Magnetic Relaxation of Single-Molecule Magnets in an External Magnetic Field: An Ising Dimer of a Terbium(III)-Phthalocyaninate Triple-Decker Complex

2010 ◽  
Vol 17 (1) ◽  
pp. 117-122 ◽  
Author(s):  
Keiichi Katoh ◽  
Takashi Kajiwara ◽  
Motohiro Nakano ◽  
Yasuhiro Nakazawa ◽  
Wolfgang Wernsdorfer ◽  
...  
2020 ◽  
Vol 49 (35) ◽  
pp. 12458-12465 ◽  
Author(s):  
Hanhan Chen ◽  
Lin Sun ◽  
Jinpeng Zhang ◽  
Zikang Xiao ◽  
Pengtao Ma ◽  
...  

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.


2015 ◽  
Vol 44 (17) ◽  
pp. 8150-8155 ◽  
Author(s):  
Jiang Liu ◽  
Yan-Cong Chen ◽  
Zhong-Xia Jiang ◽  
Jun-Liang Liu ◽  
Jian-Hua Jia ◽  
...  

Two tetranuclear dysprosium single molecule magnets under a zero applied external magnetic field showing high thermal energy barriers which are among the highest within the reported tetranuclear lanthanide-based SMMs.


2011 ◽  
Vol 25 (15) ◽  
pp. 1281-1291
Author(s):  
M. T. THOMAZ ◽  
ONOFRE ROJAS ◽  
E. V. CORRÊA-SILVA

The magnetization and the specific heat of two single molecule magnets (SMM) with spin-10, Mn 12- ac and Fe 8, are compared for Dβ ~ 0.031. The rhombic term in the Fe 8 molecule makes the x-component of its magnetization to be larger than that of the Mn 12- ac molecule. The axial symmetry of the Mn 12- ac favors the z-component of its magnetization, in comparison to the Fe 8 molecule. For T ≳ 18 K, the specific heat of the Mn 12- ac is large (80%, at most) than that of the Fe 8, at the same temperature. The corrections from the S = 9 excited states of these SMM's do not invalidate our results. An unexpected result occurs when the angle between the easy-axis and the external magnetic field equals π/4: the aforementioned percentage difference of the specific heat reaches 3% for D β ≲ 0.025 and h/k ∈[1.93, 2.04], when they are compared at distinct temperatures [Formula: see text]. This small percentage difference also happens for the average specific heat of both SMM's at those temperatures and h/D Mn ∈ [1.97, 2.1].


2015 ◽  
Vol 44 (29) ◽  
pp. 13242-13249 ◽  
Author(s):  
Malay Dolai ◽  
Mahammad Ali ◽  
Ján Titiš ◽  
Roman Boča

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.


2016 ◽  
Vol 52 (26) ◽  
pp. 4772-4775 ◽  
Author(s):  
Szymon Chorazy ◽  
Michał Rams ◽  
Anna Hoczek ◽  
Bernard Czarnecki ◽  
Barbara Sieklucka ◽  
...  

{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.


2017 ◽  
Vol 46 (25) ◽  
pp. 8259-8268 ◽  
Author(s):  
Wan-Ying Zhang ◽  
Yong-Mei Tian ◽  
Hong-Feng Li ◽  
Peng Chen ◽  
Yi-Quan Zhang ◽  
...  

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


2014 ◽  
Vol 67 (11) ◽  
pp. 1542 ◽  
Author(s):  
Michele Vonci ◽  
Colette Boskovic

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].


2020 ◽  
Vol 59 (49) ◽  
pp. 22048-22053
Author(s):  
Chihiro Kachi‐Terajima ◽  
Tasuku Eiba ◽  
Rikako Ishii ◽  
Hitoshi Miyasaka ◽  
Yuta Kodama ◽  
...  

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