A new difunctional monomer N,N'-[bis(4,4'-hydroxypropyl methacrylate phenyl ester) pyromellitimide] (BHPMEPM), was synthesized by the reaction of the bis(4-carboxyphenyl)-N,N'-pyromelli- timide acid (diaci...A new difunctional monomer N,N'-[bis(4,4'-hydroxypropyl methacrylate phenyl ester) pyromellitimide] (BHPMEPM), was synthesized by the reaction of the bis(4-carboxyphenyl)-N,N'-pyromelli- timide acid (diacid-diimide), and two molar equivalents of glycidylmethacrylate (GMA). The reaction was carried out by microwave radiation. The presence of difunctional groups, double bond groups, makes the monomer a potential material for obtaining thermosetting product. The curing and thermal stability of the crosslinked products were studied by differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA) techniques. The difunctional monomer and its thermoset polymer were characterized by FT-IR, 1</sup>H-FT-NMR and CHN elemental analysis.展开更多
文摘A new difunctional monomer N,N'-[bis(4,4'-hydroxypropyl methacrylate phenyl ester) pyromellitimide] (BHPMEPM), was synthesized by the reaction of the bis(4-carboxyphenyl)-N,N'-pyromelli- timide acid (diacid-diimide), and two molar equivalents of glycidylmethacrylate (GMA). The reaction was carried out by microwave radiation. The presence of difunctional groups, double bond groups, makes the monomer a potential material for obtaining thermosetting product. The curing and thermal stability of the crosslinked products were studied by differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA) techniques. The difunctional monomer and its thermoset polymer were characterized by FT-IR, 1</sup>H-FT-NMR and CHN elemental analysis.