Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46314
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dc.contributor.authorDash, Anadi C-
dc.contributor.authorDas, Smrutiprava-
dc.contributor.authorNanda, Rabindra K-
dc.date.accessioned2019-03-20T11:44:33Z-
dc.date.available2019-03-20T11:44:33Z-
dc.date.issued1990-03-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46314-
dc.description227-230en_US
dc.description.abstractThe (ɑβS) [(tetren)CoO2CCH2NH3]3+ ion undergoes hydrolysis at 25-40ᵒC  and pH = (6.9-8.2 via a single kinetic-controlled path. The high rate of spontaneous aquation of the glycinato complex, in contrast to the extreme inertness of its N-protonated form to aquation, is consistent with the operation of an intramolecular conjugate base mechanism (SNICB) involving the generation of a reactive conjugate base via the NH - deprotonation of the amine function of the coordinated tetren ligand by the unbound – NH2 group of the glycine ligand.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.29A(03) [March 1990]en_US
dc.titleKinetics and mechanism of hydrolysis of (ɑβS)-(glycinato-O) (tetraethylenepentamine)cobalt (III) ionen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.29A(03) [March 1990]

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