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较重的13/15族多重键体系:合成、结构与化学键活化

Heavier group 13/15 multiple bond systems: synthesis, structure and chemical bond activation.

作者信息

Dankert F, Hering-Junghans C

机构信息

Leibniz Institut für Katalyse e.V. (LIKAT), Albert-Einstein-Str. 29A, 18059 Rostock, Germany.

出版信息

Chem Commun (Camb). 2022 Jan 27;58(9):1242-1262. doi: 10.1039/d1cc06518a.

Abstract

Heavier group 13/15 multiple bonds have been under investigation since the late 80s and to date, several examples have been published, which shows the obsoleteness of the so-called double bond rule. Especially in the last few years, more and more group 13/15 multiple bonds became synthetically feasible and their application in terms of small molecule activation has been demonstrated. Our group has recently shown that the combination of the pnictinidene precursor Ter-Pn(PMe) (Pn = P, As) in combination with Al(I) synthons afforded the first examples of phospha- and arsaalumenes as isolable and thermally robust compounds. This feature article is intended to show the recent developments in the field, to outline early synthetic approaches and to discuss strategies to unlock the synthetic potential of these elusive chemical bonds.

摘要

自20世纪80年代末以来,较重的13/15族多重键一直处于研究之中,迄今为止,已有多个实例发表,这表明所谓的双键规则已过时。特别是在过去几年中,越来越多的13/15族多重键在合成上变得可行,并且它们在小分子活化方面的应用也已得到证实。我们小组最近表明,亚磷烯前体Ter-Pn(PMe)(Pn = P、As)与Al(I)合成子相结合,得到了首例作为可分离且热稳定化合物的磷铝烯和砷铝烯。这篇专题文章旨在展示该领域的最新进展,概述早期的合成方法,并讨论释放这些难以捉摸的化学键合成潜力的策略。

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