Dynamic Ultralong Organic Phosphorescence by Photoactivation

Smart materials with ultralong phosphorescence are rarely investigated and reported. Herein we report on a series of molecules with unique dynamic ultralong organic phosphorescence (UOP) features, enabled by manipulating intermolecular interactions through UV light irradiation. Our experimental data...

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Veröffentlicht in:Angewandte Chemie 2018-07, Vol.130 (28), p.8561-8567
Hauptverfasser: Gu, Long, Shi, Huifang, Gu, Mingxing, Ling, Kun, Ma, Huili, Cai, Suzhi, Song, Lulu, Ma, Chaoqun, Li, Hai, Xing, Guichuan, Hang, Xiaochun, Li, Jiewei, Gao, Yaru, Yao, Wei, Shuai, Zhigang, An, Zhongfu, Liu, Xiaogang, Huang, Wei
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container_end_page 8567
container_issue 28
container_start_page 8561
container_title Angewandte Chemie
container_volume 130
creator Gu, Long
Shi, Huifang
Gu, Mingxing
Ling, Kun
Ma, Huili
Cai, Suzhi
Song, Lulu
Ma, Chaoqun
Li, Hai
Xing, Guichuan
Hang, Xiaochun
Li, Jiewei
Gao, Yaru
Yao, Wei
Shuai, Zhigang
An, Zhongfu
Liu, Xiaogang
Huang, Wei
description Smart materials with ultralong phosphorescence are rarely investigated and reported. Herein we report on a series of molecules with unique dynamic ultralong organic phosphorescence (UOP) features, enabled by manipulating intermolecular interactions through UV light irradiation. Our experimental data reveal that prolonged irradiation of single‐component organic phosphors of PCzT, BCzT, and FCzT under ambient conditions can activate UOP with emission lifetimes spanning from 1.8 to 1330 ms. These phosphors can also be deactivated back to their original states with short‐lived phosphorescence by UV irradiation for 3 h at room temperature or through thermal treatment. Additionally, the dynamic UOP was applied successfully for a visual anti‐counterfeiting application. These findings may provide unique insight into dynamic molecular motion for optical processing and expand the scope of smart‐response materials for broader applications. Die Bestrahlung organischer Einkomponenten‐Phosphore aktiviert eine ultralange organische Phosphoreszenz mit einer Zunahme der Emissionslebensdauer von 1.8 bis 1330 ms, die über die intermolekulare Wechselwirkung modulierbar ist. Die Phosphore konnten binnen 3 h unter Umgebungsbedingungen oder durch Erhitzen zu ihrem Ursprungszustand mit kurzlebiger Phosphoreszenz deaktiviert werden. Eine Anwendung im Fälschungsschutz wurde demonstriert.
doi_str_mv 10.1002/ange.201712381
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Herein we report on a series of molecules with unique dynamic ultralong organic phosphorescence (UOP) features, enabled by manipulating intermolecular interactions through UV light irradiation. Our experimental data reveal that prolonged irradiation of single‐component organic phosphors of PCzT, BCzT, and FCzT under ambient conditions can activate UOP with emission lifetimes spanning from 1.8 to 1330 ms. These phosphors can also be deactivated back to their original states with short‐lived phosphorescence by UV irradiation for 3 h at room temperature or through thermal treatment. Additionally, the dynamic UOP was applied successfully for a visual anti‐counterfeiting application. These findings may provide unique insight into dynamic molecular motion for optical processing and expand the scope of smart‐response materials for broader applications. Die Bestrahlung organischer Einkomponenten‐Phosphore aktiviert eine ultralange organische Phosphoreszenz mit einer Zunahme der Emissionslebensdauer von 1.8 bis 1330 ms, die über die intermolekulare Wechselwirkung modulierbar ist. Die Phosphore konnten binnen 3 h unter Umgebungsbedingungen oder durch Erhitzen zu ihrem Ursprungszustand mit kurzlebiger Phosphoreszenz deaktiviert werden. Eine Anwendung im Fälschungsschutz wurde demonstriert.</description><identifier>ISSN: 0044-8249</identifier><identifier>EISSN: 1521-3757</identifier><identifier>DOI: 10.1002/ange.201712381</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Chain dynamics ; Chemistry ; Data processing ; Deactivation ; Dynamische ultralange Phosphoreszenz ; Fälschungsschutz ; Heat treatment ; Irradiation ; Kristall-Engineering ; Light irradiation ; Molecular chains ; Molecular motion ; Phosphorescence ; Phosphors ; Photoactivation ; Photoaktivierung ; Photophysik ; Smart materials ; Ultraviolet radiation</subject><ispartof>Angewandte Chemie, 2018-07, Vol.130 (28), p.8561-8567</ispartof><rights>2018 Wiley‐VCH Verlag GmbH &amp; Co. 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Die Bestrahlung organischer Einkomponenten‐Phosphore aktiviert eine ultralange organische Phosphoreszenz mit einer Zunahme der Emissionslebensdauer von 1.8 bis 1330 ms, die über die intermolekulare Wechselwirkung modulierbar ist. Die Phosphore konnten binnen 3 h unter Umgebungsbedingungen oder durch Erhitzen zu ihrem Ursprungszustand mit kurzlebiger Phosphoreszenz deaktiviert werden. Eine Anwendung im Fälschungsschutz wurde demonstriert.</description><subject>Chain dynamics</subject><subject>Chemistry</subject><subject>Data processing</subject><subject>Deactivation</subject><subject>Dynamische ultralange Phosphoreszenz</subject><subject>Fälschungsschutz</subject><subject>Heat treatment</subject><subject>Irradiation</subject><subject>Kristall-Engineering</subject><subject>Light irradiation</subject><subject>Molecular chains</subject><subject>Molecular motion</subject><subject>Phosphorescence</subject><subject>Phosphors</subject><subject>Photoactivation</subject><subject>Photoaktivierung</subject><subject>Photophysik</subject><subject>Smart materials</subject><subject>Ultraviolet radiation</subject><issn>0044-8249</issn><issn>1521-3757</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LAzEQhoMoWKtXzwXPu06ymy_wUmqtQrEe7Dmk2aTdsk1qslX237ulokdPAy_PMzO8CN1iyDEAudd-bXMCmGNSCHyGBpgSnBWc8nM0ACjLTJBSXqKrlLYAwAiXA_Tw2Hm9q81o2bRRN8GvR4u41r5P3jYh7Tch2mSsN3a06o5RG7Rp60_d1sFfowunm2RvfuYQLZ-m75PnbL6YvUzG88xg1r9gCimoJhRTXhWEOU4rWYEzYCy3QorC8MIIRhl3pWGAnREr4UglV45YyUgxRHenvfsYPg42tWobDtH3JxUBVvKSUMl7Kj9RJoaUonVqH-udjp3CoI4NqWND6rehXpAn4atubPcPrcavs-mf-w2XBmnW</recordid><startdate>20180709</startdate><enddate>20180709</enddate><creator>Gu, Long</creator><creator>Shi, Huifang</creator><creator>Gu, Mingxing</creator><creator>Ling, Kun</creator><creator>Ma, Huili</creator><creator>Cai, Suzhi</creator><creator>Song, Lulu</creator><creator>Ma, Chaoqun</creator><creator>Li, Hai</creator><creator>Xing, Guichuan</creator><creator>Hang, Xiaochun</creator><creator>Li, Jiewei</creator><creator>Gao, Yaru</creator><creator>Yao, Wei</creator><creator>Shuai, Zhigang</creator><creator>An, Zhongfu</creator><creator>Liu, Xiaogang</creator><creator>Huang, Wei</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0001-7004-6408</orcidid></search><sort><creationdate>20180709</creationdate><title>Dynamic Ultralong Organic Phosphorescence by Photoactivation</title><author>Gu, Long ; 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Die Bestrahlung organischer Einkomponenten‐Phosphore aktiviert eine ultralange organische Phosphoreszenz mit einer Zunahme der Emissionslebensdauer von 1.8 bis 1330 ms, die über die intermolekulare Wechselwirkung modulierbar ist. Die Phosphore konnten binnen 3 h unter Umgebungsbedingungen oder durch Erhitzen zu ihrem Ursprungszustand mit kurzlebiger Phosphoreszenz deaktiviert werden. Eine Anwendung im Fälschungsschutz wurde demonstriert.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/ange.201712381</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-7004-6408</orcidid></addata></record>
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subjects Chain dynamics
Chemistry
Data processing
Deactivation
Dynamische ultralange Phosphoreszenz
Fälschungsschutz
Heat treatment
Irradiation
Kristall-Engineering
Light irradiation
Molecular chains
Molecular motion
Phosphorescence
Phosphors
Photoactivation
Photoaktivierung
Photophysik
Smart materials
Ultraviolet radiation
title Dynamic Ultralong Organic Phosphorescence by Photoactivation
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