Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Vincent Ferrand"'
Autor:
Evelina Gatti, Voahirana Camosseto, Didier Marguet, Hugues Lelouard, Vincent Ferrand, Philippe Pierre, Alexandre David, Jacek Bania
Publikováno v:
The Journal of Cell Biology
In response to inflammatory stimulation, dendritic cells (DCs) have a remarkable pattern of differentiation (maturation) that exhibits specific mechanisms to control antigen processing and presentation. One of these mechanisms is the sorting of polyu
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :1063-1068
The Ligand Polyhedral Model (LPM) has been applied to the series of carbonyl species [Fe4(CO)13]2−, [Fe3Co(CO)13]−, [Ru3Co(CO)13]−, [Ru3Rh(CO)13]−, [Ru3Ir(CO)13]−, [Os3Ir(CO)13]− and [Co2Ru2(CO)13] containing thirteen carbonyl ligands. Th
Publikováno v:
Journal of Organometallic Chemistry. 601:78-86
The reaction of arene ruthenium(II) complexes [Ru(η 6 -C 6 Me 4 R 2 )(PMe 3 )Cl 2 ] ( 1 , R=Me; 1 ′, R=H) with propargyl alcohol derivatives HCC(H)(OH)( p -C 6 H 4 X) ( a , X=HCC(H)(OH); c , X=CHO; d , X=CHCH 2 ; e , X=CHCHCHC
Publikováno v:
Journal of Molecular Catalysis A: Chemical. 143:163-170
The cluster anion [Os3Ir(CO)13]− (1) was prepared in 50% yield by reaction of Os3(CO)12 with [Ir(CO)4]−. The single-crystal X-ray structure analysis of the bis(triphenylphosphoranylidene)ammonium salt shows 1 to consist of a tetrahedral metal cor
Autor:
Georg Süss-Fink, Helen Stoeckli-Evans, Antonia Neels, Isabelle Godefroy, Jean-Yves Saillard, Vincent Ferrand, Samia Kahlal, María Teresa Garland
Publikováno v:
Journal of Organometallic Chemistry. 579:285-297
The reaction of Na[HRu 3 (CO) 11 ] with an excess of tricyclohexylphosphine in methanol gives the neutral complex H 2 Ru 3 (CO) 6 (PCy 3 ) 3 which is the first 44 e − triruthenium cluster reported. This highly electron-deficient species reacts with
Publikováno v:
European Journal of Inorganic Chemistry. 1999:853-862
Publikováno v:
Scopus-Elsevier
The reaction of the mixed-metal carbonyl cluster anion [H2Ru3Ir(CO)12]− with PPh3, PMe3, P(OPh)3, AsPh3 or SbPh3 leads to the mono-substituted derivatives [H2Ru3Ir(CO)11L]− (L=PPh3 1, L=PMe3 2, L=P(OPh)3 3, L=AsPh3 4, L=SbPh3 5). Protonation of t
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :3825-3832
The mixed-metal cluster [HIrRu3(CO)13] 1 reacts with one equivalent of disubstituted alkynes RCCR to give [HIrRu3(CO)11(µ3-η2-RCCR)] (R = Ph 2; R = Me 3), with a second equivalent of the alkyne the clusters [IrRu3(CO)10(µ4-η2-RCCR)(µ-η2-RCCHR)]
Publikováno v:
Journal of Organometallic Chemistry. 549:263-274
The electron-deficient cluster (μ2-H(Ru3(CO)9[μ3-NS(O)MePh] (1) reacts with the terminal alkyne PhCH2CCH to give the vinyl complex Ru3(μ2-CO)2(CO)6[μ3-NS(O)MePh](μ2-η1,η2-PhCH2CCH2)(2). The analogous reaction with internal alkynes (RC
Autor:
Nadine Derrien, Vincent Ferrand, Carsten Bolm, Céline Gambs, Georg Süss-Fink, Helen Stoeckli-Evans
Publikováno v:
Journal of Organometallic Chemistry. 549:275-282
The reaction of the electron-deficient cluster ( μ 2 -H)Ru 3 (CO) 9 [ μ 3 -NS(O)MePh] ( 1 ) with para -nitrotolane gives, with coupling of two alkyne units and elimination of the para -nitrophenyl fragment, the trinuclear complexes Ru 3 (CO) 9 [ μ