Spectrophotometric Studies of Reactions of the Aquapentacyanoferrate(II) Ion with Ketones. Kinetics and Mechanism of the Substitution Reaction of the Aquapentacyanoferrate(II) Ion with 1-Benzoylethylpyridinium Chloride
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Jasna Lovrić
Abstract
The carbonyl group of compounds of the phenacyl- and benzoylethyl-pyridinium type is recognized as a potential σ donor ligand which can produce complexes with the aquapentacyanoferrate(II) ion. Its reactive form is the ionized one i.e. the enolate ion. A detailed spectrophotometric investigation has been made for the reaction of the aquapentacyanoferrate(II) ion with 1-benzoylethylpyridinium chloride. The equilibrium constant of the produced complex was derived using two literatury available additional types of processing the molar ratio method’s experimental data which were not found to be applied to this type of complexes. The kinetics of this substitution reaction were studied in buffered solutions at pH = 8.0 and I = 0.05 M. The obtained results are consistent with a dissociative mechanism.
© 2004 Oldenbourg Wissenschaftsverlag GmbH
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Articles in the same Issue
- Homogeneous Ice Nucleation in Water and Aqueous Solutions
- Electrochemical Lithium Insertion/Extraction in Partially Reduced α-MoO3
- Voltammetric Behaviour of Pentoxifylline at Mercury Electrode
- Spectrophotometric Studies of Reactions of the Aquapentacyanoferrate(II) Ion with Ketones. Kinetics and Mechanism of the Substitution Reaction of the Aquapentacyanoferrate(II) Ion with 1-Benzoylethylpyridinium Chloride
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- Reversible Gas Adsorption in Coated Wall Flow Tube Reactors. Model Simulations for Langmuir Kinetics
- Polyanionic Selenium Fragments and Vibrations in NaMSeN Clusters
- Book Review