Microporous coordination polymers of cobalt(II) and manganese(II) 2,6-naphthalenedicarboxylate: preparations, structures and gas sorptive and magnetic properties

被引:60
作者
Liu, Bo [1 ,2 ]
Zou, Ru-Qiang [1 ,2 ]
Zhong, Rui-Qin [1 ,2 ]
Han, Song [1 ]
Shioyama, Hiroshi [1 ]
Yamada, Tetsuya [3 ]
Maruta, Goro [3 ]
Takeda, Sadamu [3 ]
Xu, Qiang [1 ,2 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Osaka 5638577, Japan
[2] Kobe Univ, Grad Sch Engn, Kobe, Hyogo 6578501, Japan
[3] Hokkaido Univ, Dept Chem, Fac Sci & Grad Sch Sci, Sapporo, Hokkaido 0600810, Japan
关键词
metal coordination polymer; 2,6-naphthalenedicarboxylate; gas sorption; microporosity; magnetic property;
D O I
10.1016/j.micromeso.2007.08.024
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two isostructural coordination polymers M-3(NDC)(3)(DMF)(4) (M = CO (1), Mn (2); H2NDC = 2,6-naphthalenedicarboxylic acid; DMF = N,N-dimethylformamide) were prepared through conventional and microwave-assisted solvothermal methods. Single crystal X-ray analysis indicated that both complexes crystallized in the monoclinic system with space group C2/c. Powder X-ray diffraction (PXRD) patterns of the bulk samples for the two complexes obtained from microwave-assisted solvothermal syntheses matched well with the simulated ones from the single crystal data as well as the ones prepared by conventional solvothermal method. These microporous cobalt(II) and manganese(II) coordination polymers undergo reversible structural change upon desolvating, giving stable microporous frameworks containing unsaturated metal sites, and resolvating. The desolvated complexes showed different nitrogen gas adsorption capabilities but very close hydrogen adsorption behaviors. Variable-temperature magnetic susceptibilities of I and 2 revealed the weak antiferromagnetic coupling between the adjacent metal ions bridged by carboxylate. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:470 / 477
页数:8
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