首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Case study on a rare effect: The experimental and theoretical analysis of a manganese(III) spin-crossover system
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Case study on a rare effect: The experimental and theoretical analysis of a manganese(III) spin-crossover system

机译:罕见效果的案例研究:锰(III)自旋交叉系统的实验和理论分析

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The six-coordinated mononuclear manganese(III) complex [Mn(5-Br-sal-N-1,5, 8,12)]ClO_4 has been synthesized and isolated in crystalline form. Magnetic measurements and variable-temperature single-crystal X-ray crystallography corroborated with theoretical analysis provided firm evidence for the spin-crossover effects of this system. The monomeric complex cations are made by a hexadentate mixed-donor Schiff base ligand imposing a distorted octahedral geometry and subtle structural effects determining the manifestation of the variable spin properties of the manganese(III) centers. The spin crossover in [Mn(5-Br-sal-N-1,5,8,12)]ClO_4 has resulted in an unprecedented crystallographic observation of the coexistence of high-spin (HS; S = 2) and low-spin (LS; S = 1) manganese(III) complex cations in equal proportions around 100 K. At room temperature, the two crystallographically distinct manganese centers are both HS. Only one of the two slightly different units undergoes spin crossover in the temperature range ~250-50 K, whereas the other remains in the HS state down to 50 K. The density functional theory calculations, performed as relevant numerical experiments designed to identify the role of orbital and interelectron effects, revealed unedited aspects of the manganese(III) spin-conversion mechanisms, developed in the conceptual frame of ligand-field models.
机译:六配位单核锰(III)配合物[Mn(5-Br-sal-N-1,5,8,12)] ClO_4已合成并以结晶形式分离。磁测量和温度可变的单晶X射线晶体学与理论分析相佐证,为该系统的自旋交叉效应提供了有力的证据。单体配位阳离子是由六齿混合施主席夫碱配体制成的,该配体具有扭曲的八面体几何形状和微妙的结构效应,可确定锰(III)中心可变自旋特性的表现。 [Mn(5-Br-sal-N-1,5,8,12)] ClO_4中的自旋交叉导致史无前例的晶体学观察,表明高自旋(HS; S = 2)和低自旋并存(LS; S = 1)锰(III)络合物阳离子在100 K附近的比例相同。在室温下,两个晶体学上不同的锰中心均为HS。两个略有不同的单元中只有一个在〜250-50 K的温度范围内发生自旋交叉,而另一个保持在50 K以下的HS状态。密度泛函理论计算是作为相关的数值实验进行的,旨在确定其作用。轨道和电子间效应的研究揭示了配体场模型概念框架中锰(III)自旋转化机制的未编辑方面。

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