Neels, AntoniaThe mixed-metal cluster [HIrRu3(CO)13] 1 reacts with one equivalent of disubstituted alkynes RC≡CR to give [HIrRu3(CO)11(µ3-η2-RC≡CR)] (R = Ph 2; R = Me 3), with a second equivalent of the alkyne the clusters [IrRu3(CO)10(µ4-η2-RC≡CR)(µ-η2-RC=CHR)] (R = Ph 4; R = Me 5) are obtained. The single-crystal X-ray structure analyses of 2 and 3 show these clusters to have a tetrahedral Ru3Ir framework containing the alkyne ligand coordinated in a parallel fashion over the Ru3 face of the metal skeleton. In contrast, the clusters 4 and 5 consist of a butterfly arrangement of the Ru3Ir framework with the alkyne ligand coordinated to all four metal atoms, giving an overall octahedral Ru3IrC2 skeleton, as demonstrated by the single-crystal structure analysis of 4. Cluster 1 is an excellent catalyst for the hydrogenation of diphenylacetylene to give stilbene (catalytic turnover number 990 within 15 min), clusters 2 and 4 are also catalytically active but seem to represent side-channels of the catalytic cycle. - PublicationAccès libreSaturated and unsaturated triruthenium clusters containing three sterically demanding phosphine ligands : synthesis and structure of [Ru3(CO)9(PCy3)3] and [Ru3H2(CO)6(PCy3)3](1998)
; ;Godefroy, Isabelle ;Ferrand, Vincent ;Neels, AntoniaThe reaction of Na[Ru3H(CO)11] with an excess of tricyclohexylphosphine in methanol afforded, depending on the reaction conditions, the tri-substituted clusters [Ru3(CO)9(PCy3)3] (48e) and [Ru3H2(CO)6(PCy3)3] (44e), inaccessible hitherto. - PublicationAccès libreSaturated and unsaturated tetraruthenium clusters containing sterically demanding dicyclohexylphosphido ligands: synthesis and structure of [H4Ru4(CO)8(PCy2)4] and [H5Ru4(CO)8(PCy2)3](1998)
; ;Godefroy, Isabelle ;Béguin, Alain ;Rheinwald, Gerd ;Neels, AntoniaThe thermal reaction of the dinuclear complex [Ru2(CO)4(O2CH)2(PCy2H)2] with molecular hydrogen in cyclohexane afforded the tetranuclear clusters [H4Ru4(CO)8(PCy2)4] (64e) and [H5Ru4(CO)8(PCy2)3] (62e), both of which have a square-planar arrangement of the metal framework. - PublicationAccès libreMono-, di- and tetra-nuclear p-cymeneruthenium complexes containing oxalato ligands(1997)
;Yan, Hong; ;Neels, AntoniaThe oxalato complexes [Ru2(µ-η4-C2O4)Cl2(η6-p-PriC6H4Me)2] 1 and [Ru(η2-C2O4)(NH3)(η6-p-PriC6H4Me)] 2 have been prepared from the reaction of ammonium oxalate with [{RuCl2(η6-p-PriC6H4Me)}2] and [Ru(H2O)3(η6-p-PriC6H4Me)]2+, respectively. With triphenylphosphine, 1 reacted to give [Ru2 (µ-η4-C2O4)(PPh3)2 (η6-p-PriC6H4Me)2]2+3, while 2 gave [Ru(η2-C2O4)(PPh3)(η6-p-PriC6H4Me)] 4. The dichloro complex 1 can also be converted into the cationic dimethanol complex [Ru2 (µ-η4-C2O4)(MeOH)2(η6-p-PriC6H4Me)2]2+5 by precipitation of the chloride with a silver salt in methanol. Complex 5 reacted with 4,4-bipyridine to afford a novel tetranuclear metallomacrocycle [Ru4(µ-η4-C2O4)2(µ-η1:η1-bipy)2 (η6-p-PriC6H4Me)4]4+6 with alternating oxalato and 4,4-bipyridine bridges. The reaction between 1 and azide yielded the known azido-bridged complex [{Ru(µ-η1-N3)Cl(η6-p-PriC6H4Me)}2] 7. The molecular structures of 1 (two conformational isomers), 4, 5 and 6 have been solved by X-ray crystallography.