2012
DOI: 10.1016/j.electacta.2011.11.079
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Fast switching, high contrast multichromic polymers from alkyl-derivatized dithienylpyrrole and 3,4-ethylenedioxythiophene

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Cited by 43 publications
(25 citation statements)
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“…1,4-Di(2-thienyl)-1,4-butanedione and 3,3-diethyl-3,4-dihydro-2H-thieno [3,4-b] [1,4]dioxepine (ProDOT-Et 2 ) were prepared from previously published procedures [41,42]. Before electrochemical studies, all solutions were degassed with N 2 .…”
Section: Methodsmentioning
confidence: 99%
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“…1,4-Di(2-thienyl)-1,4-butanedione and 3,3-diethyl-3,4-dihydro-2H-thieno [3,4-b] [1,4]dioxepine (ProDOT-Et 2 ) were prepared from previously published procedures [41,42]. Before electrochemical studies, all solutions were degassed with N 2 .…”
Section: Methodsmentioning
confidence: 99%
“…The monomer 2,5-di(2-thienyl)pyrroles (SNS) consists of thiophene and pyrrole rings interconnected by their α-positions; the high reactivity of a pyrrole system creates the possibility of introducing a substituent into the β-position of the pyrrole ring even with the free α-positions of thiophene rings, making possible further modification to properties [27]. In recent years, a number of SNS derivatives have been synthesized with substituted branched alkyl [4], ferrocene [28], phenyl derivatives [29], aryl derivatives [30], and anthraquinone [31]. The oxidation potentials of SNS derivatives are quite low (about 0.7 V vs Ag/Ag + ) due to the conjugation of SNS in the aromatic system and the presence of electron donating atoms (S and N) in the main chain [32].…”
Section: Introductionmentioning
confidence: 99%
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“…One of the most important method of the synthesis of conducting polymers is electropolymerization. The products of polymerization reactions are deposited on various electrodes, such as metallic electrodes, steel electrodes [3,14], carbon fibers [15], glassy carbon [9] or ITO [6,[16][17][18]. A significant effect on the electrical properties, morphology and the electrode coverage have the electrode material, the solvent [19], and concentration of the electrolyte [20] used in the synthetic route.…”
Section: Introductionmentioning
confidence: 99%
“…However, the ECD does not have any absorption within the region of 600-800 nm. For practical applications, complementary ECDs, which are composed of an anodically coloring material and a cathodically coloring material [3,[29][30][31][32], are desired because of their capability of harnessing two EC materials' coloring ability without increasing the consumption of electrons. And recently, black-to-transmissive ECDs become a focused issue because they are promising to be applied in emerging commercial displays like e-papers [33,34].…”
Section: Introductionmentioning
confidence: 99%