Design, synthesis, chemical stability, packing, cyclic voltammetry, ionisation potential, and charge transport of [1]benzothieno[3,2-: B] [1]benzothiophene derivatives

Christian Ruzié, Jolanta Karpinska, Anne Laurent, Lionel Sanguinet, Simon Hunter, Thomas Anthopoulos, Vincent Lemaur, Jérôme Cornil, Alan R. Kennedy, Oliver Fenwick, Paolo Samorì, Guillaume Schweicher, Basab Chattopadhyay, Yves Henri Geerts*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Five new molecular semiconductors that differ from dioctylbenzothienobenzothiophene, by the introduction of ether or thioether side chains, have been synthesized and obtained in good yields. Their availability in sufficient quantities has allowed investigation of their electrochemical behaviour in solution and their electronic properties in solid state. Both ether and thioether compounds oxidise rather easily in solution, but nevertheless, they exhibit rather high ionisation potentials. This is a consequence of their crystal structure. Dioctylthioetherbenzothienobenzothiophene is rather sensitive to oxidation and degrades easily in close to ambient conditions. Dioctyletherbenzothienobenzothiophene is more stable. Its charge carrier mobility remains however rather moderate, on the order of 0.5 cm2 V-1 s-1, whereas that of dioctylbenzothienobenzothiophene reached 4 cm2 V-1 s-1, in the same conditions. The difference is explained by intrinsic factors as shown by a theoretical modelling.

Original languageEnglish (US)
Pages (from-to)4863-4879
Number of pages17
JournalJournal of Materials Chemistry C
Volume4
Issue number22
DOIs
StatePublished - Jan 1 2016

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Chemistry

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