Synthesis and Coordination of the New Chiral Tridentate O,N,O Ligand 2,6-Bis[(1S,2S,5R)-(−)-menthyl]pyridine to Molybdenum(VI) and Vanadium(V) Oxo Complexes: Crystal Structures of [(2,6-Bis{(−)-menthyl}pyridine)MoO2] and [(2,6-Bis{(−)-menthyl}pyridine)VO]2(μ-O)

Stéphane Bellemin‐Laponnaz, Karl S. Coleman, Peter Dierkes, Jean-Pierre Masson, John A. Osborn

European Journal of Inorganic Chemistry · 2000 · 46 citations · 12 references

Concepts

Abstract

The novel tridentate chiral ligand 2,6-bis{(−)-menthyl}pyridine (1), was readily prepared from the reaction of 2,6-dilithiopyridine with (−)-menthone. Reaction of 1 with VO(OiPr)3 and [MoO2(acac)2] resulted in the formation of the new metal-oxo complexes [VO(ONO)]2(μ-O) (2) and [MoO2(ONO)] (3) [ONO = (1 − 2 H)]. Both metal-oxo compounds 2 and 3 have demonstrated the ability to catalyze the asymmetric oxidation of prochiral olefins with tBuOOH as the oxidant. The compounds 1−3 have been fully characterized by 1H, 13C and 51V (where appropriate) NMR spectroscopy, mass spectrometry, microanalysis and IR spectroscopy. Furthermore, the molecular structures of 2 and 3 have been determined by single-crystal X-ray diffraction.

References

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