Using internal strain and mass to modulate Dy⋯Dy coupling and relaxation of magnetization in heterobimetallic metallofullerenes DyM2N@C80 and Dy2MN@C80 (M = Sc, Y, La, Lu)

dc.bibliographicCitation.date2023
dc.bibliographicCitation.firstPage468
dc.bibliographicCitation.issue2
dc.bibliographicCitation.lastPage484
dc.bibliographicCitation.volume10
dc.contributor.authorHao, Yajuan
dc.contributor.authorVelkos, Georgios
dc.contributor.authorSchiemenz, Sandra
dc.contributor.authorRosenkranz, Marco
dc.contributor.authorWang, Yaofeng
dc.contributor.authorBüchner, Bernd
dc.contributor.authorAvdoshenko, Stanislav M.
dc.contributor.authorPopov, Alexey A.
dc.contributor.authorLiu, Fupin
dc.date.accessioned2023-01-30T06:09:54Z
dc.date.available2023-01-30T06:09:54Z
dc.date.issued2022
dc.description.abstractEndohedral clusters inside metallofullerenes experience considerable inner strain when the size of the hosting cage is comparably small. This strain can be tuned in mixed-metal metallofullerenes by combining metals of different sizes. Here we demonstrate that the internal strain and mass can be used as variables to control Dy⋯Dy coupling and relaxation of magnetization in Dy-metallofullerenes. Mixed-metal nitride clusterfullerenes DyxY3−xN@Ih-C80 (x = 0-3) and Dy2LaN@Ih-C80 combining Dy with diamagnetic rare-earth elements, Y and La, were synthesized and characterized by single-crystal X-ray diffraction, SQUID magnetometry, ab initio calculations, and spectroscopic techniques. DyxY3−xN clusters showed a planar structure, but the slightly larger size of Dy3+ in comparison with that of Y3+ resulted in increased elongation of the nitrogen thermal ellipsoid, showing enhancement of the out-of-plane vibrational amplitude. When Dy was combined with larger La, the Dy2LaN cluster appeared strongly pyramidal with the distance between two nitrogen sites of 1.15(1) Å, whereas DyLa2N@C80 could not be obtained in a separable yield. Magnetic studies revealed that the relaxation of magnetization and blocking temperature of magnetization in the DyM2N@C80 series (M = Sc, Y, Lu) correlated with the mass of M, with DySc2N@C80 showing the fastest and DyLu2N@C80 the slowest relaxation. Ab initio calculations predicted very similar g-tensors for Dy3+ ground state pseudospin in all studied DyM2N@C80 molecules, suggesting that the variation in relaxation is caused by different vibrational spectra of these compounds. In the Dy2MN@C80 series (M = Sc, Y, La, Lu), the magnetic and hysteretic behavior was found to correlate with Dy⋯Dy coupling, which in turn appears to depend on the size of M3+. Across the Dy2MN@C80 series, the energy difference between ferromagnetic and antiferromagnetic states changes from 5.6 cm−1 in Dy2ScN@C80 to 3.0 cm−1 in Dy2LuN@C80, 1.0 cm−1 in Dy2YN@C80, and −0.8 cm−1 in Dy2LaN@C80. The coupling of Dy ions suppresses the zero-field quantum tunnelling of magnetization but opens new relaxation channels, making the relaxation rate dependent on the coupling strengths. DyY2N@C80 and Dy2YN@C80 were found to be non-luminescent, while the luminescence reported for DyY2N@C80 was caused by traces of Y3N@C80 and Y2ScN@C80eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/11161
dc.identifier.urihttp://dx.doi.org/10.34657/10187
dc.language.isoeng
dc.publisherCambridge : RSC
dc.relation.doihttps://doi.org/10.1039/d2qi02224a
dc.relation.essn2052-1553
dc.relation.ispartofseriesInorganic chemistry frontiers : an international journal of inorganic chemistry 10 (2023), Nr. 2
dc.rights.licenseCC BY 3.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/3.0
dc.subjectAb initio calculationseng
dc.subjectClusterfullereneseng
dc.subjectDifferent sizeseng
dc.subjectEndohedral clusterseng
dc.subjectHeterobimetallicseng
dc.subjectInternal strainseng
dc.subjectMetal nitrideseng
dc.subjectMetallofullereneseng
dc.subjectMixed-metalseng
dc.subjectRelaxation of magnetizationeng
dc.subject.ddc540
dc.titleUsing internal strain and mass to modulate Dy⋯Dy coupling and relaxation of magnetization in heterobimetallic metallofullerenes DyM2N@C80 and Dy2MN@C80 (M = Sc, Y, La, Lu)eng
dc.typearticle
dc.typeText
dcterms.bibliographicCitation.journalTitleInorganic chemistry frontiers : an international journal of inorganic chemistry
tib.accessRightsopenAccess
wgl.contributorIFWD
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
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