Hasegawa Masatoshi, Hishiki Tomoaki
Department of Chemistry, Faculty of Science, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8510, Japan.
Polymers (Basel). 2020 Apr 8;12(4):859. doi: 10.3390/polym12040859.
A series of ester-linked diamines, with different lengths and substituents, was synthesized to obtain poly(ester imide)s (PEsIs) having improved properties. A substituent-free ester-linked diamine (AB-HQ) was poorly soluble in -methyl-2-pyrrolidone at room temperature, which forced the need for polyaddition by adding tetracarboxylic dianhydride solid into a hot diamine solution. This procedure enabled the smooth progress of polymerization, however, accompanied by a significant decrease in the molecular weights of poly(amic acid)s (PAAs), particularly when using hydrolytically less stable pyromellitic dianhydride. On the other hand, the incorporation of various substituents (-CH, -OCH, and phenyl groups) to AB-HQ was highly effective in improving diamine solubility, which enabled the application of the simple polymerization process without the initial heating of the diamine solutions, and led to PAAs with sufficiently high molecular weights. The introduction of bulkier phenyl substituent tends to increase the coefficients of thermal expansion (CTE) of the PEsI films, in contrast to that of the small substituents (-CH, -OCH). The effects of ester-linked diamines, consisting of longitudinally further extended structures, were also investigated. However, this approach was unsuccessful due to the solubility problems of these diamines. Consequently, the CTE values of the PEsIs, obtained using longitudinally further extended diamines, were not as low as we had expected initially. The effects of substituent bulkiness on the target properties, and the dominant factors for water uptake () and the coefficients of hygroscopic expansion (CHE), are also discussed in this study. The PEsI derived from methoxy-sustituted AB-HQ analog and 3,3',4,4'-biphenyltetracarboxylic dianhydride achieved well-balanced properties, i.e., a very high (424 °C), a very low CTE (5.6 ppm K), a low (0.41%), a very low CHE value (3.1 ppm/RH%), and sufficient ductility, although the 26 μm-thick film narrowly missed certification of the V-0 standard in the UL-94V test. This PEsI film also displayed a moderate ε (3.18) and a low tan δ (3.14 × 10) at 10 GHz under 50% RH and at 23 °C. Thus, this PEsI system is a promising candidate as a novel dielectric substrate material for use in the next generation of high-performance flexible printed circuit boards operating at higher frequencies (≥10 GHz).
合成了一系列具有不同长度和取代基的酯键二胺,以获得性能得到改善的聚(酯酰亚胺)(PEsIs)。一种无取代基的酯键二胺(AB-HQ)在室温下在N-甲基-2-吡咯烷酮中的溶解度很差,这使得需要通过将四羧酸二酐固体加入热的二胺溶液中来进行加聚反应。该方法使聚合反应顺利进行,然而,聚(酰胺酸)(PAAs)的分子量显著降低,特别是在使用水解稳定性较差的均苯四甲酸二酐时。另一方面,在AB-HQ中引入各种取代基(-CH₃、-OCH₃和苯基)对提高二胺的溶解度非常有效,这使得可以应用简单的聚合工艺而无需预先加热二胺溶液,并得到具有足够高分子量的PAAs。与小取代基(-CH₃、-OCH₃)相比,引入体积更大的苯基取代基往往会增加PEsI薄膜的热膨胀系数(CTE)。还研究了由纵向进一步延伸结构组成的酯键二胺的影响。然而,由于这些二胺的溶解性问题,该方法未成功。因此,使用纵向进一步延伸的二胺获得的PEsIs的CTE值没有我们最初预期的那么低。本研究还讨论了取代基体积对目标性能的影响,以及吸水率()和吸湿膨胀系数(CHE)的主要影响因素。由甲氧基取代的AB-HQ类似物和联苯四甲酸二酐衍生的PEsI具有良好的平衡性能,即非常高的玻璃化转变温度(Tg,424℃)、非常低的CTE(5.6 ppm/K)、低吸水率(0.41%)、非常低的CHE值(3.1 ppm/RH%)和足够的延展性,尽管26μm厚的薄膜在UL-94V测试中勉强未能达到V-0标准的认证。该PEsI薄膜在50%RH和23℃下,在10 GHz时还显示出适中的介电常数(ε,3.18)和低损耗角正切(tanδ,3.14×10⁻³)。因此,这种PEsI体系作为一种新型介电基板材料,有望用于下一代在更高频率(≥10 GHz)下工作的高性能柔性印刷电路板。