Tetracene dicarboxylic imide and its disulfide: synthesis of ambipolar organic semiconductors for organic photovoltaic cells

Chem Asian J. 2012 Jan 2;7(1):105-11. doi: 10.1002/asia.201100590. Epub 2011 Oct 26.

Abstract

We have designed and synthesized a new donor/acceptor-type tetracene derivative by the introduction of dicarboxylic imide and disulfide groups as electron-withdrawing and -donating units, respectively. The prepared compounds, tetracene dicarboxylic imide (TI) and its disulfide (TIDS) have high chemical and electrochemical stability as well as long-wavelength absorptions of up to 886 nm in the thin films. The crystal packing structure of TIDS molecules features face-to-face π-stacking, derived from dipole-dipole interactions. Notably, TIDS exhibited ambipolar properties of both electron-donating and -accepting natures in p-n and p-i-n heterojunction organic thin-film photovoltaic devices. Accordingly, TI and TIDS are expected to be promising compounds for designing new organic semiconductors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Disulfides / chemical synthesis
  • Disulfides / chemistry*
  • Electric Power Supplies*
  • Electrochemistry
  • Imides / chemical synthesis
  • Imides / chemistry*
  • Models, Molecular
  • Molecular Structure
  • Semiconductors

Substances

  • Disulfides
  • Imides