A triple-bridged azido-Cu(II) chain compound fine-tuned by mixed carboxylate/ethanol linkers displays slow-relaxation and ferromagnetic order: synthesis, crystal structure, magnetic properties and DFT calculations.

A triple-bridged azido-Cu(II) chain compound fine-tuned by mixed carboxylate/ethanol linkers displays slow-relaxation and ferromagnetic order: synthesis, crystal structure, magnetic properties and DFT calculations.
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DOI:
10.1039/c4dt02195a
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发表时间:
2014-09
影响因子:
4
通讯作者:
Xiangyu Liu;Sanping Chen;Thais Grancha;E. Pardo;Hongshan Ke;Bing Yin;Q. Wei;G. Xie;Sheng-li Gao
Xiangyu Liu;Sanping Chen;Thais Grancha;E. Pardo;Hongshan Ke;Bing Yin;Q. Wei;G. Xie;Sheng-li Gao
中科院分区:
化学2区
文献类型:
--
作者:
Xiangyu Liu;Sanping Chen;Thais Grancha;E. Pardo;Hongshan Ke;Bing Yin;Q. Wei;G. Xie;Sheng-li Gao

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合成并表征了一种新的叠氮铜配合物[Cu(4-fba)(N3)(C2 H5 OH)](4-fba = 4-氟苯甲酸)(1)。X-射线晶体结构分析表明,1的不对称单元中只有一个晶体学上独立的Cu(II)离子,呈现伸展的八面体构型,其中两个叠氮基N原子和两个羧基O原子位于赤道正方形,而两个乙醇O原子位于顶点位置,形成一个由EO-叠氮基、syn、syn-羧基和μ2-乙醇交替组成的三维Cu(II)链.标题化合物由铁磁相互作用的铁磁链组成,具有铁磁有序性(T(c)= 7.0K)。每个链内相邻的Cu(II)离子之间的强铁磁耦合是由于超交换途径的反互补性,而铁磁链间相互作用-负责长程磁有序-最有可能是由于存在协调的乙醇分子与相邻链建立氢键。对化合物1进行了DFT计算,对磁性行为提供了定性的理论解释。
A new azido-Cu(II) compound, [Cu(4-fba)(N3)(C2H5OH)] (4-fba = 4-fluorobenzoic acid) (1), has been synthesized and characterized. The X-ray crystal structure analysis demonstrates that only one crystallographically independent Cu(II) ion in the asymmetric unit of 1 exhibits a stretched octahedral geometry in which two azido N atoms and two carboxylic O atoms locate in the equatorial square, while two ethanol O atoms occupy the apical positions, forming a 1D Cu(II) chain with an alternating triple-bridge of EO-azido, syn,syn-carboxylate, and μ2-ethanol. The title compound consists of ferromagnetically interacting ferromagnetic chains, which exhibit ferromagnetic order (T(c) = 7.0 K). The strong ferromagnetic coupling between adjacent Cu(II) ions within each chain is due to the countercomplementarity of the super-exchange pathways, whereas the ferromagnetic interchain interactions--responsible for the long-range magnetic ordering--are most likely due to the presence of coordinated ethanol molecules establishing hydrogen bonds with neighboring chains. DFT calculations have been performed on compound 1 to offer a qualitative theoretical explanation of the magnetic behavior.