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用于合理设计镝(III)单分子磁体的中性二氰基铁(II)金属配体

Neutral dicyanidoferrate(II) metalloligands for the rational design of dysprosium(III) single-molecule magnets.

作者信息

Liberka Michal, Zychowicz Mikolaj, Zychowicz Wiktor, Chorazy Szymon

机构信息

Faculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387 Krakow, Poland.

出版信息

Chem Commun (Camb). 2022 May 30;58(44):6381-6384. doi: 10.1039/d2cc02238a.

DOI:10.1039/d2cc02238a
PMID:35599588
Abstract

Diamagnetic -dicyanidoferrate(II) complexes bearing blocking aromatic diimines, -[Fe(CN)(L)] (L = 2,2'-bipyridine, 1,10'-phenanthroline) serve as metalloligands to Dy centres leading to a rigid cyanido-bridged chain of vertex-sharing {DyFe} squares which constrains the equatorial plane of embedded 4f metal ions. This results in a novel convenient route to rationally designed single-molecule magnets as the magnetic anisotropy of Dy centres can be efficiently generated by inserting aromatic -oxide ligands on labile axial positions.

摘要

带有位阻芳香二亚胺的抗磁性二氰基铁(II)配合物,-[Fe(CN)(L)](L = 2,2'-联吡啶,1,10'-菲咯啉)作为金属配体与镝中心结合,形成由顶点共享的{DyFe}正方形组成的刚性氰基桥连链,该链限制了嵌入的4f金属离子的赤道平面。这为合理设计单分子磁体提供了一条新的便捷途径,因为通过在不稳定的轴向位置插入芳香族氧化物配体,可以有效地产生镝中心的磁各向异性。

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