Y-Shaped Fluorophores Based on N(2)-Aryl-1,2,3-triazoles: Synthesis and Study of Photophysical and Chemosensor Properties for the Detection of Nitroaromatic Compounds
A five-stage method for the synthesis of Y-shaped push–pull fluorophores based on 2-(4'-methoxyphenyl)-1,2,3-triazole was proposed. The resulting molecules exhibited emission in the range from 350 to 450 nm with high quantum yields (QY) of 90–99% in solvents of various polarity. The products pr...
Gespeichert in:
Veröffentlicht in: | Doklady. Chemistry 2023-09, Vol.512 (1), p.232-241 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 241 |
---|---|
container_issue | 1 |
container_start_page | 232 |
container_title | Doklady. Chemistry |
container_volume | 512 |
creator | Lavrinchenko, I. A. Moseev, T. D. Varaksin, M. V. Seleznev, Yu. A. Sadieva, L. K. Zyryanov, G. V. Tsmokaluk, A. N. Charushin, V. N. Chupakhin, O. N. |
description | A five-stage method for the synthesis of Y-shaped push–pull fluorophores based on 2-(4'-methoxyphenyl)-1,2,3-triazole was proposed. The resulting molecules exhibited emission in the range from 350 to 450 nm with high quantum yields (QY) of 90–99% in solvents of various polarity. The products proved to be applicable as chemosensors for both aromatic and aliphatic nitro analytes in concentrations down to 300 ppb. |
doi_str_mv | 10.1134/S0012500823600682 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2905829020</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2905829020</sourcerecordid><originalsourceid>FETCH-LOGICAL-c268t-5ed734c0cfc195f26adede43260fa310b4b86cdfb0dd918f74dfd1eb033b46b03</originalsourceid><addsrcrecordid>eNp1Ub1O5DAQthAnsXA8AJ0lGpAwN7az2Swd7PFzEuKQFgqqyLHHJCgbB9spcg_Ec-JlkSjQNfNp5vsrhpADDqecy-zXEoCLKUAhZA6QF2KLTHgOBZOJ3iaTNc3W_A7ZDeEFAOYzWUzI2xNb1qpHQ6_awXnX185joBcqpJPr6N2ROGbnfmwZPxEnkkXfqH-uxXBGl2MXawxNoKozdBkHM1Jn6X3tYooZQ6NV-0Etaly5gF1wnt6nCvSxSR02rSmA_saIOjapLLnvmuid8m6lYqPpwq16N3Qm_CQ_rGoD7n_iHnm8unxY3LDbv9d_Fue3TIu8iGyKZiYzDdpqPp9akSuDBjMpcrBKcqiyqsi1sRUYM-eFnWXGGo4VSFlleYI9crjJ7b17HTDE8sUNvkuVpZjDtEhDrFV8o9LeheDRlr1vVsqPJYdy_Y7y2zuSR2w8IWm7Z_Rfyf83vQMg-Y5S</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2905829020</pqid></control><display><type>article</type><title>Y-Shaped Fluorophores Based on N(2)-Aryl-1,2,3-triazoles: Synthesis and Study of Photophysical and Chemosensor Properties for the Detection of Nitroaromatic Compounds</title><source>SpringerLink Journals - AutoHoldings</source><creator>Lavrinchenko, I. A. ; Moseev, T. D. ; Varaksin, M. V. ; Seleznev, Yu. A. ; Sadieva, L. K. ; Zyryanov, G. V. ; Tsmokaluk, A. N. ; Charushin, V. N. ; Chupakhin, O. N.</creator><creatorcontrib>Lavrinchenko, I. A. ; Moseev, T. D. ; Varaksin, M. V. ; Seleznev, Yu. A. ; Sadieva, L. K. ; Zyryanov, G. V. ; Tsmokaluk, A. N. ; Charushin, V. N. ; Chupakhin, O. N.</creatorcontrib><description>A five-stage method for the synthesis of Y-shaped push–pull fluorophores based on 2-(4'-methoxyphenyl)-1,2,3-triazole was proposed. The resulting molecules exhibited emission in the range from 350 to 450 nm with high quantum yields (QY) of 90–99% in solvents of various polarity. The products proved to be applicable as chemosensors for both aromatic and aliphatic nitro analytes in concentrations down to 300 ppb.</description><identifier>ISSN: 0012-5008</identifier><identifier>EISSN: 1608-3113</identifier><identifier>DOI: 10.1134/S0012500823600682</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Chemical compounds ; Chemical sensors ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Chemoreceptors ; Fluorescence ; Industrial Chemistry/Chemical Engineering ; Synthesis ; Triazoles</subject><ispartof>Doklady. Chemistry, 2023-09, Vol.512 (1), p.232-241</ispartof><rights>Pleiades Publishing, Ltd. 2023. ISSN 0012-5008, Doklady Chemistry, 2023, Vol. 512, Part 1, pp. 232–241. © Pleiades Publishing, Ltd., 2023. Russian Text © The Author(s), 2023, published in Doklady Rossiiskoi Akademii Nauk. Khimiya, Nauki o Materialakh, 2023, Vol. 512, pp. 21–31.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c268t-5ed734c0cfc195f26adede43260fa310b4b86cdfb0dd918f74dfd1eb033b46b03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S0012500823600682$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S0012500823600682$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,41486,42555,51317</link.rule.ids></links><search><creatorcontrib>Lavrinchenko, I. A.</creatorcontrib><creatorcontrib>Moseev, T. D.</creatorcontrib><creatorcontrib>Varaksin, M. V.</creatorcontrib><creatorcontrib>Seleznev, Yu. A.</creatorcontrib><creatorcontrib>Sadieva, L. K.</creatorcontrib><creatorcontrib>Zyryanov, G. V.</creatorcontrib><creatorcontrib>Tsmokaluk, A. N.</creatorcontrib><creatorcontrib>Charushin, V. N.</creatorcontrib><creatorcontrib>Chupakhin, O. N.</creatorcontrib><title>Y-Shaped Fluorophores Based on N(2)-Aryl-1,2,3-triazoles: Synthesis and Study of Photophysical and Chemosensor Properties for the Detection of Nitroaromatic Compounds</title><title>Doklady. Chemistry</title><addtitle>Dokl Chem</addtitle><description>A five-stage method for the synthesis of Y-shaped push–pull fluorophores based on 2-(4'-methoxyphenyl)-1,2,3-triazole was proposed. The resulting molecules exhibited emission in the range from 350 to 450 nm with high quantum yields (QY) of 90–99% in solvents of various polarity. The products proved to be applicable as chemosensors for both aromatic and aliphatic nitro analytes in concentrations down to 300 ppb.</description><subject>Chemical compounds</subject><subject>Chemical sensors</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Chemoreceptors</subject><subject>Fluorescence</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Synthesis</subject><subject>Triazoles</subject><issn>0012-5008</issn><issn>1608-3113</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1Ub1O5DAQthAnsXA8AJ0lGpAwN7az2Swd7PFzEuKQFgqqyLHHJCgbB9spcg_Ec-JlkSjQNfNp5vsrhpADDqecy-zXEoCLKUAhZA6QF2KLTHgOBZOJ3iaTNc3W_A7ZDeEFAOYzWUzI2xNb1qpHQ6_awXnX185joBcqpJPr6N2ROGbnfmwZPxEnkkXfqH-uxXBGl2MXawxNoKozdBkHM1Jn6X3tYooZQ6NV-0Etaly5gF1wnt6nCvSxSR02rSmA_saIOjapLLnvmuid8m6lYqPpwq16N3Qm_CQ_rGoD7n_iHnm8unxY3LDbv9d_Fue3TIu8iGyKZiYzDdpqPp9akSuDBjMpcrBKcqiyqsi1sRUYM-eFnWXGGo4VSFlleYI9crjJ7b17HTDE8sUNvkuVpZjDtEhDrFV8o9LeheDRlr1vVsqPJYdy_Y7y2zuSR2w8IWm7Z_Rfyf83vQMg-Y5S</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Lavrinchenko, I. A.</creator><creator>Moseev, T. D.</creator><creator>Varaksin, M. V.</creator><creator>Seleznev, Yu. A.</creator><creator>Sadieva, L. K.</creator><creator>Zyryanov, G. V.</creator><creator>Tsmokaluk, A. N.</creator><creator>Charushin, V. N.</creator><creator>Chupakhin, O. N.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20230901</creationdate><title>Y-Shaped Fluorophores Based on N(2)-Aryl-1,2,3-triazoles: Synthesis and Study of Photophysical and Chemosensor Properties for the Detection of Nitroaromatic Compounds</title><author>Lavrinchenko, I. A. ; Moseev, T. D. ; Varaksin, M. V. ; Seleznev, Yu. A. ; Sadieva, L. K. ; Zyryanov, G. V. ; Tsmokaluk, A. N. ; Charushin, V. N. ; Chupakhin, O. N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c268t-5ed734c0cfc195f26adede43260fa310b4b86cdfb0dd918f74dfd1eb033b46b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Chemical compounds</topic><topic>Chemical sensors</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Chemoreceptors</topic><topic>Fluorescence</topic><topic>Industrial Chemistry/Chemical Engineering</topic><topic>Synthesis</topic><topic>Triazoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lavrinchenko, I. A.</creatorcontrib><creatorcontrib>Moseev, T. D.</creatorcontrib><creatorcontrib>Varaksin, M. V.</creatorcontrib><creatorcontrib>Seleznev, Yu. A.</creatorcontrib><creatorcontrib>Sadieva, L. K.</creatorcontrib><creatorcontrib>Zyryanov, G. V.</creatorcontrib><creatorcontrib>Tsmokaluk, A. N.</creatorcontrib><creatorcontrib>Charushin, V. N.</creatorcontrib><creatorcontrib>Chupakhin, O. N.</creatorcontrib><collection>CrossRef</collection><jtitle>Doklady. Chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lavrinchenko, I. A.</au><au>Moseev, T. D.</au><au>Varaksin, M. V.</au><au>Seleznev, Yu. A.</au><au>Sadieva, L. K.</au><au>Zyryanov, G. V.</au><au>Tsmokaluk, A. N.</au><au>Charushin, V. N.</au><au>Chupakhin, O. N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Y-Shaped Fluorophores Based on N(2)-Aryl-1,2,3-triazoles: Synthesis and Study of Photophysical and Chemosensor Properties for the Detection of Nitroaromatic Compounds</atitle><jtitle>Doklady. Chemistry</jtitle><stitle>Dokl Chem</stitle><date>2023-09-01</date><risdate>2023</risdate><volume>512</volume><issue>1</issue><spage>232</spage><epage>241</epage><pages>232-241</pages><issn>0012-5008</issn><eissn>1608-3113</eissn><abstract>A five-stage method for the synthesis of Y-shaped push–pull fluorophores based on 2-(4'-methoxyphenyl)-1,2,3-triazole was proposed. The resulting molecules exhibited emission in the range from 350 to 450 nm with high quantum yields (QY) of 90–99% in solvents of various polarity. The products proved to be applicable as chemosensors for both aromatic and aliphatic nitro analytes in concentrations down to 300 ppb.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S0012500823600682</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0012-5008 |
ispartof | Doklady. Chemistry, 2023-09, Vol.512 (1), p.232-241 |
issn | 0012-5008 1608-3113 |
language | eng |
recordid | cdi_proquest_journals_2905829020 |
source | SpringerLink Journals - AutoHoldings |
subjects | Chemical compounds Chemical sensors Chemistry Chemistry and Materials Science Chemistry/Food Science Chemoreceptors Fluorescence Industrial Chemistry/Chemical Engineering Synthesis Triazoles |
title | Y-Shaped Fluorophores Based on N(2)-Aryl-1,2,3-triazoles: Synthesis and Study of Photophysical and Chemosensor Properties for the Detection of Nitroaromatic Compounds |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T11%3A51%3A38IST&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=Y-Shaped%20Fluorophores%20Based%20on%20N(2)-Aryl-1,2,3-triazoles:%20Synthesis%20and%20Study%20of%20Photophysical%20and%20Chemosensor%20Properties%20for%20the%20Detection%20of%20Nitroaromatic%20Compounds&rft.jtitle=Doklady.%20Chemistry&rft.au=Lavrinchenko,%20I.%20A.&rft.date=2023-09-01&rft.volume=512&rft.issue=1&rft.spage=232&rft.epage=241&rft.pages=232-241&rft.issn=0012-5008&rft.eissn=1608-3113&rft_id=info:doi/10.1134/S0012500823600682&rft_dat=%3Cproquest_cross%3E2905829020%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=2905829020&rft_id=info:pmid/&rfr_iscdi=true |