Ruthenium, copper and ruthenium-copper complexes of an unsymmetrical phosphino pyridyl 1,8-naphthyridine PNNN ligand.

A new unsymmetrical dinucleating phosphino pyridyl 1,8-naphthyridine ligand PNNN is reported. Reaction with CuCl gave the dicopper complex [Cu(μ-Cl)(PNNN)] (1). In contrast, complexation of [RuCl(cymene)] yielded a monometallic species [RuCl(cymene)(PNNN)]Cl ([2]Cl) in which the Ru is bound to the κ-N,N, rather than κ-P,N, binding pocket. The selective formation of the monoruthenium complex [2]Cl enabled synthesis of heterobimetallic complexes [RuCuCl(cymene)(PNNN)] (3) and [RuCuCl(cymene)(PNNN)][PF] ([4]2[PF6]2), which both exhibit κ-P coordination of Cu. Complexes 1 and [4]2[PF6]2 exhibit reversible dearomatisation-aromatisation behaviour at the metal-ligand cooperative methylene site upon sequential treatment with base (KOBu) and acid (HCl). Notably, deprotonation of [4]2[PF6]2 induces a shift in the coordination mode of Cu to κ-P,N.