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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...

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Autores principales: Maier, Steffen, Hippchen, Nikolai, Rominger, Frank, Freudenberg, Jan, Bunz, Uwe H. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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