ConspectusCovalent organic frameworks (COFs) represent a fascinating class of crystalline porous polymers constructed from organic building blocks linked by covalent bonds. Benefiting from their high crystallinity, large surface area, and ease of functionalization, COFs have demonstrated significant potential across various fields, including gas adsorption, luminescence, sensing, catalysis, energy storage, nanomedicine, etc. In the first decade of COF development, only those with homogeneous porosity have been constructed, and thus, their topological structures are quite limited. An exciting progress in the field of COFs is the emergence of two-dimensional (2D) COFs with hierarchical porosity, known as heteropore COFs, which have garnered considerable attention in recent years. Heteropore COFs are deliberately designed to integrate different types of pores into a single framework, resulting in heterogeneous porosity that imparts captivating properties and functions. Compared to their homopore counterparts, heteropore COFs offer a compelling platform for creating hierarchically structured porous materials, thanks to their distinctive multicompartment architectures and different pore environments. Since we achieved the construction of the first heteropore COF featuring both micropores and mesopores in 2014, substantial advancements have been achieved in the realm of heteropre COFs over the past decade, considerably increasing the topological diversity of 2D COFs. In this Account, we summarize our contributions to the development of 2D heteropore COFs. First, we review representative design strategies for the construction of 2D heteropore COFs, including the angle-specific-vertex, heterostructural-mixed-linker, multiple-linking-site, and desymmetrization-design strategies and their combinations as well as the dynamic covalent chemistry-mediated linker exchange strategy. Based on these strategies, heteroporous frameworks with two, three, and four different kinds of pores and different types of linkages have been successfully fabricated. Next, we discuss the properties and applications of heteropore COFs, including those shared with their homopore counterparts and unique ones originating from their hierarchical porous structures. Our research has shown that heteropore COFs have inherited the common features from their homopore counterparts and exhibited application potentials in gas adsorption, chemical sensing, environmental remediation, etc. More importantly, the multicompartment architecture and heterogeneous pore environment of heteropore COFs offer distinct benefits, for which exclusive applications and unique properties of heteropore COFs distinct from those of homopore COFs have been demonstrated. Finally, we highlight the current challenges and future directions of heteropore COFs, with an emphasis on the development of structural design and synthetic methodologies, precise structural characterization, and the exploration of unique properties and advanced applications. We believe that this Account will offer valuable insights into the design and synthesis of COFs with heteroporous structures, thereby accelerating their applications across a wide range of interdisciplinary research areas.
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http://dx.doi.org/10.1021/acs.accounts.4c00799 | DOI Listing |
Acc Chem Res
March 2025
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
ConspectusCovalent organic frameworks (COFs) represent a fascinating class of crystalline porous polymers constructed from organic building blocks linked by covalent bonds. Benefiting from their high crystallinity, large surface area, and ease of functionalization, COFs have demonstrated significant potential across various fields, including gas adsorption, luminescence, sensing, catalysis, energy storage, nanomedicine, etc. In the first decade of COF development, only those with homogeneous porosity have been constructed, and thus, their topological structures are quite limited.
View Article and Find Full Text PDFNano Lett
November 2024
National Key Laboratory of Uranium Resources Exploration-Mining and Nuclear Remote Sensing, East China University of Technology, Nanchang 330013, China.
Seeking novel synthetic methodology to further promote the preparation of covalent organic frameworks (COFs) has long been our pursuit but remains a challenging task. Herein, we report a new protocol, a top-down approach for facile synthesis of COFs. Interestingly, our top-down route can impressively generate extended COFs by reticular chemistry which cannot be accessed by the commonly used bottom-up synthesis route.
View Article and Find Full Text PDFPolymers (Basel)
September 2024
Key Laboratory of Ministry of Education for Advanced Materials in Tropical Island Resources, Hainan University, No. 58, Renmin Avenue, Haikou 570228, China.
Covalent organic frameworks (COFs) have garnered significant interest within the scientific community due to their distinctive ability to act as organic semiconductors responsive to visible light. This unique attribute makes them up-and-coming candidates for facilitating photocatalytic organic reactions. Herein, two donor-acceptor COFs, TPE-BSD-COF and TPE-BD-COF, have been designed and synthesized by incorporating electron-rich tetraphenylethylene and electron-deficient benzoselenadiazole and benzothiadiazole units into the framework through a Schiff-base polycondensation reaction.
View Article and Find Full Text PDFChemosphere
July 2024
Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing 100083, China.
The development of functionalized covalent organic frameworks (COFs) is crucial in expanding their potential for removing toxic heavy metals from drinking water. Here, a new sulfhydryl-modified heteroporous COF (COF) was prepared using a "bottom-up" approach in which a direct amine-aldehyde dehydration condensation between 2,5-diamino-1,4-benzenedithiol dihydrochloride (DBD) and [1,1'-biphenyl]-3,3',5,5'-tetracarbaldehyde (BTA) was occurred. The COF featured a hexagonal kagome (kgm) structure and a sheet-like morphology.
View Article and Find Full Text PDFNat Commun
January 2024
Key Laboratory of Synthetic and Self-Assembly Chemistry for Organic Functional Molecules, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, 200032, Shanghai, China.
Creating different pore environments within a covalent organic framework (COF) will lead to useful multicompartment structure and multiple functions, which however has been scarcely achieved. Herein we report designed synthesis of three two-dimensional COFs with amphiphilic porosity by steric-hindrance-mediated precision hydrophilic-hydrophobic microphase separation. Dictated by the different steric effect of the substituents introduced to a monomer, dual-pore COFs with kgm net, in which all hydroxyls locate in trigonal micropores while hydrophobic sidechains exclusively distribute in hexagonal mesopores, have been constructed to form completely separated hydrophilic and hydrophobic nanochannels.
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