Cruciform Thiophene-based Molecules as Organic Semiconductors for Field Effect Transistor Applications

  • Choi, Dong-Hoon (Department of Chemistry, Center for Electro- & Photo-responsive Molecules, Korea University) ;
  • Kim, Dae-Chul (Department of Chemistry, Center for Electro- & Photo-responsive Molecules, Korea University) ;
  • Kim, Kyung-Hwan (Department of Chemistry, Center for Electro- & Photo-responsive Molecules, Korea University) ;
  • Cho, Min-Ju (Department of Chemistry, Center for Electro- & Photo-responsive Molecules, Korea University) ;
  • Jin, Jung-Il (Department of Chemistry, Center for Electro- & Photo-responsive Molecules, Korea University)
  • Published : 2007.08.27

Abstract

Cruciform conjugated molecule, 4(DP3T)-benzene bearing terthiophene moieties has been synthesized through Horner-Emmons Reaction using 5-dodecyl-5"-aldehyde-[2,2';5',2"] terthiophene as dendrons and octaethyl benzene- 1,2,4,5-tetrayltetrakis(methylene)tetraphosphonate as the core unit; this molecule has been fully characterized. The terthiophene-based molecule exhibits good solubility in common organic solvents and good self-film forming property. They are intrinsically crystalline as they exhibit well-defined X-ray diffraction patterns from uniform orientations of molecules. Thus, intermolecular interaction can be enhanced to affect the carrier transport phenomena after annealing at $148^{\circ}C$. The semiconducting property of 4(DP3T)-benzene have been evaluated in organic field-effect transistors. 4(DP3T)-benzene exhibit carrier mobility as high as $(6.6{\pm}0.5)$ ${\times}$ $10^{-6}cm^2V^{-1}s^{-1}$.

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