主链聚酰亚胺的合成与表征

J. C. Salamone, R. E. Richard, A. C. Watterson
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引用次数: 0

摘要

制备了三种新型的主链聚芳酰亚胺,在主链上含有刚性和/或柔性基团。以双二甲基肼和二卤化物为原料,在室温下通过Menschulkin反应合成了该聚合物前驱体,得到了肼离子烯。以类似的方式,还制备了低分子量模型化合物,以确定碘烯聚合物的结构。结果发现,离子烯在水的单独存在下全部或至少部分转化为亚胺形式,而模型阳离子化合物在转化为相应的亚胺之前需要强碱。通过红外光谱和NMK光谱以及稀溶液粘度对这些新聚合物进行了表征。初步溶液性质表明,该聚合物的肼形式表现为聚电解质,而亚胺形式表现为中性聚合物。
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Synthesis and characterization of main-chain polyaminimides

Three novel main-chain polyarninimides were prepared containing rigid and/or flexible groups within the backbone. The polymer precursors were initially synthesized from bis-dimethylhydrazides and dihalides at room temperature through the Menschulkin reaction, which yielded hydrazinium ionenes. In a similar fashion, low molecular weight model compounds were also prepared in order to confirm the structures of the ionene polymers. It was found that the ionenes were totally, or at least partially, converted o the aminimide form in the presence of water alone, while the model cationic compounds required a strong base before conversion to their corresponding aminimides. These new polymers were characterized by (heir infrared and NMK spectra, as well as dilute solution viscosity. Preliminary solution properties indicate that the hydrazinium form of the polymers behave as poly electrolytes, whereas the aminimide form behaves as a neutral polymer.

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