[go: up one dir, main page]

Liou et al., 2007 - Google Patents

Synthesis and properties of wholly aromatic polymers bearing cardo fluorene moieties

Liou et al., 2007

View PDF
Document ID
13430648049907564692
Author
Liou G
Yen H
Su Y
Lin H
Publication year
Publication venue
Journal of Polymer Science Part A: Polymer Chemistry

External Links

Snippet

Three series of aromatic polyamides, polyesters, and poly (1, 3, 4‐oxadiazole) s containing bulky fluorene structures were prepared from 9, 9‐bis (4‐carboxyphenyl) fluorene. All of the polymers were readily soluble in many organic solvents and showed useful thermal stability …
Continue reading at homepage.ntu.edu.tw (PDF) (other versions)

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
    • 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
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • 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
    • C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02—Polyamines
    • 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
    • C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • 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
    • C08G79/00—Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/14—Macromolecular compounds
    • C09K2211/1441—Heterocyclic
    • 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
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands

Similar Documents

Publication Publication Date Title
Liou et al. Synthesis, photophysical, and electrochromic characterization of wholly aromatic polyamide blue-light-emitting materials
Kung et al. Fluorescent and electrochromic polyamides with pyrenylamine chromophore
Sun et al. Highly stable electrochromic and electrofluorescent dual-switching polyamide containing bis (diphenylamino)-fluorene moieties
Sun et al. Novel polyamides with fluorene-based triphenylamine: electrofluorescence and electrochromic properties
Hsiao et al. Redox-stable and visible/near-infrared electrochromic aramids with main-chain triphenylamine and pendent 3, 6-di-tert-butylcarbazole units
Wang et al. Enhancement of redox stability and electrochromic performance of aromatic polyamides by incorporation of (3, 6‐dimethoxycarbazol‐9‐yl)‐triphenylamine units
Chang et al. Novel anodic electrochromic aromatic polyamides with multi-stage oxidative coloring based on N, N, N′, N′-tetraphenyl-p-phenylenediamine derivatives
Su et al. Novel family of triphenylamine‐containing, hole‐transporting, amorphous, aromatic polyamides with stable electrochromic properties
Wang et al. Enhanced redox stability and electrochromic properties of aromatic polyamides based on N, N‐bis (4‐carboxyphenyl)‐N′, N′‐bis (4‐tert‐butylphenyl)‐1, 4‐phenylenediamine
Hsiao et al. Highly stable electrochromic polyamides based on N, N‐bis (4‐aminophenyl)‐N′, N′‐bis (4‐tert‐butylphenyl)‐1, 4‐phenylenediamine
Liou et al. Synthesis and properties of wholly aromatic polymers bearing cardo fluorene moieties
Sun et al. Novel aromatic polyamides containing 2‐diphenylamino‐(9, 9‐dimethylamine) units as multicolored electrochromic and high‐contrast electrofluorescent materials
Wang et al. Synthesis, photoluminescence, and electrochromism of polyamides containing (3, 6‐di‐tert‐butylcarbazol‐9‐yl) triphenylamine units
Chang et al. Novel anodic polyelectrochromic aromatic polyamides containing pendent dimethyltriphenylamine moieties
Hsiao et al. Synthesis and electrochromic properties of aromatic polyamides with pendent triphenylamine units
Liou et al. Synthesis and photoluminescent and electrochromic properties of aromatic poly (amine amide) s bearing pendent N‐carbazolylphenyl moieties
Hsiao et al. Solution‐processable transmissive‐to‐green switching electrochromic polyamides bearing 2, 7‐bis (diphenylamino) naphthalene units
Liou et al. Synthesis and characterization of wholly aromatic poly (azomethine) s containing donor–acceptor triphenylamine moieties
Liou et al. Synthesis and electrochromism of novel organosoluble polyarylates bearing triphenylamine moieties
Liou et al. Synthesis and evaluation of photoluminescent and electrochemical properties of new aromatic polyamides and polyimides with a kink 1, 2‐phenylenediamine moiety
Liu et al. Novel low color poly (ester imides) with triphenylamine and carbazole substituents for electrochromic applications
Lin et al. Poly (triphenylamine) s derived from oxidative coupling reaction: Substituent effects on the polymerization, electrochemical, and electro‐optical properties
Cheng et al. Novel electrochromic aromatic poly (amine–amide–imide) s with pendent triphenylamine structures
Hsiao et al. Highly redox‐stable and electrochromic aramids with morpholinyl‐substituted triphenylamine units
Liou et al. Novel thermally stable poly (amine hydrazide) s and poly (amine‐1, 3, 4‐oxadiazole) s for luminescent and electrochromic materials