Please use this identifier to cite or link to this item: https://dspace.univ-ouargla.dz/jspui/handle/123456789/27618
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dc.contributor.authorTahar DOUADI-
dc.contributor.authorTahar DOUADI-
dc.contributor.authorAli DOUADI-
dc.contributor.authorAli LOUNAS-
dc.date.accessioned2022-02-23T08:54:13Z-
dc.date.available2022-02-23T08:54:13Z-
dc.date.issued2015-10-
dc.identifier.issn2170-0672-
dc.identifier.urihttp://dspace.univ-ouargla.dz/jspui/handle/123456789/27618-
dc.descriptionAnnales des Sciences et Technologieen_US
dc.description.abstractThe azoimine ligand, bis [5-phenylazo-2- ydroxybenzaldehyde] -4, 4′- diaminophenyl ether (2) was synthesized by reducing the imine group of the azoimine form bis[5- phenylazo-2- ydroxybenzaldehyde] -4,4′-diiminophenyl ether (1), conducted by the condensation of 5-phenylazo-2-hydroxybenzaldehyde and 4,4′(diamino-diphenyl) ether. The compounds (1) and (2) were characterized using elemental analyses, IR, UV-Vis spectroscopy, 1H NMR, 13C NMR and mass spectra. The electrochemical study has been investigated by cyclic voltammetry techniqueen_US
dc.language.isofren_US
dc.relation.ispartofseriesvolume 7 numéro 2 AST 2015;-
dc.subjectAzo ligandsen_US
dc.subjectReductionen_US
dc.subjectOxidationen_US
dc.subjectScan rateen_US
dc.subjectCyclic voltammetryen_US
dc.titleCyclic voltammetry Studies of bis [5-phenylazo-2-hydroxybenzaldehyde]-4, 4′- diiminodiphenyl ether and its amine derivativeen_US
dc.typeArticleen_US
Appears in Collections:volume 7 numéro 2 AST 2015

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