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Reversible luminescence “off–on” regulation based on tunable photodimerization via crystal-to-cocrystal transformation
The photophysical properties of organic solid-state materials are inextricably linked to the molecular structures and packing modes. However, it is still a challenge to accurately tune the fluorescence color or on–off regulation of an organic material at the molecular level. Here we demonstrate a cr...
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Published in: | Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2022-01, Vol.10 (2), p.734-741 |
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creator | Wang, Yufei Shang, Hongxing Li, Bao Jiang, Shimei |
description | The photophysical properties of organic solid-state materials are inextricably linked to the molecular structures and packing modes. However, it is still a challenge to accurately tune the fluorescence color or on–off regulation of an organic material at the molecular level. Here we demonstrate a crystal engineering strategy to regulate luminescence on and off based on the control of the packing structure for photodimerization. A cyanostilbene crystal, (
Z
)-2-(3,5-bis(trifluoromethyl)phenyl)-3-(4-(pyridin-3-yl)-phenyl)acrylonitrile (1M), shows a luminescence “off” state because the packing of olefins facilitates the solid-state [2+2] photodimerization. However, the cyanostilbene cocrystal (1M–I2), consisting of 1M and 1,4-diiodotetrafluorobenzene (I2), displays a luminescence “on” state because halogen bond-induced repacking of olefins inhibits the photodimerization. A two-component cocrystal can be formed by grinding, while the rare transformation from a cocrystal to a crystal is realized by heating. With the invertible uptake and escape of halogen-bonded donors, a reversible luminescence regulation is accomplished
in situ
. Thus, we provide a simple and clarified way to accurately achieve a crystal-to-cocrystal phase transition and control the optical properties. |
doi_str_mv | 10.1039/D1TC04401J |
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Z
)-2-(3,5-bis(trifluoromethyl)phenyl)-3-(4-(pyridin-3-yl)-phenyl)acrylonitrile (1M), shows a luminescence “off” state because the packing of olefins facilitates the solid-state [2+2] photodimerization. However, the cyanostilbene cocrystal (1M–I2), consisting of 1M and 1,4-diiodotetrafluorobenzene (I2), displays a luminescence “on” state because halogen bond-induced repacking of olefins inhibits the photodimerization. A two-component cocrystal can be formed by grinding, while the rare transformation from a cocrystal to a crystal is realized by heating. With the invertible uptake and escape of halogen-bonded donors, a reversible luminescence regulation is accomplished
in situ
. Thus, we provide a simple and clarified way to accurately achieve a crystal-to-cocrystal phase transition and control the optical properties.</description><identifier>ISSN: 2050-7526</identifier><identifier>EISSN: 2050-7534</identifier><identifier>DOI: 10.1039/D1TC04401J</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Alkenes ; Crystal structure ; Crystals ; Fluorescence ; Luminescence ; Molecular structure ; Optical properties ; Packaging ; Phase transitions ; Solid state</subject><ispartof>Journal of materials chemistry. C, Materials for optical and electronic devices, 2022-01, Vol.10 (2), p.734-741</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c325t-e234f2fd0bde03f8bd1ea2d8eee62795519a49397c80d08a9ff7ddc4947452cf3</citedby><cites>FETCH-LOGICAL-c325t-e234f2fd0bde03f8bd1ea2d8eee62795519a49397c80d08a9ff7ddc4947452cf3</cites><orcidid>0000-0001-5050-3931 ; 0000-0003-0727-9764</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Wang, Yufei</creatorcontrib><creatorcontrib>Shang, Hongxing</creatorcontrib><creatorcontrib>Li, Bao</creatorcontrib><creatorcontrib>Jiang, Shimei</creatorcontrib><title>Reversible luminescence “off–on” regulation based on tunable photodimerization via crystal-to-cocrystal transformation</title><title>Journal of materials chemistry. C, Materials for optical and electronic devices</title><description>The photophysical properties of organic solid-state materials are inextricably linked to the molecular structures and packing modes. However, it is still a challenge to accurately tune the fluorescence color or on–off regulation of an organic material at the molecular level. Here we demonstrate a crystal engineering strategy to regulate luminescence on and off based on the control of the packing structure for photodimerization. A cyanostilbene crystal, (
Z
)-2-(3,5-bis(trifluoromethyl)phenyl)-3-(4-(pyridin-3-yl)-phenyl)acrylonitrile (1M), shows a luminescence “off” state because the packing of olefins facilitates the solid-state [2+2] photodimerization. However, the cyanostilbene cocrystal (1M–I2), consisting of 1M and 1,4-diiodotetrafluorobenzene (I2), displays a luminescence “on” state because halogen bond-induced repacking of olefins inhibits the photodimerization. A two-component cocrystal can be formed by grinding, while the rare transformation from a cocrystal to a crystal is realized by heating. With the invertible uptake and escape of halogen-bonded donors, a reversible luminescence regulation is accomplished
in situ
. Thus, we provide a simple and clarified way to accurately achieve a crystal-to-cocrystal phase transition and control the optical properties.</description><subject>Alkenes</subject><subject>Crystal structure</subject><subject>Crystals</subject><subject>Fluorescence</subject><subject>Luminescence</subject><subject>Molecular structure</subject><subject>Optical properties</subject><subject>Packaging</subject><subject>Phase transitions</subject><subject>Solid state</subject><issn>2050-7526</issn><issn>2050-7534</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpFkM1KAzEUhYMoWGo3PsGAO2E0f_OTpdR_CoLU9ZBJbnTKzKQmmUKLi76DW325PolTW_Ru7rnwnXvgIHRK8AXBTFxek-kYc47J4wEaUJzgOEsYP_zTND1GI-9nuJ-cpHkqBujjGRbgfFXWENVdU7XgFbQKos36yxqzWX_adrP-jhy8drUMlW2jUnrQUS9C18qtb_5mg9VVA65a7ZBFJSPllj7IOg42VnZ_RMHJ1hvrml_uBB0ZWXsY7fcQvdzeTMf38eTp7mF8NYkVo0mIgTJuqNG41ICZyUtNQFKdA0BKM5EkREgumMhUjjXOpTAm01pxwTOeUGXYEJ3t_s6dfe_Ah2JmO9f2kQVNScZISgjvqfMdpZz13oEp5q5qpFsWBBfbgov_gtkPP1pzwQ</recordid><startdate>20220107</startdate><enddate>20220107</enddate><creator>Wang, Yufei</creator><creator>Shang, Hongxing</creator><creator>Li, Bao</creator><creator>Jiang, Shimei</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0001-5050-3931</orcidid><orcidid>https://orcid.org/0000-0003-0727-9764</orcidid></search><sort><creationdate>20220107</creationdate><title>Reversible luminescence “off–on” regulation based on tunable photodimerization via crystal-to-cocrystal transformation</title><author>Wang, Yufei ; Shang, Hongxing ; Li, Bao ; Jiang, Shimei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c325t-e234f2fd0bde03f8bd1ea2d8eee62795519a49397c80d08a9ff7ddc4947452cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alkenes</topic><topic>Crystal structure</topic><topic>Crystals</topic><topic>Fluorescence</topic><topic>Luminescence</topic><topic>Molecular structure</topic><topic>Optical properties</topic><topic>Packaging</topic><topic>Phase transitions</topic><topic>Solid state</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Yufei</creatorcontrib><creatorcontrib>Shang, Hongxing</creatorcontrib><creatorcontrib>Li, Bao</creatorcontrib><creatorcontrib>Jiang, Shimei</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of materials chemistry. C, Materials for optical and electronic devices</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Yufei</au><au>Shang, Hongxing</au><au>Li, Bao</au><au>Jiang, Shimei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reversible luminescence “off–on” regulation based on tunable photodimerization via crystal-to-cocrystal transformation</atitle><jtitle>Journal of materials chemistry. C, Materials for optical and electronic devices</jtitle><date>2022-01-07</date><risdate>2022</risdate><volume>10</volume><issue>2</issue><spage>734</spage><epage>741</epage><pages>734-741</pages><issn>2050-7526</issn><eissn>2050-7534</eissn><abstract>The photophysical properties of organic solid-state materials are inextricably linked to the molecular structures and packing modes. However, it is still a challenge to accurately tune the fluorescence color or on–off regulation of an organic material at the molecular level. Here we demonstrate a crystal engineering strategy to regulate luminescence on and off based on the control of the packing structure for photodimerization. A cyanostilbene crystal, (
Z
)-2-(3,5-bis(trifluoromethyl)phenyl)-3-(4-(pyridin-3-yl)-phenyl)acrylonitrile (1M), shows a luminescence “off” state because the packing of olefins facilitates the solid-state [2+2] photodimerization. However, the cyanostilbene cocrystal (1M–I2), consisting of 1M and 1,4-diiodotetrafluorobenzene (I2), displays a luminescence “on” state because halogen bond-induced repacking of olefins inhibits the photodimerization. A two-component cocrystal can be formed by grinding, while the rare transformation from a cocrystal to a crystal is realized by heating. With the invertible uptake and escape of halogen-bonded donors, a reversible luminescence regulation is accomplished
in situ
. Thus, we provide a simple and clarified way to accurately achieve a crystal-to-cocrystal phase transition and control the optical properties.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/D1TC04401J</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-5050-3931</orcidid><orcidid>https://orcid.org/0000-0003-0727-9764</orcidid></addata></record> |
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source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
subjects | Alkenes Crystal structure Crystals Fluorescence Luminescence Molecular structure Optical properties Packaging Phase transitions Solid state |
title | Reversible luminescence “off–on” regulation based on tunable photodimerization via crystal-to-cocrystal transformation |
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