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Synthesis and Characterization of ((CCC)-C-DIPP)Fe Complexes: A Zwitterionic Metalation Method and CO2 Reactivity

机译:((CCC)-C-DIPP)Fe络合物的合成与表征:两性离子金属化方法和CO2反应性

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摘要

The synthesis and characterization of a series of novel iron complexes has been accomplished using a monoanionic pincer bis(carbene) ligand framework. Metalation first proceeded through an isolated Fe(II) zwitterionic intermediate that was subsequently reduced in situ to Fe(0) to facilitate oxidative addition of the aryl C-H bond, generating the Fe-II-H complexes. Varying the L-type ligand on these complexes exhibited profound effects, as observed by IR and H-1 NMR spectroscopy. Higher oxidation states of Fe could also be supported in this ligand framework, as evidenced by the isolation of two Fe(III) complexes. Treating an Fe-II-H complex with CO2 generated an Fe-formate complex (K-2-OOCH) from insertion into the Fe-II-H bond. The independent synthesis of this molecule was accomplished by treating Fe-II-Cl with excess NaOOCH.
机译:使用单甘油钳子双(卡贝烯)配体框架完成了一系列新的铁络合物的合成和表征。 金属化首先通过分离的Fe(II)两性离子中间体进行,随后原位还原为Fe(0)以促进氧化芳基C-H键,产生Fe-II-H络合物。 根据IR和H-1 NMR光谱观察,改变这些配合物上的L型配体表现出深刻的影响。 该配体框架中也可以支持较高的氧化态,其通过分离两种Fe(III)配合物证明。 用CO 2处理Fe-II-H络合物,产生从插入Fe-II-H键的Fe-甲酸酯复合物(K-2-OOCH)。 通过用过量的NaOOCH处理Fe-II-Cl来完成该分子的独立合成。

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  • 来源
    《Organometallics》 |2019年第15期|共10页
  • 作者单位

    Univ Illinois Sch Chem Sci 600 South Matthews Ave Urbana IL 61801 USA;

    Univ Illinois Sch Chem Sci 600 South Matthews Ave Urbana IL 61801 USA;

    Univ Illinois Sch Chem Sci 600 South Matthews Ave Urbana IL 61801 USA;

    Univ Illinois Sch Chem Sci 600 South Matthews Ave Urbana IL 61801 USA;

    Univ Illinois Sch Chem Sci 600 South Matthews Ave Urbana IL 61801 USA;

    Univ Illinois Sch Chem Sci 600 South Matthews Ave Urbana IL 61801 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 元素有机化合物;
  • 关键词

  • 入库时间 2022-08-19 17:54:46

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