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复杂硅-硅分子框架的精确合成

Precise Synthesis of Complex Si-Si Molecular Frameworks.

作者信息

Wentz Kelsie E, Gittens Alexandra F, Klausen Rebekka S

机构信息

Department of Chemistry, Johns Hopkins University, 3400 N. Charles St., Baltimore, Maryland 21218, United States.

出版信息

J Am Chem Soc. 2025 Jan 29;147(4):2938-2959. doi: 10.1021/jacs.4c12646. Epub 2025 Jan 16.

Abstract

In this Perspective, we highlight the emergence of target-oriented syntheses of complex molecules composed of Si-Si (oligosilanes) rather than C-C bonds. Saturated oligosilanes structurally resemble alkanes with respect to a tetrahedral geometry, a preference for a staggered conformation in linear chains, the ability to form stable small rings, and tetrahedral stereochemistry at asymmetrically functionalized Si centers. There are also critical differences, for example, differences in multiple bonding and the ability to form penta- and hexacoordinated structures, that mean that chemical reactivity and, in particular, rules for stereoselective synthesis do not cleanly translate from carbon to silicon. This Perspective will discuss recent achievements in the precise, controlled synthesis of complex molecules comprised mainly of Si-Si bonds and highlight the mechanistic insights enabling increased molecular complexity. New tools, such as electrochemical and catalytic reactions, will be discussed as well as the problem of controlling relative configuration in molecules containing multiple stereogenic-at-silicon centers. These synthetic achievements facilitate the discovery of new properties, including insight into light absorption, conformation, and mechanical properties.

摘要

在这篇综述中,我们重点介绍了由Si-Si键(低聚硅烷)而非C-C键构成的复杂分子的目标导向合成方法的出现。饱和低聚硅烷在结构上类似于烷烃,具有四面体几何结构、线性链中倾向于交错构象、能够形成稳定的小环以及在不对称功能化硅中心处具有四面体立体化学。但也存在一些关键差异,例如,多重键合以及形成五配位和六配位结构的能力方面的差异,这意味着化学反应性,特别是立体选择性合成规则并不能直接从碳转移到硅。这篇综述将讨论在主要由Si-Si键构成的复杂分子的精确、可控合成方面的最新进展,并突出有助于提高分子复杂性的机理见解。还将讨论新工具,如电化学反应和催化反应,以及控制含有多个硅中心立体异构中心的分子中相对构型的问题。这些合成成果有助于发现新特性,包括对光吸收、构象和机械性能的深入了解。

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