New poly(amide imide imide)s based on tetraimide dicarboxylic acid condensed from 4,4′-(hexafluoroisopropylidene)diphthalic anhydride, m-aminobenzoic acid, and 4,4″-oxydianiline and various aromatic diamines

✍ Scribed by Chin-Ping Yang; Ruei-Shin Chen; Mao-Feng Hsu

• Publisher: John Wiley and Sons
• Year: 2003
• Tongue: English
• Weight: 183 KB
• Volume: 88
• Category: Article
• ISSN: 0021-8995
• DOI: 10.1002/app.11800

✦ Synopsis

Abstract

A series of new, organosoluble, and light‐colored poly(amide imide imide)s were synthesized from tetraimide dicarboxylic acid (I) and various aromatic diamines by direct polycondensation with triphenyl phosphite and pyridine as condensing agents. I was prepared by the azeotropic condensation of 4,4′‐(hexafluoroisopropylidene)diphthalic anhydride, m‐aminobenzoic acid, and 4,4′‐oxydianiline at a 2/2/1 molar ratio in N‐methyl‐2‐pyrrolidone (NMP)/toluene. The thin films cast from N,N‐dimethylacetamide (DMAc) had cutoff wavelengths shorter than 400 nm (365–394 nm) and color coordinate b* values between 13.10 and 36.07; these polymers were lighter in color than the analogous poly(amide imide)s and isomeric polymers. All of the polymers were readily soluble in a variety of organic solvents, including NMP, DMAc, N,N‐dimethylformamide, dimethyl sulfoxide, and even less polar dioxane and tetrahydrofuran. The cast films exhibited tensile strengths of 90–104 MPa, elongations at break of 7–22%, and initial moduli of 1.9–2.4 GPa. The glass‐transition temperatures of the polymers were recorded at 274–319°C. They had 10% weight losses at temperatures beyond 520°C and left more than a 50% residue even at 800°C in nitrogen. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 669–679, 2003