The formation of complexes (x,y, z) between x tungstate ions, y o-glycero-D-gulo-heptonate ions, and z protons was studied in aqueous solution by ~3C and ZS3W NMR spectroscopy. The overall equilibrium constant for the complex-forming reaction was obtained by a competition method, showing that a (2,2
A 13C and 183W NMR study of the structures of tungstate and molybdate complexes of volemitol
✍ Scribed by Stella Chapelle; Jean-François Verchère
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 829 KB
- Volume
- 266
- Category
- Article
- ISSN
- 0008-6215
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✦ Synopsis
~H, '3(2, and ~s3W NMR spectroscopic methods were used for the structural characterization of the tungstate and molybdate complexes of volemitol (u-glycero-D-manno-heptitol) in aqueous solution.
The major species (type E) are a pair of isomeric complexes formed at the arabino site in reversed orientation, i.e., HO-1,2,3,4 and HO.4,3,2,1. A single, minor complex is formed at the HO-3,4,5,6 altro site and is shown to be isostructural with the known single complexes of ribitol and D-altritol (type E'). The present NMR results support tile hypothesis that complexes of type E' are weaker than those of type E because they are destabilized by a steric strain due to the interaction of the side chain of the ligand with the site of chelation.
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