Journal of Materials Chemistry · 2006 · 59 citations · 32 references
Natural SciencesChemistryMaterials ScienceMaterials ChemistryOrganic ChemistryPolymer ChemistryConducting PolymersConductive PolymersElectrochromic MaterialsOrganic Electronic MaterialsOrganic SemiconductorsPolymer CharacterizationConjugated PolymersElectrochromic DevicesOrganic Electrochromic MaterialsPolymer Electrochromic MaterialsPolythiopheneQuinoxaline ChemistryReduction ProcessesVoltammetry
The synthesis and electropolymerisation of a new terthiophene, 1,3-di-2-thienylthieno[3′,4′:5,6][1,4]dithiino[2,3-b]quinoxaline, is reported. The compound bears a quinoxaline unit fused to the central thiophene ring via a 1,4-dithiin ring; the latter unit ensures a non-planar structure for the molecule. The corresponding polymer, prepared electrochemically, has been characterized by cyclic voltammetry and UV-vis-NIR spectroelectrochemistry. The material is oxidised within the conjugated chain, but the reduction processes are complex and arise from both the polythiophene and the independent quinoxaline units. The polymer has two distinct colour states—orange in the neutral form and green–blue in the oxidised state. Electrochromic studies on poly(1,3-di-2-thienylthieno[3′,4′:5,6][1,4]dithiino[2,3-b]quinoxaline) reveal fast switching speeds that are superior to those of poly(3,4-ethylenedioxythiophene) (PEDOT) and a colouration efficiency of 381 cm2 C−1 at 650 nm.
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van der Waals Volumes and Radii
A. Bondì · The Journal of Physical Chemistry · 1964 · 19.2K citations
Poly(3,4-ethylenedioxythiophene) and Its Derivatives: Past, Present, and Future
L. Groenendaal, F. Jonas, D. Freitag et al. · Advanced Materials · 2000 · 3.3K citations