Fluorine-programmed nanozipping to tailored nanographenes on rutile TiO2 surfaces
Kolmer M, Zuzak R, Steiner AK, Zajac L, Engelund M, Godlewski S, Szymonski M, Amsharov K (2019)
Publication Type: Journal article, Report
Publication year: 2019
Journal
Book Volume: 363
Pages Range: 57-60
Journal Issue: 6422
Abstract
The rational synthesis of nanographenes and carbon nanoribbons directly on nonmetallic surfaces has been an elusive goal for a long time. We report that activation of the carbon (C)–fluorine (F) bond is a reliable and versatile tool enabling intramolecular aryl-aryl coupling directly on metal oxide surfaces. A challenging multistep transformation enabled by C–F bond activation led to a dominolike coupling that yielded tailored nanographenes directly on the rutile titania surface. Because of efficient regioselective zipping, we obtained the target nanographenes from flexible precursors. Fluorine positions in the precursor structure unambiguously dictated the running of the “zipping program,” resulting in the rolling up of oligophenylene chains. The high efficiency of the hydrogen fluoride zipping makes our approach attractive for the rational synthesis of nanographenes and nanoribbons directly on insulating and semiconducting surfaces.
Authors with CRIS profile
Ann-Kristin Steiner
Lehrstuhl für Organische Chemie II
Konstantin Amsharov
Lehrstuhl für Organische Chemie II
Involved external institutions
Poland (PL)
Luxembourg (LU)How to cite
APA:
Kolmer, M., Zuzak, R., Steiner, A.-K., Zajac, L., Engelund, M., Godlewski, S.,... Amsharov, K. (2019). Fluorine-programmed nanozipping to tailored nanographenes on rutile TiO2 surfaces. Science, 363(6422), 57-60. https://doi.org/10.1126/science.aav4954
MLA:
Kolmer, Marek, et al. "Fluorine-programmed nanozipping to tailored nanographenes on rutile TiO2 surfaces." Science 363.6422 (2019): 57-60.
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