Efficient Photoredox Cycles to Control Perylenediimide Self‐Assembly
Photoreduction of perylenediimide (PDI) derivatives has been widely studied for use in photocatalysis, hydrogen evolution, photo‐responsive gels, and organic semiconductors. Upon light irradiation, the radical anion (PDI⋅−) can readily be obtained, whereas further reduction to the dianion (PDI2−) is...
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Veröffentlicht in: | Chemistry : a European journal 2023-01, Vol.29 (1), p.e202202849-n/a |
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description | Photoreduction of perylenediimide (PDI) derivatives has been widely studied for use in photocatalysis, hydrogen evolution, photo‐responsive gels, and organic semiconductors. Upon light irradiation, the radical anion (PDI⋅−) can readily be obtained, whereas further reduction to the dianion (PDI2−) is rare. Here we show that full 2‐electron photoreduction can be achieved using UVC light: 1) in anaerobic conditions by ‘direct photoreduction’ of PDI aggregates, or 2) by ‘indirect photoreduction’ in aerobic conditions due to acetone ketyl radicals. The latter strategy is also efficient for other dyes, such as naphthalenediimide (NDI) and methylviologen (MV2+). Efficient photoreduction on the minute time‐scale using simple LED light in aerobic conditions is attractive for use in dissipative light‐driven systems and materials.
Photoreduction can be used to disassemble perylenediimide‐based supramolecular structures by creating repulsive dianions. Typically, photoreductions are done in oxygen‐free conditions. Here we show that ‘indirect photoreduction’ by acetone ketyl radicals is very efficient and can be done in open air. Repeated photoreduction/disassembly followed by oxidation/assembly cycles can in this way be performed by simple UV−C LED light. |
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Photoreduction can be used to disassemble perylenediimide‐based supramolecular structures by creating repulsive dianions. Typically, photoreductions are done in oxygen‐free conditions. Here we show that ‘indirect photoreduction’ by acetone ketyl radicals is very efficient and can be done in open air. Repeated photoreduction/disassembly followed by oxidation/assembly cycles can in this way be performed by simple UV−C LED light.</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.202202849</identifier><identifier>PMID: 36112270</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Aerobic conditions ; Anaerobic conditions ; Anions ; Chemical Sciences ; Gels ; Hydrogen evolution ; Irradiation ; ketyl radical ; Light irradiation ; or physical chemistry ; Organic semiconductors ; perylenediimide ; Photoreduction ; Radiation ; redox ; self-assembly ; Theoretical and</subject><ispartof>Chemistry : a European journal, 2023-01, Vol.29 (1), p.e202202849-n/a</ispartof><rights>2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH</rights><rights>2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.</rights><rights>2022. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5039-b7e36759e7eb8405bbad6606f9f3977f31b6faccb9a134b1afcff27c355af5393</citedby><cites>FETCH-LOGICAL-c5039-b7e36759e7eb8405bbad6606f9f3977f31b6faccb9a134b1afcff27c355af5393</cites><orcidid>0000-0003-1121-1754</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchem.202202849$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchem.202202849$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36112270$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-04020467$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Chunfeng</creatorcontrib><creatorcontrib>Valera, Jorge S.</creatorcontrib><creatorcontrib>Adachi, Takuji B. M.</creatorcontrib><creatorcontrib>Hermans, Thomas M.</creatorcontrib><title>Efficient Photoredox Cycles to Control Perylenediimide Self‐Assembly</title><title>Chemistry : a European journal</title><addtitle>Chemistry</addtitle><description>Photoreduction of perylenediimide (PDI) derivatives has been widely studied for use in photocatalysis, hydrogen evolution, photo‐responsive gels, and organic semiconductors. Upon light irradiation, the radical anion (PDI⋅−) can readily be obtained, whereas further reduction to the dianion (PDI2−) is rare. Here we show that full 2‐electron photoreduction can be achieved using UVC light: 1) in anaerobic conditions by ‘direct photoreduction’ of PDI aggregates, or 2) by ‘indirect photoreduction’ in aerobic conditions due to acetone ketyl radicals. The latter strategy is also efficient for other dyes, such as naphthalenediimide (NDI) and methylviologen (MV2+). Efficient photoreduction on the minute time‐scale using simple LED light in aerobic conditions is attractive for use in dissipative light‐driven systems and materials.
Photoreduction can be used to disassemble perylenediimide‐based supramolecular structures by creating repulsive dianions. Typically, photoreductions are done in oxygen‐free conditions. Here we show that ‘indirect photoreduction’ by acetone ketyl radicals is very efficient and can be done in open air. Repeated photoreduction/disassembly followed by oxidation/assembly cycles can in this way be performed by simple UV−C LED light.</description><subject>Aerobic conditions</subject><subject>Anaerobic conditions</subject><subject>Anions</subject><subject>Chemical Sciences</subject><subject>Gels</subject><subject>Hydrogen evolution</subject><subject>Irradiation</subject><subject>ketyl radical</subject><subject>Light irradiation</subject><subject>or physical chemistry</subject><subject>Organic semiconductors</subject><subject>perylenediimide</subject><subject>Photoreduction</subject><subject>Radiation</subject><subject>redox</subject><subject>self-assembly</subject><subject>Theoretical and</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNqFkc1uEzEUhS0EoqGwZYlGYlMWE_zveIWiUdogBVEJWFsej01cecbFnhRmxyPwjH0SHFICdINkyZL93XPPvQeA5wjOEYT4tdnafo4hLmdB5QMwQwyjmgjOHoIZlFTUnBF5Ap7kfAUhlJyQx-CEcIQwFnAGzlfOeePtMFaX2zjGZLv4rWomE2yuxlg1cRhTDNWlTVOwg-28731nqw82uNvvP5Y5274N01PwyOmQ7bO7-xR8Ol99bNb15v3F22a5qQ2DRNatsIQLJq2w7YJC1ra64xxyJx2RQjiCWu60Ma3UiNAWaWecw8IQxrQrc5BT8Oage71re9uZ4jvpoK6T73WaVNRe_fsz-K36HG9UWZZcCAKLwquDwvZe3Xq5Ufs3SCGGlIsbVNizu24pftnZPKreZ2ND0IONu6ywQIxSin7JvryHXsVdGsouCiWIoIzxRaHmB8qkmHOy7ugAwb1FrPZ5qmOepeDF3_Me8d8BFkAegK8-2Ok_cqpZr979Ef8J5amtag</recordid><startdate>20230102</startdate><enddate>20230102</enddate><creator>Chen, Chunfeng</creator><creator>Valera, Jorge S.</creator><creator>Adachi, Takuji B. M.</creator><creator>Hermans, Thomas M.</creator><general>Wiley Subscription Services, Inc</general><general>Wiley-VCH Verlag</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1121-1754</orcidid></search><sort><creationdate>20230102</creationdate><title>Efficient Photoredox Cycles to Control Perylenediimide Self‐Assembly</title><author>Chen, Chunfeng ; Valera, Jorge S. ; Adachi, Takuji B. M. ; Hermans, Thomas M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5039-b7e36759e7eb8405bbad6606f9f3977f31b6faccb9a134b1afcff27c355af5393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Aerobic conditions</topic><topic>Anaerobic conditions</topic><topic>Anions</topic><topic>Chemical Sciences</topic><topic>Gels</topic><topic>Hydrogen evolution</topic><topic>Irradiation</topic><topic>ketyl radical</topic><topic>Light irradiation</topic><topic>or physical chemistry</topic><topic>Organic semiconductors</topic><topic>perylenediimide</topic><topic>Photoreduction</topic><topic>Radiation</topic><topic>redox</topic><topic>self-assembly</topic><topic>Theoretical and</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Chunfeng</creatorcontrib><creatorcontrib>Valera, Jorge S.</creatorcontrib><creatorcontrib>Adachi, Takuji B. M.</creatorcontrib><creatorcontrib>Hermans, Thomas M.</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Chunfeng</au><au>Valera, Jorge S.</au><au>Adachi, Takuji B. M.</au><au>Hermans, Thomas M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient Photoredox Cycles to Control Perylenediimide Self‐Assembly</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chemistry</addtitle><date>2023-01-02</date><risdate>2023</risdate><volume>29</volume><issue>1</issue><spage>e202202849</spage><epage>n/a</epage><pages>e202202849-n/a</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><abstract>Photoreduction of perylenediimide (PDI) derivatives has been widely studied for use in photocatalysis, hydrogen evolution, photo‐responsive gels, and organic semiconductors. Upon light irradiation, the radical anion (PDI⋅−) can readily be obtained, whereas further reduction to the dianion (PDI2−) is rare. Here we show that full 2‐electron photoreduction can be achieved using UVC light: 1) in anaerobic conditions by ‘direct photoreduction’ of PDI aggregates, or 2) by ‘indirect photoreduction’ in aerobic conditions due to acetone ketyl radicals. The latter strategy is also efficient for other dyes, such as naphthalenediimide (NDI) and methylviologen (MV2+). Efficient photoreduction on the minute time‐scale using simple LED light in aerobic conditions is attractive for use in dissipative light‐driven systems and materials.
Photoreduction can be used to disassemble perylenediimide‐based supramolecular structures by creating repulsive dianions. Typically, photoreductions are done in oxygen‐free conditions. Here we show that ‘indirect photoreduction’ by acetone ketyl radicals is very efficient and can be done in open air. Repeated photoreduction/disassembly followed by oxidation/assembly cycles can in this way be performed by simple UV−C LED light.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>36112270</pmid><doi>10.1002/chem.202202849</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-1121-1754</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aerobic conditions Anaerobic conditions Anions Chemical Sciences Gels Hydrogen evolution Irradiation ketyl radical Light irradiation or physical chemistry Organic semiconductors perylenediimide Photoreduction Radiation redox self-assembly Theoretical and |
title | Efficient Photoredox Cycles to Control Perylenediimide Self‐Assembly |
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