Modulating the Relaxation Dynamics via Structural Transition From Dinuclear Dysprosium Cluster to Nonanuclear Cluster

2021 ◽  
Author(s):  
peng hu ◽  
Ling-hui Cao ◽  
Ao-gang Liu ◽  
Yi-Quan Zhang ◽  
Tianle Zhang ◽  
...  
Keyword(s):  
Energy Barrier ◽  
Magnetic Relaxation ◽  
Structural Transition ◽  
Relaxation Dynamics

Along with the transition from a dinuclear dysprosium cluster to a nonanuclear one, the variable magnetic relaxation with the energy barrier changing from 217.87 K to 9.24 K had been...

Slow magnetic relaxation in dinuclear dysprosium and holmium phenoxide bridged complexes: a Dy2 single molecule magnet with a high energy barrier

2021 ◽  
Author(s):  
Matilde Fondo ◽  
Julio Corredoira-Vázquez ◽  
Ana M. Garcia-Deibe ◽  
Jesus Sanmartin Matalobos ◽  
Silvia Gómez-Coca ◽  
...  
Keyword(s):  
Crystal Structures ◽  
Single Molecule ◽  
Energy Barrier ◽  
Magnetic Relaxation ◽  
High Energy ◽  
Single Molecule Magnet ◽  
High Energy Barrier ◽  
Slow Magnetic Relaxation

Dinuclear [M(H3L1,2,4)]2 (M = Dy, Dy2; M = Ho, Ho2) complexes were isolated from an heptadentate aminophenol ligand. The crystal structures of Dy2·2THF, and the pyridine adducts Dy2·2Py and Ho2·2Py,...

Structural anisotropy of cyanido-bridged {CoII9WV6} single-molecule magnets induced by bidentate ligands: towards the rational enhancement of an energy barrier

2016 ◽  
Vol 52 (26) ◽  
pp. 4772-4775 ◽  
Author(s):  
Szymon Chorazy ◽  
Michał Rams ◽  
Anna Hoczek ◽  
Bernard Czarnecki ◽  
Barbara Sieklucka ◽  
...  
Keyword(s):  
Single Molecule ◽  
Energy Barrier ◽  
Magnetic Relaxation ◽  
Bidentate Ligands ◽  
Single Molecule Magnets ◽  
Structural Anisotropy ◽  
Slow Magnetic Relaxation

{CoII9[WV(CN)8]6} clusters capped by odd and even number of bidentate ligands reveal the improved slow magnetic relaxation due to the significant structural anisotropy.

Polyoxometalate-Supported Lanthanoid Single-Molecule Magnets

2014 ◽  
Vol 67 (11) ◽  
pp. 1542 ◽  
Author(s):  
Michele Vonci ◽  
Colette Boskovic
Keyword(s):  
Single Molecule ◽  
Energy Barrier ◽  
Magnetic Relaxation ◽  
Donor Ligands ◽  
Single Molecule Magnets ◽  
Single Molecule Magnet ◽  
Coordination Numbers ◽  
Oxygen Donor ◽  
Slow Magnetic Relaxation

Polyoxometalates are robust and versatile multidentate oxygen-donor ligands, eminently suitable for coordination to trivalent lanthanoid ions. To date, 10 very different structural families of such complexes have been found to exhibit slow magnetic relaxation due to single-molecule magnet (SMM) behaviour associated with the lanthanoid ions. These families encompass complexes with between one and four of the later lanthanoid ions: Tb, Dy, Ho, Er, and Yb. The lanthanoid coordination numbers vary between six and eleven and a range of coordination geometries are evident. The highest energy barrier to magnetisation reversal measured to date for a lanthanoid–polyoxometalate SMM is Ueff/kB = 73 K for the heterodinuclear Dy–Eu compound (Bu4N)8H4[DyEu(OH)2(γ-SiW10O36)2].

Magnetic relaxation dynamics in thermally arrested Cr-modified Mn 2 Sb

2018 ◽  
Vol 461 ◽  
pp. 62-68 ◽  
Author(s):  
Yoshifuru Mitsui ◽  
Yoshihiro Matsumoto ◽  
Yoshiya Uwatoko ◽  
Masahiko Hiroi ◽  
Keiichi Koyama
Keyword(s):  
Magnetic Relaxation ◽  
Relaxation Dynamics

An air stable radical-bridged dysprosium single molecule magnet and its neutral counterpart: redox switching of magnetic relaxation dynamics

2017 ◽  
Vol 53 (14) ◽  
pp. 2283-2286 ◽  
Author(s):  
Brian S. Dolinar ◽  
Silvia Gómez-Coca ◽  
Dimitris I. Alexandropoulos ◽  
Kim R. Dunbar
Keyword(s):  
Magnetic Properties ◽  
Single Molecule ◽  
Quantum Tunneling ◽  
Magnetic Relaxation ◽  
Thermal Relaxation ◽  
Relaxation Dynamics ◽  
Single Molecule Magnet ◽  
Neutral Compound ◽  
Redox Switching ◽  
P Addition

Addition of a radical to the bridging tetrazine ligand of a Dy2 complex dramatically alters the magnetic properties. The radical complex undergoes magnetic relaxation via a thermal relaxation pathway, whereas the neutral compound relaxes via quantum tunneling of the magnetization.

scholarly journals Ab Initio Prediction of High-Temperature Magnetic Relaxation Rates in Single-Molecule Magnets

2021 ◽  
Author(s):  
Daniel Reta ◽  
Jon G. C. Kragskow ◽  
Nicholas Chilton
Keyword(s):  
High Temperature ◽  
Ab Initio ◽  
Single Molecule ◽  
Magnetic Relaxation ◽  
Quantitative Prediction ◽  
Relaxation Dynamics ◽  
Efficient Design ◽  
Relaxation Rates ◽  
Design Strategies ◽  
Single Molecule Magnets

<p>Organometallic molecules based on [Dy(Cp<sup>R</sup>)<sub>2</sub>]<sup>+</sup> cations have emerged as clear front-runners in the search for high-temperature single-molecule magnets. However, despite a growing family of structurally-similar molecules, these molecules show significant variations in their magnetic properties, demonstrating the importance of understanding magneto-structural relationships towards developing more efficient design strategies. Here we refine our <i>ab initio</i> spin dynamics methodology and show that it is capable of quantitative prediction of relative relaxation rates in the Orbach region. Applying it to all reported [Dy(Cp<sup>R</sup>)<sub>2</sub>]<sup>+</sup> cations allows us to tease out differences in their relaxation dynamics, highlighting that the main discriminant is the magnitude of the crystal field splitting. We subsequently employ the method to predict relaxation rates for a series of hypothetical organometallic sandwich compounds, revealing an upper limit to the effective barrier to magnetic relaxation of around 2200 K, which has been reached. However, we show that further improvements to single-molecule magnets can be made by moving vibrational modes off-resonance with electronic excitations.</p>

Hydrogen-bonding interactions and magnetic relaxation dynamics in tetracoordinated cobalt(ii) single-ion magnets

2019 ◽  
Vol 48 (2) ◽  
pp. 395-399 ◽  
Author(s):  
Ryoji Mitsuhashi ◽  
Satoshi Hosoya ◽  
Takayoshi Suzuki ◽  
Yukinari Sunatsuki ◽  
Hiroshi Sakiyama ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Magnetic Relaxation ◽  
Zero Field ◽  
Relaxation Dynamics ◽  
Hydrogen Bonding Interactions ◽  
Slow Magnetic Relaxation ◽  
Hydrogen Bonded

Zero field slow magnetic relaxation was observed in two cobalt(ii) complexes with 1-D chain hydrogen-bonded structures.

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