Cyclometalated Ir(III) complexes containing N-aryl picolinamide ancillary ligands

The reaction of the cyclometalated chloro-bridged iridium(III) dimer, [(ppy)2 Ir(μ-Cl)]2 (ppy – 2-phenyl pyridine) with N-aryl picolinamides (LH, LH–NO2, LH–CH3, LH–l, LH–F) resulted in the formation of neutral heteroleptic complexes [Ir(ppy)2L] (1), [Ir(ppy)2L–NO2](2), [Ir(ppy)2L–CH3](3), [Ir(ppy)2L–Cl](4) and [Ir(ppy)2L–F] (5). These complexes contain a six-coordinate iridium with a 2C, 4N coordination environment. The N-aryl picolinamide ligands are deprotonated during complexation and the resulting amidates bind to iridium in a chelating manner (N, N). Optical spectroscopic studies revealed that the complexes 1–5 exhibited intense π→π∗ absorptions in the ultraviolet region. In addition low energy transitions due to 1MLCT, 1LLCT and 3MLCT are also seen. The emission spectra of 1–5, upon excitation at 450 nm, show a single emission with a λmax around 513 nm. The lifetimes of this emission are in between 7.4 and 9.6 μs while the quantum yields are quite high and range from 0.2 to 0.5. Based on density functional theory (DFT) calculations on 1 and 3, the three highest occupied orbitals are composed of ligand π orbitals mixed with Ir-d orbitals while the three lowest unoccupied orbitals are mostly π orbitals of the ligands. From the time dependent DFT calculations it is revealed that the lowest energy electronic singlet and triplet excitations are a mixture of MLCT and LLCT.

The reaction of cyclometalated chloro-bridged iridium(III) dimer, [(ppy)2 Ir(μ-Cl)]2 (ppy – 2-phenyl pyridine) with N-aryl picolinamides (LH, LH–NO2, LH–CH3, LH–Cl, LH–F) in presence of sodium methoxide resulted in the formation of neutral heteroleptic complexes [Ir(ppy)2L] (1), [Ir(ppy)2L–NO2](2), [Ir(ppy)2L–CH3](3), [Ir(ppy)2L–Cl](4) and [Ir(ppy)2L–F] (5). 1–5 show a single emission with λmax at around 513 nm.Figure optionsDownload as PowerPoint slideHighlights
► Cyclometalated Ir(III) complexes containing ancillary amide ligands have been synthesized.
► All these complexes were characterized by X-ray crystallography and ESI-HRMS studies.
► The new organometallic Ir(III) complexes showed intense green phosphorescence.
► DFT calculations on these complexes were carried out to understand their photophysical properties.