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首页> 外文期刊>International Journal of Polymeric Materials >New Polymer Syntheses Part 53. Novel Polyamides of Diarylidenecycloalkanone Containing Azo Groups in the Polymer Backbone: Synthesis and Characterization
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New Polymer Syntheses Part 53. Novel Polyamides of Diarylidenecycloalkanone Containing Azo Groups in the Polymer Backbone: Synthesis and Characterization

机译:新的聚合物合成,第53部分。在聚合物主链中含有偶氮基的二亚芳基环烷酮的新型聚酰胺:合成和表征

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摘要

A new interesting class of polyamides of diarylidenecycloalkanone containing azo groups in the polymer backbone 6_(a-d) was synthesized by a solution polycondensation reaction of bis 2-aminoarylidene monomers 3_(a,b) with 4,4'-azodibenzoyl dichlorides and 3,3'-azodibenzoyl dichlorides in NMP as a solvent, using anhydrous LiCl as a catalyst at room temperature. The model compounds 4, 5 were synthesized by the interaction of one mole of bis 2-aminoarylidene monomers 3_(a,b) with two moles of benzoyl chloride using anhydrous LiCl as a catalyst in NMP at room temperature. The resulting polymers were characterized by elemental and spectral analyses, besides solubility and viscometry measurements. The thermal properties of those polymers were evaluated by TGA, DTG and DTA measurements and correlated to their structural units. X-ray analysis of the polymers showed that polyamides based on para-azo linkage have a higher degree of crystallinity than those based on meta-azo linkage in the region 20 = 5-60°. In addition, the morphological properties of selected examples were tested by SEM.
机译:通过双2-氨基亚芳基单体3_(a,b)与4,4'-偶氮二苯甲酰二氯和3,3的溶液缩聚反应,合成了新型有趣的一类在聚合物主链6_(ad)中包含偶氮基的二芳基亚环烷基酮在室温下,使用无水LiCl作为催化剂,在NMP中将'-偶氮二苯甲酰二氯化物用作溶剂。在室温下,在NMP中使用无水LiCl作为催化剂,通过使一摩尔的双2-氨基亚芳基单体3_(a,b)与两摩尔的苯甲酰氯相互作用来合成模型化合物4、5。除溶解度和粘度测定法外,所得聚合物还通过元素分析和光谱分析进行表征。这些聚合物的热性能通过TGA,DTG和DTA测量进行评估,并与它们的结构单元相关。聚合物的X射线分析表明,在20 = 5-60°的区域内,基于对偶氮键的聚酰胺比基于间偶氮键的聚酰胺具有更高的结晶度。另外,通过SEM测试了所选实施例的形态学特性。

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