Palladium(II) amido complexes with an unsymmetrical PNP′ pincer-type coordination and a new (E,E)-tetradentate diphosphinoazine coordination mode

Cationic palladium(II) complexes [PdCl{PR2CH2C(But)double bond; length as m-dashNNdouble bond; length as m-dashC(But)CH2PR2}]Cl, where R = isopropyl, cyclohexyl or tert-butyl, were synthesized by the reactions of the corresponding diphosphinoazines with bis(acetonitrile)palladium(II) dichloride. When bis(benzonitrile)palladium(II) dichloride was used instead, in the molar ratio of 2:1 to the diphosphinoazine, a new complex was isolated with the isopropyl ligand showing a previously unknown (E,E) tetradentate coordination mode. Crystal and molecular structure was determined by X-ray diffraction. The solid complex was a racemate of two axially chiral enantiomers and the chirality was preserved in solution. Reactions of the cationic complexes with triethylamine gave complexes [PdCl{PR2CHdouble bond; length as m-dashC(But)NNdouble bond; length as m-dashC(But)CH2PR2}], containing deprotonated diphosphinoazines in ene-hydrazone unsymmetrical pincer-like configuration. The complexes represent several of the still rare examples of Pd(II) amido bis(phosphine) complexes with a chlorine atom covalently bonded trans to the amide nitrogen.