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Hydration Energies of Protonated and Sodiated Thiouracils
Hydration reactions of protonated and sodiated thiouracils (2-thiouracil, 6-methyl-2-thiouracil, and 4-thiouracil) generated by electrospray ionization have been studied in a gas phase at 10 mbar using a pulsed ion-beam high-pressure mass spectrometer. The thermochemical data, ΔH (o) n, ΔS (o) n, an...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221615/ https://www.ncbi.nlm.nih.gov/pubmed/25270881 http://dx.doi.org/10.1007/s13361-014-0987-8 |
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author | Wincel, Henryk |
author_facet | Wincel, Henryk |
author_sort | Wincel, Henryk |
collection | PubMed |
description | Hydration reactions of protonated and sodiated thiouracils (2-thiouracil, 6-methyl-2-thiouracil, and 4-thiouracil) generated by electrospray ionization have been studied in a gas phase at 10 mbar using a pulsed ion-beam high-pressure mass spectrometer. The thermochemical data, ΔH (o) n, ΔS (o) n, and ΔG (o) n, for the hydrated systems were obtained by equilibrium measurements. The water binding energies of protonated thiouracils, [2SU]H(+) and [6Me2SU]H(+), were found to be of the order of 51 kJ/mol for the first, and 46 kJ/mol for the second water molecule. For [4SU]H(+), these values are 3–4 kJ/mol lower. For sodiated complexes, these energies are similar for all studied systems, and varied between 62 and 68 kJ/mol for the first and between 48 and 51 kJ/mol for the second water molecule. The structural aspects of the precursors for hydrated complexes are discussed in conjunction with available literature data. [Figure: see text] |
format | Online Article Text |
id | pubmed-4221615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-42216152014-11-11 Hydration Energies of Protonated and Sodiated Thiouracils Wincel, Henryk J Am Soc Mass Spectrom Research Article Hydration reactions of protonated and sodiated thiouracils (2-thiouracil, 6-methyl-2-thiouracil, and 4-thiouracil) generated by electrospray ionization have been studied in a gas phase at 10 mbar using a pulsed ion-beam high-pressure mass spectrometer. The thermochemical data, ΔH (o) n, ΔS (o) n, and ΔG (o) n, for the hydrated systems were obtained by equilibrium measurements. The water binding energies of protonated thiouracils, [2SU]H(+) and [6Me2SU]H(+), were found to be of the order of 51 kJ/mol for the first, and 46 kJ/mol for the second water molecule. For [4SU]H(+), these values are 3–4 kJ/mol lower. For sodiated complexes, these energies are similar for all studied systems, and varied between 62 and 68 kJ/mol for the first and between 48 and 51 kJ/mol for the second water molecule. The structural aspects of the precursors for hydrated complexes are discussed in conjunction with available literature data. [Figure: see text] Springer US 2014-10-01 2014 /pmc/articles/PMC4221615/ /pubmed/25270881 http://dx.doi.org/10.1007/s13361-014-0987-8 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Research Article Wincel, Henryk Hydration Energies of Protonated and Sodiated Thiouracils |
title | Hydration Energies of Protonated and Sodiated Thiouracils |
title_full | Hydration Energies of Protonated and Sodiated Thiouracils |
title_fullStr | Hydration Energies of Protonated and Sodiated Thiouracils |
title_full_unstemmed | Hydration Energies of Protonated and Sodiated Thiouracils |
title_short | Hydration Energies of Protonated and Sodiated Thiouracils |
title_sort | hydration energies of protonated and sodiated thiouracils |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221615/ https://www.ncbi.nlm.nih.gov/pubmed/25270881 http://dx.doi.org/10.1007/s13361-014-0987-8 |
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