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Dioxo-, Oxo-imido-, and Bis-imido-Molybdenum(VI) Complexes with a Bis-phenolate-NHC Ligand

机译:用双酚酸盐-NHC配体,二氧化硅 - ,氧代 - 咪啶 - 和双 - 咪啶 - 钼(VI)配合物

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摘要

We report the facile synthesis of five rare high-valent Mo(VI)-NHC complexes with a dianionic OCO-pincer benzimidazolylidene ligand (L-1) with the general formula (LMoO2)-Mo-1 (1), (LMo)-Mo-1(O)((NBu)-Bu-t)(THF) (2), (LMo)-Mo-1((NBu)-Bu-t)((NHBu)-Bu-t)Cl (3), (LMo)-Mo-1((NBu)-Bu-t)(2) (4), and L-1 Mo(NMes)(2) (5). These complexes represent a complete series of high-valent molybdenum(VI) complexes, obtained by consecutive exchange of the oxo for imido ligands from the dioxo complex (1) to the bis-imido complexes (4 and 5). The complexes can be synthesized in high yields following a simple deprotonation protocol, using either triethylamine or lithium diisopropylamide (LDA) as a base. All complexes have been characterized by various techniques, including H-1, C-13{H-1}, and N-15 NMR spectroscopy, IR spectroscopy, and X-ray diffraction analysis. Except for the dioxo complex 1, all complexes adopt monomeric structures in the solid state. Compounds 1, 4, and 5 are rare examples of five-coordinated molybdenum(VI) complexes in the solid state, while 2 is six-coordinated, having a weakly bound THF ligand in the axial position. The dioxo complex 1 was found to be stable under air and moisture in the solid state as well as in solution for several days. Furthermore, preliminary reactivity studies and an approximate determination of the pK(a) value of the imido ligands in 4 are presented.
机译:我们与通式表示5个罕见的高价的Mo(VI)-NHC络合物与双阴离子OCO-钳形benzimidazolylidene配体(L-1)的简便合成(LMoO2)-Mo-1(1),(LMO) - MO-1(O)((NBU)-Bu-T)(THF)(2),(LMO)-Mo-1((NBU)-Bu-T)((NHBu)-Bu-T)氯(3 ),(LMO)-Mo-1((NBU)-Bu-T)(2)(4),和L-1的Mo(NMES)(2)(5)。这些复合物代表完整的一系列高价的钼(VI)络合物,通过酰亚胺配体与双 - 酰亚胺复合物(4和5)的氧代基的连续交换从二氧络合物(1)中获得。该络合物可以以高产率以下的简单去质子化协议来合成,即使用三乙胺或二异丙基氨基锂(LDA)的位置。所有络合物已被表征通过各种技术,包括H-1,C-13 {H-1},和N-15 NMR光谱,IR光谱和X射线衍射分析。除二氧配合1,所有配合采用的固态单体结构。化合物1,图4,和图5是五配位钼(VI)在固体状态下复合物的罕见例子,而图2是六配位,具有在轴向位置的弱结合的THF配位体。络合物1的二氧被发现是在空气和湿气稳定的固态,以及在溶液中数天。此外,初步的反应性研究和4的配体亚氨基的pK(a)中的值的近似确定被呈现。

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  • 来源
    《Organometallics》 |2019年第19期|共11页
  • 作者单位

    Paderborn Univ Fac Sci Dept Chem Warburger Str 100 D-33098 Paderborn Germany;

    Paderborn Univ Fac Sci Dept Chem Warburger Str 100 D-33098 Paderborn Germany;

    Paderborn Univ Fac Sci Dept Chem Warburger Str 100 D-33098 Paderborn Germany;

    Paderborn Univ Fac Sci Dept Chem Warburger Str 100 D-33098 Paderborn Germany;

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  • 正文语种 eng
  • 中图分类 元素有机化合物;
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  • 入库时间 2022-08-19 17:54:46

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