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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 VO 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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