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Krafft temperature and enthalpy of solution of N-acyl amino acid surfactants and their racemic modifications: effect of the counter ion
Authors:Akio?Ohta  mailto:akio-o@t.kanazawa-u.ac.jp"   title="  akio-o@t.kanazawa-u.ac.jp"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Satoru?Nakashima,Hiroki?Matsuyanagi,Tsuyoshi?Asakawa,Shigeyoshi?Miyagishi
Affiliation:(1) Department of Chemistry and Chemical Engineering, Faculty of Engineering, Kanazawa University, 2-40-20 Kodatsuno, 920-8667 Kanazawa, Ishikawa, Japan
Abstract:
The Krafft temperatures and enthalpies of solution of N-hexadecanoyl alaninate and valinate, and N-tetradecanoyl phenylalaninate were obtained from differential scanning calorimetry. The Krafft temperature of N-acyl amino acid surfactant increased with decreasing size of the counter ion, with some exceptions. The enthalpy of solution was endothermic and increased with decreasing size of the counter ion except for the cases of lithium salt. The results showed that the L-L interaction in the solid state of N-hexadecanoyl amino acid surfactant salt was superior to the D-L interaction for both the alanine and valine systems when the counter ion size increased. However, the D-L interaction was still advantageous for the phenylalanine system with Cs+ as a counter ion. Both Fourier transform infrared spectroscopy studies and theoretical calculations suggested that the difference in magnitudes of the interactions between peptide and counter ion was a dominant factor for the chiral effect.
Keywords:N-Acyl amino acid surfactant  Krafft temperature  Enthalpy of solution  Counter ion  Chiral effect
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