Trimethyl-palladium(IV) and -platinum(IV) complexes containing phosphine donor ligands, including studies of 1,5,9-triethyl-1,5,9-triphosphacyclodecane and X-ray structural studies of palladium(II) and palladium(IV) complexes

Dimethyl(2,2'-bipyridine)palladium(u) reacted with methyl triflate (CF3SO3Me) at -60 °C to form a palladium(iv) complex which reacted with a range of monodentate phosphines [PPh3, PMePh2, PMe2Ph, PCy3, P(OMe)3], l,2-bis(diethylphosphino)ethane (depe), or .yv;,sj7;-l,5,9-triethyl-l,5,9-triphosphacyclodecane (s)v;,5jv;-Et3[12]aneP3) to form complexes containing octahedral palladium(iv) centresyflc-[PdMe3(2,2'-bipy)(L)]+ 1-5,11-13. The ligand depe bridges between palladium(iv) centres in a binuclear complex (11), the triphosphine forms both mononuclear (13) and binuclear species (12), and representative complexes of other bidentate nitrogen donor ligands have also been prepared, [PdMe3(N-N)(PMe2Ph)][O3SCF3] [N-N = 1,10-phenanthroline (phen) 6 or AW#',W-tetramethylethylenediamine (tmen) 7]. The first structural analysis of an organopalladium(iv) phosphine complex is reported, and octahedral 6 and platinum(iv) complexes [PtMe3(2,2'-bipy)(L)][O3SCF3] [L = PPh3 8, PMePh2 9 or PMe2Ph 10] have been isolated. All of the palladium(iv) complexes reductively eliminate ethane on decomposition to form palladium(n) species, where the monodentate phosphines form [PdMe(N-N)(L)]+ la-7a; a structural analysis of square-planar [PdMe(2,2'-bipy)(PMe2Ph)][O3SCF3] 3a is reported. The stability of palladium(iv) complexes decreases in the order PMe2Ph > PMePh2 > PPh3, and for complexes of PMe2Ph there is a stability order phen > 2,2'-bipy > tmen for [PdMe3(bidentate Iigand)(PMe2Ph)]+. © The Royal Society of Chemistry 2000.