Remanence and coercivity are the basic characteristics of permanent magnets. They are also tightly correlated with the existence of long relaxation times of magnetization in a number of molecular complexes, called accordingly single-molecule magnets (SMMs). Up to now, hysteresis loops with large coercive fields have only been observed in polynuclear metal complexes and metal-radical SMMs. On the contrary, mononuclear complexes, called single-ion magnets (SIM), have shown hysteresis loops of butterfly/phonon bottleneck type, with negligible coercivity, and therefore with much shorter relaxation times of magnetization. A mononuclear Er(III) complex is presented with hysteresis loops having large coercive fields, achieving 7000 Oe at T=1.8 K and field variation as slow as 1 h for the entire cycle. The coercivity persists up to about 5 K, while the hysteresis loops persist to 12 K. Our finding shows that SIMs can be as efficient as polynuclear SMMs, thus opening new perspectives for their applications.
The two-coordinate cationic Ni(I) bis-N-heterocyclic carbene complex [Ni(6-Mes)2]Br (1) [6-Mes =1,3-bis(2,4,6-trimethylphenyl)-3,4,5,6-tetrahydropyrimidin-2-ylidene] has been structurally characterized and displays a highly linear geometry with a C-Ni-C angle of 179.27(13)°. Density functional theory calculations revealed that the five occupied metal-based orbitals are split in an approximate 2:1:2 pattern. Significant magnetic anisotropy results from this orbital degeneracy, leading to single-ion magnet (SIM) behavior.
A dysprosium(III) sandwich complex, [Dy(III)(COT″)(2)Li(THF)(DME)], was synthesized using 1,4-bis(trimethylsilyl)cyclooctatetraenyl dianion (COT″). The complex behaves as a single-ion magnet and demonstrates unusual multiple relaxation modes. The observed relaxation pathways strongly depend on the applied static dc fields.
An organometallic building block strategy was employed to investigate the magnetic properties of a Ln III organometallic single-ion magnet (SIM) and subsequent single-molecule magnet (SMM) after coupling two of the monomeric units. New homoleptic Dy III COT″ 2 and Ln III 2 COT″ 3 (Ln = Gd, Dy) complexes have been synthesized. DFT calculations of the bimetallic Dy III complex indicate strong metal−ligand covalency and uneven donation to the Dy III ions by the terminal and internal COT″ 2− (cyclooctatetraenide) rings that correlate with the respective bond distances. Interestingly, the studies also point to a weak covalent interaction between the metal centers, despite a large separation. The ac susceptibility data indicates that both Dy III COT″ 2 and Dy III 2 COT″ 3 act as an SIM and an SMM, respectively, with complex multiple relaxation mechanisms. Ab initio calculations reveal the direction of the magnetic anisotropic axis is not perpendicular to the planar COT″ rings for both Dy III COT″ 2 and Dy III 2 COT″ 3 complexes due to the presence of trimethylsilyl groups on the COT″ rings. If these bulky groups are removed, the calculations predict reorientation of the anisotropic axis can be achieved.
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