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作 者:Hossein Mighani Mousa Ghaemy
机构地区:[1]Department of Chemistry,University of Golestan [2]Department of Chemistry,University of Mazandaran
出 处:《Chinese Journal of Polymer Science》2010年第2期147-155,共9页高分子科学(英文版)
摘 要:Aromatic/aliphatic polyamides were synthesized from a diamine monomer, 2,3-bis-p-aminophenylquinoxaline (IV), based on quinoxaline and various dicarboxylic acids of aliphatic, aromatic and heterocyclic. The diamine and polyamides were characterized by elemental analysis, FTIR and IH-NMR. The solubility of the polyamides was affected by the quinoxaline and heterocyclic groups in the polymer chain. They were all soluble in common organic solvents such as dimethylsulfoxide (DMSO), N,N-dimethylformamide (DMF) and N-methylpyrolidone (NMP). The polyamides showed inherent viscosity in the range of 0.25-0.3 dL/g in DMSO at 25℃ and good thermal stability with the char yields in the range of 65%-82% at 600℃ in nitrogen.Aromatic/aliphatic polyamides were synthesized from a diamine monomer, 2,3-bis-p-aminophenylquinoxaline (IV), based on quinoxaline and various dicarboxylic acids of aliphatic, aromatic and heterocyclic. The diamine and polyamides were characterized by elemental analysis, FTIR and IH-NMR. The solubility of the polyamides was affected by the quinoxaline and heterocyclic groups in the polymer chain. They were all soluble in common organic solvents such as dimethylsulfoxide (DMSO), N,N-dimethylformamide (DMF) and N-methylpyrolidone (NMP). The polyamides showed inherent viscosity in the range of 0.25-0.3 dL/g in DMSO at 25℃ and good thermal stability with the char yields in the range of 65%-82% at 600℃ in nitrogen.
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