4.5 Article

Synthesis and Reactivity of Bidentate N-Heterocyclic Carbene-Phosphinidene Supported Si(IV) Dicationic Complexes

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EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2022, 期 45, 页码 -

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.202201072

关键词

Coordination chemistry; Main group elements; N-Heterocyclic carbene-phosphinidene; Si(IV) Dications; Silanes

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  1. Projekt DEAL

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Here, we report the synthesis and isolation of Si(IV) dicationic complexes stabilized by a bidentate N-heterocyclic carbene-phosphinidene (NHCP). These dications exhibit high Lewis acidity and feature a tetracoordinated silicon centre. In addition, dication [2 a] is able to react with diphenylketene by insertion into the Si-P bond.
Herein, we report the synthesis and isolation of Si(IV) dications stabilized by a bidentate N-heterocyclic carbene-phosphinidene (NHCP). Treatment of the bis(NHCP) with Si(IV) bis(triflate) R2Si(OTf)(2) (with R=H, Ph) resulted in the instant formation of Si(IV) dicationic complexes [2 a] and [2 b] featuring a tetracoordinated silicon centre. The dications show expected high Lewis acidity. The bis(NHCP)-stabilized parent silyl dication 2a (SiH22+) presents the first isolable example of a parent SiH2 dication. In addition, dication [2 a] is able to react with diphenylketene by insertion into the Si-P bond.

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