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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Singh, R K | - |
| dc.contributor.author | Saxena, M C | - |
| dc.date.accessioned | 2019-03-22T10:09:48Z | - |
| dc.date.available | 2019-03-22T10:09:48Z | - |
| dc.date.issued | 1990-08 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/46423 | - |
| dc.description | 822-824 | en_US |
| dc.description.abstract | Formation Constants (log K ) of the mixed complexes of the type MAL, where M = UO + or Th4+ , A= iminodiacetate (IMDA), nitrilotriacetate (NTA), 2-hydroxyethylethylenediaminetriacetate (HEDTA), ethylenediaminetetracetate (EDTA), 1,2- diaminocyclohexanetetraacetate (CDT A) or diethylenetriaminepentaacetate (DTPA), and L=catechol (cat), 4-methylcatechol (m-cat), tiron (tir), 2,3-dihydroxynaphthalene (DHN) or chromotropic acid salt (CS), have been determined potentiometrically by the Irving-Rossotti approach at 25°C and at an ionic strength, I = 0.2 (mol dm-3, KNO3). The observed trends in solution stabilities arc (i) Th4+ > UO , (ii) CS > tir > DHN > m-cat > cat, and (iii) IMDA > NTA > HEDTA > EDTA > CDTA > DTPA with respect to the metal ions, secondary ligands (L) and primary Iigands (A), respectively. The logK values are negative. The formation constnats log K and log K have also been determined and compared with the log K values. | 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.29A(08) [August 1990] | en_US |
| dc.title | Formation constants of mixed ligand complexes of UO and Th4+ with complexones and oxygen donor ligands | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.29A(08) [August 1990] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 29A(8) 822-824.pdf | 185.12 kB | Adobe PDF | View/Open |
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) of the mixed complexes of the type MAL, where M = UO + or Th4+ , A= iminodiacetate (IMDA), nitrilotriacetate (NTA), 2-hydroxyethylethylenediaminetriacetate (HEDTA), ethylenediaminetetracetate (EDTA), 1,2- diaminocyclohexanetetraacetate (CDT A) or diethylenetriaminepentaacetate (DTPA), and L=catechol (cat), 4-methylcatechol (m-cat), tiron (tir), 2,3-dihydroxynaphthalene (DHN) or chromotropic acid salt (CS), have been determined potentiometrically by the Irving-Rossotti approach at 25°C and at an ionic strength, I = 0.2 (mol dm-3, KNO3). The observed trends in solution stabilities arc (i) Th4+ > UO
, (ii) CS > tir > DHN > m-cat > cat, and (iii) IMDA > NTA > HEDTA > EDTA > CDTA > DTPA with respect to the metal ions, secondary ligands (L) and primary Iigands (A), respectively. The
logK values are negative. The formation constnats log K
and log K
have also been determined and compared with the log K