抄録
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.
本文言語 | 英語 |
---|---|
ページ(範囲) | 1253-1260 |
ページ数 | 8 |
ジャーナル | Journal of Organometallic Chemistry |
巻 | 695 |
号 | 8 |
DOI | |
出版ステータス | 出版済み - 2010/04/15 |
ASJC Scopus 主題領域
- 生化学
- 物理化学および理論化学
- 有機化学
- 無機化学
- 材料化学