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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Spin-crossover behavior of neutral iron(iii) complexes with salicylaldehyde thio-, seleno- and semicarbazone ligands: experiment and theoretical analysis
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Spin-crossover behavior of neutral iron(iii) complexes with salicylaldehyde thio-, seleno- and semicarbazone ligands: experiment and theoretical analysis

机译:中性铁(III)配合物的旋转交叉行为与水杨醛硫脲,硒和氨基脲配体:实验与理论分析

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摘要

The iron(iii) complex [Fe(Hsemsal)(semsal)]3H(2)O (1) (H(2)semsal - salicylaldehyde semicarbazone) has been synthesized and characterized by powder and single crystal X-ray diffraction, and magnetic susceptibility measurements. Crystal structure analysis showed that the complex forms neat stacks stabilized by hydrogen-bonding through water molecules and pi-pi interactions between phenolate rings of ligands. The complex does not exhibit spin-crossover phenomena and remains in the high-spin state down to 2 K. DFT calculations were performed for a series of neutral Fe(iii) complexes, and the influence of the N2S2O2, N2Se2O2 and N2O4 coordination environment on the spin transition in these complexes was traced. The effect of substituents in the benzene ring of salicylaldehyde on the stabilization of the HS or LS states in complexes of this type was analyzed.
机译:铁(III)复合物[Fe(HSEMSAL)(SEMSAL)] 3H(2)O(1)(H(2)Semsal - SalicyldeS氨基脲)已经合成,其特征在于粉末和单晶X射线衍射,磁性 易感性测量。 晶体结构分析表明,通过氢键通过配体的酚类环之间的水分子和Pi-PI相互作用氢键稳定的复杂叠层稳定。 该复合物未表现出旋转交叉现象,并在高旋转状态下保持下降至2K.对一系列中性Fe(III)复合物进行DFT计算,以及N2S2O2,N2Se2O2和N2O4配位环境的影响 这些配合物中的旋转过渡被追踪。 分析了苯甲酰苯甲醛在苯甲酰苯甲酸苯甲酸中的效果,对该类型的复合物中HS或LS状态的稳定化。

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