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首页> 外文期刊>Zeitschrift fur Anorganische und Allgemeine Chemie >Synthesis and Characterization of Diorganocobalt Chlorides by Aliphatic Vinylic C-Cl Bond Activation
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Synthesis and Characterization of Diorganocobalt Chlorides by Aliphatic Vinylic C-Cl Bond Activation

机译:脂肪族乙烯基C-Cl键的活化合成二有机钴盐酸盐及其表征

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摘要

Three diorganocobalt chlorides [CoClMe(PMe3)(2)-{(C5H6)-CH=O}] (4), [CoClMe(PMe3)(2)-{(C6H8)-CH=O}] (5), and [CoClMe(PMe3)(2)-{(C(6)H(7)Memeta)-CH=O}] (6) were synthesized through cyclometalation reactions with aldehyde as an anchoring group involving aliphatic vinylic C-Cl bond activation. Complexes 4-6 were characterized by IR and NMR spectroscopy. The crystal and molecular structures of complexes 4 and 5 were determined by single-crystal X-ray diffraction. Complexes 4-6 are stable in solution at room temperature, but they decompose at above 30 degrees C affording C,C-couplings products with the formation of [Co(PMe3)(3)Cl]. The results of this work will be important for people to deepen the understanding of the C-Cl bond activation mechanism.
机译:三种二有机钴氯化物[CoClMe(PMe3)(2)-{(C5H6)-CH = O}](4),[CoClMe(PMe3)(2)-{(C6H8)-CH = O}](5)和[CoClMe(PMe3)(2)-{(C(6)H(7)Memeta)-CH = O}](6)是通过醛基环环化反应合成的,其中醛基为涉及脂肪族乙烯基C-Cl键活化的锚定基团。配合物4-6通过IR和NMR光谱表征。通过单晶X射线衍射确定配合物4和5的晶体和分子结构。配合物4-6在室温下在溶液中稳定,但在高于30摄氏度的温度下会分解,从而形成具有[Co(PMe3)(3)Cl]的C,C偶联产物。这项工作的结果对于人们加深对C-Cl键激活机制的了解将是重要的。

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