Issue 48, 2018

N-Cyanoimine as an electron-withdrawing functional group for organic semiconductors: example of dihydroindacenodithiophene positional isomers

Abstract

Manipulating frontier molecular orbitals by chemical design is one of the chief aspects of organic electronics. For applications in the field of n-type organic field-effect transistors (OFET), depressing the LUMO energy level is particularly important to ensure efficient charge injection. In this work, we report the incorporation of electron-withdrawing cyanoimine functional groups on the bridges of dihydroindacenodithiophene regioisomers. Cyanoimines are barely known in the field of organic electronics but herein have been found to be highly efficient in depressing the LUMO energy level of an organic semiconductor and can thus be envisaged as an attractive alternative to widely known electron-withdrawing units such as dicyanovinylene. This work focuses on a detailed structure–property relationship study, including the incorporation in n-type OFETs, of two dihydroindacenodithiophene regioisomers bearing two cyanoimine groups either in a syn- or an anti-configuration. As far as we know, this work is only the second example reported to date on N-cyanoimines incorporated in n-type OFETs, and shows the potential of these functional groups in organic electronics.

Graphical abstract: N-Cyanoimine as an electron-withdrawing functional group for organic semiconductors: example of dihydroindacenodithiophene positional isomers

Supplementary files

Article information

Article type
Paper
Submitted
28 Leq 2018
Accepted
11 Dit 2018
First published
15 Dit 2018

J. Mater. Chem. C, 2018,6, 13197-13210

N-Cyanoimine as an electron-withdrawing functional group for organic semiconductors: example of dihydroindacenodithiophene positional isomers

J. Peltier, B. Heinrich, B. Donnio, O. Jeannin, J. Rault-Berthelot, E. Jacques and C. Poriel, J. Mater. Chem. C, 2018, 6, 13197 DOI: 10.1039/C8TC04313B

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