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Thiazole fused S,N-heteroacene step-ladder polymeric semiconductors for organic transistors
Ladder-type thiazole-fused S,N-heteroacenes with an extended π-conjugation consisting of six (SN6-Tz) and nine (SN9-Tz) fused aromatic rings have been synthesized and fully characterized. To date, the synthesis of well-defined fused building blocks and polymers of π-conjugated organic compounds base...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600222/ https://www.ncbi.nlm.nih.gov/pubmed/36349116 http://dx.doi.org/10.1039/d2sc04661j |
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author | Attar, Salahuddin Yang, Rui Chen, Zhihui Ji, Xiaozhou Comí, Marc Banerjee, Sarbajit Fang, Lei Liu, Yao Al-Hashimi, Mohammed |
author_facet | Attar, Salahuddin Yang, Rui Chen, Zhihui Ji, Xiaozhou Comí, Marc Banerjee, Sarbajit Fang, Lei Liu, Yao Al-Hashimi, Mohammed |
author_sort | Attar, Salahuddin |
collection | PubMed |
description | Ladder-type thiazole-fused S,N-heteroacenes with an extended π-conjugation consisting of six (SN6-Tz) and nine (SN9-Tz) fused aromatic rings have been synthesized and fully characterized. To date, the synthesis of well-defined fused building blocks and polymers of π-conjugated organic compounds based on the thiazole moiety is a considerable synthetic challenge, due to the difficulty in their synthesis. Acceptor–donor building blocks M1 and M2 were successfully polymerized into ladder homopolymers P1–P2 and further copolymerized with a diketopyrrolopyrrole unit to afford step-ladder copolymer P3. The optical, electronic, and thermal properties, in addition to their charge transport behavior in organic thin-film transistors (OTFTs), were investigated. The results showed an interesting effect on the molecular arrangement of the thiazole-based ladder-type heteroacene in the crystal structure revealing skewed π–π-stacking, and expected to possess better p-type semiconducting performance. The polymers all possess good molecular weights and excellent thermal properties. All the polymer-based OTFT devices exhibit annealing temperature dependent performance, and among the polymers P3 exhibits the highest mobility of 0.05 cm(2) V(−1) s(−1). |
format | Online Article Text |
id | pubmed-9600222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-96002222022-11-07 Thiazole fused S,N-heteroacene step-ladder polymeric semiconductors for organic transistors Attar, Salahuddin Yang, Rui Chen, Zhihui Ji, Xiaozhou Comí, Marc Banerjee, Sarbajit Fang, Lei Liu, Yao Al-Hashimi, Mohammed Chem Sci Chemistry Ladder-type thiazole-fused S,N-heteroacenes with an extended π-conjugation consisting of six (SN6-Tz) and nine (SN9-Tz) fused aromatic rings have been synthesized and fully characterized. To date, the synthesis of well-defined fused building blocks and polymers of π-conjugated organic compounds based on the thiazole moiety is a considerable synthetic challenge, due to the difficulty in their synthesis. Acceptor–donor building blocks M1 and M2 were successfully polymerized into ladder homopolymers P1–P2 and further copolymerized with a diketopyrrolopyrrole unit to afford step-ladder copolymer P3. The optical, electronic, and thermal properties, in addition to their charge transport behavior in organic thin-film transistors (OTFTs), were investigated. The results showed an interesting effect on the molecular arrangement of the thiazole-based ladder-type heteroacene in the crystal structure revealing skewed π–π-stacking, and expected to possess better p-type semiconducting performance. The polymers all possess good molecular weights and excellent thermal properties. All the polymer-based OTFT devices exhibit annealing temperature dependent performance, and among the polymers P3 exhibits the highest mobility of 0.05 cm(2) V(−1) s(−1). The Royal Society of Chemistry 2022-09-26 /pmc/articles/PMC9600222/ /pubmed/36349116 http://dx.doi.org/10.1039/d2sc04661j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Attar, Salahuddin Yang, Rui Chen, Zhihui Ji, Xiaozhou Comí, Marc Banerjee, Sarbajit Fang, Lei Liu, Yao Al-Hashimi, Mohammed Thiazole fused S,N-heteroacene step-ladder polymeric semiconductors for organic transistors |
title | Thiazole fused S,N-heteroacene step-ladder polymeric semiconductors for organic transistors |
title_full | Thiazole fused S,N-heteroacene step-ladder polymeric semiconductors for organic transistors |
title_fullStr | Thiazole fused S,N-heteroacene step-ladder polymeric semiconductors for organic transistors |
title_full_unstemmed | Thiazole fused S,N-heteroacene step-ladder polymeric semiconductors for organic transistors |
title_short | Thiazole fused S,N-heteroacene step-ladder polymeric semiconductors for organic transistors |
title_sort | thiazole fused s,n-heteroacene step-ladder polymeric semiconductors for organic transistors |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600222/ https://www.ncbi.nlm.nih.gov/pubmed/36349116 http://dx.doi.org/10.1039/d2sc04661j |
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