On-demand Triplet-sensitized Photoswitching of Arylazopyrazoles
Triplet-sensitized Z-to-E photoisomerization of arylazopyrazole derivatives was achieved with red-light excitation of Pd(II) meso-tetraphenyltetrabenzoporphyrin (PdTPTBP) in deaerated DMSO solution. The triplet energy gap between the sensitizer and the arylazopyrazoles affects the apparent rate of Z...
Gespeichert in:
Veröffentlicht in: | Chemistry letters 2023-09, Vol.52 (9), p.727-731 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng ; jpn |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 731 |
---|---|
container_issue | 9 |
container_start_page | 727 |
container_title | Chemistry letters |
container_volume | 52 |
creator | Morikawa, Masa-aki Mizuno, Miko Harada, Naoyuki Kimizuka, Nobuo |
description | Triplet-sensitized Z-to-E photoisomerization of arylazopyrazole derivatives was achieved with red-light excitation of Pd(II) meso-tetraphenyltetrabenzoporphyrin (PdTPTBP) in deaerated DMSO solution. The triplet energy gap between the sensitizer and the arylazopyrazoles affects the apparent rate of Z-to-E photoisomerization. On-demand photoswitching of arylazopyrazoles proceeds facilely and reversibly with almost 100% efficiency despite the endothermic triplet energy transfer processes. |
doi_str_mv | 10.1246/cl.230281 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2889858834</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2889858834</sourcerecordid><originalsourceid>FETCH-LOGICAL-c370t-7f91072e5abafaf0c4dc42a43d19de20b210faa168f4d92b8f24151f2cc7eace3</originalsourceid><addsrcrecordid>eNplkM9LwzAYhoMoOKcH_4OCJw-ZyZe0TU8yhr9gMA_zHNI0cRldU5MM6f56Kxt48PJ-l-d7XngRuqVkRoEXD7qdASMg6BmaUMYFJiXNz9GEsKLAJQG4RFcxbgkhomIwQY-rDjdmp7omWwfXtybhaLrokjuYJnvf-OTjt0t647rPzNtsHoZWHXw_hDFbE6_RhVVtNDenO0Ufz0_rxSterl7eFvMl1qwkCZe2oqQEk6taWWWJ5o3moDhraNUYIDVQYpWihbC8qaAWFjjNqQWtS6O0YVN0d_T2wX_tTUxy6_ehGyslCFGJXAjGR-r-SOngYwzGyj64nQqDpET-7iN1K4_7jGxxYjdm5_Ro8tqZNGxVr7o_-__HH1aya8k</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2889858834</pqid></control><display><type>article</type><title>On-demand Triplet-sensitized Photoswitching of Arylazopyrazoles</title><source>Oxford University Press Journals All Titles (1996-Current)</source><creator>Morikawa, Masa-aki ; Mizuno, Miko ; Harada, Naoyuki ; Kimizuka, Nobuo</creator><creatorcontrib>Morikawa, Masa-aki ; Mizuno, Miko ; Harada, Naoyuki ; Kimizuka, Nobuo</creatorcontrib><description>Triplet-sensitized Z-to-E photoisomerization of arylazopyrazole derivatives was achieved with red-light excitation of Pd(II) meso-tetraphenyltetrabenzoporphyrin (PdTPTBP) in deaerated DMSO solution. The triplet energy gap between the sensitizer and the arylazopyrazoles affects the apparent rate of Z-to-E photoisomerization. On-demand photoswitching of arylazopyrazoles proceeds facilely and reversibly with almost 100% efficiency despite the endothermic triplet energy transfer processes.</description><identifier>ISSN: 0366-7022</identifier><identifier>EISSN: 1348-0715</identifier><identifier>DOI: 10.1246/cl.230281</identifier><language>eng ; jpn</language><publisher>Tokyo: The Chemical Society of Japan</publisher><subject>Endothermic reactions ; Energy gap ; Energy transfer</subject><ispartof>Chemistry letters, 2023-09, Vol.52 (9), p.727-731</ispartof><rights>The Chemical Society of Japan</rights><rights>Copyright Chemical Society of Japan 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-7f91072e5abafaf0c4dc42a43d19de20b210faa168f4d92b8f24151f2cc7eace3</citedby><cites>FETCH-LOGICAL-c370t-7f91072e5abafaf0c4dc42a43d19de20b210faa168f4d92b8f24151f2cc7eace3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Morikawa, Masa-aki</creatorcontrib><creatorcontrib>Mizuno, Miko</creatorcontrib><creatorcontrib>Harada, Naoyuki</creatorcontrib><creatorcontrib>Kimizuka, Nobuo</creatorcontrib><title>On-demand Triplet-sensitized Photoswitching of Arylazopyrazoles</title><title>Chemistry letters</title><description>Triplet-sensitized Z-to-E photoisomerization of arylazopyrazole derivatives was achieved with red-light excitation of Pd(II) meso-tetraphenyltetrabenzoporphyrin (PdTPTBP) in deaerated DMSO solution. The triplet energy gap between the sensitizer and the arylazopyrazoles affects the apparent rate of Z-to-E photoisomerization. On-demand photoswitching of arylazopyrazoles proceeds facilely and reversibly with almost 100% efficiency despite the endothermic triplet energy transfer processes.</description><subject>Endothermic reactions</subject><subject>Energy gap</subject><subject>Energy transfer</subject><issn>0366-7022</issn><issn>1348-0715</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNplkM9LwzAYhoMoOKcH_4OCJw-ZyZe0TU8yhr9gMA_zHNI0cRldU5MM6f56Kxt48PJ-l-d7XngRuqVkRoEXD7qdASMg6BmaUMYFJiXNz9GEsKLAJQG4RFcxbgkhomIwQY-rDjdmp7omWwfXtybhaLrokjuYJnvf-OTjt0t647rPzNtsHoZWHXw_hDFbE6_RhVVtNDenO0Ufz0_rxSterl7eFvMl1qwkCZe2oqQEk6taWWWJ5o3moDhraNUYIDVQYpWihbC8qaAWFjjNqQWtS6O0YVN0d_T2wX_tTUxy6_ehGyslCFGJXAjGR-r-SOngYwzGyj64nQqDpET-7iN1K4_7jGxxYjdm5_Ro8tqZNGxVr7o_-__HH1aya8k</recordid><startdate>20230905</startdate><enddate>20230905</enddate><creator>Morikawa, Masa-aki</creator><creator>Mizuno, Miko</creator><creator>Harada, Naoyuki</creator><creator>Kimizuka, Nobuo</creator><general>The Chemical Society of Japan</general><general>Chemical Society of Japan</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20230905</creationdate><title>On-demand Triplet-sensitized Photoswitching of Arylazopyrazoles</title><author>Morikawa, Masa-aki ; Mizuno, Miko ; Harada, Naoyuki ; Kimizuka, Nobuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-7f91072e5abafaf0c4dc42a43d19de20b210faa168f4d92b8f24151f2cc7eace3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; jpn</language><creationdate>2023</creationdate><topic>Endothermic reactions</topic><topic>Energy gap</topic><topic>Energy transfer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morikawa, Masa-aki</creatorcontrib><creatorcontrib>Mizuno, Miko</creatorcontrib><creatorcontrib>Harada, Naoyuki</creatorcontrib><creatorcontrib>Kimizuka, Nobuo</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Chemistry letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morikawa, Masa-aki</au><au>Mizuno, Miko</au><au>Harada, Naoyuki</au><au>Kimizuka, Nobuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>On-demand Triplet-sensitized Photoswitching of Arylazopyrazoles</atitle><jtitle>Chemistry letters</jtitle><date>2023-09-05</date><risdate>2023</risdate><volume>52</volume><issue>9</issue><spage>727</spage><epage>731</epage><pages>727-731</pages><issn>0366-7022</issn><eissn>1348-0715</eissn><abstract>Triplet-sensitized Z-to-E photoisomerization of arylazopyrazole derivatives was achieved with red-light excitation of Pd(II) meso-tetraphenyltetrabenzoporphyrin (PdTPTBP) in deaerated DMSO solution. The triplet energy gap between the sensitizer and the arylazopyrazoles affects the apparent rate of Z-to-E photoisomerization. On-demand photoswitching of arylazopyrazoles proceeds facilely and reversibly with almost 100% efficiency despite the endothermic triplet energy transfer processes.</abstract><cop>Tokyo</cop><pub>The Chemical Society of Japan</pub><doi>10.1246/cl.230281</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0366-7022 |
ispartof | Chemistry letters, 2023-09, Vol.52 (9), p.727-731 |
issn | 0366-7022 1348-0715 |
language | eng ; jpn |
recordid | cdi_proquest_journals_2889858834 |
source | Oxford University Press Journals All Titles (1996-Current) |
subjects | Endothermic reactions Energy gap Energy transfer |
title | On-demand Triplet-sensitized Photoswitching of Arylazopyrazoles |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T02%3A02%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=On-demand%20Triplet-sensitized%20Photoswitching%20of%20Arylazopyrazoles&rft.jtitle=Chemistry%20letters&rft.au=Morikawa,%20Masa-aki&rft.date=2023-09-05&rft.volume=52&rft.issue=9&rft.spage=727&rft.epage=731&rft.pages=727-731&rft.issn=0366-7022&rft.eissn=1348-0715&rft_id=info:doi/10.1246/cl.230281&rft_dat=%3Cproquest_cross%3E2889858834%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2889858834&rft_id=info:pmid/&rfr_iscdi=true |