Curcuminoid–BF2 complexes: Synthesis, fluorescence and optimization of BF2 group cleavage

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dc.bibliographicCitation.firstPage2264eng
dc.bibliographicCitation.journalTitleBeilstein Journal of Organic Chemistryeng
dc.bibliographicCitation.volume13eng
dc.contributor.authorWeiß, Henning
dc.contributor.authorReichel, Jeannine
dc.contributor.authorGörls, Helmar
dc.contributor.authorSchneider, Kilian R.A.
dc.contributor.authorMicheel, Mathias
dc.contributor.authorPröhl, Michael
dc.contributor.authorGottschaldt, Michael
dc.contributor.authorDietzek, Benjamin
dc.contributor.authorWeigand, Wolfgang
dc.date.accessioned2019-12-19T10:53:39Z
dc.date.available2019-12-19T10:53:39Z
dc.date.issued2017
dc.description.abstractEight difluoroboron complexes of curcumin derivatives carrying alkyne groups containing substituents have been synthesized following an optimised reaction pathway. The complexes were received in yields up to 98% and high purities. Their properties as fluorescent dyes have been investigated. Furthermore, a strategy for the hydrolysis of the BF2 group has been established using aqueous methanol and sodium hydroxide or triethylamine.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://doi.org/10.34657/5127
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/4711
dc.language.isoengeng
dc.publisherFrankfurt a.M. : Beilstein-Instituteng
dc.relation.doihttps://doi.org/10.3762/bjoc.13.223
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc540eng
dc.subject.ddc620eng
dc.subject.otherBF2 complexeng
dc.subject.othercurcumineng
dc.subject.otherdyeseng
dc.subject.otherfluorescenceeng
dc.subject.otherhydrolysiseng
dc.subject.otherspectroscopyeng
dc.titleCurcuminoid–BF2 complexes: Synthesis, fluorescence and optimization of BF2 group cleavageeng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPHTeng
wgl.subjectIngenieurwissenschafteneng
wgl.typeZeitschriftenartikeleng
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