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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...

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Autores principales: Danilkina, Natalia A, Vlasov, Petr S, Vodianik, Semen M, Kruchinin, Andrey A, Vlasov, Yuri G, Balova, Irina A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
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.
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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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