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Synthesis and Thermal Crosslinking Behavior of Poly(aryl ether ketone)s Containing 1,4-Naphthalene Moieties
作者姓名:NIUYa-ming  ZHANGYun-he  CHENXing-bo  WANGGui-bin  JIANGZhen-hua
作者单位:ResearchCenterofJilinUniversityforSuperEngineeringPlastics,MinistryofEducation,JilinUniversity,Changchun130012,P.R.China
摘    要:A new monomer, 1,4-bis(4-fluorobenzoyl) naphthalene (compound 2) was synthesized via a two-step reaction. 1,4-Naphthalenedicarboxylic acid chloride (compound 1) was prepared by using the acyl chlorization reaction of 1,4-naphthalenedicarboxylic acid with thionyl chloride. The Friedel-Crafts acylation of compound 1 with fluorobenzene afforded compound 2 in a 80% yield. The polycondensation of compound 2 with various bisphenols in tetramethylene sulfone(TMS) in the presence of excess potassium carbonate as a condensation reagent was carried out at 210℃ to quantitatively afford the corresponding poly(aryl ether ketone)s (compounds 3-8) containing 1,4-naphthalene moieties. Thermal analyses showed that the polymers have Tg values ranging from 496 to 500 K and are thermally stable in air with initial mass loss above 500℃. These novel polymers exhibited an excellent solubility in organic solvents including NMP, DMAc, and chloroform, etc. In addition, the glass transition temperatures of these polymers increased and the polymers became insoluble in chloroform after treated at 260℃, indicating the occurrence of a thermal crosslinking reaction.

关 键 词:合成  热交联行为  聚(芳基醚酮)s  1  4-萘  热塑性塑料
收稿时间:2004-11-10

Synthesis and Thermal Crosslinking Behavior of Poly(aryl ether ketone)s Containing 1,4-Naphthalene Moieties
NIUYa-ming ZHANGYun-he CHENXing-bo WANGGui-bin JIANGZhen-hua.Synthesis and Thermal Crosslinking Behavior of Poly(aryl ether ketone)s Containing 1,4-Naphthalene Moieties[J].Chemical Research in Chinese University,2005,21(1):109-113.
Authors:NIU Ya-ming  ZHANG Yun-he  CHEN Xing-bo  WANG Gui-bin  JIANG Zhen-Hua
Institution:Research Center of Jilin University for Super Engineering Plastics, Ministry of Education, Jilin University, Changchun 130012, P. R. China
Abstract:A new monomer, 1,4-bis(4-fluorobenzoyl) naphthalene(compound 2) was synthesized via a two-step reaction. 1,4-Naphthalenedicarboxylic acid chloride(compound 1) was prepared by using the acyl chlorization reaction of 1,4-naphthalenedicarboxylic acid with thionyl chloride. The Friedel-Crafts acylation of compound 1 with fluorobenzene afforded compound 2 in a 80% yield. The polycondensation of compound 2 with various bisphenols in tetramethylene sulfone(TMS) in the presence of excess potassium carbonate as a condensation reagent was carried out at 210 ℃ to quantitatively afford the corresponding poly(aryl ether ketone)s(compounds 3_8) containing 1,4-naphthalene moieties. Thermal analyses showed that the polymers have Tg values ranging from 496 to 500 K and are thermally stable in air with initial mass loss above 500 ℃. These novel polymers exhibited an excellent solubility in organic solvents including NMP, DMAc, and chloroform, etc. In addition, the glass transition temperatures of these polymers increased and the polymers became insoluble in chloroform after treated at 260 ℃, indicating the occurrence of a thermal crosslinking reaction.
Keywords:Poly(aryl ether ketone)  Naphthalene derivatives  Friedel-Crafts acylation  Thermal crosslinking properties
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