Synthesis of chiral calix[4]arenes bearing aminonaphthol moieties and their use in the enantiomeric recognition of carboxylic acids
dc.contributor.author | Durmaz, Mustafa | |
dc.contributor.author | Yılmaz, Mustafa | |
dc.contributor.author | Sirit, Abdülkadir | |
dc.date.accessioned | 2020-03-26T18:16:27Z | |
dc.date.available | 2020-03-26T18:16:27Z | |
dc.date.issued | 2011 | |
dc.department | Selçuk Üniversitesi | en_US |
dc.description.abstract | Two armed chiral calix[4]arenes 8-16 functionalized at the lower rim with chiral aminonaphthol units have been prepared and the structures of these receptors characterized by FTIR, H-1, and C-13, DEPT and COSY NMR spectroscopy and elemental analysis. The enantioselective recognition of these receptors with various carboxylic acids has been studied by H-1 NMR and UV/Vis spectroscopy. The receptors exhibited different chiral recognition abilities towards the enantiomers of racemic materials and formed 2 : 1 or 1 : 1 complexes between host and guest. It was also demonstrated that chiral calix[4]arenes 9 and 16 could be used as chiral NMR solvating agents to determine the enantiomeric purity of mandelic acid. | en_US |
dc.description.sponsorship | Scientific and Technical Research Council of TurkeyTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [TUBITAK-109T167]; Research Foundation of Selcuk UniversitySelcuk University [BAP-10101005] | en_US |
dc.description.sponsorship | This work was supported by the Scientific and Technical Research Council of Turkey (TUBITAK-109T167) and Research Foundation of Selcuk University (BAP-10101005). The provision of PhD studentship to M.D. by TUBITAK-BIDEB is gratefully acknowledged. | en_US |
dc.identifier.doi | 10.1039/c0ob00399a | en_US |
dc.identifier.endpage | 580 | en_US |
dc.identifier.issn | 1477-0520 | en_US |
dc.identifier.issn | 1477-0539 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.pmid | 21063630 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.startpage | 571 | en_US |
dc.identifier.uri | https://dx.doi.org/10.1039/c0ob00399a | |
dc.identifier.uri | https://hdl.handle.net/20.500.12395/26871 | |
dc.identifier.volume | 9 | en_US |
dc.identifier.wos | WOS:000285749800034 | en_US |
dc.identifier.wosquality | Q1 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | ROYAL SOC CHEMISTRY | en_US |
dc.relation.ispartof | ORGANIC & BIOMOLECULAR CHEMISTRY | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.selcuk | 20240510_oaig | en_US |
dc.title | Synthesis of chiral calix[4]arenes bearing aminonaphthol moieties and their use in the enantiomeric recognition of carboxylic acids | en_US |
dc.type | Article | en_US |