Zeolite-Encapsulated Copper(II) Amino Acid Complexes: Synthesis, Spectroscopy, and Catalysis
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Publication date
1995-12-12
Authors
Weckhuysen, B.M.
Verberckmoes, A.A.
Fu, L.
Schoonheydt, R.A.
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Abstract
The spectroscopic properties and catalytic behavior of Cu(AA)n m+ complexes (AA ) amino acid (glycine,
lysine, histidine, alanine, serine, proline, tyrosine, phenylalanine, glutamine, glutamic acid, cysteine, tryptophan,
leucine, and arginine)) in faujasite-type zeolites have been investigated. Successful immobilization was
achieved by a simple cation exchange procedure with aqueous solutions of preformed Cu(AA)n m+ complexes.
The best ion exchange results were obtained with lysine, arginine, proline (at pH ) 10), and histidine (at pH
= 7.3) as ligands and with a AA:Cu 2+ ratio of 5. The internal surface and pore volume are drastically
reduced by the uptake of the Cu(AA)n m+ complexes, and no precipitation of Cu(AA)n m+ crystals was observed
by scanning electron microscopy. Both observations suggest the location of the complexes in the supercages
of the faujasite-type zeolites. The composition of the first coordination sphere around Cu 2+ can be designed
from NNNN to NOOO by varying the type of amino acid. A free coordination site is available for catalysis,
and the oxidation of alcohols, alkanes, and alkenes with peroxides was observed at low temperatures.