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A high-spin square-planar Fe(ii) complex stabilized by a trianionic pincer-type ligand and conclusive evidence for retention of geometry and spin state in solution

机译:由三阴离子钳型配体稳定的高纺丝方平面Fe(ii)配合物并在溶液中保留了几何形状和自旋态的确凿证据

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摘要

Square-planar high-spin Fe(ii) molecular compounds are rare and the only three non-macrocyclic or sterically-driven examples reported share a common FeO4 core. Using an easily modifiable pincer-type ligand, the successful synthesis of the first compound of this type that breaks the FeO4 motif was achieved. In addition, we present the first evidence that geometry and spin state persist in solution. Extensive characterization includes the first high-field EPR and variable field/temperature Mössbauer spectra for this class of compounds. Analysis of the spectroscopic data indicates this complex exhibits a large and positive zero-field splitting tensor. Furthermore, the unusually small ΔE Q value determined for this compound is rationalized on the basis of DFT calculations.
机译:正方形平面的高自旋Fe(ii)分子化合物很少见,据报道仅有的三个非大环或空间驱动的实例共享一个共同的FeO4核。使用易于修饰的钳型配体,成功合成了破坏FeO4基序的第一类化合物。另外,我们提出了几何和自旋态在溶液中持续存在的第一个证据。广泛的表征包括此类化合物的第一个高场EPR和可变场/温度Mössbauer光谱。对光谱数据的分析表明,该复合物表现出大的正零场分裂张量。此外,基于DFT计算合理化了确定用于该化合物的异常小的ΔEQ值。

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