scholarly journals Cover Feature: Elucidation of Dual Magnetic Relaxation Processes in Dinuclear Dysprosium(III) Phthalocyaninato Triple-Decker Single-Molecule Magnets Depending on the Octacoordination Geometry (Chem. Eur. J. 61/2017)

2017 ◽  
Vol 23 (61) ◽  
pp. 15236-15236 ◽  
Author(s):  
Keiichi Katoh ◽  
Yu Aizawa ◽  
Takaumi Morita ◽  
Brian K. Breedlove ◽  
Masahiro Yamashita
Keyword(s):  
Single Molecule ◽  
Magnetic Relaxation ◽  
Relaxation Processes ◽  
Single Molecule Magnets

Cu(ii)–Dy(iii) and Co(iii)–Dy(iii) based single molecule magnets with multiple slow magnetic relaxation processes in the Cu(ii)–Dy(iii) complex

2015 ◽  
Vol 44 (29) ◽  
pp. 13242-13249 ◽  
Author(s):  
Malay Dolai ◽  
Mahammad Ali ◽  
Ján Titiš ◽  
Roman Boča
Keyword(s):  
Schiff Base ◽  
Single Molecule ◽  
Schiff Base Ligand ◽  
Magnetic Relaxation ◽  
Magnetic Behaviour ◽  
Dinuclear Complexes ◽  
Relaxation Processes ◽  
Single Molecule Magnets ◽  
Slow Magnetic Relaxation

Two CuII–DyIII and CoIII–DyIII dinuclear complexes of a Schiff base ligand (H3L) exhibit single-molecule magnetic behaviour with multiple slow magnetic relaxation processes for the former.

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.

Dramatic impact of auxiliary ligands on the two-step magnetic relaxation process in Dy4(iii) single-molecule magnets

2019 ◽  
Vol 48 (17) ◽  
pp. 5793-5799 ◽  
Author(s):  
Kun Zhang ◽  
Gao-Peng Li ◽  
Cheng Zhang ◽  
Yao-Yu Wang
Keyword(s):  
Relaxation Process ◽  
Single Molecule ◽  
Magnetic Relaxation ◽  
Relaxation Processes ◽  
Single Molecule Magnets ◽  
Coordination Sites

Two-step relaxation processes are modulated in two Dy(iii)4 SMMs through modifying the auxiliary ligands on the changeable coordination sites.

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.

Multiple-decker phthalocyaninato dinuclear lanthanoid(iii) single-molecule magnets with dual-magnetic relaxation processes

2012 ◽  
Vol 41 (44) ◽  
pp. 13582 ◽  
Author(s):  
Keiichi Katoh ◽  
Yoji Horii ◽  
Nobuhiro Yasuda ◽  
Wolfgang Wernsdorfer ◽  
Koshiro Toriumi ◽  
...  
Keyword(s):  
Single Molecule ◽  
Magnetic Relaxation ◽  
Relaxation Processes ◽  
Single Molecule Magnets

scholarly journals Series of Chloranilate-Bridged Dinuclear Lanthanide Complexes: Kramers Systems Showing Field-Induced Slow Magnetic Relaxation

2019 ◽  
Vol 5 (2) ◽  
pp. 30 ◽  
Author(s):  
Ryuta Ishikawa ◽  
Shoichi Michiwaki ◽  
Takeshi Noda ◽  
Keiichi Katoh ◽  
Masahiro Yamashita ◽  
...  
Keyword(s):  
Magnetic Susceptibility ◽  
Single Molecule ◽  
Magnetic Relaxation ◽  
Lanthanide Complexes ◽  
Relaxation Processes ◽  
X Ray Diffraction ◽  
Single Molecule Magnets ◽  
Magnetic Susceptibility Data ◽  
Susceptibility Data ◽  
Slow Magnetic Relaxation

A series of chloralilate-bridged dinuclear lanthanide complexes of formula [{LnIII(Tp)2}2(μ-Cl2An)]·2CH2Cl2, where Cl2An2− and Tp− represent the chloranilate and hydrotris (pyrazolyl)borate ligands, respectively, and Ln = Gd (1), Tb (2), Ho (3), Er (4), and Yb (5) was synthesized. All five complexes were characterized by an elemental analysis, infrared spectroscopy, single crystal X-ray diffraction, and SQUID measurements. The complexes 1–5 in the series were all isostructural. A comparison of the temperature dependence of the dc magnetic susceptibility data of these complexes revealed clear differences depending on the lanthanide center. Ac magnetic susceptibility measurements revealed that none of the five complexes exhibited a slow magnetic relaxation under a zero applied dc field. On the other hand, the Kramers systems (complexes 4 and 5) clearly displayed a slow magnetic relaxation under applied dc fields, suggesting field-induced single-molecule magnets that occur through Orbach and Raman relaxation processes.

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.

Strictly linear trinuclear Dy–Ca/Mg–Dy single-molecule magnets: the impact of long-range f–f ferromagnetic interactions on suppressing quantum tunnelling of magnetization leading to slow magnetic relaxation

2017 ◽  
Vol 46 (25) ◽  
pp. 8259-8268 ◽  
Author(s):  
Wan-Ying Zhang ◽  
Yong-Mei Tian ◽  
Hong-Feng Li ◽  
Peng Chen ◽  
Yi-Quan Zhang ◽  
...  
Keyword(s):  
Long Range ◽  
Single Molecule ◽  
Magnetic Relaxation ◽  
Single Molecule Magnets ◽  
Quantum Tunnelling ◽  
Trinuclear Complexes ◽  
Slow Magnetic Relaxation ◽  
Ferromagnetic Interactions ◽  
The Impact

A series of linear trinuclear complexes Ln2M(OQ)8 [Ln(iii) = Dy and Er, M(ii) = Ca and Mg] were structurally and magnetically investigated.

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].

Sign in / Sign up

Export Citation Format

Share Document