刘程

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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

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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.