scholarly journals Exchange Interactions at the Origin of Slow Relaxation of the Magnetization in {TbCu3} and {DyCu3} Single-Molecule Magnets

2014 ◽  
Vol 53 (17) ◽  
pp. 8970-8978 ◽  
Author(s):  
Fraser J. Kettles ◽  
Victoria A. Milway ◽  
Floriana Tuna ◽  
Rafael Valiente ◽  
Lynne H. Thomas ◽  
...  
Keyword(s):  
Single Molecule ◽  
Exchange Interactions ◽  
Slow Relaxation ◽  
Single Molecule Magnets

Magnetic field and dilution effects on the slow relaxation of {Er3} triangle-based arsenotungstate single-molecule magnets

2020 ◽  
Vol 49 (35) ◽  
pp. 12458-12465 ◽  
Author(s):  
Hanhan Chen ◽  
Lin Sun ◽  
Jinpeng Zhang ◽  
Zikang Xiao ◽  
Pengtao Ma ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Single Molecule ◽  
Magnetic Relaxation ◽  
Slow Relaxation ◽  
Relaxation Processes ◽  
Single Molecule Magnets ◽  
Thermally Activated ◽  
Slow Magnetic Relaxation ◽  
Dilution Effects

Triangular {Er3} cluster containing POM exhibits field-induced two thermally activated relaxation processes. Whereas, the diamagnetic dilution sample indicates slow magnetic relaxation with the QTM being partially suppressed.

scholarly journals Slow Relaxation of the Magnetization in Bis-Decorated Chiral Helicene-Based Coordination Complexes of Lanthanides

2018 ◽  
Vol 4 (3) ◽  
pp. 39 ◽  
Author(s):  
Jessica Flores Gonzalez ◽  
Vincent Montigaud ◽  
Nidal Saleh ◽  
Olivier Cador ◽  
Jeanne Crassous ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Ab Initio Calculations ◽  
Ab Initio ◽  
Single Molecule ◽  
Crystalline Phase ◽  
Coordination Complexes ◽  
Slow Relaxation ◽  
Single Molecule Magnets ◽  
Racemic Form

The complexes [Ln2(hfac)6(L)]·nC6H14 (Ln = Dy (1) n = 0, Yb (2) n = 1) with the L chiral 3,14-di-(2-pyridyl)-4,13-diaza[6]helicene ligand (hfac− = 1,1,1,5,5,5-hexafluoroacetylacetonate) have been synthesized in their racemic form and structurally and magnetically characterized. Both complexes behave as field-induced single molecule magnets in the crystalline phase. These magnetic properties were rationalized by ab initio calculations.

Switching slow relaxation in a MnIII3MnIV cluster: an example of grafting single-molecule magnets onto polyoxometalates

2010 ◽  
Vol 46 (16) ◽  
pp. 2760 ◽  
Author(s):  
Xikui Fang ◽  
Manfred Speldrich ◽  
Helmut Schilder ◽  
Rui Cao ◽  
Kevin P. O'Halloran ◽  
...  
Keyword(s):  
Single Molecule ◽  
Slow Relaxation ◽  
Single Molecule Magnets

scholarly journals Synthesis, structure, magnetic and luminescence properties of two dysprosium single-molecule magnets based on phenoxide dye ligands

CrystEngComm ◽  
2020 ◽  
Vol 22 (11) ◽  
pp. 1909-1913
Author(s):  
Jérôme Long ◽  
Alexander N. Selikhov ◽  
Ekaterina Mamontova ◽  
Konstantin A. Lyssenko ◽  
Yannick Guari ◽  
...  
Keyword(s):  
Single Molecule ◽  
Slow Relaxation ◽  
Luminescence Properties ◽  
Single Molecule Magnets

We report two dysprosium complexes based on phenoxide dye ligands and showing slow relaxation of their magnetization.

A remarkable energy barrier for spin reversal in a field induced dinuclear ytterbium single molecule magnet

2021 ◽  
Vol 50 (39) ◽  
pp. 13666-13670
Author(s):  
Arpan Mondal ◽  
Sanjit Konar
Keyword(s):  
Single Molecule ◽  
Energy Barrier ◽  
Slow Relaxation ◽  
Single Molecule Magnets ◽  
Single Molecule Magnet ◽  
Crystal Fields ◽  
Spin Reversal

Strong equatorial and weak axial crystal fields enhance the energy barrier for slow relaxation of magnetization in Yb-based single molecule magnets.

Mixed valency in polynuclear Mn II /Mn III , Mn III /Mn IV and Mn II /Mn III /Mn IV clusters: a foundation for high-spin molecules and single-molecule magnets

2007 ◽  
Vol 366 (1862) ◽  
pp. 113-125 ◽  
Author(s):  
Theocharis C Stamatatos ◽  
George Christou
Keyword(s):  
Single Molecule ◽  
Exchange Interactions ◽  
Zero Field ◽  
Zero Field Splitting ◽  
Single Molecule Magnets ◽  
Zero Field Splitting Parameter ◽  
Jahn Teller ◽  
Splitting Parameter ◽  
Molecular Spin ◽  
Molecular Compounds

Mixed-valent Mn/O dinuclear and polynuclear molecular compounds containing Mn III are almost without exception trapped valence. Large differences between the strengths of the exchange interactions within Mn II Mn III , Mn III Mn III and Mn III Mn IV pairs lead to situations where Mn III Mn IV interactions, the strongest of the three mentioned and antiferromagnetic in nature, dominate the intramolecular spin alignments in trinuclear and higher nuclearity mixed-valent complexes and often result in molecules that have large, and sometimes abnormally large, values of molecular spin ( S ). When coupled to a large molecular magnetoanisotropy of the easy-axis-type (negative zero-field splitting parameter, D ), also primarily resulting from individual Jahn–Teller distorted Mn III centres, such molecules will function as single-molecule magnets (molecular nanomagnets). Dissection of the structures and exchange interactions within a variety of mixed-valent Mn x cluster molecules with metal nuclearities of Mn 4 , Mn 12 and Mn 25 allows a ready rationalization of the observed S , D and overall magnetic properties in terms of competing antiferromagnetic exchange interactions within triangular subunits, resulting spin alignments and relative orientation of Mn III JT axes. Such an understanding has provided a stepping stone to the identification of a ‘magnetically soft’ Mn 25 cluster whose groundstate spin S value can be significantly altered by relatively minor structural perturbations. Such ‘spin tweaking’ has allowed this cluster to be obtained in three different forms with three different groundstate S values.

Bis-phenoxido and bis-acetato bridged heteronuclear {CoIIIDyIII} single molecule magnets with two slow relaxation branches

2016 ◽  
Vol 45 (17) ◽  
pp. 7510-7520 ◽  
Author(s):  
Susanta Hazra ◽  
Ján Titiš ◽  
Dušan Valigura ◽  
Roman Boča ◽  
Sasankasekhar Mohanta
Keyword(s):  
Schiff Base ◽  
Crystal Structures ◽  
Single Molecule ◽  
Magnetic Behaviour ◽  
Slow Relaxation ◽  
Single Molecule Magnets

Crystal structures and single molecule magnetic behaviour of two bis(μ-phenoxido)–bis(μ-acetato) {CoIIIDyIII} complexes, derived from the hexadentate Schiff base N,N′-ethylenebis(3-ethoxy- or 3-methoxysalicylaldimine), are described.

Ferromagnetic [Mn3] Single-Molecule Magnets and Their Supramolecular Networks

2009 ◽  
Vol 62 (9) ◽  
pp. 1108 ◽  
Author(s):  
Ross Inglis ◽  
Giannis S. Papaefstathiou ◽  
Wolfgang Wernsdorfer ◽  
Euan K. Brechin
Keyword(s):  
Single Molecule ◽  
Quantum Physics ◽  
Three Dimensional ◽  
Exchange Interactions ◽  
Molecular Magnets ◽  
Single Molecule Magnets ◽  
Spin Networks ◽  
Quantum Tunnelling ◽  
Field Bias ◽  
Supramolecular Networks

The complexes [MnIII3O(Et-sao)3(O2CPh(Cl)2)(MeOH)3(H2O)] (1), [MnIII3O(Et-sao)3(ClO4)(MeOH)3] (2), [MnIII3O(Et-sao)3(O2Ph(CF3)2)(EtOH)(H2O)3] (3), and [MnIII3O(Ph-sao)3(O2C-anthra)(MeOH)4]·Ph-saoH2 (4·Ph-saoH2) display dominant ferromagnetic exchange interactions leading to molecules with S = 6 ground states. The molecules are single molecule magnets (SMM) displaying large effective energy barriers for magnetization reversal. In each case their crystal structures reveal multiple intermolecular H-bonding interactions. Single crystal hysteresis loop measurements demonstrate that these interactions are strong enough to cause a clear field bias, but too weak to transform the spin networks into classical antiferromagnets. These three-dimensional networks of exchange coupled SMMs demonstrate that quantum tunnelling magnetization can be controlled using exchange interactions, suggesting supramolecular chemistry can be exploited to modulate the quantum physics of molecular magnets.

Aufbau vs. Non-Aufbau Ground States in Two-Coordinate d7 Single-Molecule Magnets

2021 ◽  
Author(s):  
Dylan Errulat ◽  
Katie L. M. Harriman ◽  
Diogo Alves Galico ◽  
Jeffrey S. Ovens ◽  
Akseli Mansikkamäki ◽  
...  
Keyword(s):  
Angular Momentum ◽  
Single Molecule ◽  
Ground States ◽  
Slow Relaxation ◽  
Single Molecule Magnets ◽  
Electronic Configurations ◽  
Large Angular Momentum

Single-molecule magnets (SMMs) with d7 electronic configurations often require designer ligands to satisfy the metal's electronic conditions to achieve large angular momentum. Herein, the slow relaxation of the magnetization in...

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