2,4-Bis(arylethynyl)-9-chloro-5,6,7,8-tetrahydroacridines: synthesis and photophysical properties

dc.bibliographicCitation.firstPage1629eng
dc.bibliographicCitation.lastPage1640eng
dc.bibliographicCitation.volume17eng
dc.contributor.authorTka, Najeh
dc.contributor.authorAyed, Mohamed Adnene Hadj
dc.contributor.authorBraiek, Mourad Ben
dc.contributor.authorJabli, Mahjoub
dc.contributor.authorChaaben, Noureddine
dc.contributor.authorAlimi, Kamel
dc.contributor.authorJopp, Stefan
dc.contributor.authorLanger, Peter
dc.date.accessioned2022-03-17T07:27:24Z
dc.date.available2022-03-17T07:27:24Z
dc.date.issued2021
dc.description.abstractAcridine derivatives have attracted considerable interest in numerous areas owing to their attractive physical and chemical properties. Herein, starting from readily available anthranilic acid, an efficient synthesis of 2,4-bis(arylethynyl)-9-chloro-5,6,7,8-tetrahydroacridine derivatives was accomplished via a one-pot double Sonogashira cross-coupling method. The UV-visible absorption and emission properties of the synthesized molecules have been examined. Additionally, theoretical studies based on density functional theory (DFT/B3LYP/6-31G(d)) were carried out.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/8252
dc.identifier.urihttps://doi.org/10.34657/7290
dc.language.isoengeng
dc.publisherFrankfurt, M. : Beilstein-Institut zur Förderung der Chemischen Wissenschafteneng
dc.relation.doihttps://doi.org/10.3762/bjoc.17.115
dc.relation.essn1860-5397
dc.relation.ispartofseriesBeilstein Journal of Organic Chemistry 17 (2021)eng
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subjectalkyneseng
dc.subjectcatalysiseng
dc.subjectcross-couplingeng
dc.subjectheterocycleseng
dc.subjectpalladiumeng
dc.subject.ddc540eng
dc.title2,4-Bis(arylethynyl)-9-chloro-5,6,7,8-tetrahydroacridines: synthesis and photophysical propertieseng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleBeilstein journal of organic chemistryeng
tib.accessRightsopenAccesseng
wgl.contributorLIKATeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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