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
Syntheses and Optoelectronic Properties of Quinoxaline Polymers: The Effect of Donor Unit
Date
2011-09-15
Author
Sendur, Merve
Balan, Abidin
Baran, Derya
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
161
views
0
downloads
Cite This
Tuning the bandgap of electrochromic polymers is one of the important research topics in electrochromism. To understand clearly the effect of donor unit in donor-acceptor-donor-type polymers, 2,3-bis(4-tert-butylphenyl)-5,8-di(thiophen-2-yl)quinoxaline and 2,3-bis(4-tert-butylphenyl)-5-(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-8-(thiophen-2-yl)quinoxaline were synthesized and polymerized potentiodynamically. Their electrochemical and spectroelectrochemical studies were performed, and the results were compared with those of poly(2,3-bis(4-tert-butylphenyl)-5,8-bis(2,3-dihydro-thieno[3,4-b][1,4]dioxin-5-yl)quinoxaline) (Gunbas et al., Adv Mater 2008, 20, 691-695). A blue shift in the polymer pi-pi* transitions revealed that the bandgap of such polymers with the same acceptor unit is related to the electron density of donor units. (C) 2011 Wiley Periodicals, Inc. J PolymSci Part A: PolymChem 49: 4065-4070, 2011
Subject Keywords
Organic Chemistry
,
Materials Chemistry
,
Polymers and Plastics
URI
https://hdl.handle.net/11511/37182
Journal
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
DOI
https://doi.org/10.1002/pola.24849
Collections
Department of Chemistry, Article
Suggestions
OpenMETU
Core
Soluble Alkyl Substituted Poly(3,4-Propylenedioxyselenophene)s: A New Platform For Optoelectronic Materials
Atak, Samed; Icli-Ozkut, Merve; Önal, Ahmet Muhtar; CİHANER, ATİLLA (Wiley, 2011-10-15)
Optical and electrochemical properties of regiosymmetric and soluble alkylenedioxyselenophene-based electrochromic polymers, namely poly(3,3-dibutyl-3,4-dihydro-2H-seleno pheno [3,4-b][1,4]dioxephine) (PProDOS-C(4)), poly(3,3-dihexyl-3,4-dihydro-2H-selenopheno[3,4-b][1,4]dioxephine) (PProDOS-C(6)), and poly(3,3-didecyl-3,4-dihydro-2H-selenopheno[3,4-b][1,4]dioxephine) (PProDOS-C(10)), are highlighted. It is noted that these unique polymers have low bandgaps (1.57-1.65 eV), and they are exceptionally stable ...
Synthesis of novel chiral thiourea derivatives and their applications, synthesis of some hdac inhibitors, addition of acyl phosphonates to ethylcyanoformate
Sağlam, Gülüzar; Demir, Ayhan Sıtkı; Department of Chemistry (2008)
The thiourea derivatives have become a main focus of research in asymmetric synthesis as an organocatalyst in recent years. In the first part, the thiourea catalysts are synthesized starting from easily available L-tartaric acid and application of the catalysts to some addition reactions showed no significant asymmetric induction. A number of HDAC inhibitors have been developed as anti-cancer agent at the present time.In the second part, some aryl butenoic acid derivatives are synthesized as HDAC inhibitors...
Electrochemical and Optical Studies of Furan and Thieno[3,2-b]thiophene End Capped Benzotriazole Derivatives
AKBASOGLU, Naime; BALAN, Abidin; BARAN, Derya; Çırpan, Ali; Toppare, Levent Kamil (Wiley, 2010-12-01)
Two new 2-dodecyl benzotriazole (BTz) based donor-acceptor-donor (DAD) type polymers were synthesized and characterized in terms of their electrochemical and spectral properties. These DAD type polymers were synthesized electrochemically from furan or thieno[3,2-b]thiophene (TT) endcapped BTz monomers. Furan based and thieno[3,2-b]thiophene based monomers showed monomer oxidations at 1.15 and 1.25 V, respectively, which eased the formation of conducting polymer films without overoxidation. Cyclic voltammetr...
MONOMER REACTIVITY RATIOS OF STYRENE-4-VINYLPYRIDINE COPOLYMERS AT LOW AND HIGH CONVERSIONS
YILMAZ, E; KUCUKYAVUZ, Z (Elsevier BV, 1993-01-01)
Monomer reactivity ratios in free-radical copolymerization of styrene and 4-vinylpyridine monomers at 80-degrees-C in toluene solution under reduced pressure were determined for low and high conversions. Finemann-Ross, Kelen-Tudos, extended Kelen-Tudos and Mayo-Lewis methods were used for this purpose. The most reliable method was found to be the extended Kelen-Tudos method. By the use of this method, for conversions below 20%, monomer reactivity values of 0.700 +/- 0.005 and 0.335 +/- 0.001 were calculated...
Syntheses, electrochemical and photophysical properties of biphenyl containing conjugated copolymers
DENIZ, Tugba Kaya; NURIOGLU, Ayda Goycek; UNLU, Naime Akbasoglu; SENDUR, Merve; Toppare, Levent Kamil; Çırpan, Ali (Elsevier BV, 2013-04-19)
Poly 4-(biphenyl-4-yl)-4'-tert butylspiro[benzo[d]imidazole-2,1'-cyclohexane] (P1), Poly 4-(biphenyl-4-yl)2-dodecyl-2H-benzo[d][1,2,3]triazole (P2), Poly(4-(5-(biphenyl-4-yl)-4-hexylthiophen-2-yl)-2-dodecyl-7(4-hexylthiophen-2-yl)-2H-benzo[d][1,2,3]triazole (P3) were synthesized via Suzuki cross coupling polycondensation reaction. Polymers are thermally stable with decomposition temperatures above 300 C. Electrochemical and optical studies revealed that P2 and P3 exhibit reversible redox behavior with multi...
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
M. Sendur, A. Balan, D. Baran, and L. K. Toppare, “Syntheses and Optoelectronic Properties of Quinoxaline Polymers: The Effect of Donor Unit,”
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
, pp. 4065–4070, 2011, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/37182.