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首页> 外文期刊>Angewandte Chemie >Unprecedented Five-Coordinate Iron(IV) Imides Generate Divergent Spin States Based on the Imide R-Groups
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Unprecedented Five-Coordinate Iron(IV) Imides Generate Divergent Spin States Based on the Imide R-Groups

机译:前所未有的五坐标铁(iv)iniDED基于酰亚胺R组产生发散的旋转状态

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摘要

Three five-coordinate iron(IV) imide complexes have been synthesized and characterized. These novel structures have disparate spin states on the iron as a function of the R-group attached to the imide, with alkyl groups leading to low-spin diamagnetic (S=0) complexes and an aryl group leading to an intermediate-spin (S=1) complex. The different spin states lead to significant differences in the bonding about the iron center as well as the spectroscopic properties of these complexes. Mossbauer spectroscopy confirmed that all three imide complexes are in the iron(IV) oxidation state. The combination of diamagnetism and N-15 labeling allowed for the first N-15 NMR resonance recorded on an iron imide. Multi-reference calculations corroborate the experimental structural findings and suggest how the bonding is distinctly different on the imide ligand between the two spin states.
机译:已经合成并表征了三种五坐标铁(IV)酰亚胺配合物。 这些新颖的结构在铁上具有不同的旋转状态,作为连接到酰亚胺的R-基团的函数,导致低自旋硅基(S = 0)络合物和导致中间旋转的芳基(S = 1)复杂。 不同的旋转状态导致铁心织物的粘合以及这些配合物的光谱性质的显着差异。 Mossbauer光谱证实,所有三个酰亚胺配合物都处于铁(IV)氧化状态。 允许在铁酰亚胺上记录的第一N-15 NMR共振的二磁场和N-15标记的组合。 多参考计算证实了实验结构发现,并表明在两个旋转状态之间的酰亚胺配体上是如何粘接的明显不同。

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