Interactions of Na+, K+, Mg2+, and Ca 2+ with benzene self-assembled monolayers

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Interactions of Na+, K+, Mg2+, and Ca 2+ with benzene self-assembled monolayers. / Pedersen, Morten Rimmen; Matthiesen, Jesper; Bovet, Nicolas Emile; Hassenkam, Tue; Pedersen, Christian Schack; Stipp, Susan Louise Svane.

In: Langmuir, Vol. 30, No. 30, 2014, p. 9115-9122.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Pedersen, MR, Matthiesen, J, Bovet, NE, Hassenkam, T, Pedersen, CS & Stipp, SLS 2014, 'Interactions of Na+, K+, Mg2+, and Ca 2+ with benzene self-assembled monolayers', Langmuir, vol. 30, no. 30, pp. 9115-9122. https://doi.org/10.1021/la5018664

APA

Pedersen, M. R., Matthiesen, J., Bovet, N. E., Hassenkam, T., Pedersen, C. S., & Stipp, S. L. S. (2014). Interactions of Na+, K+, Mg2+, and Ca 2+ with benzene self-assembled monolayers. Langmuir, 30(30), 9115-9122. https://doi.org/10.1021/la5018664

Vancouver

Pedersen MR, Matthiesen J, Bovet NE, Hassenkam T, Pedersen CS, Stipp SLS. Interactions of Na+, K+, Mg2+, and Ca 2+ with benzene self-assembled monolayers. Langmuir. 2014;30(30):9115-9122. https://doi.org/10.1021/la5018664

Author

Pedersen, Morten Rimmen ; Matthiesen, Jesper ; Bovet, Nicolas Emile ; Hassenkam, Tue ; Pedersen, Christian Schack ; Stipp, Susan Louise Svane. / Interactions of Na+, K+, Mg2+, and Ca 2+ with benzene self-assembled monolayers. In: Langmuir. 2014 ; Vol. 30, No. 30. pp. 9115-9122.

Bibtex

@article{ce9d542918fa404e9a8cc81c0a918418,
title = "Interactions of Na+, K+, Mg2+, and Ca 2+ with benzene self-assembled monolayers",
abstract = "Interactions between cations and organic molecules are found throughout nature, from the functionality and structure of proteins in humans and animals to the exchange of ions in minerals in soil and oil reservoirs with the fluid phases. We have explored the behavior of the s-block elements that are most common in the natural world, namely, Na+, K+, Mg 2+, and Ca2+. Specifically, we investigated how these ions affect the interactions between surfaces covered by self-Assembled monolayers (SAMs) terminated with benzene molecules. We used a flat oxidized silicon substrate and an atomic force microscopy (AFM) tip that were both functionalized with 11-phenoxyundecane-1-thiol and measured the adhesion force between them in solutions of each of the four chloride salts. We observed that the adhesion increased in the order of the Hofmeister series: K+ < Na + {\^a}{\^‰} Mg2+ < Ca2+. Supplementary evidence from X-ray photoelectron spectroscopy (XPS) allowed us to conclude that K+ binds in the benzene layers, creating a positive surface charge on the benzene-covered surfaces, thus leading to lower adhesion in KCl solutions than in pure water. Evidence suggested that Ca2+ does not bind to the surfaces but forms bridges between the layers, leading to higher adhesion than in pure water. In Na+ and Mg2+ solutions, adhesion is quite similar to that in pure water, indicating a lack of interaction between these two ions and the surfaces, or at least that the interaction is too weak to be detected by our measurements. The results of our studies clearly show that even a nonpolar, hydrophobic molecule, such as benzene, has a role to play in the behavior of aqueous solutions and that it interacts differently depending on which ions are present. Even ions from the same column in the periodic table behave differently.",
author = "Pedersen, {Morten Rimmen} and Jesper Matthiesen and Bovet, {Nicolas Emile} and Tue Hassenkam and Pedersen, {Christian Schack} and Stipp, {Susan Louise Svane}",
year = "2014",
doi = "10.1021/la5018664",
language = "English",
volume = "30",
pages = "9115--9122",
journal = "Langmuir",
issn = "0743-7463",
publisher = "American Chemical Society",
number = "30",

}

RIS

TY - JOUR

T1 - Interactions of Na+, K+, Mg2+, and Ca 2+ with benzene self-assembled monolayers

AU - Pedersen, Morten Rimmen

AU - Matthiesen, Jesper

AU - Bovet, Nicolas Emile

AU - Hassenkam, Tue

AU - Pedersen, Christian Schack

AU - Stipp, Susan Louise Svane

PY - 2014

Y1 - 2014

N2 - Interactions between cations and organic molecules are found throughout nature, from the functionality and structure of proteins in humans and animals to the exchange of ions in minerals in soil and oil reservoirs with the fluid phases. We have explored the behavior of the s-block elements that are most common in the natural world, namely, Na+, K+, Mg 2+, and Ca2+. Specifically, we investigated how these ions affect the interactions between surfaces covered by self-Assembled monolayers (SAMs) terminated with benzene molecules. We used a flat oxidized silicon substrate and an atomic force microscopy (AFM) tip that were both functionalized with 11-phenoxyundecane-1-thiol and measured the adhesion force between them in solutions of each of the four chloride salts. We observed that the adhesion increased in the order of the Hofmeister series: K+ < Na + â‰̂ Mg2+ < Ca2+. Supplementary evidence from X-ray photoelectron spectroscopy (XPS) allowed us to conclude that K+ binds in the benzene layers, creating a positive surface charge on the benzene-covered surfaces, thus leading to lower adhesion in KCl solutions than in pure water. Evidence suggested that Ca2+ does not bind to the surfaces but forms bridges between the layers, leading to higher adhesion than in pure water. In Na+ and Mg2+ solutions, adhesion is quite similar to that in pure water, indicating a lack of interaction between these two ions and the surfaces, or at least that the interaction is too weak to be detected by our measurements. The results of our studies clearly show that even a nonpolar, hydrophobic molecule, such as benzene, has a role to play in the behavior of aqueous solutions and that it interacts differently depending on which ions are present. Even ions from the same column in the periodic table behave differently.

AB - Interactions between cations and organic molecules are found throughout nature, from the functionality and structure of proteins in humans and animals to the exchange of ions in minerals in soil and oil reservoirs with the fluid phases. We have explored the behavior of the s-block elements that are most common in the natural world, namely, Na+, K+, Mg 2+, and Ca2+. Specifically, we investigated how these ions affect the interactions between surfaces covered by self-Assembled monolayers (SAMs) terminated with benzene molecules. We used a flat oxidized silicon substrate and an atomic force microscopy (AFM) tip that were both functionalized with 11-phenoxyundecane-1-thiol and measured the adhesion force between them in solutions of each of the four chloride salts. We observed that the adhesion increased in the order of the Hofmeister series: K+ < Na + â‰̂ Mg2+ < Ca2+. Supplementary evidence from X-ray photoelectron spectroscopy (XPS) allowed us to conclude that K+ binds in the benzene layers, creating a positive surface charge on the benzene-covered surfaces, thus leading to lower adhesion in KCl solutions than in pure water. Evidence suggested that Ca2+ does not bind to the surfaces but forms bridges between the layers, leading to higher adhesion than in pure water. In Na+ and Mg2+ solutions, adhesion is quite similar to that in pure water, indicating a lack of interaction between these two ions and the surfaces, or at least that the interaction is too weak to be detected by our measurements. The results of our studies clearly show that even a nonpolar, hydrophobic molecule, such as benzene, has a role to play in the behavior of aqueous solutions and that it interacts differently depending on which ions are present. Even ions from the same column in the periodic table behave differently.

U2 - 10.1021/la5018664

DO - 10.1021/la5018664

M3 - Journal article

C2 - 25003588

AN - SCOPUS:84905696641

VL - 30

SP - 9115

EP - 9122

JO - Langmuir

JF - Langmuir

SN - 0743-7463

IS - 30

ER -

ID: 130941597