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Anomalous Isomeric Effect on the Properties of Bisphenol F?based Benzoxazines: Toward the Molecular Design for Higher Performance

机译:对双酚F?苯并恶嗪性能的异常同构效应:更高性能的分子设计。

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摘要

A series of 2,2′-, 2,4′-, and 4,4′-substituted benzoxazine monomers based on isomeric bisphenol F and aniline has been synthesized in order to obtain a basic set of design rules toward making higher performance polybenzoxazines. All the monomer structures are confirmed by ~1H and ~(13)C NMR, and the purity is calculated by ~1H NMR. The polymerization behavior is studied by differential scanning calorimetry (DSC) and in situ Fourier transform infrared spectroscopy (FT-IR), The rate of polymerization increases in the order 4,4′-, 2,4′-, and 2,2′-substituted monomer. After polymerization, the thermal stability and glass transition temperature (T_g) of each polymer are studied by thermogravimetric analysis (TGA) and temperature-modulated DSC. The polymer obtained from 2,2′-substituted monomer gives highest thermal stability as well as T_g, which is against many of such examples available in the literature. Discussions on understanding benzoxazine structure?property relationships have been provided.
机译:合成了一系列基于异构双酚F和苯胺的2,2'-,2,4'-和4,4'-取代的苯并恶嗪单体,以便获得一套基本的设计规则,以制备更高性能的聚苯并恶嗪。所有单体结构均通过〜1H和〜(13)C NMR确认,纯度通过〜1H NMR计算。通过差示扫描量热法(DSC)和原位傅里叶变换红外光谱(FT-IR)研究了聚合行为,聚合速率按4,4'-,2,4'-和2,2'的顺序增加-取代的单体。聚合后,通过热重分析(TGA)和温度调节的DSC研究每种聚合物的热稳定性和玻璃化转变温度(T_g)。由2,2'-取代的单体获得的聚合物具有最高的热稳定性以及T_g,这与文献中可获得的许多此类实例相反。已经提供了关于理解苯并恶嗪结构-性质关系的讨论。

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