Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Open Access Guideline
Open Access Guideline
Postgraduate Thesis Guideline
Postgraduate Thesis Guideline
Communities & Collections
Communities & Collections
Help
Help
Frequently Asked Questions
Frequently Asked Questions
Guides
Guides
Thesis submission
Thesis submission
MS without thesis term project submission
MS without thesis term project submission
Publication submission with DOI
Publication submission with DOI
Publication submission
Publication submission
Supporting Information
Supporting Information
General Information
General Information
Copyright, Embargo and License
Copyright, Embargo and License
Contact us
Contact us
Synthesis and electrochromic properties of conducting polymers of 5,8-di(pyrrol-2-yl)-2,3-di(thiophen-2-yl) quinoxaline and its copolymers
Download
index.pdf
Date
2009
Author
Taşkın, Aslı Tuba
Metadata
Show full item record
Item Usage Stats
251
views
90
downloads
Cite This
A novel electroactive monomer 5,8-Di(1H-pyrrol-2-yl)-2, 3-di(thiophen-2-yl) quinoxaline (PTQ) was successfully synthesized via Stille Coupling reaction between quinoxaline and pyrrole. Nuclear magnetic resonance (1H NMR and 13C NMR) and Mass spectroscopy were used to characterize the monomer. The monomer was electrochemically polymerized in the presence of tetrabutylammonium perchlorate (TBAP) as supporting electrolyte in dichloromethane. Monomer reveals relatively low oxidation potential at +0.70V. Spectroelectrochemical behaviors and switching ability of homopolymer were investigated by UV-Vis spectroscopy and cyclic voltammetry. Two π-π* transitions were observed at 400 nm and 815 nm with a low band gap, 1.0 eV. Polymer possesses 66% optical contrast in the Near IR region, which may be promising in NIR electrochromic device applications. Spectroelectrochemical behaviors and switching ability of copolymers were investigated by UV-Vis spectroscopy and cyclic voltammetry. Copolymers of PTQ in the presence of BiEDOT and BEBT were synthesized via potentiodynamic method in DCM/TBAP (0.1 M) solvent-electrolyte couple. P(PTQ-co-BiEDOT) reveals oxidation potential at +0.45V, whereas P(PTQ-co-BEBT) reveals oxidation potential at +0.70V. The spectroelectrochemical behavior of the P(PTQ-co-BiEDOT) and P(PTQ-co-BEBT) in comparison to homopolymer revealed solid evidence of copolymerization based upon the differences in the spectral signatures. Switching time of the polymers was evaluated by kinetic studies upon measuring the percent transmittance (%T) at the maximum contrast point.
Subject Keywords
Chemistry.
,
Conducting polymers.
URI
http://etd.lib.metu.edu.tr/upload/12610600/index.pdf
https://hdl.handle.net/11511/18725
Collections
Graduate School of Natural and Applied Sciences, Thesis
Suggestions
OpenMETU
Core
Synthesis, characterization and electrochromic properties of a near infrared active conducting polymer of 1,4-di(selenophen-2-yl)-benzene
Aydemir, Kadir; Tarkuc, Simge; Durmus, Asuman; Günbaş, Emrullah Görkem; Toppare, Levent Kamil (Elsevier BV, 2008-04-15)
A novel selenophene-based monomer, 1,4-di(selenophen-2-yl)-benzene (DSB), was synthesized via Stille coupling reaction of 1,4-dibromobenzene and tributyl(2-selenophenyl)stannane. Conducting polymer (PDSB) was prepared electrochemically in the presence of tetrabutylammonium hexafluorophosphate (TBAPF(6)) as the supporting electrolyte in dichloromethane (DCM). The resulting conducting polymer was characterized by Cyclic Voltammetry, Fourier Transform Infrared and Ultraviolet-visible spectroscopy. Spectroelect...
Synthesis and electrochromic properties of a multichromic, conducting, soluble polythiophene derivative and its copolymer
Özyurt, Funda; Toppare, Levent Kamil; Department of Chemistry (2009)
A new polythiophene derivative, poly-2,3-bis(4-tert-butylphenyl)-5,8-bis(4-hexylthiophen-2-yl)quinoxaline PHTQ was synthesized by both chemical and electrochemical polymerization and its electrochemical properties were reported. The monomer was electrochemically polymerized in the presence of tetrabutylammonium hexafluorophosphate(TBAPF6) as the supporting electrolyte in dichloromethane-acetonitrile (5:95, v:v). Nuclear magnetic resonance spectroscopy (1H-NMR, 13C-NMR) was utilized for the characterization ...
Synthesis and characterization of a bifunctional amido-thiophene monomer and its copolymer with thiophene and electrochemical properties
AK, M; Çırpan, Ali; Yılmaz, Fatih; YAGCI, Y; Toppare, Levent Kamil (2005-05-01)
A bifunctional amido-thiophene namely hexamethylene (bis-3-thiophene acetamide) (HMTA) was synthesized by the reaction of 3-thiophene acetic acid with hexamethylene diamine. Copolymerization in the presence of thiophene was achieved electrochemically in tetrabutylammonium tetrafluoroborate/acetonitrile (TBAFB/AN). Spectroelectro-chemical analysis of the resulting copolymer [P(HMTA-co-Th)] reflected electronic transitions at 505 nm, 740 nm and similar to 1000 nm, revealing pi to pi* transition, polaron and b...
Synthesis and characterization of conducting copolymers of menthyl ester of 3-thiophene acetic acid with pyrrole
Kiralp, S; Alkan, S; Toppare, Levent Kamil; Cianga, I; Yagci, Y (2003-01-01)
A new thiophene derivative containing menthyl group (MM) was synthesized and polymerized via chemical and electrochemical (constant current) methods. Polymers obtained and MM itself were used to synthesize copolymers with pyrrole under conditions of constant potential electrolyses. Cyclic voltammetry (CV), thermal analysis (DSC, TGA) and scanning electron microscopy (SEM) analyses were performed for the characterization of samples.
Synthesis of novel chiral bisoxazoline ligands with a norbornadiene backbone: use in the copper-catalyzed enantioselective Henry reaction
Delikus, Rabia; Cakir, Emine; DEMİREL, NADİR; Balcı, Metin; KARATAŞ, BETÜL (The Scientific and Technological Research Council of Turkey, 2016-01-01)
Novel chiral bisoxazoline ligands based on norbornadiene were synthesized and used for the asymmetric Henry reaction. Various aromatic aldehydes were converted into chiral beta-nitro alcohols with high yields and moderate to acceptable enantioselectivities under the optimized reaction conditions.
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
A. T. Taşkın, “Synthesis and electrochromic properties of conducting polymers of 5,8-di(pyrrol-2-yl)-2,3-di(thiophen-2-yl) quinoxaline and its copolymers,” M.S. - Master of Science, Middle East Technical University, 2009.