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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...

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Autores principales: Brosius, Victor, Weigold, Svenja, Hippchen, Nikolai, Rominger, Frank, Freudenberg, Jan, Bunz, Uwe H. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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).
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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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