High-spin Schiff-base dinuclear iron(III) complexes bridged by N-oxide ligands

High-spin Schiff-base dinuclear iron(III) complexes bridged by N-oxide ligands
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DOI:
10.1016/j.ica.2009.06.057
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发表时间:
2009-10
影响因子:
2.8
通讯作者:
Ivan Nemec;R. Boča;M. Gembicky;L. Dlháň;R. Herchel;F. Renz
Ivan Nemec;R. Boča;M. Gembicky;L. Dlháň;R. Herchel;F. Renz
中科院分区:
化学3区
文献类型:
--
作者:
Ivan Nemec;R. Boča;M. Gembicky;L. Dlháň;R. Herchel;F. Renz

文献摘要

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报道了双核配合物[{FeIII(L5)}b{FeIII(L5)}](BPh4)2的合成和结构,其中L5是五齿席夫碱配体,b是基于联吡啶的二齿N-氧化物桥配体。根据磁化率、磁化强度和穆斯堡尔谱研究了磁性行为,表明配合物在整个温度范围内都具有高自旋。
Synthesis and structure of dinuclear complexes [{FeIII(L5)}b{FeIII(L5)}](BPh4)2, where L5is a pentadentate Schiff-base ligand, b is a bidentate N-oxide bridging ligand based on bipyridine, is reported. Magnetic behavior is investigated in terms of the magnetic susceptibility, magnetization, and Mössbauer spectroscopy revealing that the complexes are high-spin over the whole temperature region.