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- URN to cite this document:
- urn:nbn:de:bvb:355-epub-309652
- DOI to cite this document:
- 10.5283/epub.30965
Alternative links to fulltext:DOI
Abstract
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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