Perhalogenated tetraazaperopyrenes and their corresponding mono- and dianions
Chlorination and bromination of 2,9-perfluoropropyl-substituted tetraazaperopyrenes (TAPPs) under forcing conditions resulted in fully core-halogenated TAPP derivatives, devoid of hydrogen atoms at the polycyclic aromatic core. The octahalogenation stabilized the reduced mono- and dianionic compound...
Gespeichert in:
| Hauptverfasser: | , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
March 2, 2020
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| In: |
Organic letters
Year: 2020, Jahrgang: 22, Heft: 6, Pages: 2298-2302 |
| ISSN: | 1523-7052 |
| DOI: | 10.1021/acs.orglett.0c00478 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/acs.orglett.0c00478
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| Verfasserangaben: | Benjamin A.R. Günther, Sebastian Höfener, Robert Eichelmann, Ute Zschieschang, Hubert Wadepohl, Hagen Klauk, and Lutz H. Gade |
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| 520 | |a Chlorination and bromination of 2,9-perfluoropropyl-substituted tetraazaperopyrenes (TAPPs) under forcing conditions resulted in fully core-halogenated TAPP derivatives, devoid of hydrogen atoms at the polycyclic aromatic core. The octahalogenation stabilized the reduced mono- and dianionic compounds sufficiently to allow for their characterization. The additional ortho-chlorination led to an improvement of the electron mobility compared to the bay-substituted tetrachloro-TAPP when employed as an n-channel semiconductor in thin-film transistors. | ||
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