The dual role of self-assembled monolayers of a tetraazamacrocyclic copper(II) complex in ascorbate oxidation catalysis

The copper(II) complex with 1,4,8-trimethyl-11-(2-thioethyl)-1,4,8,11-tetraazacyclotetradecane was adsorbed on the surface of glassy carbon (GCE) and gold electrodes using the self-assembly method. More stable coverage of the electrode was obtained using a gold substrate when the complex is anchored...

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Published in:Inorganica Chimica Acta Vol. 348; pp. 129 - 134
Main Authors: Stolarczyk, Krzysztof, Bilewicz, Renata, Siegfried, Liselotte, Kaden, Thomas
Format: Journal Article
Language:English
Published: Elsevier B.V 15-05-2003
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Abstract The copper(II) complex with 1,4,8-trimethyl-11-(2-thioethyl)-1,4,8,11-tetraazacyclotetradecane was adsorbed on the surface of glassy carbon (GCE) and gold electrodes using the self-assembly method. More stable coverage of the electrode was obtained using a gold substrate when the complex is anchored to the electrode through its thioethyl substituent. The amount of the complex on the electrode surface based on the charge of the Cu 2+/Cu + peak points to the nearly monolayer coverage of the electrode surface. The catalytic effect of the monolayer towards ascorbic acid oxidation was observed in neutral and alkaline solutions, and ascribed to the electrostatic interaction of ascorbate anion with the positively charged copper complex bound to the electrode surface. In dioxygenated solutions, the copper complex adsorbed on the electrode catalyses both the electrooxidation and auto-oxidation of ascorbate. The copper-catalyzed autoxidation of ascorbic acid leads to a decrease of the ascorbate electrooxidation peak with time. The progress of this reaction was monitored based on the changes of the electrooxidation current. Copper catalyzed autoxidation of ascorbate is known to require turnover between Cu 2+ and Cu + ions. This indicates that the molecules of the copper complex anchored through the thiol groups to the gold electrode, and tightly packed on the surface play a dual role in the ascorbate oxidation process. The role of the monolayer in enhancing the autoxidation of ascorbic acid resembles the function of copper in some biological complexes catalyzing in vivo ascorbate oxidation. The copper(II) complex with 1,4,8-trimethyl-11-(2-thioethyl)tetraazacyclotetradecane was adsorbed on the surface of glassy carbon (GCE) and gold electrodes using the self-assembly method. The catalytic effect of the monolayer towards ascorbic acid oxidation was observed. In dioxygenated solutions, the copper complex adsorbed on the electrode catalyses both the electrooxidation and auto-oxidation of ascorbate.
AbstractList The copper(II) complex with 1,4,8-trimethyl-11-(2-thioethyl)-1,4,8,11-tetraazacyclotetradecane was adsorbed on the surface of glassy carbon (GCE) and gold electrodes using the self-assembly method. More stable coverage of the electrode was obtained using a gold substrate when the complex is anchored to the electrode through its thioethyl substituent. The amount of the complex on the electrode surface based on the charge of the Cu 2+/Cu + peak points to the nearly monolayer coverage of the electrode surface. The catalytic effect of the monolayer towards ascorbic acid oxidation was observed in neutral and alkaline solutions, and ascribed to the electrostatic interaction of ascorbate anion with the positively charged copper complex bound to the electrode surface. In dioxygenated solutions, the copper complex adsorbed on the electrode catalyses both the electrooxidation and auto-oxidation of ascorbate. The copper-catalyzed autoxidation of ascorbic acid leads to a decrease of the ascorbate electrooxidation peak with time. The progress of this reaction was monitored based on the changes of the electrooxidation current. Copper catalyzed autoxidation of ascorbate is known to require turnover between Cu 2+ and Cu + ions. This indicates that the molecules of the copper complex anchored through the thiol groups to the gold electrode, and tightly packed on the surface play a dual role in the ascorbate oxidation process. The role of the monolayer in enhancing the autoxidation of ascorbic acid resembles the function of copper in some biological complexes catalyzing in vivo ascorbate oxidation. The copper(II) complex with 1,4,8-trimethyl-11-(2-thioethyl)tetraazacyclotetradecane was adsorbed on the surface of glassy carbon (GCE) and gold electrodes using the self-assembly method. The catalytic effect of the monolayer towards ascorbic acid oxidation was observed. In dioxygenated solutions, the copper complex adsorbed on the electrode catalyses both the electrooxidation and auto-oxidation of ascorbate.
Author Siegfried, Liselotte
Bilewicz, Renata
Stolarczyk, Krzysztof
Kaden, Thomas
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  givenname: Krzysztof
  surname: Stolarczyk
  fullname: Stolarczyk, Krzysztof
  organization: Department of Chemistry, University of Warsaw, ul. Pasteura 1, 02-093 Warsaw, Poland
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  givenname: Renata
  surname: Bilewicz
  fullname: Bilewicz, Renata
  email: bilewicz@chem.uw.edu.pl
  organization: Department of Chemistry, University of Warsaw, ul. Pasteura 1, 02-093 Warsaw, Poland
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  givenname: Liselotte
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  fullname: Siegfried, Liselotte
  organization: Department of Chemistry, University of Basel Spitalstrasse 51, CH-4056 Basel, Switzerland
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  givenname: Thomas
  surname: Kaden
  fullname: Kaden, Thomas
  organization: Department of Chemistry, University of Basel Spitalstrasse 51, CH-4056 Basel, Switzerland
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Copyright 2003 Elsevier Science B.V.
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IngestDate Fri Aug 23 02:48:22 EDT 2024
Thu Dec 09 18:43:08 EST 2021
IsPeerReviewed true
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Keywords Ascorbate oxidation
Tetraazacyclotetradecane
SAM
Monolayers
Cyclam
Language English
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Snippet The copper(II) complex with 1,4,8-trimethyl-11-(2-thioethyl)-1,4,8,11-tetraazacyclotetradecane was adsorbed on the surface of glassy carbon (GCE) and gold...
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StartPage 129
SubjectTerms Ascorbate oxidation
Cyclam
Monolayers
SAM
Tetraazacyclotetradecane
Title The dual role of self-assembled monolayers of a tetraazamacrocyclic copper(II) complex in ascorbate oxidation catalysis
URI https://dx.doi.org/10.1016/S0020-1693(02)01514-1
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