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Diindenopyrazines: Electron‐Deficient Arenes
The syntheses, properties and application of the air‐stable electron acceptors, diindenopyrazines 4 a–g are reported demonstrating the introduction of functional aryl groups in the 6‐ and 12‐positions. The targets are accessible on the hundred milligram to gram scale. The structure of the aryl group...
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/PMC8361971/ https://www.ncbi.nlm.nih.gov/pubmed/33830516 http://dx.doi.org/10.1002/chem.202100372 |
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author | Brosius, Victor Weigold, Svenja Hippchen, Nikolai Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. |
author_facet | Brosius, Victor Weigold, Svenja Hippchen, Nikolai Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. |
author_sort | Brosius, Victor |
collection | PubMed |
description | The syntheses, properties and application of the air‐stable electron acceptors, diindenopyrazines 4 a–g are reported demonstrating the introduction of functional aryl groups in the 6‐ and 12‐positions. The targets are accessible on the hundred milligram to gram scale. The structure of the aryl groups in 4 a–g modulates their solubility, redox potentials and optical properties. The introduction of electron‐poor aryl groups to the electron‐poor diindenopyrazine backbone reduces the electron affinity to −4 eV, making the compounds attractive as n‐semiconductors. A simple organic field‐effect transistor of 4 e –without optimization– shows electron transport with a mobility of up to 0.037 cm(2) V(−1) s(−1). |
format | Online Article Text |
id | pubmed-8361971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83619712021-08-17 Diindenopyrazines: Electron‐Deficient Arenes Brosius, Victor Weigold, Svenja Hippchen, Nikolai Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. Chemistry Communications The syntheses, properties and application of the air‐stable electron acceptors, diindenopyrazines 4 a–g are reported demonstrating the introduction of functional aryl groups in the 6‐ and 12‐positions. The targets are accessible on the hundred milligram to gram scale. The structure of the aryl groups in 4 a–g modulates their solubility, redox potentials and optical properties. The introduction of electron‐poor aryl groups to the electron‐poor diindenopyrazine backbone reduces the electron affinity to −4 eV, making the compounds attractive as n‐semiconductors. A simple organic field‐effect transistor of 4 e –without optimization– shows electron transport with a mobility of up to 0.037 cm(2) V(−1) s(−1). John Wiley and Sons Inc. 2021-06-04 2021-07-12 /pmc/articles/PMC8361971/ /pubmed/33830516 http://dx.doi.org/10.1002/chem.202100372 Text en © 2021 The Authors. Published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Brosius, Victor Weigold, Svenja Hippchen, Nikolai Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. Diindenopyrazines: Electron‐Deficient Arenes |
title | Diindenopyrazines: Electron‐Deficient Arenes |
title_full | Diindenopyrazines: Electron‐Deficient Arenes |
title_fullStr | Diindenopyrazines: Electron‐Deficient Arenes |
title_full_unstemmed | Diindenopyrazines: Electron‐Deficient Arenes |
title_short | Diindenopyrazines: Electron‐Deficient Arenes |
title_sort | diindenopyrazines: electron‐deficient arenes |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361971/ https://www.ncbi.nlm.nih.gov/pubmed/33830516 http://dx.doi.org/10.1002/chem.202100372 |
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