New poly(amide-imide)s were prepared from a diimide-dicarboxylic acid, 1,4-bis(4-trimellitimidophenoxy)-2-tert-butylbenzene (BTTB), with various diamines by the direct polycondensation in N-methyl-2-pyrrolidinone (NMP) using triphenyl phosphite and pyridine as condensing agents. The new diimide-dica
Synthesis and characterization of novel aromatic poly(amide-imide)s derived from 2,2′-bis(4-trimellitimidophenoxy)biphenyl or 2,2′-bis(4-trimellitimidophenoxy)-1,1′-binaphthyl and various aromatic diamines
✍ Scribed by Ahmad Banihashemi; Hossein Behniafar
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 208 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0959-8103
- DOI
- 10.1002/pi.1205
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✦ Synopsis
Abstract
New aromatic diimide‐dicarboxylic acids having kinked and cranked structures, 2,2′‐bis(4‐trimellitimidophenoxy)biphenyl (2a) and 2,2′‐bis(4‐trimellitimidophenoxy)‐1,1′‐binaphthyl (2b), were synthesized by the reaction of trimellitic anhydride with 2,2′‐bis(4‐aminophenoxy)biphenyl (1a) and 2,2′‐bis(4‐aminophenoxy)‐1,1′‐binaphthyl (1b), respectively. Compounds 2a and 2b were characterized by FT‐IR and NMR spectroscopy and elemental analyses. Then, a series of novel aromatic poly(amide‐imide)s were prepared by the phosphorylation polycondensation of the synthesized monomers with various aromatic diamines. Owing to structural similarity, and a comparison of the characterization data, a model compound was synthesized by the reaction of 2b with aniline. The resulting polymers with inherent viscosities of 0.58–0.97 dl g^−1^ were obtained in high yield. The polymers were fully characterized by FT‐IR and NMR spectroscopy. The ultraviolet λ~max~ values of the poly(amide‐imide)s were also determined. The polymers were readily soluble in polar aprotic solvents. They exhibited excellent thermal stabilities and had 10% weight loss at temperatures above 500 °C under a nitrogen atmosphere. Copyright © 2003 Society of Chemical Industry
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A novel polymer-forming diimide-diacid, 2,6-bis(4-trimellitimidophenoxy)naphthalene, was prepared by the condensation reaction of 2,6-bis(4-aminophenoxy)naphthalene with trimellitic anhydride (TMA). A series of novel aromatic poly(amideimide)s containing 2,6-bis(phenoxy)naphthalene units were prepar
An imide ring-performed dicarboxylic acid bearing one hexafluoroisopropylidene and two ether linkages between aromatic rings, 2,2-bis[4-(4-trimellitimidophenoxy)phenyl]hexafluoropropane (II), was prepared from the condensation of 2,2-bis[4-(4-aminophenoxy)phenyl]hexafluoropropane and trimellitic anh
A diimide dicarboxylic acid, 1,4-bis(4-trimellitimidophenoxy)naphthalene (1,4-BTMPN), was prepared by condensation of 1,4-bis(4-aminophenoxy)naphthalene and trimellitic anhydride at a 1 : 2 molar ratio. A series of novel poly(amide-imide)s (IIa-k) with inherent viscosities of 0.72 to 1.59 dL/g were