McDermott, Sinead and Rooney, A. Denise and Breslin, Carmel B.
(2012)
Complexation study and spectrofluorometric determination of the binding
constant for diquat and p-sulfonatocalix[4]arene.
Tetrahedron, 60 (20).
pp. 3815-3821.
ISSN 0040-4020
Abstract
The interactions between diquat (DQ) and p-sulfonatocalix[4]arene (C4S) were studied in an aqueous solution as a function of the ionic strength. Evidence for the formation of a complex between DQ and C4S was obtained using fluorescence measurements, while the stoichiometry of the complex was confirmed as 1:1 for DQ/C4S using UV–vis spectroscopy. The ionic strength had no influence on the stoichiometry of the complex, but exerted a significant influence on the complexation constant, Kc, decreasing with an increase in the ionic strength. The thermodynamic complexation constant, Kc′, was computed as 5.25±1.11×107 using the extended Debye–Hückel law. The rate constants for the heterogeneous electron transfer for the reduction of DQ at an electrode surface were evaluated as 0.150±0.010 cm s−1 in the absence of C4S and 0.065±0.010 cm s−1 when C4S was added to the solution in a 1:1 ratio.
Item Type: |
Article
|
Keywords: |
Diquat; p-Sulfonatocalix[4]arene; Ionic strength; Complexation constant; |
Academic Unit: |
Faculty of Science and Engineering > Chemistry |
Item ID: |
7812 |
Identification Number: |
https://doi.org/10.1016/j.tet.2012.03.064 |
Depositing User: |
Dr. Denise Rooney
|
Date Deposited: |
25 Jan 2017 15:03 |
Journal or Publication Title: |
Tetrahedron |
Publisher: |
Elsevier |
Refereed: |
Yes |
Funders: |
Science Foundation Ireland (SFI) |
URI: |
|
Use Licence: |
This item is available under a Creative Commons Attribution Non Commercial Share Alike Licence (CC BY-NC-SA). Details of this licence are available
here |
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