Abstract
The synthesis of an N-heterocyclic silylene-stabilized digermanium(0) complex is described. The reaction of the amidinate-stabilized silicon(II) amide [LSiN(SiMe3)2] (1; L=PhC(NtBu)2) with GeCl2·dioxane in toluene afforded the SiII-GeII adduct [L{(Me3Si)2N}Si→GeCl2] (2). Reaction of the adduct with two equivalents of KC8 in toluene at room temperature afforded the N-heterocyclic carbene silylenestabilized digermanium(0) complex [L{(Me3Si)2N}Si← Ge=Ge Si{N(SiMe3)2}L] (3). X-ray crystallography and theoretical studies show conclusively that the N-heterocyclic silylenes stabilize the singlet digermanium(0) moiety by a weak synergic donor-acceptor interaction.
Original language | English |
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Pages (from-to) | 13155-13158 |
Number of pages | 4 |
Journal | Angewandte Chemie - International Edition |
Volume | 53 |
Issue number | 48 |
DOIs | |
Publication status | Published - Nov 24 2014 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2014 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
ASJC Scopus Subject Areas
- Catalysis
- General Chemistry
Keywords
- Carbene homologues
- Density functional calculations
- Germanium
- Silicon
- Zero oxidation state