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http://nopr.niscpr.res.in/handle/123456789/39927Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Shukla, Anju | - |
| dc.contributor.author | Upadhyay, Santosh K | - |
| dc.date.accessioned | 2017-01-31T09:53:32Z | - |
| dc.date.available | 2017-01-31T09:53:32Z | - |
| dc.date.issued | 1995-02 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/39927 | - |
| dc.description | 120-123 | en_US |
| dc.description.abstract | The kinetics of oxidation of primary amines (n-butylamine and isopropylamine) and aminoalcohols (2-aminoethanol and 3-aminopropanol) by alkaline hexacyanoferrate(III) have been studied in the presence of PdCl2 as catalyst. The order of reaction in Fe(CN) is always unity while that in substrate decreases from unity at higher [substrate]. The rate is proportional to [Pd(ll)] and is independent to [OH-] (under the conditions when [OH-]> [PdCI2]). A mechanism involving {Pd(ll)-A} and {Pd(II)-(A)2} (where A represents amine or aminoalcohol) intermediate complexes is proposed. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights | src='http://nopr.niscair.res.in/image/cc-license-sml.png'> CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-A Vol.34A(02) [February 1995] | en_US |
| dc.title | Kinetics and mechanism of Pd(II) catalysed oxidation of some primary amines and aminoalcohols by alkaline hexacyanoferrate(lll) | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.34A(02) [February 1995] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 34A(2) 120-123.pdf | 854.48 kB | Adobe PDF | View/Open |
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is always unity while that in substrate decreases from unity at higher [substrate]. The rate is proportional to [Pd(ll)] and is independent to [OH-] (under the conditions when [OH-]> [PdCI2]). A mechanism involving {Pd(ll)-A} and {Pd(II)-(A)2} (where A represents amine or aminoalcohol) intermediate complexes is proposed.