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Thiophene-based donor–acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition
Herein we present a three-component one-pot procedure to synthesize co-oligomers of a donor–acceptor–donor type, in which thiophene moieties work as donor and 1,2,3-triazoles as acceptor units. In this respect, terminally ethynylated (oligo)thiophenes were coupled to halogenated (oligo)thiophenes in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388854/ https://www.ncbi.nlm.nih.gov/pubmed/23015814 http://dx.doi.org/10.3762/bjoc.8.76 |
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author | Potratz, Stefanie Mishra, Amaresh Bäuerle, Peter |
author_facet | Potratz, Stefanie Mishra, Amaresh Bäuerle, Peter |
author_sort | Potratz, Stefanie |
collection | PubMed |
description | Herein we present a three-component one-pot procedure to synthesize co-oligomers of a donor–acceptor–donor type, in which thiophene moieties work as donor and 1,2,3-triazoles as acceptor units. In this respect, terminally ethynylated (oligo)thiophenes were coupled to halogenated (oligo)thiophenes in the presence of sodium azide and a copper catalyst. Optoelectronic properties of various thiophene-1,2,3-triazole co-oligomers were investigated by UV–vis spectroscopy and cyclic voltammetry. Several co-oligomers were electropolymerized to the corresponding conjugated polymers. |
format | Online Article Text |
id | pubmed-3388854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-33888542012-09-26 Thiophene-based donor–acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition Potratz, Stefanie Mishra, Amaresh Bäuerle, Peter Beilstein J Org Chem Full Research Paper Herein we present a three-component one-pot procedure to synthesize co-oligomers of a donor–acceptor–donor type, in which thiophene moieties work as donor and 1,2,3-triazoles as acceptor units. In this respect, terminally ethynylated (oligo)thiophenes were coupled to halogenated (oligo)thiophenes in the presence of sodium azide and a copper catalyst. Optoelectronic properties of various thiophene-1,2,3-triazole co-oligomers were investigated by UV–vis spectroscopy and cyclic voltammetry. Several co-oligomers were electropolymerized to the corresponding conjugated polymers. Beilstein-Institut 2012-05-03 /pmc/articles/PMC3388854/ /pubmed/23015814 http://dx.doi.org/10.3762/bjoc.8.76 Text en Copyright © 2012, Potratz 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 Potratz, Stefanie Mishra, Amaresh Bäuerle, Peter Thiophene-based donor–acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition |
title | Thiophene-based donor–acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition |
title_full | Thiophene-based donor–acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition |
title_fullStr | Thiophene-based donor–acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition |
title_full_unstemmed | Thiophene-based donor–acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition |
title_short | Thiophene-based donor–acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition |
title_sort | thiophene-based donor–acceptor co-oligomers by copper-catalyzed 1,3-dipolar cycloaddition |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388854/ https://www.ncbi.nlm.nih.gov/pubmed/23015814 http://dx.doi.org/10.3762/bjoc.8.76 |
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