TY - JOUR
T1 - Synthesis and characterization of novel aromatic poly(imide-benzoxazole) copolymers
AU - Hsu, Steve Lien Chung
AU - Luo, Guo Wei
AU - Chen, Hui Tzu
AU - Chuang, Shih Wei
PY - 2005/12/1
Y1 - 2005/12/1
N2 - New poly(imide-benzoxazole) copolymers were prepared directly from a dianhydride, a diacid chloride, and a bis(o-diaminophenol) monomer in a two-step method. In the first step, poly(amic acid-hydroxyamide) precursors were synthesized by low-temperature solution polymerization in an organic solvent. Subsequently, the thermal cyclodehydration of the poly(amic acid-hydroxyamide) precursors at 350 °C produced the corresponding poly(imide-benzoxazole) copolymers. The inherent viscosities of the precursor polymers were around 0.19-0.33 dL/g. The cyclized poly(imide-benzoxazole) copolymers had glass-transition temperatures in the range of 331-377 °C. The 5% weight loss temperatures ranged from 524 to 535 °C in nitrogen and from 500 to 514 °C in air. The poly(imide-benzoxazole) copolymers were amorphous, as evidenced by the wide-angle X-ray diffraction measurements. The structures of the precursor copolymers and the fully cyclized copolymers were characterized by Fourier transform infrared, 1H NMR, and elemental analysis.
AB - New poly(imide-benzoxazole) copolymers were prepared directly from a dianhydride, a diacid chloride, and a bis(o-diaminophenol) monomer in a two-step method. In the first step, poly(amic acid-hydroxyamide) precursors were synthesized by low-temperature solution polymerization in an organic solvent. Subsequently, the thermal cyclodehydration of the poly(amic acid-hydroxyamide) precursors at 350 °C produced the corresponding poly(imide-benzoxazole) copolymers. The inherent viscosities of the precursor polymers were around 0.19-0.33 dL/g. The cyclized poly(imide-benzoxazole) copolymers had glass-transition temperatures in the range of 331-377 °C. The 5% weight loss temperatures ranged from 524 to 535 °C in nitrogen and from 500 to 514 °C in air. The poly(imide-benzoxazole) copolymers were amorphous, as evidenced by the wide-angle X-ray diffraction measurements. The structures of the precursor copolymers and the fully cyclized copolymers were characterized by Fourier transform infrared, 1H NMR, and elemental analysis.
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U2 - 10.1002/pola.21093
DO - 10.1002/pola.21093
M3 - Article
AN - SCOPUS:30544432776
SN - 0887-624X
VL - 43
SP - 6020
EP - 6027
JO - Journal of Polymer Science, Part A: Polymer Chemistry
JF - Journal of Polymer Science, Part A: Polymer Chemistry
IS - 23
ER -