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Chiral Memory in Silyl-Pyridinium and Quinolinium Cations

机译:甲硅烷基吡啶鎓和喹啉鎓阳离子中的手性记忆

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Pyridine- and quinoline-stabilized silyl cations have been prepared, and their structure in condensed phases unambiguously assigned using ~1H, ~(13)C, ~(15)N, ~(29)Si, and ~1H DOSY NMR as well as X-ray diffraction studies. Solid state structures thus show in both cases a stabilization of the cationic silicon center through an N—Si interaction and formation of a highly strained four-membered ring system. Chiral memory at the silicon atom in these heterocycle-stabilized silyl cations was also established, leading to various levels of selectivity depending on the nature of the heterocycle. Lowest energy conformations of the starting silanes obtained through DFT calculations, along with the isolation and characterization of the Si-centered chiral silyl cation intermediates, finally allowed to propose a plausible hypothesis as to the configurational stability of these silyl cations.
机译:制备了吡啶和喹啉稳定的甲硅烷基阳离子,并使用〜1H,〜(13)C,〜(15)N,〜(29)Si和〜1H DOSY NMR明确指定了它们在缩合相中的结构X射线衍射研究。因此,在两种情况下,固态结构均显示出通过N-Si相互作用和形成高应变四元环系统形成的阳离子硅中心的稳定性。还建立了在这些杂环稳定的甲硅烷基阳离子中硅原子上的手性记忆,从而根据杂环的性质导致不同程度的选择性。通过DFT计算获得的起始硅烷的最低能级构象,以及以硅为中心的手性甲硅烷基阳离子中间体的分离和表征,最终使人们提出了关于这些甲硅烷基阳离子的构型稳定性的合理假说。

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