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Speciation in the aqueous H+/H2VO4–/H2O2/picolinate system relevant to diabetes research

Andersson, Ingegärd (author)
Umeå universitet,Kemiska institutionen
Gorzsás, András (author)
Umeå universitet,Kemiska institutionen
Pettersson, Lage (author)
Umeå universitet,Kemiska institutionen
 (creator_code:org_t)
Cambridge : Royal Society of Chemistry, Thomas Graham House, 2004
2004
English.
In: Dalton Transactions. - Cambridge : Royal Society of Chemistry, Thomas Graham House. - 1477-9226 .- 1477-9234. ; :3, s. 421-428
  • Journal article (peer-reviewed)
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  • A detailed study of the quaternary aqueous H+/H2VO4−/H2O2/picolinate (Pi−) system has been performed at 25 °C in 0.150 M Na(Cl) medium using quantitative 51V NMR (500 MHz) and potentiometric data (glass electrode). In the ternary H+/H2VO4−/Pi− system, six complexes have been found in the pH region 1–10. In the quaternary H+/H2VO4−/H2O2/Pi−system, eight additional complexes have been found. Generally, equilibria are fast in both systems. The rate of peroxide decomposition depends on the species in solution. Chemical shifts, compositions and formation constants for the species are given. Equilibrium conditions and the fit of the model to the experimental data are illustrated in distribution diagrams. Possible formation of mixed ligand species with imidazole, lactic acid and citric acid have been investigated and ruled out under the same experimental conditions. Structural proposals are given, based on 13C NMR data and available crystal structures.

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