DFT Investigation of the Mechanism of Phosphine-Thioether Isomerization in the Triosmium Cluster Os3(CO)10(Ph2PCH2CH2SMe): Migratory Preference for the Formation of an Edge-Bridged Thioether versus a Phosphine Moiety

• Autores: David A. Hrovat, Ebbe Nordlander, Michael G. Richmond
• Localización: Organometallics, ISSN 0276-7333, Vol. 31, Nº. 18, 2012, págs. 6608-6613
• Idioma: inglés
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• Resumen

  • The rearrangement of the phosphine-thioether ligand in 1,2-(Peq,Seq)-Os3(CO)10(Ph2PCH2CH2SMe) to 1,1-(Peq,Sax)-Os3(CO)10(Ph2PCH2CH2SMe) was investigated by electronic structure calculations. The chelated isomer lies 2.5 kcal/mol lower in energy than its bridged counterpart, and the barrier computed for the mechanism is in agreement with the results from our earlier experimental study. Phosphine-thioether isomerization occurs via three distinct steps that involve the migration of the CO and SMe groups in a plane that is perpendicular to the trimetallic core. One of the intermediates on the reaction surface corresponds to the 50e cluster Os3(CO)9(μ-CO)(μ-Ph2PCH2CH2SMe), whose edge-bridging thioether moiety functions as a 4e donor ligand. Alternative mechanisms involving ligand dissociation/association and merry-go-round sequences are energetically prohibitive.