Synthesis and properties of new thermosetting oligoimides containing terminal propargyl groups

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Russian Chemical Bulletin Pub Date : 2024-10-26 DOI:10.1007/s11172-024-4386-4
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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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.

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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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