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dc.contributor.authorYu, JS-
dc.contributor.authorRyoo, JW-
dc.contributor.authorLee, CW-
dc.contributor.authorKim, SJ-
dc.contributor.authorHong, SB-
dc.contributor.authorKevan, L-
dc.date.accessioned2024-01-21T18:35:34Z-
dc.date.available2024-01-21T18:35:34Z-
dc.date.created2021-09-04-
dc.date.issued1997-03-21-
dc.identifier.issn0956-5000-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/143886-
dc.description.abstractThe location of Cu-II and its interaction with deuteriated adsorbates in Cu-II-exchanged K-offretite aluminosilicate zeolite have been investigated by electron paramagnetic resonance (EPR) and electron spin echo modulation (ESEM) spectroscopies and compared with those in Cu-II-exchanged K-offretite gallosilicate. Basically similar Cu-II locations to those in CuK-offretite gallosilicate are observed in CuK-offretite aluminosilicate, but there are some interesting differences. It is found that in the fresh hydrated sample, Cu-II is, in the main channel, coordinated to three water molecules and three framework oxygens in a six-ring window of an epsilon-cage to form a distorted octahedral complex. Upon evacuation at increasing temperature, Cu-II ions move from the main channel through the E-cages to hexagonal prism sites. However, the water coordinated to Cu-II is more tightly bound in the aluminosilicate than in the gallosilicate. Dehydration produces two different Cu-II species in the aluminosilicate, both believed to be located in recessed sites owing to the lack of broadening of its EPR lines by oxygen, while only one Cu-II species is located in a recessed site in the gallosilicate. Adsorption of polar molecules such as water, alcohols, dimethyl sulfoxide, acetonitrile and ammonia cause changes in the EPR spectrum of the Cu-II indicating migration into cation positions in the main channels where adsorbate coordination can occur. However, non-polar ethene does not cause migration of Cu-II. Cu-II forms complexes with two molecules of methanol, ethanol and propanol, and one molecule of dimethyl sulfoxide based on ESEM data. Cu-II forms a trigonal bipyramidal complex with two ammonias in axial positions and three framework oxygens in a six-ring window of an epsilon-cage based on EPR parameters and ESEM data, which is the same for Cu-II in CuK-offretite gallosilicate.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.subjectNUCLEAR MAGNETIC-RESONANCE-
dc.subjectSTRUCTURAL CHARACTERIZATION-
dc.subjectTEMPERATURE-DEPENDENCE-
dc.subjectPROPYLENE OXIDATION-
dc.subjectY ZEOLITES-
dc.subjectX-ZEOLITE-
dc.subjectSIMULATION-
dc.subjectMIGRATION-
dc.subjectSPECTRA-
dc.subjectMAZZITE-
dc.titleCopper(II) ionic species in Cu-II-exchanged K-offretite aluminosilicate and comparison with Cu-II-exchanged K-offretite gallosilicate determined by electron paramagnetic resonance and electron spin echo modulation spectroscopies-
dc.typeArticle-
dc.identifier.doi10.1039/a606011k-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, v.93, no.6, pp.1225 - 1231-
dc.citation.titleJOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS-
dc.citation.volume93-
dc.citation.number6-
dc.citation.startPage1225-
dc.citation.endPage1231-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1997WQ18000029-
dc.identifier.scopusid2-s2.0-33751194889-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryPhysics, Atomic, Molecular & Chemical-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPhysics-
dc.type.docTypeArticle-
dc.subject.keywordPlusNUCLEAR MAGNETIC-RESONANCE-
dc.subject.keywordPlusSTRUCTURAL CHARACTERIZATION-
dc.subject.keywordPlusTEMPERATURE-DEPENDENCE-
dc.subject.keywordPlusPROPYLENE OXIDATION-
dc.subject.keywordPlusY ZEOLITES-
dc.subject.keywordPlusX-ZEOLITE-
dc.subject.keywordPlusSIMULATION-
dc.subject.keywordPlusMIGRATION-
dc.subject.keywordPlusSPECTRA-
dc.subject.keywordPlusMAZZITE-
dc.subject.keywordAuthorCu**I**I ions-
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