کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1325277 | 1499945 | 2009 | 7 صفحه PDF | دانلود رایگان |

Reaction of acetato-bridged dinuclear palladacycles, [Pd(iminoisoindoline)(μ-OAc)]2, with stoichiometric amounts of PR3 (where R = Ph or Cy) resulted in formation of the corresponding mononuclear phosphine-ligated, six-membered palladacycles with the general formula [Pd(iminoisoindoline)(OAc)PR3]. The analogous chloride complexes were synthesized by reaction of [Pd(iminoisoindoline)(μ-OAc)]2 with LiCl in acetone followed by addition of phosphine to afford the monomeric derivatives [Pd(iminoisoindoline)(Cl)PR3]. Representative crystal structures of both types of mononuclear palladacycles confirmed the mononuclear nature of the complexes and showed a trans-arrangement of the phosphine ligand to the heterocyclic imine-nitrogen of the palladacycles.
The synthesis of mononuclear phosphine-ligated, six-membered palladacycles with the general formula [Pd(iminoisoindoline)(X)PR3], where X = OAc or Cl and R = Ph or Cy, are described.Figure optionsDownload as PowerPoint slide
Journal: Journal of Organometallic Chemistry - Volume 694, Issues 9–10, 15 April 2009, Pages 1542–1548