首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Direct oxide transfer from an eta(2)-keto ligand to generate a cobalt PCcarbeneP(O) pincer complex
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Direct oxide transfer from an eta(2)-keto ligand to generate a cobalt PCcarbeneP(O) pincer complex

机译:从ETA(2) - 酮配体的直接氧化物转移,产生钴PcCarbenep(O)钳子复合物

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摘要

We report the direct carbonyl cleavage in a kappa(3)-P ',(eta(2)-C,O),P '' ligand by a monomeric cobalt centre through metal-ligand cooperativity. C-O cleavage leads to the formation of a PCcarbeneP(O) pincer ligand with a central alkylidene anchor. A DFT analysis, supported by kinetic studies, suggests that decoordination of a pincer phosphino arm to generate a kinetically accessible free phosphine may be critical in transfer of the oxide to a phosphorus position. Thus, oxide transfer to bisphosphino bidentate co-ligands was also found to be viable, allowing access to the previously reported PCcarbeneP pincer complex (2), where bisphosphines were used as oxide sequestering agents.
机译:我们通过金属 - 配体协作,通过金属 - 配体中心在Kappa(3)-P',(ETA(2)-C,O),P''配体中报告直接羰基裂解。 C-O裂解导致形成具有中央亚烷基锚的PcCarbenep(O)钳子配体。 通过动力学研究支持的DFT分析表明,渗滤体臂的解构以产生动力学上可偏转的游离膦可以在氧化物转移到磷位置至关重要。 因此,还发现氧化物转移到二磷亚二齿共配体的可行性,允许进入先前报道的PcCarbenep钳子复合物(2),其中二膦用作氧化物螯合剂。

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