Central to the performance of commercialized green and red OLEDs is the organometallic phosphorescent emitter, [2] which is responsible for the conversion of electrical energy into light with near unity internal quantum efficiency (IQE), as these complexes show simultaneously high photoluminescence quantum yields (Φ PL ) and can efficiently harvest both singlet and triplet excitons to produce light in the device. However, the blue sub-pixel in OLEDs presently uses an organic fluorophore as there do not exist phosphorescent OLEDs that are sufficiently stable or bright for commercial use, and few reported examples of phosphorescent emitters that are close to the BT.2020 industry standard for blue, [3] defined as CIE coordinates of (0.131, 0.046). [4] Among the most promising phosphorescent blue emitters are iridium(III) complexes with cyclometallating N-heterocyclic carbene (NHC) ligands. In these complexes the strongly σ-donating and weakly π-accepting NHC contributes to greatly destabilize the LUMO of the Ir(C^C) 3 complex and thus increase the energy of the emissive triplet state. Luminescent Ir(C^C) 3 complexes were first reported by Thompson and co-workers in 2005; [3a,5] however, in these early examples [fac-Ir(pmi) 3 and fac-Ir(pmb) 3 ] the photo luminescence quantum yields, Φ PL , were very low, and the complexes emitted in the near UV. A step change in the photophysical properties of Ir(C^C) 3 complex occurred in 2016 where Forrest and co-workers reported a bright, blue complex, mer-Ir(pmp) 3 , (λ PL = 465 nm, Φ PL = 78% in degassed 2-MeTHF) and the OLEDs showed unprecedentedly high maximum external quantum efficiencies (EQE max = 14.4%) and blue electroluminescence [CIE = (0.16, 0.15)], (Figure 1). [6] Since this publication, there has been a growing number of blueemitting Ir(C^C) 3 complexes reported and used as emitters in OLEDs, [3b,7] the diversity of iridium(III) NHC complexes has recently been reviewed. [8] A detracting feature of many phosphorescent iridium complexes is the presence of thermally accessible 3 MC excited states. Their population leads to increased nonradiative decay and degradation of the complex induced by the lengthening of the Irligand bonds resulting in deligation. [10] The strongly coordinating and σ-donating NHC ligands in Ir(C^C) 3 complexes possess a much larger octahedral splitting gap, destabilizing Four new deep-blue-emitting iridium(III) NHC complexes containing sterically demanding ligands are synthesized. The four complexes show bright, deep-blue emission, with emission maxima between 420 and 427 nm in both acetonitrile solution and 30 wt% doped films in TSPO1; the two meridional isomers showing photoluminescence quantum yields, Φ PL , in doped films of 80% and 89%. The two meridional isomers are used to assess the impact of emitters containing bulky, sterically demanding ligands on the performance of organic light-emitting diodes (OLEDs). OLEDs employing a stepped doping profile with mer-Ir(tfpi_tmBn) 3 as the emitter produce the highest performing devices in this...