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Synthesis and Polymerization of Bismaleimide Derived from 5(6)-amino-1(4′-aminophenyl)-1,3,3′-trimethyl indane

机译:5(6)-氨基-1(4€-氨基苯基)-1,3,3€-三甲基茚满衍生的双马来酰亚胺的合成和聚合

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摘要

The acid-catalyzed dimerization of α-methyl styrene led to the formation of trimethyl phenyl indane, which on nitration followed by reduction using hydrazine hydrate gave 5(6)-amino-1(4′-aminophenyl)-1,3,3′-trimethyl indane. This aromatic diamine was used to synthesize bismaleamic acid and imidized to yield bismaleimide. The bismaleamic acid was converted to prepolymer directly by imidizing it in refluxing toluene. All the materials synthesized were characterized using FTIR, 1H and 13C NMR. The direct inlet mass spectral characterizations were carried out for bismaleamic acid, bismaleimide and bismaleimide prepolymer. The fragmentation pattern was discussed in detail and the structure proposed was confirmed. The thermogravimetric studies were done for all the materials and kinetic parameters (energy of activation and frequency factor) were calculated using Dharwadkar and Kharkhanavala method. The structural changes occurring in the thermally polymerized bismaleimide and bismaleimide prepolymer were discussed.
机译:α-甲基苯乙烯的酸催化二聚导致形成的三甲基苯基茚满,硝化后再还原使用水合肼得到5(6)-氨基-1(4€-氨基苯基)-1,3, 3€-三甲基茚满。该芳族二胺用于合成双马来酰胺酸并被酰亚胺化以生成双马来酰亚胺。通过在回流的甲苯中将其酰亚胺化,将双马来酰胺酸直接转化为预聚物。使用FTIR, 1 H和 13 C NMR对所有合成的材料进行表征。对双马来酰胺酸,双马来酰亚胺和双马来酰亚胺预聚物进行直接入口质谱表征。详细讨论了碎片模式,并确定了所提出的结构。对所有材料进行了热重研究,并使用Dharwadkar和Kharkhanavala方法计算了动力学参数(活化能和频率因子)。讨论了在热聚合的双马来酰亚胺和双马来酰亚胺预聚物中发生的结构变化。

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  • 来源
    《Polymer-Plastics Technology and Engineering》 |2009年第2期|p.141-151|共11页
  • 作者单位

    Department of Polymer Technology, Kamaraj College of Engineering and Technology, India;

    Defense Materials and Stores Research and Development Establishment (DMSRDE), Kanpur, India;

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