First synthesis of naphthalene annulated oxepins

Dobelmann, L. and Parham, A. H. and Buesing, A. and Buchholz, H. and Koenig, B. (2014) First synthesis of naphthalene annulated oxepins. RSC ADVANCES, 4 (105). pp. 60473-60477. ISSN 2046-2069,

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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.

Item Type: Article
Uncontrolled Keywords: FIELD-EFFECT TRANSISTORS; ORGANIC SEMICONDUCTORS; DERIVATIVES; EMISSION; HETEROCYCLES; MOBILITY;
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König
Depositing User: Dr. Gernot Deinzer
Date Deposited: 28 Nov 2019 13:53
Last Modified: 28 Nov 2019 13:53
URI: https://pred.uni-regensburg.de/id/eprint/10887

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