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Field-Induced Multiple Relaxation Mechanism of Co<sup>III</sup><sub>2</sub>Dy<sup>III</sup> Compound with the Dysprosium Ion in a Low-Symmetrical Environment

Shufang XueState Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, P. R. ChinaLiviu UngurTheory of Nanomaterials Group, Department of Chemistry, Katholieke Universiteit Leuven, Celestijnenlaan 200F, 3001 Leuven, BelgiumYun‐Nan GuoSchool of Science, Xi’an Jiaotong University, Xi’an, 710049, P. R. ChinaJinkui TangState Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, P. R. ChinaLiviu F. ChibotaruTheory of Nanomaterials Group, Department of Chemistry, Katholieke Universiteit Leuven, Celestijnenlaan 200F, 3001 Leuven, Belgium
2014en
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A defective cubane-shaped heterometallic trinuclear Co(III)2Dy(III) compound with only one magnetically interesting ion (Dy(III)) has been assembled by virtue of a multifunctional acylhydrazone ligand. Because of the nonaxial ground state of Dy(III) ion derived from a low-symmetrical crystal field, the title compound displays field-induced multiple relaxation processes which are of molecular and a dipolar-dipolar coupling origin, as revealed by combined experimental and theoretical investigations. The results demonstrate that such a mononuclear dysprosium(III) compound with a low-symmetrical environment of magnetic center appears to be a model system for further investigations to shed light on the complex relaxation mechanism of lanthanide-based single ion magnets.

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