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http://nopr.niscpr.res.in/handle/123456789/43902Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Karweer, S B | - |
| dc.contributor.author | Mhatre, S N | - |
| dc.contributor.author | Pillai, B P | - |
| dc.contributor.author | Iyer, R K | - |
| dc.contributor.author | Moorthy, P N | - |
| dc.date.accessioned | 2018-03-20T04:27:18Z | - |
| dc.date.available | 2018-03-20T04:27:18Z | - |
| dc.date.issued | 1993-06 | - |
| dc.identifier.issn | IJC-A Vol.32A(06) [June 1993] | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/43902 | - |
| dc.description | 502-505 | en_US |
| dc.description.abstract | High field variable pH 27Al NMR spectral studies of AlCl3-malic acid system show the formation of as many as four complex species in the pH range 2-8. The binding of malate to aluminium takes place through the hydroxyl and carboxyl groups resulting in five- and six-membered chelate rings with deprotonation of the hydroxyl group. Malate functions either as a bidentate or a tridentate ligand. The 1:1 AI-malate chelate has been isolated and characterised by elemental analysis, potentiometric titration and IR spectroscopy. The results indicate deprotonation of hydroxyl group and bidentate nature of carboxylate groups. A bridged polymeric structure has been proposed for the chelate. | 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.32A(06) [June 1993] | en_US |
| dc.title | Studies on speciation of aluminium complexes with malic acid by high field 27Al NMR spectroscopy | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.32A(06) [June 1993] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 32A(6) 502-505.pdf | 3.31 MB | Adobe PDF | View/Open |
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