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http://nopr.niscpr.res.in/handle/123456789/41303Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Ghosh, Alak Kumar | - |
| dc.contributor.author | Ghosh, Shyamal | - |
| dc.contributor.author | De, G S | - |
| dc.date.accessioned | 2017-04-19T06:10:45Z | - |
| dc.date.available | 2017-04-19T06:10:45Z | - |
| dc.date.issued | 1996-04 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/41303 | - |
| dc.description | 342-345 | en_US |
| dc.description.abstract | The kinetics of anation of [Rh(OH2)5(OH)]2+ by ![]() -methionine has been studied spectrophotometrically by monitoring the characteristic absorption peak of the product complex (λmax = 262 nm) as a function of substrate and ligand concentrations in the 50-65°C temperature range and in the pH range 2.5-4.3. The rate law involving the outersphere complex formation has been established at pH 4.3 as . The activation parameters have been calculated and compared with those for water exchange reaction and other substitution reactions. A mechanism· involving the prior formation of an outersphere complex followed by associative interchange (Ia) is suggested where both bond making and bond breaking are equally important in the transition state. | 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.35A(04) [April 1996] | en_US |
| dc.title | Kinetics and mechanism of anation of hydroxopentaaquarhodium(III) ion by ![]() -methionine | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.35A(04) [April 1996] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 35A(4) 342-345.pdf | 792.54 kB | Adobe PDF | View/Open |
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-methionine has been studied spectrophotometrically by monitoring the characteristic absorption peak of the product complex (λmax = 262 nm) as a function of substrate and ligand concentrations in the 50-65°C temperature range and in the pH range 2.5-4.3. The rate law involving the outersphere complex formation has been established at pH 4.3 as
. The activation parameters have been calculated and compared with those for water exchange reaction and other substitution reactions. A mechanism· involving the prior formation of an outersphere complex followed by associative interchange (Ia) is suggested where both bond making and bond breaking are equally important in the transition state.