HEAT-RESISTANT, PYRIDINE-BASED POLYAMIDES CONTAINING ETHER AND ESTER UNITS WITH IMPROVED SOLUBILITY
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HEAT-RESISTANT, PYRIDINE-BASED POLYAMIDES CONTAINING ETHER AND ESTER UNITS WITH IMPROVED SOLUBILITY
HEAT-RESISTANT, PYRIDINE-BASED POLYAMIDES CONTAINING ETHER AND ESTER UNITS WITH IMPROVED SOLUBILITY
高分子科学(英文版)2010年28卷第1期 页码:29-37
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纸质出版:2010-01-20
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Hassan Ebadi a, Shahram Mehdipour-Ataei b. HEAT-RESISTANT, PYRIDINE-BASED POLYAMIDES CONTAINING ETHER AND ESTER UNITS WITH IMPROVED SOLUBILITY[J]. 高分子科学(英文版), 2010,28(1):29-37.
Hassan Ebadi a, Shahram Mehdipour-Ataei b. HEAT-RESISTANT, PYRIDINE-BASED POLYAMIDES CONTAINING ETHER AND ESTER UNITS WITH IMPROVED SOLUBILITY[J]. 2010, 28(1): 29-37.
Hassan Ebadi a, Shahram Mehdipour-Ataei b. HEAT-RESISTANT, PYRIDINE-BASED POLYAMIDES CONTAINING ETHER AND ESTER UNITS WITH IMPROVED SOLUBILITY[J]. 高分子科学(英文版), 2010,28(1):29-37.DOI:
Hassan Ebadi a, Shahram Mehdipour-Ataei b. HEAT-RESISTANT, PYRIDINE-BASED POLYAMIDES CONTAINING ETHER AND ESTER UNITS WITH IMPROVED SOLUBILITY[J]. 2010, 28(1): 29-37.DOI:
HEAT-RESISTANT, PYRIDINE-BASED POLYAMIDES CONTAINING ETHER AND ESTER UNITS WITH IMPROVED SOLUBILITY
as basic monomer for the preparation of polyamides
was prepared via three consecutive reactions. Nucleophilic substitution reaction of 1
4-dihydroxy benzene with 4-nitrobenzoyl chloride produced 4-hydroxyphenyl 4-nitrobenzoate (HPNB). Reduction of nitro groups to amino groups using Fe and HCl resulted in preparation of 4-hydroxyphenyl 4-aminobenzoate (HPAB). The diamine was synthesized through nucleophilic substitution reaction of HPAB with 2
6-dichloropyridine. The precursors and diamine were fully characterized by common methods
and the diamine was polycondensed with different diacid chlorides in the presence of an acid scavenger to prepare new polyamides. The polyamides were characterized
and their physical properties including thermal stability and behavior
inherent viscosity and solubility were studied.
Abstract
A diamine containing ether and ester units
as basic monomer for the preparation of polyamides
was prepared via three consecutive reactions. Nucleophilic substitution reaction of 1
4-dihydroxy benzene with 4-nitrobenzoyl chloride produced 4-hydroxyphenyl 4-nitrobenzoate (HPNB). Reduction of nitro groups to amino groups using Fe and HCl resulted in preparation of 4-hydroxyphenyl 4-aminobenzoate (HPAB). The diamine was synthesized through nucleophilic substitution reaction of HPAB with 2
6-dichloropyridine. The precursors and diamine were fully characterized by common methods
and the diamine was polycondensed with different diacid chlorides in the presence of an acid scavenger to prepare new polyamides. The polyamides were characterized
and their physical properties including thermal stability and behavior
inherent viscosity and solubility were studied.
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