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Three new carbazole-based diamines, 3,6-diaminocarbazole ( 2 ), 3,6-diamino- N -phenylcarbazole ( 4 ) and N -(4‘-aminophenyl)-3-aminocarbazole ( 7 ), were prepared from carbazole or N -phenylcarbazole. Homopolyimides and copolyimides derived from these three diamines as well as 4,4‘-diamineodiphenyl ether (DDE), with 4,4‘-(hexafluoroisopropylidene)diphthalic anhydride (6FDA) in 1-methyl-2-pyrrolidinone (NMP) via a two-step condensation reaction, were obtained. These polyimides, especially those derived from monomers 4 and 7, were readily soluble in many organic polar solvents. They had weight-average molecular weights ranging from 1.5 × 10 4 to 5.9 × 10 4 . DSC analyses indicated that (co)polyimides derived from diamine 4 had glass transition temperatures and others derived from diamines 2 and 7 did not show any glass transition prior to thermal decomposition in air.
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Chen et al. (1999) studied this question.
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