Diazapentacenes from Quinacridones

Bis(silylethynylated) 5,7‐ and 5,12‐diazapentacenes were synthesized from cis‐ and trans‐quinacridone using protection, alkynylation and deoxygenation. The solid‐state packing of the targets is determined by choice and position of the silylethynyl substituents. The position of the substituents and n...

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Autores principales: Wiesner, Thomas, Ahrens, Lukas, Rominger, Frank, Freudenberg, Jan, Bunz, Uwe H. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986698/
https://www.ncbi.nlm.nih.gov/pubmed/33289942
http://dx.doi.org/10.1002/chem.202004761
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author Wiesner, Thomas
Ahrens, Lukas
Rominger, Frank
Freudenberg, Jan
Bunz, Uwe H. F.
author_facet Wiesner, Thomas
Ahrens, Lukas
Rominger, Frank
Freudenberg, Jan
Bunz, Uwe H. F.
author_sort Wiesner, Thomas
collection PubMed
description Bis(silylethynylated) 5,7‐ and 5,12‐diazapentacenes were synthesized from cis‐ and trans‐quinacridone using protection, alkynylation and deoxygenation. The solid‐state packing of the targets is determined by choice and position of the silylethynyl substituents. The position of the substituents and nitrogen atoms influence the optical properties of the targets.
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spelling pubmed-79866982021-03-25 Diazapentacenes from Quinacridones Wiesner, Thomas Ahrens, Lukas Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. Chemistry Communications Bis(silylethynylated) 5,7‐ and 5,12‐diazapentacenes were synthesized from cis‐ and trans‐quinacridone using protection, alkynylation and deoxygenation. The solid‐state packing of the targets is determined by choice and position of the silylethynyl substituents. The position of the substituents and nitrogen atoms influence the optical properties of the targets. John Wiley and Sons Inc. 2021-02-17 2021-03-08 /pmc/articles/PMC7986698/ /pubmed/33289942 http://dx.doi.org/10.1002/chem.202004761 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://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
Wiesner, Thomas
Ahrens, Lukas
Rominger, Frank
Freudenberg, Jan
Bunz, Uwe H. F.
Diazapentacenes from Quinacridones
title Diazapentacenes from Quinacridones
title_full Diazapentacenes from Quinacridones
title_fullStr Diazapentacenes from Quinacridones
title_full_unstemmed Diazapentacenes from Quinacridones
title_short Diazapentacenes from Quinacridones
title_sort diazapentacenes from quinacridones
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986698/
https://www.ncbi.nlm.nih.gov/pubmed/33289942
http://dx.doi.org/10.1002/chem.202004761
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AT bunzuwehf diazapentacenesfromquinacridones

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