β-SiH-Containing Tris(silazido) Rare-Earth Complexes as Homogeneous and Grafted Single-Site Catalyst Precursors for Hydroamination

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A series of homoleptic rare-earth silazido compounds and their silica-grafted derivatives were prepared to compare spectroscopic and catalytic features under homogeneous and interfacial conditions. Trivalent tris(silazido) compounds Ln{N(SiHMe2)tBu}3 (Ln = Sc (1), Y (2), Lu (3)) are prepared in high yield by salt metathesis reactions. Solution-phase and solid-state characterization of 1–3 by NMR and IR spectroscopy and X-ray diffraction reveals Ln↼H–Si interactions. These features are retained in solvent-coordinated 2·Et2O, 2·THF, and 3·THF. The change in spectroscopic features characterizing the secondary interactions (νSiH, 1JSiH) from the unactivated SiH in the silazane HN(SiHMe2)tBu follows the trend 3 > 2 > 1 ≈ 2·Et2O > 2·THF ≈ 3·THF. Ligand lability follows the same pattern, with Et2O readily dissociating from 2·Et2O while THF is displaced only during surface grafting reactions. 1 and 2·THF graft onto mesoporous silica nanoparticles (MSN) to give Ln{N(SiHMe2)tBu}n@MSN (Ln = Sc (1@MSN), Y (2@MSN)) al...