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Hydration of Heavy Alkaline-Earth Cations Studied by Molecular Dynamics Simulations and X-ray Absorption Spectroscopy

[Image: see text] The physicochemical properties of the three heaviest alkaline-earth cations, Sr(2+), Ba(2+), and Ra(2+) in water have been studied by means of classical molecular dynamics (MD) simulations. A specific set of cation–water intermolecular potentials based on ab initio potential energy...

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Autores principales: Pappalardo, Rafael R., Caralampio, Daniel Z., Martínez, José M., Sánchez Marcos, Enrique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8512670/
https://www.ncbi.nlm.nih.gov/pubmed/34387993
http://dx.doi.org/10.1021/acs.inorgchem.1c01888
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author Pappalardo, Rafael R.
Caralampio, Daniel Z.
Martínez, José M.
Sánchez Marcos, Enrique
author_facet Pappalardo, Rafael R.
Caralampio, Daniel Z.
Martínez, José M.
Sánchez Marcos, Enrique
author_sort Pappalardo, Rafael R.
collection PubMed
description [Image: see text] The physicochemical properties of the three heaviest alkaline-earth cations, Sr(2+), Ba(2+), and Ra(2+) in water have been studied by means of classical molecular dynamics (MD) simulations. A specific set of cation–water intermolecular potentials based on ab initio potential energy surfaces has been built on the basis of the hydrated ion concept. The polarizable and flexible model of water MCDHO2 was adopted. The theoretical–experimental comparison of structural, dynamical, energetic, and spectroscopical properties of Sr(2+) and Ba(2+) aqueous solutions is satisfactory, which supports the methodology developed. This good behavior allows a reasonable reliability for the predicted Ra(2+) physicochemical data not experimentally determined yet. Simulated extended X-ray absorption fine-structure (EXAFS) and X-ray absorption near-edge spectroscopy spectra have been computed from the snapshots of the MD simulations and compared with the experimental information available for Sr(2+) and Ba(2+). For the Ra(2+) case, the Ra L(3)-edge EXAFS spectrum is proposed. Structural and dynamical properties of the aqua ions for the three cations have been obtained and analyzed. Along the [M(H(2)O)(n)](m+) series, the M–O distance for the first-hydration shell is 2.57, 2.81, and 2.93 Å for Sr(2+), Ba(2+), and Ra(2+), respectively. The hydration number also increases when one is going down along the group: 8.1, 9.4, and 9.8 for Sr(2+), Ba(2+), and Ra(2+), respectively. Whereas [Sr(H(2)O)(8)](2+) is a typical aqua ion with a well-defined structure, the Ba(2+) and Ra(2+) hydration provides a picture exhibiting an average between the ennea- and the deca-hydration. These results show a similar chemical behavior of Ba(2+) and Ra(2+) aqueous solutions and support experimental studies on the removal of Ra-226 of aquifers by different techniques, where Ra(2+) is replaced by Ba(2+). A comparison of the heavy alkaline ions, Rb(+) and Cs(+), with the heavy alkaline-earth ions is made.
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spelling pubmed-85126702021-10-13 Hydration of Heavy Alkaline-Earth Cations Studied by Molecular Dynamics Simulations and X-ray Absorption Spectroscopy Pappalardo, Rafael R. Caralampio, Daniel Z. Martínez, José M. Sánchez Marcos, Enrique Inorg Chem [Image: see text] The physicochemical properties of the three heaviest alkaline-earth cations, Sr(2+), Ba(2+), and Ra(2+) in water have been studied by means of classical molecular dynamics (MD) simulations. A specific set of cation–water intermolecular potentials based on ab initio potential energy surfaces has been built on the basis of the hydrated ion concept. The polarizable and flexible model of water MCDHO2 was adopted. The theoretical–experimental comparison of structural, dynamical, energetic, and spectroscopical properties of Sr(2+) and Ba(2+) aqueous solutions is satisfactory, which supports the methodology developed. This good behavior allows a reasonable reliability for the predicted Ra(2+) physicochemical data not experimentally determined yet. Simulated extended X-ray absorption fine-structure (EXAFS) and X-ray absorption near-edge spectroscopy spectra have been computed from the snapshots of the MD simulations and compared with the experimental information available for Sr(2+) and Ba(2+). For the Ra(2+) case, the Ra L(3)-edge EXAFS spectrum is proposed. Structural and dynamical properties of the aqua ions for the three cations have been obtained and analyzed. Along the [M(H(2)O)(n)](m+) series, the M–O distance for the first-hydration shell is 2.57, 2.81, and 2.93 Å for Sr(2+), Ba(2+), and Ra(2+), respectively. The hydration number also increases when one is going down along the group: 8.1, 9.4, and 9.8 for Sr(2+), Ba(2+), and Ra(2+), respectively. Whereas [Sr(H(2)O)(8)](2+) is a typical aqua ion with a well-defined structure, the Ba(2+) and Ra(2+) hydration provides a picture exhibiting an average between the ennea- and the deca-hydration. These results show a similar chemical behavior of Ba(2+) and Ra(2+) aqueous solutions and support experimental studies on the removal of Ra-226 of aquifers by different techniques, where Ra(2+) is replaced by Ba(2+). A comparison of the heavy alkaline ions, Rb(+) and Cs(+), with the heavy alkaline-earth ions is made. American Chemical Society 2021-08-13 2021-09-06 /pmc/articles/PMC8512670/ /pubmed/34387993 http://dx.doi.org/10.1021/acs.inorgchem.1c01888 Text en © 2021 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Pappalardo, Rafael R.
Caralampio, Daniel Z.
Martínez, José M.
Sánchez Marcos, Enrique
Hydration of Heavy Alkaline-Earth Cations Studied by Molecular Dynamics Simulations and X-ray Absorption Spectroscopy
title Hydration of Heavy Alkaline-Earth Cations Studied by Molecular Dynamics Simulations and X-ray Absorption Spectroscopy
title_full Hydration of Heavy Alkaline-Earth Cations Studied by Molecular Dynamics Simulations and X-ray Absorption Spectroscopy
title_fullStr Hydration of Heavy Alkaline-Earth Cations Studied by Molecular Dynamics Simulations and X-ray Absorption Spectroscopy
title_full_unstemmed Hydration of Heavy Alkaline-Earth Cations Studied by Molecular Dynamics Simulations and X-ray Absorption Spectroscopy
title_short Hydration of Heavy Alkaline-Earth Cations Studied by Molecular Dynamics Simulations and X-ray Absorption Spectroscopy
title_sort hydration of heavy alkaline-earth cations studied by molecular dynamics simulations and x-ray absorption spectroscopy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8512670/
https://www.ncbi.nlm.nih.gov/pubmed/34387993
http://dx.doi.org/10.1021/acs.inorgchem.1c01888
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