Some new hydroxo-enyl derivatives of palladium(II) of the type [Pd(C7H8 · OH)Br]2, and [Pd(diene · OH)(LL)]PF6 (C7H8 = norbornadiene, diene = norbornadiene or 1,5-cyclooctadiene; LL = 2,2′-bipyridyl or 1,10-phenanthroline) have been made by nucleophilic attack of H2O on the diene coordinated to the metal in dipositively charged complexes. Evidence is presented to show that the hydroxonorbornenyl-1,2-bis(diphenylphosphino)ethane palladium(II) is involved as an intermediate, in an unusual example of oxidation of the alcoholic group through a palladium(II)-mediated intramolecular hydrogen transfer.
"Preparation and reactions of Hydroxo-enyl palladium(II) derivatives” J.Organometallic Chemistry ,() - / E., Rotondo; F., CUSMANO PRIOLO; A., Donato; R., Pietropaolo; Donato, Andrea. - In: JOURNAL OF ORGANOMETALLIC CHEMISTRY. - ISSN 0022-328X. - 251:(1983), pp. 273-279.
"Preparation and reactions of Hydroxo-enyl palladium(II) derivatives” J.Organometallic Chemistry ,() -
DONATO, Andrea
1983-01-01
Abstract
Some new hydroxo-enyl derivatives of palladium(II) of the type [Pd(C7H8 · OH)Br]2, and [Pd(diene · OH)(LL)]PF6 (C7H8 = norbornadiene, diene = norbornadiene or 1,5-cyclooctadiene; LL = 2,2′-bipyridyl or 1,10-phenanthroline) have been made by nucleophilic attack of H2O on the diene coordinated to the metal in dipositively charged complexes. Evidence is presented to show that the hydroxonorbornenyl-1,2-bis(diphenylphosphino)ethane palladium(II) is involved as an intermediate, in an unusual example of oxidation of the alcoholic group through a palladium(II)-mediated intramolecular hydrogen transfer.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.