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Recently, numerous efforts have been devoted to sky blue or greenish blue organic light-emitting diodes (OLEDs), nevertheless, the deep blue and pure blue OLEDs still remain a formidable challenge. Herein, a series of deep blue and pure blue donor–acceptor–donor (D–A–D) type emitters, namely Cz-DMTD, PhCz-DMTD and TMCz-DMTD, were constructed. For PhCz-DMTD which exhibited no delayed fluorescence component, the extended delocalization of donors and the enhancement of oscillator strength were both observed through theoretical calculation. For methyl-engineered TMCz-DMTD, the degenerate charge transfer singlet excited (1CT) and triplet excited (3CT) states and localized triplet excited (3LE) state endowed a thermally activated delayed fluorescence (TADF) character. Moreover, PhCz-DMTD and TMCz-DMTD based OLEDs displayed emission with Commission Internationale de l'Eclairage (CIE) coordinates of (0.164, 0.077) and (0.157, 0.107) and with maximum external quantum efficiencies (EQEmax) of 4.6% and 8.7%, respectively. It is the first time that the electroluminescence wavelength of TMCz based OLEDs reached below 450 nm with a CIEy below 0.11. Molecular engineering of the carbazole moiety is expected to provide a valuable strategy for molecular design of more deep blue emitters. [ABSTRACT FROM AUTHOR]

Two novel heteroleptic iridium complexes containing 4-phenylquinazoline (pqz) as a cyclometalating ligand, namely Ir1 and Ir2, are designed and synthesized. Methoxy groups are incorporated into the 6- and 7-sites of pqz rings to tune the physical properties and the emission performance of the complexes. The introduction of methoxy groups in Ir1 and Ir2 causes a slight blue shift by 3–5 nm relative to the reference complex Ir(pqz)2(acac) (630 nm), and moderate photoluminescence quantum yields of 0.35 and 0.38 and short lifetimes of 0.79 and 0.64 μs, respectively, are obtained. Ir1 and Ir2 are used as doped emitters to fabricate phosphorescence organic light-emitting diodes and pure red electroluminescence (EL) is achieved. In comparison with the reference complex Ir(pqz)2(acac), dramatically improved EL performance with color purity and efficiencies are realized for both Ir1 and Ir2. In particular, the Ir2 device exhibits a maximum external quantum efficiency of 26.22% with Commission Internationale de l'Eclairage (CIE) coordinates of (0.65, 0.34), which is close to the best efficiencies reported for other pqz based red iridium phosphors but advantageous in terms of a simple device structure with a single emitting layer. [ABSTRACT FROM AUTHOR]