Spectrometric and electrochemical investigation of vanadium(V) and vanadium(IV) tartrate complexes in solution

Spectroscopic and electrochemical studies were carried out to characterize the vanadium(IV) and (V) complexes that form in solution and their interconversions. 51V NMR spectroscopy coupled with ¹H NMR, 13C NMR and EPR spectroscopy were used to characterize the vanadium(V)-tartrate complexes that form in the vanadium-tartrate system. The major complex that forms over most of the pH range is a 1:1 complex. In addition a minor 1:2 complex forms. The 1:2 complex formed from enantiomerically pure tartaric acid was less stable than complex formed from racemic tartaric acid. These complexes are different than the 2:2 complex that is the major contributor in the vanadium(IV)-tartrate system. The polarographic and cyclic voltammetic investigations of the electrochemical behavior of V(V) in the presence of tartrate demonstrated a complex formation. The diffusion coefficient values of free vanadium ions and vanadium-tartrate complexes were determined. The minimum average values for the diffusion coefficient for the vanadium(IV)-tartrate 2:2 complexes were determined to range from 3 <FONT FACE=Symbol>´</FONT> 10-6 cm² s-1 to 17 <FONT FACE=Symbol>´</FONT> 10-6 cm² s-1 depending on pH.

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Main Authors: Khan,Ahmad R., Crans,Debbie C., Pauliukaite,Rasa, Norkus,Eugenijus
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Química 2006
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000500012
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spelling oai:scielo:S0103-505320060005000122006-12-01Spectrometric and electrochemical investigation of vanadium(V) and vanadium(IV) tartrate complexes in solutionKhan,Ahmad R.Crans,Debbie C.Pauliukaite,RasaNorkus,Eugenijus vanadium(V) vanadium(IV) tartrate complexes NMR and EPR spectroscopy electrochemistry Spectroscopic and electrochemical studies were carried out to characterize the vanadium(IV) and (V) complexes that form in solution and their interconversions. 51V NMR spectroscopy coupled with ¹H NMR, 13C NMR and EPR spectroscopy were used to characterize the vanadium(V)-tartrate complexes that form in the vanadium-tartrate system. The major complex that forms over most of the pH range is a 1:1 complex. In addition a minor 1:2 complex forms. The 1:2 complex formed from enantiomerically pure tartaric acid was less stable than complex formed from racemic tartaric acid. These complexes are different than the 2:2 complex that is the major contributor in the vanadium(IV)-tartrate system. The polarographic and cyclic voltammetic investigations of the electrochemical behavior of V(V) in the presence of tartrate demonstrated a complex formation. The diffusion coefficient values of free vanadium ions and vanadium-tartrate complexes were determined. The minimum average values for the diffusion coefficient for the vanadium(IV)-tartrate 2:2 complexes were determined to range from 3 <FONT FACE=Symbol>´</FONT> 10-6 cm² s-1 to 17 <FONT FACE=Symbol>´</FONT> 10-6 cm² s-1 depending on pH.info:eu-repo/semantics/openAccessSociedade Brasileira de QuímicaJournal of the Brazilian Chemical Society v.17 n.5 20062006-10-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000500012en10.1590/S0103-50532006000500012
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Khan,Ahmad R.
Crans,Debbie C.
Pauliukaite,Rasa
Norkus,Eugenijus
spellingShingle Khan,Ahmad R.
Crans,Debbie C.
Pauliukaite,Rasa
Norkus,Eugenijus
Spectrometric and electrochemical investigation of vanadium(V) and vanadium(IV) tartrate complexes in solution
author_facet Khan,Ahmad R.
Crans,Debbie C.
Pauliukaite,Rasa
Norkus,Eugenijus
author_sort Khan,Ahmad R.
title Spectrometric and electrochemical investigation of vanadium(V) and vanadium(IV) tartrate complexes in solution
title_short Spectrometric and electrochemical investigation of vanadium(V) and vanadium(IV) tartrate complexes in solution
title_full Spectrometric and electrochemical investigation of vanadium(V) and vanadium(IV) tartrate complexes in solution
title_fullStr Spectrometric and electrochemical investigation of vanadium(V) and vanadium(IV) tartrate complexes in solution
title_full_unstemmed Spectrometric and electrochemical investigation of vanadium(V) and vanadium(IV) tartrate complexes in solution
title_sort spectrometric and electrochemical investigation of vanadium(v) and vanadium(iv) tartrate complexes in solution
description Spectroscopic and electrochemical studies were carried out to characterize the vanadium(IV) and (V) complexes that form in solution and their interconversions. 51V NMR spectroscopy coupled with ¹H NMR, 13C NMR and EPR spectroscopy were used to characterize the vanadium(V)-tartrate complexes that form in the vanadium-tartrate system. The major complex that forms over most of the pH range is a 1:1 complex. In addition a minor 1:2 complex forms. The 1:2 complex formed from enantiomerically pure tartaric acid was less stable than complex formed from racemic tartaric acid. These complexes are different than the 2:2 complex that is the major contributor in the vanadium(IV)-tartrate system. The polarographic and cyclic voltammetic investigations of the electrochemical behavior of V(V) in the presence of tartrate demonstrated a complex formation. The diffusion coefficient values of free vanadium ions and vanadium-tartrate complexes were determined. The minimum average values for the diffusion coefficient for the vanadium(IV)-tartrate 2:2 complexes were determined to range from 3 <FONT FACE=Symbol>´</FONT> 10-6 cm² s-1 to 17 <FONT FACE=Symbol>´</FONT> 10-6 cm² s-1 depending on pH.
publisher Sociedade Brasileira de Química
publishDate 2006
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000500012
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AT cransdebbiec spectrometricandelectrochemicalinvestigationofvanadiumvandvanadiumivtartratecomplexesinsolution
AT pauliukaiterasa spectrometricandelectrochemicalinvestigationofvanadiumvandvanadiumivtartratecomplexesinsolution
AT norkuseugenijus spectrometricandelectrochemicalinvestigationofvanadiumvandvanadiumivtartratecomplexesinsolution
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