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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Synthesis and lanthanide coordination chemistry of trifluoromethyl derivatives of phosphinoylmethyl pyridine N-oxides
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Synthesis and lanthanide coordination chemistry of trifluoromethyl derivatives of phosphinoylmethyl pyridine N-oxides

机译:膦酰基甲基吡啶N-氧化物的三氟甲基衍生物的合成及镧系配位化学

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摘要

A synthetic route for the formation of 2-[bis(2-trifluoromethylphenyl)phosphinoylmethyl]pyridine N-oxide (1c) and 2-[bis(3,5-trifluoromethylphenyl)phosphinoylmethyl]pyridineN-oxide (1d) was developed and the new ligands characterized by spectroscopic methods and single-crystal X-ray diffraction analyses. The coordination chemistry of 1c was examined with Yb(NO3)(3) and the molecular structure of one complex, [Yb(1c)(NO3)(3)(DMF)]center dot DMF center dot 0.5H(2)O, was determined by single-crystal X-ray diffraction methods. The ligand is found to coordinate in a bidentate fashion, and this is compared against lanthanide coordination chemistry observed for the related ligand, [Ph2P(O)CH2]C5H4NO.
机译:开发了形成2- [双(2-(三三氟甲基苯基)膦酰基甲基]吡啶N-氧化物(1c)和2- [双(3,5-三氟甲基苯基)膦酰基甲基]吡啶N-氧化物(1d)的合成途径。通过光谱方法和单晶X射线衍射分析表征的配体。用Yb(NO3)(3)和一种配合物[Yb(1c)(NO3)(3)(DMF)]中心点DMF中心点0.5H(2)O的分子结构检查了1c的配位化学。通过单晶X射线衍射法测定。发现该配体以双齿形式配位,并将其与观察到的相关配体[Ph2P(O)CH2] C5H4NO的镧系元素配位化学进行比较。

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