Abstract

AbstractA novel chiral nanographene (i.e.EP9H) with a pentadecabenzo[9]helicene core fragment has been synthesized and fully characterized. Single‐crystal X‐ray diffraction unambiguously confirms the helical structure. The fluorescence emission ofEP9His located in the near infrared region (λem=684 nm) with a medium quantum yield (0.10) for helicene derivatives. Cyclic voltammetry reveals its seven quasi‐reversible redox states from −2 to +5. Furthermore, enantiopureEP9Hdisplays distinct CD signals in a broad spectral range from 300 to 700 nm. Notably, compared to the reported small organic molecules,EP9Hdisplays an outstanding |glum| value of 4.50×10−2andBCPLas 304 M−1cm−1.

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