Department of Chemistry, University of California-Irvine, 1102 Natural Sciences II, Irvine, California 92697, USA.
J Am Chem Soc. 2012 Feb 1;134(4):1996-9. doi: 10.1021/ja210957u. Epub 2012 Jan 20.
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 FeCp(2) 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)(Δ(18)O = 31 cm(-1)). Mn Kβ X-ray emission spectra showed Kβ' and Kβ(1,3) bands at 6475.92 and 6490.50 eV, respectively, which are characteristic of a high-spin Mn(V) center.
氧合锰(V)物种在各种生物和合成过程中都有涉及,包括它们在光合作用中氧气释放复合物的关键反应中心的作用。几乎所有单核 Mn(V)-氧合配合物都具有四方对称,产生低自旋物种。现在报道了一种新的高自旋 Mn(V)-氧合配合物,它是由具有三角对称的 well-characterized oxomanganese(III) 配合物制备的。用 FeCp(2) 进行的氧化实验通过光学和电子顺磁共振(EPR)光谱进行监测,并支持高自旋氧合锰(V)配合物的配方。平行模式的 EPR 谱在 g = 4.01 处具有独特的 S = 1 信号,具有 A(z) = 113 MHz 的六线超精细图案。共振拉曼光谱支持存在氧配体,其在 737 和 754 cm(-1) 处显示出 O-同位素敏感峰,分配为以 746 cm(-1)(Δ(18)O = 31 cm(-1))为中心的费米双重态。Mn Kβ X 射线发射光谱显示 Kβ'和 Kβ(1,3) 带分别在 6475.92 和 6490.50 eV 处,这是高自旋 Mn(V)中心的特征。