First synthesis of naphthalene annulated oxepins
Highly condensed oxepins have been prepared in good yields from their corresponding diols by etherification using p -toluenesulfonic acid. Their intriguing twisted structures were unambiguously determined by X-ray crystallography. Substitution effects of a novel highly aromatic naphthalene annulated...
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Veröffentlicht in: | RSC advances 2014-01, Vol.4 (105), p.60473-60477 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Highly condensed oxepins have been prepared in good yields from their corresponding diols by etherification using
p
-toluenesulfonic acid. Their intriguing twisted structures were unambiguously determined by X-ray crystallography. Substitution effects of a novel highly aromatic naphthalene annulated oxepin indicate that structural and conjugative effects have an influence on the optoelectronic properties. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/C4RA10652K |