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Synthesis and chemosensing properties of cinnoline-containing poly(arylene ethynylene)s
Novel poly(arylene ethynylene)s comprising a cinnoline core were prepared in high yields via a three-step methodology. A Richter-type cyclization of 2-ethynyl- and 2-(buta-1,3-diynyl)aryltriazenes was used for cinnoline ring formation, followed by a Sonogashira coupling for the introduction of trime...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419556/ https://www.ncbi.nlm.nih.gov/pubmed/25977711 http://dx.doi.org/10.3762/bjoc.11.43 |
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author | Danilkina, Natalia A Vlasov, Petr S Vodianik, Semen M Kruchinin, Andrey A Vlasov, Yuri G Balova, Irina A |
author_facet | Danilkina, Natalia A Vlasov, Petr S Vodianik, Semen M Kruchinin, Andrey A Vlasov, Yuri G Balova, Irina A |
author_sort | Danilkina, Natalia A |
collection | PubMed |
description | Novel poly(arylene ethynylene)s comprising a cinnoline core were prepared in high yields via a three-step methodology. A Richter-type cyclization of 2-ethynyl- and 2-(buta-1,3-diynyl)aryltriazenes was used for cinnoline ring formation, followed by a Sonogashira coupling for the introduction of trimethylsilylethynyl moieties and a sila-Sonogashira coupling as the polycondensation technique. The fluorescence of the cinnoline-containing polymers in THF was highly sensitive to quenching by Pd(2+) ions. |
format | Online Article Text |
id | pubmed-4419556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-44195562015-05-14 Synthesis and chemosensing properties of cinnoline-containing poly(arylene ethynylene)s Danilkina, Natalia A Vlasov, Petr S Vodianik, Semen M Kruchinin, Andrey A Vlasov, Yuri G Balova, Irina A Beilstein J Org Chem Full Research Paper Novel poly(arylene ethynylene)s comprising a cinnoline core were prepared in high yields via a three-step methodology. A Richter-type cyclization of 2-ethynyl- and 2-(buta-1,3-diynyl)aryltriazenes was used for cinnoline ring formation, followed by a Sonogashira coupling for the introduction of trimethylsilylethynyl moieties and a sila-Sonogashira coupling as the polycondensation technique. The fluorescence of the cinnoline-containing polymers in THF was highly sensitive to quenching by Pd(2+) ions. Beilstein-Institut 2015-03-20 /pmc/articles/PMC4419556/ /pubmed/25977711 http://dx.doi.org/10.3762/bjoc.11.43 Text en Copyright © 2015, Danilkina et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Danilkina, Natalia A Vlasov, Petr S Vodianik, Semen M Kruchinin, Andrey A Vlasov, Yuri G Balova, Irina A Synthesis and chemosensing properties of cinnoline-containing poly(arylene ethynylene)s |
title | Synthesis and chemosensing properties of cinnoline-containing poly(arylene ethynylene)s |
title_full | Synthesis and chemosensing properties of cinnoline-containing poly(arylene ethynylene)s |
title_fullStr | Synthesis and chemosensing properties of cinnoline-containing poly(arylene ethynylene)s |
title_full_unstemmed | Synthesis and chemosensing properties of cinnoline-containing poly(arylene ethynylene)s |
title_short | Synthesis and chemosensing properties of cinnoline-containing poly(arylene ethynylene)s |
title_sort | synthesis and chemosensing properties of cinnoline-containing poly(arylene ethynylene)s |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419556/ https://www.ncbi.nlm.nih.gov/pubmed/25977711 http://dx.doi.org/10.3762/bjoc.11.43 |
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