Post-synthetic modification of covalent organic frameworks

Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

Tornøe, C. W., Christensen, C., & Meldal, M. (2002) · The Journal of Organic Chemistry · doi:10.1021/jo011148j · Cited by 8,696

Porous, Crystalline, Covalent Organic Frameworks

Côté, A. P., Benin, A. I., Ockwig, N. W., O'Keeffe, M., Matzger, A. J., & Yaghi, O. M. (2005) · Science · doi:10.1126/science.1120411 · Cited by 8,357

Metal–Organic Frameworks (MOFs)

Zhou, H.-C. “., & Kitagawa, S. (2014) · Chem. Soc. Rev. · doi:10.1039/c4cs90059f · Cited by 4,125

Covalent organic frameworks (COFs): from design to applications

Ding, S.-Y., & Wang, W. (2013) · Chem. Soc. Rev. · doi:10.1039/c2cs35072f · Cited by 4,020

The atom, the molecule, and the covalent organic framework

Diercks, C. S., & Yaghi, O. M. (2017) · Science · doi:10.1126/science.aal1585 · Cited by 3,482

Covalent organic frameworks

Feng, X., Ding, X., & Jiang, D. (2012) · Chemical Society Reviews · doi:10.1039/c2cs35157a · Cited by 3,098

Metal–Organic Frameworks and Self-Assembled Supramolecular Coordination Complexes: Comparing and Contrasting the Design, Synthesis, and Functionality of Metal–Organic Materials

Cook, T. R., Zheng, Y.-R., & Stang, P. J. (2013) · Chemical Reviews · doi:10.1021/cr3002824 · Cited by 2,950

Supramolecular Coordination: Self-Assembly of Finite Two- and Three-Dimensional Ensembles

Chakrabarty, R., Mukherjee, P. S., & Stang, P. J. (2011) · Chemical Reviews · doi:10.1021/cr200077m · Cited by 2,926

Covalent organic frameworks comprising cobalt porphyrins for catalytic CO 2 reduction in water

Lin, S., Diercks, C. S., Zhang, Y.-B., Kornienko, N., Nichols, E. M., Zhao, Y., Paris, A. R., Kim, D., Yang, P., Yaghi, O. M., et al. (2015) · Science · doi:10.1126/science.aac8343 · Cited by 2,644

Applications of hybrid organic–inorganic nanocomposites

Sanchez, C., Julián, B., Belleville, P., & Popall, M. (2005) · Journal of Materials Chemistry · doi:10.1039/b509097k · Cited by 2,636

Synthesis, Structure, and Carbon Dioxide Capture Properties of Zeolitic Imidazolate Frameworks

Phan, A., Doonan, C. J., Uribe-Romo, F. J., Knobler, C. B., O’Keeffe, M., & Yaghi, O. M. (2010) · Accounts of Chemical Research · doi:10.1021/ar900116g · Cited by 2,618

Dynamic Covalent Chemistry

Rowan, S. J., Cantrill, S. J., Cousins, G. R. L., Sanders, J. K. M., & Stoddart, J. F. (2002) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20020315)41:6<898::aid-anie898>3.0.co;2-e · Cited by 2,588

Designed Synthesis of 3D Covalent Organic Frameworks

El-Kaderi, H. M., Hunt, J. R., Mendoza-Cortés, J. L., Côté, A. P., Taylor, R. E., O'Keeffe, M., & Yaghi, O. M. (2007) · Science · doi:10.1126/science.1139915 · Cited by 2,575

Construction of Covalent Organic Framework for Catalysis: Pd/COF-LZU1 in Suzuki–Miyaura Coupling Reaction

Ding, S.-Y., Gao, J., Wang, Q., Zhang, Y., Song, W.-G., Su, C.-Y., & Wang, W. (2011) · Journal of the American Chemical Society · doi:10.1021/ja206846p · Cited by 2,443

Construction of Crystalline 2D Covalent Organic Frameworks with Remarkable Chemical (Acid/Base) Stability via a Combined Reversible and Irreversible Route

Kandambeth, S., Mallick, A., Lukose, B., Mane, M. V., Heine, T., & Banerjee, R. (2012) · Journal of the American Chemical Society · doi:10.1021/ja308278w · Cited by 2,156

Covalent organic frameworks: a materials platform for structural and functional designs

Huang, N., Wang, P., & Jiang, D. (2016) · Nature Reviews Materials · doi:10.1038/natrevmats.2016.68 · Cited by 2,017

Metal–Salen Schiff base complexes in catalysis: practical aspects

Cozzi, P. G. (2004) · Chem. Soc. Rev. · doi:10.1039/b307853c · Cited by 1,978

Functional Molecular Flasks: New Properties and Reactions within Discrete, Self‐Assembled Hosts

Yoshizawa, M., Klosterman, J. K., & Fujita, M. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200805340 · Cited by 1,930

Dynamic Combinatorial Chemistry

Corbett, P. T., Leclaire, J., Vial, L., West, K. R., Wietor, J.-L., Sanders, J. K. M., & Otto, S. (2006) · Chemical Reviews · doi:10.1021/cr020452p · Cited by 1,922

Chemistry of Covalent Organic Frameworks

Waller, P. J., Gándara, F., & Yaghi, O. M. (2015) · Accounts of Chemical Research · doi:10.1021/acs.accounts.5b00369 · Cited by 1,897

dynamic covalent chemistry

Ruhland, K. (2020) · Catalysis from A to Z · doi:10.1002/9783527809080.cataz06077 · Cited by 1,724

A Crystalline Imine-Linked 3-D Porous Covalent Organic Framework

Uribe-Romo, F. J., Hunt, J. R., Furukawa, H., Klöck, C., O’Keeffe, M., & Yaghi, O. M. (2009) · Journal of the American Chemical Society · doi:10.1021/ja8096256 · Cited by 1,715

Conjugated microporous polymers: design, synthesis and application

Xu, Y., Jin, S., Xu, H., Nagai, A., & Jiang, D. (2013) · Chemical Society Reviews · doi:10.1039/c3cs60160a · Cited by 1,683

Stable, crystalline, porous, covalent organic frameworks as a platform for chiral organocatalysts

Xu, H., Gao, J., & Jiang, D. (2015) · Nature Chemistry · doi:10.1038/nchem.2352 · Cited by 1,643

Covalent Organic Frameworks: Chemistry beyond the Structure

Kandambeth, S., Dey, K., & Banerjee, R. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.8b10334 · Cited by 1,575

Covalent Organic Frameworks: Structures, Synthesis, and Applications

Lohse, M. S., & Bein, T. (2018) · Advanced Functional Materials · doi:10.1002/adfm.201705553 · Cited by 1,527

Recent advances in dynamic covalent chemistry

Jin, Y., Yu, C., Denman, R. J., & Zhang, W. (2013) · Chemical Society Reviews · doi:10.1039/c3cs60044k · Cited by 1,487

Privileged Chiral Catalysts

Yoon, T. P., & Jacobsen, E. N. (2003) · Science · doi:10.1126/science.1083622 · Cited by 1,459

The use of elemental sulfur as an alternative feedstock for polymeric materials

Chung, W. J., Griebel, J. J., Kim, E. T., Yoon, H., Simmonds, A. G., Ji, H. J., Dirlam, P. T., Glass, R. S., Wie, J. J., Nguyen, N. A., et al. (2013) · Nature Chemistry · doi:10.1038/nchem.1624 · Cited by 1,455

Covalent organic frameworks based on Schiff-base chemistry: synthesis, properties and potential applications

Segura, J. L., Mancheño, M. J., & Zamora, F. (2016) · Chemical Society Reviews · doi:10.1039/c5cs00878f · Cited by 1,409

Two-dimensional sp 2 carbon–conjugated covalent organic frameworks

Jin, E., Asada, M., Xu, Q., Dalapati, S., Addicoat, M. A., Brady, M. A., Xu, H., Nakamura, T., Heine, T., Chen, Q., et al. (2017) · Science · doi:10.1126/science.aan0202 · Cited by 1,334

The convergence of synthetic organic and polymer chemistries

Hawker, C. J., & Wooley, K. L. (2005) · Science · doi:10.1126/science.1109778 · Cited by 1,298

β-Ketoenamine-Linked Covalent Organic Frameworks Capable of Pseudocapacitive Energy Storage

DeBlase, C. R., Silberstein, K. E., Truong, T.-T., Abruña, H. D., & Dichtel, W. R. (2013) · Journal of the American Chemical Society · doi:10.1021/ja409421d · Cited by 1,249

Covalent organic frameworks for membrane separation

Yuan, S., Li, X., Zhu, J., Zhang, G., Van Puyvelde, P., & Van der Bruggen, B. (2019) · Chemical Society Reviews · doi:10.1039/c8cs00919h · Cited by 1,201

Bipyridine: The Most Widely Used Ligand. A Review of Molecules Comprising at Least Two 2,2‘-Bipyridine Units

Kaes, C., Katz, A., & Hosseini, M. W. (2000) · Chemical Reviews · doi:10.1021/cr990376z · Cited by 1,174

Postsynthetically Modified Covalent Organic Frameworks for Efficient and Effective Mercury Removal

Sun, Q., Aguila, B., Perman, J., Earl, L. D., Abney, C. W., Cheng, Y., Wei, H., Nguyen, N., Wojtas, L., & Ma, S. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.6b12885 · Cited by 1,056

Exfoliation of Covalent Organic Frameworks into Few-Layer Redox-Active Nanosheets as Cathode Materials for Lithium-Ion Batteries

Wang, S., Wang, Q., Shao, P., Han, Y., Gao, X., Ma, L., Yuan, S., Ma, X., Zhou, J., Feng, X., et al. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b02648 · Cited by 1,030

Rationally synthesized two-dimensional polymers

Colson, J. W., & Dichtel, W. R. (2013) · Nature Chemistry · doi:10.1038/nchem.1628 · Cited by 1,016

Crystalline Covalent Organic Frameworks with Hydrazone Linkages

Uribe-Romo, F. J., Doonan, C. J., Furukawa, H., Oisaki, K., & Yaghi, O. M. (2011) · Journal of the American Chemical Society · doi:10.1021/ja204728y · Cited by 977

From precision polymers to complex materials and systems

Lutz, J.-F., Lehn, J.-M., Meijer, E. W., & Matyjaszewski, K. (2016) · Nature Reviews Materials · doi:10.1038/natrevmats.2016.24 · Cited by 969

An Azine-Linked Covalent Organic Framework

Dalapati, S., Jin, S., Gao, J., Xu, Y., Nagai, A., & Jiang, D. (2013) · Journal of the American Chemical Society · doi:10.1021/ja4103293 · Cited by 924

Beyond post-synthesis modification: evolution of metal–organic frameworks via building block replacement

Deria, P., Mondloch, J. E., Karagiaridi, O., Bury, W., Hupp, J. T., & Farha, O. K. (2014) · Chem. Soc. Rev. · doi:10.1039/c4cs00067f · Cited by 877

Click Chemistry beyond Metal‐Catalyzed Cycloaddition

Becer, C. R., Hoogenboom, R., & Schubert, U. S. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200900755 · Cited by 866

Reticular Synthesis of Microporous and Mesoporous 2D Covalent Organic Frameworks

Côté, A. P., El-Kaderi, H. M., Furukawa, H., Hunt, J. R., & Yaghi, O. M. (2007) · Journal of the American Chemical Society · doi:10.1021/ja0751781 · Cited by 812

Thiol–ene “click” reactions and recent applications in polymer and materials synthesis: a first update

Lowe, A. B. (2014) · Polym. Chem. · doi:10.1039/c4py00339j · Cited by 768

Fe-Porphyrin-Based Metal–Organic Framework Films as High-Surface Concentration, Heterogeneous Catalysts for Electrochemical Reduction of CO2

Hod, I., Sampson, M. D., Deria, P., Kubiak, C. P., Farha, O. K., & Hupp, J. T. (2015) · ACS Catalysis · doi:10.1021/acscatal.5b01767 · Cited by 765

Two‐Dimensional Covalent Organic Frameworks for Carbon Dioxide Capture through Channel‐Wall Functionalization

Huang, N., Chen, X., Krishna, R., & Jiang, D. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201411262 · Cited by 762

Designed synthesis of large-pore crystalline polyimide covalent organic frameworks

Fang, Q., Zhuang, Z., Gu, S., Kaspar, R. B., Zheng, J., Wang, J., Qiu, S., & Yan, Y. (2014) · Nature Communications · doi:10.1038/ncomms5503 · Cited by 753

Catechol‐Based Biomimetic Functional Materials

Sedó, J., Saiz‐Poseu, J., Busqué, F., & Ruiz‐Molina, D. (2013) · Advanced Materials · doi:10.1002/adma.201202343 · Cited by 752

Chemically stable polyarylether-based covalent organic frameworks

Guan, X., Li, H., Ma, Y., Xue, M., Fang, Q., Yan, Y., Valtchev, V., & Qiu, S. (2019) · Nature Chemistry · doi:10.1038/s41557-019-0238-5 · Cited by 749

Lewis acid-catalysed formation of two-dimensional phthalocyanine covalent organic frameworks

Spitler, E. L., & Dichtel, W. R. (2010) · Nature Chemistry · doi:10.1038/nchem.695 · Cited by 747

A net-based approach to coordination polymers †

Robson, R. (2000) · Journal of the Chemical Society, Dalton Transactions · doi:10.1039/b003591m · Cited by 726

DYNAMERS: dynamic polymers as self-healing materials

Roy, N., Bruchmann, B., & Lehn, J.-M. (2015) · Chemical Society Reviews · doi:10.1039/c5cs00194c · Cited by 717

2D Covalent Organic Frameworks as Intrinsic Photocatalysts for Visible Light-Driven CO2 Reduction

Yang, S., Hu, W., Zhang, X., He, P., Pattengale, B., Liu, C., Cendejas, M., Hermans, I., Zhang, X., Zhang, J., et al. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b09705 · Cited by 705

Chiral Salen Complexes: An Overview to Recoverable and Reusable Homogeneous and Heterogeneous Catalysts

Baleizão, C., & Garcia, H. (2006) · Chemical Reviews · doi:10.1021/cr050973n · Cited by 697

Synthesis of Ultrafine and Highly Dispersed Metal Nanoparticles Confined in a Thioether-Containing Covalent Organic Framework and Their Catalytic Applications

Lu, S., Hu, Y., Wan, S., McCaffrey, R., Jin, Y., Gu, H., & Zhang, W. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b07918 · Cited by 646

Covalent Organic Frameworks as a Decorating Platform for Utilization and Affinity Enhancement of Chelating Sites for Radionuclide Sequestration

Sun, Q., Aguila, B., Earl, L. D., Abney, C. W., Wojtas, L., Thallapally, P. K., & Ma, S. (2018) · Advanced Materials · doi:10.1002/adma.201705479 · Cited by 641

Multivalency and Cooperativity in Supramolecular Chemistry

Badjić, J. D., Nelson, A., Cantrill, S. J., Turnbull, W. B., & Stoddart, J. F. (2005) · Accounts of Chemical Research · doi:10.1021/ar040223k · Cited by 635

Weaving of organic threads into a crystalline covalent organic framework

Liu, Y., Ma, Y., Zhao, Y., Sun, X., Gándara, F., Furukawa, H., Liu, Z., Zhu, H., Zhu, C., Suenaga, K., et al. (2016) · Science · doi:10.1126/science.aad4011 · Cited by 616

A Photoconductive Covalent Organic Framework: Self‐Condensed Arene Cubes Composed of Eclipsed 2D Polypyrene Sheets for Photocurrent Generation

Wan, S., Guo, J., Kim, J., Ihee, H., & Jiang, D. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200900881 · Cited by 614

Chemical Conversion of Linkages in Covalent Organic Frameworks

Waller, P. J., Lyle, S. J., Osborn Popp, T. M., Diercks, C. S., Reimer, J. A., & Yaghi, O. M. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b08377 · Cited by 604

Targeted Drug Delivery in Covalent Organic Nanosheets (CONs) via Sequential Postsynthetic Modification

Mitra, S., Sasmal, H. S., Kundu, T., Kandambeth, S., Illath, K., Díaz Díaz, D., & Banerjee, R. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b00925 · Cited by 587

Opportunities of Covalent Organic Frameworks for Advanced Applications

Song, Y., Sun, Q., Aguila, B., & Ma, S. (2019) · Advanced Science · doi:10.1002/advs.201801410 · Cited by 586

Facile transformation of imine covalent organic frameworks into ultrastable crystalline porous aromatic frameworks

Li, X., Zhang, C., Cai, S., Lei, X., Altoé, V., Hong, F., Urban, J. J., Ciston, J., Chan, E. M., & Liu, Y. (2018) · Nature Communications · doi:10.1038/s41467-018-05462-4 · Cited by 573

Crystal engineering of topochemical solid state reactions

Biradha, K., & Santra, R. (2013) · Chem. Soc. Rev. · doi:10.1039/c2cs35343a · Cited by 539

Pore surface engineering in covalent organic frameworks

Nagai, A., Guo, Z., Feng, X., Jin, S., Chen, X., Ding, X., & Jiang, D. (2011) · Nature Communications · doi:10.1038/ncomms1542 · Cited by 523

3D Porphyrin-Based Covalent Organic Frameworks

Lin, G., Ding, H., Chen, R., Peng, Z., Wang, B., & Wang, C. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b04141 · Cited by 517

Nanocrystal bilayer for tandem catalysis

Yamada, Y., Tsung, C.-K., Huang, W., Huo, Z., Habas, S. E., Soejima, T., Aliaga, C. E., Somorjai, G. A., & Yang, P. (2011) · Nature Chemistry · doi:10.1038/nchem.1018 · Cited by 516

Supramolecular Chemistry and Self-Assembly in Organic Materials Design

Stupp, S. I., & Palmer, L. C. (2014) · Chemistry of Materials · doi:10.1021/cm403028b · Cited by 513

Advances in Inorganic Chemistry

Henderson, R. A. (2001) · Journal of Organometallic Chemistry · doi:10.1016/s0022-328x(01)00721-5 · Cited by 492

Flexibility Matters: Cooperative Active Sites in Covalent Organic Framework and Threaded Ionic Polymer

Sun, Q., Aguila, B., Perman, J., Nguyen, N., & Ma, S. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b10629 · Cited by 487

Cobalt-Modified Covalent Organic Framework as a Robust Water Oxidation Electrocatalyst

Aiyappa, H. B., Thote, J., Shinde, D. B., Banerjee, R., & Kurungot, S. (2016) · Chemistry of Materials · doi:10.1021/acs.chemmater.6b01370 · Cited by 483

Removal of GenX and Perfluorinated Alkyl Substances from Water by Amine-Functionalized Covalent Organic Frameworks

Ji, W., Xiao, L., Ling, Y., Ching, C., Matsumoto, M., Bisbey, R. P., Helbling, D. E., & Dichtel, W. R. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b06958 · Cited by 451

Radical Covalent Organic Frameworks: A General Strategy to Immobilize Open‐Accessible Polyradicals for High‐Performance Capacitive Energy Storage

Xu, F., Xu, H., Chen, X., Wu, D., Wu, Y., Liu, H., Gu, C., Fu, R., & Jiang, D. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201501706 · Cited by 449

Locking Covalent Organic Frameworks with Hydrogen Bonds: General and Remarkable Effects on Crystalline Structure, Physical Properties, and Photochemical Activity

Chen, X., Addicoat, M., Jin, E., Zhai, L., Xu, H., Huang, N., Guo, Z., Liu, L., Irle, S., & Jiang, D. (2015) · Journal of the American Chemical Society · doi:10.1021/ja509602c · Cited by 448

Covalent Organic Framework Electrocatalysts for Clean Energy Conversion

Lin, C., Zhang, D., Zhao, Z., & Xia, Z. (2018) · Advanced Materials · doi:10.1002/adma.201703646 · Cited by 443

H2 Evolution with Covalent Organic Framework Photocatalysts

Banerjee, T., Gottschling, K., Savasci, G., Ochsenfeld, C., & Lotsch, B. V. (2018) · ACS Energy Letters · doi:10.1021/acsenergylett.7b01123 · Cited by 440

Tailor-Made Pore Surface Engineering in Covalent Organic Frameworks: Systematic Functionalization for Performance Screening

Huang, N., Krishna, R., & Jiang, D. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b04300 · Cited by 437

Tessellated multiporous two-dimensional covalent organic frameworks

Jin, Y., Hu, Y., & Zhang, W. (2017) · Nature Reviews Chemistry · doi:10.1038/s41570-017-0056 · Cited by 421

Emerging crystalline porous materials as a multifunctional platform for electrochemical energy storage

Zhou, J., & Wang, B. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00283a · Cited by 418

Metalation of a Mesoporous Three-Dimensional Covalent Organic Framework

Baldwin, L. A., Crowe, J. W., Pyles, D. A., & McGrier, P. L. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b10316 · Cited by 403

Crystalline Lithium Imidazolate Covalent Organic Frameworks with High Li-Ion Conductivity

Hu, Y., Dunlap, N., Wan, S., Lu, S., Huang, S., Sellinger, I., Ortiz, M., Jin, Y., Lee, S.-H., & Zhang, W. (2019) · Journal of the American Chemical Society · doi:10.1021/jacs.9b02448 · Cited by 402

Covalent Triazine Framework as Catalytic Support for Liquid Phase Reaction

Chan-Thaw, C. E., Villa, A., Katekomol, P., Su, D. S., Thomas, A., & Prati, L. (2010) · Nano Letters · doi:10.1021/nl904082k · Cited by 390

Conjugated Covalent Organic Frameworks via Michael Addition–Elimination

Rao, M. R., Fang, Y., De Feyter, S., & Perepichka, D. F. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.6b12005 · Cited by 374

Postsynthetic Functionalization of Three‐Dimensional Covalent Organic Frameworks for Selective Extraction of Lanthanide Ions

Lu, Q., Ma, Y., Li, H., Guan, X., Yusran, Y., Xue, M., Fang, Q., Yan, Y., Qiu, S., & Valtchev, V. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201712246 · Cited by 358

Highly stable covalent organic framework–Au nanoparticles hybrids for enhanced activity for nitrophenol reduction

Pachfule, P., Kandambeth, S., Díaz Díaz, D., & Banerjee, R. (2014) · Chem. Commun. · doi:10.1039/c3cc49176e · Cited by 352

Constructing Crystalline Covalent Organic Frameworks from Chiral Building Blocks

Xu, H.-S., Ding, S.-Y., An, W.-K., Wu, H., & Wang, W. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b07516 · Cited by 350

Salen-Based Covalent Organic Framework

Li, L.-H., Feng, X.-L., Cui, X.-H., Ma, Y.-X., Ding, S.-Y., & Wang, W. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b01523 · Cited by 350

Applications of covalent organic frameworks (COFs): From gas storage and separation to drug delivery

Wu, M.-X., & Yang, Y.-W. (2017) · Chinese Chemical Letters · doi:10.1016/j.cclet.2017.03.026 · Cited by 348

Covalent Organic Frameworks as a Platform for Multidimensional Polymerization

Bisbey, R. P., & Dichtel, W. R. (2017) · ACS Central Science · doi:10.1021/acscentsci.7b00127 · Cited by 345

Metal/covalent–organic frameworks-based electrocatalysts for water splitting

Yan, Y., He, T., Zhao, B., Qi, K., Liu, H., & Xia, B. Y. (2018) · Journal of Materials Chemistry A · doi:10.1039/c8ta05985c · Cited by 318

Design of Vanadium Complex Catalysts for Precise Olefin Polymerization

Nomura, K., & Zhang, S. (2011) · Chemical Reviews · doi:10.1021/cr100207h · Cited by 310

Toward Covalent Organic Frameworks Bearing Three Different Kinds of Pores: The Strategy for Construction and COF-to-COF Transformation via Heterogeneous Linker Exchange

Qian, C., Qi, Q.-Y., Jiang, G.-F., Cui, F.-Z., Tian, Y., & Zhao, X. (2017) · Journal of the American Chemical Society · doi:10.1021/jacs.7b02303 · Cited by 308

Porphyrins as Catalysts in Scalable Organic Reactions

Barona-Castaño, J., Carmona-Vargas, C., Brocksom, T., & De Oliveira, K. (2016) · Molecules · doi:10.3390/molecules21030310 · Cited by 306

Highly Fluorescent Polyimide Covalent Organic Nanosheets as Sensing Probes for the Detection of 2,4,6-Trinitrophenol

Zhang, C., Zhang, S., Yan, Y., Xia, F., Huang, A., & Xian, Y. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6b16423 · Cited by 304

Chiral induction in covalent organic frameworks

Han, X., Zhang, J., Huang, J., Wu, X., Yuan, D., Liu, Y., & Cui, Y. (2018) · Nature Communications · doi:10.1038/s41467-018-03689-9 · Cited by 290

Recent progress in two-dimensional COFs for energy-related applications

Zhan, X., Chen, Z., & Zhang, Q. (2017) · Journal of Materials Chemistry A · doi:10.1039/c7ta02105d · Cited by 275

Catalysis using multifunctional organosiliceous hybrid materials

Díaz, U., Brunel, D., & Corma, A. (2013) · Chemical Society Reviews · doi:10.1039/c2cs35385g · Cited by 267

Thiol grafted imine-based covalent organic frameworks for water remediation through selective removal of Hg(ii)

Merí-Bofí, L., Royuela, S., Zamora, F., Ruiz-González, M. L., Segura, J. L., Muñoz-Olivas, R., & Mancheño, M. J. (2017) · Journal of Materials Chemistry A · doi:10.1039/c7ta05588a · Cited by 237

Metal Doped Core–Shell Metal‐Organic Frameworks@Covalent Organic Frameworks (MOFs@COFs) Hybrids as a Novel Photocatalytic Platform

Sun, D., Jang, S., Yim, S., Ye, L., & Kim, D. (2018) · Advanced Functional Materials · doi:10.1002/adfm.201707110 · Cited by 237

Surface Pore Engineering of Covalent Organic Frameworks for Ammonia Capture through Synergistic Multivariate and Open Metal Site Approaches

Yang, Y., Faheem, M., Wang, L., Meng, Q., Sha, H., Yang, N., Yuan, Y., & Zhu, G. (2018) · ACS Central Science · doi:10.1021/acscentsci.8b00232 · Cited by 237

Sequential Pore Wall Modification in a Covalent Organic Framework for Application in Lactic Acid Adsorption

Lohse, M. S., Stassin, T., Naudin, G., Wuttke, S., Ameloot, R., De Vos, D., Medina, D. D., & Bein, T. (2016) · Chemistry of Materials · doi:10.1021/acs.chemmater.5b04388 · Cited by 233

Dynamic covalent polymers

García, F., & Smulders, M. M. J. (2016) · Journal of Polymer Science Part A: Polymer Chemistry · doi:10.1002/pola.28260 · Cited by 229

Synthesis of ‘unfeasible’ zeolites

Mazur, M., Wheatley, P. S., Navarro, M., Roth, W. J., Položij, M., Mayoral, A., Eliášová, P., Nachtigall, P., Čejka, J., & Morris, R. E. (2016) · Nature Chemistry · doi:10.1038/nchem.2374 · Cited by 228

Immobilization of ionic liquids to covalent organic frameworks for catalyzing the formylation of amines with CO2 and phenylsilane

Dong, B., Wang, L., Zhao, S., Ge, R., Song, X., Wang, Y., & Gao, Y. (2016) · Chemical Communications · doi:10.1039/c6cc03058k · Cited by 209

From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks—A Modulation Approach

Calik, M., Sick, T., Dogru, M., Döblinger, M., Datz, S., Budde, H., Hartschuh, A., Auras, F., & Bein, T. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.5b10708 · Cited by 208

Design Principles for Covalent Organic Frameworks in Energy Storage Applications

Alahakoon, S. B., Thompson, C. M., Occhialini, G., & Smaldone, R. A. (2017) · ChemSusChem · doi:10.1002/cssc.201700120 · Cited by 192

Covalent Organic Frameworks: From Materials Design to Biomedical Application

Zhao, F., Liu, H., Mathe, S., Dong, A., & Zhang, J. (2017) · Nanomaterials · doi:10.3390/nano8010015 · Cited by 190

Recent advances in AIEgen-based luminescent metal–organic frameworks and covalent organic frameworks

Ma, L., Feng, X., Wang, S., & Wang, B. (2017) · Materials Chemistry Frontiers · doi:10.1039/c7qm00254h · Cited by 186

Towards covalent organic frameworks with predesignable and aligned open docking sites

Chen, X., Huang, N., Gao, J., Xu, H., Xu, F., & Jiang, D. (2014) · Chem. Commun. · doi:10.1039/c4cc01825g · Cited by 183

Ultrathin two-dimensional covalent organic framework nanoprobe for interference-resistant two-photon fluorescence bioimaging

Wang, P., Zhou, F., Zhang, C., Yin, S.-Y., Teng, L., Chen, L., Hu, X.-X., Liu, H.-W., Yin, X., & Zhang, X.-B. (2018) · Chemical Science · doi:10.1039/c8sc03393e · Cited by 167

Thiol–ene chemistry for polymer coatings and surface modification – building in sustainability and performance

Resetco, C., Hendriks, B., Badi, N., & Du Prez, F. (2017) · Mater. Horiz. · doi:10.1039/c7mh00488e · Cited by 158

Covalent-Organic Frameworks Composed of Rhenium Bipyridine and Metal Porphyrins: Designing Heterobimetallic Frameworks with Two Distinct Metal Sites

Johnson, E. M., Haiges, R., & Marinescu, S. C. (2018) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.8b07795 · Cited by 143

The Nanomaterial Characterization Bottleneck

Richman, E. K., & Hutchison, J. E. (2009) · ACS Nano · doi:10.1021/nn901112p · Cited by 141

Two-dimensional metal-organic framework and covalent-organic framework: synthesis and their energy-related applications

Zheng, W., Tsang, C., Lee, L. Y. S., & Wong, K. (2019) · Materials Today Chemistry · doi:10.1016/j.mtchem.2018.12.002 · Cited by 141

Covalent organic frameworks (COFs): perspectives of industrialization

Zhao, W. J., Xia, L., & Liu, X. (2018) · CrystEngComm · doi:10.1039/c7ce02079a · Cited by 140

Zwitterionic Covalent Organic Frameworks as Catalysts for Hierarchical Reduction of CO 2 with Amine and Hydrosilane

Mu, Z., Ding, X., Chen, Z., & Han, B. (2018) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.8b14671 · Cited by 136

Luminescent Porous Polymers Based on Aggregation‐Induced Mechanism: Design, Synthesis and Functions

Dalapati, S., Gu, C., & Jiang, D. (2016) · Small · doi:10.1002/smll.201602427 · Cited by 135

3D Covalent Organic Frameworks of Interlocking 1D Square Ribbons

Liu, Y., Diercks, C. S., Ma, Y., Lyu, H., Zhu, C., Alshmimri, S. A., Alshihri, S. M., & Yaghi, O. M. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b12177 · Cited by 134

Model Reactions for Synthesis of Pharmacologically Active Polymers by Way of Monomeric and Polymeric Reactive Esters

Batz, H. G., Franzmann, G., & Ringsdorf, H. (1972) · Angewandte Chemie International Edition in English · doi:10.1002/anie.197211031 · Cited by 123

ortho-Arene Cyclynes, Related Heterocyclynes, and Their Metal Chemistry

Youngs, W. J., Tessier, C. A., & Bradshaw, J. D. (1999) · Chemical Reviews · doi:10.1021/cr9902446 · Cited by 119

Postsynthetic Functionalization of Zr4+-Immobilized Core–Shell Structured Magnetic Covalent Organic Frameworks for Selective Enrichment of Phosphopeptides

Gao, C., Bai, J., He, Y., Zheng, Q., Ma, W., Lei, Z., Zhang, M., Wu, J., Fu, F., & Lin, Z. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b03330 · Cited by 119

Metal-functionalized covalent organic frameworks as precursors of supercapacitive porous N-doped graphene

Romero, J., Rodríguez‐San‐Miguel, D., Ribera, A., Mas‐Ballesté, R., Otero, T. F., Manet, I. G. J., Liscio, F., Abellán, G., Zamora, F., & Coronado, E. (2016) · Journal of Materials Chemistry A · doi:10.1039/c6ta09296a · Cited by 112

MasterChem: cooking 2D-polymers

Rodríguez‐San‐Miguel, D., Amo‐Ochoa, P., & Zamora, F. (2016) · Chemical Communications · doi:10.1039/c5cc10283a · Cited by 108

Highly Stable COF‐Supported Co/Co(OH)2 Nanoparticles Heterogeneous Catalyst for Reduction of Nitrile/Nitro Compounds under Mild Conditions

Mullangi, D., Chakraborty, D., Pradeep, A., Koshti, V. S., Vinod, C. P., Panja, S. N., Nair, S., & Vaidhyanathan, R. (2018) · Small · doi:10.1002/smll.201801233 · Cited by 106

Fe-Porphyrin-Based Covalent Organic Framework As a Novel Peroxidase Mimic for a One-Pot Glucose Colorimetric Assay

Wang, J., Yang, X., Wei, T., Bao, J., Zhu, Q., & Dai, Z. H. (2018) · ACS Applied Bio Materials · doi:10.1021/acsabm.8b00104 · Cited by 104

A covalent organic framework-based route to the in situ encapsulation of metal nanoparticles in N-rich hollow carbon spheres

Chen, L., Zhang, L., Chen, Z., Liu, H., Luque, R., & Li, Y. (2016) · Chemical Science · doi:10.1039/c6sc01659f · Cited by 100

Transition Metal Decorated Graphyne: An Efficient Catalyst for Oxygen Reduction Reaction

Kancharlapalli, S., & Ghosh, S. K. (2013) · The Journal of Physical Chemistry C · doi:10.1021/jp407007n · Cited by 96

A new azodioxy-linked porphyrin-based semiconductive covalent organic framework with I 2 doping-enhanced photoconductivity

Nath, B., Li, W., Huang, J., Wang, G., Fu, Z., Yao, M., & Xu, G. (2016) · CrystEngComm · doi:10.1039/c6ce00168h · Cited by 86

Covalent triazine framework-supported palladium nanoparticles for catalytic hydrogenation of N-heterocycles

He, T., Liu, L., Wu, G., & Chen, P. (2015) · Journal of Materials Chemistry A · doi:10.1039/c5ta03056k · Cited by 83

A quaternary-ammonium-functionalized covalent organic framework for anion conduction

Guo, H., Wang, J., Fang, Q., Zhao, Y., Gu, S., Zheng, J., & Yan, Y. S. (2017) · CrystEngComm · doi:10.1039/c7ce00042a · Cited by 77

Intensified synthesis and post-synthetic modification of covalent organic frameworks using a continuous flow of microdroplets technique

Singh, V. P., Jang, S., Vishwakarma, N. K., & Kim, D. (2018) · NPG Asia Materials · doi:10.1038/am.2017.209 · Cited by 55

Acid/hydrazide-appended covalent triazine frameworks for low-pressure CO 2 capture: pre-designable or post-synthesis modification

Fu, Y., Wang, Z., Fu, X., Yan, J., Liu, C., Pan, C., & Yu, G. (2017) · Journal of Materials Chemistry A · doi:10.1039/c7ta05416e · Cited by 53

Immobilization of dioxomolybdenum(VI) complex bearing salicylidene 2-picoloyl hydrazone on chloropropyl functionalized SBA-15: A highly active, selective and reusable catalyst in olefin epoxidation

Bagherzadeh, M., Zare, M., Salemnoush, T., Özkâr, S., & Akbayrak, S. (2014) · Applied Catalysis A General · doi:10.1016/j.apcata.2014.01.020 · Cited by 50

Catalytic oxidation of hydroquinone to quinone using molecular oxygen

Radel, R. J., Sullivan, J. M., & Hatfield, J. D. (1982) · Industrial & Engineering Chemistry Product Research and Development · doi:10.1021/i300008a010 · Cited by 47

Pore wall fluorescence labeling of covalent organic frameworks

Rager, S., Doḡru, M., Werner, V., Gavryushin, A. E., Götz, M., Engelke, H., Medina, D. D., Knochel, P., & Bein, T. (2017) · CrystEngComm · doi:10.1039/c7ce00684e · Cited by 43

Highly Efficient Oxygen Reduction Electrocatalyst Derived from a New Three-Dimensional PolyPorphyrin

Ren, S., Wang, J., & Xia, X. (2016) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6b05560 · Cited by 40

Photoactivatable Anthracenes

Thapaliya, E. R., Captain, B., & Raymo, F. M. (2014) · The Journal of Organic Chemistry · doi:10.1021/jo5004482 · Cited by 22

A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective ligation of azides and terminal alkynes

Rostovtsev, V. V., Green, L. G., Fokin, V. V., & Sharpless, K. B. (2002) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20020715)41:14<2596::aid-anie2596>3.0.co;2-4

Untitled work

Kolb (2001) · doi:10.1002/1521-3773(20010601)40:11<2004::aid-anie2004>3.0.co;2-5

Metal–Covalent Organic Frameworks (MCOFs): A Bridge Between Metal–Organic Frameworks and Covalent Organic Frameworks

Dong, J., Han, X., Liu, Y., Li, H., & Cui, Y. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202004796 · Cited by 561

Chiral covalent organic frameworks: design, synthesis and property

Han, X., Yuan, C., Hou, B., Liu, L., Li, H., Liu, Y., & Cui, Y. (2020) · Chemical Society Reviews · doi:10.1039/d0cs00009d · Cited by 478

Nanoscale covalent organic frameworks: from controlled synthesis to cancer therapy

He, X., Jiang, Z., Akakuru, O. U., Li, J., & Wu, A. (2021) · Chemical Communications · doi:10.1039/d1cc04846e · Cited by 303

Metallodrugs in cancer nanomedicine

Peña, Q., Wang, A., Zaremba, O., Shi, Y., Scheeren, H. W., Metselaar, J. M., Kiessling, F., Pallares, R. M., Wuttke, S., & Lammers, T. (2022) · Chemical Society Reviews · doi:10.1039/d1cs00468a · Cited by 259

Mixed-valence Pt(0)/Pt2+ nanoassemblies as high-Z radiosensitizers and metallo-immune regulators for potent radiotherapy of breast cancer

Zhang, F., Feng, L., Jia, C., Wu, Y., Liu, J., Shuai, X., & Cao, Z. (2023) · Nano Today · doi:10.1016/j.nantod.2022.101708 · Cited by 26