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首页> 外文期刊>Organometallics >Aminolysis of bis[bis(trimethylsilyl)amido]iron and -cobalt as a versatile route to N-heterocyclic carbene complexes
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Aminolysis of bis[bis(trimethylsilyl)amido]iron and -cobalt as a versatile route to N-heterocyclic carbene complexes

机译:双[双(三甲基硅烷基)酰胺基]铁和钴的氨解反应是制备N-杂环卡宾络合物的通用途径

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摘要

A range of new N-heterocyclic carbene complexes of iron(II) and cobalt(II) have been conveniently obtained by the aminolysis of bis[bis(trimethylsilyl) amido]iron and -cobalt precursors with imidazol(in)ium salts. Whereas sterically less hindered salts produced the tetrahedral complexes [M(carbene) _2Cl_2] (M = Fe), bulkier salts gave the three-coordinate [M(carbene){N(SiMe_3)_2}Cl] (M = Fe, Co), which serve as versatile precursors to a range of derivatives; mechanistic aspects of the reaction are discussed.
机译:通过将双[双(三甲基甲硅烷基)酰胺]铁和-钴前体与咪唑(铟)盐进行氨解,可方便地获得一系列新的铁(II)和钴(II)的N-杂环卡宾配合物。位阻较少的盐生成四面体络合物[M(卡宾)_2Cl_2](M = Fe),而体积较大的盐生成三坐标[M(卡宾){N(SiMe_3)_2} Cl](M = Fe,Co) ,可作为多种衍生物的通用前体;讨论了反应机理。

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