THz-EPR-based Magneto-Structural Correlations for Cobalt(II) Single-Ion Magnets With Bis-Chelate Coordination

被引:3
作者
Pohle, Maximilian H. [1 ]
Lohmiller, Thomas [2 ,3 ]
Boehme, Michael [1 ]
Rams, Michal [4 ]
Ziegenbalg, Sven [1 ]
Goerls, Helmar [1 ]
Schnegg, Alexander [5 ]
Plass, Winfried [1 ]
机构
[1] Friedrich Schiller Univ Jena, Inst Anorgan & Analyt Chem, Humboldtstr 8, D-07743 Jena, Germany
[2] Helmholtz Zentrum Berlin Materialien & Energie Gmb, Dept Spins Energy Convers & Quantum Informat Sci, Energy Joint Lab EPR4, Albert Einstein Str 16, D-12489 Berlin, Germany
[3] Humboldt Univ, Inst Chem, Brook Taylor Str 2, D-12489 Berlin, Germany
[4] Jagiellonian Univ, Inst Phys, PL-30348 Krakow, Poland
[5] Max Planck Inst Chem Energy Convers, EPR Res Grp, Stiftstr 34-36, D-45470 Mulheim An Der Ruhr, Germany
关键词
cobalt; magnetic properties; EPR spectroscopy; ab initio calculations; electronic structure; INDUCED SLOW RELAXATION; ZERO-FIELD; MOLECULE MAGNETS; ELECTRONIC-STRUCTURE; COMPLEXES; ANISOTROPY; MAGNETIZATION; SYMMETRY; DYNAMICS; SPECTRA;
D O I
10.1002/chem.202401545
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New cobalt(II)-based complexes with [N2O2] coordination formed by two bis-chelate ligands were synthesized and characterized by a multi-technique approach. The complexes possess an easy-axis anisotropy (D<0) and magnetic measurements show a field-induced slow relaxation of magnetization. The spin-reversal barriers, i. e., the splitting of the two lowest Kramers doublets (U-ZFS), have been measured by THz-EPR spectroscopy, which allows to distinguish the two crystallographically independent species present in one of the complexes. Based on these experimental U-ZFS energies together with those for related complexes reported in literature, it was possible to establish magneto-structural correlations. U-ZFS linearly depends on the elongation parameter epsilon(T) of the (pseudo-)tetrahedral coordination, which is given by the ratio between the average obtuse and acute angles at the cobalt(II) ion, while U-ZFS was found to be virtually independent of the twist angle of the chelate planes. With increasing deviation from the orthogonality of the latter, the rhombicity (|E/D|) increases.
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页数:14
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