Authentic-blue phosphorescent iridium(III) complexes bearing both hydride and benzyl diphenylphosphine; control of the emission efficiency by ligand coordination geometry.

Sequential treatment of IrCl(3) x nH(2)O with 2 equiv of benzyl diphenylphosphine (bdpH) and then 1 equiv of 3-trifluoromethyl-5-(2-pyridyl) pyrazole (fppzH) in 2-methoxyethanol gave formation to three isomeric complexes with formula [Ir(bdp)(fppz)(bdpH)H] (1-3). Their molecular structures were established by single crystal X-ray diffraction studies, showing existence of one monodentate phosphine bdpH, one terminal hydride, a cyclometalated bdp chelate, and a fppz chelate. Variation of the metal-ligand bond distances showed good agreement with those predicted by the trans effect.

Syntheses, photophysics, and application of iridium(III) phosphorescent emitters for highly efficient, long-life organic light-emitting diodes.

Rational design and synthesis of Ir(III) complexes (1-3) bearing two cyclometalated ligands (C--N) and one 2-(diphenylphosphino)phenolate chelate (P--O) as well as the corresponding Ir(III) derivatives (4-6) with only one (C--N) ligand and two P--O chelates are reported, where (C--NH)=phenylpyridine (ppyH), 1-phenylisoquinoline (piqH), and 4-phenylquinazoline (nazoH). Single crystal X-ray diffraction studies of 3 reveal a distorted octahedral coordination geometry, in which two nazo ligands adopt an eclipsed configuration, with the third P--O ligand located trans to the phenyl group of both nazo ligands, confirming the general skeletal pattern for 1-3. In sharp contrast, complex 4 reveals a trans-disposition for the PPh2 groups, along with the phenolate groups residing opposite the unique cyclometalated ppy ligand, which is the representative structure for 4-6.

Blue to true-blue phosphorescent Ir(III) complexes bearing a nonconjugated ancillary phosphine chelate: strategic synthesis, photophysics, and device integration.

We report the design and synthesis of Ir(III) complexes functionalized with substituted pyridyl cyclometalate or azolate chromophores, plus one newly designed nonconjugated phosphine chelate, which not only greatly restricts its participation in the lowest-lying electronic transition but also enhances the coordination strength. These two key factors lead to fine-tuning of the phosphorescence chromaticity toward authentic blue and simultaneously suppress, in part, the nonradiative deactivation. This conceptual design presents a novel strategy in achieving heretofore uncommon, high-efficiency blue and true-blue phosphorescence.

Reactions of the (2-pyridyl) pyrrolide platinum(II) complex driven by sterically encumbered chelation: a model for the reversible attack of alcohol at the coordinated carbon monoxide.

Treatment of 3,5-bis(trifluoromethyl)-2-(2'-pyridyl)pyrrole (fpyroH) with Pt(DMSO)2Cl2 and Na2CO3 in THF solution gave a light-yellow complex denoted as [Pt(fpyro)2] (1). A single-crystal X-ray diffraction study on 1 revealed a large conformational distortion around the platinum(II) center, which is attributed to interligand repulsion between the pyridyl groups and the CF3 substituents of the nearby pyrrolides. Reaction of 1 with N- and C-donor ligands such as acetonitrile, pyridine, isocyanide, and CO affords the adducts [Pt(fpyro)2(L)], L = NCMe (2), pyridine (3), CNBut (4), and CO (5), showing formation of one monodentate fpyro ligand by release of the strain energy.

Phosphorescent iridium(III) complexes with nonconjugated cyclometalated ligands.

A series of blue phosphorescent iridium(III) complexes 1-4 with nonconjugated N-benzylpyrazole ligands were synthesized and their structural, electrochemical, and photophysical properties were investigated. Complexes 1-4 exhibit phosphorescence with yields of 5-45 % in degassed CH2Cl2. Of the compounds, 1 showed emission that was nearly true blue at 460 nm with a lack of vibronic progression.

New CVD precursors capable of depositing copper metal under mixed O2/Ar atmosphere.

Volatile low-melting CuII metal complexes Cu[OC(CF3)2CH2C(Me)=NMe]2 (4) and Cu[OC(CF3)2CH2CHMeNHMe]2 (5) were synthesized and characterized by spectroscopic methods. A single-crystal X-ray diffraction study on complex 4 shows the anticipated N2O2 square-planar geometry with the imino alcoholate ligand arranged in the all-trans orientation. In contrast, a highly distorted N2O2 geometry with a dihedral angle of 33 degrees was observed for complex 5, suggesting that the fully saturated amino alcoholate ligand produces a much greater steric congestion around the metal ion.