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Triptycene End‐Capped Benzothienobenzothiophene and Naphthothienobenzothiophene
Previously it was demonstrated that triptycene end‐capping can be used as a crystal engineering strategy to direct the packing of quinoxalinophenanthrophenazines (QPPs) towards cofacially stacked π dimers with large molecular overlap resulting in high charge transfer integrals. Remarkably, this pack...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589444/ https://www.ncbi.nlm.nih.gov/pubmed/32368815 http://dx.doi.org/10.1002/chem.202001125 |
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author | Ueberricke, Lucas Schwarz, Julia Ghalami, Farhad Matthiesen, Maik Rominger, Frank Elbert, Sven M. Zaumseil, Jana Elstner, Marcus Mastalerz, Michael |
author_facet | Ueberricke, Lucas Schwarz, Julia Ghalami, Farhad Matthiesen, Maik Rominger, Frank Elbert, Sven M. Zaumseil, Jana Elstner, Marcus Mastalerz, Michael |
author_sort | Ueberricke, Lucas |
collection | PubMed |
description | Previously it was demonstrated that triptycene end‐capping can be used as a crystal engineering strategy to direct the packing of quinoxalinophenanthrophenazines (QPPs) towards cofacially stacked π dimers with large molecular overlap resulting in high charge transfer integrals. Remarkably, this packing motif was formed under different crystallization conditions and with a variety of derivatives bearing additional functional groups or aromatic substituents. Benzothienobenzothiophene (BTBT) and its derivatives are known as some of the best performing compounds for organic field‐effect transistors. Here, the triptycene end‐capping concept is introduced to this class of compounds and polymorphic crystal structures are investigated to evaluate the potential of triptycene end‐caps as synthons for crystal engineering. |
format | Online Article Text |
id | pubmed-7589444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75894442020-10-30 Triptycene End‐Capped Benzothienobenzothiophene and Naphthothienobenzothiophene Ueberricke, Lucas Schwarz, Julia Ghalami, Farhad Matthiesen, Maik Rominger, Frank Elbert, Sven M. Zaumseil, Jana Elstner, Marcus Mastalerz, Michael Chemistry Full Papers Previously it was demonstrated that triptycene end‐capping can be used as a crystal engineering strategy to direct the packing of quinoxalinophenanthrophenazines (QPPs) towards cofacially stacked π dimers with large molecular overlap resulting in high charge transfer integrals. Remarkably, this packing motif was formed under different crystallization conditions and with a variety of derivatives bearing additional functional groups or aromatic substituents. Benzothienobenzothiophene (BTBT) and its derivatives are known as some of the best performing compounds for organic field‐effect transistors. Here, the triptycene end‐capping concept is introduced to this class of compounds and polymorphic crystal structures are investigated to evaluate the potential of triptycene end‐caps as synthons for crystal engineering. John Wiley and Sons Inc. 2020-09-11 2020-10-01 /pmc/articles/PMC7589444/ /pubmed/32368815 http://dx.doi.org/10.1002/chem.202001125 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 | Full Papers Ueberricke, Lucas Schwarz, Julia Ghalami, Farhad Matthiesen, Maik Rominger, Frank Elbert, Sven M. Zaumseil, Jana Elstner, Marcus Mastalerz, Michael Triptycene End‐Capped Benzothienobenzothiophene and Naphthothienobenzothiophene |
title | Triptycene End‐Capped Benzothienobenzothiophene and Naphthothienobenzothiophene |
title_full | Triptycene End‐Capped Benzothienobenzothiophene and Naphthothienobenzothiophene |
title_fullStr | Triptycene End‐Capped Benzothienobenzothiophene and Naphthothienobenzothiophene |
title_full_unstemmed | Triptycene End‐Capped Benzothienobenzothiophene and Naphthothienobenzothiophene |
title_short | Triptycene End‐Capped Benzothienobenzothiophene and Naphthothienobenzothiophene |
title_sort | triptycene end‐capped benzothienobenzothiophene and naphthothienobenzothiophene |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589444/ https://www.ncbi.nlm.nih.gov/pubmed/32368815 http://dx.doi.org/10.1002/chem.202001125 |
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