Abstract
Potentiometric and electrochemical studies have been carried out with a family of ferrocene redox-functionalised polyamines (L-1-L-5) and have been directed towards the discrimination, using electrochemical techniques, between the two oxoanions phosphate and sulfate and the electrochemical sensing of ATP. Potentiometric titrations were carried out in THF-water (70 : 30 v/v, 0.1 mol dm(-3) tetrabutylammonium perchlorate, 25 degrees C) for L-1, L-2, L-3, L-5 and in water (0.1 mol dm(-3) potassium nitrate, 25 degrees C) for L-4. Potentiometric data indicate that all receptors studied form stable complexes with sulfate, phosphate and ATP. Distribution for the ternary diagram system sulfate-phosphate-L-2 shows pH dependent selectivity patterns; [L2HjSO4](j - 2) species exist at greater than 90% in the pH range 3-4, whereas the corresponding phosphate complexes are the main species in the neutral and the basic pH range. The electrochemical studies are in agreement with speciation results. Sulfate produces in all cyclic receptors maximum cathodic shifts of the redox potential of the ferrocenyl groups around pH 3-4, whereas maximum cathodic shifts for phosphate were found between pH 7 and 8. This behaviour is not observed for the open-chain tetraamine L-5. Selective quantitative electrochemical recognition of sulfate and phosphate in the presence of competing anions in aqueous solution has been achieved using the redox-active polyaza ferrocene macrocyclic L-2, L-3 and L-4 receptors. Additionally ATP is able to cathodically shift the oxidation potential of the ferrocenyl groups of L-2 and L-3 receptors by up to 100 mV. The electrochemical response of L-3 against ADP and AMP is also reported.
| Original language | English |
|---|---|
| Pages (from-to) | 127-133 |
| Number of pages | 7 |
| Journal | JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS |
| Issue number | 2 |
| Publication status | Published - 21 Jan 1999 |
Keywords
- CRYSTAL-STRUCTURE
- MOLECULES
- ANIONS
- BINDING
- LIGANDS
- WATER