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一种由三阴离子钳型配体稳定的高自旋平面四方铁(II)配合物以及溶液中几何结构和自旋态保持的确凿证据。

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.

作者信息

Pascualini M E, Di Russo N V, Thuijs A E, Ozarowski A, Stoian S A, Abboud K A, Christou G, Veige A S

机构信息

Department of Chemistry , Center for Catalysis , University of Florida , Gainesville , FL 32611 , USA . Email:

National High Magnetic Field Laboratory , Florida State University , Tallahassee , FL 32310 , USA.

出版信息

Chem Sci. 2015 Jan 1;6(1):608-612. doi: 10.1039/c4sc02634a. Epub 2014 Oct 15.

Abstract

Square-planar high-spin Fe(ii) molecular compounds are rare and the only three non-macrocyclic or sterically-driven examples reported share a common FeO core. Using an easily modifiable pincer-type ligand, the successful synthesis of the first compound of this type that breaks the FeO 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 Δ value determined for this compound is rationalized on the basis of DFT calculations.

摘要

平面正方形高自旋Fe(ii)分子化合物很罕见,已报道的仅有的三个非大环或空间驱动的例子都有一个共同的FeO核心。通过使用一种易于修饰的钳型配体,成功合成了首例打破FeO基序的此类化合物。此外,我们首次证明了其几何结构和自旋态在溶液中保持不变。广泛的表征包括此类化合物的首个高场电子顺磁共振(EPR)和可变场/温度穆斯堡尔光谱。光谱数据分析表明该配合物表现出一个大的正零场分裂张量。此外,基于密度泛函理论(DFT)计算,解释了该化合物异常小的Δ值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b1a/5491960/3d2e63f9cf5e/c4sc02634a-s1.jpg

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