Multi-Functionalization of Solid Support via Zn(II)-Mediated Chirality-Directed Self-Assembly

Max S. Overshiner, Shuyuan Tian, Kegan B. Morrow, Jailyn R. Wendt, John Zhou, Hannah M. Briggs, Gerardo B. Márquez, K. Kilway, S. Moteki
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Abstract

Establishing a strategy for realizing programmed self-assembly is critical in manufacturing materials with functional hybrid structures. In this work, we introduce a robust methodology for enabling multi-component self-assembly using the concept of chirality-directed self-assembly. A specific combination of heterochiral Zn(II) methylene bis(oxazoline) (BOX) complexes can be selectively generated when combinations of enantiomers of chiral BOX ligands are mixed in the presence of Zn(Oac)2. The resulting Zn(II) BOX complexes, unlike non-covalent bonds, are highly stable and stay intact at elevated temperatures, yet can be reversibly disintegrated under mild conditions using EDTA. This approach can be easily applied to multi-functionalize various solid supports enabling the one-pot generation of multi-functional hybrid struc-

Abstract Image

Zn(II)介导的手性定向自组装实现固体载体的多功能化
建立实现程序自组装的策略对于制造具有功能杂化结构的材料至关重要。在这项工作中,我们介绍了一种使用手性定向自组装概念实现多组分自组装的稳健方法。当手性BOX配体的对映体的组合在Zn(Oac)2的存在下混合时,可以选择性地产生异手性Zn(II)亚甲基双(恶唑啉)(BOX)配合物的特定组合。与非共价键不同,得到的Zn(II)BOX复合物高度稳定,在高温下保持完整,但可以在使用EDTA的温和条件下可逆分解。这种方法可以很容易地应用于多种功能化的固体载体,从而实现多功能杂化结构的一锅生产-
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来源期刊
CiteScore
3.70
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0.00%
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审稿时长
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