Halide abstraction from tetrylidene complexes [TbbE(Br)IrH(PMe3)3] [E =Ge (1), Sn (2)] and [Ar*E(Cl)IrH(PMe3)3] gives the salts [TbbEIrH(PMe3)3][BArF4] [E =Ge (3), Sn (4)] and [Ar*EIrH(PMe3)3][BArF4] [E = Ge (3’), E =...

In reaction of tantalocene trihydride with the low valent aryl tin cation [Ar*Sn(C6H6)][Al(OC{CF3}3)4] (1a) the hydridostannylene complex [Cp2TaH2-Sn(H)Ar*][Al(OC{CF3}3)4] (2) was synthesized. Hydride bridged adducts [Cp2WH2EAr*][Al(OC{CF3}3)4] (E = Sn 3a,...

The organogermanium and organotin trihydrides (TbbEH3) [E = Ge (3), Sn (7)] with the Tbb substituent were synthesized by hydride substitution (Tbb = 2,6-[CH(SiMe3)2]2-4-(t-Bu)C6H2). Deprotonation of the organoelement trihydrides 3...

Allylmagnesium chloride and methyl-propenyl-magnesium bromide were reacted with bulky substituted organolead and organotin halides (Ar*PbBr)2, (Ar′PbBr)2, (Ar*SnCl)2 (Ar* = 2,6-trip2C6H3-, trip = 2,4,6-triisopropylphenyl, Ar′ = 2,6-mes2C6H3-, mes = 2,4,6-trimethylphenyl). The allyl ligand coordinates in an η3-coordination mode at organoplumbylene fragments. In the solid state as well as in solution, η3-coordination was characterized by crystal structure analysis and Saunders’ isotopic perturbation technique. For the plumbylene Ar*Pb­(C3H5), a solid state 207Pb magic angle spinning (MAS) NMR spectrum could be obtained. The isotropic chemical shift is −435 ppm, and the magnitude of the 207Pb chemical shift tensor of 7000­(500) ppm is among the greatest observed experimentally. The methylallyl ligand coordinated at a plumbylene fragment exhibits two short and one long Pb–C interaction. In reaction with aniline, the allyl ligand reacts as a leaving group to give amidoplumbylenes.

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