Azaacenes bearing five-membered rings

We report the synthesis of processible (dihydro)pyracyclene- and acenaphthylene-substituted azaacenes using condensation reactions in solution. The targets are characterized via cyclic voltammetry, X-ray crystallography, UV/Vis, fluorescence spectroscopy and DFT/NICS calculations. Formal hydrogenati...

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Hauptverfasser: Ganschow, Michael (VerfasserIn) , Koser, Silke (VerfasserIn) , Hodecker, Manuel (VerfasserIn) , Rominger, Frank (VerfasserIn) , Freudenberg, Jan (VerfasserIn) , Dreuw, Andreas (VerfasserIn) , Bunz, Uwe H. F. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: August10, 2018
In: Chemistry - a European journal
Year: 2018, Jahrgang: 24, Heft: 51, Pages: 13667-13675
ISSN:1521-3765
DOI:10.1002/chem.201802900
Online-Zugang:Verlag, Volltext: https://doi.org/10.1002/chem.201802900
Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201802900
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Verfasserangaben:Michael Ganschow, Silke Koser, Manuel Hodecker, Frank Rominger, Jan Freudenberg, Andreas Dreuw, and Uwe H.F. Bunz
Beschreibung
Zusammenfassung:We report the synthesis of processible (dihydro)pyracyclene- and acenaphthylene-substituted azaacenes using condensation reactions in solution. The targets are characterized via cyclic voltammetry, X-ray crystallography, UV/Vis, fluorescence spectroscopy and DFT/NICS calculations. Formal hydrogenation of the annulated five-membered ring surprisingly alters emission in the solid-state as a consequence of modulation of aromaticity and HOMO-LUMO overlap. Five highly fluorescent, crystalline azaacenes were investigated as emitters in organic light-emitting diodes, and their performance with respect to luminance and efficiency was compared to that of structurally related azaacenes.
Beschreibung:Gesehen am 24.09.2019
Beschreibung:Online Resource
ISSN:1521-3765
DOI:10.1002/chem.201802900