| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 7757309 | Journal of Organometallic Chemistry | 2014 | 31 Pages |
Abstract
Transmetallation of iminophosphoranes from [Li{C6H4(PPh2NPh)-2}]2 to chloride-bridge dimers [Pd(μ-Cl)(CËN)]2 affords mixed bis-cyclopalladated complexes, which were obtained regioselectively as cis(C,C)-isomers. Complex [Pd{C6H4(PPh2NPh)-2}}(C6H4-(2â²-NC5H4)-2)] is regioselectively oxidized to the stable Pd(IV) derivative [Pd(OAc)2{C6H4(PPh2NPh)-2}(C6H4-(2â²-NC5H4)-2)] by treatment with PhI(OAc)2. This compound undergoes reductive elimination, releasing the acetoxylated phenylpyridine and keeping the orthopalladated iminophosphorane.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
David Aguilar, Greco González, Pedro Villuendas, Esteban P. Urriolabeitia,
