首页> 外文期刊>WSEAS Transactions on Biology and Biomedicine >Grafted Copolymer Based on Chitosan and Poly(N-Isopropylacryl Amide) via Click Technique. I. Synthesis and Characterization
【24h】

Grafted Copolymer Based on Chitosan and Poly(N-Isopropylacryl Amide) via Click Technique. I. Synthesis and Characterization

机译:基于壳聚糖和聚(N-异丙基丙烯酰胺)的接枝共聚物通过咔哒技术。 I.合成和表征

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

As chitosan's solubility represents a drawback for further applications, the functionalization of chitosan became attractive by a variety of chemical methods. The present study deals with the chemical modification of chitosan by using click chemistry technique as versatile tool being easy to perform with high yields and no additional by products. The approach used herein was to attach a responsive moiety (e.g. NIPAAm, HEMA or DMAEMA) on the macromolecular chain of chitosan via an azide-alkyne coupled reaction. More specifically, the reaction occurred between azide-chitosan and alkyne terminated responsive polymer. The method includes the modification of chain transfer agent with alkyne terminated groups, polymerization of responsive monomer, azidation steps of chitosan and final click reaction between two end products. Structure of end products and intermediaries were confirmed by the FT-IR and H-NMR spectra. Thermal characterization was performed showing different thermal behavior with the chemical modification. As main outcome, chitosan-g-PNIPAAm was obtained, the structure being confirmed by the disappearance of azide group and the presence of triazole moiety within the final product. The new approach of advancing the reaction via alkyne terminated-PNIPAAm, synthesized by RAFT, seemed to be successful as verified by 1H-NMR. Thermal properties revealed a better thermal stability for the new polymeric materials as the structure was more complex.
机译:由于壳聚糖的溶解度代表了进一步应用的缺点,壳聚糖的官能化因各种化学方法而变得有吸引力。本研究涉及壳聚糖的化学改性,通过使用咔哒化化学技术作为多功能工具,易于高产率,并且产品不额外。这里使用的方法是通过叠氮化物 - 炔烃偶联反应在壳聚糖的大分子链上附着响应部分(例如Nipaam,Hema或Dmaema)。更具体地,反应发生在叠氮化物 - 壳聚糖和炔烃之间的反应性响应聚合物之间。该方法包括用炔烃封端基团的链转移剂的改性,响应式单体的聚合,壳聚糖的蒸叠步骤和两端产物之间的反应。通过FT-IR和H-NMR光谱证实了最终产品和中间体的结构。进行热表征,显示出不同的热行为与化学改性。作为主要结果,获得了壳聚糖-G-PNIPAAM,通过叠氮基团的消失和最终产物中的三唑部分存在来证实该结构。通过筏合成的炔烃终止-PnipAam推进反应的新方法似乎是成功的,如1H-NMR验证。热性能显示新型聚合物材料的更好的热稳定性,因为该结构更复杂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号