Synthesis and electropolymerisation of 3,4-ethylenedioxythiophene functionalised with alkoxy groups

A. Czardybon; M. Lapkowski

doi:10.1016/S0379-6779(00)01309-6

Synthesis and electropolymerisation of 3,4-ethylenedioxythiophene functionalised with alkoxy groups

A. Czardybon
, M. Lapkowski

Department of Physical Chemistry and Technology of Polymers (RCH/RCH4)

Silesian University of Technology
Polish Academy of Sciences

Research output: Contribution to journal › Article › peer-review

45 Citations (Scopus)

Abstract

We prepared 3,4-ethylenedioxythiophene (EDOT) functionalised with hydroxyl, hexyloxymethyl and dodecyloxymethyl groups. These monomers were polymerised and examined on account of their stability using cyclic voltammetry. Obtained polymers are stable in the range of potentials 0 - 1.8 V. PEDOT functionalised with a dodecyloxymethyl group was soluble in chloroform and benzene.

Original language	English
Pages (from-to)	161-162
Number of pages	2
Journal	Synthetic Metals
Volume	119
Issue number	1-3
DOIs	https://doi.org/10.1016/S0379-6779(00)01309-6
Publication status	Published - 15 Mar 2001

Keywords

Electrochemical methods
Electropolymerisation
Heterocycle synthesis
Solution processing

ASJC Scopus subject areas

Electronic, Optical and Magnetic Materials
Condensed Matter Physics
Mechanics of Materials
Mechanical Engineering
Metals and Alloys
Materials Chemistry

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10.1016/S0379-6779(00)01309-6

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abstract = "We prepared 3,4-ethylenedioxythiophene (EDOT) functionalised with hydroxyl, hexyloxymethyl and dodecyloxymethyl groups. These monomers were polymerised and examined on account of their stability using cyclic voltammetry. Obtained polymers are stable in the range of potentials 0 - 1.8 V. PEDOT functionalised with a dodecyloxymethyl group was soluble in chloroform and benzene.",

keywords = "Electrochemical methods, Electropolymerisation, Heterocycle synthesis, Solution processing",

author = "A. Czardybon and M. Lapkowski",

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TY - JOUR

T1 - Synthesis and electropolymerisation of 3,4-ethylenedioxythiophene functionalised with alkoxy groups

AU - Czardybon, A.

AU - Lapkowski, M.

PY - 2001/3/15

Y1 - 2001/3/15

N2 - We prepared 3,4-ethylenedioxythiophene (EDOT) functionalised with hydroxyl, hexyloxymethyl and dodecyloxymethyl groups. These monomers were polymerised and examined on account of their stability using cyclic voltammetry. Obtained polymers are stable in the range of potentials 0 - 1.8 V. PEDOT functionalised with a dodecyloxymethyl group was soluble in chloroform and benzene.

AB - We prepared 3,4-ethylenedioxythiophene (EDOT) functionalised with hydroxyl, hexyloxymethyl and dodecyloxymethyl groups. These monomers were polymerised and examined on account of their stability using cyclic voltammetry. Obtained polymers are stable in the range of potentials 0 - 1.8 V. PEDOT functionalised with a dodecyloxymethyl group was soluble in chloroform and benzene.

KW - Electrochemical methods

KW - Electropolymerisation

KW - Heterocycle synthesis

KW - Solution processing

UR - https://www.scopus.com/pages/publications/0035867823

U2 - 10.1016/S0379-6779(00)01309-6

DO - 10.1016/S0379-6779(00)01309-6

M3 - Article

AN - SCOPUS:0035867823

SN - 0379-6779

VL - 119

SP - 161

EP - 162

JO - Synthetic Metals

JF - Synthetic Metals

IS - 1-3

ER -

Synthesis and electropolymerisation of 3,4-ethylenedioxythiophene functionalised with alkoxy groups

Abstract

Keywords

ASJC Scopus subject areas

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