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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....

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Bibliographic Details
Main Authors: Reiß, Hilmar (Author) , Han, Jie (Author) , Koser, Silke (Author) , Tverskoy, Olena (Author) , Freudenberg, Jan (Author) , Hinkel, Felix Peter (Author) , Dreuw, Andreas (Author) , Bunz, Uwe H. F. (Author)
Format: Article (Journal)
Language:English
Published: 31 May 2018
In: Angewandte Chemie. International edition
Year: 2018, Volume: 57, Issue: 30, Pages: 9543-9547
ISSN:1521-3773
DOI:10.1002/anie.201805728
Online Access:Verlag, Volltext: https://doi.org/10.1002/anie.201805728
Verlag: https://onlinelibrary.wiley.com/doi/10.1002/anie.201805728
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Author Notes: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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Summary: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....
Item Description:Gesehen am 27.01.2020
Physical Description:Online Resource
ISSN:1521-3773
DOI:10.1002/anie.201805728

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