کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1338187 | 979661 | 2012 | 7 صفحه PDF | دانلود رایگان |

The Schiff base ligand N-salicylidin-2-bromoethylimine (L) and its vanadium(IV) complex, VOL2 (1), were synthesized and characterized by using X-ray, CHN, 1H NMR and FT-IR methods. X-ray analysis shows the Schiff base ligand L acts as a bidentate (O, N) chelating ligand and coordinates via imine nitrogen and phenolato oxygen atoms to the V(IV) center. The coordination geometry around the V(IV) center in 1 is approximately square pyramidal, as indicated by the unequal metal–ligand bond distances and angles, with the basal plane formed by the N2O2 donors of the two bidentate Schiff base ligands, the two phenolato O atoms and the two imine N atoms are in the trans position. The coordination sphere of the V(IV) is completed by one oxygen atom in apical position. In the Schiff base ligand, L, there are some classical intramolecular O1–H1⋯N1 and non-classical intermolecular C9–H9b⋯O1 hydrogen bonds, while in 1, there are two non-classical intermolecular C7–H7⋯O3 and C8–H8b⋯O3 hydrogen bonds. The catalytic activity of 1 in epoxidation of cyclooctene was investigated in different conditions to obtain optimum conditions. The effects of solvent, oxidant, catalyst concentration and alkene/oxidant ratio were studied and the results showed that in CCl4 in the presence of tert-butylhydroperoxide in 1:3 alkene/oxidant ratio, high epoxide yield was obtained. The epoxidation of alkenes was also carried out in optimized conditions that high catalytic activity and selectivity were obtained.
A new bidentate O, N Schiff base ligand (L) and its vanadyl complex (VOL2) were prepared. The ligand and complex was characterized by FT-IR, CHN analysis and 1H NMR. The crystal structure of the ligand and vanadyl complex was determined by X-ray analysis. The vanadyl complex showed high activity and selectivity in epioxidation of alkenes.Figure optionsDownload as PowerPoint slide
Journal: Polyhedron - Volume 31, Issue 1, 4 January 2012, Pages 265–271