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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Dash, Anadi C | - |
| dc.contributor.author | Acharya, Achyutananda | - |
| dc.contributor.author | Sahoo, Rama K | - |
| dc.date.accessioned | 2017-02-08T11:14:46Z | - |
| dc.date.available | 2017-02-08T11:14:46Z | - |
| dc.date.issued | 1998-09 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/40267 | - |
| dc.description | 759-764 | en_US |
| dc.description.abstract | The reversible complexation of cobalt(II) with 2-(irnidaioleazo) benzene (lAB) and 2-(2-aminoethyl)benzimidazole (AEB) has been studied at l=0.3 mol dm-3. At 25°C the values of log KM (KM is the stability constant), ∆H0/KJ mol-1, and ∆S0/JK-1 mol'! are 2.09±0.03, 14.4±2.4, 88±8 for Co(IAB)2+ and 2.65±0.01, 20.0±7.2, 120±21 for Co(AEB)2+ respectively. The rate constants of formation of COL2+chelate via the reaction: CO(OH2)62++L Co(OH2)4L2+., (10-4 k/dm-3 mol-1 s-1=11.7±0.4 (lAB), 1.01±0.03 (AEB) at 10°C) are at least 10 times smallerthan the rate constant of water exchange from Co(OH2)62+.Data analysis further indicates that the chelate formation involves Chelation Controlled Substitution mechanism. The dissociation of Co(AEB)2+ is strongly acid catalysed unlike that for Co(IAB)2+. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-A Vol.37A(09) [September 1998] | en_US |
| dc.title | Complex formation of cobalt(II) with 2-(imidazoleazo )benzene and 2-(2-aminoethyl)benzimidazole: A kinetic and equilibrium study | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.37A(09) [September 1998] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 37A(9) 759-764.pdf | 565.92 kB | Adobe PDF | View/Open |
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