2019/10/16 by Baishakhi Mondal, Dibyajyoti Borah, Rakesh Mazumdar +1 · 1 citation
Biochemistry, Genetics and Molecular Biology · Materials Science · Chemistry · #Electron Spin Resonance Studies #Porphyrin and Phthalocyanine Chemistry #Metal-Catalyzed Oxygenation Mechanisms
paper · doi:10.1021/acs.inorgchem.9b02359
A nitrosyl complex of MnII-porphyrinate, [(F20TPP)MnII(NO)], 1 (F20TPPH2 = 5,10,15,20 tetrakis(pentafluorophenyl)porphyrin), was synthesized and characterized. Spectroscopic and structural characterization revealed complex 1 as a penta-coordinated MnII-nitrosyl with a linear Mn–N–O (180.0°) moiety. Complex 1 does not react with O2. However, it reacts with superoxide (O2–) in THF at −80 °C to result in the corresponding nitrate (NO3–) complex, 2, via the formation of a presumed MnIII-peroxynitrite intermediate. ESI-mass spectrometry and UV–visible and X-band EPR spectroscopic studies suggest the generation of MnIV-oxo species in the reaction through homolytic cleavage of the O–O bond of the peroxynitrite ligand as proposed in NOD activity. The intermediate formation of the MnIII-peroxynitrite was further supported by the well accepted phenol ring nitration which resembles the biologically well-established tyrosine nitration.