投稿者:
Unknown
- First published: Full publication history
- DOI: 10.1002/anie.201508372View/save citation
- Cited by: 0 articles Check for new citations
-
[*] Dr. C. Deville, Dr. J. Sundberg, Prof. Dr. V. McKee, Prof. Dr. C. J. McKenzie
Department of Physics, Chemistry and Pharmacy University of Southern Denmark
S. K. Padamati, Prof. Dr. W. R. Browne
Molecular Inorganic Chemistry, Stratingh Institute for Chemistry University of Groningen
Abstract
A MnII complex, [Mn(dpeo)2]2+ (dpeo=1,2-di(pyridin-2-yl)ethanone oxime), activates O2, with ensuing stepwise oxidation of the methylene group in the ligands providing an alkoxide and ultimately a ketone group. X-ray crystal-structure analysis of an intermediate homoleptic alkoxide MnIII complex shows tridentate binding of the ligand via the two pyridyl groups and the newly installed alkoxide moiety, with the oxime group no longer coordinated. The structure of a MnII complex of the final ketone ligand, cis-[MnBr2(hidpe)2] (hidpe=2-(hydroxyimino)-1,2-di(pyridine-2-yl)ethanone) shows that bidentate oxime/pyridine coordination has been resumed. H218O and 18O2 labeling experiments suggest that the inserted O atoms originate from two different O2 molecules. The progress of the oxygenation was monitored through changes in the resonance-enhanced Raman bands of the oxime unit.
コメント