2010
DOI: 10.1002/app.33317
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Synthesis and characterization of conducting copolymers of quinoxaline derivatives

Abstract: Electrochemical copolymerizations of 2,3-di(2-thienyl)quinoxaline (M1), 6-methyl-2,3-di(2-thienyl)-quinoxaline (M2), and 2,3-di(2-thienyl)quinoxaline-6-yl)-(phenyl)methanone (M3) with 3,4-ethylenedioxy thiophene (EDOT) were carried out in CH 3 CN/TBABF 4 (0.1M) solvent-electrolyte couple via potentiodynamic electrolysis. The obtained copolymers were characterized by cyclic voltammetry (CV), Fourier transform-infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and thermogravimetry analyses (TGA). … Show more

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Cited by 8 publications
(11 citation statements)
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“…Differences in FTIR spectra between copolymer and monomer reveal the complete disappearance of CH peaks between 3102 cm −1 and out‐of‐plane bending CH peaks at 875 cm −1 . Disappearance of these peaks is the evidence of polymerization from 2‐ and 5‐positions of the thiophene moiety of monomer 5. The presence of a new peak at 950 cm −1 for copolymer is due to asymmetric COC stretching of etheric units that stems from comonomer EDOT 5.…”
Section: Resultsmentioning
confidence: 95%
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“…Differences in FTIR spectra between copolymer and monomer reveal the complete disappearance of CH peaks between 3102 cm −1 and out‐of‐plane bending CH peaks at 875 cm −1 . Disappearance of these peaks is the evidence of polymerization from 2‐ and 5‐positions of the thiophene moiety of monomer 5. The presence of a new peak at 950 cm −1 for copolymer is due to asymmetric COC stretching of etheric units that stems from comonomer EDOT 5.…”
Section: Resultsmentioning
confidence: 95%
“…Disappearance of these peaks is the evidence of polymerization from 2‐ and 5‐positions of the thiophene moiety of monomer 5. The presence of a new peak at 950 cm −1 for copolymer is due to asymmetric COC stretching of etheric units that stems from comonomer EDOT 5. The peak at 1141 cm −1 belongs to perchlorate ions.…”
Section: Resultsmentioning
confidence: 96%
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“…On the other hand, thanks to its structural diversity, nitrogen containing heterocycles have also attracted considerable interest in recent years due to their unique properties [3][4][5] . Thiophene and quinoxaline copolymers have been employed as electronic carriers in electroluminescent devices 6 and as material for organic light-emitting devices 7 , among others.…”
Section: Introductionmentioning
confidence: 99%
“…Conducting polymers have been extensively investigated due to their potential applications in advanced electronic devices . Among these, polyaniline, polypyrrole, polythiophene, and their derivatives are of particular importance because they may be synthesized by electrochemical polymerization.…”
Section: Introductionmentioning
confidence: 99%