Organic thermally activated delayed fluorescence (TADF) materials have been widely investigated due to their impressive electronic properties and applied potential for the third generation of organic light-emitting diodes (OLED). We present organic TADF material () based on the strained benzoguanidine donor and compare it with the benchmark carbazole-based material (). Extended π-conjugation in material results in yellow-green luminescence at 512 nm with a fast radiative rate of 5.5 × 10 s and a photoluminescence quantum yield of 46% in methylcyclohexane solution. Such a nitrogen-rich material has a significantly stabilized highest occupied molecular orbital (HOMO) at -6.4 eV while the lowest unoccupied molecular orbital (LUMO) at -4.0 eV, indicating potential suitability for application as the electron transport layer or TADF class III emitter in OLEDs.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494236PMC
http://dx.doi.org/10.3762/bjoc.19.95DOI Listing

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