6533b871fe1ef96bd12d0d85

RESEARCH PRODUCT

Preparation and reactions of 1-methylpyrid-6-one-2-yl compounds of palladium(II) and platinum(II)

Bruno CrocianiAlberto ScrivantiFrancesca Di BiancaAmalia Giovenco

subject

Steric effectsStereochemistryOrganic ChemistryMigratory insertionchemistry.chemical_elementProtonationBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundAcetic acidchemistryMaterials ChemistryElectronic effectPhysical and Theoretical ChemistryTriphenylphosphineTriethylaminePalladium

description

Abstract The compounds trans -[MCl{(1-Me)C 5 H 3 (6-O)N- C 2 }(L) 2 ] (M = Pd, Pt; L = PPh 3 , PMe 2 Ph), can be prepared from the reaction of the corresponding 1-methyl-6-chloro-2-pyridylium cationic complexes, trans -[MCl{(1-Me)C 5 H 3 (6-Cl)N- C 2 }(L) 2 ]ClO 4 , with a mixture of acetic acid, ethanol, and triethylamine in the molar ratio M/MeCO 2 H/EtOH/NEt 3 of 1/3/3/4. The rate is slow compared to that of the 1-methyl-2-chloropyridinium cation under similar conditions, and is markedly affected by the steric and electronic effects of the trans -MCl(L) 2 unit. The novel 1-methylpyrid-6-one-2-yl derivatives have been characterized by conventional spectroscopic techniques and by reactions involving either protonation and methylation of the carbonyl group or migratory insertion of isocyanides into the Pd C 2 bond.

https://doi.org/10.1016/0022-328x(84)80316-2