Mononuclear Fe(III) Schiff Base Complex with Trans-FeO4N2 Chromophore of o-Aminophenol Origin: Synthesis, Characterisation, Crystal Structure, and Spin State Investigation

Dawit Tesfaye, Jonas Braun, Mamo Gebrezgiabher, J. Kuchár, J. Černák, Taju Sani, A. Gismelseed, Tim Hochdörffer, Volker Schünemann, C. Anson, Annie K. Powell, Madhu Thomas
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Abstract

A new iron(III) complex (Et3NH)2[Fe(L)2](ClO4)·MeOH (1) where H2L = 2-{(E)-[2-hydroxyphenyl)imino]methyl}phenol has been synthesised and characterised by single crystal XRD, elemental analysis and DC magnetic susceptibility measurements. The dianionic ligands L2− coordinate in a tridentate fashion with the Fe(III) through their deprotonated phenolic oxygens and azomethine nitrogen atoms, resulting in a trans-FeO4N2 chromophore. Variable-temperature magnetic measurements were performed between 300 and 5 K under an applied field of 0.1 T and show that 1 is in the high spin state (S = 5/2) over the whole measured temperature range. This is confirmed by Mössbauer spectroscopy at 77 and 300 K.
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邻氨基苯酚来源的反式 FeO4N2 色素的单核 Fe(III) 希夫碱配合物:合成、表征、晶体结构和自旋态研究
我们合成了一种新的铁(III)配合物 (Et3NH)2[Fe(L)2](ClO4)-MeOH (1),其中 H2L = 2-{(E)-[2-羟基苯基)亚氨基]甲基}苯酚,并通过单晶 XRD、元素分析和直流磁感应强度测量对其进行了表征。二阴离子配体 L2- 通过其去质子化的酚氧原子和偶氮甲基氮原子与铁(III)以三叉配位方式配位,形成反式-FeO4N2 发色团。在 0.1 T 的外加磁场下,在 300 至 5 K 之间进行了变温磁性测量,结果表明 1 在整个测量温度范围内都处于高自旋状态(S = 5/2)。在 77 和 300 K 温度下进行的莫斯鲍尔光谱分析也证实了这一点。
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