Triptycene end-capped indigo derivatives: turning insoluble pigments to soluble dyes
The synthesis of a highly soluble triptycene end-capped indigo and its bay annulated derivative is reported. Both compounds have been studied by absorption and emission spectroscopy cyclic voltammetry, as well as theoretical calculations and compared to the parent indigo and bay annulated indigo. Be...
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| Hauptverfasser: | , , , , |
|---|---|
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2021
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| In: |
European journal of organic chemistry
Year: 2021, Heft: 1, Pages: 72-76 |
| ISSN: | 1099-0690 |
| DOI: | 10.1002/ejoc.202001362 |
| Online-Zugang: | Verlag, kostenfrei, Volltext: https://doi.org/10.1002/ejoc.202001362 Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.202001362 |
| Verfasserangaben: | Bahiru P. Benke, Leif Hertwig, Xuan Yang, Frank Rominger, and Michael Mastalerz |
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| 520 | |a The synthesis of a highly soluble triptycene end-capped indigo and its bay annulated derivative is reported. Both compounds have been studied by absorption and emission spectroscopy cyclic voltammetry, as well as theoretical calculations and compared to the parent indigo and bay annulated indigo. Besides a large improvement of solubility in organic solvents by the factor of approx. 70(!) the compounds also show a pronounced tendency to form crystals. Both properties, making these compounds promising electron acceptors for organic electronics. | ||
| 650 | 4 | |a Dyes | |
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