期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 55, 期 37, 页码 11082-11085出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201604346
关键词
cyclopentadienyl ligands; dysprosium; molecular magnetism; organometallics; rare-earth elements
The single-molecule magnet (SMM) properties of the isocarbonyl-ligated dysprosium metallocene [Cp*Dy-2{-(OC)(2)FeCp}](2) (1(Dy)), which contains a rhombus-shaped Dy2Fe2 core, are described. Combining a strong axial [Cp*](-) ligand field with a weak equatorial field consisting of the isocarbonyl ligands leads to an anisotropy barrier of 662cm(-1) in zero applied field. The dominant thermal relaxation pathways in 1(Dy) involves at least the fourth-excited Kramers doublet, thus demonstrating that prominent SMM behavior can be observed for dysprosium in low-symmetry environments.
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