Laboratoire Léon Brillouin, CEA-CNRS, UMR12, CEA Saclay, 91191, Gif-sur-Yvette, France.
Institut Parisien de Chimie Moléculaire (IPCM), Sorbonne Universités, UPMC Paris 6, UMR 8232, 4 place Jussieu, 75252, Paris cedex 5, France.
Angew Chem Int Ed Engl. 2016 Mar 14;55(12):3963-7. doi: 10.1002/anie.201511354. Epub 2016 Feb 17.
We have determined by polarized neutron diffraction (PND) the low-temperature molecular magnetic susceptibility tensor of the anisotropic low-spin complex PPh4 [Fe(III) (Tp)(CN)3]⋅H2O. We found the existence of a pronounced molecular easy magnetization axis, almost parallel to the C3 pseudo-axis of the molecule, which also corresponds to a trigonal elongation direction of the octahedral coordination sphere of the Fe(III) ion. The PND results are coherent with electron paramagnetic resonance (EPR) spectroscopy, magnetometry, and ab initio investigations. Through this particular example, we demonstrate the capabilities of PND to provide a unique, direct, and straightforward picture of the magnetic anisotropy and susceptibility tensors, offering a clear-cut way to establish magneto-structural correlations in paramagnetic molecular complexes.
我们通过偏振中子衍射(PND)确定了各向异性低自旋配合物 PPh4[Fe(III)(Tp)(CN)3]⋅H2O 的低温分子磁 susceptibility张量。我们发现存在一个明显的分子易磁化轴,几乎与分子的 C3 假轴平行,这也对应于 Fe(III)离子八面体配位球的三角拉长方向。PND 结果与电子顺磁共振(EPR)光谱、磁测量和从头算研究一致。通过这个特殊的例子,我们展示了 PND 提供独特、直接和简单的磁各向异性和磁化率张量的能力,为确定顺磁分子配合物中的磁结构相关性提供了明确的方法。