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Molecular Features of Reline and Homologous Deep Eutectic Solvents Contributing to Nonideal Mixing Behavior

Cite this: J. Phys. Chem. B 2020, 124, 35, 7586–7597
Publication Date (Web):August 3, 2020
https://doi.org/10.1021/acs.jpcb.0c03091
Copyright © 2020 American Chemical Society

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Abstract

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Deep eutectic solvents based on choline chloride and a series of urea derivatives are studied by molecular dynamics simulations with the aim to identify molecular features contributing to nonideal mixing behavior of these compounds. In case of reline, a mixture of choline chloride and urea in 1:2 ratio, urea molecules provide sufficient hydrogen bond donor sites to take up the chloride anions into their polar network. Replacing any of the hydrogen atoms of urea by a methyl group strongly pushes the anion to interact with these alkyl chains, resulting in a positive deviation of the activity coefficients of choline chloride compared to reline. Furthermore, the oxygen atom of urea can interact with the nitrogen atom of the cation. This enables the chloride anion to move off-center of the cation toward the hydrogen atom of its hydroxyl group, possessing stronger directional Coulomb interactions than the nitrogen atom of the cation. The substitution of urea’s hydrogen atoms in cis position to the carbonyl group as in 1,3-dimethylurea, pushes the newly introduced nonpolar alkyl chains toward the nitrogen atom of the cation. This effect can be responsible for the experimentally observed increase of the activity coefficient of the urea derivative compared to urea. Additionally, indications for formation of nonpolar domains within the liquid and, thus, nanoscale segregation is visible as soon as one hydrogen atom of urea is replaced by an alkyl group.

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The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acs.jpcb.0c03091.

  • Complete list of force field parameters, detailed validation of the force field, fitting of the dihedral potential energy surface of thiourea to the first-principles reference, computational details of first-principles MD simulations, box lengths from NPT simulations, and additional MSDs and RDFs (PDF)

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Cited By

This article is cited by 12 publications.

  1. Akshay Malik, Hemant K. Kashyap. Solvent Organization around Methane Dissolved in Archetypal Reline and Ethaline Deep Eutectic Solvents as Revealed by AIMD Investigation. The Journal of Physical Chemistry B 2022, 126 (34) , 6472-6482. https://doi.org/10.1021/acs.jpcb.2c02406
  2. Yong Zhang, Henry Squire, Burcu Gurkan, Edward J. Maginn. Refined Classical Force Field for Choline Chloride and Ethylene Glycol Mixtures over Wide Composition Range. Journal of Chemical & Engineering Data 2022, 67 (8) , 1864-1871. https://doi.org/10.1021/acs.jced.1c00841
  3. Omid Shayestehpour, Stefan Zahn. Ion Correlation in Choline Chloride–Urea Deep Eutectic Solvent (Reline) from Polarizable Molecular Dynamics Simulations. The Journal of Physical Chemistry B 2022, 126 (18) , 3439-3449. https://doi.org/10.1021/acs.jpcb.1c10671
  4. Burcu E. Gurkan, Edward J. Maginn, Emily B. Pentzer. Deep Eutectic Solvents: A New Class of Versatile Liquids. The Journal of Physical Chemistry B 2020, 124 (50) , 11313-11315. https://doi.org/10.1021/acs.jpcb.0c10099
  5. Dinis O. Abranches, João A.P. Coutinho. Everything You Wanted to Know about Deep Eutectic Solvents but Were Afraid to Be Told. Annual Review of Chemical and Biomolecular Engineering 2023, 14 (1) , 141-163. https://doi.org/10.1146/annurev-chembioeng-101121-085323
  6. Kayleigh R. Barlow, Gregory S. Tschumper. Conformational comparison of urea and thiourea near the CCSD ( T ) complete basis set limit. International Journal of Quantum Chemistry 2023, 123 (8) https://doi.org/10.1002/qua.27075
  7. Morteza Asemani, Behnam Ranjbar. Other thermal methods. 2023, 315-354. https://doi.org/10.1016/B978-0-12-821933-1.00004-5
  8. A. Sanati, M.R. Malayeri, O. Busse, J.J. Weigand. Utilization of ionic liquids and deep eutectic solvents in oil operations: Progress and challenges. Journal of Molecular Liquids 2022, 361 , 119641. https://doi.org/10.1016/j.molliq.2022.119641
  9. Caroline Velez, Orlando Acevedo. Simulation of deep eutectic solvents: Progress to promises. WIREs Computational Molecular Science 2022, 12 (4) https://doi.org/10.1002/wcms.1598
  10. Joshua J. Buzolic, Hua Li, Zachary M. Aman, Gregory G. Warr, Rob Atkin. Self-assembled nanostructure induced in deep eutectic solvents via an amphiphilic hydrogen bond donor. Journal of Colloid and Interface Science 2022, 616 , 121-128. https://doi.org/10.1016/j.jcis.2022.02.029
  11. Dmitry Tolmachev, Natalia Lukasheva, Ruslan Ramazanov, Victor Nazarychev, Natalia Borzdun, Igor Volgin, Maria Andreeva, Artyom Glova, Sofia Melnikova, Alexey Dobrovskiy, Steven A. Silber, Sergey Larin, Rafael Maglia de Souza, Mauro Carlos Costa Ribeiro, Sergey Lyulin, Mikko Karttunen. Computer Simulations of Deep Eutectic Solvents: Challenges, Solutions, and Perspectives. International Journal of Molecular Sciences 2022, 23 (2) , 645. https://doi.org/10.3390/ijms23020645
  12. Mert Atilhan, Santiago Aparicio. Review on chemical enhanced oil recovery: Utilization of ionic liquids and deep eutectic solvents. Journal of Petroleum Science and Engineering 2021, 205 , 108746. https://doi.org/10.1016/j.petrol.2021.108746

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