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Reduced Acid Dissociation of Amino-Acids at the Surface of Water

[Image: see text] We use surface-specific intensity vibrational sum-frequency generation and attenuated total reflection spectroscopy to probe the ionization state of the amino-acids l-alanine and l-proline at the air/water surface and in the bulk. The ionization state is determined by probing the v...

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Autores principales: Strazdaite, Simona, Meister, Konrad, Bakker, Huib J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355887/
https://www.ncbi.nlm.nih.gov/pubmed/28177623
http://dx.doi.org/10.1021/jacs.6b12079
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author Strazdaite, Simona
Meister, Konrad
Bakker, Huib J.
author_facet Strazdaite, Simona
Meister, Konrad
Bakker, Huib J.
author_sort Strazdaite, Simona
collection PubMed
description [Image: see text] We use surface-specific intensity vibrational sum-frequency generation and attenuated total reflection spectroscopy to probe the ionization state of the amino-acids l-alanine and l-proline at the air/water surface and in the bulk. The ionization state is determined by probing the vibrational signatures of the carboxylic acid group, representing the nondissociated acid form, and the carboxylate anion group, representing the dissociated form, over a wide range of pH values. We find that the carboxylic acid group deprotonates at a significantly higher pH at the surface than in the bulk.
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spelling pubmed-53558872017-03-22 Reduced Acid Dissociation of Amino-Acids at the Surface of Water Strazdaite, Simona Meister, Konrad Bakker, Huib J. J Am Chem Soc [Image: see text] We use surface-specific intensity vibrational sum-frequency generation and attenuated total reflection spectroscopy to probe the ionization state of the amino-acids l-alanine and l-proline at the air/water surface and in the bulk. The ionization state is determined by probing the vibrational signatures of the carboxylic acid group, representing the nondissociated acid form, and the carboxylate anion group, representing the dissociated form, over a wide range of pH values. We find that the carboxylic acid group deprotonates at a significantly higher pH at the surface than in the bulk. American Chemical Society 2017-02-08 2017-03-15 /pmc/articles/PMC5355887/ /pubmed/28177623 http://dx.doi.org/10.1021/jacs.6b12079 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Strazdaite, Simona
Meister, Konrad
Bakker, Huib J.
Reduced Acid Dissociation of Amino-Acids at the Surface of Water
title Reduced Acid Dissociation of Amino-Acids at the Surface of Water
title_full Reduced Acid Dissociation of Amino-Acids at the Surface of Water
title_fullStr Reduced Acid Dissociation of Amino-Acids at the Surface of Water
title_full_unstemmed Reduced Acid Dissociation of Amino-Acids at the Surface of Water
title_short Reduced Acid Dissociation of Amino-Acids at the Surface of Water
title_sort reduced acid dissociation of amino-acids at the surface of water
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5355887/
https://www.ncbi.nlm.nih.gov/pubmed/28177623
http://dx.doi.org/10.1021/jacs.6b12079
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