Abstract
The dream to prepare well-defined materials drives the methodological evolution for molecular synthesis, structural control and materials manufacturing. Among various methods, chemical approaches to design, synthesize, control and engineer small molecules, polymers and networks offer the fundamental strategies. Merging covalent bonds and non-covalent interactions into one method to establish a complex structural composition for specific functions, mimicking biological systems such as DNA, RNA and proteins, is at the centre of chemistry and materials science. Covalent organic frameworks (COFs) are a class of crystalline porous polymers that enable the integration of organic units into highly ordered structures via polymerization. This polymerization system is unique as it deploys covalent bonds to construct the primary order structures of polymeric backbones via polycondensation and leverages on non-covalent interactions to create the high order structures of polymeric networks via supramolecular polymerization in a one-pot reaction system. This Primer covers all aspects of the field of COFs from chemistry to physics, materials and applications, and outlines the design principle, experimental methods, characterization and applications, with an aim to show a concise yet full picture of the field. The key fundamental issues to be addressed are analysed with an outlook on the future major directions from different perspectives.
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References
Saikia, I., Borah, A. J. & Phukan, P. Use of bromine and bromo-organic compounds in organic synthesis. Chem. Rev. 116, 6837–7042 (2016).
Faure, E. et al. Catechols as versatile platforms in polymer chemistry. Prog. Polym. Sci. 38, 236–270 (2013).
Diner, C. & Szabó, K. J. Recent advances in the preparation and application of allylboron species in organic synthesis. J. Am. Chem. Soc. 139, 2–14 (2017).
Song, Y., Sun, Q., Aguila, B. & Ma, S. Opportunities of covalent organic frameworks for advanced applications. Adv. Sci. 6, 1801410 (2019).
Hisaki, I., Xin, C., Takahashi, K. & Nakamura, T. Designing hydrogen-bonded organic frameworks (HOFs) with permanent porosity. Angew. Chem. Int. Ed. 58, 11160–11170 (2019).
Wang, S., Yao, W., Lin, J., Ding, Z. & Wang, X. Cobalt imidazolate metal–organic frameworks photosplit CO2 under mild reaction conditions. Angew. Chem. Int. Ed. 53, 1034–1038 (2014).
Manrao, E. A. et al. Reading DNA at single-nucleotide resolution with a mutant MspA nanopore and phi29 DNA polymerase. Nat. Biotechnol. 30, 349–353 (2012).
Gao, Y. et al. Structure of the RNA-dependent RNA polymerase from COVID-19 virus. Science 368, 779–782 (2020).
Warner, K. D., Hajdin, C. E. & Weeks, K. M. Principles for targeting RNA with drug-like small molecules. Nat. Rev. Drug Discov. 17, 547–558 (2018).
Verkman, A. S. & Mitra, A. K. Structure and function of aquaporin water channels. Am. J. Physiol. Ren. Physiol. 278, F13–F28 (2000).
Kühlbrandt, W. Structure and mechanisms of F-type ATP synthases. Annu. Rev. Biochem. 88, 515–549 (2019).
Hanson, M. A. et al. Crystal structure of a lipid G protein-coupled receptor. Science 335, 851–855 (2012).
Perrier, S. 50th anniversary perspective: RAFT polymerization — a user guide. Macromolecules 50, 7433–7447 (2017).
Mohapatra, H., Kleiman, M. & Esser-Kahn, A. P. Mechanically controlled radical polymerization initiated by ultrasound. Nat. Chem. 9, 135–139 (2017).
Kang, J. et al. A rational strategy for the realization of chain-growth supramolecular polymerization. Science 347, 646–651 (2015).
Hashim, P. K., Bergueiro, J., Meijer, E. W. & Aida, T. Supramolecular polymerization: a conceptual expansion for innovative materials. Prog. Polym. Sci. 105, 101250 (2020).
Feng, X., Ding, X. & Jiang, D. Covalent organic frameworks. Chem. Soc. Rev. 41, 6010–6022 (2012).
Diercks, C. S. & Yaghi, O. M. The atom, the molecule, and the covalent organic framework. Science 355, eaal1585 (2017).
Xing, C. et al. Enhancing enzyme activity by the modulation of covalent interactions in the confined channels of covalent organic frameworks. Angew. Chem. Int. Ed. 61, e202201378 (2022).
Traxler, M. et al. Acridine-functionalized covalent organic frameworks (COFs) as photocatalysts for metallaphotocatalytic C−N cross-coupling. Angew. Chem. Int. Ed. 61, e202117738 (2022).
Zhang, W. et al. Reconstructed covalent organic frameworks. Nature 604, 72–79 (2022).
Guo, J. et al. Conjugated organic framework with three-dimensionally ordered stable structure and delocalized π clouds. Nat. Commun. 4, 2736 (2013). This work reports the discovery of the phenazine linkage to synthesize fully π-conjugated and robust COFs.
Jin, E. et al. Two-dimensional sp2 carbon-conjugated covalent organic frameworks. Science 357, 673–676 (2017). This work reports the discovery of ferromagnetism in carbon-conjugated COFs.
Geng, K. et al. Covalent organic frameworks: design, synthesis, and functions. Chem. Rev. 120, 8814–8933 (2020).
Mu, Z. et al. Covalent organic frameworks with record pore apertures. J. Am. Chem. Soc. 144, 5145–5154 (2022).
Côté, A. P., El-Kaderi, H. M., Furukawa, H., Hunt, J. R. & Yaghi, O. M. Reticular synthesis of microporous and mesoporous 2D covalent organic frameworks. J. Am. Chem. Soc. 129, 12914–12915 (2007).
Ding, X. et al. Synthesis of metallophthalocyanine covalent organic frameworks that exhibit high carrier mobility and photoconductivity. Angew. Chem. Int. Ed. 50, 1289–1293 (2011).
Chen, X., Addicoat, M., Irle, S., Nagai, A. & Jiang, D. Control of crystallinity and porosity of covalent organic frameworks by managing interlayer interactions based on self-complementary π-electronic force. J. Am. Chem. Soc. 135, 546–549 (2013).
Yue, Y., Li, H., Chen, H. & Huang, N. Piperazine-linked covalent organic frameworks with high electrical conductivity. J. Am. Chem. Soc. 144, 2873–2878 (2022).
Jin, E. et al. Designed synthesis of stable light-emitting two-dimensional sp2 carbon-conjugated covalent organic frameworks. Nat. Commun. 9, 4143 (2018).
Li, L. et al. Isoreticular series of two-dimensional covalent organic frameworks with the kgd topology and controllable micropores. J. Am. Chem. Soc. 144, 6475–6482 (2022).
Dalapati, S. et al. Rational design of crystalline supermicroporous covalent organic frameworks with triangular topologies. Nat. Commun. 6, 7786 (2015).
Krishnaraj, C. et al. Strongly reducing (diarylamino)benzene-based covalent organic framework for metal-free visible light photocatalytic H2O2 generation. J. Am. Chem. Soc. 142, 20107–20116 (2020).
Huang, N. et al. Multiple-component covalent organic frameworks. Nat. Commun. 7, 12325 (2016).
Chen, X. et al. Designed synthesis of double-stage two-dimensional covalent organic frameworks. Sci. Rep. 5, 14650 (2015).
Yu, X. et al. Gating effects for ion transport in three-dimensional functionalized covalent organic frameworks. Angew. Chem. Int. Ed. 61, e202200820 (2022).
Wang, S. et al. A three-dimensional sp2 carbon-conjugated covalent organic framework. J. Am. Chem. Soc. 143, 15562–15566 (2021).
Uribe-Romo, F. J. et al. A crystalline imine-linked 3-D porous covalent organic framework. J. Am. Chem. Soc. 131, 4570–4571 (2009).
Xie, Y. et al. Tuning the topology of three-dimensional covalent organic frameworks via steric control: from pts to unprecedented ljh. J. Am. Chem. Soc. 143, 7279–7284 (2021).
Li, H. et al. Three-dimensional tetrathiafulvalene-based covalent organic frameworks for tunable electrical conductivity. J. Am. Chem. Soc. 141, 13324–13329 (2019).
El-Kaderi Hani, M. et al. Designed synthesis of 3D covalent organic frameworks. Science 316, 268–272 (2007).
Baldwin, L. A., Crowe, J. W., Pyles, D. A. & McGrier, P. L. Metalation of a mesoporous three-dimensional covalent organic framework. J. Am. Chem. Soc. 138, 15134–15137 (2016).
Sun, R., Wang, X., Wang, X. & Tan, B. Three-dimensional crystalline covalent triazine frameworks via a polycondensation approach. Angew. Chem. Int. Ed. 61, e202117668 (2022).
Yahiaoui, O. et al. 3D anionic silicate covalent organic framework with srs topology. J. Am. Chem. Soc. 140, 5330–5333 (2018).
Ma, T. et al. Diverse crystal size effects in covalent organic frameworks. Nat. Commun. 11, 6128 (2020).
Han, B. et al. Maximizing electroactive sites in a three-dimensional covalent organic framework for significantly improved carbon dioxide reduction electrocatalysis. Angew. Chem. Int. Ed. 61, e202114244 (2022).
Liu, Y. et al. Weaving of organic threads into a crystalline covalent organic framework. Science 351, 365–369 (2016).
Lan, Y. et al. Materials genomics methods for high-throughput construction of COFs and targeted synthesis. Nat. Commun. 9, 5274 (2018).
Kang, X. et al. Reticular synthesis of tbo topology covalent organic frameworks. J. Am. Chem. Soc. 142, 16346–16356 (2020).
Nguyen, H. L., Gropp, C., Ma, Y., Zhu, C. & Yaghi, O. M. 3D covalent organic frameworks selectively crystallized through conformational design. J. Am. Chem. Soc. 142, 20335–20339 (2020).
Martínez-Abadía, M. et al. π-Interpenetrated 3D covalent organic frameworks from distorted polycyclic aromatic hydrocarbons. Angew. Chem. Int. Ed. 60, 9941–9946 (2021).
Gropp, C., Ma, T., Hanikel, N. & Yaghi Omar, M. Design of higher valency in covalent organic frameworks. Science 370, eabd6406 (2020).
Ma, J.-X. et al. Cage based crystalline covalent organic frameworks. J. Am. Chem. Soc. 141, 3843–3848 (2019).
Zhu, Q. et al. 3D cage COFs: a dynamic three-dimensional covalent organic framework with high-connectivity organic cage nodes. J. Am. Chem. Soc. 142, 16842–16848 (2020).
Côté, A. P. et al. Porous, crystalline, covalent organic frameworks. Science 310, 1166–1170 (2005). This work reports the synthesis of the early example of COFs.
Nagai, A. et al. A squaraine-linked mesoporous covalent organic framework. Angew. Chem. Int. Ed. 52, 3770–3774 (2013).
Ding, S.-Y. et al. Construction of covalent organic framework for catalysis: Pd/COF-LZU1 in Suzuki–Miyaura coupling reaction. J. Am. Chem. Soc. 133, 19816–19822 (2011).
Chen, X. et al. Locking covalent organic frameworks with hydrogen bonds: general and remarkable effects on crystalline structure, physical properties, and photochemical activity. J. Am. Chem. Soc. 137, 3241–3347 (2015).
Ascherl, L. et al. Molecular docking sites designed for the generation of highly crystalline covalent organic frameworks. Nat. Chem. 8, 310–316 (2016).
Li, Z. et al. A 2D azine-linked covalent organic framework for gas storage applications. Chem. Commun. 50, 13825–13828 (2014).
Han, X., Huang, J., Yuan, C., Liu, Y. & Cui, Y. Chiral 3D covalent organic frameworks for high performance liquid chromatographic enantioseparation. J. Am. Chem. Soc. 140, 892–895 (2018).
Lyu, H., Diercks, C. S., Zhu, C. & Yaghi, O. M. Porous crystalline olefin-linked covalent organic frameworks. J. Am. Chem. Soc. 141, 6848–6852 (2019).
Huang, N. et al. A stable and conductive metallophthalocyanine framework for electrocatalytic carbon dioxide reduction in water. Angew. Chem. Int. Ed. 59, 16587–16593 (2020).
Li, X. et al. Dynamic covalent synthesis of crystalline porous graphitic frameworks. Chem 6, 933–944 (2020).
Zhuang, X. et al. A two-dimensional conjugated polymer framework with fully sp2-bonded carbon skeleton. Polym. Chem. 7, 4176–4181 (2016).
Xu, S., Richter, M. & Feng, X. Vinylene-linked two-dimensional covalent organic frameworks: synthesis and functions. Acc. Mater. Res. 2, 252–265 (2021).
Cui, W.-R. et al. Regenerable and stable sp2 carbon-conjugated covalent organic frameworks for selective detection and extraction of uranium. Nat. Commun. 11, 436 (2020).
Meng, F. et al. Synthesis of ionic vinylene-linked covalent organic frameworks through quaternization-activated Knoevenagel condensation. Angew. Chem. Int. Ed. 60, 13614–13620 (2021).
Acharjya, A., Longworth-Dunbar, L., Roeser, J., Pachfule, P. & Thomas, A. Synthesis of vinylene-linked covalent organic frameworks from acetonitrile: combining cyclotrimerization and aldol condensation in one pot. J. Am. Chem. Soc. 142, 14033–14038 (2020).
Acharjya, A., Pachfule, P., Roeser, J., Schmitt, F.-J. & Thomas, A. Vinylene-linked covalent organic frameworks by base-catalyzed aldol condensation. Angew. Chem. Int. Ed. 58, 14865–14870 (2019). This work reports the synthesis of a C=C COF with base conditions.
Jadhav, T. et al. 2D poly(arylene vinylene) covalent organic frameworks via aldol condensation of trimethyltriazine. Angew. Chem. Int. Ed. 58, 13753–13757 (2019).
Bi, S. et al. Two-dimensional semiconducting covalent organic frameworks via condensation at arylmethyl carbon atoms. Nat. Commun. 10, 2467 (2019).
Pastoetter, D. L. et al. Synthesis of vinylene-linked two-dimensional conjugated polymers via the Horner–Wadsworth–Emmons reaction. Angew. Chem. Int. Ed. 59, 23620–23625 (2020).
Grunenberg, L. et al. Amine-linked covalent organic frameworks as a platform for postsynthetic structure interconversion and pore-wall modification. J. Am. Chem. Soc. 143, 3430–3438 (2021).
Li, X.-T. et al. Construction of covalent organic frameworks via three-component one-pot Strecker and Povarov reactions. J. Am. Chem. Soc. 142, 6521–6526 (2020).
Liu, H. et al. Covalent organic frameworks linked by amine bonding for concerted electrochemical reduction of CO2. Chem 4, 1696–1709 (2018).
Stewart, D. et al. Stable and ordered amide frameworks synthesised under reversible conditions which facilitate error checking. Nat. Commun. 8, 1102 (2017).
Waller, P. J. et al. Chemical conversion of linkages in covalent organic frameworks. J. Am. Chem. Soc. 138, 15519–15522 (2016).
Zhou, Z.-B. et al. A facile, efficient, and general synthetic method to amide-linked covalent organic frameworks. J. Am. Chem. Soc. 144, 1138–1143 (2022).
Qian, H.-L., Meng, F.-L., Yang, C.-X. & Yan, X.-P. Irreversible amide-linked covalent organic framework for selective and ultrafast gold recovery. Angew. Chem. Int. Ed. 59, 17607–17613 (2020).
Lyle, S. J. et al. Multistep solid-state organic synthesis of carbamate-linked covalent organic frameworks. J. Am. Chem. Soc. 141, 11253–11258 (2019).
Li, C. et al. Asymmetric photocatalysis over robust covalent organic frameworks with tetrahydroquinoline linkage. Chin. J. Catal. 41, 1288–1297 (2020).
Zhou, Z.-B. et al. Toward azo-linked covalent organic frameworks by developing linkage chemistry via linker exchange. Nat. Commun. 13, 2180 (2022).
Feng, J. et al. Fused-ring-linked covalent organic frameworks. J. Am. Chem. Soc. 144, 6594–6603 (2022).
Wang, Y. et al. Construction of fully conjugated covalent organic frameworks via facile linkage conversion for efficient photoenzymatic catalysis. J. Am. Chem. Soc. 142, 5958–5963 (2020).
Ren, S. et al. Porous, fluorescent, covalent triazine-based frameworks via room-temperature and microwave-assisted synthesis. Adv. Mater. 24, 2357–2361 (2012).
Yang, Z. et al. Transformation strategy for highly crystalline covalent triazine frameworks: from staggered AB to eclipsed AA stacking. J. Am. Chem. Soc. 142, 6856–6860 (2020).
Wang, K. et al. Covalent triazine frameworks via a low-temperature polycondensation approach. Angew. Chem. Int. Ed. 56, 14149–14153 (2017).
Liu, M. et al. Crystalline covalent triazine frameworks by in situ oxidation of alcohols to aldehyde monomers. Angew. Chem. Int. Ed. 57, 11968–11972 (2018).
Zhang, S. et al. Strong-base-assisted synthesis of a crystalline covalent triazine framework with high hydrophilicity via benzylamine monomer for photocatalytic water splitting. Angew. Chem. Int. Ed. 59, 6007–6014 (2020).
Guo, L. et al. Crystallization of covalent triazine frameworks via a heterogeneous nucleation approach for efficient photocatalytic applications. Chem. Mater. 33, 1994–2003 (2021).
Pyles, D. A., Crowe, J. W., Baldwin, L. A. & McGrier, P. L. Synthesis of benzobisoxazole-linked two-dimensional covalent organic frameworks and their carbon dioxide capture properties. ACS Macro Lett. 5, 1055–1058 (2016).
Wei, P.-F. et al. Benzoxazole-linked ultrastable covalent organic frameworks for photocatalysis. J. Am. Chem. Soc. 140, 4623–4631 (2018).
Seo, J.-M., Noh, H.-J., Jeong, H. Y. & Baek, J.-B. Converting unstable imine-linked network into stable aromatic benzoxazole-linked one via post-oxidative cyclization. J. Am. Chem. Soc. 141, 11786–11790 (2019).
Li, T. et al. A 2D covalent organic framework involving strong intramolecular hydrogen bonds for advanced supercapacitors. Polym. Chem. 11, 47–52 (2020).
Wang, K. et al. Synthesis of stable thiazole-linked covalent organic frameworks via a multicomponent reaction. J. Am. Chem. Soc. 142, 11131–11138 (2020).
Haase, F. et al. Topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis. Nat. Commun. 9, 2600 (2018).
Waller, P. J., AlFaraj, Y. S., Diercks, C. S., Jarenwattananon, N. N. & Yaghi, O. M. Conversion of imine to oxazole and thiazole linkages in covalent organic frameworks. J. Am. Chem. Soc. 140, 9099–9103 (2018).
Wang, P.-L., Ding, S.-Y., Zhang, Z.-C., Wang, Z.-P. & Wang, W. Constructing robust covalent organic frameworks via multicomponent reactions. J. Am. Chem. Soc. 141, 18004–18008 (2019).
Ranjeesh, K. C. et al. Imidazole-linked crystalline two-dimensional polymer with ultrahigh proton-conductivity. J. Am. Chem. Soc. 141, 14950–14954 (2019).
Jiang, Y. et al. Partial oxidation-induced electrical conductivity and paramagnetism in a Ni(II) tetraaza[14]annulene-linked metal organic framework. J. Am. Chem. Soc. 141, 16884–16893 (2019).
Howarth, A. J. et al. Best practices for the synthesis, activation, and characterization of metal–organic frameworks. Chem. Mater. 29, 26–39 (2017).
Ma, T. et al. Single-crystal X-ray diffraction structures of covalent organic frameworks. Science 361, 48–52 (2018). This work reports a seeded growth strategy to prepare single-crystal 3D COFs 100 μm in size.
Liang, L. et al. Non-interpenetrated single-crystal covalent organic frameworks. Angew. Chem. Int. Ed. 59, 17991–17995 (2020).
Evans, A. M. et al. Seeded growth of single-crystal two-dimensional covalent organic frameworks. Science 361, 52–57 (2018). This work reports a seeded growth strategy to prepare single-crystal 2D COFs 1 μm in size.
Zhang, L. et al. Covalent organic framework for efficient two-photon absorption. Matter 2, 1049–1063 (2020).
Peng, L. et al. Ultra-fast single-crystal polymerization of large-sized covalent organic frameworks. Nat. Commun. 12, 5077 (2021).
Liu, K. et al. On-water surface synthesis of crystalline, few-layer two-dimensional polymers assisted by surfactant monolayers. Nat. Chem. 11, 994–1000 (2019).
Zhang, T. et al. Engineering crystalline quasi-two-dimensional polyaniline thin film with enhanced electrical and chemiresistive sensing performances. Nat. Commun. 10, 4225 (2019). This work showcases a rare example of COFs as a chemiresistive sensor.
Karak, S. et al. Constructing ultraporous covalent organic frameworks in seconds via an organic terracotta process. J. Am. Chem. Soc. 139, 1856–1862 (2017).
Martín-Illán, J. Á. et al. Macroscopic ultralight aerogel monoliths of imine-based covalent organic frameworks. Angew. Chem. Int. Ed. 60, 13969–13977 (2021).
Vazquez-Molina, D. A. et al. Mechanically shaped two-dimensional covalent organic frameworks reveal crystallographic alignment and fast Li-ion conductivity. J. Am. Chem. Soc. 138, 9767–9770 (2016).
Rodríguez-San-Miguel, D. et al. Crystalline fibres of a covalent organic framework through bottom-up microfluidic synthesis. Chem. Commun. 52, 9212–9215 (2016).
Zhang, M. et al. Hierarchical-coassembly-enabled 3D-printing of homogeneous and heterogeneous covalent organic frameworks. J. Am. Chem. Soc. 141, 5154–5158 (2019).
Franco, C. et al. Biomimetic synthesis of sub-20 nm covalent organic frameworks in water. J. Am. Chem. Soc. 142, 3540–3547 (2020). This work reports COF nanoparticle synthesis in water.
Burke, D. W. et al. Acid exfoliation of imine-linked covalent organic frameworks enables solution processing into crystalline thin films. Angew. Chem. Int. Ed. 59, 5165–5171 (2020).
Colson, J. W. et al. Oriented 2D covalent organic framework thin films on single-layer graphene. Science 332, 228–231 (2011).
Hussain, S. A., Dey, B., Bhattacharjee, D. & Mehta, N. Unique supramolecular assembly through Langmuir–Blodgett (LB) technique. Heliyon 4, e01038 (2018).
Shinde, D. B. et al. Crystalline 2D covalent organic framework membranes for high-flux organic solvent nanofiltration. J. Am. Chem. Soc. 140, 14342–14349 (2018).
Dong, R., Zhang, T. & Feng, X. Interface-assisted synthesis of 2D materials: trend and challenges. Chem. Rev. 118, 6189–6235 (2018).
Jin, Y. et al. Confined growth of ordered organic frameworks at an interface. Chem. Soc. Rev. 49, 4637–4666 (2020).
Lafferentz, L. et al. Controlling on-surface polymerization by hierarchical and substrate-directed growth. Nat. Chem. 4, 215–220 (2012).
Galeotti, G. et al. Synthesis of mesoscale ordered two-dimensional π-conjugated polymers with semiconducting properties. Nat. Mater. 19, 874–880 (2020).
Grossmann, L. et al. On-surface photopolymerization of two-dimensional polymers ordered on the mesoscale. Nat. Chem. 13, 730–736 (2021).
Bieri, M. et al. Two-dimensional polymer formation on surfaces: insight into the roles of precursor mobility and reactivity. J. Am. Chem. Soc. 132, 16669–16676 (2010).
Telychko, M. et al. Ultrahigh-yield on-surface synthesis and assembly of circumcoronene into a chiral electronic Kagome-honeycomb lattice. Sci. Adv. 7, eabf0269 (2021).
Liu, X.-H. et al. On-surface synthesis of single-layered two-dimensional covalent organic frameworks via solid–vapor interface reactions. J. Am. Chem. Soc. 135, 10470–10474 (2013).
Bieri, M. et al. Porous graphenes: two-dimensional polymer synthesis with atomic precision. Chem. Commun. 45, 6919–6921 (2009).
Sahabudeen, H. et al. Wafer-sized multifunctional polyimine-based two-dimensional conjugated polymers with high mechanical stiffness. Nat. Commun. 7, 13461 (2016).
Dey, K. et al. Selective molecular separation by interfacially crystallized covalent organic framework thin films. J. Am. Chem. Soc. 139, 13083–13091 (2017).
Wang, Z. et al. Viologen-immobilized 2D polymer film enabling highly efficient electrochromic device for solar-powered smart window. Adv. Mater. 34, 2106073 (2022).
Qi, H. et al. Near-atomic-scale observation of grain boundaries in a layer-stacked two-dimensional polymer. Sci. Adv. 6, eabb5976 (2020).
Park, S. et al. Two‐dimensional boronate ester covalent organic framework thin films with large single crystalline domains for neuromorphic memory device. Angew. Chem. Int. Ed. 132, 2–9 (2020).
Wang, Z. et al. On-water surface synthesis of charged two-dimensional polymer single crystals via the irreversible Katritzky reaction. Nat. Synth. 1, 69–76 (2022). This work reports an on-surface synthesis of membranes.
Sahabudeen, H. et al. Highly crystalline and semiconducting imine-based two-dimensional polymers enabled by interfacial synthesis. Angew. Chem. Int. Ed. 59, 2–11 (2020).
Fan, H. et al. Covalent organic framework–covalent organic framework bilayer membranes for highly selective gas separation. J. Am. Chem. Soc. 140, 10094–10098 (2018).
Ying, Y. et al. Ultrathin two-dimensional membranes assembled by ionic covalent organic nanosheets with reduced apertures for gas separation. J. Am. Chem. Soc. 142, 4472–4480 (2020).
Fu, J. et al. Fabrication of COF–MOF composite membranes and their highly selective separation of H2/CO2. J. Am. Chem. Soc. 138, 7673–7680 (2016).
Ma, H.-C., Zou, J., Li, X.-T., Chen, G.-J. & Dong, Y.-B. Homochiral covalent organic frameworks for asymmetric catalysis. Chem. Eur. J. 26, 13754–13770 (2020).
Sun, X. et al. In-situ anchoring bimetallic nanoparticles on covalent organic framework as an ultrasensitive electrochemical sensor for levodopa detection. Talanta 225, 122072 (2021).
Huang, Y. et al. Filling COFs with bimetallic nanoclusters for CO2-to-alcohols conversion with H2O oxidation. Appl. Catal. B 288, 120001 (2021).
Liao, Y., Li, J. & Thomas, A. General route to high surface area covalent organic frameworks and their metal oxide composites as magnetically recoverable adsorbents and for energy storage. ACS Macro Lett. 6, 1444–1450 (2017).
Fan, H., Gu, J., Meng, H., Knebel, A. & Caro, J. High‐flux membranes based on the covalent organic framework COF‐LZU1 for selective dye separation by nanofiltration. Angew. Chem. Int. Ed. 57, 4083–4087 (2018).
Chakraborty, D. et al. Cu/Cu2O nanoparticles supported on a phenol–pyridyl COF as a heterogeneous catalyst for the synthesis of unsymmetrical diynes via glaser–hay coupling. ACS Appl. Mater. Interfaces 11, 15670–15679 (2019).
Wen, L. et al. Solid-phase microextraction using a β-ketoenamine-linked covalent organic framework coating for efficient enrichment of synthetic musks in water samples. Anal. Methods. 12, 2434–2442 (2020).
Chen, X., Zhang, H., Ci, C., Sun, W. & Wang, Y. Few-layered boronic ester based covalent organic frameworks/carbon nanotube composites for high-performance K-organic batteries. ACS Nano 13, 3600–3607 (2019).
Zha, Z. et al. 3D graphene functionalized by covalent organic framework thin film as capacitive electrode in alkaline media. ACS Appl. Mater. Interfaces 7, 17837–17843 (2015).
Luo, M. et al. Defects engineering leads to enhanced photocatalytic H2 evolution on graphitic carbon nitride–covalent organic framework nanosheet composite. Small 16, 2001100 (2020).
Kang, Z. et al. Mixed matrix membranes (MMMs) comprising exfoliated 2D covalent organic frameworks (COFs) for efficient CO2 separation. Chem. Mater. 28, 1277–1285 (2016).
Cheng, Y. et al. Highly efficient CO2 capture by mixed matrix membranes containing three-dimensional covalent organic framework fillers. J. Mater. Chem. A 7, 4549–4560 (2019).
Li, Z. et al. Light-emitting covalent organic frameworks: fluorescence improving via pinpoint surgery and selective switch-on sensing of anions. J. Am. Chem. Soc. 140, 12374–12377 (2018).
Tao, S. et al. Confining H3PO4 network in covalent organic frameworks enables proton super flow. Nat. Commun. 11, 1981 (2020).
Ghosh, S. et al. Band-like transport of charge carriers in oriented two-dimensional conjugated covalent organic frameworks. Chem. Mater. 34, 736–745 (2022).
Zhang, Y.-B. et al. Single-crystal structure of a covalent organic framework. J. Am. Chem. Soc. 135, 16336–16339 (2013).
Xu, H., Tao, S. & Jiang, D. Proton conduction in crystalline and porous covalent organic frameworks. Nat. Mater. 15, 722–726 (2016).
Zhang, J., Han, X., Wu, X., Liu, Y. & Cui, Y. Multivariate chiral covalent organic frameworks with controlled crystallinity and stability for asymmetric catalysis. J. Am. Chem. Soc. 139, 8277–8285 (2017).
Jin, E. et al. A nanographene-based two-dimensional covalent organic framework as a stable and efficient photocatalyst. Angew. Chem. Int. Ed. 61, e202114059 (2022).
Huang, N., Wang, P., Addicoat, M. A., Heine, T. & Jiang, D. Ionic covalent organic frameworks: design of a charged interface aligned on 1D channel walls and its unusual electrostatic functions. Angew. Chem. Int. Ed. 56, 4982–4986 (2017).
Jin, E. et al. Module-patterned polymerization towards crystalline 2D sp2-carbon covalent organic framework semiconductors. Angew. Chem. Int. Ed. 61, e202115020 (2022).
Aradi, B., Hourahine, B. & Frauenheim, T. DFTB+, a sparse matrix-based implementation of the DFTB method. J. Phys. Chem. A 111, 5678–5684 (2007).
Rietveld, H. M. A profile refinement method for nuclear and magnetic structures. J. Appl. Cryst. 2, 65–71 (1969).
Xu, H., Gao, J. & Jiang, D. Stable, crystalline, porous, covalent organic frameworks as a platform for chiral organocatalysts. Nat. Chem. 7, 905–912 (2015). This work reports highly stable and porous COFs as well as chiral COFs for chiral organocatalysts that are used and featured in various latter research studies.
Banerjee, T. et al. Single-site photocatalytic H2 evolution from covalent organic frameworks with molecular cobaloxime co-catalysts. J. Am. Chem. Soc. 139, 16228–16234 (2017).
Wan, S., Guo, J., Kim, J., Ihee, H. & Jiang, D. A belt-shaped, blue luminescent, and semiconducting covalent organic framework. Angew. Chem. Int. Ed. 47, 8826–8830 (2008). This work reports the first semiconducting, luminescence and photoconductive COFs that are featured in many latter research works.
Dalapati, S., Jin, E., Addicoat, M., Heine, T. & Jiang, D. Highly emissive covalent organic frameworks. J. Am. Chem. Soc. 138, 5797–5800 (2016).
Li, X. et al. Partitioning the interlayer space of covalent organic frameworks by embedding pseudorotaxanes in their backbones. Nat. Chem. 12, 1115–1122 (2020).
Xu, L. et al. Surface-confined crystalline two-dimensional covalent organic frameworks via on-surface Schiff-base coupling. ACS Nano 7, 8066–8073 (2013).
Chen, J. et al. Synthesis of bipyridine-based covalent organic frameworks for visible-light-driven photocatalytic water oxidation. Appl. Catal. B 262, 118271 (2020).
Jin, E. et al. Exceptional electron conduction in two-dimensional covalent organic frameworks. Chem 7, 3309–3324 (2021).
Ding, X. et al. An n-channel two-dimensional covalent organic framework. J. Am. Chem. Soc. 133, 14510–14513 (2011).
Hou, X., Geng, K., Li, J., Wu, S. & Wu, J. Dibenzylidene-s-indacenetetraone linked n-type semiconducting covalent organic framework via aldol condensation. ACS Mater. Lett. 4, 1154–1159 (2022).
Jin, S. et al. Charge dynamics in a donor–acceptor covalent organic framework with periodically ordered bicontinuous heterojunctions. Angew. Chem. Int. Ed. 52, 2017–2021 (2013). This work reports the donor–acceptor COFs for electron transfer and charge separation.
Jin, S. et al. Creation of superheterojunction polymers via direct polycondensation: segregated and bicontinuous donor–acceptor π-columnar arrays in covalent organic frameworks for long-lived charge separation. J. Am. Chem. Soc. 137, 7817–7827 (2015).
Jin, S. et al. Large pore donor–acceptor covalent organic frameworks. Chem. Sci. 4, 4505–4511 (2013).
Feng, X. et al. An ambipolar conducting covalent organic framework with self-sorted and periodic electron donor–acceptor ordering. Adv. Mater. 24, 3026–3031 (2012).
Wan, S., Guo, J., Kim, J., Ihee, H. & Jiang, D. A photoconductive covalent organic framework: self-condensed arene cubes composed of eclipsed 2D polypyrene sheets for photocurrent generation. Angew. Chem. Int. Ed. 48, 5439–5442 (2009).
Slot, M. R. et al. Experimental realization and characterization of an electronic Lieb lattice. Nat. Phys. 13, 672 (2017).
Meng, Z., Stolz, R. M. & Mirica, K. A. Two-dimensional chemiresistive covalent organic framework with high intrinsic conductivity. J. Am. Chem. Soc. 141, 11929–11937 (2019).
Wan, S. et al. Covalent organic frameworks with high charge carrier mobility. Chem. Mater. 23, 4094–4097 (2011).
Wang, M. et al. Unveiling electronic properties in metal–phthalocyanine-based pyrazine-linked conjugated two-dimensional covalent organic frameworks. J. Am. Chem. Soc. 141, 16810–16816 (2019).
Tao, S. & Jiang, D. Covalent organic frameworks for energy conversions: current status, challenges, and perspectives. CCS Chem. 3, 2003–2024 (2020).
Jin, E. et al. 2D sp2 carbon-conjugated covalent organic frameworks for photocatalytic hydrogen production from water. Chem 5, 1632–1647 (2019).
Liu, W. et al. A scalable general synthetic approach toward ultrathin imine-linked two-dimensional covalent organic framework nanosheets for photocatalytic CO2 reduction. J. Am. Chem. Soc. 141, 17431–17440 (2019).
Bi, S. et al. Vinylene-bridged two-dimensional covalent organic frameworks via Knoevenagel condensation of tricyanomesitylene. J. Am. Chem. Soc. 142, 11893–11900 (2020).
Xu, Q. et al. Template conversion of covalent organic frameworks into 2D conducting nanocarbons for catalyzing oxygen reduction reaction. Adv. Mater. 30, 1706330 (2018).
Xu, H. et al. Catalytic covalent organic frameworks via pore surface engineering. Chem. Commun. 50, 1292–1294 (2014).
Wang, X. et al. Homochiral 2D porous covalent organic frameworks for heterogeneous asymmetric catalysis. J. Am. Chem. Soc. 138, 12332–12335 (2016).
Ma, H.-C., Chen, G.-J., Huang, F. & Dong, Y.-B. Homochiral covalent organic framework for catalytic asymmetric synthesis of a drug intermediate. J. Am. Chem. Soc. 142, 12574–12578 (2020).
Han, X. et al. Chiral covalent organic frameworks with high chemical stability for heterogeneous asymmetric catalysis. J. Am. Chem. Soc. 139, 8693–8697 (2017).
Tan, K. T., Tao, S., Huang, N. & Jiang, D. Water cluster in hydrophobic crystalline porous covalent organic frameworks. Nat. Commun. 12, 6747 (2021). This work showcases water confinement control in the COF channels.
Nguyen, H. L. et al. A porous covalent organic framework with voided square grid topology for atmospheric water harvesting. J. Am. Chem. Soc. 142, 2218–2221 (2020).
Biswal, B. P. et al. Pore surface engineering in porous, chemically stable covalent organic frameworks for water adsorption. J. Mater. Chem. A 3, 23664–23669 (2015).
Sun, Q. et al. Covalent organic frameworks as a decorating platform for utilization and affinity enhancement of chelating sites for radionuclide sequestration. Adv. Mater. 30, 1705479 (2018).
Li, Y., Yang, C.-X., Qian, H.-L., Zhao, X. & Yan, X.-P. Carboxyl-functionalized covalent organic frameworks for the adsorption and removal of triphenylmethane dyes. ACS Appl. Nano Mater. 2, 7290–7298 (2019).
Furukawa, H. & Yaghi, O. M. Storage of hydrogen, methane, and carbon dioxide in highly porous covalent organic frameworks for clean energy applications. J. Am. Chem. Soc. 131, 8875–8883 (2009).
Kahveci, Z., Islamoglu, T., Shar, G. A., Ding, R. & El-Kaderi, H. M. Targeted synthesis of a mesoporous triptycene-derived covalent organic framework. CrystEngComm 15, 1524–1527 (2013).
Zhai, L., Huang, N., Xu, H., Chen, Q. & Jiang, D. A backbone design principle for covalent organic frameworks: the impact of weakly interacting units on CO2 adsorption. Chem. Commun. 53, 4242–4245 (2017).
Huang, N., Chen, X., Krishna, R. & Jiang, D. Two-dimensional covalent organic frameworks for carbon dioxide capture through channel-wall functionalization. Angew. Chem. Int. Ed. 54, 2986–2990 (2015).
Huang, N., Zhai, L., Xu, H. & Jiang, D. Stable covalent organic frameworks for exceptional mercury removal from aqueous solutions. J. Am. Chem. Soc. 139, 2428–2434 (2017).
Ding, S.-Y. et al. Thioether-based fluorescent covalent organic framework for selective detection and facile removal of mercury(II). J. Am. Chem. Soc. 138, 3031–3037 (2016).
Sun, Q. et al. Postsynthetically modified covalent organic frameworks for efficient and effective mercury removal. J. Am. Chem. Soc. 139, 2786–2793 (2017).
Li, Z. et al. Three-dimensional ionic covalent organic frameworks for rapid, reversible, and selective ion exchange. J. Am. Chem. Soc. 139, 17771–17774 (2017).
Garai, B. et al. Taming the topology of calix[4]arene-based 2D-covalent organic frameworks: interpenetrated vs noninterpenetrated frameworks and their selective removal of cationic dyes. J. Am. Chem. Soc. 143, 3407–3415 (2021).
Wang, P. et al. High-precision size recognition and separation in synthetic 1D nanochannels. Angew. Chem. Int. Ed. 58, 15922–15927 (2019).
Ning, G.-H. et al. Salicylideneanilines-based covalent organic fframeworks as chemoselective molecular sieves. J. Am. Chem. Soc. 139, 8897–8904 (2017).
Qian, H.-L., Yang, C.-X. & Yan, X.-P. Bottom-up synthesis of chiral covalent organic frameworks and their bound capillaries for chiral separation. Nat. Commun. 7, 12104 (2016).
Li, X. et al. Tuneable near white-emissive two-dimensional covalent organic frameworks. Nat. Commun. 9, 2335 (2018).
Li, Z. et al. Editing light emission with stable crystalline covalent organic frameworks via wall surface perturbation. Angew. Chem. Int. Ed. 60, 19419–19427 (2021).
Jhulki, S. et al. Humidity sensing through reversible isomerization of a covalent organic framework. J. Am. Chem. Soc. 142, 783–791 (2020).
Koh, J. X., Geng, K. & Jiang, D. Smart covalent organic frameworks: dual channel sensors for acids and bases. Chem. Commun. 57, 9418–9421 (2021).
Han, X. et al. Chiral induction in covalent organic frameworks. Nat. Commun. 9, 1294 (2018).
Peng, Y. et al. Ultrathin two-dimensional covalent organic framework nanosheets: preparation and application in highly sensitive and selective DNA detection. J. Am. Chem. Soc. 139, 8698–8704 (2017).
Chen, S., Yuan, B., Liu, G. & Zhang, D. Electrochemical sensors based on covalent organic frameworks: a critical review. Front. Chem. 8, 601044 (2020).
Kandambeth, S., Kale, V. S., Shekhah, O., Alshareef, H. N. & Eddaoudi, M. 2D covalent-organic framework electrodes for supercapacitors and rechargeable metal-ion batteries. Adv. Energy Mater. 12, 2100177 (2022).
Li, J. et al. Bulk COFs and COF nanosheets for electrochemical energy storage and conversion. Chem. Soc. Rev. 49, 3565–3604 (2020).
Zhao, X., Pachfule, P. & Thomas, A. Covalent organic frameworks (COFs) for electrochemical applications. Chem. Soc. Rev. 50, 6871–6913 (2021).
Xu, F. et al. Radical covalent organic frameworks: a general strategy to immobilize open-accessible polyradicals for high-performance capacitive energy storage. Angew. Chem. Int. Ed. 54, 6814–6818 (2015).
Xu, F. et al. Electrochemically active, crystalline, mesoporous covalent organic frameworks on carbon nanotubes for synergistic lithium-ion battery energy storage. Sci. Rep. 5, 8225 (2015).
Haldar, S., Roy, K., Kushwaha, R., Ogale, S. & Vaidhyanathan, R. Chemical exfoliation as a controlled route to enhance the anodic performance of COF in LIB. Adv. Energy Mater. 9, 1902428 (2019).
Yang, D.-H. et al. Structure-modulated crystalline covalent organic frameworks as high-rate cathodes for Li-ion batteries. J. Mater. Chem. A 4, 18621–18627 (2016).
Xu, F. et al. Energy-storage covalent organic frameworks: improving performance via engineering polysulfide chains on walls. Chem. Sci. 10, 6001–6006 (2019).
Xu, Q. et al. Boosting lithium–sulfur battery performance by integrating a redox-active covalent organic framework in the separator. ACS Appl. Energy Mater. 2, 5793–5798 (2019).
Jiang, C. et al. Constructing universal ionic sieves via alignment of two-dimensional covalent organic frameworks (COFs). Angew. Chem. Int. Ed. 57, 16072–16076 (2018).
Peng, Y. et al. Mechanoassisted synthesis of sulfonated covalent organic frameworks with high intrinsic proton conductivity. ACS Appl. Mater. Interfaces 8, 18505–18512 (2016).
Sasmal, H. S. et al. Superprotonic conductivity in flexible porous covalent organic framework membranes. Angew. Chem. Int. Ed. 57, 10894–10898 (2018).
Li, J., Wang, J., Wu, Z., Tao, S. & Jiang, D. Ultrafast and stable proton conduction in polybenzimidazole covalent organic frameworks via confinement and activation. Angew. Chem. Int. Ed. 60, 12918–12923 (2021).
Feriante, C. et al. New mechanistic insights into the formation of imine-linked two-dimensional covalent organic frameworks. J. Am. Chem. Soc. 142, 18637–18644 (2020).
Xu, Q., Tao, S., Jiang, Q. & Jiang, D. Ion conduction in polyelectrolyte covalent organic frameworks. J. Am. Chem. Soc. 140, 7429–7432 (2018).
Xu, Q., Tao, S., Jiang, Q. & Jiang, D. Designing covalent organic frameworks with a tailored ionic interface for ion transport across one-dimensional channels. Angew. Chem. Int. Ed. 59, 4557–4563 (2020).
Zhang, G. et al. Accumulation of glassy poly(ethylene oxide) anchored in a covalent organic framework as a solid-state Li+ electrolyte. J. Am. Chem. Soc. 141, 1227–1234 (2018).
Hu, Y. et al. Crystalline lithium imidazolate covalent organic frameworks with high Li-ion conductivity. J. Am. Chem. Soc. 141, 7518–7525 (2019).
Tao, S. et al. Hydroxide anion transport in covalent organic frameworks. J. Am. Chem. Soc. 143, 8970–8975 (2021). This meticulous work describes anion transport in COFs with a detailed investigation.
Huang, N., Wang, P. & Jiang, D. Covalent organic frameworks: a materials platform for structural and functional designs. Nat. Rev. Mater. 1, 16068 (2016).
Lohse, M. S. & Bein, T. Covalent organic frameworks: structures, synthesis, and applications. Adv. Funct. Mater. 28, 1705553 (2018).
Chen, X. et al. Covalent organic frameworks: chemical approaches to designer structures and built-In functions. Angew. Chem. Int. Ed. 59, 5050–5091 (2020).
Spitzer, S. et al. Solvent-free on-surface synthesis of boroxine COF monolayers. Chem. Commun. 53, 5147–5150 (2017).
Cai, Z. F. et al. Electric-field-mediated reversible transformation between supramolecular networks and covalent organic frameworks. J. Am. Chem. Soc. 141, 11404–11408 (2019).
Wang, S., Yang, L., Xu, K., Chen, H. & Huang, N. De Novo fabrication of large-area and self-standing covalent organic framework films for efficient separation. ACS Appl. Mater. Interfaces 13, 44806–44813 (2021).
Li, R. L. et al. Controlled growth of imine-linked two-dimensional covalent organic framework nanoparticles. Chem. Sci. 10, 3796–3801 (2019).
Nagai, A. et al. Pore surface engineering in covalent organic frameworks. Nat. Commun. 2, 536 (2011). This work reports the pore surface engineering strategy for designing and constructing COFs with tailor-made pores that are used in many latter studies.
Li, Z., He, T., Gong, Y. & Jiang, D. Covalent organic frameworks: pore design and interface engineering. Acc. Chem. Res. 53, 1672–1685 (2020).
Emmerling, S. T. et al. In situ monitoring of mechanochemical covalent organic framework formation reveals templating effect of liquid additive. Chem 7, 1639–1652 (2021).
Seki, T. et al. Real-time study of on-water chemistry: surfactant monolayer-assisted growth of a crystalline quasi-2D polymer. Chem 7, 2758–2770 (2021).
Zhan, G. et al. Observing polymerization in 2D dynamic covalent polymers. Nature 603, 835–840 (2022).
Sanchez-Lengeling, B. & Aspuru-Guzik, A. Inverse molecular design using machine learning: generative models for matter engineering. Science 361, 360–365 (2018).
Wang, Y. et al. Toward designing highly conductive polymer electrolytes by machine learning assisted coarse-grained molecular dynamics. Chem. Mater. 32, 4144–4151 (2020).
Chen, Z., Kirlikovali, K. O., Li, P. & Farha, O. K. Reticular chemistry for highly porous metal–organic frameworks: the chemistry and applications. Acc. Chem. Res. 55, 579–591 (2022).
Ma, N. & Horike, S. Metal–organic network-forming glasses. Chem. Rev. 122, 4163–4203 (2022).
Kang, S., Kim, G.-H. & Park, S.-J. Conjugated block copolymers for functional nanostructures. Acc. Chem. Res. 55, 2224–2234 (2022).
Li, J., Zhou, X., Wang, J. & Li, X. Two-dimensional covalent organic frameworks (COFs) for membrane separation: a mini review. Ind. Eng. Chem. Res. 58, 15394–15406 (2019).
Dogru, M. & Bein, T. On the road towards electroactive covalent organic frameworks. Chem. Commun. 50, 5531–5546 (2014).
Wang, S. et al. Semiconductive covalent organic frameworks: structural design, synthesis, and application. Small Struct. 1, 2000021 (2020).
Esrafili, A., Wagner, A., Inamdar, S. & Acharya, A. P. Covalent organic frameworks for biomedical applications. Adv. Healthc. Mater. 10, 2002090 (2021).
Liu, X. et al. Recent advances in covalent organic frameworks (COFs) as a smart sensing material. Chem. Soc. Rev. 48, 5266–5302 (2019).
Acknowledgements
D.J. acknowledges Singapore Ministry of Education (MOE) Tier 2 grants (MOE-T2EP10220-0004 and MOE-T2EP10221-0006), MOE Tier 1 grants (A-0008368-00-00 and A-0008369-00-00) and an A* star grant (U2102d2004). A.T. is grateful for support from the Deutsche Forschungsgemeinschaft (DFG; German Research Foundation) under Germany′s Excellence Strategy — EXC 2008-390540038 — UniSysCat. S.G. acknowledges the Alexander von Humboldt Stiftung for a postdoctoral fellowship. Z.W. and X.F. acknowledge the EU Graphene Flagship (GrapheneCore3, no. 881603), ERC Consolidator Grant (T2DCP), DFG project (2D polyanilines, no. 426572620), CRC 1415 (Chemistry of Synthetic Two-Dimensional Materials, no. 417590517) and SPP 2244 (2DMP). F.Z. and D.R.-S.-M. acknowledge Ministerio de Ciencia e Innovación through project PID2019-106268GB-C32. W.W. acknowledges financial support by the National Natural Science Foundation of China (Nos. 92056202 and 21903041) and the 111 project 2.0 (BP1221004). N.H. acknowledges the National Natural Science Foundation of China (No. 92163131).
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All authors researched data for the article. All authors contributed substantially to discussion of the content. S.G. and A.T. wrote Irreversible reactions. Z.W. and X.F. wrote Thin films, Composites and Outlook. F.W. and N.H. wrote Reproducibility and data deposition, Limitations and optimizations, and Outlook. D.R.-S.-M. and F.Z. wrote Processable COFs and Energy storage. J.F. and W.W. wrote Single-crystal formation. D.J. and K.T.T. wrote the rest of the sections, reviewed and edited the manuscript and prepared the figures before submission.
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Glossary
- π interactions
-
Non-covalent interactions that involve the π system.
- Covalent bonds
-
Regions of relatively high electron density between nuclei that arise at least partly from sharing of electrons and give rise to an attractive force and characteristic internuclear distance.
- Knots
-
Organic molecules with multiple reactive points to enable the branching of a polymeric backbone and that locate on the lattice vertex.
- Linkers
-
Organic molecules with multiple reactive points that connect knots.
- Non-covalent interactions
-
Forces that do not involve the sharing of electrons but involve dispersed electromagnetic interactions.
- Polycondensation reactions
-
Polymerizations in which the growth of polymer chains proceeds by condensation reactions between molecules of all degrees of polymerization.
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Tan, K.T., Ghosh, S., Wang, Z. et al. Covalent organic frameworks. Nat Rev Methods Primers 3, 1 (2023). https://doi.org/10.1038/s43586-022-00181-z
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DOI: https://doi.org/10.1038/s43586-022-00181-z