化学
超级交换
抗磁性
镧系元素
结晶学
离子
羟甲基
配体(生物化学)
密度泛函理论
无机化学
立体化学
计算化学
磁场
物理
受体
有机化学
量子力学
生物化学
作者
Gavin A. Craig,Gunasekaran Velmurugan,Claire Wilson,Rafael Valiente,Gopalan Rajaraman,Mark Murrie
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2019-10-07
卷期号:58 (20): 13815-13825
被引量:16
标识
DOI:10.1021/acs.inorgchem.9b01592
摘要
The chelating ligand 1,3-bis(tris(hydroxymethyl)methylamino)propane (H6L) has been used to synthesize a family of octanuclear heterometallic complexes with the formula (NMe4)3[Mn4Ln4(H2L)3(H3L)(NO3)12] (Ln = La (1), Ce (2), Pr (3), Nd (4)). Encapsulation by the ligand causes the Mn(III) centers to lie in an unusually distorted (∼C2v) environment, which is shown by density functional theory and complete active space self-consistent field calculations to impact on the magnetic anisotropy of the Mn(III) ion. The theoretical study also supports the experimental observation of a ferromagnetic superexchange interaction between the Mn(III) ions in 1, despite the ions being separated by the diamagnetic La(III) ion. The optical properties of the compounds show that the distortion of the Mn(III) ions leads to three broad absorption bands originating from the transition metal ion, while the Nd(III) containing complex also displays some weak sharp features arising from the lanthanide f-f transitions.
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