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通过点击化学对仿生组装进行后修饰来获得先进功能材料。

Access to Advanced Functional Materials through Postmodification of Biomimetic Assemblies via Click Chemistry.

机构信息

Physical Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99354, United States.

Department of Chemical Engineering, University of Washington, Seattle, Washington 98195, United States.

出版信息

Biomacromolecules. 2024 Mar 11;25(3):1391-1407. doi: 10.1021/acs.biomac.3c01454. Epub 2024 Feb 29.

Abstract

The design, synthesis, and fabrication of functional nanomaterials with specific properties remain a long-standing goal for many scientific fields. The self-assembly of sequence-defined biomimetic synthetic polymers presents a fundamental strategy to explore the chemical space beyond biological systems to create advanced nanomaterials. Moreover, subsequent chemical modification of existing nanostructures is a unique approach for accessing increasingly complex nanostructures and introducing functionalities. Of these modifications, covalent conjugation chemistries, such as the click reactions, have been the cornerstone for chemists and materials scientists. Herein, we highlight some recent advances that have successfully employed click chemistries for the postmodification of assembled one-dimensional (1D) and two-dimensional (2D) nanostructures to achieve applications in molecular recognition, mineralization, and optoelectronics. Specifically, biomimetic nanomaterials assembled from sequence-defined macromolecules such as peptides and peptoids are described.

摘要

具有特定性质的功能纳米材料的设计、合成和制造仍然是许多科学领域的长期目标。序列定义的仿生合成聚合物的自组装为探索超越生物系统的化学空间以创造先进的纳米材料提供了一种基本策略。此外,对现有纳米结构的后续化学修饰是获得越来越复杂的纳米结构和引入功能的独特方法。在这些修饰中,点击反应等共价键合化学已成为化学家材料科学家的基石。在此,我们重点介绍了一些最近的进展,这些进展成功地将点击化学用于组装的一维(1D)和二维(2D)纳米结构的后修饰,以实现分子识别、矿化和光电应用。具体来说,描述了由肽和肽类似物等序列定义的大分子组装而成的仿生纳米材料。

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