Synthetic, Structural, and Mechanistic Studies on the Oxidative Addition of Aromatic Chlorides to a Palladium (<i>N</i>-Heterocyclic Carbene) Complex: Relevance to Catalytic Amination

The oxidative addition products trans-[Pd(NHC)2(Ar)Cl] (NHC = cyclo-C{NtBuCH}2; Ar = Me-4-C6H4, MeO-4-C6H4, CO2Me-4-C6H4) have been isolated in good yields from the reactions of ArCl with the amination precatalyst [Pd(NHC)2] and structurally characterized. The former undergo reversible dissociation of one NHC ligand at elevated temperatures, and a value of 25.57 kcal mol-1 has been determined for the Pd−NHC dissociation enthalpy in the case where Ar = Me-4-C6H4. Detailed kinetic studies have established that the oxidative addition reactions proceed by a dissociative mechanism. Rate data for the oxidation addition of Me-4-C6H4Cl to [Pd(NHC)2] compared to that obtained for the [Pd(NHC)2]-catalyzed coupling of morpholine with 4-chlorotoluene are consistent with a rate-determining oxidative addition in the catalytic amination reaction. The relative rates of oxidative addition of the three aryl chlorides to [Pd(NHC)2] (CO2Me-4-C6H4Cl > Me-4-C6H4Cl > MeO-4-C6H4Cl) reflect the electronic nature of the substituents and also parallel observed trends in coupling efficiency for these aryl halides in aminations.