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      Multifunctional Porous Hydrogen-Bonded Organic Frameworks: Current Status and Future Perspectives

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          Abstract

          Hydrogen-bonded organic frameworks (HOFs), self-assembled from organic or metalated organic building blocks (also termed as tectons) by hydrogen bonding, π–π stacking, and other intermolecular interactions, have become an emerging class of multifunctional porous materials. So far, a library of HOFs with high porosity has been synthesized based on versatile tectons and supramolecular synthons. Benefiting from the flexibility and reversibility of H-bonds, HOFs feature high structural flexibility, mild synthetic reaction, excellent solution processability, facile healing, easy regeneration, and good recyclability. However, the flexible and reversible nature of H-bonds makes most HOFs suffer from poor structural designability and low framework stability. In this Outlook, we first describe the development and structural features of HOFs and summarize the design principles of HOFs and strategies to enhance their stability. Second, we highlight the state-of-the-art development of HOFs for diverse applications, including gas storage and separation, heterogeneous catalysis, biological applications, sensing, proton conduction, and other applications. Finally, current challenges and future perspectives are discussed.

          Abstract

          HOFs are emerging as a unique type of multifunctional porous material. Herein, we summarize the design principles and various applications of HOFs as well as the prospect of their future development.

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          Multifunctional porous hydrogen-bonded organic framework materials

          This review provides an overview of development in the design, synthesis, and application of multifunctional porous hydrogen-bonded organic framework (HOF) materials. Hydrogen-bonded organic frameworks (HOFs) represent an interesting type of polymeric porous materials that can be self-assembled through H-bonding between organic linkers. To realize permanent porosity in HOFs, stable and robust open frameworks can be constructed by judicious selection of rigid molecular building blocks and hydrogen-bonded units with strong H-bonding interactions, in which the framework stability might be further enhanced through framework interpenetration and other types of weak intermolecular interactions such as π⋯π interactions. Owing to the reversible and flexible nature of H-bonding connections, HOFs show high crystallinity, solution processability, easy healing and purification. These unique advantages enable HOFs to be used as a highly versatile platform for exploring multifunctional porous materials. Here, the bright potential of HOF materials as multifunctional materials is highlighted in some of the most important applications for gas storage and separation, molecular recognition, electric and optical materials, chemical sensing, catalysis, and biomedicine.
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            Hydrogen-Bonded Organic Frameworks as a Tunable Platform for Functional Materials

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              Designing Hydrogen‐Bonded Organic Frameworks (HOFs) with Permanent Porosity

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                Author and article information

                Journal
                ACS Cent Sci
                ACS Cent Sci
                oc
                acscii
                ACS Central Science
                American Chemical Society
                2374-7943
                2374-7951
                16 December 2022
                28 December 2022
                : 8
                : 12
                : 1589-1608
                Affiliations
                []State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences , Fuzhou 350002, P. R. China
                []College of Life Science, Fujian Agriculture and Forestry University , Fuzhou, Fujian 350002, P. R. China
                [§ ]Fujian Science & Technology Innovation Laboratory for Optoelectronic Information of China , Fuzhou, Fujian 350108, P. R. China
                Author notes
                Author information
                https://orcid.org/0000-0003-2515-3356
                https://orcid.org/0000-0001-9096-6981
                https://orcid.org/0000-0002-2398-399X
                Article
                10.1021/acscentsci.2c01196
                9801510
                36589879
                b80c6a81-57c6-47ea-8106-3a4c92464002
                © 2022 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 10 October 2022
                Funding
                Funded by: National Natural Science Foundation of China, doi 10.13039/501100001809;
                Award ID: 2033008
                Funded by: Fujian Provincial Department of Science and Technology, doi 10.13039/501100005270;
                Award ID: 2021ZZ103
                Funded by: Fujian Provincial Department of Science and Technology, doi 10.13039/501100005270;
                Award ID: 2021ZR105
                Funded by: Natural Science Foundation of Fujian Province, doi 10.13039/501100003392;
                Award ID: 2020J01549
                Funded by: Ministry of Science and Technology of the People''s Republic of China, doi 10.13039/501100002855;
                Award ID: 2018YFA0208600
                Funded by: National Natural Science Foundation of China, doi 10.13039/501100001809;
                Award ID: 22220102005
                Categories
                Outlook
                Custom metadata
                oc2c01196
                oc2c01196

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