Intermolecular Electronic Coupling of Organic Units for Efficient Persistent Room-Temperature Phosphorescence

Although persistent room‐temperature phosphorescence (RTP) emission has been observed for a few pure crystalline organic molecules, there is no consistent mechanism and no universal design strategy for organic persistent RTP (pRTP) materials. A new mechanism for pRTP is presented, based on combining...

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Published inAngewandte Chemie International Edition Vol. 55; no. 6; pp. 2181 - 2185
Main Authors Yang, Zhiyong, Mao, Zhu, Zhang, Xuepeng, Ou, Depei, Mu, Yingxiao, Zhang, Yi, Zhao, Cunyuan, Liu, Siwei, Chi, Zhenguo, Xu, Jiarui, Wu, Yuan-Chun, Lu, Po-Yen, Lien, Alan, Bryce, Martin R.
Format Journal Article
LanguageEnglish
Published WEINHEIM Blackwell Publishing Ltd 05.02.2016
Wiley
Wiley Subscription Services, Inc
John Wiley and Sons Inc
EditionInternational ed. in English
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Summary:Although persistent room‐temperature phosphorescence (RTP) emission has been observed for a few pure crystalline organic molecules, there is no consistent mechanism and no universal design strategy for organic persistent RTP (pRTP) materials. A new mechanism for pRTP is presented, based on combining the advantages of different excited‐state configurations in coupled intermolecular units, which may be applicable to a wide range of organic molecules. By following this mechanism, we have developed a successful design strategy to obtain bright pRTP by utilizing a heavy halogen atom to further increase the intersystem crossing rate of the coupled units. RTP with a remarkably long lifetime of 0.28 s and a very high quantum efficiency of 5 % was thus obtained under ambient conditions. This strategy represents an important step in the understanding of organic pRTP emission. Persistence pays off: Bright persistent room‐temperature phosphorescence from pure organic molecules was achieved by intermolecular electronic coupling of selected units in crystals. The combined advantages of their different excited‐state configurations (i.e., the nπ* state with a high intersystem crossing rate and the ππ* state with a low radiative rate) results in a hybrid intersystem‐crossing process that leads to efficient persistent room‐temperature phosphorescence.
Bibliography:863 Program - No. SS2015AA031701
CSC
Science and Technology Planning Project of Guangdong - No. 2015B090913003
NSFC - No. 51173210; No. 51473185
EPSRC
istex:B63E7CA6E87F53CE8992D72B01DB1A22F6DB6739
ark:/67375/WNG-SPQZBMZ0-3
ArticleID:ANIE201509224
These authors contributed equally to this work.
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ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201509224