Enantioselevtive compexation of chiral lariat crown ethers and chiral primary alkylamonum perchlorates

dc.authorid0000-0002-6612-2751en_US
dc.contributor.authorAral, Tarık
dc.contributor.authorKöylü, Mehmet Zafer
dc.contributor.authorKocakaya, Şafak Özhan
dc.contributor.authorKarakaplan, Mehmet
dc.contributor.authorHoşgören, Halil
dc.date.accessioned2021-03-29T10:14:39Z
dc.date.available2021-03-29T10:14:39Z
dc.date.issued2011-02-01en_US
dc.departmentBatman Üniversitesi Fen - Edebiyat Fakültesi Kimya Bölümüen_US
dc.description.abstractIn order to investigate the enantiomeric recognition abilities toward 2 chiral alkylammonium perchlorates (AmI, AmII) by 1 H-NMR titration method in CDCl 3, 4 chiral lariat ethers 8-11 with a (p-methoxyphenoxy) methyl flexible side arm were used. The most effective enantiomeric recognition was obtained by LCEs 9 and 11 toward AmII, by KR /KS 6.58 and KS /KR 6.63, respectively. The effect of macroring size, subunit of macroring, and side arm appeared to have strong influence on the binding ability of these alkylammonium ions.en_US
dc.identifier.citationAral, T., Köylü, M.Z., Kocakaya, Ş.Ö., Hoşgören, H. (2011). Enantioselevtive compexation of chiral lariat crown ethers and chiral primary alkylamonum perchlorates. Turkish Journal Chemistry 25 (2) , pp.171-179en_US
dc.identifier.endpage179en_US
dc.identifier.issn1303-6130
dc.identifier.issn1300-0527
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage171en_US
dc.identifier.urihttps://dergipark.org.tr/tr/pub/tbtkchem/issue/11893/142148
dc.identifier.urihttps://hdl.handle.net/20.500.12402/2795
dc.identifier.volume35en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherTurkish Journal Chemistryen_US
dc.relation.isversionof10.3906/kim-1008-844en_US
dc.relation.journalTurkish Journal Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.subjectChiral Lariat Crown Ethersen_US
dc.subjectEnantioselectivityen_US
dc.subjectComplexation Propertiesen_US
dc.subjectMolecular Recognitionen_US
dc.subjectNMR Titrationen_US
dc.titleEnantioselevtive compexation of chiral lariat crown ethers and chiral primary alkylamonum perchloratesen_US
dc.typeArticleen_US

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