Gold-catalyzed facile synthesis and crystal structures of benzene-/naphthalene-based bispentalenes as organic semiconductors

The gold-catalyzed facile synthesis of U-shaped and S-shaped bispentalenes is described from easily available tetra(arylethynyl)-benzenes and -naphthalenes. The optoelectronic and transistor properties were also investigated. The selectivity between the U-shaped and S-shaped bispentalene isomers can...

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Hauptverfasser: Sekine, Kohei (VerfasserIn) , Schulmeister, Jürgen (VerfasserIn) , Paulus, Fabian (VerfasserIn) , Goetz, Katelyn (VerfasserIn) , Rominger, Frank (VerfasserIn) , Rudolph, Matthias (VerfasserIn) , Zaumseil, Jana (VerfasserIn) , Hashmi, A. Stephen K. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2019
In: Chemistry - a European journal
Year: 2018, Jahrgang: 25, Heft: 1, Pages: 216-220
ISSN:1521-3765
DOI:10.1002/chem.201805637
Online-Zugang:Resolving-System, Volltext: http://dx.doi.org/10.1002/chem.201805637
Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201805637
Volltext
Verfasserangaben:Kohei Sekine, Jürgen Schulmeister, Fabian Paulus, Katelyn P. Goetz, Frank Rominger, Matthias Rudolph, Jana Zaumseil, and A. Stephen K. Hashmi
Beschreibung
Zusammenfassung:The gold-catalyzed facile synthesis of U-shaped and S-shaped bispentalenes is described from easily available tetra(arylethynyl)-benzenes and -naphthalenes. The optoelectronic and transistor properties were also investigated. The selectivity between the U-shaped and S-shaped bispentalene isomers can be tuned by the bulkiness of the ligand and the substrates. The S-shaped naphthalene-based bispentalene shows a one-dimensional face-to-face packing pattern in solid state and a good hole mobility, indicating that the S-shaped bispentalene core is highly suitable for transistor applications. The gold-catalyzed annulation of tetraynes provides a useful protocol in the synthesis of bispentalenes for organic semiconductors.
Beschreibung:Version of record online: December 17, 2018
Gesehen am 05-02-2019
Beschreibung:Online Resource
ISSN:1521-3765
DOI:10.1002/chem.201805637