Covalent organic frameworks (COFs) represent a highly versatile class of crystalline porous materials, formed by the deliberate assembly of organic building units into ordered two-dimensional (2D) and three-dimensional (3D) structures. Their unique combination of topological precision and tunable micro- or mesoporous architectures offers unmatched flexibility in material design. By selecting specific building units, reactive sites, and functional groups, COFs can be engineered to achieve customized skeletal, porous, and interfacial properties, opening the door to materials with optimized performance for diverse applications. Among recent advances, high-connectivity 3D COFs have emerged as a particularly exciting development, with their intricate network structures enabling unprecedented levels of structural complexity, stability, and functionality. This review provides a comprehensive overview of the synthesis strategies, topological design principles, structural characterization techniques, and emerging applications of high-connectivity 3D COFs. We explore their potential across a broad range of cutting-edge applications, including gas adsorption and separation, macromolecule adsorption, dye removal, photocatalysis, electrocatalysis, lithium-sulfur batteries, and charge transport. By examining these key areas, we aim to deepen the understanding of the intricate relationship between structure and function, guiding the rational design of next-generation COF materials. The continued advancements in this field hold immense promise for revolutionizing sectors such as energy storage, catalysis, and molecular separation, making high-connectivity 3D COFs a cornerstone for future technological innovations.
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http://dx.doi.org/10.1039/d4cs00703d | DOI Listing |
Chem Soc Rev
November 2024
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun 130012, P. R. China.
Covalent organic frameworks (COFs) represent a highly versatile class of crystalline porous materials, formed by the deliberate assembly of organic building units into ordered two-dimensional (2D) and three-dimensional (3D) structures. Their unique combination of topological precision and tunable micro- or mesoporous architectures offers unmatched flexibility in material design. By selecting specific building units, reactive sites, and functional groups, COFs can be engineered to achieve customized skeletal, porous, and interfacial properties, opening the door to materials with optimized performance for diverse applications.
View Article and Find Full Text PDFJ Am Chem Soc
September 2024
Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization, School of Chemistry, South China Normal University, Guangzhou 510006, P.R. China.
The connectivity (valency) of building blocks for constructing 3D covalent organic frameworks (COFs) has long been limited to 4, 6, 8, and 12. Developing a higher connectivity remains a great challenge in the field of COF structural design. Herein, this work reports a hierarchical expansion strategy for making 16-connected building blocks to construct 3D COFs with sqc topology.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
April 2024
Beijing Advanced Innovation Center for Materials Genome Engineering, Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials, Department of Chemistry and Chemical Engineering, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing, 100083, China.
Developing high connectivity (>8) three-dimensional (3D) covalent organic frameworks (COFs) towards new topologies and functions remains a great challenge owing to the difficulty in getting high connectivity organic building blocks. This however represents the most important step towards promoting the diversity of COFs due to the still limited dynamic covalent bonds available for constructing COFs at this stage. Herein, highly connected phthalocyanine-based (Pc-based) 3D COFs MPc-THHI-COFs (M=H, Ni) were afforded from the reaction between 2,3,9,10,16,17,23,24-octacarboxyphthalocyanine M(TAPc) (M=H, Ni) and 5,5',5'',5''',5'''',5'''''-(triphenylene-2,3,6,7,10,11-hexayl)hexa(isophthalohydrazide) (THHI) with 12 connecting sites.
View Article and Find Full Text PDFJ Am Chem Soc
February 2024
Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.
The structural exploration of three-dimensional covalent organic frameworks (3D COFs) is of great significance to the development of COF materials. Different from structurally diverse MOFs, which have a variety of connectivity (3-24), now the valency of 3D COFs is limited to only 4, 6, and 8. Therefore, the exploration of organic building blocks with higher connectivity is a necessary path to broaden the scope of 3D COF structures.
View Article and Find Full Text PDFJ Am Chem Soc
April 2022
Key Laboratory for Soft Chemistry and Functional Materials of Ministry of Education, School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China.
The connectivity of building units for 3D covalent organic frameworks (COFs) has long been primarily 4 and 6, which have severely curtailed the structural diversity of 3D COFs. Here we demonstrate the successful design and synthesis of a porphyrin based, 8-connected building block with cubic configuration, which could be further reticulated into an unprecedented interpenetrated pcb topology by imine condensation with linear amine monomers. This study presents the first case of high-connectivity building units bearing 8-connected cubic nodes, thus greatly enriching the topological possibilities of 3D COFs.
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