Three‐Centre Oxidative Addition of Phosphorus Ylides to Ru3(CO)12 Phosphorus ylides undergo oxidative addition to Ru3(CO)12 to yield a wide range of Ru3 clusters with triply bridging organic ligands derived from the ylides. Ph3PCH2 forms HRu3(CO)9(μ31‐Ph3P — CH — CO) (1) containing a phosphonio enolate. Ph3PCH — CHO yields a product mixture containing the phosphonio enolate‐bridged cluster and its PPh3 derivative 6, the phosphoniomethylidyne‐bridged compound H2Ru3(CO)9(μ31‐C — PPh3) (5), and the ketenylidene‐bridged compound H2Ru3(CO)8(PPh3)(μ31‐C — CO) (7). Thermal treatment converts the phosphonio enolate ligand (in 1) into the phosphoniomethylidyne ligand (in 5), and the latter into the ketenylidene ligand (in 7). With Ph3PCH — C(O)Me and Ru3(CO)12 ortho1‐metalated Ru3 derivatives 10, 11 of the phosphonio ketone R3P — C — C(O)Me are produced, and likewise with Ph3PCH — COOEt the ortho1‐metalated derivative 12 of the phosphonio ester R3P — C — CO2Et. Me3PCH — COOtBu is oxidatively added to form HRu3(CO)9(μ31‐Me3P — C — COOtBu) (13) bearing a phosphonio ester ligand. — The crystal structures of 6 and 13 are reported. The sequence of Ru3 clusters and the bonding modes of the μ3 ligands can be related to the surface reactions during Fischer‐Tropsch catalysis.
No takes yet. Share an insight, caveat, or question.
Heineke et al. (1993) studied this question.
Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context: