Reactivity of Cr(III) μ-oxo compounds: catalyst regeneration and atom transfer processes.

Oxidation of CpCr[(XylNCMe)(2)CH] (Xyl = 2,6-Me(2)C(6)H(3)) with pyridine N-oxide or air generated the μ-oxo dimer, {CpCr[(XylNCMe)(2)CH]}(2)(μ-O). The μ-oxo dimer was converted to paramagnetic Cr(III) CpCr[(XylNCMe)(2)CH](X) complexes (X = OH, O(2)CPh, Cl, OTs) via protonolysis reactions. The related Cr(III) alkoxide complexes (X = OCMe(3), OCMe(2)Ph) were prepared by salt metathesis and characterized by single crystal X-ray diffraction. The interconversion of the Cr(III) complexes and their reduction back to Cr(II) with Mn powder were monitored using UV-vis spectroscopy. The related CpCr[(DepNCMe)(2)CH] (Dep = 2,6-Et(2)C(6)H(3)) Cr(II) complex was studied for catalytic oxygen atom transfer reactions with PPh(3) using O(2) or air. Both Cr(II) complexes reacted with pyridine N-oxide and γ-terpinene to give the corresponding Cr(III) hydroxide complexes. When CpCr[(DepNCMe)(2)CH] was treated with pyridine N-oxide in benzene in the absence of hydrogen atom donors, a dimeric Cr(III) hydroxide product was isolated and structurally characterized, apparently resulting from intramolecular hydrogen atom abstraction of a secondary benzylic ligand C-H bond followed by intermolecular C-C bond formation. The use of very bulky hexaisopropylterphenyl ligand substituents did not preclude the formation of the analogous μ-oxo dimer, which was characterized by X-ray diffraction. Attempts to develop a chromium-catalyzed intermolecular hydrogen atom transfer process based on these reactions were unsuccessful. The protonolysis and reduction reactions of the μ-oxo dimer were used to improve the previously reported Cr-catalyzed radical cyclization of a bromoacetal.