Australian Journal of Chemistry · 1968 · 12 citations · 0 references
Natural SciencesChemistryInorganic ChemistryOrganic ChemistrySolid-state ChemistryCarbon MonoxideChemical BondingCoordination ChemistryMetal-ligand BondingTransition Metal ChemistryTransition Metal ComplexesBidentate Ligand BindingCarbon Monoxide CoordinationCarbon Monoxide LigandsCarbon Monoxide SourcesLanthanide HalidesMetal-ligand Bond StrengthMonodentate Ligand BindingTransition Metal Carbonyls
Complexes of the types MX2(CO)3(dam)2 and MX2(CO)2(dam)2 [M = Mo, W; X = Cl, Br; dam = bis(diphenylarsino)methane] have been prepared and characterized. The compounds are all non-electrolytes; in the tricarbonyls both of the potentially bidentate arsenic ligands are in fact acting only as monodentates, but in the dicarbonyls there is mixed coordination with one ligand monodentate and the other bidentate. The dicarbonyl complexes absorb carbon monoxide in solution at room temperature and pressure, a metal-arsenic bond of the bidentate ligand is broken, and the corresponding tricarbonyl compound is produced. The reaction is readily reversible; thus the system is an example of a carbon monoxide carrier.