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In contrast to the common intramolecular charge transfer (ICT) emission, planarized intramolecular charge transfer (PLICT) based materials usually possess higher proportion radiative decay for their flat and rigid conformation in excited states. Herein, a strategy for designing PLICT‐based emitters by the excited state quinone‐conformation induced planarization is proposed. By virtue of RIR mechanism on TPP (tetraphenylpyrazinyl) unit, the newcomers named as TPP‐PPI (1‐phenyl‐2‐(4′‐(3,5,6‐triphenylpyrazin‐2‐yl)‐[1,1′‐biphenyl]‐4‐yl)‐1H‐phenanthro[9,10‐d] imidazole) and TPP‐PI (1‐phenyl‐2‐(4‐(3,5,6‐triphenylpyrazin‐2‐yl)phenyl)‐1H‐phenanthro[9,10‐d]imidazole) exhibit aggregation‐induced emission (AIE) characteristics. TPP‐PPI and TPP‐PI have obvious PLICT properties via series of spectral measurements. Employing theoretical calculation in ground and excited states in different solvents, their PLICT process is confirmed further, and TPP's contribution on PLICT formation becomes clear. In non‐doped organic light‐emitting diodes, these two emitters with AIE and PLICT characteristic exhibit good performance with external quantum efficiency (4.85% and 4.36%) as blue emitters. [ABSTRACT FROM AUTHOR]

Organic luminophores of narrowband emission are considered a filter-less light resource, promising for high-resolution organic light-emitting diode (OLED) display technology. It is essentially feasible to achieve narrowband emission by manipulating the intrinsic structural relaxation and vibronic coupling in the excited state. On this basis, by the introduction of single bond-linked peripheral moieties of 4-methoxyphenyl into the benzo[c]benzo [7,8]quinolino[1,2,3-fg]acridine-7,11-dione (BAO) core, the resulting BAO-PMO is observed to exhibit better performance, achieving a full width at half-maximum (FWHM) of down to 27 nm/0.14 eV in toluene for the narrowest band compared with that of BAO (35 nm/0.20 eV). An effective strategy is thus proposed by the significant enhancement of the low-frequency vibronic coupling strength with simultaneous mitigation of the high-frequency ones to realize the control of structural relaxation. In consequence, the BAO-PMO based OLED device exhibits a narrowband green emission with an FWHM of 37 nm/0.18 eV. • Organic narrowband luminophores based on carbonyl-bridged triarylamine were shown. • The emission narrowing was achieved via vibronic coupling regulation of the excited-state configuration. • Doped OLEDs exhibit narrowband green emission with a full width at half-maximum of down to 37 nm. [ABSTRACT FROM AUTHOR]

In this work, a novel green emitter, namely 16,16-dimethylbenzo[ a ]quinolino[3,2,1- de ]acridin-10(16 H)-one (GACQ), with amine‒carbonyl fused structure has been designed and synthesized. The single-crystal structure analysis confirmed that the fused structure shows non-planar conformation with dihedral angle of 48.97° from the front-view direction. The photophysical and theoretical results confirmed that GACQ exhibited hybridized local and charge-transfer (HLCT) feature with strong green emissions of 513 and 535 nm in solution and film, respectively. The non-doped device based on GACQ achieved high luminance (15810 cd m−2) and good efficiency stability with negligible external quantum efficiency (EQE) roll-off. Furthermore, the doped device exhibited high maximum EQE of 4.8% with CIE coordinate of (0.38, 0.58). [Display omitted] • A novel amine‒carbonyl fused emitter, GACQ, has been successfully constructed. • GACQ possesses hybridized local and charge-transfer characteristic. • Non-doped device of GACQ exhibited high luminance and negligible EQE roll-off. • Doped device based on GACQ achieved maximum EQE of up to 4.8%. [ABSTRACT FROM AUTHOR]