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Advances on the Determination of the Astatine Pourbaix Diagram: Predomination of AtO(OH)2− over At− in Basic Conditions
Authors:Dumitru‐Claudiu Sergentu  Dr David Teze  Dr Andréa Sabatié‐Gogova  Dr Cyrille Alliot  Ning Guo  Dr Fadel Bassal  Dr Isidro Da Silva  Prof?Dr David Deniaud  Dr Rémi Maurice  Dr Julie Champion  Dr Nicolas Galland  Dr Gilles Montavon
Institution:1. SUBATECH, UMR CNRS 6457, IN2P3/EMN Nantes/Université de Nantes, Nantes Cedex 3, France;2. CEISAM, UMR CNRS 6230, Université de Nantes, Nantes Cedex 3, France;3. GIP ARRONAUX, Saint-Herblain Cedex, France;4. CEMHTI, UPR CNRS 3079, Site Cyclotron CS30058, Orléans Cedex 2, France
Abstract:It is generally assumed that astatide (At?) is the predominant astatine species in basic aqueous media. This assumption is questioned in non‐complexing and non‐reductive aqueous solutions by means of high‐pressure anion‐exchange chromatography. Contrary to what is usually believed, astatide is found to be a minor species at pH=11. A different species, which also bears a single negative charge, becomes predominant when the pH is increased beyond 7. Using competition experiments, an equilibrium constant value of 10?6.9 has been determined for the formation of this species from AtO(OH) with the exchange of one proton. The identification of this species, AtO(OH)2?, is achieved through relativistic quantum mechanical calculations, which rule out the significant formation of the AtO2? species, while leading to a hydrolysis constant of AtO(OH) in excellent agreement with experiment when the AtO(OH)2? species is considered. Beyond the completion of the Pourbaix diagram of astatine, this new information is of interest for the development of 211At radiolabeling protocols.
Keywords:astatine  competition experiments  hydrolysis constants  Pourbaix diagrams  quantum mechanical calculations
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