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Photoisomerization of 1,2‐Di(4‐pyridyl)ethylene According to NMR and UV Spectroscopy Data and Density Functional Modeling
Photoisomerization of 1,2‐di(4‐pyridyl)ethylene under UV irradiation was studied by NMR and UV spectroscopy in solutions of acetone, acetonitrile and chloroform. It has been established that in the studied solutions under irradiation, geometric photoisomerization occurs: the trans‐isomer transforms...
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Published in: | Photochemistry and photobiology 2023-11, Vol.99 (6), p.1378-1383 |
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container_title | Photochemistry and photobiology |
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creator | Shaidullina, Amina F. Sharipova, Alsu R. Volkov, Michael Yu Savostina, Liudmila I. Gafiyatullin, Linar G. Turanova, Olga A. Turanov, Alexander N. |
description | Photoisomerization of 1,2‐di(4‐pyridyl)ethylene under UV irradiation was studied by NMR and UV spectroscopy in solutions of acetone, acetonitrile and chloroform. It has been established that in the studied solutions under irradiation, geometric photoisomerization occurs: the trans‐isomer transforms into the cis‐isomer and then cyclization occurs. DFT modeling of the listed processes, states and UV absorption spectra of the sample in an acetonitrile solution was performed.
Photoisomerization of 1,2‐di(4‐pyridyl)ethylene under UV irradiation was studied by NMR and UV spectroscopy in solutions of acetone, acetonitrile and chloroform. It has been established that in the studied solutions under irradiation, geometric photoisomerization occurs: the trans‐isomer transforms into the cis‐isomer and then cyclization occurs. DFT modeling of the listed processes, states and UV absorption spectra of the sample in an acetonitrile solution was performed. |
doi_str_mv | 10.1111/php.13785 |
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Photoisomerization of 1,2‐di(4‐pyridyl)ethylene under UV irradiation was studied by NMR and UV spectroscopy in solutions of acetone, acetonitrile and chloroform. It has been established that in the studied solutions under irradiation, geometric photoisomerization occurs: the trans‐isomer transforms into the cis‐isomer and then cyclization occurs. DFT modeling of the listed processes, states and UV absorption spectra of the sample in an acetonitrile solution was performed.</description><identifier>ISSN: 0031-8655</identifier><identifier>EISSN: 1751-1097</identifier><identifier>DOI: 10.1111/php.13785</identifier><identifier>PMID: 36702750</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Absorption spectra ; Acetonitrile ; Chloroform ; Ethylene ; Irradiation ; Isomers ; Modelling ; NMR ; Nuclear magnetic resonance ; Radiation ; Spectroscopy ; Ultraviolet radiation ; Ultraviolet spectroscopy</subject><ispartof>Photochemistry and photobiology, 2023-11, Vol.99 (6), p.1378-1383</ispartof><rights>2023 American Society for Photobiology.</rights><rights>Copyright © 2023 American Society for Photobiology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3535-4b2c8a5de041be9b1d107cf82ed237de94387f5492ec28d0f676ba74860d87713</citedby><cites>FETCH-LOGICAL-c3535-4b2c8a5de041be9b1d107cf82ed237de94387f5492ec28d0f676ba74860d87713</cites><orcidid>0000-0002-7759-7832</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36702750$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shaidullina, Amina F.</creatorcontrib><creatorcontrib>Sharipova, Alsu R.</creatorcontrib><creatorcontrib>Volkov, Michael Yu</creatorcontrib><creatorcontrib>Savostina, Liudmila I.</creatorcontrib><creatorcontrib>Gafiyatullin, Linar G.</creatorcontrib><creatorcontrib>Turanova, Olga A.</creatorcontrib><creatorcontrib>Turanov, Alexander N.</creatorcontrib><title>Photoisomerization of 1,2‐Di(4‐pyridyl)ethylene According to NMR and UV Spectroscopy Data and Density Functional Modeling</title><title>Photochemistry and photobiology</title><addtitle>Photochem Photobiol</addtitle><description>Photoisomerization of 1,2‐di(4‐pyridyl)ethylene under UV irradiation was studied by NMR and UV spectroscopy in solutions of acetone, acetonitrile and chloroform. It has been established that in the studied solutions under irradiation, geometric photoisomerization occurs: the trans‐isomer transforms into the cis‐isomer and then cyclization occurs. DFT modeling of the listed processes, states and UV absorption spectra of the sample in an acetonitrile solution was performed.
Photoisomerization of 1,2‐di(4‐pyridyl)ethylene under UV irradiation was studied by NMR and UV spectroscopy in solutions of acetone, acetonitrile and chloroform. It has been established that in the studied solutions under irradiation, geometric photoisomerization occurs: the trans‐isomer transforms into the cis‐isomer and then cyclization occurs. DFT modeling of the listed processes, states and UV absorption spectra of the sample in an acetonitrile solution was performed.</description><subject>Absorption spectra</subject><subject>Acetonitrile</subject><subject>Chloroform</subject><subject>Ethylene</subject><subject>Irradiation</subject><subject>Isomers</subject><subject>Modelling</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Radiation</subject><subject>Spectroscopy</subject><subject>Ultraviolet radiation</subject><subject>Ultraviolet spectroscopy</subject><issn>0031-8655</issn><issn>1751-1097</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kc9u1DAQhy0EokvhwAsgS1xaibT-GzvHqkspUgsroFwjx56wrrJxaidCQarUR-AZeRK83cIBibnMYb75NKMfQi8pOaK5jof1cES50vIRWlAlaUFJpR6jBSGcFrqUcg89S-maECoqRZ-iPV4qwpQkC3S7Wocx-BQ2EP0PM_rQ49Bi-ob9uvu59Acit2GO3s3dIYzruYMe8Im1ITrff8NjwB8uP2HTO3z1FX8ewI4xJBuGGS_NaO4HS-iTH2d8NvV26zcdvgwOurz_HD1pTZfgxUPfR1dnb7-cnhcXH9-9Pz25KCyXXBaiYVYb6YAI2kDVUEeJsq1m4BhXDirBtWqlqBhYph1pS1U2RgldEqeVonwfHey8Qww3E6Sx3vhkoetMD2FKNVOKUEa0EBl9_Q96HaaYj86UrpjmrNJb4eGOsvndFKGth-g3Js41JfU2kzpnUt9nktlXD8ap2YD7S_4JIQPHO-C772D-v6lena92yt8e_ZcG</recordid><startdate>202311</startdate><enddate>202311</enddate><creator>Shaidullina, Amina F.</creator><creator>Sharipova, Alsu R.</creator><creator>Volkov, Michael Yu</creator><creator>Savostina, Liudmila I.</creator><creator>Gafiyatullin, Linar G.</creator><creator>Turanova, Olga A.</creator><creator>Turanov, Alexander N.</creator><general>Blackwell Publishing Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>4T-</scope><scope>7TM</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7759-7832</orcidid></search><sort><creationdate>202311</creationdate><title>Photoisomerization of 1,2‐Di(4‐pyridyl)ethylene According to NMR and UV Spectroscopy Data and Density Functional Modeling</title><author>Shaidullina, Amina F. ; Sharipova, Alsu R. ; Volkov, Michael Yu ; Savostina, Liudmila I. ; Gafiyatullin, Linar G. ; Turanova, Olga A. ; Turanov, Alexander N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3535-4b2c8a5de041be9b1d107cf82ed237de94387f5492ec28d0f676ba74860d87713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Absorption spectra</topic><topic>Acetonitrile</topic><topic>Chloroform</topic><topic>Ethylene</topic><topic>Irradiation</topic><topic>Isomers</topic><topic>Modelling</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Radiation</topic><topic>Spectroscopy</topic><topic>Ultraviolet radiation</topic><topic>Ultraviolet spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shaidullina, Amina F.</creatorcontrib><creatorcontrib>Sharipova, Alsu R.</creatorcontrib><creatorcontrib>Volkov, Michael Yu</creatorcontrib><creatorcontrib>Savostina, Liudmila I.</creatorcontrib><creatorcontrib>Gafiyatullin, Linar G.</creatorcontrib><creatorcontrib>Turanova, Olga A.</creatorcontrib><creatorcontrib>Turanov, Alexander N.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Docstoc</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Photochemistry and photobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shaidullina, Amina F.</au><au>Sharipova, Alsu R.</au><au>Volkov, Michael Yu</au><au>Savostina, Liudmila I.</au><au>Gafiyatullin, Linar G.</au><au>Turanova, Olga A.</au><au>Turanov, Alexander N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photoisomerization of 1,2‐Di(4‐pyridyl)ethylene According to NMR and UV Spectroscopy Data and Density Functional Modeling</atitle><jtitle>Photochemistry and photobiology</jtitle><addtitle>Photochem Photobiol</addtitle><date>2023-11</date><risdate>2023</risdate><volume>99</volume><issue>6</issue><spage>1378</spage><epage>1383</epage><pages>1378-1383</pages><issn>0031-8655</issn><eissn>1751-1097</eissn><abstract>Photoisomerization of 1,2‐di(4‐pyridyl)ethylene under UV irradiation was studied by NMR and UV spectroscopy in solutions of acetone, acetonitrile and chloroform. It has been established that in the studied solutions under irradiation, geometric photoisomerization occurs: the trans‐isomer transforms into the cis‐isomer and then cyclization occurs. DFT modeling of the listed processes, states and UV absorption spectra of the sample in an acetonitrile solution was performed.
Photoisomerization of 1,2‐di(4‐pyridyl)ethylene under UV irradiation was studied by NMR and UV spectroscopy in solutions of acetone, acetonitrile and chloroform. It has been established that in the studied solutions under irradiation, geometric photoisomerization occurs: the trans‐isomer transforms into the cis‐isomer and then cyclization occurs. DFT modeling of the listed processes, states and UV absorption spectra of the sample in an acetonitrile solution was performed.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>36702750</pmid><doi>10.1111/php.13785</doi><tpages>1383</tpages><orcidid>https://orcid.org/0000-0002-7759-7832</orcidid></addata></record> |
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subjects | Absorption spectra Acetonitrile Chloroform Ethylene Irradiation Isomers Modelling NMR Nuclear magnetic resonance Radiation Spectroscopy Ultraviolet radiation Ultraviolet spectroscopy |
title | Photoisomerization of 1,2‐Di(4‐pyridyl)ethylene According to NMR and UV Spectroscopy Data and Density Functional Modeling |
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