Synthesis of a bimetallic P-N bridged rhodium (I)-ruthenium (II) complex: Application in the hydroformylation reaction
Résumé
The reaction of [Rh(acac)(PPh2Py)(2)] (acac = acetylacetonate, PPh2Py = 2 (diphenylphosphino)pyridine) with [Cp*Ru(CH3CN)(3)][OTf] (Cp* = pentamethylcyclopentadienyl, OTf = trifluoromethanesulfonate) provides a cationic bimetallic complex [Cp*Ru(PPh2Py)(2)Rh(acac)][OTf], in which a ruthenium rhodium coordinate (dative covalent) bond is formed. The structure was ascertained by single crystal X-ray diffraction. The catalytic performances of the bimetallic complex were evaluated in the hydroformylation reaction of 1-octene and compared to those of the in situ formed catalysts and the mononuclear counterparts. The catalysis results point out that the bimetallic complex is fragmenting under hydroformylation conditions, which was confirmed by NMR analysis.