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苯乙炔封端的可交联含氟聚芳醚的合成及性能 被引量:6

Synthesis and Properties of Crosslinkable Fluorinated Poly(aryl ethers) Terminated with Phenylethynyl Moieties
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摘要 The crosslinkable trifluoromethylated poly(aryl ethers) terminated with phenylethynyl moieties(11F-PAE-PEP)s were prepared in two step syntheses. The structure of 11F-PAE-PEP was confirmed by FTIR and 1H NMR. The crosslinking behavior was studied by DSC. There is a remarkable increase of T g after crosslinking of the poly(aryl ethers). The T g values of crosslinked polymers were 437 and 446 K, respectively. The crosslinked polymers could not be soluble in common organic solvents, such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidinone, chloroform, and tetrahydrofuran. The temperatures at a 5% mass loss of the crosslinked polymers in air were above 789 K. They showed a good optical property, too. This kind of polymers will be the promising materials used as the microelectronics and optical waveguide devices. The crosslinkable trifluoromethylated poly(aryl ethers) terminated with phenylethynyl moieties(11F-PAE-PEP)s were prepared in two step syntheses. The structure of 11F-PAE-PEP was confirmed by FTIR and 1H NMR. The crosslinking behavior was studied by DSC. There is a remarkable increase of T g after crosslinking of the poly(aryl ethers). The T g values of crosslinked polymers were 437 and 446 K, respectively. The crosslinked polymers could not be soluble in common organic solvents, such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-2-pyrrolidinone, chloroform, and tetrahydrofuran. The temperatures at a 5% mass loss of the crosslinked polymers in air were above 789 K. They showed a good optical property, too. This kind of polymers will be the promising materials used as the microelectronics and optical waveguide devices.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2003年第8期1522-1524,共3页 Chemical Journal of Chinese Universities
基金 国家自然科学基金 (批准号 :5 0 2 0 30 0 4)资助
关键词 苯乙炔端基 交联 含氟聚芳醚 合成 性能 含氟聚合物 光电集成器件 Poly(aryl ether) Fluorinated polymer Cross-linkage
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