The formation of dinuclear tungstate and molybdate complexes of D-glycero-L-manno-heptose was studied in aqueous solution by J3C and t83W NMR spectroscopy. The chelating aldose is always tetradentate and occurs exclusively in furanose or acyclic hydrated forms, the proportions of which depend on the
A multinuclear NMR spectroscopy study of the tungstate and molybdate complexes of d-fructose and l-sorbose
✍ Scribed by Jean-Paul Sauvage; Jean-François Verchère; Stella Chapelle
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 486 KB
- Volume
- 286
- Category
- Article
- ISSN
- 0008-6215
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✦ Synopsis
The formation of dinuclear tungstate and molybdate complexes of D-fructose and L-sorbose was studied in aqueous solution by I H, ~3C, and ~83W NMR spectroscopy. These ketoses react only in acyclic forms, because HO-3,4 are trans in the cyclic lbrms. With tungstate, both sugars form a major complex of the same type in which the hydrated ketose is bound through the O-1,2,4 site of chelation. The ligands are tetradentate, since both 0-2 atoms bridge the metal atoms. Complexes of the same type prevail in the molybdate systems, but are accompanied by one (sorbose) or two (fructose) minor complexes formed by the acyclic keto forms in which the sites of chelation are the 0-3,4,5,6 systems. Multinuclear NMR data are provided for the identification of the various types of complexes.
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~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 orien
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