1998
DOI: 10.1016/s0022-0728(97)00548-2
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Electrochemical behaviour of 3, 4-ethylenedioxythiophene functionalized by a sulphonate group. Application to the preparation of poly(3, 4-ethylenedioxythiophene) having permanent cation-exchange properties

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Cited by 109 publications
(85 citation statements)
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“…Failure to purify the monomer leads to inferior materials properties. The alcoholic precursor, 2,3-dihydrothieno[3,4-b] [1,4]dioxin-2-yl methanol (EDOT±CH 2 OH), was synthesized according to Stephan et al [37]. It should be noted that this procedure leads to a mixture of approximately 90 % six-membered (EDOT±CH 2 OH) and 10 % seven-membered ring isomers (ProDOT), as verified through gas chromatography.…”
Section: Methodsmentioning
confidence: 99%
“…Failure to purify the monomer leads to inferior materials properties. The alcoholic precursor, 2,3-dihydrothieno[3,4-b] [1,4]dioxin-2-yl methanol (EDOT±CH 2 OH), was synthesized according to Stephan et al [37]. It should be noted that this procedure leads to a mixture of approximately 90 % six-membered (EDOT±CH 2 OH) and 10 % seven-membered ring isomers (ProDOT), as verified through gas chromatography.…”
Section: Methodsmentioning
confidence: 99%
“…Water-soluble PEDOT has been synthesized by adding an alkoxysulphonate functionality to the EDOT monomer, [50,51] resulting in the derivative poly(4-(2,3-…”
Section: Pedot-smentioning
confidence: 99%
“…16 Compound 7 was synthesized so that it could be functionalized through the hydroxy-group and used as the monomer unit in the polymer fabrication. Methanol-EDOT is a derivative of 3,4-ethylenedioxythiophene (EDOT), and as such, the polymer of this monomer is a high stability conducting polymer.…”
Section: Initial Synthesismentioning
confidence: 99%