Pt–M complexes (M=Ag, Au) as models for intermediates in transmetalation processes

Abstract

Heteropolynuclear complexes [(CNC)(PPh3)PtM(PPh3)]ClO4 [M=Au (1), Ag (2)] and [{Pt(CNC)(PPh3)}2M]ClO4 [M=Ag (3), Au (4); CNC=2,6‐diphenylpyridinate] were prepared and studied by X‐ray crystallography, spectroscopic techniques, and DFT calculations. The X‐ray crystal structures of 1, 3, and 4 confirmed the existence of Pt−M bonds and M⋅⋅⋅Cipso interactions involving one of the phenyl fragments of CNC. Their NMR spectra showed the persistence of the Pt−M interactions in solution and also revealed an intramolecular metronome‐like dynamic process consisting of back‐and‐forth motion of the acidic M fragments along the C‐Pt‐C axis. DFT calculations on these complexes identified two main orbital interactions between the [PtCNC] and [M]+ fragments, namely, donation from the former to a vacant orbital of the latter and much weaker backdonation from the acidic M to the Pt fragment. Overall, the strength of the [Pt]⋅⋅⋅M interactions is higher for the gold compounds than for their silver counterparts. The interaction between the acidic center (silver or gold) and the carbon atom of one of the phenylene rings in these heteropolymetallic complexes can be envisaged as the first step in a process of interchange of aryl ligands. However, the ligand exchange cannot progress further due to the polydentate nature of the CNC ligand, and therefore these structures can be considered as frozen snapshots of a transmetalation reaction that has been arrested at different stages of the process.