Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1975
Title: Slow Magnetic Relaxation in an Asymmetrically Coupled Heptanuclear Dysprosium(III)-Nickel(II) Architecture
Authors: Mukherjee, Soumya
JOARDER, BIPLAB
Xue, Shufang
Tang, Jinkui
GHOSH, SUJIT K.
Dept. of Chemistry
Keywords: Dysprosium
Nickel
Cluster compounds
Asymmetry Slow
Magnetic relaxation
Heptanuclear Dysprosium
Architecture
2014
Issue Date: Mar-2014
Publisher: Springer Nature
Citation: Proceedings of the National Academy of Sciences, India Section A: Physical Sciences, 84(2), 151-156.
Abstract: A new dysprosium(III)–nickel(II) heterometallic cluster, namely, [Dy III3Ni II4(L)6(OH)4(CH3OH)3(CH3CN)(NO3)(OH2)]·(CH3CN)3(CH3OH)2 (H2O)2 (1), has been synthesized from the schiff-base ligand H2L (L = o-phenolsalicylimine), dysprosium nitrate and nickel nitrate. A single-crystal X-ray diffraction study reveals that the highly asymmetric core of 1 consists of an unprecedented edge-sharing arrangement of three dissimilar Dy2Ni triangles, along with one Dy2Ni2 rectangle, connected to one side of the central metallic core. Both static (dc) and dynamic (ac) magnetic properties of 1 have been studied. The results reveal that compound 1 exhibits slow relaxation of the magnetization, making 1 a remarkable new addition to the family of Ln–Ni single molecule magnets, having a new asymmetric Ni4Dy3-architecture.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1975
https://doi.org/10.1007/s40010-013-0116-2
ISSN: 0369-8203
2250-1762
Appears in Collections:JOURNAL ARTICLES

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