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N-Heterocyclic Carbene Piano-Stool Iron Complexes as Efficient Catalysts for Hydrosilylation of Carbonyl Derivatives

机译:N-杂环卡宾钢琴凳铁配合物作为羰基衍生物氢化硅烷化的有效催化剂

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摘要

Hydrosilylation with well defined pianostooliron(II) complexes bearing both N-heterocycliccarbene and cyclopentadienyl ligands was accomplished with both aldehydes and ketones. Typically, the reduction of aldehydes exhibited good activities (full reduction at 30℃ in 3 h), whereas for ketones, the reaction need 16 h at 70℃ to obtain good conversions. Of notable interest is the use of visible light irradiation to generate one of the active catalyst.
机译:用既带有N-杂环卡宾又带有环戊二烯基配体的明确定义的二茂铁(II)配合物进行氢化硅烷化反应,同时使用醛和酮。通常,醛的还原表现出良好的活性(在30℃下3小时内完全还原),而对于酮类,在70℃下反应需要16小时才能获得良好的转化率。值得注意的是使用可见光辐照产生一种活性催化剂。

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