Abstract

The ionic methylpalladium complexes [Pd(Me)(bppy)]X {X = Cl 1a, SO3CF3 1b, [3,5-(CF3)2C6H3]4B 1c}, containing the novel flexible terdentate nitrogen ligand 2,6-bis(pyrimidin-2-yl)pyridine, have been synthesised. Complexes 1a–1c reacted quantitatively with carbon monoxide, resulting in formation of the acylpalladium complexes [Pd{C(O)Me}(bppy)]X {X = Cl 2a, SO3CF3 2b, [3,5-(CF3)2C6H3]4B 2c}. Complexes 1a–1c and 2a–2c have been isolated and fully characterised. In chloroform as well as in methanol, all the complexes show dynamic behaviour due to exchange of the co-ordinated and unco-ordinated pyrimidinyl nitrogen atoms. The influence of solvent, methyl and acyl ligand, counter ion and the presence of free Cl– and CO on the dynamic behaviour has been studied and the thermodynamic parameters have been determined. A mechanism for the observed exchange process has been proposed. This mechanism involves (a) dissociation of one of the pyrimidinyl nitrogen atoms, which may be initiated by chloride, solvent or CO co-ordination, (b) rotation about the pyrimidinyl–pyridine bond and (c) reformation of the nitrogen–palladium bond.

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