Complexation of Some Amino Acids and Peptides by p-Sulfonatocalix[4]arene and Hexasodium p-Sulfonatocalix[6]arene in Aqueous Solution |
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Authors: | H-J Buschmann L Mutihac E Schollmeyer |
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Institution: | (1) Deutsches Textilforschungzentrum Nord-West e. V., Adlerstrasse 1, D-47798 Krefeld, Germany;(2) Faculty of Chemistry, University of Bucharest, 4-12 Regina Elisabeta, Bucharest, 703461, Romania |
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Abstract: | The stability constants (log K), the reaction enthalpy( H) and entropy ( S) of the complexesformed between some amino acids (glycine, L-alanine,L-valine, L-leucine, L-phenylalanine, L-tryptophan,L-threonine, and L-lysine) and peptides (glycyl-glycine,glycyl-L-alanine, glycyl-L-leucine, glycyl-L-phenylalanine,L-leucyl-glycine, L-leucyl-L-alanine, glycyl-L-valine,L-leucyl-glycyl-glycine, and glycyl-glycyl-glycine) withp-sulfonatocalix4]arene and hexasodiump-sulfonatocalix6]arene in aqueous solutions by meansof calorimetric titration have been investigated. The reportedresults demonstrate that the amino acids and peptides under studyform complexes with both p-sulfonatocalix4]areneand hexasodium p-sulfonatocalix6]arene. In the case of theamino acids and peptides the complexation with water-solublecalixarenes in aqueous solution is favored by enthalpiccontributions and disfavored by entropic contributions. However,no influence of the ring size of the calixarenes upon thecomplexation is observed. By comparison with the reaction ofthe sodium salt of phenol-4-sulfonic acid with amino acids amacrocyclic effect in case of the calixarenes is possible. |
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Keywords: | aqueous solution amino acids calorimetric titration peptides p-sulfonatocalix[n]arenes |
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