Abstract

Emissive electron donor–acceptor (D–A) conjugates have a wide variety of applications in biophotonics, two-photon absorption materials, organic lasers, long wavelength emitters, and so forth. However, it is still a challenge to synthesize high solid-state efficiency D–A structured emitters due to the notorious aggregation-caused quenching (ACQ) effect. Though some D–A systems are reported to show aggregation-induced emission (AIE) behaviors, most are only selectively AIE-active in highly polar solvents, showing decreased solid-sate emission efficiencies compared to those in nonpolar solvents. Here we report the triphenylamine (TPA) and 2,3,3-triphenylacrylonitrile (TPAN) based D–A architectures, namely, TPA3TPAN and DTPA4TPAN. Decoration of arylamines with TPAN changes their emission behaviors from ACQ to AIE, making resulting TPA3TPAN and DTPA4TPAN nonluminescent in common solvents but highly emissive when aggregated as nanoparticles, solid powders, and thin films owing to their highly twisted configurat...

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