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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >A rhodium(I) dicarbonyl complex with a redox-active ferrocenyl phosphine-NHC ligand: Enhanced reactivity of the metal centre through ferrocene oxidation
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A rhodium(I) dicarbonyl complex with a redox-active ferrocenyl phosphine-NHC ligand: Enhanced reactivity of the metal centre through ferrocene oxidation

机译:具有氧化还原活性的二茂铁基膦-NHC配体的铑(I)二羰基配合物:通过二茂铁氧化提高金属中心的反应性

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摘要

A rhodium(l) dicarbonyl complex bearing a bidentate ferrocenyl phosphine-NHC ligand has been synthesized and characterized by NMR, IR spectroscopy, mass spectrometry and X-ray diffraction methods. Its behaviour towards oxidation was investigated and revealed that changing the oxidation state of ferrocene can significantly modify the electron density at rhodium. Oxidation of the rhodium(I) dicarbonyl complex in acetonitrile furnished an air-stable rhodium(III) complex, stabilized by acetonitrile molecules and with an interesting C-H bond activation at ferrocene. This new rhodium(III) complex is active for the hydrosilylation of acetophenone and its derivatives. (C) 2014 Elsevier Ltd. All rights reserved.
机译:合成了带有二齿二茂铁基膦-NHC配体的铑(l)二羰基配合物,并通过NMR,IR光谱,质谱和X射线衍射法表征。研究了其对氧化的行为,发现改变二茂铁的氧化态可以显着改变铑的电子密度。乙腈中二羰基铑(I)配合物的氧化提供了一种空气稳定的铑(III)配合物,该配合物由乙腈分子稳定并且在二茂铁上具有令人感兴趣的C-H键活化。这种新的铑(III)配合物对苯乙酮及其衍生物的氢化硅烷化具有活性。 (C)2014 Elsevier Ltd.保留所有权利。

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