Low-transition-temperature mixtures (LTTMs): A new generation of designer solvents

Novel solvent properties of choline chloride/urea mixturesElectronic supplementary information (ESI) available: spectroscopic data. See http://www.rsc.org/suppdata/cc/b2/b210714g/

Abbott, A. P., Capper, G., Davies, D. L., Rasheed, R. K., & Tambyrajah, V. (2003) · Chemical Communications · doi:10.1039/b210714g · Cited by 5,738

Deep eutectic solvents: syntheses, properties and applications

Zhang, Q., De Oliveira Vigier, K., Royer, S., & Jérôme, F. (2012) · Chemical Society Reviews · doi:10.1039/c2cs35178a · Cited by 4,899

Deep eutectic solvents formed between choline chloride and carboxylic acids: Versatile alternatives to ionic liquids

Abbott, A. P., Boothby, D., Capper, G., Davies, D. L., & Rasheed, R. K. (2004) · Journal of the American Chemical Society · doi:10.1021/ja048266j · Cited by 4,340

ANALYSIS OF RECENT MEASUREMENTS OF THE VISCOSITY OF GLASSES

Fulcher, G. S. (1925) · Journal of the American Ceramic Society · doi:10.1111/j.1151-2916.1925.tb16731.x · Cited by 4,199

Ionic liquids. Green solvents for the future

Earle, M. J., & Seddon, K. R. (2000) · Pure and Applied Chemistry · doi:10.1351/pac200072071391 · Cited by 2,813

Origins, Current Status, and Future Challenges of Green Chemistry

Anastas, P. T., & Kirchhoff, M. M. (2002) · Accounts of Chemical Research · doi:10.1021/ar010065m · Cited by 2,221

What is a green solvent? A comprehensive framework for the environmental assessment of solvents

Capello, C., Fischer, U., & Hungerbühler, K. (2007) · Green Chemistry · doi:10.1039/b617536h · Cited by 1,917

The properties of organic liquids that are relevant to their use as solvating solvents

Marcus, Y. (1993) · Chemical Society Reviews · doi:10.1039/cs9932200409 · Cited by 1,637

Are Natural Deep Eutectic Solvents the Missing Link in Understanding Cellular Metabolism and Physiology?

Choi, Y. H., van Spronsen, J., Dai, Y., Verberne, M., Hollmann, F., Arends, I. W. C. E., Witkamp, G.-J., & Verpoorte, R. (2011) · Plant Physiology · doi:10.1104/pp.111.178426 · Cited by 1,368

Organic chemistry in water

LI, C. ‐., & Chen, L. (2005) · Chemical Society Reviews · doi:10.1039/b507207g · Cited by 1,335

Acetaminophen solubility in aqueous solutions of betaine-propylene glycol natural deep eutectic solvent at different temperatures

Barzegar-Jalali, M., Jafari, P., & Jouyban, A. (2021) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2021.118199 · Cited by 14

Insights into the Play of Novel Brønsted Acid-Based Deep Eutectic Solvents for the Conversion of Glucose into 5-Hydroxymethylfurfural without Additional Catalysts

Tao, S., Hu, L., Zhang, X., Mai, Y., Xian, X., Zheng, X., & Lin, X. (2022) · Industrial & Engineering Chemistry Research · doi:10.1021/acs.iecr.2c01193 · Cited by 15

Chemiluminescent gels of G-quadruplexes in deep eutectic solvents

Qi, P., Jia, L., Yi, M., Zhao, E., Liu, Y., Song, A., & Hao, J. (2022) · Colloids and Surfaces A Physicochemical and Engineering Aspects · doi:10.1016/j.colsurfa.2022.130319 · Cited by 14

Morita–Baylis–Hillman reaction in eutectic solvent under aqueous medium

Zhao, S., Zhi, H., Zhang, M., Yan, Q., Fan, J., & Guo, J. (2016) · RSC Advances · doi:10.1039/c6ra04710f · Cited by 14

Morpholinium and Piperidinium Based Deep Eutectic Solvents for Synthesis of Pyrazole‐5‐Carbonitriles, Indoles and Tetrazoles: Bulk Properties via Molecular Dynamics Simulations

Sanam, Bux, K., al‐Rashida, M., Alharthy, R. D., Moin, S. T., & Hameed, A. (2018) · ChemistrySelect · doi:10.1002/slct.201803265 · Cited by 14

Choline Chloride/Urea as an Eco‐Friendly Deep Eutectic Solvent for TCT‐Mediated Amide Coupling at Room Temperature

Kimiya, S., & Saberi, D. (2019) · ChemistrySelect · doi:10.1002/slct.201804066 · Cited by 14

ZnCl 2 +Urea, the deep eutectic solvent promoted synthesis of the spirooxindolopyrans and xanthenes through a pseudo-three-component approach

Nishtala, V. B., & Basavoju, S. (2019) · Synthetic Communications · doi:10.1080/00397911.2019.1620784 · Cited by 14

Valorization of monosaccharides towards fructopyrazines in a new sustainable and efficient eutectic medium

Filonenko, S., Völkel, A., & Antonietti, M. (2019) · Green Chemistry · doi:10.1039/c9gc02176k · Cited by 14

Deep Eutectic Solvents as a New Reaction Medium for Biotransformations

Yang, Z., & Wen, Q. (2015) · Wiley eBooks · doi:10.1002/9781118854501.ch25 · Cited by 14

Solute rotation and solvation dynamics in deep eutectic solvents

Hossain, S. S., & Samanta, A. (2021) · Chemical Physics Impact · doi:10.1016/j.chphi.2021.100043 · Cited by 13

Silver‐catalysed A3‐coupling reactions in phenylacetic acid/alkylamineN‐oxide eutectic mixture under dielectric heating: An alternative approach to propargylamines

Brambilla, E., Bortolla, A., Pirovano, V., Caselli, A., TIECCO, M., & Abbiati, G. (2022) · Applied Organometallic Chemistry · doi:10.1002/aoc.6669 · Cited by 14

Predicting the Thermal Behavior in the Design of Type V Deep Eutectic Solvents: The Combined Role of Polarity and Steric Asymmetry

Mannucci, G., Teixeira, G., Sosa, F. H. B., Palluzzi, M., Busato, M., Coutinho, J. A. P., & D’Angelo, P. (2024) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.3c07965 · Cited by 13

The Variety of Deep Eutectic Solvents

Marcus, Y. (2018) · Springer eBooks · doi:10.1007/978-3-030-00608-2_2 · Cited by 15

Role of Solvent System in Green Synthesis of Nanoparticles

Ali, K., Cherian, T., Fatima, S., Saquib, Q., Faisal, M., Alatar, A. A., Musarrat, J., & Al-Khedhairy, A. A. (2020) · Springer eBooks · doi:10.1007/978-981-15-5179-6_3 · Cited by 13

Molecular dynamics investigation of wetting–dewetting behavior of reline DES nanodroplet at model carbon material

Malik, A., Dhattarwal, H. S., & Kashyap, H. K. (2020) · The Journal of Chemical Physics · doi:10.1063/5.0023460 · Cited by 13

Physically Cross-Linked Titania-Supported Novel Eutectogels as Solid-State Electrolytes: An Experimental and Quantum Chemical Investigation

Dutta, A., Kundu, D., Sharma, S., Paul, N., Naik, P. K., Silvester, D. S., & Banerjee, T. (2023) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.3c05551 · Cited by 13

Combination of a Deep Eutectic Solvent and Macroporous Resin for Green Recovery of Iridoids, Chlorogenic Acid, and Flavonoids from Eucommia ulmoides Leaves

Liao, Y., Chen, F., Tang, H., Dessie, W., & Qin, Z. (2024) · Molecules · doi:10.3390/molecules29030737 · Cited by 14

Low-Transition-Temperature Mixtures (LTTMs) for Dissolving Proteins and for Drug Formulation

Su, E., & Klibanov, A. M. (2015) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-015-1777-x · Cited by 14

Proton conducting electrolytes composed of chondroitin sulfate polysaccharide and citric acid

Santos, F. M., Barbosa, P., Pereira, R. F. P., Silva, M. M. P., Gonçalves, H. M. R., Nunes, S. C., Figueiredo, F. L., Valente, A. J. M., & Bermudez, V. D. Z. (2019) · European Polymer Journal · doi:10.1016/j.eurpolymj.2019.109453 · Cited by 13

Efficient synthesis of bio‐based monomer 2,5‐bishydroxymethylfuran by the solvent‐free hydrogenation of 5‐hydroxymethylfurfural‐based deep eutectic mixture

Wang, T., Wei, J., Feng, Y., Liu, H., Tang, X., Zeng, X., Sun, Y. Q., Lei, T., & Lin, L. (2020) · Journal of Chemical Technology & Biotechnology · doi:10.1002/jctb.6373 · Cited by 13

Organic Salts Based on Isoniazid Drug: Synthesis, Bioavailability and Cytotoxicity Studies

Santos, F., Branco, L. C., & Duarte, A. R. C. (2020) · Pharmaceutics · doi:10.3390/pharmaceutics12100952 · Cited by 13

Measurements of the Thermal Conductivity of l -Menthol–Decanoic Acid Deep Eutectic Solvents in the Temperature Range from 283.15 to 363.15 K at Pressures up to 15.1 MPa

Yu, L., Hou, X., Wu, K., & He, C. (2021) · Journal of Chemical & Engineering Data · doi:10.1021/acs.jced.0c01099 · Cited by 13

Therapeutic Liquid Formulations Based on Low Transition Temperature Mixtures for the Incorporation of Anti-Inflammatory Drugs

Roda, A., Paiva, A., & Duarte, A. R. C. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13101620 · Cited by 17

Synthesis and Characterisation of Thymol‐Based Hydrophobic Deep Eutectic Solvents

Adeoye, D. O., Gano, Z. S., Ahmed, O. U., Shuwa, S. M., Atta, A. Y., & Jubril, B. Y. (2023) · ECSOC 2023 · doi:10.3390/ecsoc-27-16380 · Cited by 12

New hydrophobic DES based on tri–n-octylphosphine oxide and dicarboxylic acids: synthesis, spectroscopy and liquid–liquid extraction of actinides

Kshirsagar, A., Verma, P. K., & Murali, M. S. (2021) · Journal of Radioanalytical and Nuclear Chemistry · doi:10.1007/s10967-021-07994-4 · Cited by 12

Novel hydrophobic acetanilide-based deep eutectic solvents. Preparation, properties, their applications in liquid–liquid extraction

Kianpoor, A., & Sadeghi, R. (2024) · Chemical Engineering Science · doi:10.1016/j.ces.2024.119866 · Cited by 12

Analyzing the Effect of Extraction Parameters on Phenolic Composition and Selected Compounds in Clove Buds Using Choline Chloride and Lactic Acid as Extraction Agents

Strižincová, P., Šurina, I., Jablonský, M., Majová, V., Ház, A., Hroboňová, K., & Špačková, A. (2024) · Processes · doi:10.3390/pr12040653 · Cited by 13

Aqueous biphasic systems developed with deep eutectic solvents and polymer for the efficient extraction of pigments from beverages

Xu, K., Zhao, Y., Chen, K., Dong, H., Sun, S., Ni, Z., & Wang, Y. (2024) · Food Chemistry · doi:10.1016/j.foodchem.2024.139206 · Cited by 12

Recent Progress in Non-Aqueous Biocatalysis of Immobilized Enzymes

Ma, J., Wang, L., Chu, Y., Wang, Y., Chen, K., & Li, H. (2024) · Processes · doi:10.3390/pr12081571 · Cited by 12

Enhancing separation of Y( III ) from Sr( II ) using tributyl phosphate in a novel deep eutectic solvent media

Zhao, Q., Wu, F. P., Shih, A. A., Fung, C. K., Gao, P., & Liu, M. (2024) · AIChE Journal · doi:10.1002/aic.18552 · Cited by 12

Insights into DES Stability and Reactivity with Carboxylic Acids: A Computational Approach

Yadav, S., Prajapat, A., Aslam, M., Kumar, S., Kabane, B., Bahadur, I., Rahaman, M., Singh, P., & Singh, T. (2024) · Journal of Computational Biophysics and Chemistry · doi:10.1142/s2737416524500443 · Cited by 12

Infinite Dilution Activity Coefficients and Thermodynamic Properties of Various Organic Solutes in a Choline Chloride + Oxalic Acid Deep Eutectic Solvent

Wang, C., Wang, Q., Yalikun, N., Fu, J., & Wang, B. (2022) · Journal of Chemical & Engineering Data · doi:10.1021/acs.jced.2c00016 · Cited by 12

Effect of temperature and composition on solubility and thermodynamics of salicylic acid in aqueous mixtures of betaine-based deep eutectic solvents

Jafari, P., Barzegar-Jalali, M., & Jouyban, A. (2023) · Korean Journal of Chemical Engineering · doi:10.1007/s11814-022-1284-z · Cited by 12

Separation of methanol and ethanol from azeotropic MTBE mixtures using choline chloride-based deep eutectic solvents

Esfahani, H. S., Khoshsima, A., Pazuki, G., & Hosseini, A. (2023) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2023.121641 · Cited by 13

Sustainable polar aprotic/poly-deep eutectic solvent systems for highly efficient dissolution of lignin

Liu, Q., Wang, Y., Bian, J., Li, M., Ren, J., Hao, X., & Peng, F. (2023) · Green Chemistry · doi:10.1039/d3gc00733b · Cited by 13

Mechanistic Investigation of Isobutanol/Isobutyl Acetate Separation by Extraction Using Low-Transition Temperature Mixtures

Yan, J., Li, X., Meng, M., Zhao, C., Li, J., & Sun, L. (2023) · Industrial & Engineering Chemistry Research · doi:10.1021/acs.iecr.3c02200 · Cited by 12

Carbon–GO Composites with Preferential Water versus Ethanol Uptake

Guan, L., Patiño, J., Collados, C. C., Tamayo, A., Gutiérrez, M. C., Ferrer, M. L., Silvestre‐Albero, J., & del Monte, F. (2019) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.9b02745 · Cited by 12

Selection of Anti‐gluten DNA Aptamers in a Deep Eutectic Solvent

Svigelj, R., Dossi, N., Toniolo, R., Miranda‐Castro, R., de-los-Santos-Álvarez, N., & Lobo-Castañón, M. J. (2018) · Angewandte Chemie · doi:10.1002/ange.201804860 · Cited by 12

Deep Eutectic Solvent Membranes Designed by the Same-Anion Strategy for Highly Efficient Ethylene/Ethane Separation

Xu, M., Dou, H., Ren, Y., Peng, F., Xiao, X., Tantai, X., Sun, Y., Jiang, B., Yang, N., & Zhang, L. (2022) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.2c00253 · Cited by 11

Preparation of Ammonium Persulfate/Glycerol based Novel Deep Eutectic Solvent under controlled conditions; Characterizations, Physical properties

Zaman, S. U., Mehdi, M. S., Umar, M., Rafiq, S., Saif-ur-Rehman, Zaman, M. K. U., Javed, M. D., Waseem, M. A., & Tahir, N. (2023) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2023.135265 · Cited by 11

The hydrophobic collapse of thermoresponsive polymer poly( N -vinyl caprolactam): a new class of biocompatible solvents

Rawat, P., Mor, S., Yadav, R., Narang, P., Bisht, M., & Venkatesu, P. (2023) · New Journal of Chemistry · doi:10.1039/d3nj04754g · Cited by 11

Molecular interaction between three novel amino acid based deep eutectic solvents with surface active ionic liquid: A comparative study

Banjare, M. K., Barman, B., Behera, K., Khan, J. M., Banjare, R. K., Pandey, S., & Ghosh, K. K. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e35598 · Cited by 11

Covalent organic frameworks and related innovative materials in chiral separation and recognition

Qin, Y., Li, D., Yao, T., Ali, A., Wu, J., & Yao, S. (2024) · Biomedical Chromatography · doi:10.1002/bmc.6008 · Cited by 11

Quantum chemical investigations into the structural and spectroscopic properties of choline chloride-based deep eutectic solvents

Hasan, M. A., Rahman, I. M. M., Hossain, M., & Chowdhury, F. I. (2024) · Chemical Physics Impact · doi:10.1016/j.chphi.2024.100777 · Cited by 11

High-performance functionalized keratin for efficient lithium recovery: Experimental and statistical physics insights

Abujayyab, M., Hasan, S. W., Lemaoui, T., AlNashef, I. M., Arafat, H. A., & BANAT, F. A. (2025) · Desalination · doi:10.1016/j.desal.2025.118782 · Cited by 11

The complex world of eutectic solvents: Guidelines for a correct characterization and use in sample preparation

Bosco, C. D., Cesaris, M. G. D., Antonelli, L., Felli, N., & Gentili, A. (2025) · Advances in Sample Preparation · doi:10.1016/j.sampre.2025.100189 · Cited by 11

Controlled Growth of Rubrene Nanowires by Eutectic Melt Crystallization

Chung, J., Hyon, J., Park, K.-S., Cho, B., Baek, J., Kim, J., Lee, S. U., Sung, M. M., & Kang, Y. (2016) · Scientific Reports · doi:10.1038/srep23108 · Cited by 11

Investigation of SO2 solubilities in some biobased solvents and their thermodynamic properties

Deng, D., Liu, X., Cui, Y., & Jiang, Y. (2017) · The Journal of Chemical Thermodynamics · doi:10.1016/j.jct.2017.12.021 · Cited by 11

Enhanced one-step sample pretreatment method for extraction of ginsenosides from rat plasma using tailor-made deep eutectic mixture solvents

Zhao, N., Liu, S., Xing, J., Zheng, Z., Pi, Z., Song, F., & Liu, Z. (2019) · Analytical Methods · doi:10.1039/c8ay02433b · Cited by 11

Scrutiny of the supramolecular structure of bio-sourced fructose/glycerol/water ternary mixtures: Towards green low transition temperature mixtures

Caprin, B., Charton, V., Rodier, J.-D., Vogelgesang, B., Charlot, A., Boisson, F., & Fleury, É. (2021) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2021.116428 · Cited by 12

Insights into therapeutic liquid mixtures and formulations towards tuberculosis therapy

Santos, F., Pires, D., Anes, E., & Duarte, A. R. C. (2023) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2023.122862 · Cited by 11

What the anion tells us about the structure of tetrabutylammonium salt/phenol-based deep eutectic solvents? A combined infrared spectroscopic and DFT study

Mahi, M.-R., Nicolov, N., Coma, L., Grondin, J., Aupetit, C., Méreau, R., & Tassaing, T. (2023) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2023.122505 · Cited by 11

DBS‐Based Eutectogels: Organized Vessels to Perform the Michael Addition Reaction**

Rizzo, C., Marullo, S., Benaglia, M., & D’Anna, F. (2023) · European Journal of Organic Chemistry · doi:10.1002/ejoc.202300263 · Cited by 11

Does Viscosity Decoupling Guarantee Dynamic Heterogeneity? A Clue through an Excitation and Emission Wavelength-Dependent Time-Resolved Fluorescence Anisotropy Study

Tarif, E., Das, N., & Sen, P. (2023) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.3c00334 · Cited by 11

Highly Selective CO2/CH4Membranes Based on Ethanolamine Ionic Liquids

Alcantara, M. L., Oliveira, G. D. A. R., Lião, L. M., Ortiz, A., & Mattedi, S. (2024) · Industrial & Engineering Chemistry Research · doi:10.1021/acs.iecr.3c04533 · Cited by 11

Influence of Betaine- and Choline-based Eutectic Solvents on Lipase Activity

Ribeiro, B. D., Iff, L. D. C., Coelho, M. A. Z., & Marrucho, I. M. (2019) · Current Biochemical Engineering · doi:10.2174/2212711906666190710181629 · Cited by 12

Deep eutectic solvent mediated rapid and selective one-pot synthesis of 5-alkylidene-Thiazolones

Azizi, N., Qomi, M., Asghari, M., & Farhadi, E. (2021) · Sustainable Chemistry and Pharmacy · doi:10.1016/j.scp.2021.100457 · Cited by 11

SUBSTITUTION OF SOLVENTS BY SAFER PRODUCTS

(2019) · Elsevier eBooks · doi:10.1016/b978-1-927885-41-3.50010-3 · Cited by 14

Experimental determination and correlation of naproxen solubility in biodegradable low-toxic betaine-based deep eutectic solvents and water mixtures at 293.15 K to 313.15 K

Barzegar-Jalali, M., Jafari, P., & Jouyban, A. (2022) · Fluid Phase Equilibria · doi:10.1016/j.fluid.2022.113508 · Cited by 11

Scientific specialties in Green Chemistry

Marcelino, L. V., Pinto, A. L., & Marques, C. A. (2020) · Iberoamerican Journal of Science Measurement and Communication · doi:10.47909/ijsmc.06 · Cited by 11

Structure and Implications

Hammond, O. S., & Edler, K. J. (2019) · Wiley eBooks · doi:10.1002/9783527818488.ch2 · Cited by 11

Tailorable Antibacterial Activity and Biofilm Eradication Properties of Biocompatible α-Hydroxy Acid-Based Deep Eutectic Solvents

Dubinenko, G. E., Ивановна, С. Е., Golovina, K. S., Myshova, A. E., Igumnova, O. A., Plotnikov, E., Badaraev, A. D., Rutkowski, S., Filimonov, V. D., & Tverdokhlebov, S. I. (2025) · Pharmaceutics · doi:10.3390/pharmaceutics18010016 · Cited by 10

Chiral Eutectic Mixtures and Deep Eutectic Solvents for Induced Circularly Polarized Luminescence

Nelson, B. P., VandenElzen, L., Whitacre, G., & Hopkins, T. A. (2021) · ChemPhotoChem · doi:10.1002/cptc.202100139 · Cited by 10

Ultrasound- and heat-assisted extraction of glycyrrhizin from licorice by two glycerol-based DESs - Modeling and optimization as per response surface methodology

Kubra, K. T., Ahmed, D., Aydar, A. Y., & Qamar, M. T. (2022) · Sustainable Chemistry and Pharmacy · doi:10.1016/j.scp.2022.100910 · Cited by 10

Water Induced Alterations in Self‐Assembly of a Bio‐Surfactant in Deep Eutectic Solvent for Enhanced Enzyme Activity

Sethi, O., Singh, M., Sood, A. K., & Kang, T. S. (2023) · ChemPhysChem · doi:10.1002/cphc.202300293 · Cited by 10

Balancing the strength and toughness in delignified bamboo through the changing of silicon composition

Wang, Y., Jia, S., Ling, Z., Ma, J., Ma, X., & Fang, C. (2024) · Materials & Design · doi:10.1016/j.matdes.2024.113408 · Cited by 10

Hydrophobic Deep Eutectic Solvents as New Supported Liquid Membranes for Extraction of β‐Blockers by Hollow Fiber–Electromembrane Extraction

Beiranvand, M., Yamini, Y., & Khataei, M. M. (2025) · Journal of Separation Science · doi:10.1002/jssc.70102 · Cited by 10

Extraction, purification, and functionality of proteins using deep eutectic solvents: a review

Khanalipour, A., Tabibiazar, M., Masoumi, B., Azar, S. T., Allahyari, A., & Borji, M. (2025) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2025.127623 · Cited by 12

Prognostication of advanced CO2 capture using tunable solvents with an ensemble learning-based decision tree model

Soleimani, R., Dehaghani, A. H. S., Behtouei, Z., Farahani, H., & Hashemi, S. M. (2025) · Scientific Reports · doi:10.1038/s41598-025-04318-4 · Cited by 10

Design of a Ɛ-caprolactam-based ionic liquids for the extraction of lipids from starved Parachlorella kessleri microalgae for sustainable aviation fuels (SAF)

Rivas-Navia, D., Cheikhwafa, J., Zurita, A., Torrens, E., & Bengoa, C. (2025) · Algal Research · doi:10.1016/j.algal.2025.104369 · Cited by 10

Norharmane prototropism in choline chloride-based deep eutectic solvents

Bhawna, B., Dhingra, D., Pandey, A., & Pandey, S. (2019) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/j.jphotochem.2019.112138 · Cited by 10

Mild depolymerization of alkaline lignin in a formic acid-choline chloride type deep eutectic solvent system

Li, P., Li, X., Jiang, Z., Xu, X., Jin, Y., & Wu, W. (2023) · Holzforschung · doi:10.1515/hf-2022-0145 · Cited by 10

Isobaric Vapor–Liquid Equilibria for the Quaternary System Water + Ethanol + Ethylene Glycol + Choline Chloride and the Ternary System Water + Ethanol + Choline Chloride at 101.3 kPa

Zhang, Y., Fang, J., & Zhang, L. (2019) · Journal of Chemical & Engineering Data · doi:10.1021/acs.jced.9b00254 · Cited by 10

Preparation and physico-chemical studies of Ag2O nanoparticles using newly formed malonic acid and ZnCl2-based deep eutectic solvents

Sarjuna, K., & Ilangeswaran, D. (2021) · Materials Today Proceedings · doi:10.1016/j.matpr.2021.11.355 · Cited by 10

Deep eutectic solvents: green solvents for the removal of degraded gelatin on cellulose nitrate cinematographic films

Lozano, M. V. C., Sciutto, G., Prati, S., & Mazzeo, R. (2022) · Heritage Science · doi:10.1186/s40494-022-00748-9 · Cited by 10

Deep Eutectic Solvent: An Efficient Catalyst for C‐O Coupling Reactions.

Pant, P. L., & Shankarling, G. S. (2017) · ChemistrySelect · doi:10.1002/slct.201700584 · Cited by 10

Organic Synthesis in DES s

Perna, F. M., Vitale, P., & Capriati, V. (2019) · Wiley eBooks · doi:10.1002/9783527818488.ch7 · Cited by 10

Thermal and Physical Properties of CO2-Reactive Binary Mixtures

Cagli, E., Liu, H., Khokhar, V., Klemm, A., & Gurkan, B. (2024) · Journal of Chemical & Engineering Data · doi:10.1021/acs.jced.3c00653 · Cited by 9

Integrated dilute acid-ternary deep eutectic solvents treatment for efficient component separation and sugar platform from lignocellulose

Yan, B., Fu, Y., Ding, W., Shi, G., Wang, Z., & Zhang, S. (2024) · Industrial Crops and Products · doi:10.1016/j.indcrop.2024.119808 · Cited by 9

Hydrogen-bond induced non-linear size dependence of lysozyme under the influence of aqueous glyceline

Sarkar, I., Sil, A., Guchhait, B., & Das, S. (2025) · The Journal of Chemical Physics · doi:10.1063/5.0251283 · Cited by 10

Synthesis of Novel Deep Eutectic Solvents for Ultralow Wear Performance at the Steel/Steel Interface under High Pressure

Gao, Y., Du, C., Zhang, L., Wang, L., Jia, Y., Fang, L., Li, X., Liu, Y., & Wang, D. (2025) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.5c05698 · Cited by 9

Exploring the Synergy between π–π Interactions and Hydrogen-Bonding in the Formation of Type V Deep Eutectic Solvents

Pietropaoli, E., Mannucci, G., Cirillo, L., Palluzzi, M., Busato, M., & D’Angelo, P. (2025) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.5c05276 · Cited by 10

Advancements in low-carbon biofuel production from agricultural waste valorization

Kusmayadi, A., Leong, Y. K., Ong, H. C., Hidayatullah, I. M., Budiastuti, H., & Ridwan, I. M. (2025) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2025.108726 · Cited by 10

Recent Developments in the Lithiation Reactions of Oxygen Heterocycles

Perna, F. M., Salomone, A., & Capriati, V. (2015) · Advances in heterocyclic chemistry · doi:10.1016/bs.aihch.2015.10.003 · Cited by 9

One-Pot Synthesis of Highly Functionalized Indole in Choline Chloride/Oxalic Acid as a Deep Eutectic Solvent

Berjis, A., Mirza, B., & Anaraki‐Ardakani, H. (2022) · Polycyclic aromatic compounds · doi:10.1080/10406638.2022.2089172 · Cited by 9

Performance evaluation and molecular dynamics simulation in the Liquid–liquid extraction process of low transition temperature mixture + n-hexane + 1,2-Dichloroethane

Zhang, W., Yi, X., Yi, Q., & Sun, L. (2022) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2022.119913 · Cited by 9

HFIP-promoted halo-carbocyclizations of N - and O -tethered arene–alkene substrates to access all halo (X = Br, I, Cl)-functionalized tetrahydroquinoline and chroman cores

Shukla, P. M., Bhattacharya, A., Pratap, A., Pradhan, A., Sinha, P., Soni, T., & Maji, B. (2022) · Organic & Biomolecular Chemistry · doi:10.1039/d2ob01597h · Cited by 9

Effect of temperature and composition on physical properties of deep eutectic solvents based on 2-(methylamino)ethanol – measurement and prediction

Nowosielski, B., Jamrógiewicz, M., Łuczak, J., Tercjak, A., & Warmińska, D. (2022) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2022.121069 · Cited by 9

Study of intermolecular interactions present in ternary mixtures containing sugar alcohol and choline chloride at different temperatures

Gaba, R., Kaur, N., Urvika, Pal, A., & Sharma, D. (2023) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2023.121766 · Cited by 9

Solvent-free, photoinduced block copolymer synthesis from polymerizable eutectics by simultaneous PET-RAFT and ring-opening polymerization in air

Nahar, Y., Stanfield, M. K., Bissember, A. C., & Thickett, S. C. (2023) · Polymer Chemistry · doi:10.1039/d3py00294b · Cited by 9

The interaction of pseudo-binary system of DES (1TEAB: 3EG) with acetonitrile, ethanol and water by volumetric properties, surface properties and refractive properties

Wei, J., Sun, X., Zhang, Y., Gao, P., Ren, C., Fang, D., & Li, L. (2023) · Journal of Thermal Analysis and Calorimetry · doi:10.1007/s10973-023-12221-1 · Cited by 9

Synergistic utilization of cold caustic extraction and deep eutectic solvent for the production of dissolving pulp from corn stalks

Liu, F., Qi, T., Wei, Q., Zhang, J., Li, Y., & Qu, Y. (2024) · Biomass and Bioenergy · doi:10.1016/j.biombioe.2024.107184 · Cited by 9

Tunable Properties of Non‐Volatile Magnetic Mixtures on Different Surfaces

Abellán-Martín, S. J., Zapater, C., González‐Gallardo, N., Aguirre, M. Á., Vidal, L., Ramón, D. J., & Canals, A. (2024) · ChemPhysChem · doi:10.1002/cphc.202400458 · Cited by 9

The deep eutectic melt of sorbitol and metformin hydrochloride: synthesis of 3-substituted 2-aminonaphtho[2,3-b]furan-4,9-diones and their photophysical properties

Rad‐Moghadam, K., Hassani, S. A. R. M., & Roudsari, S. T. (2016) · RSC Advances · doi:10.1039/c5ra19619a · Cited by 9

Life cycle assessment of oil palm empty fruit bunch delignification using natural malic acid-based low-transition-temperature mixtures: a gate-to-gate case study

Yiin, C. L., Yusup, S. B., Quitain, A. T., Uemura, Y., Sasaki, M., & Kida, T. (2018) · Clean Technologies and Environmental Policy · doi:10.1007/s10098-018-1590-7 · Cited by 9

Optimization and control of CO2 capture using low transition temperature mixtures

Ma, S., Shang, X., Li, L., Pan, Q., Xue, C., Ji, K., & Sun, L. (2018) · International journal of greenhouse gas control · doi:10.1016/j.ijggc.2018.12.016 · Cited by 9

Isobaric Liquid–Liquid Equilibrium Measurements and Thermodynamics Modeling for Systems: Benzene + Cyclohexane + DESs at 303.15 and 323.15 K

Sun, L., Luo, F., Liu, R., Yang, H., Huang, L., & Li, J. (2019) · Journal of Chemical & Engineering Data · doi:10.1021/acs.jced.8b01029 · Cited by 9

Performance of the Glycerol–Choline Chloride Deep Eutectic Solvent as an Entrainer for Separation of Ethanol and Water

Li, P., Wu, Y., Hao, X., & Zhang, L. (2021) · Journal of Chemical & Engineering Data · doi:10.1021/acs.jced.1c00207 · Cited by 9

DFT study of interaction of Palladium Pdn (n = 1–6) nanoparticles with deep eutectic solvents

Ghenaatian, H. R., Shakourian‐Fard, M., Alizadeh, V., & Kamath, G. (2021) · Journal of Molecular Graphics and Modelling · doi:10.1016/j.jmgm.2021.108072 · Cited by 9

Imidazolium-urea low transition temperature mixtures for the UHP-promoted oxidation of boron compounds

Martos, M., & Pastor, I. M. (2021) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2021.118349 · Cited by 10

Mischungen mit niedriger Übergangstemperatur (LTTMs) – eine neue Generation von Designer‐Lösungsmitteln

Francisco, M., van den Bruinhorst, A., & Kroon, M. C. (2013) · Angewandte Chemie · doi:10.1002/ange.201207548 · Cited by 57

ChemInform Abstract: Low‐Transition‐Temperature Mixtures (LTTMs): A New Generation of Designer Solvents.

Francisco, M., van den Bruinhorst, A., & Kroon, M. C. (2013) · ChemInform · doi:10.1002/chin.201327237 · Cited by 2

Low-melting mixture solvents: extension of deep eutectic solvents and ionic liquids for broadening green solvents and green chemistry

Chen, Y., & Yu, Z. (2023) · Green Chemical Engineering · doi:10.1016/j.gce.2023.11.001 · Cited by 134

Enhancing sustainable green chemistry using low‐transition‐temperature mixtures with deep eutectic solvents and ionic liquids for eco applications

Prakash, D. (2026) · Environmental Progress & Sustainable Energy · doi:10.1002/ep.70441

Novel Green Solvents: From Deep Eutectic Solvents and Ionic Liquids to Low-Melting Mixture Solvents

Chen, Y., Zhang, Q., Wang, T., Liu, Z., & Shi, Z. (2025) · ACS symposium series · doi:10.1021/bk-2025-1504.ch004 · Cited by 2