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Broadly Applicable Synthesis of Arylated Dithieno[3,2‐b:2′,3′‐d]pyrroles as Building Blocks for Organic Electronic Materials
A novel and versatile method for the N‐arylation of dithieno[3,2‐b:2′,3′‐d]pyrrole (DTP) is presented. By Pd‐ or Cu‐catalyzed coupling a variety of arenes and acenes were directly attached at the DTP−nitrogen yielding a variety of functionalized DTPs. Investigations on optical and redox properties l...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456814/ https://www.ncbi.nlm.nih.gov/pubmed/34152046 http://dx.doi.org/10.1002/chem.202101478 |
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author | Vogt, Astrid Schwer, Fabian Förtsch, Sebastian Lorenz, Christoph Mena‐Osteritz, Elena Aubele, Anna Kraus, Teresa Bäuerle, Peter |
author_facet | Vogt, Astrid Schwer, Fabian Förtsch, Sebastian Lorenz, Christoph Mena‐Osteritz, Elena Aubele, Anna Kraus, Teresa Bäuerle, Peter |
author_sort | Vogt, Astrid |
collection | PubMed |
description | A novel and versatile method for the N‐arylation of dithieno[3,2‐b:2′,3′‐d]pyrrole (DTP) is presented. By Pd‐ or Cu‐catalyzed coupling a variety of arenes and acenes were directly attached at the DTP−nitrogen yielding a variety of functionalized DTPs. Investigations on optical and redox properties led to valuable structure‐property relationships, which were corroborated by quantum chemical calculations. Further functionalization and elongation of the conjugation of an acceptor‐substituted DTP was elaborated to result in complex cruciform‐type donor−acceptor oligomers, which were investigated and implemented in single material organic solar cells. |
format | Online Article Text |
id | pubmed-8456814 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84568142021-09-27 Broadly Applicable Synthesis of Arylated Dithieno[3,2‐b:2′,3′‐d]pyrroles as Building Blocks for Organic Electronic Materials Vogt, Astrid Schwer, Fabian Förtsch, Sebastian Lorenz, Christoph Mena‐Osteritz, Elena Aubele, Anna Kraus, Teresa Bäuerle, Peter Chemistry Full Papers A novel and versatile method for the N‐arylation of dithieno[3,2‐b:2′,3′‐d]pyrrole (DTP) is presented. By Pd‐ or Cu‐catalyzed coupling a variety of arenes and acenes were directly attached at the DTP−nitrogen yielding a variety of functionalized DTPs. Investigations on optical and redox properties led to valuable structure‐property relationships, which were corroborated by quantum chemical calculations. Further functionalization and elongation of the conjugation of an acceptor‐substituted DTP was elaborated to result in complex cruciform‐type donor−acceptor oligomers, which were investigated and implemented in single material organic solar cells. John Wiley and Sons Inc. 2021-07-29 2021-08-25 /pmc/articles/PMC8456814/ /pubmed/34152046 http://dx.doi.org/10.1002/chem.202101478 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Vogt, Astrid Schwer, Fabian Förtsch, Sebastian Lorenz, Christoph Mena‐Osteritz, Elena Aubele, Anna Kraus, Teresa Bäuerle, Peter Broadly Applicable Synthesis of Arylated Dithieno[3,2‐b:2′,3′‐d]pyrroles as Building Blocks for Organic Electronic Materials |
title | Broadly Applicable Synthesis of Arylated Dithieno[3,2‐b:2′,3′‐d]pyrroles as Building Blocks for Organic Electronic Materials |
title_full | Broadly Applicable Synthesis of Arylated Dithieno[3,2‐b:2′,3′‐d]pyrroles as Building Blocks for Organic Electronic Materials |
title_fullStr | Broadly Applicable Synthesis of Arylated Dithieno[3,2‐b:2′,3′‐d]pyrroles as Building Blocks for Organic Electronic Materials |
title_full_unstemmed | Broadly Applicable Synthesis of Arylated Dithieno[3,2‐b:2′,3′‐d]pyrroles as Building Blocks for Organic Electronic Materials |
title_short | Broadly Applicable Synthesis of Arylated Dithieno[3,2‐b:2′,3′‐d]pyrroles as Building Blocks for Organic Electronic Materials |
title_sort | broadly applicable synthesis of arylated dithieno[3,2‐b:2′,3′‐d]pyrroles as building blocks for organic electronic materials |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456814/ https://www.ncbi.nlm.nih.gov/pubmed/34152046 http://dx.doi.org/10.1002/chem.202101478 |
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