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Chemical exchange of hydroxyl protons in quercetin measured by pulsed field gradient NMR

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dc.contributor.authorHong, Y. -S.-
dc.contributor.authorHong, K. S.-
dc.contributor.authorCho, J. -H.-
dc.contributor.authorVolkov, V. I.-
dc.contributor.authorLee, C. -H.-
dc.date.accessioned2021-09-08T20:22:10Z-
dc.date.available2021-09-08T20:22:10Z-
dc.date.created2021-06-19-
dc.date.issued2009-02-
dc.identifier.issn0937-9347-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/120687-
dc.description.abstractThe diffusion behavior of hydroxyl protons (OH) in quercetin in 100% DMSO-d(6) (deuterium dimethylsulfoxide) and a 90% DMSO-d(6) solution containing 10% H2O was investigated with 600 MHz H-1 pulsed field gradient (PFG) nuclear magnetic resonance (NMR). Only resonances of the 5-hydroxyl protons (OH5) were well resolved in NMR spectra of quercetin for all solutions under study. This phenomenon is explained by the intramolecular hydrogen bonding between OH5 protons and the 4-carbonyl oxygen (CO4). During diffusion experiments, the OH5 protons showed a biexponential diffusion decay, indicating an exchange process with water. As water content in the solvents increased, the lifetime (tau (q)) of the OH5 protons decreased from 96.7 +/- 10.0 ms in 100% DMSO-d(6) to 14.3 +/- 1.4 ms in the 90% DMSO-d(6) solution containing 10% H2O, indicating an increase in the exchange rate (k (q) = l/tau (q)) of the OH5 protons. This study demonstrates that the diffusion approach with PFG-NMR is much faster and easier for estimating the short lifetime or fast exchange rate of hydroxyl protons in quercetin.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherSPRINGER WIEN-
dc.subjectANTIOXIDANT ACTIVITY-
dc.subjectLIPID-PEROXIDATION-
dc.subjectDIFFUSION-
dc.subjectFLAVONOIDS-
dc.subjectCOMPLEXES-
dc.subjectALUMINUM-
dc.subjectMETABOLISM-
dc.subjectDEPENDENCE-
dc.subjectMEMBRANE-
dc.subjectMODEL-
dc.titleChemical exchange of hydroxyl protons in quercetin measured by pulsed field gradient NMR-
dc.typeArticle-
dc.contributor.affiliatedAuthorHong, Y. -S.-
dc.contributor.affiliatedAuthorLee, C. -H.-
dc.identifier.doi10.1007/s00723-008-0160-2-
dc.identifier.scopusid2-s2.0-65449145616-
dc.identifier.wosid000265497600006-
dc.identifier.bibliographicCitationAPPLIED MAGNETIC RESONANCE, v.35, no.2, pp.261 - 270-
dc.relation.isPartOfAPPLIED MAGNETIC RESONANCE-
dc.citation.titleAPPLIED MAGNETIC RESONANCE-
dc.citation.volume35-
dc.citation.number2-
dc.citation.startPage261-
dc.citation.endPage270-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalResearchAreaSpectroscopy-
dc.relation.journalWebOfScienceCategoryPhysics, Atomic, Molecular & Chemical-
dc.relation.journalWebOfScienceCategorySpectroscopy-
dc.subject.keywordPlusANTIOXIDANT ACTIVITY-
dc.subject.keywordPlusLIPID-PEROXIDATION-
dc.subject.keywordPlusDIFFUSION-
dc.subject.keywordPlusFLAVONOIDS-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusALUMINUM-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusDEPENDENCE-
dc.subject.keywordPlusMEMBRANE-
dc.subject.keywordPlusMODEL-
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