journal article·2019-04

Electrochromic properties of multifunctional conductive polymer based on naphthalene

Hakan Can Soyleyici

Optical Materials· Volume 90
Publisher page

Abstract

Abstract Conductive polymers are high-tech materials with high energy efficiency, bright colors, compatible with ambient conditions and superior optical properties. The properties of the polymer vary depending on the properties of the monomer used in polymer synthesis. For this reason, the use of multifunctional new monomers with high π-electron density and branching, containing different functional groups, is important in the formation of different types of conductive polymers. In this study, a new monomer suitable for double-sided polymerization on the thiophene groups in the center with the naphthalene molecule has been synthesized (DPN) and polymer P(DPN) has been obtained via this new monomer. P(DPN) is very stable and has the best optical properties. Also it is a special material with the potential to be used for sensor studies with amide groups and active amine protons that can be derivated.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Conducting polymers and applications · Analytical Chemistry and Sensors · Advanced Chemical Sensor Technologies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (39)

Show source-provided references
1. Electrochemical synthesis and characterization of 1,4-benzodioxan-Based electrochromic polymer and its application in electrochromic devices10.1149/2.0381510jes ↗
2. Recent advances in electropolymerized conducting polymers in amperometric biosensors10.1007/s00604-003-0067-4 ↗
3. Navy-to-transmissive electrochromic polymer based on 3,4-propylenedioxythiophene10.1007/s10854-018-9740-6 ↗
4. Conductive polymers: opportunities and challenges in biomedical applications10.1021/acs.chemrev.6b00275 ↗
5. Post polymerization functionalization of a soluble poly(2,5-dithienylpyrrole) derivative via click chemistry10.1149/2.0301707jes ↗
6. Applications of three dithienylpyrroles-based electrochromic polymers in high-contrast electrochromic devices
7. Electrochemistry of secondary amine substituted 2,5-di(2-thienyl)pyrrole derivative and its copolymer10.1149/2.0291707jes ↗
8. Phenylthiophene-containing poly(2,5-dithienylpyrrole)s as potential anodic layers for high-contrast electrochromic devices10.1149/2.0401805jes ↗
9. An amide substituted dithienylpyrrole based copolymer: its electrochromic properties10.1149/2.0631602jes ↗
10. Online · 2016 · 1744
11. Fast switching, high contrast multichromic polymers from alkyl-derivatized dithienylpyrrole and 3,4-ethylenedioxythiophene10.1016/j.electacta.2011.11.079 ↗
12. High contrast electrochromic polymer and copolymer materials based on amide-substituted poly(dithienyl pyrrole)10.1149/2.0111702jes ↗
13. A processable rainbow mimic fluorescent polymer and its unprecedented coloration efficiency in electrochromic device10.1016/j.electacta.2007.10.030 ↗
14. New class of 2,5-di(2-thienyl)pyrrole compounds and novel optical properties of its conducting polymer10.1016/j.matchemphys.2013.07.019 ↗
15. Optoelectrochromic characterization and smart windows application of bi-functional amid substituted thienyl pyrrole derivative10.1016/j.polymer.2017.04.060 ↗
16. Processable amide substituted 2,5-Bis(2-thienyl)pyrrole based conducting polymer and its fluorescent and electrochemical properties10.1149/2.0071614jes ↗
17. A soluble and fluorescent new type thienylpyrrole based conjugated polymer: optical, electrical and electrochemical properties10.1039/C6CP02214F ↗
18. Synthesis of highly branched conducting polymer architecture for electrochromic applications
19. Efficient synthesis of EDOT modified ABBB-type unsymmetrical zinc phthalocyanine: optoelectrochromic and glucose sensing properties of its copolymerized film10.1039/C7NJ03250A ↗
20. Heterogeneity of chemokine cell-surface receptor expression in triple-negative breast cancer
21. π-Conjugated polymers bearing electronic and optical functionalities. Preparation, properties and their applications10.1016/S1381-5148(97)00140-5 ↗
22. Multielectrochromic copolymers of 3,4-ethylenedioxythiophene and naphthalene prepared via electropolymerization in boron trifluoride diethyl etherate10.1016/j.jelechem.2012.10.033 ↗
23. Skotheim · 2007
24. Electrochemical and optical properties of new soluble dithienylpyrroles based on azo dyes10.1016/j.electacta.2008.09.067 ↗
25. A novel electrochromic and fluorescent polythienylpyrrole bearing 1,1′-bipyrrole10.1016/j.electacta.2008.09.008 ↗
26. An electrochromic and fluorescent polymer based on 1-(1-naphthyl)-2,5-di-2-thienyl-1H-pyrrole10.1016/j.jelechem.2007.11.024 ↗
27. Processable electrochromic and fluorescent polymers based on N-substituted thienylpyrrole10.1016/j.electacta.2008.07.013 ↗
28. Optical, electrical and electrochemical properties of heteroaromatic copolymers10.1016/0032-3861(89)90054-2 ↗
29. Luminescent network film deposited electrochemically from a carbazole functionalized AIE molecule and its application for OLEDs10.1039/C4TC02475C ↗
30. A novel multielectrochromic copolymer based on 1-(4-nitrophenyl)-2,5-di(2-thienyl)-1H-pyrrole and EDOT10.1016/j.jelechem.2007.02.002 ↗
31. Reactivity of 2,5-dithienyl-pyrroles and thiophenes10.1016/0379-6779(93)90296-9 ↗
32. A new processable donor-acceptor polymer displaying neutral state yellow electrochromism10.1016/j.polymer.2013.09.033 ↗
33. N-substituted 2,5-di(2-thienyl)pyrroles: application, production, properties, and electrochemical polymerization (review)10.1007/s10593-011-0735-y ↗
34. Ferrocene-functionalized 4-(2,5-Di(thiophen-2-yl)-1H-pyrrol-1-yl)aniline: a novel design in conducting polymer-based electrochemical biosensors10.3390/s150101389 ↗
35. A new conducting polymer of 2,5-bis(2-thienyl)-1H-(pyrrole) (SNS) containing carbazole subunit: electrochemical, optical and electrochromic properties10.1016/j.synthmet.2009.07.027 ↗
36. Synthesis and electropolymerization of N-(4′-carboxyphenyl)-2,5-di(2″-thienyl)pyrrole10.1016/j.synthmet.2009.09.035 ↗
37. Effect of alkyl side-chain length and solvent on the luminescent characteristics of poly(3-n-alkylthiophene)10.1016/S0379-6779(03)00361-8 ↗
38. A new approach to the Schiff base-substituted oligophenols: the electrochromic application of 2-[3-thienylmethylene]aminophenol based co-polythiophenes
39. Electrosynthesis of anthracene clicked poly(thienylpyrrole)s and investigation of their electrochromic properties10.1016/j.polymer.2015.07.005 ↗