A new dicarboxylic acid having a kinked structure was synthesized from the condensation of 2,2 -bis (4-aminophenoxy ) biphenyl and trimellitic anhydride. A series of biphenyl-2,2 -diyl-containing aromatic poly ( amide-imide ) s having inherent viscosities of 0.23 -0.94 dL / g was prepared by the tri
Preparation and characterization of colorless alternate poly(amide-imide)s based on trimellitic anhydride and 2,2-bis[4-(3-aminophenoxy)phenyl]sulfone
โ Scribed by Chin-Ping Yang; Ruei-Shin Chen; Chi-Chi Huang
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 148 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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โฆ Synopsis
Alternate poly(amide-imide) [P(A-alt-I)] was synthesized from two aromatic diamines and trimellitic anhydride (TMA). When the diamine was 2,2-bis[4-(3aminophenoxy)phenyl]sulfone (BAPS), the resulted P(A-alt-I) was found to be of light color. Specifically, when BAPS was located between two amide groups in the P(A-alt-I) chain, the P(A-alt-I) was almost colorless. A series of P(A-alt-I)s (Series III) containing BAPS was synthesized through direct polycondensation of an aromatic dicarboxylic acid prepared from various aromatic diamines and TMA, as well as BAPS. Polymers of Series III were much lighter in color than those of the isomeric series (BAPS was located between two imide group). The series of P(A-alt-I)s III had inherent viscosities ranging 0.69 -1.35 dL/g and good solubility in various solvents. The tensile strengths, elongations to break, and initial moduli of the films were 72-107 MPa, 7-12% and 1.93-2.39 GPa, respectively, and most of the films had no yielding. Polymers of Series III had glass transition temperatures 210 -272ยฐC and 10% weight loss temperatures in nitrogen 518 -545ยฐC, indicating excellent thermal stability.
๐ 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
A series of new aromatic poly(amide-imide)s were synthesized by the triphenyl phosphite-activated polycondensation of the diimide-diacid, 1,4-bis(trimellitimido)-2,5-dichlorobenzene (I), with various aromatic diamines in a medium consisting of N-methyl-2-pyrrolidone (NMP), pyridine, and calcium chlo
## Abstract Five new poly(amideโimide)s **8aโe** were synthesized through the direct polycondensation reaction of five chiral __N__,__N__โฒโ(pyromellitoyl)โbisโLโamino acids **3aโe** with 1,3โbis(4โaminophenoxy) propane **7** in a medium consisting of __N__โmethylโ2โpyrrolidone, triphenyl phosfite,
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