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.

The near-infrared luminescence and magnetism of dinuclear complexes with different local symmetries constructed from a β-diketonate co-ligand and bis-Schiff base ligand

2020 ◽  
Vol 44 (6) ◽  
pp. 2561-2570 ◽  
Author(s):  
Huan-Huan Chen ◽  
Dong-Fang Wu ◽  
Yao-Yao Duan ◽  
Ling Li ◽  
Yun-Juan Wang ◽  
...  
Keyword(s):  
Schiff Base ◽  
Schiff Base Ligand ◽  
Magnetic Relaxation ◽  
Near Infrared ◽  
Relaxation Behavior ◽  
Dinuclear Complexes ◽  
Infrared Luminescence ◽  
Slow Magnetic Relaxation ◽  
Local Symmetries

A DyIII-complex based on a β-diketonate co-ligand and bi-Schiff base ligand displays slow magnetic relaxation behavior.

Modulating single-molecule magnet behavior towards multiple magnetic relaxation processes through structural variation in Dy4 clusters

2018 ◽  
Vol 5 (8) ◽  
pp. 1876-1885 ◽  
Author(s):  
Wen-Min Wang ◽  
Xiao-Min Kang ◽  
Hai-Yun Shen ◽  
Zhi-Lei Wu ◽  
Hong-Ling Gao ◽  
...  
Keyword(s):  
Schiff Base ◽  
Single Molecule ◽  
Schiff Base Ligand ◽  
Magnetic Relaxation ◽  
Structural Variation ◽  
Slow Relaxation ◽  
Relaxation Processes ◽  
Magnetic Studies ◽  
Single Molecule Magnet

Three Dy4 clusters based on a flexible and attractive Schiff base ligand HL have been synthesized, and they showed different tetranuclear core arrangements. Magnetic studies reveal that clusters 1–3 display distinct slow relaxation of magnetization.

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.

Single molecule magnetic behaviour in lanthanide naphthalenesulfonate complexes

2018 ◽  
Vol 47 (48) ◽  
pp. 17349-17356 ◽  
Author(s):  
Guo Peng ◽  
Ying-Ying Zhang ◽  
Bo Li ◽  
Xiao-Fan Sun ◽  
Hong-Ling Cai ◽  
...  
Keyword(s):  
Single Molecule ◽  
Magnetic Relaxation ◽  
Lanthanide Complexes ◽  
Magnetic Behaviour ◽  
Single Molecule Magnets ◽  
Slow Magnetic Relaxation

A family of mononuclear lanthanide complexes exhibiting slow magnetic relaxation is reported, providing the first examples of pure 4f sulfonate-based single molecule magnets.

Designing asymmetric Dy2 single-molecule magnets with two-step relaxation processes by the modification of the coordination environments of Dy(iii) ions

2020 ◽  
Vol 49 (26) ◽  
pp. 8976-8984
Author(s):  
Yuan Huang ◽  
Jia-Xin Li ◽  
Yu Ge ◽  
Xia-Mei Zhang ◽  
Yang Xu ◽  
...  
Keyword(s):  
Schiff Base ◽  
Single Molecule ◽  
Schiff Base Ligand ◽  
Slow Relaxation ◽  
Relaxation Processes ◽  
Single Molecule Magnets ◽  
Single Molecule Magnet

The reaction of Dy(NO3)3·6H2O and an asymmetric Schiff-base ligand H2L afforded two asymmetric dinuclear compound. Both complexes exhibit single-molecule magnet behavior with two-step slow 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].

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