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Fluorination and chlorination effects on quinoxalineimides as an electron-deficient building block for n-channel organic semiconductors

The quinoxalineimide (QI) unit, containing the electron-withdrawing quinoxaline and imide groups, is an electron-deficient building block for organic semiconductor materials. In this study, three fluorinated or chlorinated QIs (QI-1F, QI-2F, and QI-2Cl), have been designed and developed. We report t...

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Autores principales: Hasegawa, Tsukasa, Ashizawa, Minoru, Kawauchi, Susumu, Masunaga, Hiroyasu, Ohta, Noboru, Matsumoto, Hidetoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062530/
https://www.ncbi.nlm.nih.gov/pubmed/35515293
http://dx.doi.org/10.1039/c9ra02413a
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author Hasegawa, Tsukasa
Ashizawa, Minoru
Kawauchi, Susumu
Masunaga, Hiroyasu
Ohta, Noboru
Matsumoto, Hidetoshi
author_facet Hasegawa, Tsukasa
Ashizawa, Minoru
Kawauchi, Susumu
Masunaga, Hiroyasu
Ohta, Noboru
Matsumoto, Hidetoshi
author_sort Hasegawa, Tsukasa
collection PubMed
description The quinoxalineimide (QI) unit, containing the electron-withdrawing quinoxaline and imide groups, is an electron-deficient building block for organic semiconductor materials. In this study, three fluorinated or chlorinated QIs (QI-1F, QI-2F, and QI-2Cl), have been designed and developed. We report the impact of the fluorination or chlorination of the QI unit on the electronic structures and charge carrier transport properties as compared to unsubstituted QI (QI-2H) bearing the same n-hexyl side chains. The frontier molecular orbital energy levels downshifted with the incorporation of fluorine or chlorine atoms onto the π-framework of QI. Single-crystal structure analyses revealed that all QI-based molecules have an entirely planar backbone and are packed into two-dimensional slipped stacks with diagonal electronic coupling that enables two-dimensional charge carrier transport. Notably, the doubly fluorinated or chlorinated QIs formed compact molecular packing in the single-crystal structures through an infinite intermolecular network relative to unsubstituted QI (QI-2H). The field-effect transistor-based QI molecules exhibited typical n-channel transport properties. As compared to unsubstituted QI (QI-2H), the chlorinated QI exhibited improved electron mobilities up to 7.1 × 10(−3) cm(2) V(−1) s(−1). The threshold voltages of the fluorinated or chlorinated QI devices were clearly smaller than that of QI-2H, which reflects the lowest unoccupied molecular orbital levels of the molecules. This study demonstrates that the fluorinated or chlorinated QIs are versatile building blocks in creating n-channel organic semiconductor materials.
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spelling pubmed-90625302022-05-04 Fluorination and chlorination effects on quinoxalineimides as an electron-deficient building block for n-channel organic semiconductors Hasegawa, Tsukasa Ashizawa, Minoru Kawauchi, Susumu Masunaga, Hiroyasu Ohta, Noboru Matsumoto, Hidetoshi RSC Adv Chemistry The quinoxalineimide (QI) unit, containing the electron-withdrawing quinoxaline and imide groups, is an electron-deficient building block for organic semiconductor materials. In this study, three fluorinated or chlorinated QIs (QI-1F, QI-2F, and QI-2Cl), have been designed and developed. We report the impact of the fluorination or chlorination of the QI unit on the electronic structures and charge carrier transport properties as compared to unsubstituted QI (QI-2H) bearing the same n-hexyl side chains. The frontier molecular orbital energy levels downshifted with the incorporation of fluorine or chlorine atoms onto the π-framework of QI. Single-crystal structure analyses revealed that all QI-based molecules have an entirely planar backbone and are packed into two-dimensional slipped stacks with diagonal electronic coupling that enables two-dimensional charge carrier transport. Notably, the doubly fluorinated or chlorinated QIs formed compact molecular packing in the single-crystal structures through an infinite intermolecular network relative to unsubstituted QI (QI-2H). The field-effect transistor-based QI molecules exhibited typical n-channel transport properties. As compared to unsubstituted QI (QI-2H), the chlorinated QI exhibited improved electron mobilities up to 7.1 × 10(−3) cm(2) V(−1) s(−1). The threshold voltages of the fluorinated or chlorinated QI devices were clearly smaller than that of QI-2H, which reflects the lowest unoccupied molecular orbital levels of the molecules. This study demonstrates that the fluorinated or chlorinated QIs are versatile building blocks in creating n-channel organic semiconductor materials. The Royal Society of Chemistry 2019-04-08 /pmc/articles/PMC9062530/ /pubmed/35515293 http://dx.doi.org/10.1039/c9ra02413a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Hasegawa, Tsukasa
Ashizawa, Minoru
Kawauchi, Susumu
Masunaga, Hiroyasu
Ohta, Noboru
Matsumoto, Hidetoshi
Fluorination and chlorination effects on quinoxalineimides as an electron-deficient building block for n-channel organic semiconductors
title Fluorination and chlorination effects on quinoxalineimides as an electron-deficient building block for n-channel organic semiconductors
title_full Fluorination and chlorination effects on quinoxalineimides as an electron-deficient building block for n-channel organic semiconductors
title_fullStr Fluorination and chlorination effects on quinoxalineimides as an electron-deficient building block for n-channel organic semiconductors
title_full_unstemmed Fluorination and chlorination effects on quinoxalineimides as an electron-deficient building block for n-channel organic semiconductors
title_short Fluorination and chlorination effects on quinoxalineimides as an electron-deficient building block for n-channel organic semiconductors
title_sort fluorination and chlorination effects on quinoxalineimides as an electron-deficient building block for n-channel organic semiconductors
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062530/
https://www.ncbi.nlm.nih.gov/pubmed/35515293
http://dx.doi.org/10.1039/c9ra02413a
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