个人信息Personal Information
研究员
博士生导师
硕士生导师
任职 : 高分子材料系副系主任
性别:男
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A407室
联系方式:Tel.: 0411-84986191
电子邮箱:liuch1115@dlut.edu.cn
Phthalonitrile-functional multiple arylene ether nitrile-containing phthalazinone moiety: facile synthesis, curing, and properties
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论文类型:期刊论文
发表时间:2014-08-01
发表刊物:HIGH PERFORMANCE POLYMERS
收录刊物:SCIE、EI
卷号:26
期号:5
页面范围:540-549
ISSN号:0954-0083
关键字:Cross-linking; phthalonitrile; solubility; high-performance polymer
摘要:This article discloses a series of processable multiple phthalazinone-based ether nitriles with various contents of phthalonitrile ends (compounds 4a-4e) and compares the cyclization feasibility of terminal phthalonitrile and pendant cyano group. Compounds 4a-4e were synthesized by facile polycondensation of excess 4-(4-hydroxyphenyl)-2,3-phthalazine-1-one (compound 1) with 2,6-difluorobenzonitrile (compound 2), followed by end-capping of 4-nitrophthalonitrile (compound 4). Their number-averaged molecular weights (M(n)s) and glass transitions can be well tailored by adjusting reactant ratio. Compounds 4a-4e are readily soluble in N-methyl-2-pyrrolidone, N, N-dimethylacetamide, dimethyl sulfoxide, N, N-dimethylformamide, and chloroform and hence can be processed either from their solutions or from melts. On mixing with trace amount of bis(4-aminophenyl) sulfone (compound 5), all oligomers were cross-linked to insoluble networks (compounds 6a-6d) except the high-molecular-weight 4e with the lowest phthalonitrile content. The phthalonitrile is found to be an effectively reactive site for cross-linking, whereas the pendant cyano group in multiple ether nitriles hardly undergoes any reaction confirmed by model reaction. Compounds 6a-6d maintain good structural integrity upon heating to 450 degrees C and exhibit superior thermal stabilities compared with the known phthalazinone polymers. Compounds 6a-6d exhibit high flexural strength (98-111 MPa) as well as limited water absorption (2.2-2.7 wt%) under ambient conditions over a course of 30 days, permitting them to be promising candidates for organic electronics and automotives.