Hossein Mighani a, Mousa Ghaemy b. SYNTHESIS AND CHARACTERIZATION OF ORGANOSOLUBLE POLYAMIDES FROM QUINOXALINE BASED DIAMINE[J]. 高分子科学(英文版), 2010,28(2):147-155.
Hossein Mighani a, b. SYNTHESIS AND CHARACTERIZATION OF ORGANOSOLUBLE POLYAMIDES FROM QUINOXALINE BASED DIAMINE[J]. 2010, 28(2): 147-155.
Hossein Mighani a, Mousa Ghaemy b. SYNTHESIS AND CHARACTERIZATION OF ORGANOSOLUBLE POLYAMIDES FROM QUINOXALINE BASED DIAMINE[J]. 高分子科学(英文版), 2010,28(2):147-155.DOI: 10.1007/s10118-010-8231-x.
Hossein Mighani a, b. SYNTHESIS AND CHARACTERIZATION OF ORGANOSOLUBLE POLYAMIDES FROM QUINOXALINE BASED DIAMINE[J]. 2010, 28(2): 147-155.DOI: 10.1007/s10118-010-8231-x.
SYNTHESIS AND CHARACTERIZATION OF ORGANOSOLUBLE POLYAMIDES FROM QUINOXALINE BASED DIAMINE
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 1H-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°C and good thermal stability with the char yields in the range of 65%-82% at 600°C in nitrogen.
Abstract
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 1H-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°C and good thermal stability with the char yields in the range of 65%-82% at 600°C in nitrogen.
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