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KINETICS AND MECHANISM OF THE REVERSIBLE FORMATION OF THE BINUCLEAR SPECIES BETWEEN PYRIDINE-2-CARBOXYLATO(PENTAAMMINE)COBALT(III) AND COBALT(II) IN AQUEOUS-SOLUTION

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dc.contributor.author Das, N.
dc.date.accessioned 2018-10-01T12:19:34Z
dc.date.available 2018-10-01T12:19:34Z
dc.date.issued 1993
dc.identifier.citation Proceedings Of The Indian Academy Of Sciences-Chemical Sciences, 105(4-5), 1993: 245-252
dc.identifier.issn 0253-4134
dc.identifier.uri http://ore.immt.res.in/handle/2018/408
dc.description.abstract The kinetics of formation and dissociation of the binuclear complex of cobalt(II) with pyridine-2-carboxylato(pentaammine) cobalt(III) have been studied in the temperature range 10-25-degrees-C and at I = 0.3 mol dm-3 (ClO4-). The formation of (NH3)5CoO2CC5H4NCo4+ in the pH range 2.35-3.20 involves the reaction of Co(OH2)62+ with the protonated (pyridine-N) and the deprotonated forms of the complex. The rate and activation parameters for the formation reaction are consistent with an I(d) mechanism. The binuclear species undergoes dissociation to yield the parent cobalt(III) substrate and cobalt(II) via spontaneous and acid-catalysed paths. The rate data at 20-degrees-C for the spontaneous dissociation of the binuclear complex and of mono(pyridine-2-carboxylato) cobalt(II) are comparable indicating the chelating nature of the binuclear species.
dc.language en
dc.publisher Indian Academy Of Science
dc.relation.isreferencedby SCI
dc.rights Copyright [1993]. All efforts have been made to respect the copyright to the best of our knowledge. Inadvertent omissions, if brought to our notice, stand for correction and withdrawal of document from this repository.
dc.subject Chemical Sciences
dc.title KINETICS AND MECHANISM OF THE REVERSIBLE FORMATION OF THE BINUCLEAR SPECIES BETWEEN PYRIDINE-2-CARBOXYLATO(PENTAAMMINE)COBALT(III) AND COBALT(II) IN AQUEOUS-SOLUTION
dc.type Journal Article
dc.affiliation.author CSIR-IMMT, Bhubaneswar 751013, Odisha, India


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