Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 134, Issue 4, Pages 1996-1999Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja210957u
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Funding
- NIH [GM50781, GM77387, GM47365, GM55302]
- Office of Science, Office of Basic Energy Sciences (OBES), Division of Chemical Sciences, Geosciences and Biosciences, Department of Energy (DOE) [DE-AC02-05CH11231]
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Oxomanganese(V) species have been implicated in a variety of biological and synthetic processes, including their role as a key reactive center within the oxygen-evolving complex in photosynthesis. Nearly all mononuclear Mn-V-oxo complexes have tetragonal symmetry, producing low-spin species. A new high-spin Mn-V-oxo complex that was prepared from a well-characterized oxomanganese(III) complex having trigonal symmetry is now reported. Oxidation experiments with [FeCp2](+) were monitored with optical and electron paramagnetic resonance (EPR) spectroscopies and support a high-spin oxomanganese(V) complex formulation. The parallel-mode EPR spectrum has a distinctive S = 1 signal at g = 4.01 with a six-line hyperfine pattern having A(z) = 113 MHz. The presence of an oxo ligand was supported by resonance Raman spectroscopy, which revealed O-isotope-sensitive peaks at 737 and 754 cm(-1) assigned as a Fermi doublet centered at 746 cm(-1) (Delta O-18 = 31 cm(-1)). Mn K beta X-ray emission spectra showed K beta' and K beta(1,3) bands at 6475.92 and 6490.50 eV, respectively, which are characteristic of a high-spin Mn-V center.
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