C2-Symmetric chiral diamine ligands for enantiomeric recognition of amino acid esters and mandelic acid by proton nmr titration method
dc.authorid | 0000-0001-7811-8816 | en_US |
dc.contributor.author | Aral, Hayriye | |
dc.contributor.author | Aral, Tarık | |
dc.contributor.author | Çolak, Mehmet | |
dc.contributor.author | Ziyadanoğulları, Berrin | |
dc.contributor.author | Ziyadanoğulları, Recep | |
dc.date.accessioned | 2019-06-21T12:12:57Z | |
dc.date.available | 2019-06-21T12:12:57Z | |
dc.date.issued | 2013-07-08 | en_US |
dc.department | Batman Üniversitesi Fen - Edebiyat Fakültesi Kimya Bölümü | en_US |
dc.description.abstract | Two novel C2 -symmetric chiral diamines containing α-phenylethyl and α-(1-naphthyl)ethyl chiral subunits were prepared with quantitative yields. Enantiomeric recognition properties of these simple structured diamine ligands towards D- and L-amino acid esters and D- and L-mandelic acid were examined by the 1H NMR titration method. These ligands exhibited strong complexation (with Kf up to 2481 M-1) and good enantioselectivity (up to KL /KD = 4.08) towards the mandelic acid enantiomers. The results show that simple structured and easily accessible acyclic C2 -symmetrical compounds can also be used for enantiomeric recognition of racemic amino acids and mandelic acid in addition to complex molecules such as crown ethers and other cyclic molecules. | en_US |
dc.identifier.citation | Aral, H., Aral, T., Colak, M., ZİYADANOĞULLARI, B., ZİYADANOĞULLARI, R. (2013). C_2-Symmetric chiral diamine ligands for enantiomeric recognition of amino acid esters and mandelic acid by proton NMR titration method. Turkish Journal of Chemistry, 37(3), pp. 374-382. https://doi.org/10.3906/kim-1207-58 | en_US |
dc.identifier.endpage | 382 | en_US |
dc.identifier.issn | 1300-0527 | |
dc.identifier.issn | 1303-6130 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 374 | en_US |
dc.identifier.uri | https://doi.org/10.3906/kim-1207-58 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12402/2102 | |
dc.identifier.volume | 37 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | TÜBİTAK | en_US |
dc.relation.isversionof | 10.3906/kim-1207-58 | en_US |
dc.relation.journal | Turkish Journal of Chemistry | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Attribution-ShareAlike 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by-sa/3.0/us/ | * |
dc.subject | Amino Acids | en_US |
dc.subject | C2 Symmetric | en_US |
dc.subject | Chiral Diamines | en_US |
dc.subject | Enantiomeric Recognition | en_US |
dc.subject | Mandelic Acid | en_US |
dc.subject | NMR Titration | en_US |
dc.title | C2-Symmetric chiral diamine ligands for enantiomeric recognition of amino acid esters and mandelic acid by proton nmr titration method | en_US |
dc.type | Article | en_US |