Magnesium-catalyzed hydrosilylation of α,β-unsaturated esters.

ToMgHB(CF) (, To = tris(4,4-dimethyl-2-oxazolinyl)phenylborate) catalyzes the 1,4-hydrosilylation of α,β-unsaturated esters. This magnesium hydridoborate compound is synthesized by the reaction of ToMgMe, PhSiH, and B(CF). Unlike the transient ToMgH formed from the reaction of ToMgMe and PhSiH, the borate adduct persists in solution and in the solid state.

Piano-Stool Lutetium Amido and Imido Compounds Supported by a Constrained Bis(oxazoline)cyclopentadienyl Ligand.

{Bo(M)Cp(tet)}Lu(CH2Ph)2 (1; Bo(M)Cp(tet) = MeC(Ox(Me2))2C5Me4; Ox(Me2) = 4,4-dimethyl-2-oxazoline) was prepared in 95% yield from the reaction of Bo(M)Cp(tet)H and Lu(CH2Ph)3THF3. Compound 1 reacts with 1 or 2 equiv of H2NCH2R (R = C6H5, 1-C10H7) to give the corresponding imido complexes [{Bo(M)Cp(tet)}LuNCH2R]2 (R = C6H5 (2a), 1-C10H7 (2b)) or amido complexes {Bo(M)Cp(tet)}Lu(NHCH2R)2 (R = C6H5 (3a), 1-C10H7 (3b)). Once isolated, the imido species are insoluble in nonprotic organic solvents.

Divergent reaction pathways of tris(oxazolinyl)borato zinc and magnesium silyl compounds.

Synthesis and reactivity of monomeric magnesium and zinc silyl compounds To(M)M-Si(SiHMe2)3 and To(M)M-Si(SiMe3)3 are described (To(M) = tris(4,4-dimethyl-2-oxazolinyl)phenylborate). The magnesium compounds react slowly with water and air, while the zinc compounds are inert. With CO2, To(M)Mg-Si(SiHMe2)3 provides To(M)MgO2CSi(SiHMe2)3 through CO2 insertion, whereas To(M)Zn-Si(SiHMe2)3 affords To(M)ZnOCHO.