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
Preparation and properties of new poly(amide-imide)s based on 1,4-bis(4-trimellitimidophenoxy)naphthalene and aromatic diamines
✍ Scribed by Chin-Ping Yang; Ruei-Shin Chen; Jhy-An Chen
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 128 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0887-624X
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✦ Synopsis
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 prepared by triphenyl phosphite-activated polycondensation from the diimide-diacid 1,4-BTMPN with various aromatic diamines (Ia-k) in a medium consisting of N-methyl-2-pyrrolidinone (NMP), pyridine, and calcium chloride. The poly(amide-imide)s showed good solubility in NMP, N,N-dimethylacetamide, and N,N-dimethylformamide. The thermal properties of the obtained poly(amide-imide)s were examined with differential scanning calorimetry and thermogravimetry analysis. The synthesized poly(amide-imide)s possessed glass-transition temperatures in the range of 215 to 263°C. The poly(amide-imide)s exhibited excellent thermal stabilities and had 10% weight losses at temperatures in the range of 538 to 569°C under a nitrogen atmosphere. A comparative study of some corresponding poly(amide-imide)s also is presented.
📜 SIMILAR VOLUMES
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
## Abstract Six new poly(amide‐imide)s **8a–f** containing trimethylene moiety in the main chain were synthesized by the polycondensation reactions of 1,3‐bis[4,4'‐(trimellitimido) phenoxy] propane **6** with six different aromatic diamines **7a–f** in a medium constituting __N__‐methyl‐2‐pyrrolido
A series of new alternative poly(amide-imide)s (PAIs, III a-j ) was synthesized by the direct polycondensation of 1,4-bis(4-aminophenoxy)naphthalene (1,4-BAPON) with various aromatic diimide-diacids. These polymers were obtained in quantitative yields with inherent viscosities of 0.71-1.03 dL/g. Exc
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
A series of poly(amide-imide)s III a-m containing flexible isopropylidene and ether groups in the backbone were synthesized by the direct polycondensation of 4,4Ј-[1,4-phenylenebis(isopropylidene-1,4-phenyleneoxy)]dianiline (PIDA) with various bis(trimellitimide)s II a-m in N-methyl-2-pyrrolidone (N