Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/43811
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dc.contributor.authorNandel, Fateh S-
dc.contributor.authorJain, Dharam V S-
dc.date.accessioned2018-03-13T09:33:28Z-
dc.date.available2018-03-13T09:33:28Z-
dc.date.issued1993-04-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/43811-
dc.description323-325en_US
dc.description.abstractThe intermediate [Fe(CN)6SO3]4- is formed in the reaction between [Fe(CN)6]3- and [SO3]2-. The oxidation of the intermediate to [Fe(CN)6]3- in presence of H2O2 has been studied by monitoring the increase in the [Fe(CN)6]3- absorbance at 420 nm. The rate constant thus obtained is found similar to that for the hydrolysis of the intermediate under comparable conditions. The kinetic data reveal that iron is in + 3 oxidation state in the intermediate and electron is transferred from the bound SO to [Fe(CN)6]3- during hydrolysis. These results are supported by the semi-empirical quantum mechanical calculations for the [Fe(CN)6]4- + SO3 system.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.32A(04) [April 1993]en_US
dc.titleOxidation state of iron in [Fe(CN)6SO3]4-en_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.32A(04) [April 1993]

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