Several ion-exchange resins and resin precursor materials formed from natural polysaccharides have been examined by solid-state NMR spectroscopy. NMR spectra of the dry resin contained broad, featureless bands due to the polysaccharide backbone of the resin and additional broad bands due to attached
Coordination-site exchange and solid-state 13C NMR studies of bis(oxalato)dioxovanadate(V) ion
✍ Scribed by Man-Ho Lee; Kjeld Schaumburg
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 376 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Activation parameters were determined for the exchange between the two types of carboxylate groups which are cis and trans to the VO bonds in the bis(oxalato)dioxovanadate(V) ion, [VO~2~(C~2~O~4~)~2~]^3−^. Kinetic data were obtained from the ^13^C NMR spectra at eleven temperatures between 268 and 306 K by the total line‐shape method. The coordination‐site exchange mechanism, involving chelate ring opening and closing in the ion, is proposed. The solid‐state ^13^C NMR spectra of the oxalato complexes, (NH~4~)~3~[VO~2~(C~2~O~4~)~2~]·2H~2~O and K~3~[VO~2~(C~2~O~4~)~2~]·3H~2O~, are also discussed in relation to the structures.
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