Strongly Luminescent Pt(Iv) Complexes With A Mesoionic N-Heterocyclic Carbene Ligand: Tuning Their Photophysical Properties

The synthesis, electrochemistry, and photophysical properties of a series of bis-cyclometalated Pt(IV) complexes that combine the mesoionic aryl-NHC ligand 4-butyl-3-methyl-1-phenyl-1H-1,2,3-triazol-5-ylidene (trz) with either 1-phenylpyrazole or 2-arylpyridine (C boolean AND N) are reported. The complexes (OC-6-54)-[PtCl2(C boolean AND N)(trz)] bearing cyclometalating 2-arylpyridines present phosphorescent emissions in the blue to yellow color range, which essentially arise from (LC)-L-3(C boolean AND N) states, and reach quantum yields of ca. 0.3 in fluid solutions and almost unity in poly(methyl methacrylate) (PMMA) matrices at 298 K, thus representing a class of strong emitters with tunable properties. A systematic comparison with the homologous C-2-symmetrical species (OC-6-33)-[PtCl2(C boolean AND N)(2)], which contains two equal 2-arylpyridine ligands, shows that the introduction of a trz ligand leads to significantly lower nonradiative decay rates and higher quantum efficiencies. Computational calculations substantiate the effect of the carbene ligand, which raises the energy of d sigma* orbitals in these derivatives and results in the higher energies of nonemissive deactivating (LMCT)-L-3 states. In contrast, the isomers (OC-6-42)-[PtCl2(C boolean AND N)(trz)] are not luminescent because they present a (LMCT)-L-3 state as the lowest triplet.