Geometry and magnetic interaction modulations in dinuclear Dy2 single-molecule magnets

2017 ◽  
Vol 46 (25) ◽  
pp. 8252-8258 ◽  
Author(s):  
Mei Guo ◽  
Yonghui Xu ◽  
Jianfeng Wu ◽  
Lang Zhao ◽  
Jinkui Tang
Keyword(s):  
Single Molecule ◽  
Magnetic Interaction ◽  
Coordination Geometry ◽  
Single Molecule Magnets

A series of dinuclear dysprosium compounds were synthesized, in which compound 3 combines the bridging modes of 1 and coordination geometry of 2, resulting in better SMM performance.

scholarly journals High-Coordinate Mononuclear Ln(III) Complexes: Synthetic Strategies and Magnetic Properties

2020 ◽  
Vol 7 (1) ◽  
pp. 1
Author(s):  
Joydev Acharya ◽  
Pankaj Kalita ◽  
Vadapalli Chandrasekhar
Keyword(s):  
Magnetic Properties ◽  
Single Molecule ◽  
Fine Tuning ◽  
Coordination Geometry ◽  
Single Molecule Magnets ◽  
Magnetization Relaxation ◽  
Quantum Tunneling Of Magnetization ◽  
Structural Correlation ◽  
High Coordination Number ◽  
High Coordination

Single-molecule magnets involving monometallic 4f complexes have been investigated extensively in last two decades to understand the factors that govern the slow magnetization relaxation behavior in these complexes and to establish a magneto-structural correlation. The prime goal in this direction is to suppress the temperature independent quantum tunneling of magnetization (QTM) effect via fine-tuning the coordination geometry/microenvironment. Among the various coordination geometries that have been pursued, complexes containing high coordination number around Ln(III) are sparse. Herein, we present a summary of the various synthetic strategies that were used for the assembly of 10- and 12-coordinated Ln(III) complexes. The magnetic properties of such complexes are also described.

scholarly journals Relationship between the Coordination Geometry and Spin Dynamics of Dysprosium(III) Heteroleptic Triple-Decker Complexes

2019 ◽  
Vol 5 (4) ◽  
pp. 65 ◽  
Author(s):  
Tetsu Sato ◽  
Satoshi Matsuzawa ◽  
Keiichi Katoh ◽  
Brian K. Breedlove ◽  
Masahiro Yamashita
Keyword(s):  
Single Molecule ◽  
Magnetic Relaxation ◽  
Spin Dynamics ◽  
Twist Angle ◽  
Magnetic Interactions ◽  
Relaxation Processes ◽  
Coordination Geometry ◽  
Single Molecule Magnets ◽  
Spin Lattice ◽  
The Relationship

When using single molecule magnets (SMMs) in spintronics devices, controlling the quantum tunneling of the magnetization (QTM) and spin-lattice interactions is important. To improve the functionality of SMMs, researchers have explored the effects of changing the coordination geometry of SMMs and the magnetic interactions between them. Here, we report on the effects of the octa-coordination geometry on the magnetic relaxation processes of dinuclear dysprosium(III) complexes in the low-temperature region. Mixed ligand dinuclear Dy3+ triple-decker complexes [(TPP)Dy(Pc)Dy(TPP)] (1), which have crystallographically equivalent Dy3+ ions, and [(Pc)Dy(Pc)Dy(TPP)] (2), which have non-equivalent Dy3+ ions, (Pc2− = phthalocyaninato; TPP2− = tetraphenylporphyrinato), undergo dual magnetic relaxation processes. This is due to the differences in the ground states due to the twist angle (φ) between the ligands. The relationship between the off-diagonal terms and the dual magnetic relaxation processes that appears due to a deviation from D4h symmetry is discussed.

Coordination anion effects on the geometry and magnetic interaction of binuclear Dy2 single-molecule magnets

2021 ◽  
Author(s):  
Jinjiang Wu ◽  
Xiao-Lei Li ◽  
Léo La Droitte ◽  
Olivier Cador ◽  
Boris Le Guennic ◽  
...  
Keyword(s):  
Single Molecule ◽  
Magnetic Interaction ◽  
Single Molecule Magnets ◽  
Multidentate Ligand

Two new dimeric dysprosium(III) complexes [Dy2(HL)2(SCN)2]·2CH3CN (1) and [Dy2(HL)2(NO3)2]·2CH3CN·2H2O (2) have been assembled using the H3L multidentate ligand (H3L = 2,2'-((((2-hydroxy-5-methyl-1,3-phenylene)bis(methylene))bis((pyridin-2-ylmethyl)azanediyl))bis(methylene))diphenol). The use of different coordination anions for the two...

Carboxylate-Bridged Dinuclear Dy2 Single-Molecule Magnets: Synthesis, Structure, and Magnetic Studies

2013 ◽  
Vol 66 (1) ◽  
pp. 98 ◽  
Author(s):  
Yu-mei Song ◽  
Feng Luo ◽  
Yan Zhu ◽  
Xiao-zhao Tian ◽  
Gong-ming Sun
Keyword(s):  
Magnetic Properties ◽  
Single Molecule ◽  
Coordination Geometry ◽  
Magnetic Studies ◽  
Single Molecule Magnets ◽  
Chlorobenzoic Acid ◽  
Ferromagnetic Interaction ◽  
Single Molecule Magnet ◽  
The Difference

In this work, the synthesis, structure, and magnetic studies of three dinuclear Dy2 compounds, namely Dy2(bpy)2(L)6 (1), Dy2(phen)2(L)6 (2), Dy2(μ-H2O)2(bpy)2(L)6 (3) are reported in detail, where HL, phen, and bpy are 4-chlorobenzoic acid, 1,10-phenanthroline, and 2,2′-bipyridine. Magnetic studies reveal the intramolecular ferromagnetic interaction and single-molecule magnetic properties of these compounds. The fine-tuned single-molecule magnet properties of compounds 1–3, mainly due to the difference of the coordination geometry of DyIII ions, are highlighted.

High local coordination symmetry around the spin center and the alignment between magnetic and symmetric axes together play a crucial role in single-molecule magnet performance

2019 ◽  
Vol 48 (15) ◽  
pp. 4931-4940 ◽  
Author(s):  
Zhao-Fu Yang ◽  
Yong-Mei Tian ◽  
Wan-Ying Zhang ◽  
Peng Chen ◽  
Hong-Feng Li ◽  
...  
Keyword(s):  
Single Molecule ◽  
Crucial Role ◽  
Pentagonal Bipyramid ◽  
Coordination Geometry ◽  
Single Molecule Magnets ◽  
Single Molecule Magnet ◽  
Local Coordination ◽  
Spin Center

A tetradentate 8-hydroxyquinoline-based acyl hydrazine ligand was used to construct a series of mono/di-nuclear dysprosium single-molecule magnets (SMMs) with nearly ideal pentagonal bipyramid coordination geometry (D5h).

Modulating the Magnetic Interaction in New Triple-Decker Dysprosium(III) Single-Molecule Magnets

2018 ◽  
Vol 57 (3) ◽  
pp. 1408-1416 ◽  
Author(s):  
Jing-Yuan Ge ◽  
Hai-Ying Wang ◽  
Jian Su ◽  
Jing Li ◽  
Bao-Lin Wang ◽  
...  
Keyword(s):  
Single Molecule ◽  
Magnetic Interaction ◽  
Single Molecule Magnets

scholarly journals Macrocycle Based Dinuclear Dysprosium(III) Single Molecule Magnets with Local D5h Coordination Geometry

2021 ◽  
Author(s):  
Jianfeng Wu ◽  
Serhiy Demeshko ◽  
Sebastian Dechert ◽  
Franc Meyer
Keyword(s):  
Single Molecule ◽  
High Performance ◽  
Lanthanide Ions ◽  
Coordination Geometry ◽  
Single Molecule Magnets

Targeted approaches for manipulating the coordination geometry of lanthanide ions is a promising way to synthesize high-performance single-molecule magnets (SMMs), but most of the successful examples reported to date focus...

Seeking Magneto-Structural Correlations in Easily Tailored Pentagonal Bipyramid Dy(III) Single-Ion Magnets

2019 ◽  
Author(s):  
Guo-Zhang Huang ◽  
Ze-Yu Ruan ◽  
Jie-Yu Zheng ◽  
Yan-Cong Chen ◽  
Si-Guo Wu ◽  
...  
Keyword(s):  
Single Molecule ◽  
Structural Engineering ◽  
Magnetic Hysteresis ◽  
Sweep Rate ◽  
Coordination Bond ◽  
Pentagonal Bipyramid ◽  
Single Molecule Magnets ◽  
Crystal Field Theory ◽  
Bond Angles ◽  
Axial Coordination

<p><a></a>Controlling molecular magnetic anisotropy via structural engineering is delicate and fascinating, especially for single-molecule magnets (SMMs). Herein a family of dysprosium single-ion magnets (SIMs) sitting in pentagonal bipyramid geometry have been synthesized with the variable-size terminal ligands and counter anions, through which the subtle coordination geometry of Dy(III) can be finely tuned based on the size effect. The effective energy barrier (Ueff) successfully increases from 439 K to 632 K and the magnetic hysteresis temperature (under a 200 Oe/s sweep rate) raises from 11 K to 24 K. Based on the crystal-field theory, a semi-quantitative magneto-structural correlation deducing experimentally for the first time is revealed that the Ueff is linearly proportional to the structural-related value S2<sup>0</sup> corresponding to the axial coordination bond lengths and the bond angles. Through the evaluation of the remanent magnetization from hysteresis, quantum tunneling of magnetization (QTM) is found to exhibit negative correlation with the structural-related value S<sub>tun</sub> corresponding to the axial coordination bond angles.<br></p>

Correlating Blocking Temperatures in Single Molecule Magnets with Raman Relaxation

2018 ◽  
Author(s):  
Marcus J. Giansiracusa ◽  
Andreas Kostopoulos ◽  
George F. S. Whitehead ◽  
David Collison ◽  
Floriana Tuna ◽  
...  
Keyword(s):  
Relaxation Time ◽  
Single Molecule ◽  
Energy Barrier ◽  
Thermal Relaxation ◽  
Relaxation Mechanism ◽  
Blocking Temperature ◽  
Single Molecule Magnets ◽  
Single Molecule Magnet ◽  
Key Parameter

We report a six coordinate DyIII single-molecule magnet<br>(SMM) with an energy barrier of 1110 K for thermal relaxation of<br>magnetization. The sample shows no retention of magnetization<br>even at 2 K and this led us to find a good correlation between the<br>blocking temperature and the Raman relaxation regime for SMMs.<br>The key parameter is the relaxation time (𝜏<sub>switch</sub>) at the point where<br>the Raman relaxation mechanism becomes more important than<br>Orbach.

A Combined Spin-Flip and IP/EA Approach for Handling Spin and Spatial Degeneracies: Application to Double Exchange Systems

2018 ◽  
Author(s):  
Shannon Houck ◽  
Nicholas Mayhall
Keyword(s):  
Single Molecule ◽  
Double Exchange ◽  
Computational Effort ◽  
Strongly Correlated ◽  
Single Molecule Magnets ◽  
New Approach ◽  
Spin Flip ◽  
Model Hamiltonian ◽  
Simultaneous Existence ◽  
Exchange Parameters

<div>Many multiconfigurational systems, such as single-molecule magnets, are difficult to study using traditional computational methods due to the simultaneous existence of both spin and spatial degeneracies. In this work, a new approach termed n-spin-flip Ionization Potential/Electron Affinity (<i>n</i>SF-IP or <i>n</i>SF-EA) is introduced which combines the spin-flip method of Anna Krylov with particle-number changing IP/EA methods. We demonstrate the efficacy of the approach by applying it to the strongly-correlated N<sub>2</sub><sup>+</sup> as well as several double exchange systems. We also demonstrate that when these systems are well-described by a double exchange model Hamiltonian, only 1SF-IP/EA is required to extract the double exchange parameters and accurately predict energies for the low-spin states. This significantly reduces the computational effort for studying such systems. The effects of including additional excitations (using a RAS-<i>n</i>SF-IP/EA scheme) are also examined, with particular emphasis on hole and particle excitations.</div>

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