Ferromagnetically coupled single-chain magnets exhibiting a magnetic hysteresis of 0.42 Tesla in cyano-bridged Fe2III MII (M = Ni, Fe) coordination polymers

被引:2
|
作者
Wang, Jin-Hua [1 ,2 ]
Javed, Mohammad Khurram [1 ]
Li, Jia-Xin [3 ]
Zhang, Yi-Quan [3 ]
Li, Zhao-Yang [1 ]
Yamashita, Masahiro [4 ]
机构
[1] Nankai Univ, Sch Mat Sci & Engn, Tianjin 300350, Peoples R China
[2] Dezhou Univ, Coll Med & Nursing, Shandong Engn Res Ctr Novel Pharmaceut Excipients, Dezhou 253023, Peoples R China
[3] Nanjing Normal Univ, Sch Phys Sci & Technol, 1 Wenyuan Rd, Nanjing 210023, Peoples R China
[4] Tohoku Univ, Grad Sch Sci, Dept Chem, 6-3 Aramaki Aza Aoba,Aoba Ku, Sendai 9808578, Japan
基金
中国国家自然科学基金;
关键词
CRYSTAL-STRUCTURES; BEHAVIOR; METAMAGNETISM; ANISOTROPY; COEXISTENCE; RELAXATION;
D O I
10.1039/d3dt01043k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis, single-crystal structures and magnetic properties of two new double-zigzag-chain cyanobridged heterobimetallic {[M-II( Py-NOH)(2)][Fe-III( Tp*)(CN)(3)](2)}center dot H2O ([(Fe2MII)-M-III]) (Py-NOH = 4-pyridinealdoxime, Tp* = tris(3,5-dimethylpyrazol-1-yl)borohydride, M = Ni (1), Fe (2)) compounds are reported. The crystal structures of both compounds were determined by single-crystal X-ray diffraction. Complexes 1 and 2 are isostructural, with the crystal structure comprising neutral double-zigzag (4,2-ribbon-like) bimetallic chains. The Fe-III ion is coordinated by three cyanide carbon atoms and three nitrogen atoms of Tp* anions. However, the M-II ion is surrounded by four cyanide nitrogen atoms and two nitrogen atoms from two Py-NOH ligands. The crystal structures and magnetic studies demonstrate that both complexes behave as single-chain magnetics (SCMs) with intrachain ferromagnetic coupling. Furthermore, [(Fe2NiII)-Ni-III] exhibits an excellent coercive field of 0.42 T at 1.8 K, among cyano-bridged 3d transition-metal-based SCMs reported thus far. Preliminary theoretical calculations provide a deep understanding of the magnetic properties of [(Fe2NiII)-Ni-III].
引用
收藏
页码:15510 / 15517
页数:8
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