SCHEDULED MAINTENANCE
Racemic monoperoxovanadium(v) complexes with achiral OO and ON donor set heteroligands: synthesis, crystal structure and stereochemistry of [NH3(CH2)2NH3][VO(O2)(ox)(pic)]·2H2O and [NH3(CH2)2NH3][VO(O2)(ox)(pca)]
Abstract
Monoperoxovanadium(V) complexes, [NH3(CH2)2NH3][VO(O2)(ox)(pic)]·2H2O (1) and [NH3(CH2)2NH3][VO(O2)(ox)(pca)] (2) [NH3(CH2)2NH3 = ethane-1,2-diammonium(2+), ox = oxalate(2−), pic = pyridine-2-carboxylate(1−), pca = pyrazine-2-carboxylate(1−)], were synthesized and characterized by X-ray analysis, IR and Raman spectroscopies. The five equatorial positions of the pentagonal bipyramid around the vanadium atoms are occupied by the η2-peroxo ligand, two oxygen atoms of the ox, and the nitrogen atom of the pic or pca ligands, respectively. The oxo ligand and the oxygen atom of pic or pca are in the axial positions. Networks of X–H⋯O (X = C, N or O) hydrogen bonds, and π–π interactions between aromatic rings in 1 and anion–π interactions in 2, determine the molecular packings and build up the supramolecular architecture. Three stereochemical rules for occupation of the donor sites in two-heteroligand [VO(O2)(L1)(L2)] complexes (L1, L2 are bidentate neutral or differently charged anionic heteroligands providing an OO, NN or ON donor set) are discussed. 1 and 2 crystallize as racemic compounds. The 51V NMR spectra proved that the parent complex anions of 1 and 2 partially decompose on dissolution in water to the monoperoxo–ox, –pic or –pca complexes.
![Graphical abstract: Racemic monoperoxovanadium(v) complexes with achiral OO and ON donor set heteroligands: synthesis, crystal structure and stereochemistry of [NH3(CH2)2NH3][VO(O2)(ox)(pic)]·2H2O and [NH3(CH2)2NH3][VO(O2)(ox)(pca)]](/en/Image/Get?imageInfo.ImageType=GA&imageInfo.ImageIdentifier.ManuscriptID=B504211A&imageInfo.ImageIdentifier.Year=2005)
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