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dc.contributor.authorBaşaran, İsmet
dc.contributor.authorÇakır, Ümit
dc.date.accessioned2019-10-17T10:51:25Z
dc.date.available2019-10-17T10:51:25Z
dc.date.issued2014en_US
dc.identifier.issn1388-3127
dc.identifier.issn1573-1111
dc.identifier.urihttps://doi.org/10.1007/s10847-013-0286-1
dc.identifier.urihttps://hdl.handle.net/20.500.12462/8282
dc.descriptionÇakır, Ümit (Balıkesir Author)en_US
dc.description.abstracto-Dihydroxy-3-(methylphenyl)-chromenones (coumarins; 3a-3c) were synthesized from trimethoxy-benzaldehydes through a reaction with the corresponding methylphenyl-acrylonitrile in pyridine center dot HCl and then H3O+. Dihydroxycoumarins reacted with the ditosylate or dichloride derivatives of tri-or tetraethyleneglycols in the presence of CH3CN/Na2CO3 and macrocyclic ethers with a coumarin moiety were obtained. The chromatographically purified new coumarin-crown ethers (5a-5f) were identified by IR, H-1 NMR, and Mass spectrometry. The binding constants of Na+ with the coumarin-crown ethers were determined in an 80 % dioxane/water binary solvent system at 25 degrees C from conductance measurements.en_US
dc.description.sponsorshipyoken_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.relation.isversionof10.1007/s10847-013-0286-1en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectCoumarin-Crown Ethersen_US
dc.subjectSynthesisen_US
dc.subjectComplexationen_US
dc.subjectConductometryen_US
dc.titleThe synthesis, Na+ binding properties of new coumarin-crown ethersen_US
dc.typearticleen_US
dc.relation.journalJournal of Inclusion Phenomena and Macrocyclic Chemistryen_US
dc.contributor.departmentFen Edebiyat Fakültesien_US
dc.contributor.authorID0000-0001-7641-8938en_US
dc.identifier.volume78en_US
dc.identifier.issue1-4en_US
dc.identifier.startpage179en_US
dc.identifier.endpage184en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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