1D and 2D Cobalt(II) Coordination Polymers, Co(ox)(en): Synthesis, Structures and Magnetic Properties

被引:9
作者
Kang, Jaeun [1 ]
Lee, Yumi [1 ]
Kim, Seungjoo [2 ]
Yun, Hoseop [2 ]
Do, Junghwan [1 ]
机构
[1] Konkuk Univ, Dept Chem, Seoul 143701, South Korea
[2] Ajou Univ, Dept Chem, Suwon 441749, South Korea
关键词
Hydrothermal synthesis; Cobalt complex; Oxalate; Ethylenediamine; Magnetic properties; CRYSTAL-STRUCTURES; OXALATE; COMPLEXES; ZN(II); CU(II); CO(II); ETHYLENEDIAMINE; BEHAVIOR; LIGANDS; SYSTEMS;
D O I
10.5012/bkcs.2014.35.11.3244
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two ethylenediamine cobalt(II) oxalate complexes Co(ox)(en), 1 and Co(ox)(en)center dot 2H(2)O, 2 have been hydrothermally synthesized and characterized by single crystal X ray diffraction, IR spectrum, TG analysis, and magnetic measurements. In 1, Co atoms are coordinated by two bis-bidentate oxalate ions in trans-configuration to form Co(ox) chains, which are further bridged by ethylenediamine molecules to produce 2D grid layers, Co(ox)(en). In 2, Co atoms are coordinated by bridging oxalate ions in cis-configuration to form Co(ox) chains, and the additional chelation of ethylenediamine to Co atoms completes 1D zigzag chain, Co(en)(ox). Two lattice water molecules stabilize the chains through hydrogen bonding. Magnetic susceptibility measurements indicate that both complexes exhibit weak antiferromagnetic coupling between cobalt(II) ions with the susceptibility maxima at 23 K for 1 and 20 K for 2, respectively. In 1 and 2, the oxalate ligands afford: a much shorter and more effective pathway for the magnetic interaction between cobalt ions compared to the ethylenediamine ligands, so the magnetic behaviors of both complexes could be well described with 1D infinite magnetic chain model.
引用
收藏
页码:3244 / 3248
页数:5
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