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Synthesis and characterization of novel soluble triphenylamine‐containing aromatic polyamides based on <i>N</i>,<i>N</i>′‐bis(4‐aminophenyl)‐<i>N</i>,<i>N</i>′‐diphenyl‐1,4‐phenylenediamine
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2002
Year
EngineeringSmart PolymerResponsive PolymersOrganic ChemistryChemistryPolymersChemical EngineeringPolymer TechnologyMacromolecular EngineeringPolymer ProcessingHybrid MaterialsThermal StabilityPolymer ChemistryNovel Aromatic PolyamidesOrganic Material ChemistryPolymer ScienceAromatic PolyamidesConjugated PolymerTriphenylamine UnitsPolymer Synthesis
Abstract A new triphenylamine‐containing aromatic diamine, N , N ′‐bis(4‐aminophenyl)‐ N , N ′‐diphenyl‐1,4‐phenylenediamine, was prepared by the condensation of N , N ′‐diphenyl‐1,4‐phenylenediamine with 4‐fluoronitrobenzene, followed by catalytic reduction. A series of novel aromatic polyamides with triphenylamine units were prepared from the diamine and various aromatic dicarboxylic acids or their diacid chlorides via the direct phosphorylation polycondensation or low‐temperature solution polycondensation. All the polyamides were amorphous and readily soluble in many organic solvents such as N , N ‐dimethylacetamide and N ‐methyl‐2‐pyrrolidone. These polymers could be solution cast into transparent, tough, and flexible films with good mechanical properties. They had useful levels of thermal stability associated with relatively high glass‐transition temperatures (257–287 °C), 10% weight‐loss temperatures in excess of 550 °C, and char yields at 800 °C in nitrogen higher than 72%. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2810–2818, 2002
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