Preparation and characterization of highly transparent and colorless semi-aromatic polyimide films derived from alicyclic dianhydride and aromatic diamines

Abstract

A novel meta-substituted aromatic diamine containing trifluoromethyl and sulfonyl groups in the backbone, i.e., 2,2′-bis[4-(3-amino-5-trifluoromethylphenoxy)phenyl]sulfone (m-6FBAPS), was synthesized and characterized. A series of semi-aromatic polyimides were prepared from 1,2,4,5-cyclohexanetetracarboxylic dianhydride (CHDA) and various aromatic diamines. These polymers exhibited excellent solubility, high thermal stabilities and good mechanical properties. All semi-aromatic polyimide films showed considerably improved optical transparency as comparing with traditional aromatic ones due to the incorporation of alicyclic moieties. They gave the UV cutoff wavelengths of 292–314 nm, transmittance at 450 nm > 91% and yellowness indices <3.8. The extremely transparent and entirely colorless films were obtained from the polymers incorporated with bulky electron-withdrawing trifluoromethyl and sulfonyl groups in diamine moieties, such as PI-2, PI-5 and PI-6. Their excellent optical properties are attributed to the distorted molecular conformation combined with the weakened electron-accepting and electron-donating properties of dianydride and diamines, which significantly restrained the formation of inter-/intra-molecular charge transfer interactions.