Cyclodimers and cyclotrimers of 2,3 -bisalkynylated anthracenes, phenazines and diazatetracenes
The synthesis of novel (N−)acene-based cyclooligomers is reported. Glaser-Hay coupling of the bisethynylated monomers results in cyclodimers and cyclotrimers that are separable by column and gel-permeation chromatographies. For the diazatetracene, the use of sec-butyl-silylethynyl groups is necessar...
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| Hauptverfasser: | , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
06 October 2021
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| In: |
Chemistry - a European journal
Year: 2021, Jahrgang: 27, Heft: 66, Pages: 16320-16324 |
| ISSN: | 1521-3765 |
| DOI: | 10.1002/chem.202103193 |
| Online-Zugang: | Verlag, kostenfrei, Volltext: https://doi.org/10.1002/chem.202103193 Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.202103193 
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| Verfasserangaben: | Steffen Maier, Nikolai Hippchen, Frank Rominger, Jan Freudenberg, and Uwe H.F. Bunz |
MARC
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| 520 | |a The synthesis of novel (N−)acene-based cyclooligomers is reported. Glaser-Hay coupling of the bisethynylated monomers results in cyclodimers and cyclotrimers that are separable by column and gel-permeation chromatographies. For the diazatetracene, the use of sec-butyl-silylethynyl groups is necessary to achieve solubility. Diazatetracene-based cyclodimers and cyclotrimers were used as semiconductors in thin-film transistors. Although their optoelectronic properties are quite similar, their electron mobilities in proof-of-concept thin-film transistors differ by an order of magnitude. | ||
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