Ascherl L, Sick T, Margraf J, Lapidus SH, Calik M, Hettstedt C, Karaghiosoff K, Doeblinger M, Clark T, Chapman KW, Auras F, Bein T (2016)
Publication Status: Published
Publication Type: Journal article
Publication year: 2016
Publisher: Nature Publishing Group
Book Volume: 8
Pages Range: 310-316
Journal Issue: 4
DOI: 10.1038/NCHEM.2444
Covalent organic frameworks (COFs) formed by connecting multidentate organic building blocks through covalent bonds provide a platform for designing multifunctional porous materials with atomic precision. As they are promising materials for applications in optoelectronics, they would benefit from a maximum degree of long-range order within the framework, which has remained a major challenge. We have developed a synthetic concept to allow consecutive COF sheets to lock in position during crystal growth, and thus minimize the occurrence of stacking faults and dislocations. Hereby, the three-dimensional conformation of propeller-shaped molecular building units was used to generate well-defined periodic docking sites, which guided the attachment of successive building blocks that, in turn, promoted long-range order during COF formation. This approach enables us to achieve a very high crystallinity for a series of COFs that comprise tri- and tetradentate central building blocks. We expect this strategy to be transferable to a broad range of customized COFs.
APA:
Ascherl, L., Sick, T., Margraf, J., Lapidus, S.H., Calik, M., Hettstedt, C.,... Bein, T. (2016). Molecular docking sites designed for the generation of highly crystalline covalent organic frameworks. Nature Chemistry, 8(4), 310-316. https://doi.org/10.1038/NCHEM.2444
MLA:
Ascherl, Laura, et al. "Molecular docking sites designed for the generation of highly crystalline covalent organic frameworks." Nature Chemistry 8.4 (2016): 310-316.
BibTeX: Download