Abstract
Organic π-conjugated materials exhibiting violet-blue emissions are of great interest for diverse applications. Helicenes and stilbenes hold great potential as compounds capable of achieving violet-blue fluorescence. In this study, aza[6]helicenes THNI and DHNC, along with their planar precursors DFVHI and HHIVC, were successfully synthesized using indole, carbazole, and fluorene units as building blocks. The molecular structures were verified through the utilization of 1H and 13C nuclear magnetic resonance (NMR), high resolution mass spectroscopies (HRMS), and the crystal structure of THNI was further elucidated via X-ray analysis. The synthesized material exhibited exceptional thermal stability with a Td value of ≥350 °C. The HOMO and LUMO energy levels were determined through cyclic voltammetry analysis, while density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations at the B3LYP/6-31G(d) level were employed to investigate ground-state geometries and vertical electronic transitions. Optical properties were characterized using UV–vis absorption spectroscopy as well as single- and two-photon excited photoluminescence. The UV–vis absorption spectra indicate that helicenes possess superior light-harvesting capabilities compared to their planar precursors, owing to the former's higher molar extinction coefficients. These compounds exhibit violet-blue emissions in various solvents and solid-state films. In addition, aza[6]helicenes exhibit higher photoluminescence quantum yields (PLQYs) and shorter maximum emission peaks compared to their planar precursors. However, the maximum two-photon absorption (TPA) cross section (δ) values of aza[6]helicenes are lower than those of their planar counterparts. Therefore, THNI and DHNC may be promising candidates for violet-blue emitters in OLEDs due to their curved confined π-electron systems, high thermal and optical stability, and high PLQYs. Meanwhile, DFVHI and HHIVC exhibit potential as two-photon fluorescent probes for bioimaging.
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