Bimetallic Cleavage of Aromatic C–H Bonds by Rare-Earth-Metal Complexes

Rare-earth metal hydroxylamide complexes.

The rare-earth metal hydroxylamide compound Y[N(SiHMe2)2]2[ONBn2][THF] (1) was prepared by the silylamide elimination pathway from the reaction of N,N-dibenzylhydroxylamine, Bn2NOH (Bn = CH2C6H5), with Y[N(SiHMe2)2]3[THF]2 and was characterised by multinuclear NMR spectroscopy and elemental analysis. The compounds [Cp2Y(ONBn2)]2 (2a) [Cp2Sm(ONBn2)]2 (2b) were obtained by the reactions of MCp3 (...

Metal-metal bonds in bimetallic surfaces.

Cleavage of unreactive bonds with pincer metal complexes.

Since the first reports some three decades ago, the chemistry of pincer metal complexes has seen a tremendous development with impact on materials chemistry, supramolecular chemistry, bioorganometallics, and, presumably most significantly, on (catalytic) bond making and breaking processes. The remarkable progress is due to a large extent to the well-defined nature and tunability of the pincer l...

Tetrahydropentalenyl-phosphazene constrained geometry complexes of rare-earth metal alkyls.

Reactions of Cp™HPPh2 (1, diphenyl(4,4,6,6-tetramethyl-1,4,5,6-tetrahydropentalen-2-yl)phosphane) with the organic azides AdN3 and DipN3 (Ad = 1-adamantyl; Dip = 2,6-di-iso-propylphenyl) led to the formation of two novel CpPN ligands: P-amino-cyclopentadienylidene-phosphorane (Cp™PPh2NHAd; L(Ad)H) and P-cyclopentadienyl-iminophosphorane (Cp™HPPh2NDip; L(Dip)H). Both were characterized by NMR sp...

Chiral poly-rare earth metal complexes in asymmetric catalysis

Asymmetric catalysis is a powerful component of modern synthetic organic chemistry. To further broaden the scope and utility of asymmetric catalysis, new basic concepts for the design of asymmetric catalysts are crucial. Because most chemical reactions involve bond-formation between two substrates or moieties, high enantioselectivity and catalyst activity should be realized if an asymmetric cat...