What is it about?
The length of the conjugated chain and the type and number of substituents were controlled for several types of oligothiophenes. These controls dramatically changed the optical, electrochemical, and electrical properties of the oligothiophenes. Applications to field-effect transistors and smart windows were also investigated.
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Why is it important?
Poly(3,4-ethylenedioxythiophene) (PEDOT), whose monomer unit is a thiophene ring bearing an ethylenedioxy group in the side chain (3,4-ethylenedioxythiophene, EDOT), has been widely used in organic electronic devices in recent years because of its excellent charge transport properties. However, the degree of polymerization of PEDOT obtained by oxidative polymerization is not controlled, and it is known that the degree of polymerization is in the range of 6-13mers. In this study, we synthesized several types of EDOT-containing oligothiophenes (3, 6, 7, 9, and 11mers), which are composed solely of EDOT. Oligothiophenes composed only of EDOT are chemically unstable (easily oxidized by air) and have poor solubility, but the oligothiophenes synthesized in this study partially contain EDOT, which solves these problems. The introduction of a partial EDOT unit into the oligothiophene also resulted in a significant red shift in the absorption wavelength region and a negative shift in the oxidation potential compared to the EDOT-free oligothiophene. They also found that the material can be applied as a field-effect transistor and smart window.
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This page is a summary of: Synthesis and electrical properties of novel oligothiophenes partially containing 3,4-ethylenedioxythiophenes, RSC Advances, January 2014, Royal Society of Chemistry,
DOI: 10.1039/c3ra44129f.
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