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
Conducting polymers of terepthalic acid bis-(2-thiophen-3-yl-ethyl) ester and their electrochromic properties
Date
2004-07-12
Author
Coskun, Y
Çırpan, Ali
Toppare, Levent Kamil
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
275
views
0
downloads
Cite This
Terepthalic acid bis-(2-thiophen-3-yl-ethyl)ester (TATE) was synthesized through the reaction of 2-thiophen-3-yl-ethanol and terepthaloyl chloride. Homopolymer of TATE was synthesized via potentiostatic and potentiodynamic methods by using tetrabutylammonium tetrafluoroborate (TBAFB) as the supporting electrolyte in dichloromethane/borontrifluoride ethylether solvent mixture(DM/BFEE) (8:2, v/v). Copolymerisation of TATE with thiophene was achieved in DM/BFEE solvent mixture (8:2, v/v) by using TBAFB as the supporting electrolyte in the presence of thiophene. The chemical structure of monomer is characterised via NMR and FTIR. Both homopolymer (PTATE) and copolymer P(TATE-co-Th) were characterised by various techniques including cyclic voltammetry, FTIR, scanning electron microscopy and UV-VIS spectroscopy. Conductivities of samples were measured by four probe technique. Optoelectrochemical analysis indicates that the homopolymer and copolymer have an electronic band gap, measured as the onset of the pi-to-pi* transition, as 2.17 and 2.00 eV, respectively.
Subject Keywords
Organic Chemistry
,
Polymers and Plastics
URI
https://hdl.handle.net/11511/37896
Journal
POLYMER
DOI
https://doi.org/10.1016/j.polymer.2004.05.038
Collections
Department of Chemistry, Article
Suggestions
OpenMETU
Core
A new soluble conducting polymer and its electrochromic devices
YİLDİZ, UMİT HAKAN; SAHİN, ELİF; Akhmedov, IM; Tanyeli, Cihangir; Toppare, Levent Kamil (Wiley, 2006-04-01)
A new polythiophene derivative was synthesized by both chemical and electrochemical oxidative polymerization of 1-(1-phenylethyl)-2,5-di(2-thienyl)-1H-pyrrole (PETPy). Of which the chemical method produces a polymer that is completely soluble in organic solvents. The structures of both the monomer and the soluble polymer were elucidated by nuclear magnetic resonance (H-1 and C-13 NMR) and Fourier transform infrared (FTIR) spectroscopy. The average molecular weight has been determined by gel permeation chrom...
Electrochromic properties of copolymer of terephthalic acid bis-(thiophen-3-yl-methyl) thioester with pyrrole
Tuerkarslan, Oezlem; Toppare, Levent Kamil (Informa UK Limited, 2007-01-01)
Terephthalic acid bis-(thiophen-3-yl-methyl) thioester ( TTMT) was synthesized via the reaction of thiophen-3-yl methanethiol with terephthaloyl dichloride. This 3-functionalized thiophene monomer was polymerized in the presence of pyrrole (Py) upon constant potential application. Spectroelectrochemistry experiments reflected a pi to pi* transition with a band gap energy of 2.4 eV for the copolymer. A dual type electrochromic device (ECD) of P(TTMT-co-Py) and poly(3,4-ethylenedioxythiophene) (PEDOT) was con...
A soluble and multichromic conducting polythiophene derivative
Varis, Serhat; Ak, Metin; Tanyeli, Cihangir; Akhmedov, Idris Mecidoglu; Toppare, Levent Kamil (Elsevier BV, 2006-10-01)
A new soluble polythiophene derivative was synthesized by both chemical and electrochemical oxidative polymerization of 1-4-nitrophenyl-2,5-di(2-thienyl)-1H-pyrrole (SNSNO2). Chemical method produces a polymer which is completely soluble in organic solvents. The structures of both the monomer and the soluble polymer were elucidated by H-1 and C-13-NMR and FTIR. The average molecular weight has been determined by GPC to be Mn = 6.3 x 10(3) for the chemically synthesized polymer. P(SNSNO2) was also synthesize...
Poly(ethylene terephthalate)/Carbon Nanotube Composites Prepared With Chemically Treated Carbon Nanotubes
Yesil, Sertan; Bayram, Göknur (Wiley, 2011-07-01)
Surfaces of multiwalled carbon nanotubes (CNT) were functionalized by treatment with strong acid mixture (purification) followed by modification with sodium dodecyl sulfate, poly(ethylene glycol) (PEG), and diglycidyl ether of Bisphenol A (DGEBA). Poly(ethylene terephthalate) (PET)-based conductive polymer composites were prepared by using these CNT by means of melt mixing with a twin screw extruder. Amount of carboxylic acid groups on the CNT surface increased after acid treatment but decreased with surfac...
Polymerization of propylene oxide by the Pruitt-Baggett catalyst
Çolak, Nureddin; Alyürük, Kemal (Elsevier BV, 1989-9)
The Pruitt-Baggett adduct (PBA) which formed from the reaction of FeCl3 with propylene oxide (PO) was hydrolysed in diethyl ether (ether) solutions at different mole ratios. Although the hydrolysates were insoluble in ether they could be converted into PO-soluble form (PBC) by a thermal treatment providing that the r value was kept smaller or equal to unity. PBC polymerized PO concurrently into a mixture of high molecular weight crystalline polymer with low molecular weight non-crystallizable oligomers. Th...
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
Y. Coskun, A. Çırpan, and L. K. Toppare, “Conducting polymers of terepthalic acid bis-(2-thiophen-3-yl-ethyl) ester and their electrochromic properties,”
POLYMER
, pp. 4989–4995, 2004, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/37896.