TY - JOUR
T1 - Synthesis of Novel Fluorinated Poly(aryl ether ketone)s and Their Properties
AU - Qingze Jiao, Jiao
AU - Li, Na
AU - Zhang, Pei
AU - Wang, Shanshan
AU - Zhao, Yun
AU - Feng, Caihong
AU - Lv, Yuzhen
N1 - Publisher Copyright:
© 2021, Pleiades Publishing, Ltd.
PY - 2021/7
Y1 - 2021/7
N2 - Abstract: A novel bisphenol monomer, (4-trifluoromethyl) phenylhydroquinone, was synthesized using a three-step synthetic procedure. Two aromatic poly(aryl ether ketone)s were then prepared via a nucleophilic polycondensation reaction of (4-trifluoromethyl) phenylhydroquinone and two difluorinated aromatic ketones, respectively. As-synthesized poly(aryl ether ketone)s show a high thermal stability, and the temperatures at 5% weight loss are above 530°C in N2 atmosphere. The solubility of the polymers is improved by introduction of bulky pendant groups. All the polymers form transparent, strong, and flexible films with tensile strengths of 65–70 MPa, Young’s moduli of 1.6–2.0 GPa, and elongations at break of 36–42%. Polymer films have low dielectric constants of 2.6–2.7 at 1 MHz and low water absorption of 0.21–0.25%. In addition, they have low absorptions at the telecommunication wavelengths of 1300 and 1550 nm.
AB - Abstract: A novel bisphenol monomer, (4-trifluoromethyl) phenylhydroquinone, was synthesized using a three-step synthetic procedure. Two aromatic poly(aryl ether ketone)s were then prepared via a nucleophilic polycondensation reaction of (4-trifluoromethyl) phenylhydroquinone and two difluorinated aromatic ketones, respectively. As-synthesized poly(aryl ether ketone)s show a high thermal stability, and the temperatures at 5% weight loss are above 530°C in N2 atmosphere. The solubility of the polymers is improved by introduction of bulky pendant groups. All the polymers form transparent, strong, and flexible films with tensile strengths of 65–70 MPa, Young’s moduli of 1.6–2.0 GPa, and elongations at break of 36–42%. Polymer films have low dielectric constants of 2.6–2.7 at 1 MHz and low water absorption of 0.21–0.25%. In addition, they have low absorptions at the telecommunication wavelengths of 1300 and 1550 nm.
UR - http://www.scopus.com/inward/record.url?scp=85114022152&partnerID=8YFLogxK
U2 - 10.1134/S1560090421040059
DO - 10.1134/S1560090421040059
M3 - Article
AN - SCOPUS:85114022152
SN - 1560-0904
VL - 63
SP - 333
EP - 340
JO - Polymer Science - Series B
JF - Polymer Science - Series B
IS - 4
ER -