Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/46051
Title: Hydrogen bonding or transient coordination of pendant group: Cause for lability in ligand substitution reaction of aminopolycarboxylatoruthenium(III) complexes
Authors: Khan, M M Taqui
Bajaj, H C
Chatterjee, Debabrata
Issue Date: Mar-1992
Publisher: NISCAIR-CSIR, India
Abstract: The rate of substitution of water molecule in [LRuIII(H2O)l complexes [L= ethylenediaminetetraacetate (EDTA) anion and N-hydroxyethylethylenediaminetriacetate (HEDTRA) anion] with CI- ion has been studied spectrophotometrically in aqueous medium at 30°C. The rates of substitutions of CI- in [LRuCI] with thiocyanate (SCN-) have also been studied as a function of SCN- concentration in the temperature range 30-50°C. In both the cases, ruthenium(III)-EDTA is found to be more reactive than the corresponding HEDTRA complex. Activation parameters H and S for the substitution of [LRuIIICI]- complexes with SCN- are determined and a suitable mechanism is proposed. The reactivity of [LRuIIICI]- towards SCN- substitution is discussed in terms of the transient coordination of the uncoordinated - COOH or -CH2 - OH pendant group which assists in the elimination of leaving group and ligation of substituting nucleophiles.
Page(s): 152-155
URI: http://nopr.niscair.res.in/handle/123456789/46051
ISSN: 0975-0975(Online); 0376-4710(Print)
Appears in Collections:IJC-A Vol.31A(03) [March 1992]

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