Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3645
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dc.contributor.authorJOARDER, BIPLABen_US
dc.contributor.authorChaudhari, Abhijeet K.en_US
dc.contributor.authorRogez, Guillaumeen_US
dc.contributor.authorGHOSH, SUJIT K.en_US
dc.date.accessioned2019-07-23T11:09:21Z
dc.date.available2019-07-23T11:09:21Z
dc.date.issued2012-05en_US
dc.identifier.citationDalton Transactions, 41(25), 7695-7699.en_US
dc.identifier.issn1477-9226en_US
dc.identifier.issn1477-9234en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3645-
dc.identifier.urihttps://doi.org/10.1039/C2DT30643Cen_US
dc.description.abstractHerein, we present a carboxylate-based dinuclear dysprosium compound, namely [Dy2L6(MeOH)2(H2O)2] (LH = n-butyric acid) from the reaction of Dy(NO3)3·xH2O with n-butyric acid and triethylamine in MeOH solvent. The single crystal X-ray diffraction analysis demonstrate that a total of six monocarboxylate ligands formed this dimeric compound by carboxylate bridging along with coordination from solvent molecules (water and methanol). Each DyIII ion is coordinated by nine donor atoms forming a mono-capped antiprismatic coordination environment. Alternating current (AC) magnetic measurements show a frequency dependence of the out-of-phase magnetic susceptibilities (χ′′) indicating a slow relaxation behaviour of the magnetization.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectCarboxylate-based dinuclearen_US
dc.subjectRelaxation behaviouren_US
dc.subjectDinuclear dysprosium compounden_US
dc.subject2012en_US
dc.titleA carboxylate-based dinuclear dysprosium(III) cluster exhibiting slow magnetic relaxation behaviouren_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleDalton Transactionsen_US
dc.publication.originofpublisherForeignen_US
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