A 3D Compound Based on Semi-rigid Tricarboxylato-Bridged Co(II): Synthesis, Crystal Structure and Magnetism

被引:1
|
作者
An, Yan-Yan [1 ,2 ]
Guo, Ting-Ting [1 ]
Bian, Jian-Hong [1 ]
Yan, Juan-Zhi [1 ]
机构
[1] Taiyuan Univ, Dept Mat & Chem Engn, Taiyuan 030032, Peoples R China
[2] Shanxi Univ, Inst Mol Sci, Key Lab Chem Biol & Mol Engn, Educ Minist, Taiyuan 030006, Shanxi, Peoples R China
关键词
Compound; Crystal structure; Magnetism; Co(II) ion; SINGLE-CHAIN; CO-II; COORDINATION; LUMINESCENCE; FRAMEWORKS; CATALYSIS;
D O I
10.1007/s10870-023-00993-1
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
With the assistance of N-donor ligand 1,4-bi(1H-imidazol-1-yl)benzene (1,4-bib), Co(II) reacts with 5-((4-carboxyphenoxy)-methyl)isophthalic acid (H3L) under hydrothermal condition to form a compound [Co3(L3-)2(1,4-bib)4]& BULL;4H2O (1). The both contributions of semi-rigid tricarboxylic ligand L3- and rigid 1,4-bib leads to predictably high dimensional structure. Compound 1 crystallizes in a complicated 3D network, which can be simplified as 3,6,8-conn topology. For the correlation between structure and property, the structural feature is well reflected in the magnetic property: a carboxylato group bridges two Co(II) paramagnetic ions. Within the dinuclear subunit, significant anti-ferromagnetic interactions are observed.Graphical AbstractA novel 3D Co(II) compound 1 is formed via hydrothermal reaction in this work. Antiferromagnetic interactions between two neighbour cations coordinated by one carboxylato group are observed.
引用
收藏
页码:540 / 546
页数:7
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