A nine-ring fused terrylene diimide exhibits switching between red TADF and near-IR room temperature phosphorescence.

Herein, we report the first example of a terrylene diimide derivative that switches emission between thermally activated delayed fluorescence (TADF) and room temperature phosphorescence (RTP) in the red region. By design, the molecule TDI-cDBT boasts a symmetrical, consecutively fused nine-ring motif with a kite-like structure. The rigid core formed by the annulated dibenzothiophene moiety favoured efficient intersystem crossing and yielded a narrow-band emission with a full-width half maxima (FWHM) of 0.09 eV, along with high colour purity. A small ΔE S1-T1 of 0.04 eV facilitated thermally activated delayed fluorescence, enhancing the quantum yield to 88% in the red region. Additionally, it also prefers a direct triplet emission from the aggregated state. The room temperature phosphorescence observed from the aggregates has a longer emission lifetime of 1.8 ms, which is further prolonged to 8 ms at 77 K in the NIR region. Thus, the current strategy is successful in not only reducing ΔE S1-T1 to favour TADF but also serves as a novel platform that can switch emission from TADF to RTP depending upon the concentration.

The deeper it goes, the brighter it glows: NIR emissive nitro-terrylene diimides with deep LUMOs.

Herein, we present the first examples of air-stable, deep-lowest unoccupied molecular orbital (LUMO) polycyclic aromatic molecules with emission in the near-infrared (NIR) region, using nitration as a strategy. Despite the fact that nitroaromatics are non-emissive, the choice of a comparatively electron-rich terrylene core proved to be beneficial for achieving fluorescence in these molecules. The extent of nitration proportionately stabilized the LUMOs. Tetra-nitrated terrylene diimide exhibited a deep-LUMO (≤-4.5 eV) of -5.0 eV vs. Fc/Fc+, the lowest for any larger RDIs. These are also the only examples of emissive nitro-RDIs, with larger quantum yields.

Isolation and Structural Characterization of Regioisomers of Dibrominated Terrylene Diimides.

Diverse applications of rylenediimides are attributed to the accessibility of simple methodologies to obtain versatile halogenated precursors. Terrylene diimides are important molecular platforms to achieve materials with NIR absorption and emission. In this work, we present a simple synthesis for the hitherto unknown di- and tribromo-TDIs. Regioisomerically pure dibromo TDIs, including an elusive 1,14-derivative, could be successfully isolated and structurally characterized along with tribromo-TDI. The utility of these bromo derivatives has also been demonstrated with a redox anchoring.