首页> 外文期刊>Journal of Polymer Science, Part A. Polymer Chemistry >Isomeric compositions in amide acids and poly(amic acid)s derived from 1-(trifluouomethyl)-2,3,5,6-benzenetetracarboxylic dianhydride
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Isomeric compositions in amide acids and poly(amic acid)s derived from 1-(trifluouomethyl)-2,3,5,6-benzenetetracarboxylic dianhydride

机译:1-(三氟甲基)-2,3,5,6-苯四甲酸二酐衍生的酰胺酸和聚(酰胺酸)中的异构体组成

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Two different poly(amic acid)s were synthesized by the polycondensations of 1-(trifluoromethyl)-2,3,5,6-benzenetetracarboxylic dianhydride (CF3DAN) with p-phenylene diamine and benzidine. In addition, an amide acid model compound was prepared from CF3DAN and aniline. Isomeric units in the poly(amic acid)s as well as the amide acid were investigated by H-1 and C-13-nuclear magnetic resonance (NMR) spectroscopies. Spectroscopic results indicate that the major isomeric component was a CF3-meta-isomeric unit centered on the aromatic carbon substituted with the trifluoromethyl group. In particular, the amide acid compound was determined to be composed of 80 mol % CFS-meta-isomer and 20 mol % H-meta-isomer. Therefore, for the poly(amic acid)s, the minor isomeric component is speculated to be a H-meta-isomeric unit rather than a para-isomeric unit. The result might result mainly from the strong electron-withdrawable and bulky trifluoromethyl substituent in the CF3DAN monomer. The strong electron withdrawability might significantly enhance the reactivities of the adjacent carbons in the monomer to the nucleophilic attack of the amino nitrogen in the aniline and diamines, and consequently overcome the role of the bulkyness, ultimately leading to the amide acid and poly(amic acid)s rich with the CF3-meta-isomeric unit. In addition, a portion of the imide form was detected in the dried AN-CF3DAM-AN amide acid. Thus, the formation of imide linkage might be involved in a small portion for the dried poly(amic acid)s. (C) 1998 John Wiley & Sons, Inc. [References: 41]
机译:通过1-(三氟甲基)-2,3,5,6-苯四甲酸二酐(CF3DAN)与对苯二胺和联苯胺的缩聚反应合成了两种不同的聚酰胺酸。另外,由CF 3 DAN和苯胺制备酰胺酸模型化合物。通过H-1和C-13核磁共振(NMR)光谱研究了聚(酰胺酸)和酰胺酸中的异构体单元。光谱结果表明,主要的异构体组分是CF 3-元异构体单元,其中心位于被三氟甲基取代的芳族碳上。特别地,确定酰胺酸化合物由80mol%的CFS-元异构体和20mol%的H-元异构体组成。因此,对于聚(酰胺酸),推测其次要异构成分是H-元异构单元而不是对位异构单元。结果可能主要来自CF3DAN单体中的强吸电子性和庞大的三氟甲基取代基。强的电子吸收性可能会显着提高单体中相邻碳原子对苯胺和二胺中氨基氮的亲核攻击的反应性,因此克服了笨重的作用,最终导致了酰胺酸和聚酰胺酸)富含CF3-元异构单元。另外,在干燥的AN-CF 3 DAM-AN酰胺酸中检测到一部分酰亚胺形式。因此,对于干燥的聚(酰胺酸),酰亚胺键的形成可能涉及一小部分。 (C)1998 John Wiley&Sons,Inc. [参考:41]

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