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      The influence of the molecular packing on the room temperature phosphorescence of purely organic luminogens

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          Abstract

          Organic luminogens with persistent room temperature phosphorescence (RTP) have attracted great attention for their wide applications in optoelectronic devices and bioimaging. However, these materials are still very scarce, partially due to the unclear mechanism and lack of designing guidelines. Herein we develop seven 10-phenyl-10H-phenothiazine-5,5-dioxide-based derivatives, reveal their different RTP properties and underlying mechanism, and exploit their potential imaging applications. Coupled with the preliminary theoretical calculations, it is found that strong π–π interactions in solid state can promote the persistent RTP. Particularly, CS-CF 3 shows the unique photo-induced phosphorescence in response to the changes in molecular packing, further confirming the key influence of the molecular packing on the RTP property. Furthermore, CS-F with its long RTP lifetime could be utilized for real-time excitation-free phosphorescent imaging in living mice. Thus, our study paves the way for the development of persistent RTP materials, in both the practical applications and the inherent mechanism.

          Abstract

          Organic luminogens with persistent room temperature phosphorescence will find wide applications in optoelectronic devices and bioimaging, but they are still scarce. Here, the authors synthesize seven organic luminogens and investigate their different properties and potential imaging applications.

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          The nature of .pi.-.pi. interactions

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            Excitation energies from time-dependent density-functional theory.

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              A New Long Phosphorescent Phosphor with High Brightness, SrAl[sub 2]O[sub 4]:Eu[sup 2+],Dy[sup 3+]

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                Author and article information

                Contributors
                kypu@ntu.edu.sg
                lizhen@whu.edu.cn
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                26 February 2018
                26 February 2018
                2018
                : 9
                : 840
                Affiliations
                [1 ]ISNI 0000 0001 2331 6153, GRID grid.49470.3e, Department of Chemistry, , Wuhan University, ; Wuhan, 430072 China
                [2 ]ISNI 0000 0001 2224 0361, GRID grid.59025.3b, School of Chemical and Biomedical Engineering Nanyang Technological University, ; Singapore, 637457 Singapore
                [3 ]ISNI 0000 0000 9040 3743, GRID grid.28703.3e, Department of Chemistry and Chemical Engineering, , Beijing University of Technology, ; Beijing, 100124 China
                [4 ]ISNI 0000000119573309, GRID grid.9227.e, Key Laboratory of Organic Solids, Beijing National Laboratory for Molecular Science (BNLMS), Institute of Chemistry, , Chinese Academy of Sciences, ; Beijing, 100190 China
                Author information
                http://orcid.org/0000-0002-8064-6009
                Article
                3236
                10.1038/s41467-018-03236-6
                5826932
                29483501
                79293769-d800-452a-868c-1ebac6547185
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 1 February 2017
                : 30 January 2018
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