The reactions of A13+ ion with a series of aminopolycarboxylic acids containing coordinating sites (denticity, n) ranging from 3 to 8 were studied by potentiometric and "A1 NMR methods. Hydrolysis constants of the complexes were determined by potentiometry. The 27Al {'H} NMR data indicate a nearly l
Studies on complex species of aluminium with aminocarboxylic acids by 27Al NMR spectroscopy
✍ Scribed by S. B. Karweer; B. P. Pillai; R. K. Iyer
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 214 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The reactions of Al^3+^ ion with glycine, picolinic acid, 1,2‐propylenediaminetetraacetic acid and triethylenetetra‐minehexaacetic acid (H~p~L) were studied by potentiometric and ^27^Al NMR methods, and the complex species in solution at different pH values were identified. Acidic hydrolysis of the Al‐PDTA complex results in the formation of [AIL]^−^, [Al(H~2~O)LH] and [Al(H~2~O)~2~LH~2~]^+^ prior to dissociation, while base hydrolysis takes place through the monohydroxo species. Although TTHA is a decadentate ligand, the maximum number of donor sites utilized in the formation of the 1:1 Al‐TTHA complex is only five.
📜 SIMILAR VOLUMES
## Abstract Proton spin‐spin coupling values measured for a wide range of tetrasubstituted tetrahydropyran ring‐systems obtained from aldopentopyranose sugars have been correlated with values calculated from a generalized version of the Karplus equation which takes into account the electronegativit