Abstract
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.
Original language | English |
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Pages (from-to) | 1253-1260 |
Number of pages | 8 |
Journal | Journal of Organometallic Chemistry |
Volume | 695 |
Issue number | 8 |
DOIs | |
State | Published - 2010/04/15 |
Keywords
- Kinetics
- Phosphine sulfide formation
- Phosphine-bridging reaction
- Steric conversion mechanism
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
- Materials Chemistry