Abstract
AbstractA series of ethynyl‐terminated aromatic imide monomers containing phosphine oxide in the backbone were synthesized by the reaction of tris(3‐aminophenyl) phosphine oxide (TAP) or bis(3‐aminophenyl)methyl phosphine oxide (BAP) with pyromellitic dianhydride (PMDA) or 3, 3′,4, 4′‐benzophenone tetracarboxylic acid dianhydride (BTDA) or 4, 4′‐perfluoroisopropylidenebis(phthalic anhydride), and 3‐ethynyl aniline. Structural characterization was done by infrared, nuclear magnetic resonance spectroscopy and elemental analysis. Thermal characterization was done by differential scanning calorimetry and thermogravimetric analysis. The decomposition temperatures of cured resins were above 500°C in nitrogen atmosphere. Char yield at 800°C ranged from 52–63.5%.
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