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Custom Coordination Environments for Lanthanoids: Tripodal Ligands Achieve Near-Perfect Octahedral Coordination for Two Dysprosium-Based Molecular Nanomagnets

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dc.contributor.authorLim, Kwang Soo-
dc.contributor.authorBaldovi, Jose J.-
dc.contributor.authorJiang, ShangDa-
dc.contributor.authorKoo, Bong Ho-
dc.contributor.authorKang, Dong Won-
dc.contributor.authorLee, Woo Ram-
dc.contributor.authorKoh, Eui Kwan-
dc.contributor.authorGaita-Arino, Alejandro-
dc.contributor.authorCoronado, Eugenio-
dc.contributor.authorSlota, Michael-
dc.contributor.authorBogani, Lapo-
dc.contributor.authorHong, Chang Seop-
dc.date.accessioned2021-09-03T06:21:59Z-
dc.date.available2021-09-03T06:21:59Z-
dc.date.created2021-06-16-
dc.date.issued2017-05-01-
dc.identifier.issn0020-1669-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/83501-
dc.description.abstractControlling the coordination sphere of lanthanoid complexes is a challenging critical step toward controlling their relaxation properties. Here we present the synthesis of hexacoordinated dysprosium single-molecule magnets, where tripodal ligands achieve a near-perfect octahedral coordination. We perform a complete experimental and theoretical investigation of their magnetic properties, including a full single-crystal magnetic anisotropy analysis. The combination of electrostatic and crystal-field computational tools (SIMPRE and CONDON codes) allows us to explain the static behavior of these systems in detail.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.subjectSINGLE-ION MAGNETS-
dc.subjectSPIN QUBITS-
dc.subjectRELAXATION-
dc.subjectANISOTROPY-
dc.subjectCOMPLEXES-
dc.subjectSYMMETRY-
dc.subjectDY(III)-
dc.subjectBARRIER-
dc.subjectCROSSOVER-
dc.subjectCOHERENCE-
dc.titleCustom Coordination Environments for Lanthanoids: Tripodal Ligands Achieve Near-Perfect Octahedral Coordination for Two Dysprosium-Based Molecular Nanomagnets-
dc.typeArticle-
dc.contributor.affiliatedAuthorHong, Chang Seop-
dc.identifier.doi10.1021/acs.inorgchem.6b03118-
dc.identifier.scopusid2-s2.0-85018984560-
dc.identifier.wosid000400633200017-
dc.identifier.bibliographicCitationINORGANIC CHEMISTRY, v.56, no.9, pp.4911 - 4917-
dc.relation.isPartOfINORGANIC CHEMISTRY-
dc.citation.titleINORGANIC CHEMISTRY-
dc.citation.volume56-
dc.citation.number9-
dc.citation.startPage4911-
dc.citation.endPage4917-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Inorganic & Nuclear-
dc.subject.keywordPlusSINGLE-ION MAGNETS-
dc.subject.keywordPlusSPIN QUBITS-
dc.subject.keywordPlusRELAXATION-
dc.subject.keywordPlusANISOTROPY-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusSYMMETRY-
dc.subject.keywordPlusDY(III)-
dc.subject.keywordPlusBARRIER-
dc.subject.keywordPlusCROSSOVER-
dc.subject.keywordPlusCOHERENCE-
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