等结构
化学
席夫碱
结晶学
配体(生物化学)
乙二胺
磁化率
单晶
晶体结构
镧系元素
立体化学
无机化学
离子
有机化学
生物化学
受体
作者
Andrea Koščíková,Juraj Černák,Larry R. Falvello,Milagros Tomás,Irene Ara,Ján Titiš,Roman Boča
标识
DOI:10.1002/chem.202500376
摘要
Three new dinuclear complexes [CuCl(o‐van‐en)Ln(H2O)3 Cl]Cl·C2H6O (Ln = Sm (1), Eu (2), Gd (3); H2(o‐van‐en) is the Schiff base formed by 2/1 condensation of o‐vanillin and ethylenediamine) were prepared in single crystal form by the method of horizontal diffusion. The prepared complexes were characterized by chemical analyses and IR spectroscopy. The three complexes are isostructural and the Cu(II) is situated in the smaller cavities while the larger cavities accommodate larger Ln(III) atoms. The pentacoordination of the Cu(II) atoms is completed by a chlorido ligand in the apical position, while the octacoordination of the Ln(III) atoms is achieved by three additional aqua and one chlorido co‐ligands. AC susceptibility studies have shown that complexes 2 and 3 exhibit field supported slow magnetic relaxation while the complex 1 does not display AC activity.
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