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Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Solid-State Emissive Triarylborane-Based [2.2]Paracyclophanes Displaying Circularly Polarized Luminescence and
Meng-Yuan Zhang1, Zhi-Yi Li2, Bo Lu1
1School of Chemistry and Chemical Engineering , Shandong University , Jinan 250100 , P. R. China.
Abstract:
New types of [2.2]paracyclophane derivatives, g-BNMe2-Cp and m-BNMe2-Cp, in which electron-donating NMe2 and the electron-accepting BMes2 are introduced at the pseudo -gem and pseudo -meta positions, were designed and synthesized. The efficient through-space charge transfer enables the intense fluorescence with thermally activated delayed fluorescence characteristics. The quantum yields are up to 0.72 and 0.39 in cyclohexane. In addition, no significant fluorescence quenching was observed in the solid state with fluorescence quantum yields of powder up to 0.53 and 0.33. Moreover, the enantiomerically pure forms of g-BNMe2-Cp exhibit strong CPL signals with glum up to 4.24 × 10-3.
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