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Peralkynylated Tetraazaacene Derivatives
The synthesis of a decaethynylated tetraazapentacene is described. It was obtained by a combination of condensation reactions giving the two pyrazine rings and subsequent consecutive Stille‐type couplings. This is the first example of any higher (hetero)acene that is peralkynylated. The presence of...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028064/ https://www.ncbi.nlm.nih.gov/pubmed/31609484 http://dx.doi.org/10.1002/chem.201904087 |
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author | Reiss, Hilmar Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. |
author_facet | Reiss, Hilmar Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. |
author_sort | Reiss, Hilmar |
collection | PubMed |
description | The synthesis of a decaethynylated tetraazapentacene is described. It was obtained by a combination of condensation reactions giving the two pyrazine rings and subsequent consecutive Stille‐type couplings. This is the first example of any higher (hetero)acene that is peralkynylated. The presence of the four nitrogen atoms removes the peri interaction of the substituted alkyne groups, giving this rock‐stable and highly twisted heteroacene. |
format | Online Article Text |
id | pubmed-7028064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70280642020-02-25 Peralkynylated Tetraazaacene Derivatives Reiss, Hilmar Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. Chemistry Communications The synthesis of a decaethynylated tetraazapentacene is described. It was obtained by a combination of condensation reactions giving the two pyrazine rings and subsequent consecutive Stille‐type couplings. This is the first example of any higher (hetero)acene that is peralkynylated. The presence of the four nitrogen atoms removes the peri interaction of the substituted alkyne groups, giving this rock‐stable and highly twisted heteroacene. John Wiley and Sons Inc. 2019-12-16 2020-01-22 /pmc/articles/PMC7028064/ /pubmed/31609484 http://dx.doi.org/10.1002/chem.201904087 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Reiss, Hilmar Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. Peralkynylated Tetraazaacene Derivatives |
title | Peralkynylated Tetraazaacene Derivatives |
title_full | Peralkynylated Tetraazaacene Derivatives |
title_fullStr | Peralkynylated Tetraazaacene Derivatives |
title_full_unstemmed | Peralkynylated Tetraazaacene Derivatives |
title_short | Peralkynylated Tetraazaacene Derivatives |
title_sort | peralkynylated tetraazaacene derivatives |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7028064/ https://www.ncbi.nlm.nih.gov/pubmed/31609484 http://dx.doi.org/10.1002/chem.201904087 |
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