Formation of palladium(0) complexes from Pd(OAc)(2) and a bidentate phosphine ligand (dppp) and their reactivity in oxidative addition

Citation
C. Amatore et al., Formation of palladium(0) complexes from Pd(OAc)(2) and a bidentate phosphine ligand (dppp) and their reactivity in oxidative addition, ORGANOMETAL, 20(15), 2001, pp. 3241-3249
Citations number
31
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANOMETALLICS
ISSN journal
02767333 → ACNP
Volume
20
Issue
15
Year of publication
2001
Pages
3241 - 3249
Database
ISI
SICI code
0276-7333(20010723)20:15<3241:FOPCFP>2.0.ZU;2-8
Abstract
A Pd-0 complex is spontaneously generated from Pd(OAc)(2) and a bidentate p hosphine such as dppp (1,3-bis(diphenylphosphino)propane). dppp is the redu cing agent and is oxidized to the hemioxide dppp(O). The intramolecular red uction step is reversible. A stable Pd-0 complex is quantitatively formed i n the presence of 2 equiv of dppp, water, and a base (NEt3). The oxidative addition of PhI gives a cationic complex, PhPd(dppp)(dppp(O))(+), in which dppp(O) behaves as a monodentate ligand. PhPd(OAc)(dppp) is formed in the p resence of added AcO-. The oxidative addition of PhI is an intricate reacti on whose kinetics has been investigated only in the presence of added AcO-. It involves reactive dimeric or/and monomeric Pd-0 complexes ligated by Ac O- whose relative reactivity is a function of the PhI concentration.