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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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5064736/
https://www.ncbi.nlm.nih.gov/pubmed/26836346
http://dx.doi.org/10.1002/anie.201509224
Descripción
Sumario: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.