38
Meng X, Ballerat-Busserolles K, Husson P, Andanson J-M (2016) Impact of water on the melting
temperature of urea + choline chloride deep eutectic solvent. New J Chem 40(5):4492–4499.
https://doi.org/10.1039/C5NJ02677F
Mitar A, Panić M, Prlić Kardum J, Halambek J, Sander A, Zagajski Kučan K, Radojčić
Redovniković I, Radošević K (2019) Physicochemical properties, cytotoxicity, and antioxidative activity of natural deep eutectic solvents containing organic acid. Chem Biochem Eng Q
33(1):1–18. https://doi.org/10.15255/CABEQ.2018.1454
Mjalli FS (2016) Mass connectivity index-based density prediction of deep eutectic solvents. Fluid
Phase Equilib 409:312–317. https://doi.org/10.1016/j.fluid.2015.09.053
Mjalli FS, Shahbaz K, AlNashef IM (2015) Modified Rackett equation for modelling the molar
volume of deep eutectic solvents. Thermochim Acta 614:185–190. https://doi.org/10.1016/j.
tca.2015.06.026
Mulia K, Fauzia F, Krisanti EA (2019) Polyalcohols as hydrogen-bonding donors in choline
chloride- based deep eutectic solvents for extraction of Xanthones from the pericarp of Garcinia
mangostana L. Molecules 24(3):636. https://doi.org/10.3390/molecules24030636
Nunes RJ, Saramago B, Marrucho IM (2019) Surface tension of dl-menthol:octanoic acid eutectic
mixtures. J Chem Eng Data 64(11):4915–4923. https://doi.org/10.1021/acs.jced.9b00424
Paiva A, Craveiro R, Aroso I, Martins M, Reis RL, Duarte ARC (2014) Natural deep eutectic
solvents – solvents for the 21st century. ACS Sustain Chem Eng 2(5):1063–1071. https://doi.
org/10.1021/sc500096j
Pandey A, Pandey S (2014) Solvatochromic probe behavior within choline chloride-based deep
eutectic solvents: effect of temperature and water. J Phys Chem B 118(50):14652–14661.
https://doi.org/10.1021/jp510420h
Pandey A, Rai R, Pal M, Pandey S (2013) How polar are choline chloride-based deep eutectic solvents? Phys Chem Chem Phys 16(4):1559–1568. https://doi.org/10.1039/C3CP53456A
Posada E, López-Salas N, Riobóo RJJ, Ferrer ML, Gutiérrez MC, Monte F d (2017) Reline aqueous solutions behaving as liquid mixtures of H-bonded co-solvents: microphase segregation
and formation of co-continuous structures as indicated by Brillouin and 1H NMR spectroscopies. Phys Chem Chem Phys 19(26):17103–17110. https://doi.org/10.1039/C7CP02180A
Posada E, Roldán-Ruiz MJ, Jiménez Riobóo RJ, Gutiérrez MC, Ferrer ML, del Monte F (2019)
Nanophase separation in aqueous dilutions of a ternary DES as revealed by Brillouin and NMR
spectroscopy. J Mol Liq 276:196–203. https://doi.org/10.1016/j.molliq.2018.11.139
Reichardt C (1994) Solvatochromic dyes as solvent polarity indicators. Chem Rev 94(8):2319–2358.
https://doi.org/10.1021/cr00032a005
Ribeiro BD, Florindo C, Iff LC, Coelho MAZ, Marrucho IM (2015) Menthol-based eutectic mixtures: hydrophobic low viscosity solvents. ACS Sustain Chem Eng 3(10):2469–2477. https://
doi.org/10.1021/acssuschemeng.5b00532
Rodriguez Rodriguez N, van den Bruinhorst A, Kollau LJBM, Kroon MC, Binnemans K (2019)
Degradation of deep-eutectic solvents based on choline chloride and carboxylic acids. ACS
Sustain Chem Eng 7(13):11521–11528. https://doi.org/10.1021/acssuschemeng.9b01378
Roldán-Ruiz MJ, Jiménez-Riobóo RJ, Gutiérrez MC, Ferrer ML, del Monte F (2019) Brillouin and
NMR spectroscopic studies of aqueous dilutions of malicine: determining the dilution range
for transition from a “water-in-DES” system to a “DES-in-water” one. J Mol Liq 284:175–181.
https://doi.org/10.1016/j.molliq.2019.03.133
Rublova Y, Kityk A, Danilov F, Protsenko V (2020) Mechanistic study on surface tension of binary
and ternary mixtures containing choline chloride, ethylene glycol and water (components of
aqueous solutions of a deep eutectic solvent, ethaline). Z Phys Chem 234(3):399–413. https://
doi.org/10.1515/zpch-2019-1492
Sanchez-Fernandez A, Hammond OS, Jackson AJ, Arnold T, Doutch J, Edler KJ (2017)
Surfactant–solvent interaction effects on the micellization of cationic surfactants in a carboxT. El Achkar et al.
Meng X, Ballerat-Busserolles K, Husson P, Andanson J-M (2016) Impact of water on the melting
temperature of urea + choline chloride deep eutectic solvent. New J Chem 40(5):4492–4499.
https://doi.org/10.1039/C5NJ02677F
Mitar A, Panić M, Prlić Kardum J, Halambek J, Sander A, Zagajski Kučan K, Radojčić
Redovniković I, Radošević K (2019) Physicochemical properties, cytotoxicity, and antioxidative activity of natural deep eutectic solvents containing organic acid. Chem Biochem Eng Q
33(1):1–18. https://doi.org/10.15255/CABEQ.2018.1454
Mjalli FS (2016) Mass connectivity index-based density prediction of deep eutectic solvents. Fluid
Phase Equilib 409:312–317. https://doi.org/10.1016/j.fluid.2015.09.053
Mjalli FS, Shahbaz K, AlNashef IM (2015) Modified Rackett equation for modelling the molar
volume of deep eutectic solvents. Thermochim Acta 614:185–190. https://doi.org/10.1016/j.
tca.2015.06.026
Mulia K, Fauzia F, Krisanti EA (2019) Polyalcohols as hydrogen-bonding donors in choline
chloride- based deep eutectic solvents for extraction of Xanthones from the pericarp of Garcinia
mangostana L. Molecules 24(3):636. https://doi.org/10.3390/molecules24030636
Nunes RJ, Saramago B, Marrucho IM (2019) Surface tension of dl-menthol:octanoic acid eutectic
mixtures. J Chem Eng Data 64(11):4915–4923. https://doi.org/10.1021/acs.jced.9b00424
Paiva A, Craveiro R, Aroso I, Martins M, Reis RL, Duarte ARC (2014) Natural deep eutectic
solvents – solvents for the 21st century. ACS Sustain Chem Eng 2(5):1063–1071. https://doi.
org/10.1021/sc500096j
Pandey A, Pandey S (2014) Solvatochromic probe behavior within choline chloride-based deep
eutectic solvents: effect of temperature and water. J Phys Chem B 118(50):14652–14661.
https://doi.org/10.1021/jp510420h
Pandey A, Rai R, Pal M, Pandey S (2013) How polar are choline chloride-based deep eutectic solvents? Phys Chem Chem Phys 16(4):1559–1568. https://doi.org/10.1039/C3CP53456A
Posada E, López-Salas N, Riobóo RJJ, Ferrer ML, Gutiérrez MC, Monte F d (2017) Reline aqueous solutions behaving as liquid mixtures of H-bonded co-solvents: microphase segregation
and formation of co-continuous structures as indicated by Brillouin and 1H NMR spectroscopies. Phys Chem Chem Phys 19(26):17103–17110. https://doi.org/10.1039/C7CP02180A
Posada E, Roldán-Ruiz MJ, Jiménez Riobóo RJ, Gutiérrez MC, Ferrer ML, del Monte F (2019)
Nanophase separation in aqueous dilutions of a ternary DES as revealed by Brillouin and NMR
spectroscopy. J Mol Liq 276:196–203. https://doi.org/10.1016/j.molliq.2018.11.139
Reichardt C (1994) Solvatochromic dyes as solvent polarity indicators. Chem Rev 94(8):2319–2358.
https://doi.org/10.1021/cr00032a005
Ribeiro BD, Florindo C, Iff LC, Coelho MAZ, Marrucho IM (2015) Menthol-based eutectic mixtures: hydrophobic low viscosity solvents. ACS Sustain Chem Eng 3(10):2469–2477. https://
doi.org/10.1021/acssuschemeng.5b00532
Rodriguez Rodriguez N, van den Bruinhorst A, Kollau LJBM, Kroon MC, Binnemans K (2019)
Degradation of deep-eutectic solvents based on choline chloride and carboxylic acids. ACS
Sustain Chem Eng 7(13):11521–11528. https://doi.org/10.1021/acssuschemeng.9b01378
Roldán-Ruiz MJ, Jiménez-Riobóo RJ, Gutiérrez MC, Ferrer ML, del Monte F (2019) Brillouin and
NMR spectroscopic studies of aqueous dilutions of malicine: determining the dilution range
for transition from a “water-in-DES” system to a “DES-in-water” one. J Mol Liq 284:175–181.
https://doi.org/10.1016/j.molliq.2019.03.133
Rublova Y, Kityk A, Danilov F, Protsenko V (2020) Mechanistic study on surface tension of binary
and ternary mixtures containing choline chloride, ethylene glycol and water (components of
aqueous solutions of a deep eutectic solvent, ethaline). Z Phys Chem 234(3):399–413. https://
doi.org/10.1515/zpch-2019-1492
Sanchez-Fernandez A, Hammond OS, Jackson AJ, Arnold T, Doutch J, Edler KJ (2017)
Surfactant–solvent interaction effects on the micellization of cationic surfactants in a carboxT. El Achkar et al.