|کد مقاله||کد نشریه||سال انتشار||مقاله انگلیسی||ترجمه فارسی||نسخه تمام متن|
|1401140||984677||2016||6 صفحه PDF||سفارش دهید||دانلود کنید|
• Sonochemical synthesis of a new tetradentate oxovanadium complex.
• Highest yield and Shorter reaction time than in conventional pathway.
• The complex crystallises in the monoclinic system.
• The metal center exhibits a quasi reversible redox system on GC electrode.
The oxovanadium (IV) complex “VOL” of a tetradentate Schiff base ligand derived from the condensation of diaminoethane and 2-hydroxy-1-naphthaldehyde was efficiently prepared via ultrasound irradiation and the template effect of VO(acac)2.The resulting product was characterized by elemental analysis, infrared, electronic absorption and molar conductance measurement. Single X-ray structure analysis showed that the complex is a monomeric five-coordinate with a distorted square pyramidal geometry. It crystallizes in monoclinic system having unit cell parameters a = 8.3960 (5) Å; b = 12.5533 (8) Å and c = 18.7804 (11) Å; α = γ = 90°; β = 104.843°(2), with P 21/c space group.Cyclic voltammetry of the complex, carried out on a glassy carbon (GC) electrode in DMF, showed reversible cyclic voltammograms response in the potential range 0.15–0.60 V involving a single electron redox wave VV/VIV, the diffusion coefficient is determinedusing GC rotating disk electrode. The Levich plot Ilim = f(ω1/2), was used to calculate the diffusion-convection controlled currents.
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Journal: Journal of Molecular Structure - Volume 1120, 15 September 2016, Pages 239–244