Strong Circularly‐Polarized Room‐Temperature Phosphorescence from a Feasibly Separable Scaffold of Bidibenzo[b,d]furan with Locked Axial Chirality

Novel accessible scaffold featuring circularly‐polarized room‐temperature phosphorescence (RTP) is attractive but challenging. Herein, we report a new feasibly separable bidibenzo[b,d]furan compound with strong circularly‐polarized RTP when doping into the rigid polymer matrix. The simple silica‐gel...

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Veröffentlicht in:Angewandte Chemie International Edition 2022-07, Vol.61 (30), p.e202202977-n/a
Hauptverfasser: Huang, Wenbin, Fu, Chunya, Liang, Zhiwei, Zhou, Kang, He, Zikai
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Sprache:eng
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Zusammenfassung:Novel accessible scaffold featuring circularly‐polarized room‐temperature phosphorescence (RTP) is attractive but challenging. Herein, we report a new feasibly separable bidibenzo[b,d]furan compound with strong circularly‐polarized RTP when doping into the rigid polymer matrix. The simple silica‐gel column can separate the absolute chiral R‐isomer with excellent chiroptical properties. The experimental data reveal that the treated films exhibit an RTP efficiency of 14.8 %, a largest dissymmetric factor of 0.12, and a longest lifetime of 0.56 s under ambient conditions. It is found that reducing the nonradiative decays boosts the intrinsic circularly‐polarized RTP emission. The impressive results indicate that the locked axial chirality skeleton endows the potential of achieving superior circularly‐polarized emission for the small organic optoelectronic molecules. A feasibly separable bidibenzofuran compound exhibits strong circularly‐polarized room‐temperature phosphorescence (RTP) when doping into poly(vinyl alcohol) (PVA). The silica‐gel column can separate the absolute chiral R‐isomer. The treated PVA films have a RTP efficiency of 14.8 %, a largest glum of 0.12, and a lifetime of 0.56 s. The impressive results indicate that the locked axial chirality skeleton endows the potential of achieving superior circularly‐polarized emission for the small molecules.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.202202977