Hierarchical-Coassembly-Enabled 3D-Printing of Homogeneous and Heterogeneous Covalent Organic Frameworks

亚胺 聚合物 无定形固体 化学工程 自愈水凝胶 结晶度 化学 纳米技术 共价键 多孔性 材料科学 共价有机骨架 高分子化学 有机化学 催化作用 工程类
作者
Mingshi Zhang,Longyu Li,Qianming Lin,Miao Tang,Yuyang Wu,Chenfeng Ke
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:141 (13): 5154-5158 被引量:167
标识
DOI:10.1021/jacs.9b01561
摘要

Covalent organic frameworks (COFs) are crystalline polymers with permanent porosity. They are usually synthesized as micrometer-sized powders or two-dimensional thin films and membranes for applications in molecular storage, separation, and catalysis. In this work, we report a general method to integrate COFs with imine or β-ketoenamine linkages into three-dimensional (3D)-printing materials. A 3D-printing template, Pluronic F127, was introduced to coassemble with imine polymers in an aqueous environment. By limitation of the degree of imine polycondensation during COF formation, the amorphous imine polymer and F127 form coassembled 3D-printable hydrogels with suitable shear thinning and rapid self-healing properties. After the removal of F127 followed by an amorphous-to-crystalline transformation, three β-ketoenamine- and imine-based COFs were fabricated into 3D monoliths possessing high crystallinity, hierarchical pores with high surface areas, good structural integrity, and robust mechanical stability. Moreover, when multiple COF precursor inks were employed for 3D printing, heterogeneous dual-component COF monoliths were fabricated with high spatial precision. This method not only enables the development of COFs with sophisticated 3D macrostructure but also facilitates the heterogeneous integration of COFs into devices with interconnected interfaces at the molecular level.
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