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Branching Ratio and L2+L3 Intensities of 3d-Transition Metals in Phthalocyanines and the Amine Complexes (STATES AND STRUCTURES-Crystal Information Analysis)

机译:酞菁和胺配合物中3d过渡金属的支化比和L2 + L3强度(状态和结构-晶体信息分析)

摘要

L2,3 inner-shell excitation spectra were obtained by electron energy-loss spectroscopy (EELS) for the divalent first transition series metals in phthalocyanine complexes. It was found that the value of normalized total intensity of I(L2+L3) was nearly proportional to the formal electron vacancies of each 3d-state, and the values of the branching ratio, I(L3)/I((L2+L3), represented a high spin state rather than low spin state. EELS was also applied to charge-transfer complexes of FePc with amine. It was concluded that their I(L2+L3) intensity of Fe showed the decrease in vacancies of 3d-states on the formation of the charge transfer complex, which suggests some electron transfer from the amine to Fe in phthalocyanine.
机译:通过电子能量损失谱(EELS)获得了酞菁配合物中二价第一过渡系列金属的L2,3内壳激发光谱。发现I(L2 + L3)的归一化总强度值与每个3d态的形式电子空位几乎成正比,支化比I(L3)/ I((L2 + L3 )表示高自旋态而不是低自旋态。EELS还用于FePc与胺的电荷转移络合物,结论是它们的Fe的I(L2 + L3)强度显示3d态的空位降低电荷转移络合物的形成,表明在酞菁中电子从胺转移到Fe。

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