首页> 外文期刊>Inorganica Chimica Acta >C-P bond forming reactivity of N-heteropentacene: Isolation and characterization of a phospho-ylide complex of ruthenium(II)
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C-P bond forming reactivity of N-heteropentacene: Isolation and characterization of a phospho-ylide complex of ruthenium(II)

机译:N-杂戊并苯的C-P键形成反应性:钌(II)的磷-叶立德络合物的分离和表征

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摘要

In an unusual reaction of H_2L~2 (H_2L ~2 = N-heteropentacene) with Ru(PPh_3)_3Cl _2 a phospho-ylide ruthenium(II) complex (1) was obtained via unprecedented chemical transformations of the conjugate base [L ~2]~(2-). A bidentated phospho-ylide ligand is formed with concomitant aromatic ring hydroxylation and new C-P bond formation reactions. The new ligand, binds to Ru~(II) as a neutral N, O-donor. Crystal structure determination by single crystal X-ray diffraction has been used to characterize the compound. The phospho-ylide Ru(II) description of the complex was established based on ~(13)C as well as ~(31)P NMR studies. The complex shows rich spectral and redox properties. UV-Vis-NIR spectrum consisted of multiple low-energy transitions in the visible and near IR regions. Preliminary density functional theory calculations were employed to understand the electronic structure and to assign the spectral transitions. Cyclic voltammogram and EPR-spectrum of the electrogenerated oxidized compound are reported and used to characterize the redox properties.
机译:在H_2L〜2(H_2L〜2 = N-异戊四烯)与Ru(PPh_3)_3Cl _2的不寻常反应中,通过共轭碱[L〜2]的空前化学转化获得了磷酰钌(II)配合物]〜(2-)。与伴随的芳环羟基化和新的C-P键形成反应形成二齿的磷酸-叶立德配体。新的配体作为中性的N,O供体与Ru(II)结合。通过单晶X射线衍射测定晶体结构已用于表征该化合物。基于〜(13)C和〜(31)P NMR研究建立了配合物的磷酰化Ru(II)描述。该配合物显示出丰富的光谱和氧化还原特性。 UV-Vis-NIR光谱由可见光和近红外区域的多个低能跃迁组成。初步的密度泛函理论计算用于了解电子结构并指定光谱跃迁。报告了电生成的氧化化合物的循环伏安图和EPR光谱,并将其用于表征氧化还原特性。

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