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RESEARCH LETTERS

New natural deep eutectic solvents based on aromatic organic acids

, , ORCID Icon, &
Pages 713-719 | Received 01 Sep 2021, Accepted 17 Nov 2021, Published online: 02 Dec 2021

References

  • Abbott, A.P.; Capper, G.; Davies, D.L.; Rasheed, R.K.; Tambyrajah, V. Novel Solvent Properties of Choline Chloride/Urea Mixtures. Chem. Commun. 2003, 1, 70–71.
  • Paiva, A.; Craveiro, R.; Aroso, I.; Martins, M. Natural Deep Eutectic Solvents - Solvents for the 21st Century. ACS Sustain. Chem. Eng. 2014, 2, 1063–1071.
  • Liu, Y.; Friesen, J.B.; McAlpine, J.B.; Lankin, D.C. Natural Deep Eutectic Solvents: Properties, Applications, and Perspectives. J. Nat. Prod. 2018, 81, 679–690.
  • Fernández, M.; Boiteux, J.; Espino, M.; Gomez, F.V.; Silva, M.F. Natural Deep Eutectic Solvents-Mediated Extractions: The Way Forward for Sustainable Analytical Developments. Anal. Chim. Acta 2018, 1038, 1–10.
  • Smith, E.L.; Abbott, A.P.; Ryder, K.S. Deep Eutectic Solvents (DESs) and Their Applications. Chem. Rev. 2014, 114, 11060–11082.
  • Tome, L.I.N.; Baiao, V.; da Silva, W.; Brett, C.M.A. Deep Eutectic Solvents for the Production and Application of New Materials. Appl. Mater. Today. 2018, 10, 30–50.
  • Chen, B.L.; Peng, Z.Q.; Li, C.; Feng, Y.C. Catalytic Conversion of Biomass to Furanic Derivatives with Deep Eutectic Solvents. ChemSusChem. 2021, 14, 1496–1506.
  • Clarke, C.J.; Tu, W.C.; Levers, O.; Brohl, A.; Hallett, J.P. Green and Sustainable Solvents in Chemical Processes. Chem. Rev. 2018, 118, 747–800.
  • Abranches, D.O.; Martins, M.A.R.; Silva, L.P.; Schaeffer, N. Phenolic Hydrogen Bond Donors in the Formation of Non-Ionic Deep Eutectic Solvents: The Quest for Type V DES. Chem. Commun. 2019, 55, 10253–10256.
  • Fan, C.; Liu, Y.; Sebbah, T.; Cao, X.L. A Theoretical Study on Terpene-Based Natural Deep Eutectic Solvent: Relationship Between Viscosity and Hydrogen-Bonding Interactions. Glob. Chall. 2021, 5, 1–8.
  • Prausnitz, J.M.; Lichtenthaler, R.N.; Azevedo, E.G. Molecular Thermodynamics of Fluid-Phase Equilibria; Prentice Hall PTR: Upper Saddle River, NJ, 1999.
  • Parker, T.M.; Burns, L.A.; Parrish, R.M.; Ryno, A.G.; Sherrill, C.D. Levels of Symmetry Adapted Perturbation Theory (SAPT). I. Efficiency and Performance for Interaction Energies. J. Chem. Phys. 2014, 140, 1–16.
  • Parrish, R.M.; Burns, L.A.; Smith, D.G.A.; Simmonett, A.C. PSI4 1.1: An Open-Source Electronic Structure Program Emphasizing Automation, Advanced Libraries, and Interoperability. J. Chem. Theory Comput. 2017, 13, 3185–3197.
  • Riley, K.E.; Hobza, P. Noncovalent Interactions in Biochemistry. Wires Comput. Mol. Sci. 2011, 1, 3–17.
  • Eckert, F.; Klamt, A. Fast Solvent Screening Via Quantum Chemistry: COSMO-RS Approach. AIChE J. 2002, 48, 369–385.
  • Schaeffer, N.; Abranches, D.O.; Silva, L.P.; Martins, M.A.R. Non-ideality in Thymol Plus Menthol Type v Deep Eutectic Solvents. ACS Sustain. Chem. Eng. 2021, 9, 2203–2211.
  • Abranches, D.O.; Martins, R.O.; Silva, L.P.; Martins, M.A.R. Liquefying Compounds by Forming Deep Eutectic Solvents: A Case Study for Organic Acids and Alcohols. J. Phys. Chem. B 2020, 124, 4174–4184.
  • Martins, M.A.R.; Silva, L.P.; Schaeffer, N.; Abranches, D.O.; Maximo, G.J.; Pinho, S.P.; Coutinho, J.A.P. Greener Terpene–Terpene Eutectic Mixtures as Hydrophobic Solvents. ACS Sustain. Chem. Eng. 2019, 7, 17414–17423.
  • Omar, K.A.; Sadeghi, R. Can Isopiestic Method Predict the Formation of Deep Eutectic Solvents? J. Mol. Liq. 2021, 333, 1–9.
  • Al-Kadhemy, M.F.H.; Rasheed, Z.S.; Salim, S.R. Fourier Transform Infrared Spectroscopy for Irradiation Coumarin Doped Polystyrene Polymer Films by Alpha ray. J. Radiat. Res. Appl. Sci. 2019, 9, 321–331.
  • Babij, M.; Mondry, A. Synthesis, Structure and Spectroscopic Studies of Europium Complex with S(+)-Mandelic Acid. J. Rare Earth 2011, 29, 1188–1191.
  • Fan, C.; Sebbah, T.; Liu, Y.; Cao, X. Terpenoid-Capric Acid Based Natural Deep Eutectic Solvent: Insight Into the Nature of Low Viscosity. Cleaner Eng. Technol. 2021, 3, 1–9.
  • Abranches, D.O.; Silva, L.P.; Martins, M.A.R.; Pinho, S.P.; Coutinho, J.A.P. Understanding the Formation of Deep Eutectic Solvents: Betaine as a Universal Hydrogen Bond Acceptor. ChemSusChem. 2020, 13, 4916–4921.
  • Turner, A.H.; Holbrey, J.D. Investigation of Glycerol Hydrogen-Bonding Networks in Choline Chloride/Glycerol Eutectic-Forming Liquids Using Neutron Diffraction. Phys. Chem. Chem. Phys. 2019, 21, 21782–21789.
  • Malik, A.; Kashyap, H.K. Heterogeneity in Hydrophobic Deep Eutectic Solvents: SAXS Prepeak and Local Environments. Phys. Chem. Chem. Phys. 2021, 23, 3915–3924.