Polymeric Manganese(II) Acetate Derivatives: Syntheses, Crystal Structures and Magnetic Properties

被引:0
作者
Li, Dong-Yang [1 ]
Zhang, Xiao-Nan [1 ]
Chen, Wei-Peng [1 ]
Zhai, Yuan-Qi [1 ]
Zheng, Yan-Zhen [1 ]
机构
[1] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Sch Chem, State Key Lab Elect Insulat & Power Equipment,Xian, Xian, Peoples R China
基金
中国国家自然科学基金;
关键词
Polymer; Manganese(II); Magnetic coupling; Magnetic order; Magnetocaloric effect; SINGLE-MOLECULE-MAGNET; COORDINATION POLYMER; REFRIGERATION CAPACITY; MN; NI;
D O I
10.1002/ejic.202400360
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Three novel polymeric Mn(II) acetate derivatives, identified as {[Mn2.5(OH)(CH3COO)4] & sdot; 0.5CH3OH & sdot; 0.5CH3CN}n (1), {[Mn3(CH3CO O)6] & sdot; 0.5CH3CN}n (2) and {Mn1.5K(CH3COO)4}n (3), have been successfully prepared by systematically adjusting the ratio of reactants and using the 2-mercapto-5-methyl-1,3,4-thiadiazole (Hmmt) as the template agent. These three complexes can be regarded as the different crystalline forms of Mn(CH3COO)2 under different reaction conditions. Single-crystal X-ray diffraction analyses revealed that 1 and 2 feature the unique three-dimensional (3D) framework. For 3, it displays a 2D structure, which is further assembled to form a 3D extended network via the weak hydrogen bond interactions. Magnetic studies confirmed that 1 and 2 show antiferromagnetic interactions, and 1 displays a long-range ordering phase below the critical temperature (Tc) of 7.8 K. In addition, magnetisation data collected for 1-2 yield low magnetic entropy changes, which can be attributed to the strong antiferromagnetic interactions among the Mn(II) centres.
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页数:7
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