Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46688
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dc.contributor.authorReddy, M Shankar-
dc.contributor.authorRam, Kashi-
dc.contributor.authorReddy, M G Ram-
dc.date.accessioned2019-03-26T06:05:45Z-
dc.date.available2019-03-26T06:05:45Z-
dc.date.issued1989-05-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46688-
dc.description437-439en_US
dc.description.abstractThe formation constants of 1 : 1 and 1 : 2 binary (Cu-A and Cu-A2) and 1: 1 : 1 ternary (Cu-A-L) chelates [where A= 4-amino-5-mercapto-l,2,4-triazole (AMT) or 4-amino-5-mercapto- 3-methyl-l ,2,4-triazole (AMMT) and L= ethylenediamine (en); 1,10-phenanthroline (Phen); 2,2'-bipyridyl (Bipy), o-phenylenediamine (OPDA); glycine (Gly); o-aminophenol (o-AP); catechol (Cat); oxalic acid (Oxa) or thiodiacetic acid (TDA)] have been determined potentiometrically in aqueous medium. The ligands AMT and AMMT behave as primary ligands in presence of en, Gly, o-AP and Cat, while in presence of Phen, Bipy, NTA, IMDA and Oxa, they act as secondary ligands. They coordinate simultaneously in presence of OPDA and TDA. The overall stability constants, Log βAL, are discussed in terms of the basicity of ligands, statistical aspects, electrostatic interaction, metal-ligand π-interaction, denticity, nature of donor sites and stereochemical aspects.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.28A(05) [May 1989]en_US
dc.titleFormation constants of binary & ternary complexes of Cu (II) with substituted 1,2,4-triazoles & some O,O; O,N & N,N donors in aqueous mediumen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.28A(05) [May 1989]

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