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Immobilization of Cobalt Complexes on Mesoporous MCM-41 Support Materials

Published online by Cambridge University Press:  10 February 2011

J. F. Diaz
Affiliation:
Department of Chemistry, University of Texas at Dallas, Richardson TX 75083–0688, USAbalkus@utdallas.edu
F. Bedioui
Affiliation:
Laboratoire d'Electrochimie et de Chimie Analytique (URA n°216 du CNRS), Ecole Nationale Supérieure de Chimie de Paris, 11 rue Pierre et Marie Curie, 75231 Paris cedex 05, France33 1 44 27 67 51; bedioui@ext.jussieu.fr.
E. Briot
Affiliation:
Laboratoire d'Electrochimie et de Chimie Analytique (URA n°216 du CNRS), Ecole Nationale Supérieure de Chimie de Paris, 11 rue Pierre et Marie Curie, 75231 Paris cedex 05, France33 1 44 27 67 51; bedioui@ext.jussieu.fr.
J. Devynck
Affiliation:
Laboratoire d'Electrochimie et de Chimie Analytique (URA n°216 du CNRS), Ecole Nationale Supérieure de Chimie de Paris, 11 rue Pierre et Marie Curie, 75231 Paris cedex 05, France33 1 44 27 67 51; bedioui@ext.jussieu.fr.
K. J. Balkus Jr
Affiliation:
Department of Chemistry, University of Texas at Dallas, Richardson TX 75083–0688, USAbalkus@utdallas.edu
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Abstract

The pore surface of mesoporous MCM-41 type materials have been functionalized with silanes to yield surface bound chelate ligands that include ethylenediamine (ED), diethylenetriamine (DET) and ethylenediaminetriacetic acid salt (EDT). Additionally, The grafted DET ligand was reacted with salicylaldehyde to generate the supported tetradentate Schiff base ligand designated as DES. The MCM-41 bound ligands were used to prepare a series of covalently attached cobalt(II) complexes that potential as oxygen carriers and catalysts. These materials were characterized by FTIR and cyclic voltammetry as well as elemental analysis.

Type
Research Article
Copyright
Copyright © Materials Research Society 1996

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References

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