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首页> 外文期刊>Journal of Organometallic Chemistry >Synthesis and structural characterization of new piano-stool ruthenium(II) complexes bearing 1-butylimidazole heteroaromatic ligand
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Synthesis and structural characterization of new piano-stool ruthenium(II) complexes bearing 1-butylimidazole heteroaromatic ligand

机译:含1-丁基咪唑杂芳族配体的新型钢琴凳钌(II)配合物的合成与结构表征

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New cationic ruthenium(II) complexes with the formula [Ru(η ~5-C _5H _5)(LL)(1-BuIm)] [Z], with (LL) = 2PPh _3 or DPPE, and Z = CF _3SO _3 ~-, PF _6 ~-, BPh _4 ~-, have been synthesized and fully characterized. Spectroscopic and electrochemical studies revealed that the electronic properties of the coordinated 1-butylimidazole were clearly influenced by the nature of the phosphane coligands (LL) and also by the different counter ions. The solid state structures of the six complexes determined by X-ray crystallographic studies, confirmed the expected distorted three-legged piano stool structure. However the geometry of the 1-butylimidazole ligand was found considerably different in all six compounds, being governed by the stereochemistry of the mono and bidentate coligands (PPh _3 or DPPE).
机译:新的阳离子钌(II)配合物,其化学式为[Ru(η〜5-C _5H _5)(LL)(1-BuIm)] [Z],其中(LL)= 2PPh _3或DPPE,Z = CF _3SO _3合成了~~,PF _6〜-,BPh _4〜-。光谱和电化学研究表明,配位的1-丁基咪唑的电子性质明显受膦大分子配体(LL)的性质以及不同的抗衡离子的影响。通过X射线晶体学研究确定的六种配合物的固态结构,证实了预期的扭曲的三足钢琴凳结构。然而,发现1-丁基咪唑配体的几何形状在所有六个化合物中均存在显着差异,这受单和双齿大肠菌(PPh _3或DPPE)的立体化学控制。

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