chromaticity standards defined by the National Television System Committee (NTSC) and European Broadcasting Union (EBU) with Commission Internationale de l'Éclairage (CIE) coordinates of (0.14, 0.08) and (0.15, 0.06), respectively; 2) possess high photoluminescence quantum yields (Φ PL ) that translate into high external quantum efficiencies in the OLED, particularly at useful brightnesses (at least 100 cd m −2 for displays and 1000 cd m −2 for lighting); and 3) exhibit competitive device stabilities to fluorescent complexes. [1] Of the phosphorescent complexes studied, iridium(III) compounds have attracted the widest interest as emitters in electroluminescent devices due to their high Φ PL , short phosphorescence lifetimes (τ PL ) and facile color tunability based on the choice of ligands around the metal center. [2] Despite these properties, the design of highly efficient pure blue phosphorescent iridium complexes remains a challenging target to achieve. [3] In order to tune the emission to the blue, electronwithdrawing substituents are typically incorporated on the cyclometalating ligands of the iridium complexes. Three issues arise when employing this strategy. The first is that the electrochemical stability of fluoro substituents, the most popular electron-withdrawing substituent, such as in the widely studied FIrpic [iridium(III)bis(4,6-difluopyridinato-N,C 2′ )picolinate] sky blue emitter, [4] is poor, translating to greatly reduced device stability; [5] while the use of other more strongly electron-withdrawing substituents do not necessarily translate into blueremitting complexes, despite deepening the highest occupied molecular orbital (HOMO) of the compound. [6] The second is that as the energy of the emissive triplet state increases, nonradiative recombination via thermally accessible metal-centered excited states becomes increasingly problematic, leading to emitter degradation. [7] Finally, most iridium(III) complexes do not meet the deep blue chromaticity requirements, and instead possess CIE y ordinates greater than 0.1 as their triplet energies are not sufficiently high (at least 2.8 eV); [3b,8] those that do possess maximal external quantum efficiency (EQE max ) values < 10%. [9] Another strategy to tune the emission of charge-neutral iridium(III) complexes to the blue is to replace the coordinating pyridine rings that are typically employed with more sigma-donating heterocycles that serve to destabilize the lowest unoccupied molecular orbital (LUMO) of the complexes, such as imidazoles [10] and N-heterocyclic carbene (NHC) ligands. [9b,10b,11] High-efficiency pure blue phosphorescent organic light-emitting diodes (OLEDs) remain one of the grand challenges, principally because the emissive complexes employed either do not possess sufficiently high photoluminescence quantum yields or exhibit unsatisfactory Commission International de l'Éclairage (CIE) coordinates. Here two deep-blue-emitting homoleptic iridium(III) complexes are reported and OLEDs are demonstrated with CIE coordinates of ...