通过点击化学和自动色谱的高通量生成嵌段共聚物库

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Elizabeth A. Murphy, Katherine G. Roth, Morgan W. Bates, Megan C. Murphy, Jerrick Edmund, Christopher M. Bates* and Craig J. Hawker*, 
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引用次数: 0

摘要

设计特定应用的嵌段共聚物具有挑战性,因为分子结构、自组装行为和体性能之间存在复杂的关系,而且设计空间大,传统上需要耗时、迭代的合成。为了克服这些挑战,本文报告了一种基于库的策略,利用活性酯基嵌段共聚物和自动化色谱,可以在不需要特定样品优化的情况下对广泛的成分和化学景观进行高通量探索。通过将自动化色谱与机器人合成和正交聚合后修饰化学相结合,我们有效地从单个合成的“母体”共聚物中生成了90个定义良好的嵌段共聚物的多样化文库。这种适应性强的方法能够有效地获得具有广泛组成、分子量、功能和性质的材料。通过将实验室自动化与点击化学相结合,这些见解将加速高性能应用的先进嵌段共聚物的发现和设计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-Throughput Generation of Block Copolymer Libraries via Click Chemistry and Automated Chromatography

High-Throughput Generation of Block Copolymer Libraries via Click Chemistry and Automated Chromatography

Designing block copolymers for specific applications is challenging because of the intricate relationship among molecular structure, self-assembly behavior, and bulk properties, which is compounded by a large design space that traditionally requires time-consuming, iterative synthesis. To overcome these challenges, here we report a library-based strategy leveraging an active ester-based block copolymer and automated chromatography which enables the high-throughput exploration of broad compositional and chemical landscapes without requiring sample-specific optimization. By integrating automated chromatography with robotic synthesis and orthogonal postpolymerization modification chemistry, we efficiently generated a diverse library of 90 well-defined block copolymers from a single as-synthesized “parent” copolymer. This adaptable method enables efficient access to materials with a wide range of compositions, molecular weights, functionalities, and properties. By integrating laboratory automation with click chemistry, these insights will accelerate the discovery and design of advanced block copolymers for high-performance applications.

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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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