The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.
3D Porphyrin-Based Covalent Organic Frameworks
Abstract
The design and synthesis of three-dimensional covalent organic frameworks (3D COFs) bearing photoelectric units have been considered as a big challenge. Herein, for the first time, we reported the targeted synthesis of two 3D porphyrin-based COFs (3D-Por-COF and 3D-CuPor-COF), starting from tetrahedral (3D- T d ) and square (2D- C 4 ) building blocks connected through [4 + 4] imine condensation reactions. On the basis of structural characterizations, 3D-Por-COF and 3D-CuPor-COF are microporous materials with high surface areas, and are proposed to adopt a 2-fold interpenetrated pts topology with Pmc 2 1 space group. Interestingly, both 3D COFs are photosensitive and can be used as heterogeneous catalyst for generating singlet oxygen under photoirradiation. However, 3D-Por-COF shows enhanced photocatalytic activity compared with 3D-CuPor-COF, indicating the properties of 3D porphyrin-based COFs can be tuned by metalation of porphyrin rings. The results reported here will greatly inspire us to design and synthesize 3D COFs bearing other metalloporphyrins for interesting applications (e.g., catalysis) in the future.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
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 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
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
The Reticular Chemistry Structure Resource (RCSR) Database of, and Symbols for, Crystal Nets
O’Keeffe, M., Peskov, M. A., Ramsden, S. J., & Yaghi, O. M. (2008) · Accounts of Chemical Research · doi:10.1021/ar800124u · Cited by 2,313
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
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
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
Segura, J. L., Mancheño, M. J., & Zamora, F. (2016) · Chemical Society Reviews · doi:10.1039/c5cs00878f · Cited by 1,409
Ding, S.-Y., Dong, M., Wang, Y.-W., Chen, Y.-T., Wang, H.-Z., Su, C.-Y., & Wang, W. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.5b10754 · Cited by 1,333
Porous Organic Materials: Strategic Design and Structure–Function Correlation
Das, S., Heasman, P., Ben, T., & Qiu, S. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00439 · Cited by 1,286
A tunable azine covalent organic framework platform for visible light-induced hydrogen generation
Vyas, V. S., Haase, F., Stegbauer, L., Savasci, G., Podjaski, F., Ochsenfeld, C., & Lotsch, B. V. (2015) · Nature Communications · doi:10.1038/ncomms9508 · Cited by 1,263
Covalent Organic Frameworks for CO2 Capture
Zeng, Y., Zou, R., & Zhao, Y. (2016) · Advanced Materials · doi:10.1002/adma.201505004 · Cited by 1,140
3D Porous Crystalline Polyimide Covalent Organic Frameworks for Drug Delivery
Fang, Q., Wang, J., Gu, S., Kaspar, R. B., Zhuang, Z., Zheng, J., Guo, H., Qiu, S., & Yan, Y. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b04147 · Cited by 1,065
Covalent Organic Frameworks with High Charge Carrier Mobility
Wan, S., Gándara, F., Asano, A., Furukawa, H., Saeki, A., Dey, S. K., Liao, L., Ambrogio, M. W., Botros, Y. Y., Duan, X., et al. (2011) · Chemistry of Materials · doi:10.1021/cm201140r · Cited by 843
A Pyrene-Based, Fluorescent Three-Dimensional Covalent Organic Framework
Lin, G., Ding, H., Yuan, D., Wang, B., & Wang, C. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b00652 · Cited by 797
Self-citationLewis 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
Conjugated porphyrin arrays: synthesis, properties and applications for functional materials
Tanaka, T., & Osuka, A. (2015) · Chemical Society Reviews · doi:10.1039/c3cs60443h · Cited by 699
Ionic Covalent Organic Frameworks with Spiroborate Linkage
Du, Y., Yang, H., Whiteley, J. M., Wan, S., Jin, Y., Lee, S., & Zhang, W. (2016) · Angewandte Chemie International Edition · doi:10.1002/anie.201509014 · Cited by 674
Kang, Z., Peng, Y., Qian, Y., Yuan, D., Addicoat, M. A., Heine, T., Hu, Z., Tee, L., Guo, Z., & Zhao, D. (2016) · Chemistry of Materials · doi:10.1021/acs.chemmater.5b02902 · Cited by 672
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
Metal–metalloporphyrin frameworks: a resurging class of functional materials
Gao, W.-Y., Chrzanowski, M., & Ma, S. (2014) · Chem. Soc. Rev. · doi:10.1039/c4cs00001c · Cited by 613
Chemical sensing in two dimensional porous covalent organic nanosheets
Das, G., Biswal, B. P., Kandambeth, S., Venkatesh, V., Kaur, G., Addicoat, M. A., Heine, T., Verma, S. K., & Banerjee, R. (2015) · Chemical Science · doi:10.1039/c5sc00512d · Cited by 600
Porphyrins as excellent dyes for dye-sensitized solar cells: recent developments and insights
Higashino, T., & Imahori, H. (2015) · Dalton Transactions · doi:10.1039/c4dt02756f · Cited by 582
Ascherl, L., Sick, T., Margraf, J. T., Lapidus, S. H., Calik, M., Hettstedt, C., Karaghiosoff, K., Döblinger, M., Clark, T., Chapman, K. W., et al. (2016) · Nature Chemistry · doi:10.1038/nchem.2444 · Cited by 543
Homochiral 2D Porous Covalent Organic Frameworks for Heterogeneous Asymmetric Catalysis
Wang, X., Han, X., Zhang, J., Wu, X., Liu, Y., & Cui, Y. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b07714 · Cited by 524
One-Step Construction of Two Different Kinds of Pores in a 2D Covalent Organic Framework
Zhou, T.-Y., Xu, S.-Q., Wen, Q., Pang, Z.-F., & Zhao, X. (2014) · Journal of the American Chemical Society · doi:10.1021/ja5092936 · Cited by 501
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
Constructing monocrystalline covalent organic networks by polymerization
Beaudoin, D., Maris, T., & Wuest, J. D. (2013) · Nature Chemistry · doi:10.1038/nchem.1730 · Cited by 435
Reticular Synthesis of Covalent Organic Borosilicate Frameworks
Hunt, J. R., Doonan, C. J., LeVangie, J. D., Côté, A. P., & Yaghi, O. M. (2008) · Journal of the American Chemical Society · doi:10.1021/ja805064f · Cited by 433
Feng, X., Liu, L., Honsho, Y., Saeki, A., Seki, S., Irle, S., Dong, Y., Nagai, A., & Jiang, D. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201106203 · Cited by 411
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
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
Pang, Z.-F., Xu, S.-Q., Zhou, T.-Y., Liang, R.-R., Zhan, T.-G., & Zhao, X. (2016) · Journal of the American Chemical Society · doi:10.1021/jacs.6b01244 · Cited by 323
Smith, B. J., & Dichtel, W. R. (2014) · Journal of the American Chemical Society · doi:10.1021/ja5037868 · Cited by 316
Che, C.-M., & Huang, J.-S. (2009) · Chemical Communications · doi:10.1039/b901221d · Cited by 223
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
Ma, H., Ren, H., Meng, S., Yan, Z., Zhao, H., Sun, F., & Zhu, G. (2013) · Chemical Communications · doi:10.1039/c3cc45217d · Cited by 190
Zhu, Y., Wan, S., Jin, Y., & Zhang, W. (2015) · Journal of the American Chemical Society · doi:10.1021/jacs.5b09487 · Cited by 175
Ma, W., Yu, P., Ohsaka, T., & Mao, L. (2015) · Electrochemistry Communications · doi:10.1016/j.elecom.2015.01.021 · Cited by 117
Design and Properties of Porphyrin‐based Singlet Oxygen Generator
Jeong, H., & Choi, M. (2015) · Israel Journal of Chemistry · doi:10.1002/ijch.201500026 · Cited by 90
EPR STUDIES ON SINGLET OXYGEN PRODUCTION BY PORPHYRINS
Cannistraro, S., VORST, A. V. D., & Jori, G. (1978) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.1978.tb07704.x · Cited by 72
Cited by
Covalent Organic Framework Photocatalysts: Structures and Applications
Wang, H., Wang, H., Wang, Z., Tang, L., Zeng, G., Xu, P., Chen, M., Xiong, T., Zhou, C., Li, X., et al. (2020) · Chemical Society Reviews · doi:10.1039/d0cs00278j · Cited by 1,301
Liu, R., Tan, K. T., Gong, Y., Chen, Y., Li, Z., Xie, S., He, T., Lu, Z., Yang, H., & Jiang, D. (2021) · Chemical Society Reviews · doi:10.1039/d0cs00620c · Cited by 1,083
Post-synthetic modification of covalent organic frameworks
Segura, J. L., Royuela, S., & Mar Ramos, M. (2019) · Chemical Society Reviews · doi:10.1039/c8cs00978c · Cited by 832
Benzoxazole-Linked Ultrastable Covalent Organic Frameworks for Photocatalysis
Wei, P.-F., Qi, M.-Z., Wang, Z.-P., Ding, S.-Y., Yu, W., Liu, Q., Wang, L.-K., Wang, H.-Z., An, W.-K., & Wang, W. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b00571 · Cited by 771
Chen, R., Shi, J., Ma, Y., Lin, G., Lang, X., & Wang, C. (2019) · Angewandte Chemie International Edition · doi:10.1002/anie.201902543 · Cited by 697
Self-citation
Metadata
- Authors
- Lin, G., Ding, H., Chen, R., Peng, Z., Wang, B., & Wang, C.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2017-06-15
- Volume
- 139
- Issue
- 25
- Pages
- 8705-8709
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2622519202
- Cited by
- 517
- References
- 43
- FWCI
- 19.20
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
