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DOI:
https://doi.org/10.34804/supra.20210928170 Cc Cc by 4.0

Title:
Calorimetric, NMR, and UV Investigations of Aliphatic l-Amino Acids Complexation by Calix[4]arene Bis-hydroxymethylphosphous Acid

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Description:
The stability constants, enthalpy ΔH 0, entropy ΔS 0, and Gibbs energy ΔG 0 were determined for the host–guest complexes (1:1) of calix[4]arene bis-hydroxymethylphosphous acid with glycine, l-alanine, l-valine, l-leucine, l-isoleucine residues in methanol solution with the aid of the titration experiments followed by calorimetric and spectroscopic (1H NMR, UV) methods. The experimental data indicated that the host–guest complexation was under control of the direct electrostatic interaction between negatively charged calixarene phosphoryl group and amino acid residue NH 3 + group, modulated by the hydrophobic interaction, which drive the inclusion of the residue alkyl side-chain into the calixarene cavity. The stability of the inclusion complexes was found correlated with the size of the aliphatic amino acid’s side-chain. The experimental data were additionally analyzed in the terms of the three state model corresponding to coexistence of 2:1 and 1:1 complexation equilibria.

Citation:

W. Zielenkiewicz, A. Marcinowicz, J. Poznański, S. Cherenok, V. Kalchenko, SupraBank 2024, Calorimetric, NMR, and UV Investigations of Aliphatic l-Amino Acids Complexation by Calix[4]arene Bis-hydroxymethylphosphous Acid (dataset). https://doi.org/10.34804/supra.20210928170

Link: https://doi.org/10.34804/supra.20210928170
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Citation:

W. Zielenkiewicz, A. Marcinowicz, J. Poznański, S. Cherenok, V. Kalchenko, J Incl Phenom Macrocycl Chem 2006, 55, 11–19.

Link: https://doi.org/10.1007/s10847-005-9012-y
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Creators:
Orcidid | Ror | W. Zielenkiewicz
Orcidid | Ror | A. Marcinowicz
Orcidid | Ror | J. Poznański
Orcidid | Ror | S. Cherenok
Orcidid | Ror | V. Kalchenko

Contributers:
Orcidid | Ror | Mary Maguire | DataManager

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