Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/39927
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dc.contributor.authorShukla, Anju-
dc.contributor.authorUpadhyay, Santosh K-
dc.date.accessioned2017-01-31T09:53:32Z-
dc.date.available2017-01-31T09:53:32Z-
dc.date.issued1995-02-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/39927-
dc.description120-123en_US
dc.description.abstractThe kinetics of oxidation of primary amines (n-butylamine and isopropylamine) and aminoalcohols (2-aminoethanol and 3-aminopropanol) by alkaline hexacyanoferrate(III) have been studied in the presence of PdCl2 as catalyst. The order of reaction in Fe(CN) is always unity while that in substrate decreases from unity at higher [substrate]. The rate is proportional to [Pd(ll)] and is independent to [OH-] (under the conditions when [OH-]> [PdCI2]). A mechanism involving {Pd(ll)-A} and {Pd(II)-(A)2} (where A represents amine or aminoalcohol) intermediate complexes is proposed.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rightssrc='http://nopr.niscair.res.in/image/cc-license-sml.png'> CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.34A(02) [February 1995]en_US
dc.titleKinetics and mechanism of Pd(II) catalysed oxidation of some primary amines and aminoalcohols by alkaline hexacyanoferrate(lll)en_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.34A(02) [February 1995]

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