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In this work, new di-acid monomers 4, 4’-di-carboxillic-2â€-chloro-4â€- nitro triphenylamine (Di-CO2H-1), 4, 4’- di-carboxylic -2â€,4â€,6â€-trichloro-triphenylamine (Di-CO2H-2) were synthesized by reaction of p-cyanobenzofluride with two aromatic amines (2-chloro 4-nitro aniline and 2,4,6-trichloro aniline by aromatic nucleophilc substitution method to produce two di cyano intermediates compounds 4, 4’-Dicyano-2â€-chloro-4â€- nitro triphenylamine (Di-CN1) and 4, 4’-dicyano-2â€,4â€,6â€-trichloro-triphenylamine (Di-CN2) which form final di-carboxylic monomers after alkaline hydrolysis. Finally, these monomers react with two different arom
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