Bromination improves the electron mobility of Tetraazapentacene
A fully air‐stable radical anion is formed from a bis‐TIPS‐ethynyl‐substituted tetraazapentacene with four bromine substituents attached in the 2‐, 3‐, 9‐, and 10‐positions. The deep‐lying LUMO (i.e....
Gespeichert in:
| Hauptverfasser: | , , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
31 May 2018
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| In: |
Angewandte Chemie. International edition
Year: 2018, Jahrgang: 57, Heft: 30, Pages: 9543-9547 |
| ISSN: | 1521-3773 |
| DOI: | 10.1002/anie.201805728 |
| Online-Zugang: | Verlag, Volltext: https://doi.org/10.1002/anie.201805728 Verlag: https://onlinelibrary.wiley.com/doi/10.1002/anie.201805728 |
| Verfasserangaben: | Hilmar Reiss, Lei Ji, Jie Han, Silke Koser, Olena Tverskoy, Jan Freudenberg, Felix Hinkel, Michael Moos, Alexandra Friedrich, Ivo Krummenacher, Christoph Lambert, Holger Braunschweig, Andreas Dreuw, Todd B. Marder, and Uwe H.F. Bunz |
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| 520 | |a A fully air‐stable radical anion is formed from a bis‐TIPS‐ethynyl‐substituted tetraazapentacene with four bromine substituents attached in the 2‐, 3‐, 9‐, and 10‐positions. The deep‐lying LUMO (i.e.... | ||
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