Synthesis and properties of new thermosetting oligoimides containing terminal propargyl groups

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
V. S. Bochenkov, A. I. Ryzhkov, R. N. Shamsutdinova, M. S. Piskarev, V. L. Baklagin, A. Yu. Tsegelskaya, I. G. Abramov, A. I. Buzin, A. A. Kuznetsov
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引用次数: 0

Abstract

A series of new oligoimides based on 4,4- and 3,4-oxydianiline and 2,2-bis[(3,4-dicarboxyphenoxy)phenyl]propane dianhydride, possessing different average chain lengths, and containing terminal propargyl groups were synthesized according to an efficient single-step high-temperature polycyclocondensation method. Their molecular weight characteristics, solubility in organic solvents, thermal (DSC, TMA, and TGA), and rheological properties were studied. The synthesized oligoimides exhibited a significantly lower exothermic effect upon curing due to their elongated chain as compared to diimides. The oligoimides upon increasing the temperature enter into a viscous fluid state, in which they remain up to the curing onset temperature of 270–320 °C. The symmetry of structure of the diamine moiety (4,4-ODA or 3,4-ODA) and the molecular weight of oligoimides affect the temperature of transition to the viscous fluid state.

含端丙炔基团的新型热固性低聚酰亚胺的合成及其特性
采用高效的单步高温缩聚法合成了一系列基于 4,4- 和 3,4- 氧二苯胺和 2,2- 双[(3,4-二羧基苯氧基)苯基]丙烷二酐的新型低聚亚胺,它们具有不同的平均链长,并含有末端丙炔基团。研究了它们的分子量特性、在有机溶剂中的溶解性、热学(DSC、TMA 和 TGA)和流变学特性。与二亚胺相比,合成的低聚亚胺在固化时的放热效应明显较低,这是因为它们的链条较长。当温度升高时,低聚亚胺进入粘性流体状态,并一直保持到 270-320 °C 的固化起始温度。二胺分子结构的对称性(4,4-ODA 或 3,4-ODA)和低聚亚胺的分子量会影响向粘性流体状态转变的温度。
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来源期刊
Russian Chemical Bulletin
Russian Chemical Bulletin 化学-化学综合
CiteScore
2.70
自引率
47.10%
发文量
257
审稿时长
3-8 weeks
期刊介绍: Publishing nearly 500 original articles a year, by leading Scientists from Russia and throughout the world, Russian Chemical Bulletin is a prominent international journal. The coverage of the journal spans practically all areas of fundamental chemical research and is presented in five sections: General and Inorganic Chemistry; Physical Chemistry; Organic Chemistry; Organometallic Chemistry; Chemistry of Natural Compounds and Bioorganic Chemistry.
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