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首页> 外文期刊>Angewandte Chemie >Olefin Cyclopropanation by Radical Carbene Transfer Reactions Promoted by Cobalt(II)/Porphyrinates: Active-Metal-Template Synthesis of [2]Rotaxanes
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Olefin Cyclopropanation by Radical Carbene Transfer Reactions Promoted by Cobalt(II)/Porphyrinates: Active-Metal-Template Synthesis of [2]Rotaxanes

机译:通过钴(II)/卟啉酸盐促进的自由基切菜转移反应的烯烃环丙烷:活性金属 - 模板合成[2]轮烷基

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摘要

A Co-II/porphyrinate-based macrocycle in the presence of a 3,5-diphenylpyridine axial ligand functions as an endotopic ligand to direct the assembly of [2]rotaxanes from diazo and styrene half-threads, by radical-carbene-transfer reactions, in excellent 95% yield. The method reported herein applies the active-metal-template strategy to include radical-type activation of ligands by the metal-template ion during the organometallic process which ultimately yields the mechanical bond. A careful quantitative analysis of the product distribution afforded from the rotaxane self-assembly reaction shows that the Co-II/porphyrinate subunit is still active after formation of the mechanical bond and, upon coordination of an additional diazo half-thread derivative, promotes a novel intercomponent C-H insertion reaction to yield a new rotaxane-like species. This unexpected intercomponent C-H insertion illustrates the distinct reactivity brought to the Co-II/porphyrinate catalyst by the mechanical bond.
机译:在存在3,5-二苯基吡啶轴配体的情况下,基于CO-II /卟啉基宏环用作内甲烷配体,以通过自由基 - 切菜转移反应将[2]旋转丁烷的组装从Diazo和苯乙烯半螺纹组成,优异的95%收率。本文报道的方法适用于有机金属过程中的金属模板离子包括由金属模板离子的自由基型活化,最终产生机械键。仔细定量分析来自甲烷自组装反应得到的产物分布表明,在形成机械键后,CO-II /卟啉酶仍然活跃,并在协调另外的重氮半线衍生物后,促进新颖嵌段性CH插入反应,得到新的旋石刀状物种。这种意外的相块性C-H插入说明了通过机械键合给CO-II /卟啉催化剂的不同反应性。

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