Please use this identifier to cite or link to this item:
|Type:||Artigo de periódico|
|Title:||Molecular structure of the molybdenum oxo-diperoxo compound MoO(O-2)(2)(OPy)(H2O): A computational and X-ray study|
|Abstract:||We have carded out a combined experimental and theoretical study of the molecular structure of the-MoO(O-2)(2)- (OPy)(H2O) coordination compound using X-ray crystallography and DFT-B3LYP computational method, respectively. The MoO(O-2)(2)(OPY)(H2O) Complex crystallizes in the orthorhombic space group Pmna with Z = 4, a = 6.9001(9) Angstrom, b =8.0471(1) Angstrom, c = 16.227(2) Angstrom, V = 901.0(2) Angstrom (3), and the X-ray data analysis yields a bipyramidal-pentagonal coordination polyhedron for the Mo atom. The pyridine N-oxide (OPy) ligand occupies the equatorial position, with the oxygen atom of this ligand being located in the same plane as the four peroxo oxygen atoms. The H2O ligand is situated trans to the oxo group, forming intermolecular hydrogen bonds with peroxo groups belonging,to two adjacent complexes. In our theoretical approach these intermolecular interactions were taken into account by including two methanol molecules which form hydrogen bonds with the water ligand leading to a good agreement between the calculated and the experimental geometry. Our results suggest that it is necessary to take into account the presence of these interactions in order to reconcile the theoretical results to the experimental data, in particular the distance between Mo and the oxygen of water ligand. These results seem,to be a general feature for analogous bis-peroxo complexes that have been reported in the literature.|
|Editor:||Amer Chemical Soc|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.