Nanba Yūsuke, Asakura Daisuke, Okubo Masashi, Zhou Haoshen, Amemiya Kenta, Okada Kozo, Glans Per-Anders, Jenkins Catherine A, Arenholz Elke, Guo Jinghua
Energy Technology Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki 305-8568, Japan.
Phys Chem Chem Phys. 2014 Apr 21;16(15):7031-6. doi: 10.1039/c3cp55471f. Epub 2014 Mar 7.
The electronic structure of Na2[Fe(CN)5NO]·2H2O (sodium nitroprusside: SNP) was investigated by using soft X-ray absorption (XA) spectroscopy. The Fe L2,3-edge XA spectrum of SNP exhibited distinct and very large satellite peaks for L3 and L2 regions, which is different from the spectra of hexacyanoferrates and the other iron compounds. A configuration-interaction full-multiplet calculation, in which the ligand molecular orbitals for the C4v symmetry were taken into account, revealed the Fe(2+) low-spin state with very strong effects of metal-to-ligand charge-transfer from the Fe 3d to NO 2p orbitals.
通过软X射线吸收(XA)光谱研究了Na2[Fe(CN)5NO]·2H2O(硝普钠:SNP)的电子结构。SNP的Fe L2,3边XA光谱在L3和L2区域表现出明显且非常大的卫星峰,这与六氰合铁酸盐和其他铁化合物的光谱不同。一种考虑了C4v对称性配体分子轨道的组态相互作用全多重态计算揭示了Fe(2+)低自旋态,具有从Fe 3d到NO 2p轨道的非常强的金属到配体电荷转移效应。