具有可调水溶性的多糖氨基甲酸酯和混合氨基甲酸酯的合成与表征

IF 6.2 Q1 CHEMISTRY, APPLIED
Martin Gericke, Zakaria Atmani, Lennart Hendrik Skodda, Thomas Heinze
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引用次数: 0

摘要

我们合成了具有两类功能性的多糖衍生物:用于点击化学方法的活性基团和可调节产物水溶性的基团。以取代度(DS)在 0.6 至 3.0 之间的木聚糖苯基碳酸盐(XPCs)和纤维素苯基碳酸盐(CPCs)为起始材料进行了制备。通过模块化合成方法,这些碳酸酯衍生物与不同的胺进行转化,得到了具有(i)活性炔基或糠基和/或(ii)亲水性羟烷基或叔氨基的功能性木聚糖氨基甲酸酯(XCs)和纤维素氨基甲酸酯(CCs)。这两种官能团可通过方便的一锅法分别或同时引入。成功制备了具有低、中和高 DS 值(0.6 至 2.5)的混合多糖氨基甲酸酯,并对其进行了表征。通过改变两个亲水取代基的类型和 DS 值,可以调节氨基甲酸酯和混合氨基甲酸酯的水溶性。令人惊讶的是,一些产物显示出较低或较高的临界溶液温度(LCSTs、UCSTs)。因此,我们对水溶液中的热可逆相变进行了研究。这项工作中获得的产品在通过选择性共价交联制备水凝胶以及制备热致伸缩性生物材料方面大有可为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis and characterization of polysaccharide carbamates and mixed carbamates with tunable water solubility

Synthesis and characterization of polysaccharide carbamates and mixed carbamates with tunable water solubility

Polysaccharide derivatives with two types of functionalities were synthesized; reactive groups for click-chemistry approaches and groups that can tune the water solubility of the products. Xylan phenylcarbonates (XPCs) and cellulose phenylcarbonates (CPCs) with degrees of substitution (DS) ranging from 0.6 to 3.0 were prepared as starting materials. In a modular synthesis approach, these carbonate derivatives were converted with different amines to obtain functional xylan carbamates (XCs) and cellulose carbamates (CCs) with (i) reactive alkynyl- or furfuryl groups and / or (ii) hydrophilic hydroxyalkyl or tertiary amino groups. Both types of functionalities were introduced separately or simultaneously in a convenient one-pot-approach. Mixed polysaccharide carbamates with low, intermediate, and high DS values (0.6 to 2.5) were successfully prepared and characterized. The water solubility of the carbamates and mixed carbamates was tuned by variation of the type and DS of the two hydrophilic substituents. Surprisingly, some of the products showed lower or upper critical solution temperatures (LCSTs, UCSTs). Thus, the thermoreversible phase transition in aqueous solutions was studied. The products obtained in this work are very promising for the preparation of hydrogels through selective covalent crosslinking as well as for the fabrication of thermoresponsive biomaterials.

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