The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks—A Modulation Approach
Open accessAbstract
Crystallinity and porosity are of central importance for many properties of covalent organic frameworks (COFs), including adsorption, diffusion, and electronic transport. We have developed a new method for strongly enhancing both aspects through the introduction of a modulating agent in the synthesis. This modulator competes with one of the building blocks during the solvothermal COF growth, resulting in highly crystalline frameworks with greatly increased domain sizes reaching several hundreds of nanometers. The obtained materials feature fully accessible pores with an internal surface area of over 2000 m(2) g(-1). Compositional analysis via NMR spectroscopy revealed that the COF-5 structure can form over a wide range of boronic acid-to-catechol ratios, thus producing frameworks with compositions ranging from highly boronic acid-deficient to networks with catechol voids. Visualization of an -SH-functionalized modulating agent via iridium staining revealed that the COF domains are terminated by the modulator. Using functionalized modulators, this synthetic approach thus also provides a new and facile method for the external surface functionalization of COF domains, providing accessible sites for post-synthetic modification reactions. We demonstrate the feasibility of this concept by covalently attaching fluorescent dyes and hydrophilic polymers to the COF surface. We anticipate that the realization of highly crystalline COFs with the option of additional surface functionality will render the modulation concept beneficial for a range of applications, including gas separations, catalysis, and optoelectronics.
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Sing, K. S. W. (1985) · Pure and Applied Chemistry · doi:10.1351/pac198557040603 · Cited by 24,485
Cited by
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
Self-citationSingle-crystal x-ray diffraction structures of covalent organic frameworks
Ma, T., Kapustin, E. A., Yin, S. X., Liang, L., Zhou, Z., Niu, J., Li, L.-H., Wang, Y., Su, J., Li, J., et al. (2018) · Science · doi:10.1126/science.aat7679 · Cited by 1,381
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
Zhang, F., Sheng, J., Yang, Z., Sun, X., Tang, H., Lu, M., Dong, H., Shen, F., Liu, J., & Lan, Y. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201806862 · Cited by 719
Metadata
- Authors
- Calik, M., Sick, T., Dogru, M., Döblinger, M., Datz, S., Budde, H., Hartschuh, A., Auras, F., & Bein, T.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2016-01-23
- Volume
- 138
- Issue
- 4
- Pages
- 1234-1239
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2268566230
- Cited by
- 208
- References
- 1
- FWCI
- 5.73
- Type
- journal article
- Language
- en
- Open access
- hybrid
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- Calik, M., Sick, T., Dogru, M., Döblinger, M., Datz, S., Budde, H., Hartschuh, A., Auras, F., & Bein, T. (2016). From Highly Crystalline to Outer Surface-Functionalized Covalent Organic Frameworks—A Modulation Approach. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.5b10708
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