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Styrene Aziridination by Iron(IV) Nitrides

机译:氮化铁(IV)对苯乙烯的氮杂氮化

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Thermolysis of the iron(IV) nitride complex [PhB(tBuIm)(3)FeN] with styrene leads to formation of the high-spin iron(II) aziridino complex [PhB(tBuIm)(3)Fe-N(CH2CHPh)]. Similar aziridination occurs with both electron-rich and electron-poor styrenes, while bulky styrenes hinder the reaction. The aziridino complex [PhB(tBuIm)(3)Fe-N(CH2CHPh)] acts as a nitride synthon, reacting with electron-poor styrenes to generate their corresponding aziridino complexes, that is, aziridine cross-metathesis. Reaction of [PhB(tBuIm)(3)Fe-N(CH2CHPh)] with Me3SiCl releases the N-functionalized aziridine Me3SiN(CH2CHPh) while simultaneously generating [PhB(tBuIm)(3)FeCl]. This closes a synthetic cycle for styrene azirdination by a nitride complex. While the less hindered iron(IV) nitride complex [PhB(MesIm)(3)FeN] reacts with styrenes below room temperature, only bulky styrenes lead to tractable aziridino products.
机译:氮化铁(IV)络合物[PhB(tBuIm)(3)FeN]与苯乙烯的热解导致形成高旋转铁(II)叠氮基络合物[PhB(tBuIm)(3)Fe-N(CH2CHPh)] 。富电子苯乙烯和贫电子苯乙烯都会发生类似的叠氮化,而笨重的苯乙烯会阻碍反应。叠氮基络合物[PhB(tBuIm)(3)Fe-N(CH2CHPh)]充当氮化物合成子,与电子贫乏的苯乙烯反应生成相应的叠氮基络合物,即氮丙啶交叉复分解。 [PhB(tBuIm)(3)Fe-N(CH2CHPh)]与Me3SiCl反应生成N-官能化氮丙啶Me3SiN(CH2CHPh),同时生成[PhB(tBuIm)(3)FeCl]。这样就关闭了氮化物络合物进行苯乙烯叠氮化的合成循环。虽然受阻较小的氮化铁(IV)络合物[PhB(MesIm)(3)FeN]与室温以下的苯乙烯反应,但只有大体积的苯乙烯才能生成易处理的叠氮基产物。

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