A stable bis(benzocyclobutadiene)-annelated tetraazapentacene derivative

Abstract Biphenylene-2,3-dione is a powerful reagent to build up cyclobutadiene-containing azapolyheterocycles. The target structures are formed in high yields through classical condensation of suitable aromatic diamines with the biphenylenedione. To achieve the title compound, the biphenylenedione...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Biegger, Philipp (VerfasserIn) , Schaffroth, Manuel (VerfasserIn) , Tverskoy, Olena (VerfasserIn) , Rominger, Frank (VerfasserIn) , Bunz, Uwe H. F. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 15 September 2016
In: Chemistry - a European journal
Year: 2016, Jahrgang: 22, Heft: 44, Pages: 15896-15901
ISSN:1521-3765
DOI:10.1002/chem.201602675
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/chem.201602675
Verlag, lizenzpflichtig, Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/chem.201602675
Volltext
Verfasserangaben:Philipp Biegger, Manuel Schaffroth, Olena Tverskoy, Frank Rominger, and Uwe H. F. Bunz
Beschreibung
Zusammenfassung:Abstract Biphenylene-2,3-dione is a powerful reagent to build up cyclobutadiene-containing azapolyheterocycles. The target structures are formed in high yields through classical condensation of suitable aromatic diamines with the biphenylenedione. To achieve the title compound, the biphenylenedione is coupled with a diaminobenzothiadiazole derivative. Reductive cleavage of the thiadiazole ring and subsequent condensation with the biphenylenedione gives the title compound in which a central tetraazapentacene is flanked by two benzocyclobutadiene units. This compound is stable despite its extended π-system and its optical features are blueshifted in comparison to those of the symmetrical tetraazapentacene.
Beschreibung:Gesehen am 11.05.2020
Beschreibung:Online Resource
ISSN:1521-3765
DOI:10.1002/chem.201602675