Chemical Imidization Study by Spectroscopic Techniques. 2. Polyamic Acids

1998 
Chemical imidization of polyamic acid based on 1,5-diaminonaphthalene and a dianhydride was studied by UV−visible and FT-IR ATR techniques under various reaction conditions, such as polyamic acid concentration, solvent condition (dry vs humidity-exposed NMP), catalysts of tertiary amines with different degrees of steric crowding and base strength, and the concentration of the acetic anhydride and pyridine. With acetic anhydride and pyridine, the reaction was very similar to that of the model amic acids, with the simultaneous formation of bisimide groups and bisisoimide groups, followed by isomerization of bisisoimde groups to bisimide groups, which is very sensitive to the dryness of the solvent. The reaction with polymer films supported a similar trend. Chemical imidization seems to proceed by nucleophilic catalysis by tertiary amines, depending on the steric crowding as well as the base strength. Reducing steric crowding in the catalyst facilitates the formation of an acylammonium (or pyridinium) cation...
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