A pyrene-fused N-heteroacene with eleven rectilinearly annulated aromatic rings

A highly soluble pyrene-fused undecacene is realized by end-capping the rectilinear aromatic π-plane with triptycenylene units. Besides the good solubility, the compound shows a high tendency to crystallize. Two polymorphs from dichlorobenzene and chloroform are described. In the polymorph from chlo...

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Hauptverfasser: Kohl, Bernd (VerfasserIn) , Rominger, Frank (VerfasserIn) , Mastalerz, Michael (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: March 27, 2015
In: Angewandte Chemie. International edition
Year: 2015, Jahrgang: 54, Heft: 20, Pages: 6051-6056
ISSN:1521-3773
DOI:10.1002/anie.201411972
Online-Zugang:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1002/anie.201411972
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/anie.201411972
Volltext
Verfasserangaben:Bernd Kohl, Frank Rominger, and Michael Mastalerz
Beschreibung
Zusammenfassung:A highly soluble pyrene-fused undecacene is realized by end-capping the rectilinear aromatic π-plane with triptycenylene units. Besides the good solubility, the compound shows a high tendency to crystallize. Two polymorphs from dichlorobenzene and chloroform are described. In the polymorph from chloroform, half of the molecules are strongly bent out of the π-plane by 26.4°.
Beschreibung:Gesehen am 14.07.2020
Beschreibung:Online Resource
ISSN:1521-3773
DOI:10.1002/anie.201411972