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First synthesis of naphthalene annulated oxepins
Article
Dobelmann, Lars, Parham, A. H., Büsing, A., Buchholz, H. and König, Burkhard
(2014)
First synthesis of naphthalene annulated oxepins.
RSC Advances 4, pp. 60473-60477.
DOI to cite this document: 10.5283/epub.30965
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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| Item type | Article | ||||
| Journal or Publication Title | RSC Advances | ||||
| Publisher | ROYAL SOC CHEMISTRY | ||||
| Place of Publication | CAMBRIDGE | ||||
| Volume | 4 | ||||
| Page Range | pp. 60473-60477 | ||||
| Date | 2014 | ||||
| Date of publication | 17 Nov 2014 07:09 | ||||
| Additional Information (public) | Open-Access-Komponente aus der Allianzlizenz | ||||
| Institutions | Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König | ||||
| Identification Number |
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| Keywords | FIELD-EFFECT TRANSISTORS; ORGANIC SEMICONDUCTORS; DERIVATIVES; EMISSION; HETEROCYCLES; MOBILITY; | ||||
| Dewey Decimal Classification | 500 Science > 540 Chemistry & allied sciences | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| URN of the UB Regensburg | urn:nbn:de:bvb:355-epub-309652 | ||||
| Item ID | 30965 |
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