Abstract
The monoatomic zero-valent tin complex (stannylone) {[SiII(Xant)SiII]Sn0} 5 stabilized by a bis(silylene)xanthene ligand, [SiII(Xant)SiII=PhC(NtBu)2Si(Xant)Si(NtBu)2CPh], and its bis-tetracarbonyliron complex {[SiII(Xant)SiII]Sn0[Fe(CO)4]2} 4 are reported. The stannylone 5 bearing a two-coordinate zero-valent tin atom is synthesized by reduction of the precursor 4 with potassium graphite. Compound 4 results from the SnII halide precursor {[SiII(Xant)SiII]SnIICl}Cl 2 or {[SiII(Xant)SiII]SnBr2} 3 through reductive salt-metathesis reaction with K2Fe(CO)4. According to density functional theory (DFT) calculations, the highest occupied molecular orbital (HOMO) and HOMO-1 of 5 correspond to a π-type lone pair with delocalization into both adjacent vacant orbitals of the SiII atoms and a σ-type lone pair at the Sn0 center, respectively, indicating genuine stannylone character.
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CITATION STYLE
Xu, J., Dai, C., Yao, S., Zhu, J., & Driess, M. (2022). A Genuine Stannylone with a Monoatomic Two-Coordinate Tin(0) Atom Supported by a Bis(silylene) Ligand. Angewandte Chemie - International Edition, 61(3). https://doi.org/10.1002/anie.202114073
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