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Cyclodimers and Cyclotrimers of 2,3 ‐Bisalkynylated Anthracenes, Phenazines and Diazatetracenes
The synthesis of novel (N−)acene‐based cyclooligomers is reported. Glaser‐Hay coupling of the bisethynylated monomers results in cyclodimers and cyclotrimers that are separable by column and gel‐permeation chromatographies. For the diazatetracene, the use of sec‐butyl‐silylethynyl groups is necessar...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297893/ https://www.ncbi.nlm.nih.gov/pubmed/34612544 http://dx.doi.org/10.1002/chem.202103193 |
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author | Maier, Steffen Hippchen, Nikolai Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. |
author_facet | Maier, Steffen Hippchen, Nikolai Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. |
author_sort | Maier, Steffen |
collection | PubMed |
description | The synthesis of novel (N−)acene‐based cyclooligomers is reported. Glaser‐Hay coupling of the bisethynylated monomers results in cyclodimers and cyclotrimers that are separable by column and gel‐permeation chromatographies. For the diazatetracene, the use of sec‐butyl‐silylethynyl groups is necessary to achieve solubility. Diazatetracene‐based cyclodimers and cyclotrimers were used as semiconductors in thin‐film transistors. Although their optoelectronic properties are quite similar, their electron mobilities in proof‐of‐concept thin‐film transistors differ by an order of magnitude. |
format | Online Article Text |
id | pubmed-9297893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92978932022-07-21 Cyclodimers and Cyclotrimers of 2,3 ‐Bisalkynylated Anthracenes, Phenazines and Diazatetracenes Maier, Steffen Hippchen, Nikolai Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. Chemistry Communications The synthesis of novel (N−)acene‐based cyclooligomers is reported. Glaser‐Hay coupling of the bisethynylated monomers results in cyclodimers and cyclotrimers that are separable by column and gel‐permeation chromatographies. For the diazatetracene, the use of sec‐butyl‐silylethynyl groups is necessary to achieve solubility. Diazatetracene‐based cyclodimers and cyclotrimers were used as semiconductors in thin‐film transistors. Although their optoelectronic properties are quite similar, their electron mobilities in proof‐of‐concept thin‐film transistors differ by an order of magnitude. John Wiley and Sons Inc. 2021-11-05 2021-11-25 /pmc/articles/PMC9297893/ /pubmed/34612544 http://dx.doi.org/10.1002/chem.202103193 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Maier, Steffen Hippchen, Nikolai Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. Cyclodimers and Cyclotrimers of 2,3 ‐Bisalkynylated Anthracenes, Phenazines and Diazatetracenes |
title | Cyclodimers and Cyclotrimers of 2,3 ‐Bisalkynylated Anthracenes, Phenazines and Diazatetracenes |
title_full | Cyclodimers and Cyclotrimers of 2,3 ‐Bisalkynylated Anthracenes, Phenazines and Diazatetracenes |
title_fullStr | Cyclodimers and Cyclotrimers of 2,3 ‐Bisalkynylated Anthracenes, Phenazines and Diazatetracenes |
title_full_unstemmed | Cyclodimers and Cyclotrimers of 2,3 ‐Bisalkynylated Anthracenes, Phenazines and Diazatetracenes |
title_short | Cyclodimers and Cyclotrimers of 2,3 ‐Bisalkynylated Anthracenes, Phenazines and Diazatetracenes |
title_sort | cyclodimers and cyclotrimers of 2,3 ‐bisalkynylated anthracenes, phenazines and diazatetracenes |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297893/ https://www.ncbi.nlm.nih.gov/pubmed/34612544 http://dx.doi.org/10.1002/chem.202103193 |
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