Synthesis and properties of new polyimides derived from 1,5‐bis(4‐aminophenoxy)naphthalene and aromatic tetracarboxylic dianhydrides

Abstract

AbstractNovel aromatic polyimides containing bis(phenoxy)naphthalene units were synthesized from 1,5‐bis(4‐aminophenoxy)naphthalene (APN) and various aromatic tetracarboxylic dianhydrides by the usual two‐step procedure that included ring‐opening polyaddition in a polar solvent such as N,N‐dimethylacetamide (DMAc) to give poly(amic acid)s, followed by cyclodehydration to polyimides. The poly(amic acid)s had inherent viscosities between 0.72 and 1.94 dL/g, depending on the tetracarboxylic dianhydrides used. Excepting the polyimide IVb obtained from 3,3′,4,4′‐biphenyltetracarboxylic dianhydride (BPDA), all other polyimides formed brown, flexible, and tough films by casting from the poly(amic acid) solutions. The polyimide synthesized from BPDA was characterized as semicrystalline, whereas the other polyimides showed amorphous patterns as shown by the x‐ray diffraction studies. Tensile strength, initial moduli, and elongation at break of the APN‐based polyimide films ranged from 105–135 MPa, 1.92–2.50 GPa, and 6–7%, respectively. These polyimides had glass transition temperatures between 228 and 317°C. Thermal analyses indicated that these polymers were fairly stable, and the 10% weight loss temperatures by TGA were recorded in the range of 543–574°C in nitrogen and 540–566°C in air atmosphere, respectively. © 1993 John Wiley & Sons, Inc.