Stepwise phosphine sulfide formation and metal-bridging reaction of tetradentate and tridentate phosphine ligands on palladium(II)

Kinetic studies on the stepwise phosphine sulfide formation reaction of the five-coordinate trigonal-bipyramidal Pd(II) complexes with the tripodal tetradentate phosphine ligand, [PdCl(pp3)]Cl and [Pd(4-Cltp)(pp3)](BF4) (pp3 = tris[2-(diphenylphosphino)ethyl]phosphine; 4-Cltp = 4-chlorothiophenolate), were carried out, and it was revealed that the reactions proceeded via the intermediate with a pendant dissociated phosphino group. Formation of the intermediate was utilized for the bridging reaction onto Pt(II) to form the phosphine-bridged linear trinuclear and cyclic tetranuclear mixed-metal complexes. Difference in the steric conversion mechanism in the phosphine-bridging reaction between the linear tridentate phosphine (bis[2-(diphenylphosphino)ethyl]phenylphosphine) and pp3 is also reported.

Kinetic studies revealed that the phosphine sulfide formation reactions of the Pd(II) complexes with tripodal tetradentate phosphine proceed via the intermediate with a pendant dissociated phosphino group. The steric conversion mechanism of the phosphine-bridging reaction onto Pt(II) for the tetradentate phosphine was compared with that for the linear tridentate one.Figure optionsDownload as PowerPoint slide