[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Chahma et al., 2007 - Google Patents

Linear and branched electroactive polymers based on ethylenedioxythiophene–triarylamine conjugates

Chahma 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) …
Continue reading at pubs.rsc.org (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C08G61/122Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
    • C08G61/123Macromolecular 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
    • C08G61/124Macromolecular 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
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid 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
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0034Organic 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