Luminescent Platinum(II) Complexes with Terdentate N∧C∧C Ligands

Abstract

The synthesis, structure, and luminescence of Pt(II) complexes of the type [Pt(N∧C∧C)(L)] are reported, where N∧C∧C is a terdentate ligand resulting from the cycloplatination of 2-(3,5-diphenoxyphenyl)pyridine or 2-(4,4″-dimethyl-[1,1′:3′,1″-Terphenyl]-5′-yl)pyridine, and L represents a monodentate ancillary ligand, which can be γ-picoline, 4-pyridinecarboxaldehyde, PPh3, n-butyl or 2,6-dimethylphenyl isocyanide, CO, or the N-heterocyclic carbenes 1-butyl-3-methylimidazol-2-ylidene or 4-butyl-3-methyl-1-phenyl-1H-1,2,3-Triazol-5-ylidene. Derivatives bearing CO, isocyanides, or carbenes showed the highest stabilities in solution, whereas the pyridine and PPh3 derivatives establish ligand-exchange equilibria in acetonitrile. Different supramolecular structures are observed in the solid state, which largely depend on the nature of the ancillary ligand. Isocyanides and CO favor π interactions between the aromatic rings, metallophilic Pt···Pt contacts, or a combination of both. In contrast, pyridine ligands may lead to bimolecular assemblies driven by C-H···O, C-H···Pt, or C-H/π hydrogen bonds. Luminescence was examined in fluid solution, poly(methyl methacrylate) matrices, and the solid state at 298 K, and in 2-methyltetrahydrofuran glasses at 77 K. The majority of derivatives show highly efficient emissions from 3ILCT/MLCT or 3ILCT/MLCT/LLCT excited states of monomeric species. The formation of excimers and different types of emissive aggregates are demonstrated, which lead to red-shifted emissions of different origins and characteristics depending on the involved noncovalent interactions.