Organic Thin Film Transistors from a Soluble Oligothiophene Derivative Containing Thermally Removable Solubilizing Groups
Journal of the American Chemical Society2004Vol. 126(6), pp. 1596–1597
Citations Over TimeTop 1% of 2004 papers
Abstract
A symmetrical alpha,omega-substituted sexithiophene derivative containing thermally removable branched ester solubilizing groups has been prepared. These oligomers can be solution cast into thin films and then thermolyzed to remove the solubilizing group, leaving short pendant alkene groups on the oligomer. Device testing of thin film transistors shows an increase in hole mobility from 1 x 10-5 cm2/(V s) with on/off ratios of approximately 100 before thermolysis to 5 x 10-2 cm2/(V s) with on/off ratios >105 after thermolysis. This method offers an attractive route to easily processed and highly performing thiophene oligomers.
Related Papers
- → Fundamental vibrations of thiophene and its deuterated derivatives(1965)181 cited
- → Synthesis of phenanthro[b]thiophenes(1980)76 cited
- → Angular polycyclic thiophenes containing two thiophene rings. Part II(1984)15 cited
- → Synthesis of benzo[4,5]phenaleno[1,9‐bc]thiophene and benzo[4,5]phenaleno[9,1–6c]thiophene(1982)23 cited
- → Naphthothiophenes and Other Thiophene Compounds Containing Two Carbocyclic Fused Rings(1954)