The development of rigid polyaromatic
building blocks for narrowband
violet fluorophores has received tremendous attention. Herein, we
designed and synthesized two new triangle-shaped rigid building blocks,
namely, 2,5-di-tert-butylindolo[3,2,1-jk]carbazole (tBuICz) and 2,11-di-tert-butylindolo[3,2,1-jk]carbazole-4-carbonitrile (tBuICzCN), and tethered them with different chromophores to
yield a series of violet–blue fluorophores, viz., ICzTPA–ICzPICN, and studied their structure–function
relationship. The appended chromophores and cyano unit played a vital
role in controlling the optical and electrical properties of the compounds.
Except triphenylamine-substituted derivatives, the compounds showed
pure violet emission (λem ≤ 403 nm). Intriguingly,
the compounds exhibited narrow-band emission with a full-width at
half-maximum ≤ 40 nm, attributed to the rigidity of the ICz
core. The emission of the compounds displayed positive solvatochromism,
which is ascribed to the photoinduced intramolecular charge transfer
in the excited state. The compounds revealed excellent thermal robustness
with T
5d ≥ 363 °C. The triphenylamine-featuring
derivatives displayed a high-lying HOMO compared to their congeners
due to their electron-rich nature. When we applied these materials
in organic light-emitting diodes, ICzPI outperformed
in the series with an EQEmax of 3.07% and a current efficiency
of 1.04 cd/A. Notably, its CIEy ∼ 0.046 precisely matched with
the Rec.2020 standard of deep-blue color (CIEy ∼ 0.046).