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首页> 外文期刊>Chemistry - A European Journal >Ir-Catalysed Asymmetric Allylic Substitutions with Cyclometalated (Phosphoramidite)Ir Complexes—Resting States, Catalytically Active (π-Allyl)Ir Complexes and Computational Exploration
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Ir-Catalysed Asymmetric Allylic Substitutions with Cyclometalated (Phosphoramidite)Ir Complexes—Resting States, Catalytically Active (π-Allyl)Ir Complexes and Computational Exploration

机译:环金属化(亚磷酰胺)Ir配合物的Ir催化不对称烯丙基取代基—重整态,催化活性(π-烯丙基)Ir配合物和计算探索

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摘要

Mechanistic aspects of allylic substitutions with iridium catalysts derived from phosphoramidites by cyclometalation were investigated. The determination of resting states by 31P NMR spectroscopy led to the conclusion that the cyclometalation process is reversible. A novel, one-pot procedure for the preparation of (π- allyl)Ir complexes was developed, and these complexes were characterised by X-ray crystal structure analyses and spectral data. They are fully active catalysts of the allylic substitution reaction. DFT calculations on the allyl complexes, transition states of the allylic substitution and product olefin complexes gave further mechanistic insight.
机译:研究了通过环金属化衍生自亚磷酰胺的铱催化剂进行烯丙基取代的机理。用 31 P NMR光谱法测定静止态得出的结论是环金属化过程是可逆的。开发了一种新颖的一锅法制备(π-烯丙基)Ir配合物,并通过X射线晶体结构分析和光谱数据对这些配合物进行了表征。它们是烯丙基取代反应的全活性催化剂。对烯丙基配合物,烯丙基取代基的过渡态和产物烯烃配合物的DFT计算提供了进一步的机理研究。

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