The tuning of oxalato-bridge on magnetic interaction and field-induced phase transition in Ba2Co2Cl2(C2O4)3•4H2O

被引:1
作者
Song, Yujie [1 ,2 ]
Niu, Haoyu [1 ,2 ]
Zeng, Zhuo [1 ,2 ]
Jiang, Dequan [1 ,2 ]
Liang, Youyuan [1 ,2 ]
Huang, Hao [1 ,2 ]
Xiao, Lixia [3 ]
Xia, Zhengcai [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Wuhan Natl High Magnet Field Ctr, Wuhan, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Phys, Wuhan, Peoples R China
[3] Wenhua Coll, Dept Phys, Wuhan, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Oxalato-bridged; Spin dimer; Phase transition; Pulsed high magnetic field; COPPER(II) BINUCLEAR COMPLEXES; ONE SINGLE-CRYSTAL; HYDROTHERMAL SYNTHESIS; EXCHANGE; NI(II); CU(II); 3-HYDROXYPYRIDINE; SPECTROSCOPY; LIGAND; CO(II);
D O I
10.1016/j.jmmm.2022.169475
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The crystal structure of the oxalato-bridged compound Ba2Co2Cl2(C2O4)(3)center dot 4H(2)O has C2/c symmetry and contains two types of oxalate-bridged modes. We have investigated the magnetization behavior of the Ba2Co2Cl2(C2O4)(3)center dot 4H(2)O sample with both the static and pulsed magnetic fields. The Bleaney-Bowers fitting for the temperature dependence of magnetization shows that there are two different spin-dimers with the different intra-and inter-dimer interactions. Using the high field sweep rate of the pulsed magnetic field, magnetization measurements show four continuous phase transitions (with four different critical magnetic fields) in a smaller magnetic field range from 5.5 to 7 T, which also confirms there are two different dimers. Based on the structure analysis, the four phase transitions might result from four different magnetic exchange interactions (J(1), J(1)', J(2) and J(2)') in the two different dimers. Thus, in the design of the molecular-based magnetic materials, the oxalato-bridged and its various bridging modes can be used to mediate the magnetic interaction of the intra- and interdimers, the electronic effect between the metal ions and induce new phases.
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页数:7
相关论文
共 43 条
[1]   Infinite two-dimensional sheet-like array of a 2,2′-bipyrimidine-bis(oxalato)chromate(III) complex:: synthesis, crystal structure and magnetic properties of [K(H2O)Cr(C2O4)2(bpym)] [J].
Bérézovsky, F ;
Hajem, AA ;
Triki, S ;
Pala, JS ;
Molinié, P .
INORGANICA CHIMICA ACTA, 1999, 284 (01) :8-13
[2]   Ab initio study of the exchange coupling in oxalato-bridged Cu(II) dinuclear complexes [J].
Cabrero, J ;
Ben Amor, N ;
de Graaf, C ;
Illas, F ;
Caballol, R .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (44) :9983-9989
[3]  
Cano J, 1998, CHEM-EUR J, V4, P476, DOI 10.1002/(SICI)1521-3765(19980310)4:3<476::AID-CHEM476>3.0.CO
[4]  
2-8
[5]   Slow Relaxation of the Magnetization in Non-Linear Optical Active Layered Mixed Metal Oxalate Chains [J].
Cariati, Elena ;
Ugo, Renato ;
Santoro, Giuseppe ;
Tordin, Elisa ;
Sorace, Lorenzo ;
Caneschi, Andrea ;
Sironi, Angelo ;
Macchi, Piero ;
Casati, Nicola .
INORGANIC CHEMISTRY, 2010, 49 (23) :10894-10901
[6]   A novel one-dimensional oxalato-bridged copper(II) complex with 2,2′-bipyridine [J].
Castillo, O ;
Luque, A ;
Iglesias, S ;
Guzmán-Miralles, C ;
Román, P .
INORGANIC CHEMISTRY COMMUNICATIONS, 2001, 4 (11) :640-642
[7]   One-dimensional oxalato-bridged copper(II) complexes with 3-hydroxypyridine and 2-amino-4-methylpyridine [J].
Castillo, O ;
Luque, A ;
Julve, M ;
Lloret, F ;
Román, P .
INORGANICA CHIMICA ACTA, 2001, 315 (01) :9-17
[8]   Synthesis, characterisation, crystal structures, and magnetic properties of one-dimensional oxalato-bridged metal(II) complexes with 3-hydroxypyridine and isoquinoline [J].
Castillo, O ;
Luque, A ;
Lloret, F ;
Román, P .
INORGANICA CHIMICA ACTA, 2001, 324 (1-2) :141-149
[9]   Synthesis, crystal structure, and magnetic properties of a one-dimensional polymeric copper(II) complex containing an unusual 1,1′-bicoordinated oxalato bridge [J].
Castillo, O ;
Luque, A ;
Sertucha, J ;
Román, P ;
Lloret, F .
INORGANIC CHEMISTRY, 2000, 39 (26) :6142-+
[10]   Syntheses, crystal structures, and magnetic properties of one-dimensional oxalato-bridged Co(II), Ni(II), and Cu(II) complexes with n-aminopyridine (n=2-4) as terminal ligand [J].
Castillo, O ;
Luque, A ;
Román, P ;
Lloret, F ;
Julve, M .
INORGANIC CHEMISTRY, 2001, 40 (22) :5526-5535