Reactivity of a Unique Si(I)–Si(I)-Based η <sup>2</sup> -Bis(silylene) Iron Complex
Zhiyuan He, Lingyu Liu, Felix J. de Zwart, Xiaolian Xue, Andreas W. Ehlers, KaKing Yan, Serhiy Demeshko, Jarl Ivar van der Vlugt, Bas de Bruin, Jeremy P. Krogman
Abstract
In this paper, we report the synthesis of a unique silicon(I)-based metalla-disilirane and report on its reactivity toward TMS-azide and benzophenone. Metal complexes containing disilylenes ((bis)silylenes with a Si–Si bond) are known, but direct ligation of the Si(I) centers to transition metals always generated dinuclear species. To overcome this problem, we targeted the formation of a mononuclear iron(0)–silicon(I)-based disilylene complex via templated synthesis, starting with ligation of two Si(II) centers to iron(II), followed by a two-step reduction. The DFT structure of the resulting η2-disilylene-iron complex reveals metal-to-silicon π-back donation and a delocalized three-center–two-electron (3c–2e) aromatic system. The Si(I)–Si(I) bond displays unusual but well-defined reactivity. With TMS-azide, both the initial azide adduct and the follow-up four-membered nitrene complex could be isolated. Reaction with benzophenone led to selective 1,4-addition into the Si–Si bond. This work reveals that selective reactions of Si(I)–Si(I) bonds are made possible by metal ligation.