structural relaxation and vibronic coupling of the excited states. For pure organic materials, donor-acceptor typed thermally activated delayed fluorescence (TADF) emitters are able to realize 100% internal quantum efficiency via efficient reverse intersystem crossing (RISC) process, but the geometrical deformation between D and A units typically causes broad intramolecular charge-transfer emission with substantial Stokes shift in devices. [2] A promising molecular design strategy termed multiresonance TADF (MR-TADF) that fully addressed the aforementioned obstacle has been lately proposed by Hatakeyama et al. [3] This is made possible by atomic separation of frontier molecular orbitals (FMOs) via opposite resonance effect of electron-rich nitrogen and electron-deficient boron in a rigid molecular framework, which promises i) limited excited-state reorganization and minimized bonding/antibonding characteristics of FMOs, leading to compressed full width at half maximum (FWHM) of emission band; ii) adequate separation and overlap of the electron/hole wavefunctions to induce small singlet-triplet energy difference (ΔE ST ) and intense oscillating strength (f), leading to high luminescence efficiency. [4][5][6][7] An additional merit for most MR-TADF emitters is their tendency to adopt horizontal anisotropic orientation in vacuum-evaporated organic thin films, which would benefit light extraction from device and enhance efficiency. [5,8] For instance, by employing a state-of-the-art MR-TADF emitter ν-DABNA, maximum external quantum efficiency (EQE max ) up to 34.4% with high color purity (FWHM = 18 nm and Commission International de l'Éclairage (CIE) coordinates of (0.12, 0.11)) was realized in deep-blue OLED. [8,9] An important issue to be addressed for MR-TADF emitters is the severe aggregation-caused quenching (ACQ) and spectral broadening in solid state due to intense π-π interactions. [6,10,11] In a recent photophysical study, Monkman's group unveiled the strong prevalence for ν-DABNA to form less emissive aggregates/excimers even at extremely low doping concentrations, resulting in broadened linewidth and lower-than-expected device performances. [12] These findings offer a clear explanation to the fact that, though many MR-TADF emitters present narrowband photoluminescence (PL) emission with quantum Multiresonance thermally activated delayed fluorescence (MR-TADF) emitters manifest great potential for organic light-emitting diodes (OLEDs) due to their high exciton-utilization efficiency and narrowband emission. Nonetheless, their tendency toward self-quenching caused by strong interchromophore interactions would induce doping sensitivity and deteriorate the device performances, and effective strategy to construct quenching-resistant emitters without sacrifycing color purity is still to be developed. By segregating the planar MR-TADF skeleton using two bulky carbazolyl units, herein a highly emissive molecule with enhanced quenching resistance is reported. The steric effect largely removes the formation of de...