The differential magnetic relaxation behaviours of slightly distorted triangular dodecahedral dysprosium analogues in a type of cyano-bridged 3d–4f zig-zag chain compounds

2020 ◽  
Vol 49 (20) ◽  
pp. 6867-6875 ◽  
Author(s):  
An-Qi Xue ◽  
Yang-Yu Liu ◽  
Jia-Xin Li ◽  
Yan Zhang ◽  
Yin-Shan Meng ◽  
...  

Differential magnetic properties were observed for triangular dodecahedral dysprosium analogues in a type of cyano-bridged 3d–4f zig-zag chain compound.

2017 ◽  
Vol 46 (23) ◽  
pp. 7556-7566 ◽  
Author(s):  
Xiangyu Liu ◽  
Xiaohui Ma ◽  
Peipei Cen ◽  
Yuewei Wu ◽  
Chengcheng Zhang ◽  
...  

Two triple-bridged azido-Cu(ii) chains exhibit distinct magnetic behaviors.


Inorganics ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 51
Author(s):  
Lin Miao ◽  
Mei-Jiao Liu ◽  
Man-Man Ding ◽  
Yi-Quan Zhang ◽  
Hui-Zhong Kou

The complexes of lanthanide metals, especially dysprosium, can generally exhibit excellent magnetic properties. By means of modifying ligands, dual functions or even multi-functions can be achieved. Here, we synthesized an eight-coordinate Dy(III) complex 1, [Dy(HL-o)2(MeOH)2](ClO4)3·4.5MeOH, which is single-molecule magnet (SMM), and the introduction of the rhodamine 6G chromophore in the ring-opened ligand HL-o realizes ligand-centered fluorescence in addition to SMM. Magnetic measurements and ab initio calculations indicate that the magnetic relaxation for complex 1 should be due to the Raman relaxation process. Studies on magneto-structural correlationship of the rhodamine salicylaldehyde hydrazone Dy(III) complexes show that the calculated energy of the first Kramers Doublet (EKD1) is basically related to the Ophenoxy-Dy-Ophenoxy bond angle, i.e., the larger Ophenoxy-Dy-Ophenoxy bond angle corresponds to a larger EKD1.


2005 ◽  
Vol 159 ◽  
pp. 1-10 ◽  
Author(s):  
Hikomitsu Kikuchi ◽  
Yutaka Fujii ◽  
Meiro Chiba ◽  
Seitaro Mitsudo ◽  
Toshitaka Idehara ◽  
...  

2019 ◽  
Vol 43 (33) ◽  
pp. 12941-12949 ◽  
Author(s):  
Wen-Min Wang ◽  
Li Zhang ◽  
Xian-Zhen Li ◽  
Li-Yuan He ◽  
Xin-Xin Wang ◽  
...  

A family LnIII4 clusters were successfully synthesized and structurally characterized. Magnetic studies show that Gd4 cluster displays magnetic refrigeration, while Dy4 cluster demonstrates two distinct slow magnetic relaxation processes.


2020 ◽  
Vol 6 (4) ◽  
pp. 48
Author(s):  
Lu Xi ◽  
Jing Han ◽  
Xiaohui Huang ◽  
Licun Li

Employing a new nitronyl nitroxide biradical NITPhPzbis(NITPhPzbis = 5-(1-pyrazolyl)-1,3-bis(1’-oxyl-3’-oxido-4’,4’,5’,5’-tetramethyl-4,5-hydro-1H-imidazol-2-yl)benzene), a series of 2p-4f complexes [Ln2(hfac)6(H2O)(NITPhPzbis)] (LnIII = Gd1, Tb2, Dy3; hfac = hexafluoroacetylacetonate) were successfully synthesized. In complexes 1–3, the designed biradical NITPhPzbis coordinates with two LnIII ions in chelating and bridging modes to form a four-spin binuclear structure. Direct-current magnetic study of Gd analogue indicates that ferromagnetic exchange exists between the Gd ion and the radical while antiferromagnetic coupling dominates between two mono-radicals. Dynamic magnetic data show that the χ” signals of complex 3 exhibit frequency dependence under zero field, demonstrating slow magnetic relaxation behavior in complex 3. And the estimated values of Ueff and τ0 are about 8.4 K and 9.1 × 10−8 s, respectively.


1988 ◽  
Vol 49 (C8) ◽  
pp. C8-861-C8-862 ◽  
Author(s):  
C. Benelli ◽  
A. Caneschi ◽  
D. Gatteschi ◽  
L. Pardi ◽  
P. Rey

2019 ◽  
Vol 48 (15) ◽  
pp. 4774-4778 ◽  
Author(s):  
Hao Miao ◽  
Miao Li ◽  
Hong-Qing Li ◽  
Fu-Xing Shen ◽  
Yi-Quan Zhang ◽  
...  

A new bis-tridentate nitronyl nitroxide radical was synthesized and characterized. Field-induced slow magnetic relaxation was observed in the radical-bridged CoII complex.


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