A linear trinuclear ferrous single molecule magnet

2018 ◽  
Vol 47 (46) ◽  
pp. 16704-16708
Author(s):  
Shihao Liu ◽  
Yi-Fei Deng ◽  
Chang'An Li ◽  
Xiaoyong Chang ◽  
Yuan-Zhu Zhang

A linear trinuclear ferrous [FeII3] SMM exhibited clear magnetic hysteresis loops and a significant higher effective energy barrier in comparison with its cobalt(ii) analogue.

2019 ◽  
Author(s):  
Tian Han ◽  
Marcus J. Giansiracusa ◽  
Zi-Han Li ◽  
You-Song Ding ◽  
Nicholas F. Chilton ◽  
...  

A dichlorido-bridged dinuclear dysprosium(III) single-molecule magnet [Dy<sub>2</sub>L<sub>2</sub>(<i>µ</i>-Cl)<sub>2</sub>(THF)<sub>2</sub>] has been made using a diamine-bis(phenolate) ligand, H<sub>2</sub>L. Magnetic studies show an energy barrier for magnetization reversal (<i>U</i><sub>eff</sub>) around 1000 K. Exchange-biasing effect is clearly seen in magnetic hysteresis with steps up to 4 K. <i>Ab</i> initio calculations exclude the possibility of pure dipolar origin of this effect leading to the conclusion that super-exchange <i>via</i> the chloride bridging ligands is important.


2019 ◽  
Vol 55 (55) ◽  
pp. 7930-7933 ◽  
Author(s):  
Tian Han ◽  
You-Song Ding ◽  
Zi-Han Li ◽  
Ke-Xin Yu ◽  
Yuan-Qi Zhai ◽  
...  

A large energy barrier for magnetization reversal of about 623 K is observed in a dichlorido-bridged Dy(iii) dimer.


2014 ◽  
Vol 67 (11) ◽  
pp. 1581 ◽  
Author(s):  
Stuart K. Langley ◽  
Daniel P. Wielechowski ◽  
Boujemaa Moubaraki ◽  
Brendan F. Abrahams ◽  
Keith S. Murray

The synthesis and magnetic characterisation of four new heterometallic {CrIII2DyIII2} complexes 2–5 are described. The present work follows on from a recently isolated complex [CrIII2DyIII2(OMe)2(O2CPh)4(mdea)2(NO3)2] (1) (mdeaH2 = N-methyldiethanolamine), which displayed impressive single molecule magnet (SMM) properties, notably highly coercive magnetic hysteresis loops below 3.5 K. Compounds 1–5 all display a planar butterfly type metallic core arrangement, with the DyIII ions occupying the central body positions and the CrIII ion the outer wing positions. The core is stabilized by the amine–diolate, and carboxylate bridging ligands. Variation of the amine–diolate ligand resulted in several structural analogues which maintain the same metallic core, but differ from the parent 1 in the outer ligand coordination environment. Magnetic studies reveal complexes 2–5 also display SMM behaviour, unambiguously confirmed via low temperature magnetic hysteresis loops, each displaying wide coercive fields, a rare occurrence for lanthanoid-based SMMs.


2020 ◽  
Vol 56 (27) ◽  
pp. 3887-3890 ◽  
Author(s):  
Jianfeng Wu ◽  
Serhiy Demeshko ◽  
Sebastian Dechert ◽  
Franc Meyer

A hexanuclear cluster containing six {Cp*Dy} units shows a high energy barrier (Ueff = 561 K) for magnetic relaxation and butterfly-shaped hysteresis loops up to 4.5 K.


2016 ◽  
Vol 7 ◽  
pp. 126-137 ◽  
Author(s):  
Wen Yu ◽  
Frank Schramm ◽  
Eufemio Moreno Pineda ◽  
Yanhua Lan ◽  
Olaf Fuhr ◽  
...  

A series of 2,2’-bipyrimidine-bridged dinuclear lanthanide complexes with the general formula [Ln(tmhd)3]2bpm (tmhd = 2,2,6,6-tetramethyl-3,5-heptanedionate, bpm = 2,2’-bipyrimidine, Ln = Gd(III), 1; Tb(III), 2; Dy(III), 3; Ho(III), 4 and Er(III), 5) has been synthesized and characterized. Sublimation of [Tb(tmhd)3]2bpm onto a Au(111) surface leads to the formation of a homogeneous film with hexagonal pattern, which was studied by scanning tunneling microscopy (STM). The bulk magnetic properties of all complexes have been studied comprehensively. The dynamic magnetic behavior of the Dy(III) and Er(III) compounds clearly exhibits single molecule magnet (SMM) characteristics with an energy barrier of 97 and 25 K, respectively. Moreover, micro-SQUID measurements on single crystals confirm their SMM behavior with the presence of hysteresis loops.


2015 ◽  
Vol 39 (5) ◽  
pp. 3467-3473 ◽  
Author(s):  
Xing-Yun Lu ◽  
Yu-Qing Liu ◽  
Xiao-Wei Deng ◽  
Zhao-Xia Zhu ◽  
Min-Xia Yao ◽  
...  

Three isomorphous Ni–Ln heterodinuclear complexes were synthesized and structurally characterized. The Dy derivative exhibits field-induced single-molecule magnet behavior with an effective energy barrier of 16.9 K under a 1000 Oe dc field.


2019 ◽  
Vol 48 (29) ◽  
pp. 10795-10798 ◽  
Author(s):  
Marcus J. Giansiracusa ◽  
Susan Al-Badran ◽  
Andreas K. Kostopoulos ◽  
George F. S. Whitehead ◽  
David Collison ◽  
...  

We report a six coordinate DyIII single-molecule magnet (SMM) with an energy barrier of 1110 K for thermal relaxation of magnetization, but no magnetic hysteresis above 2 K.


2019 ◽  
Author(s):  
Tian Han ◽  
Marcus J. Giansiracusa ◽  
Zi-Han Li ◽  
You-Song Ding ◽  
Nicholas F. Chilton ◽  
...  

A dichlorido-bridged dinuclear dysprosium(III) single-molecule magnet [Dy<sub>2</sub>L<sub>2</sub>(<i>µ</i>-Cl)<sub>2</sub>(THF)<sub>2</sub>] has been made using a diamine-bis(phenolate) ligand, H<sub>2</sub>L. Magnetic studies show an energy barrier for magnetization reversal (<i>U</i><sub>eff</sub>) around 1000 K. Exchange-biasing effect is clearly seen in magnetic hysteresis with steps up to 4 K. <i>Ab</i> initio calculations exclude the possibility of pure dipolar origin of this effect leading to the conclusion that super-exchange <i>via</i> the chloride bridging ligands is important.


2018 ◽  
Author(s):  
Marcus J. Giansiracusa ◽  
Andreas Kostopoulos ◽  
George F. S. Whitehead ◽  
David Collison ◽  
Floriana Tuna ◽  
...  

We report a six coordinate DyIII single-molecule magnet<br>(SMM) with an energy barrier of 1110 K for thermal relaxation of<br>magnetization. The sample shows no retention of magnetization<br>even at 2 K and this led us to find a good correlation between the<br>blocking temperature and the Raman relaxation regime for SMMs.<br>The key parameter is the relaxation time (𝜏<sub>switch</sub>) at the point where<br>the Raman relaxation mechanism becomes more important than<br>Orbach.


Author(s):  
Matilde Fondo ◽  
Julio Corredoira-Vázquez ◽  
Ana M. Garcia-Deibe ◽  
Jesus Sanmartin Matalobos ◽  
Silvia Gómez-Coca ◽  
...  

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,...


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