首页> 外文期刊>Microporous and mesoporous materials: The offical journal of the International Zeolite Association >Microporous coordination polymers of cobalt(II) and manganese(II) 2,6-naphthalenedicarboxylate: preparations, structures and gas sorptive and magnetic properties
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Microporous coordination polymers of cobalt(II) and manganese(II) 2,6-naphthalenedicarboxylate: preparations, structures and gas sorptive and magnetic properties

机译:2,6-萘二甲酸钴(II)和锰(II)的微孔配位聚合物:制备,结构及气体吸附和磁性

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摘要

Two isostructural coordination polymers M3(NDC)3(DMF)4 (M = Co (1), Mn (2); H2NDC = 2,6-naphthalenedicarboxylic acid; DMF = N,N'-dimethylfonnamide) 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 1 and 2 revealed the weak antiferromagnetic coupling between the adjacent metal ions bridged by carboxylate.
机译:通过常规方法和微波法制备了两种同构配位聚合物M3(NDC)3(DMF)4(M = Co(1),Mn(2); H2NDC = 2,6-萘二甲酸; DMF = N,N'-二甲基甲酰胺)辅助溶剂热法。单晶X射线分析表明,两种配合物在单斜体系中均以C2 / c空间群结晶。微波辅助溶剂热合成得到的两种配合物的大块样品的粉末X射线衍射(PXRD)图谱与单晶数据和常规溶剂热法制备的样品的模拟X谱图相吻合。这些微孔钴(II)和锰(II)配位聚合物在去溶剂化后会发生可逆的结构变化,产生稳定的包含不饱和金属位点的微孔骨架,并重新溶解。脱溶剂的配合物显示出不同的氮气吸附能力,但氢吸附行为非常接近。 1和2的可变温度磁化率显示了由羧酸盐桥接的相邻金属离子之间的弱反铁磁耦合。

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