Issue 44, 2019

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

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

Supplementary files

Article information

Article type
Communication
Submitted
13 Apr 2019
Accepted
07 May 2019
First published
07 May 2019

Chem. Commun., 2019,55, 6253-6256

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, 55, 6253 DOI: 10.1039/C9CC02872B

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