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2,7,11,16‐Tetra‐tert‐Butyl Tetraindenopyrene Revisited by an “Inverse” Synthetic Approach

A new synthetic route to tetraindenopyrene (TIP)—a bowl‐shaped cut‐out structure of C(70)—is reported. The key step in this approach is a fourfold palladium‐catalyzed C−H activation that increases the yield more than 50 times in comparison to the approach originally described by Scott and co‐workers...

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Autores principales: Elbert, Sven M., Haidisch, Anika, Kirschbaum, Tobias, Rominger, Frank, Zschieschang, Ute, Klauk, Hagen, Mastalerz, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496754/
https://www.ncbi.nlm.nih.gov/pubmed/32314830
http://dx.doi.org/10.1002/chem.202001555
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author Elbert, Sven M.
Haidisch, Anika
Kirschbaum, Tobias
Rominger, Frank
Zschieschang, Ute
Klauk, Hagen
Mastalerz, Michael
author_facet Elbert, Sven M.
Haidisch, Anika
Kirschbaum, Tobias
Rominger, Frank
Zschieschang, Ute
Klauk, Hagen
Mastalerz, Michael
author_sort Elbert, Sven M.
collection PubMed
description A new synthetic route to tetraindenopyrene (TIP)—a bowl‐shaped cut‐out structure of C(70)—is reported. The key step in this approach is a fourfold palladium‐catalyzed C−H activation that increases the yield more than 50 times in comparison to the approach originally described by Scott and co‐workers. Besides examination of its optoelectronic properties and study of its aggregation in solution, TIP was also re‐investigated by dispersion‐corrected DFT methods, which showed that dispersion interactions significantly increase the bowl‐to‐bowl inversion barrier. Furthermore, TIP was used as a semiconductor in p‐channel thin‐film transistors (TFTs).
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spelling pubmed-74967542020-09-25 2,7,11,16‐Tetra‐tert‐Butyl Tetraindenopyrene Revisited by an “Inverse” Synthetic Approach Elbert, Sven M. Haidisch, Anika Kirschbaum, Tobias Rominger, Frank Zschieschang, Ute Klauk, Hagen Mastalerz, Michael Chemistry Full Papers A new synthetic route to tetraindenopyrene (TIP)—a bowl‐shaped cut‐out structure of C(70)—is reported. The key step in this approach is a fourfold palladium‐catalyzed C−H activation that increases the yield more than 50 times in comparison to the approach originally described by Scott and co‐workers. Besides examination of its optoelectronic properties and study of its aggregation in solution, TIP was also re‐investigated by dispersion‐corrected DFT methods, which showed that dispersion interactions significantly increase the bowl‐to‐bowl inversion barrier. Furthermore, TIP was used as a semiconductor in p‐channel thin‐film transistors (TFTs). John Wiley and Sons Inc. 2020-07-20 2020-08-17 /pmc/articles/PMC7496754/ /pubmed/32314830 http://dx.doi.org/10.1002/chem.202001555 Text en © 2020 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-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
Elbert, Sven M.
Haidisch, Anika
Kirschbaum, Tobias
Rominger, Frank
Zschieschang, Ute
Klauk, Hagen
Mastalerz, Michael
2,7,11,16‐Tetra‐tert‐Butyl Tetraindenopyrene Revisited by an “Inverse” Synthetic Approach
title 2,7,11,16‐Tetra‐tert‐Butyl Tetraindenopyrene Revisited by an “Inverse” Synthetic Approach
title_full 2,7,11,16‐Tetra‐tert‐Butyl Tetraindenopyrene Revisited by an “Inverse” Synthetic Approach
title_fullStr 2,7,11,16‐Tetra‐tert‐Butyl Tetraindenopyrene Revisited by an “Inverse” Synthetic Approach
title_full_unstemmed 2,7,11,16‐Tetra‐tert‐Butyl Tetraindenopyrene Revisited by an “Inverse” Synthetic Approach
title_short 2,7,11,16‐Tetra‐tert‐Butyl Tetraindenopyrene Revisited by an “Inverse” Synthetic Approach
title_sort 2,7,11,16‐tetra‐tert‐butyl tetraindenopyrene revisited by an “inverse” synthetic approach
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496754/
https://www.ncbi.nlm.nih.gov/pubmed/32314830
http://dx.doi.org/10.1002/chem.202001555
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