Abstract

Fine tuning the energy gaps of red emitters and promoting the fluorescence efficiencies are especially highly desired considering their specific applications. Herein, by varying the molecular symmetry from D-A-D to D-A structures, the red fluorescent emitters with triphenylamine (TPA) donor and 2,3-dicyanopyrazino phenanthrene (DCPP) acceptor realized increased fluorescence quantum yield (ΦPL) from 2TPA-DCPP to TPA-DCPP due to the decreased non-radiative paths. Moreover, fine control of the emitting color from orange to red and then to deep-red was achieved depending on the intermolecular packing patterns of TPA-DCPP in the aggregation state. Taking the advantages, TPA-DCPP-based OLED exhibited red emission (λ = 640 nm, CIE coordinate of (0.62, 0.38)) with an excellent maximum EQE of 8.30%. The TPA-DCPP@F-127 nanoparticles showed deep-red emission (λ = 684 nm) and were successfully used for cellular imaging of Hela cells. Our results demonstrated that “the simpler, the better” strategy may be feasible to construct D-A structured red emitters with high efficiencies for diverse applications.

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