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Dinuclear dysprosium SMMs bridged by a neutral bipyrimidine ligand: two crystal systems that depend on different lattice solvents lead to a distinct slow relaxation behaviour.
Sun, Wen-Bin; Yan, Bing; Jia, Li-Hui; Wang, Bing-Wu; Yang, Qian; Cheng, Xin; Li, Hong-Feng; Chen, Peng; Wang, Zhe-Ming; Gao, Song.
Affiliation
  • Sun WB; Beijing National Laboratory of Molecular Science State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China. wangbw@pku.edu.cn gaosong@pku.edu.cn.
Dalton Trans ; 45(21): 8790-4, 2016 Jun 07.
Article in En | MEDLINE | ID: mdl-27143486
ABSTRACT
Two dinuclear dysprosium complexes with the Dy(iii) ions bridged by the neutral bipyrimidine (BPYM) ligand were synthesized and magnetically characterized. They crystallized in a monoclinic and triclinic crystal system, respectively, with almost the same structural core, only differing in the lattice solvent molecules. Alternating current (ac) susceptibility measurements revealed that they exhibit significant slow relaxation of magnetization until 25 K in the absence of a dc field. The single and double relaxation processes were assigned to one and two types of Dy(iii) environments in the two dimmers, respectively, with barriers of 266 and 345 K under zero field conditions. The magnetic hysteresis loops of 1 and 2 were both observed up to 2.5 K.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2016 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2016 Document type: Article