Abstract

AbstractThe 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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