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Fluorine-substituted quinoidal thiophene with a F–H hydrogen bond locked conformation for high-performance n-channel organic transistors

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Abstract

The novel dicyanomethylene-substituted 1,2-bis(thieno[3,2-b]thiophene-2-yl)ethene based quinoidal compounds QBTTE and F2-QBTTE are reported. The F⋯H (vinylene) hydrogen bonds lock the backbone conformation and greatly improve the transistor performance of F2-QBTTE.

Graphical abstract: Fluorine-substituted quinoidal thiophene with a F–H hydrogen bond locked conformation for high-performance n-channel organic transistors

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Publication details

The article was received on 13 Apr 2019, accepted on 07 May 2019 and first published on 07 May 2019


Article type: Communication
DOI: 10.1039/C9CC02872B
Chem. Commun., 2019, Advance Article

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    Fluorine-substituted quinoidal thiophene with a F–H hydrogen bond locked conformation for high-performance n-channel organic transistors

    D. Wang, X. Qiao, G. Ouyang, H. Wu and H. Li, Chem. Commun., 2019, Advance Article , DOI: 10.1039/C9CC02872B

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