Carbon dioxide reduction by dinuclear Yb(ii) and Sm(ii) complexes supported by siloxide ligands.

Two dinuclear homoleptic complexes of lanthanides(ii) supported by the polydentate tris(tertbutoxy) siloxide ligand ([Yb2L4], 1-Yb and [Sm2L4], 1-Sm, (L = (OtBu)3SiO-)) were synthesized in 70-80% yield and 1-Sm was crystallographically characterized. 1-Yb and 1-Sm are stable in solution at -40 °C but cleave the DME C-O bond over time at room temperature affording the crystal of [Yb2L4(µ-OMe)2(DME)2], 2. The 1-Yb and 1-Sm complexes effect the reduction of CO2 under ambient conditions leading to carbonate and oxalate formation. The selectivity of the reduction towards oxalate or carbonate changes depend on the solvent polarity and on the nature of the ion. For both the lanthanides, carbonate formation is favoured but oxalate formation increases if a non-polar solvent is used. Computational studies suggest that the formation of oxalate is favoured with respect to carbonate formation in the reaction of the dimeric lanthanide complexes with CO2. Crystals of the tetranuclear mixed-valence oxalate intermediate [Yb4L8(C2O4)], 3 were isolated from hexane and the presence of a C2O42- ligand bridging two [YbIIL2YbIIIL2] dinuclear moieties was shown. Crystals of the tetranuclear di-carbonate product [Sm4L8(µ3-CO3-κ4-O,O',O'')2], 4 were isolated from hexane. The structures of 3 and 4 suggest that the CO2 activation in non-polar solvents involves the interaction of two dimers with CO2 molecules at least to some extent. Such a cooperative interaction results in both oxalate and carbonate formation.

Grafting of a new bis-silylamido aluminum species on silica: insight from solid-state NMR into interactions with the surface.

The new bisamido aluminum species [AlCl{N(SiMe3)2}2(THF)] (1) was prepared and fully characterized by 27Al and 35Cl solid-state NMR, along with X-ray diffraction studies. 1 was grafted on silica partially dehydroxylated at 700 °C, affording silica-supported Al species. The resulting material (2) was characterized by IR, elemental analysis and 1H, 13C and 27Al solid-state MAS NMR. The 1D and 2D 27Al MAS NMR studies showed the occurrence of two types of species, where the Al center adopts a tetracoordinated coordination sphere, with as an additional coordinated Lewis base, either a THF ligand or a silica-surface siloxane moiety. DFT calculations allowed understanding the grafting mechanism and the spectroscopic properties of the material.