基于纤维素的新型多两性电解质的合成与结构表征

IF 9.9 Q1 MATERIALS SCIENCE, COMPOSITES Advanced Industrial and Engineering Polymer Research Pub Date : 2022-01-01 DOI:10.1016/j.aiepr.2021.06.001
Annett Pfeifer, Agnes Kemmer, Thomas Heinze
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引用次数: 1

摘要

以甲磺酸纤维素为原料,采用高分子模拟反应合成了新型氨基纤维素磺酸基聚合物。为了获得不同的氨基纤维素作为起始构建块,对不对称和对称n -烷基化二胺进行了全面的研究。在与不对称二胺的反应中,结果表明,主要的氨基部分反应较好。由此得到的衍生物由中性主结构单元和阳离子侧结构单元组成,目前尚未描述。为了研究氨基纤维素6-脱氧-6-(N,N,N ',N ' -四亚甲基乙二胺)的反应性,以纤维素为原料,通过与1,3-propansultone的转化,设计了新型多两性聚合物。通过1D和2d核磁共振光谱进行了详细的结构表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Synthesis and structure characterization of novel polyampholytes based on cellulose

Sulfobetainic polymers were synthesized by polymeranalogous reaction of new amino celluloses starting from cellulose tosylate. To obtain different amino celluloses as starting building blocks, a comprehensive study with a selection of asymmetric and symmetric N-alkylated diamines was performed. For reaction with asymmetric diamines, it turned out that the primary amino moiety reacts preferably. Derivatives thus obtained consist in a neutral main structural unit and a cationic side structural unit, which is not described up to now. In order to investigate the reactivity of the amino celluloses 6-deoxy-6-(N,N,N′,N′-tetramethylethylenediamino) cellulose was used as uniform starting material for the design of novel polyampholytes by conversion with 1,3-propansultone. Detailed structure characterization was implemented by means of 1D and 2D-NMR spectroscopy.

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来源期刊
Advanced Industrial and Engineering Polymer Research
Advanced Industrial and Engineering Polymer Research Materials Science-Polymers and Plastics
CiteScore
26.30
自引率
0.00%
发文量
38
审稿时长
29 days
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