Please use this identifier to cite or link to this item: http://repository.aaup.edu/jspui/handle/123456789/625
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dc.contributor.authorismail warad, $Other$Palestinian-
dc.contributor.authormohammed al-nuri, $Other$Palestinian-
dc.contributor.authormaher abu eid, $Other$Palestinian-
dc.contributor.authorzeid al-othman, $Other$Other-
dc.contributor.authorsaud al-resayes, $Other$Other-
dc.contributor.authornizam diab-
dc.date.accessioned2020-02-05T07:25:44Z-
dc.date.available2020-02-05T07:25:44Z-
dc.date.issued2010-
dc.identifier.urihttp://repository.aaup.edu/jspui/handle/123456789/625-
dc.description.abstractThe kinetics of oxidation of L-cysteine by 3-di-2-pyridylketone-2-thiophenylhydrazone-iron(III), [Fe(DPKTH)2]3+ complex in acidic medium was studied spectrophotometrically at 36 oC temperature. The molar ratios of DPKTH to iron(III) and iron(II) individually, were found to be [2:1] [DPKTH : iron(III)/(II)]. The reaction was stroked to be first-order with respect to iron(III) and L-cysteine, second-order with respected to DPKTH ligand and reversed second-order with respected to hydrogen ion concentration. Added salts did not affect the rate and no free radical was detected when radical detector was placed in the reaction mixture. Ethanol solvent ratio was found to effect both the initial rate and the maximum absorbance (?max) of [Fe(DPKTH)2]2+ complex. The initial rate rose when the temperature was increased which empowered to calculate the activation parameters. A suitable reaction mechanism was proposed.en_US
dc.publisherE-Journal of Chemistry, 2010, 7(S1), S527-S535.en_US
dc.subjectIron(II)en_US
dc.subjectKineticsen_US
dc.subjectL -cysteineen_US
dc.subject3- Di -2-pyridylketone-2-thiophenylhydrazone ligand.en_US
dc.titleKinetics and Mechanism of Oxidation of L-Cysteine by Bis-3-di-2-pyridylketone-2-thiophenylhydrazone- iron(III) Complex in Acidic Mediumen_US
dc.typeArticleen_US
Appears in Collections:Faculty & Staff Scientific Research publications

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