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Complexes de métaux non-nobles de fer et de nickel portant des ligands redox non-innocents et leurs applications en catalyse : de l'activation C-H aux réactions de couplages croisés

机译:携带非纯氧化还原配体的非贵金属铁和镍金属配合物及其在催化中的应用:从C-H活化到交叉偶联反应

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摘要

This PhD work has focused on the development of complexes of non-noble metals bearing non-innocent ligands and their catalytic applications as efficient alternatives to noble metal complexes, in the light of increasing concerns regarding cost and sustainability-related issues of noble metals. Towards this goal, we have developed and characterized complexes of non-noble metals (Fe, Ni) with non-innocent ligands using multiple spectroscopic techniques. This work was aimed at broadening the field of useful catalytic applications of these particular complexes. For our dedicated program in iron catalysis, a new method for tandem C–H activation/arylation of unactivated arenes catalyzed by iron complexes bearing redox-active bis(imino)pyridine ligands was developed. Preliminary mechanistic insights were gained based on combined spectroscopic data (NMR, in situ IR, EPR), reactivity studies as well as DFT calculations. The results obtained are clearly in favor of a mechanism distinct to that previously reported for iron-based catalytic systems and are not compatible with homolytic aromatic substitution (HAS). We have also focused on another challenging field in catalysis: cross-coupling reactions catalyzed by nickel as base metal, bearing redox non-innocent ligands. Several challenges in cross-coupling reactions remain among which coupling of non-activated alkyl halides. Mechanisms involving nickel catalysts often differ from those involved in palladium catalyzed cross-coupling reactions. The behavior of nickel complexes bearing redox non-innocent ligands was studied in order to unveil new reactivites and gain a better understanding of the catalytic cycles at stake.
机译:鉴于对贵金属的成本和可持续性相关问题的关注日益增加,这项博士学位研究的重点是带有非无价配体的非贵金属配合物的开发及其催化应用,可以替代贵金属配合物。为了实现这一目标,我们使用多种光谱技术开发并鉴定了非贵金属(Fe,Ni)与非纯配体的配合物。这项工作旨在拓宽这些特殊配合物的有用催化应用领域。对于我们的铁催化专用程序,开发了一种新的串联C–H活化/芳构化的新方法,该方法由带有氧化还原活性的双(亚氨基)吡啶配体的铁配合物催化。基于组合的光谱数据(NMR,原位红外,EPR),反应性研究以及DFT计算,获得了初步的力学见解。获得的结果显然有利于与先前报道的基于铁的催化体系不同的机理,并且与均溶芳族取代(HAS)不兼容。我们还专注于催化领域中另一个具有挑战性的领域:以镍为贱金属并带有氧化还原非纯配体的镍催化的交叉偶联反应。交叉偶联反应中的几个挑战仍然存在,其中包括未活化的烷基卤化物的偶联。涉及镍催化剂的机理通常不同于涉及钯催化的交叉偶联反应的机理。研究了带有氧化还原非纯配体的镍配合物的行为,以揭示新的活性物质并更好地了解所涉及的催化循环。

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    Salanouve Elise;

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  • 年度 2014
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  • 原文格式 PDF
  • 正文语种 fr
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