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dc.contributor.authorEffenberger, Franzde
dc.contributor.authorMack, Karl-Ernstde
dc.contributor.authorNiess, Rolfde
dc.contributor.authorReisinger, Friedrichde
dc.contributor.authorSteinbach, Adalbertde
dc.contributor.authorStohrer, Wolf-Dieterde
dc.contributor.authorStezowski, John J.de
dc.contributor.authorRommel, Ilsede
dc.contributor.authorMaier, Andreasde
dc.date.accessioned2009-07-30de
dc.date.accessioned2016-03-31T07:47:40Z-
dc.date.available2009-07-30de
dc.date.available2016-03-31T07:47:40Z-
dc.date.issued1988de
dc.identifier.other316154377de
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-43544de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/1128-
dc.identifier.urihttp://dx.doi.org/10.18419/opus-1111-
dc.description.abstractDimeric σ-complexes 2, postulated intermediates in the oxidative dimerization of aromatics, were obtained by oxidation of tripprolidin-1-ylbenzenes 1a-f with silver nitrate. Treatment of 2 with strong base gave biphenyls 4. In solution, especially under the influence of light, compounds 2 dissociate to radical cations 1o+,which react irreversibly with solvent under H abstraction to give σ-complexes 3. Crystal structures were determined by X-ray diffraction methods for compounds 2a and 2c. Reactions of triaminobenzenes 8 and 9 with bromine and halocyanogens gave mixtures of substitution (10/ 11) and dimerization products (12/ 13). This product formation can be plausibly explained in terms of known steric and electronic factors of both reaction partners.en
dc.language.isoende
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.subject.classificationAromaten , Anilinde
dc.subject.ddc540de
dc.titleDimeric σ-complexes : intermediates in the oxidative dimerization of aromatics (Aminobenzenes ; 19)en
dc.typearticlede
dc.date.updated2013-05-08de
ubs.fakultaetFakultät Chemiede
ubs.institutInstitut für Organische Chemiede
ubs.opusid4354de
ubs.publikation.sourceJournal of Organic Chemistry 53 (1988), S. 4379-4386. URL http://dx.doi.org./10.1021/jo00253a035de
ubs.publikation.typZeitschriftenartikelde
Enthalten in den Sammlungen:03 Fakultät Chemie

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