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Lewis base-stabilized silyliumylidene ions in transition metal coordination chemistry

机译:Lewis碱稳定的甲硅烷基亚氨基离子在过渡金属配位化学中

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Base stabilized silyliumylidene ions are starting to gather more and more interest from academia and industry because of their intriguing possibilities as synthons in organosilicon chemistry, facile activation of small molecules and possible applications in transition metal-free catalysis. Furthermore, with the presence of a stereochemically active lone pair on the low-valent silicon center, they can act as ligands in transition metal complexes comparable to carbenes and silylenes. Utilization of the incredible synthetic potential of Si(II) cations - the possible formation of up to three new bonds in a single reaction - can also give facile access to dative, single, double and triple bonds between silicon and a transition metal. Over the past years we have invested in further developing the area of base-stabilized silyliumylidene ions and have contributed significantly to their potential coordination chemistry and their intriguing reactivities with transition metals. This Frontier article discusses the recent developments in the chemistry of base-stabilized Si(II) cations as ligands and highlights our contributions to this field.
机译:基础稳定的甲硅烷基亚氨基离子开始收集学术界和工业的越来越多的兴趣,因为它们作为有机硅化学的合成器的兴趣可能性,小分子的体内激活以及过渡金属催化作用可能的应用。此外,在低Ventry硅中心存在立体化学活性孤独对的情况下,它们可以用作与碳纤维剂和甲硅烷烯的过渡金属配合物中的配体。利用Si(II)阳离子的令人难以置信的合成电位 - 在单一反应中可以形成最多三种新键 - 还可以在硅和过渡金属之间进行嵌合的DIT,单,双和三键。在过去几年中,我们投入了进一步发展碱稳定的甲硅烷基亚氨基区的面积,并对其潜在的协调化学和具有过渡金属的有趣重塑作出显着贡献。这个边界文章讨论了基础稳定的Si(II)阳离子的最新发展成为配体,并强调了我们对该领域的贡献。

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