Electrochemical evidence that pyranopterin redox chemistry controls the catalysis of YedY, a mononuclear Mo enzyme

A Tetracoordinated Phosphasalen Nickel(III) Complex Angewandte Chemie International Edition by Thi-Phuong-Anh Cao, Grégory Nocton, Louis Ricard, Xavier F. Le Goff, Audrey Auffrant  /  2d  //  keep unread  //  hide  //  preview Abstract The oxidation of a NiII complex bearing a tetradentate phosphasalen ligand, which differs from salen by the presence of an iminophosphorane (PN) in place of an imine unit, was easily achieved by addition of a silver salt. The site of this oxidation was investigated with a combination of techniques (NMR, EPR, UV/Vis spectroscopy, X-ray diffraction, magnetic measurements) as well as DFT calculations. All data are in agreement with a high-valent NiIII center concentrating the spin density. This markedly differs from precedents in the salen series for which oxidation on the metal was only observed at low temperature or in the presence of additional ligands or anions. Therefore, thanks to the good electron-donating properties of the phosphasalen ligand, [Ni(Psalen)]+ represents a rare example of a tetracoordinated high-valent nickel complex in presence of a phenoxide ligand. P=N does not equal C=N: A rare tetracoordinated NiIIIcomplex is obtained in the one-electron oxidation of a nickel(II) complex containing a novel phosphasalen ligand. The metal center as the oxidation site, and not the ligand as is the case for nickel salen complexes, is demonstrated by various techniques such as X-ray diffraction, EPR spectrocopy, and DFT calculations (see picture). Visit Website +TAG