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首页> 外文期刊>Chemistry - A European Journal >A Family of Four-Coordinate Iron(II) Complexes Bearing the Sterically Hindered Tris(pyrazolyl)borato Ligand TptBu,Me?
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A Family of Four-Coordinate Iron(II) Complexes Bearing the Sterically Hindered Tris(pyrazolyl)borato Ligand TptBu,Me?

机译:带有立体受阻的三(吡唑基)硼酸酯配体Tp tBu,Me 的四坐标铁(II)配合物族

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摘要

A new family of 14-electron, four-coordinate iron(II) complexes of the general formula [TptBu,MeFeX] (TptBu,Me is the sterically hindered hydrotris(3-tert-butyl-5-methyl-pyrazolyl) borate ligand and X=Cl (1), Br, I) were synthesized by salt metathesis of FeX2 with TptBu,MeK. The related fluoride complex was prepared by reaction of 1 with AgBF4. Chloride 1 proved to be a good precursor for ligand substitution reactions, generating a series of four-coordinate iron(II) complexes with carbon, oxygen, and sulphur ligands. All of these complexes were fully characterized by conventional spectroscopic methods and most were characterized by single-crystal X-ray crystallographic analysis. Magnetic measurements for all complexes agreed with a high-spin (d6, S=2) electronic configuration. The halide series enabled the estimation of the covalent radius of iron in these complexes as 1.24 Å.
机译:通式[Tp tBu,Me FeX](Tp tBu,Me )的一个新的14电子,四配位铁(II)配合物是位阻通过FeX 2 与Tp tBu的盐复分解反应合成了氢三(3-叔丁基-5-甲基-吡唑基)硼酸酯配体和X = Cl(1),Br,I)。我 K。 1与AgBF 4 反应制得相关的氟化物配合物。氯化物1被证明是配体取代反应的良好前体,可生成一系列具有碳,氧和硫配体的四配位铁(II)配合物。所有这些配合物均已通过常规的光谱学方法进行了充分表征,而大多数则通过单晶X射线晶体学分析进行了表征。所有复合物的磁测量结果均符合高旋转(d 6 ,S = 2)电子结构。卤化物系列使得这些配合物中铁的共价半径估计为1.24Å。

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