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An aromatic diamine monomer,4,4’-bis(3-amino-5-trifluoromethyl phenoxy)-biphenyl (TFBPDA),wassynthesized via the nucleophilic displacement reaction of 3,5-dinitrobenzotrifluoride and 4,4’-biphenol.The monomer wasreacted with various aromatic dianhydrides via the high temperature polycondensation procedure to provide a series ofpolyimides.The polyimides,PI-1 to PI-4,show good solubility not only in aprotic solvents,such as N-methyl-2-pyrrolidinone and N,N-dimethylacetamide,but also in many common solvents,such as m-cresol,chloroform andcyclopentanone.PI-4,derived from 4,4’-(hexafluoroisopropylidene)diphthalic anhydride and TFBPDA,was even soluble intoluene.Moreover,PI films exhibit good thermal stability,outstanding transparency in the visible light region and acceptablemechanical and electrical properties.The excellent combined properties of the polyimides make them as a good candidate forfabricating microelectronics.
An aromatic diamine monomer, 4,4’-bis (3-amino-5-trifluoromethyl phenoxy) -biphenyl (TFBPDA), wassynthesized via the nucleophilic displacement reaction of 3,5-dinitrobenzotrifluoride and 4,4’-biphenol. with various aromatic dianhydrides via the high temperature polycondensation procedure to provide a series of polyimides. the polyimides, PI-1 to PI-4, show good solubility not only in aprotic solvents, such as N-methyl-2-pyrrolidinone and N, N- dimethylacetamide, but also in many common solvents such as m-cresol, chloroform andcyclopentanone. PI-4, derived from 4,4 ’- (hexafluoroisopropylidene) diphthalic anhydride and TFBPDA, was even soluble intoluene. , outstanding transparency in the visible light region and acceptable mechanical and electrical properties. The excellent combined properties of the polyimides make them as a good candidate for fabricating microelectronics.