Go to content
UR Home

First synthesis of naphthalene annulated oxepins

URN to cite this document:
urn:nbn:de:bvb:355-epub-309652
Dobelmann, Lars ; Parham, A. H. ; Büsing, A. ; Buchholz, H. ; König, Burkhard
[img]
Preview
License: Creative Commons Attribution 3.0
PDF - Published Version
(790kB)
Date of publication of this fulltext: 17 Nov 2014 07:09


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.


Owner only: item control page
  1. Homepage UR

University Library

Publication Server

Contact:

Publishing: oa@ur.de

Dissertations: dissertationen@ur.de

Research data: daten@ur.de

Contact persons