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Crystal structure and magnetic properties of a Ce-III-Cu-II heterodinuclear complex

机译:Ce-III-Cu-II异双核配合物的晶体结构和磁性

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Crystal structure and magnetic properties of a heterodinuclear complex, LCu(Me2CO)Ce(NO3)O-3 (L = (N,N'-propylene-bis(3-methoxysalicylideneimine)) are reported. (C19H22N2O4)Cu(C3H6O) Ce(NO3)(3), monoclinic, space group P2(1)/c, with a = 9.8295(4), b 19.049(3), c = 15.668(3) Angstrom, beta = 94.873(12)degrees, V = 2923.2(7) Angstrom(3), Z = 4. The central region of the complex is occupied by Cu-II and Ce-III ions which are bridged by two phenolato oxygen atoms of the ligand. The copper ion adopts a square-based 4+1 coordination made, the equatorial N2O2 donors being afforded by the ligand while the axial position is occupied by an oxygen atom of the acetone molecule. The Ce-III ion is deca-coordinated. In addition to the two phenolate oxygen atoms, the coordination sphere contains two oxygen atoms of the OMe side arms of L and six oxygen atoms from the three bidentate nitrate ions. The Ce...Cu separation is 3.601(2) Angstrom. and the dihedral angle between the CeO(2)Cu and CeO(3)Cu planes is 17.4(1)degrees. The magnetic susceptibility of the complex was measured over the range 5-350 K. The magnetic properties of the investigated compound are dominated by the crystal field effect on the Ce-III site, masking the magnetic interaction between the paramagnetic centers. [References: 17]
机译:报告了异双核配合物LCu(Me2CO)Ce(NO3)O-3(L =(N,N'-丙烯-双(3-甲氧基水杨亚胺))的晶体结构和磁性。(C19H22N2O4)Cu(C3H6O)Ce (NO3)(3),单斜面,空间群P2(1)/ c,a = 9.8295(4),b 19.049(3),c = 15.668(3)埃,beta = 94.873(12)度,V = 2923.2(7)埃(3),Z =4。配合物的中心区域被Cu-II和Ce-III离子占据,它们被配体的两个酚基氧原子桥接,铜离子采用基于正方形的进行了4 + 1配位,赤道型N2O2供体由配体提供,而轴向位置被丙酮分子的氧原子占据,Ce-III离子被十位配位。配位球包含L的OMe侧臂的两个氧原子和来自三个双齿硝酸根离子的六个氧原子,Ce ... Cu间距为3.601(2)埃,CeO(2)Cu与CeO(3)Cu计划es是17.4(1)度。在5-350 K的范围内测量了该复合物的磁化率。所研究化合物的磁性能受Ce-III位置上的晶场效应支配,掩盖了顺磁中心之间的磁相互作用。 [参考:17]

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