个人信息Personal Information
教授
博士生导师
硕士生导师
性别:女
毕业院校:大连理工大学
学位:博士
所在单位:化工学院
学科:高分子材料. 高分子化学与物理. 功能材料化学与化工
办公地点:大连理工大学西部校区化工实验楼A405
联系方式:手机:13009436945
电子邮箱:wangjinyan@dlut.edu.cn
Soluble and crosslinkable poly(phthalazinone ether ketone)s with pendent terminal ethynyl groups: synthesis, characterization and click modification
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论文类型:期刊论文
发表时间:2015-07-01
发表刊物:POLYMER INTERNATIONAL
收录刊物:SCIE、EI、Scopus
卷号:64
期号:7
页面范围:875-883
ISSN号:0959-8103
关键字:poly(arylene ether)s; ethynyl group; crosslinkable; click modification
摘要:New poly(phthalazinone ether ketone)s (PPEKs) with pendent terminal ethynyl groups were synthesized by the aromatic nucleophilic substitution (SNAr) polycondensation reaction of a new bisphenol monomer, 2-(3-ethynylphenyl)hydroquinone, with 4-(4-hydroxyphenyl)phthalazin-1(2H)-one and 4,4-bis(4-fluorophenyl) ketone, followed by click modification reaction with 1-azidopyrene. Fourier transform infrared and NMR spectral data of the model compound indicated that the terminal ethynyl groups were stable in SNAr reaction conditions, thus allowing the synthesis of the desired polymers. The PPEKs obtained with glass transition temperature (T-g) in the range 152-245 degrees C were amorphous, characterized by wide-angle X-ray diffraction, and dissolved in organic solvent to cast into transparent and flexible films. Differential scanning calorimetry results indicated that the curing reaction of the terminal ethynyl groups of the copolymers took place upon heating to 250 degrees C. The T-g of cured PPEKs was increased to about 260 degrees C. They also exhibited excellent thermal stability with 5% weight loss temperatures ranging from 448 to 527 degrees C in various atmospheres. The PPEKs with pendent terminal ethynyl groups were subsequently functionalized with pyrene through click reaction. A dilute chloroform solution displayed a red-shifted emission profile. (c) 2014 Society of Chemical Industry