Yamamoto coupling for the synthesis of benzophenes and acene-based cyclooctatetraenes

Two TIPS-ethynylated dibromoacenes were used in a shotgun Yamamoto-reaction with 1,2-dibromobenzene or 4,5-dibromoveratrol. Four soluble benzononaphenes/benzoundecaphenes were isolated in satisfactory yields. Examples of tetracene- and pentacene-fused tetrabenzocyclooctatetraenes also isolated from...

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Hauptverfasser: Rüdiger, Elias (VerfasserIn) , Koser, Silke (VerfasserIn) , Rominger, Frank (VerfasserIn) , Freudenberg, Jan (VerfasserIn) , Bunz, Uwe H. F. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 17 April 2018
In: Chemistry - a European journal
Year: 2018, Jahrgang: 24, Heft: 39, Pages: 9919-9927
ISSN:1521-3765
DOI:10.1002/chem.201801459
Online-Zugang:Verlag, Volltext: https://doi.org/10.1002/chem.201801459
Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201801459
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Verfasserangaben:Elias C. Rüdiger, Silke Koser, Frank Rominger, Jan Freudenberg, and Uwe H.F. Bunz
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Zusammenfassung:Two TIPS-ethynylated dibromoacenes were used in a shotgun Yamamoto-reaction with 1,2-dibromobenzene or 4,5-dibromoveratrol. Four soluble benzononaphenes/benzoundecaphenes were isolated in satisfactory yields. Examples of tetracene- and pentacene-fused tetrabenzocyclooctatetraenes also isolated from this reaction are reported. All compounds were characterized by UV/Vis and fluorescence spectroscopy, cyclic voltammetry, X-ray crystallography as well as DFT and NICS calculations.
Beschreibung:Gesehen am 25.04.2019
Beschreibung:Online Resource
ISSN:1521-3765
DOI:10.1002/chem.201801459