Growth of single-crystal imine-linked covalent organic frameworks in water using amphiphilic amino-acid derivatives

Zhipeng Zhou, Lei Zhang, Yonghang Yang, Iñigo J. Vitorica-Yrezabal, Honglei Wang, Fanglin Tan, Li Gong, Yuyao Li, Pohua Chen, Xin Dong, Zihao Liang, Jing Yang, Chao Wang, Yuexian Hong, Yi Qiu, Armin Gölzhäuser, Xudong Chen, Haoyuan Qi, Sihai Yang, Wei Liu, Junliang Sun, Zhikun Zheng
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Abstract

Abstract Living organisms explored functional biomolecules such as proteins bearing glycine to create single-crystals of minerals in water without resorting to low levels of supersaturation. However, this strategy remains poorly effective in the crystallization of organic polymers. Here, we report a biomimetic strategy and its implementation to synthesize single-crystals of an important class of organic polymers - covalent organic frameworks (COFs) in water under ambient conditions. The strategy explores assemblies of amphiphilic molecules of glycine derivatives as dynamic barriers to separate monomers in water and oil phases, thereby regulating the polymerization and crystallization processes. Monomers first polymerized into disordered solids regardless of concentration variations over five orders of magnitude, then transformed into crystals in a step-by-step fashion with monomers and dimers as main building units, affording six types of single-crystals at the gram-scale with yields of ≥ 92% besides a two-dimensional COF-366. This study will be a valuable addition to the repertoire of crystallization path and methodology of organic polymers and promote their industrial applications.
用两亲性氨基酸衍生物在水中生长单晶亚胺连接的共价有机框架
生物体探索了功能生物分子,如含有甘氨酸的蛋白质,以在水中产生矿物质单晶,而不需要求助于低水平的过饱和。然而,这种策略在有机聚合物的结晶中仍然效果不佳。在这里,我们报道了一种仿生策略及其在环境条件下在水中合成一类重要有机聚合物-共价有机框架(COFs)的单晶。该策略探索了甘氨酸衍生物的两亲分子组装作为分离水相和油相单体的动态屏障,从而调节聚合和结晶过程。单体首先聚合成无序固体,无论浓度变化超过5个数量级,然后以单体和二聚体为主要构建单元逐步转化为晶体,除了二维COF-366外,还提供了6种克级单晶,产率≥92%。本研究将为有机聚合物的结晶路径和结晶方法提供有价值的补充,并促进其工业应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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