Photoisomerisierung von trans-l-(3.5-Di-JerJ-butyl-4-hydroxyphenyl)-2-phenyldiazen

Hofer, Edgar

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dc.identifier.uri	http://dx.doi.org/10.15488/2460
dc.identifier.uri	http://www.repo.uni-hannover.de/handle/123456789/2486
dc.contributor.author	Hofer, Edgar
dc.date.accessioned	2017-11-24T11:46:30Z
dc.date.available	2017-11-24T11:46:30Z
dc.date.issued	1980
dc.identifier.citation	Hofer, E.: Photoisomerisierung von trans-l-(3.5-Di-JerJ-butyl-4-hydroxyphenyl)-2-phenyldiazen. In: Zeitschrift für Naturforschung - Section B Journal of Chemical Sciences 35 (1980), Nr. 2, S. 233-236. DOI: https://doi.org/10.1515/znb-1980-0220
dc.description.abstract	Light induced isomerizations of the title compound have been studied. The thermal cis-trans isomerization 3→1 occurs via the tautomeric quinonephenylhydrazone (2) as shown by 1H NMR, spectroscopy. The influence of solvent on the thermal cis-trans isomerization is discussed. 1H NMR data of 1, 2 and 3 are given. Values of the tautomeric equilibrium 1⇋2 are determined for various solvents and different temperatures.	eng
dc.language.iso	ger
dc.publisher	Berlin : De Gruyter
dc.relation.ispartofseries	Zeitschrift für Naturforschung - Section B Journal of Chemical Sciences 35 (1980), Nr. 2
dc.rights	CC BY-NC-ND 3.0 Unported
dc.rights.uri	https://creativecommons.org/licenses/by-nc-nd/3.0/
dc.subject	Light Induced Isomerizations	eng
dc.subject	Tautomeric Diaryldiazenes	eng
dc.subject.ddc	540 \| Chemie	ger
dc.title	Photoisomerisierung von trans-l-(3.5-Di-JerJ-butyl-4-hydroxyphenyl)-2-phenyldiazen
dc.type	Article
dc.type	Text
dc.relation.essn	1865-7117
dc.relation.issn	0932-0776
dc.relation.doi	https://doi.org/10.1515/znb-1980-0220
dc.bibliographicCitation.issue	2
dc.bibliographicCitation.volume	35
dc.bibliographicCitation.firstPage	233
dc.bibliographicCitation.lastPage	236
dc.description.version	publishedVersion
tib.accessRights	frei zug�nglich