Liu et al., 2014 - Google Patents
New triphenylamine-based poly (amine-imide) s with carbazole-substituents for electrochromic applicationsLiu et al., 2014
- Document ID
- 8519456459534387881
- Author
- Liu Y
- Chao D
- Yao H
- Publication year
- Publication venue
- Organic Electronics
External Links
Snippet
A new carbazole-derived triphenylamine-containing diimide-diacid monomer (5), 4, 4′-bis (trimellitimido)-4 ″-N-carbazolytriphenylamine, is prepared by the condensation of 4, 4′- diamino-4 ″-N-carbazolytriphenylamine (4) and two molar equivalents of trimellitic …
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 C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 0 title abstract description 9
Classifications
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- 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
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/14—Polyamide-imides
-
- 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
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
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- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
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- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
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- C09B1/28—Dyes with amino groups substituted by hydrocarbon radicals substituted by alkyl, aralkyl or cyclo alkyl groups
- C09B1/30—Dyes with amino groups substituted by hydrocarbon radicals substituted by alkyl, aralkyl or cyclo alkyl groups sulfonated
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| Hsiao et al. | Novel aromatic polyamides and polyimides functionalized with 4‐tert‐butyltriphenylamine groups | |
| Sun et al. | Highly stable electrochromic and electrofluorescent dual-switching polyamide containing bis (diphenylamino)-fluorene moieties | |
| Hsiao et al. | Redox-stable and visible/near-infrared electrochromic aramids with main-chain triphenylamine and pendent 3, 6-di-tert-butylcarbazole units | |
| Kung et al. | Fluorescent and electrochromic polyamides with pyrenylamine chromophore | |
| Wang et al. | Enhancement of redox stability and electrochromic performance of aromatic polyamides by incorporation of (3, 6‐dimethoxycarbazol‐9‐yl)‐triphenylamine units | |
| Liou et al. | Synthesis and electrochemical properties of novel aromatic poly (amine− amide) s with anodically highly stable yellow and blue electrochromic behaviors | |
| Hsiao et al. | Synthesis and electro-optical properties of aromatic polyamides and polyimides bearing pendent 3, 6-dimethoxycarbazole units | |
| Sun et al. | Novel polyamides with fluorene-based triphenylamine: electrofluorescence and electrochromic properties | |
| Hsiao et al. | New electroactive and electrochromic aromatic polyamides with ether‐linked bis (triphenylamine) units | |
| Kung et al. | Synthesis and characterization of novel electroactive polyamides and polyimides with bulky 4‐(1‐adamantoxy) triphenylamine moieties | |
| Chang et al. | Novel anodic polyelectrochromic aromatic polyamides containing pendent dimethyltriphenylamine moieties | |
| Hsiao et al. | Synthesis and electrochromic properties of aromatic polyimides bearing pendent triphenylamine units | |
| Hsiao et al. | Electroactive aromatic polyamides and polyimides with adamantylphenoxy-substituted triphenylamine units | |
| Hsiao et al. | Synthesis and electrochromic properties of aromatic polyamides with pendent triphenylamine units | |
| 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 | |
| Wang et al. | Substituent effects on electrochemical and electrochromic properties of aromatic polyimides with 4‐(carbazol‐9‐yl) triphenylamine moieties | |
| Sun et al. | Novel aromatic polyamides containing 2‐diphenylamino‐(9, 9‐dimethylamine) units as multicolored electrochromic and high‐contrast electrofluorescent materials | |
| Hsiao et al. | A comparative study on the properties of aromatic polyamides with methyl-or trifluoromethyl-substituted triphenylamine groups | |
| Hsiao et al. | Solution‐processable transmissive‐to‐green switching electrochromic polyamides bearing 2, 7‐bis (diphenylamino) naphthalene units | |
| Hsiao et al. | Synthesis and characterization of electrochromic poly (amide–imide) s based on the diimide-diacid from 4, 4′-diamino-4 ″-methoxytriphenylamine and trimellitic anhydride | |
| Yen et al. | Mixed‐valence class I transition and electrochemistry of bis (triphenylamine)‐based aramids containing isolated ether‐linkage | |
| Liu et al. | Novel triphenylamine polyamides bearing carbazole and aniline substituents for multi-colored electrochromic applications |