Chahma et al., 2007 - Google Patents
Linear and branched electroactive polymers based on ethylenedioxythiophene–triarylamine conjugatesChahma et al., 2007
- Document ID
- 15902079361194059647
- Author
- Chahma M
- Gilroy J
- Hicks R
- Publication year
- Publication venue
- Journal of Materials Chemistry
External Links
Snippet
Triphenylamines with one, two, or three 3, 4-ethylenedioxythiophene (EDOT) substituents attached to the para-phenyl carbons have been prepared via metal-catalyzed cross- coupling reactions. The amines with two or three EDOTs (compounds 4 and 3, respectively) …
- 229920001746 Electroactive polymer 0 title description 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
- C08G61/124—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one nitrogen atom in the ring
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0034—Organic polymers or oligomers
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Jayakannan et al. | Synthesis and structure‐property relationship of new donor–acceptor‐type conjugated monomers and polymers on the basis of thiophene and benzothiadiazole | |
Jestin et al. | Synthesis and characterization of the electronic and electrochemical properties of thienylenevinylene oligomers with multinanometer dimensions | |
Berrouard et al. | Low-cost synthesis and physical characterization of thieno [3, 4-c] pyrrole-4, 6-dione-based polymers | |
Yamamoto et al. | π-conjugated donor− acceptor copolymers constituted of π-excessive and π-deficient arylene units. Optical and electrochemical properties in relation to CT structure of the polymer | |
Kitamura et al. | Design of narrow-bandgap polymers. Syntheses and properties of monomers and polymers containing aromatic-donor and o-quinoid-acceptor units | |
Oyaizu et al. | Linear ladder-type π-conjugated polymers composed of fused thiophene ring systems | |
Sotzing et al. | Electrochromic conducting polymers via electrochemical polymerization of bis (2-(3, 4-ethylenedioxy) thienyl) monomers | |
Trouillet et al. | Synthesis and characterization of a new soluble, structurally well-defined conjugated polymer alternating regioregularly alkylated thiophene oligomer and 2, 2 ‘-bipyridine units: metal-free form and Ru (II) complex | |
Yamamoto et al. | Poly (aryleneethynylene) type polymers containing a ferrocene unit in the π-conjugated main chain. Preparation, optical properties, redox behavior, and Mössbauer spectroscopic analysis | |
Sumi et al. | Synthesis and properties of a series of the longest oligothiophenes up to the 48-mer | |
Liu et al. | Multifaceted regioregular oligo (thieno [3, 4-b] thiophene) s enabled by tunable quinoidization and reduced energy band gap | |
Frère et al. | Effect of local molecular structure on the chain-length dependence of the electronic properties of thiophene-based π-conjugated systems | |
Reddinger et al. | Site specific electropolymerization to form transition-metal-containing, electroactive polythiophenes | |
Aubert et al. | Copolymers of 3, 4-ethylenedioxythiophene and of pyridine alternated with fluorene or phenylene units: Synthesis, optical properties, and devices | |
Bolduc et al. | Insight into the isoelectronic character of azomethines and vinylenes using representative models: a spectroscopic and electrochemical study | |
Vangeneugden et al. | Synthesis and characterization of a poly (1, 3-dithienylisothianaphthene) derivative for bulk heterojunction photovoltaic cells | |
van Haare et al. | π-Dimers of prototype high-spin polaronic oligomers | |
Algı et al. | An ambipolar low band gap material based on BODIPY and EDOT | |
İçli-Özkut et al. | A neutral state yellow to navy polymer electrochrome with pyrene scaffold | |
Alkan et al. | The impact of [1, 2, 5] chalcogenazolo [3, 4‐f]‐benzo [1, 2, 3] triazole structure on the optoelectronic properties of conjugated polymers | |
Chahma et al. | Linear and branched electroactive polymers based on ethylenedioxythiophene–triarylamine conjugates | |
Pammer et al. | Synthesis, Structures, and Hydroboration of Oligo-and Poly (3-alkynylthiophene) s | |
Guven et al. | Tuning of electrochromic properties of electrogenerated polythiophenes through Ru (II) complex tethering and backbone derivatization | |
Imae et al. | Electrosynthesis and charge-transport properties of poly (3′, 4′-ethylenedioxy-2, 2′: 5′, 2′′-terthiophene) | |
Lère‐Porte et al. | Highly Conjugated Poly (thiophene) s− Synthesis of Regioregular 3‐Alkylthiophene Polymers and 3‐Alkylthiophene/Thiophene Copolymers |