悬垂的异氰酸酯和含环氧化物共聚物:合成,与胺的顺序双官能团化,和表面修饰

Nisa Demirbilek, Nergiz Cengiz, Tugce N. Gevrek
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引用次数: 0

摘要

摘要聚合物携带不同的反应基团,可以正交功能化是设计多功能材料所需要的。虽然已经报道了几种正交功能化聚合物,但大多数工作使用的是对不同官能团反应的手柄。然而,聚合物对具有相同官能团的分子具有正交反应的例子很少。在这项工作中,我们报告了可以使用不同的含胺分子依次功能化的聚合物材料。本文合成了含异氰酸酯和环氧化物基团的共聚物,并研究了它们与含胺分子的顺序官能化。我们表明,这种共聚物可以首先在室温下通过异氰酸酯基团缀合与特定的含胺分子官能化。然后,在65℃下通过环氧胺反应,可以附着不同的含胺分子。通过1H NMR和FTIR光谱技术对母体和随后的官能化共聚物进行了化学表征,以建立正交官能化。此外,通过异氰酸-胺反应,环氧侧链被用作聚合物的表面锚定基团。这种获得正交反应性胺功能化共聚物及其衍生表面的直接方法将成为各种生物医学应用的有吸引力的材料。图形抽象
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pendant isocyanate and epoxide-containing copolymers: synthesis, sequential dual-functionalization with amines, and surface modifications
Abstract Polymers carrying different reactive groups that can be orthogonally functionalized are desirable for the design of multi-functionalizable materials. While several orthogonally functionalizable polymers have been reported, most of the work utilizes handles that are reactive toward different functional groups. However, examples of polymers that are orthogonally reactive toward molecules bearing the same functional group are rare. In this work, we report polymeric materials that can be sequentially functionalized using different amine-bearing molecules. Herein, we synthesized isocyanate and epoxide group containing copolymers, and investigated their sequential functionalization with amine-containing molecules. We show that such copolymers can be first functionalized with a particular amine-bearing molecule at room temperature, using conjugation through the isocyanate group. Thereafter, a different amine-containing molecule can be attached through the epoxy-amine reaction at 65 °C. Chemical characterizations of parent and subsequently functionalized copolymers were done by 1H NMR and FTIR spectroscopy techniques, to establish orthogonal functionalization. Additionally, the epoxide side chains were utilized as surface anchoring group after the functionalization of the polymer via isocyanate-amine reaction. This straightforward approach for obtaining orthogonally reactive amine-functionalizable copolymers, and surfaces derived thereof, would be attractive materials for various biomedical applications. Graphical abstract
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