N‐Acenoacenes: Synthesis and Solid‐State Properties

Four N‐acenoacenes were synthesized and analyzed for their optoelectronic properties and solid‐state packings. Two of the regioisomeric acridinoacridines are TIPS‐ethynylated, whereas the other pair are Boc‐ and triflate substituted derivatives. The two TIPS‐ethynyldiazaacenoacenes were processed in...

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Autores principales: Wiesner, Thomas, Pardon, Marcel, Maier, Steffen, Rominger, Frank, Freudenberg, Jan, Bunz, Uwe H. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091707/
https://www.ncbi.nlm.nih.gov/pubmed/35947374
http://dx.doi.org/10.1002/chem.202201916
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author Wiesner, Thomas
Pardon, Marcel
Maier, Steffen
Rominger, Frank
Freudenberg, Jan
Bunz, Uwe H. F.
author_facet Wiesner, Thomas
Pardon, Marcel
Maier, Steffen
Rominger, Frank
Freudenberg, Jan
Bunz, Uwe H. F.
author_sort Wiesner, Thomas
collection PubMed
description Four N‐acenoacenes were synthesized and analyzed for their optoelectronic properties and solid‐state packings. Two of the regioisomeric acridinoacridines are TIPS‐ethynylated, whereas the other pair are Boc‐ and triflate substituted derivatives. The two TIPS‐ethynyldiazaacenoacenes were processed into organic thin‐film transistors with saturation hole mobilities reaching 2.9×10(−2) cm(2)(Vs)(−1).
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spelling pubmed-100917072023-04-13 N‐Acenoacenes: Synthesis and Solid‐State Properties Wiesner, Thomas Pardon, Marcel Maier, Steffen Rominger, Frank Freudenberg, Jan Bunz, Uwe H. F. Chemistry Research Articles Four N‐acenoacenes were synthesized and analyzed for their optoelectronic properties and solid‐state packings. Two of the regioisomeric acridinoacridines are TIPS‐ethynylated, whereas the other pair are Boc‐ and triflate substituted derivatives. The two TIPS‐ethynyldiazaacenoacenes were processed into organic thin‐film transistors with saturation hole mobilities reaching 2.9×10(−2) cm(2)(Vs)(−1). John Wiley and Sons Inc. 2022-10-25 2022-12-09 /pmc/articles/PMC10091707/ /pubmed/35947374 http://dx.doi.org/10.1002/chem.202201916 Text en © 2022 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 Research Articles
Wiesner, Thomas
Pardon, Marcel
Maier, Steffen
Rominger, Frank
Freudenberg, Jan
Bunz, Uwe H. F.
N‐Acenoacenes: Synthesis and Solid‐State Properties
title N‐Acenoacenes: Synthesis and Solid‐State Properties
title_full N‐Acenoacenes: Synthesis and Solid‐State Properties
title_fullStr N‐Acenoacenes: Synthesis and Solid‐State Properties
title_full_unstemmed N‐Acenoacenes: Synthesis and Solid‐State Properties
title_short N‐Acenoacenes: Synthesis and Solid‐State Properties
title_sort n‐acenoacenes: synthesis and solid‐state properties
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091707/
https://www.ncbi.nlm.nih.gov/pubmed/35947374
http://dx.doi.org/10.1002/chem.202201916
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