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Novel choline-chloride-based deep-eutectic-solvents with renewable hydrogen bond donors: levulinic acid and sugar-based polyols
Abstract
Choline chloride (ChCl) has been combined with renewable hydrogen bond donors (HBD) to form novel deep eutectic solvents (DES) with melting points lower than 100 °C. In some cases (e.g. sorbitol or isosorbide as HBDs) chiral DES can be easily produced. Moreover, the addition of glycerol decreases the viscosity of DES significantly. In the ChCl : levulinic acid DES case, singular properties were observed. Thus, equimolecular mixtures of ChCl : levulinic acid (1 : 1) formed a crystal at room temperature, rapidly melting in contact with air humidity. Addition of excess of acetone to ChCl : levulinic acid (1 : 2) leads to the almost quantitative precipitation of choline chloride, which can be used again to form a DES.
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Cites
Abbott, A. P., Capper, G., Davies, D. L., Rasheed, R. K., & Tambyrajah, V. (2003) · Chemical Communications · doi:10.1039/b210714g · Cited by 5,738
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
Abbott, A. P., Capper, G., Davies, D. L., Munro, H. L., Rasheed, R. K., & Tambyrajah, V. (2001) · Chemical Communications · doi:10.1039/b106357j · Cited by 1,100
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Deep eutectic solvents: A review of fundamentals and applications
Hansen, B. B., Spittle, S., Chen, B., Poe, D., Zhang, Y., Klein, J. M., Horton, A., Adhikari, L., Zelovich, T., Doherty, B. W., et al. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00385 · Cited by 3,422
Low-transition-temperature mixtures (LTTMs): A new generation of designer solvents
Francisco, M., van den Bruinhorst, A., & Kroon, M. C. (2013) · Angewandte Chemie International Edition · doi:10.1002/anie.201207548 · Cited by 1,378
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García, G., Aparicio, S., Ullah, R., & Atilhan, M. (2015) · Energy & Fuels · doi:10.1021/ef5028873 · Cited by 1,112
Florindo, C., Oliveira, F. S., Rebelo, L. P. N., Fernandes, A. M., & Marrucho, I. M. (2014) · ACS Sustainable Chemistry & Engineering · doi:10.1021/sc500439w · Cited by 977
Low melting mixtures in organic synthesis–an alternative to ionic liquids?
Ruß, C., & König, B. (2012) · Green Chemistry · doi:10.1039/c2gc36005e · Cited by 654
Zhao, B.-Y., Xu, P., Yang, F.-X., Wu, H., Zong, M.-H., & Lou, W.-Y. (2015) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.5b00619 · Cited by 617
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Overview of acidic deep eutectic solvents on synthesis, properties and applications
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Pena-Pereira, F., Kloskowski, A., & Namieśnik, J. (2015) · Green Chemistry · doi:10.1039/c5gc00611b · Cited by 257
Jeong, K. M., Ko, J., Zhao, J., Jin, Y., Yoo, D. E., Han, S. Y., & Lee, J. (2017) · Journal of Cleaner Production · doi:10.1016/j.jclepro.2017.03.038 · Cited by 235
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Mirzajani, R., Kardani, F., & Ramezani, Z. (2020) · Food Chemistry · doi:10.1016/j.foodchem.2020.126179 · Cited by 153
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Silva, J. M., Reis, R. L., Paiva, A., & Duarte, A. R. C. (2018) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.8b01687 · Cited by 142
Cardellini, F., Tiecco, M., Germani, R., Cardinali, G., Corte, L., Roscini, L., & Spreti, N. (2014) · RSC Adv. · doi:10.1039/c4ra10628h · Cited by 140
Wang, M., Wang, J., Zhang, Y., Xia, Q., Bi, W., Yang, X., & Chen, D. D. Y. (2016) · Journal of Chromatography A · doi:10.1016/j.chroma.2016.03.061 · Cited by 108
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Ghanemi, K., Navidi, M.-A., Fallah-Mehrjardi, M., & Dadolahi-Sohrab, A. (2014) · Anal. Methods · doi:10.1039/c3ay41843j · Cited by 79
Altamash, T., Nasser, M. S., Elhamarnah, Y., Magzoub, M., Ullah, R., Anaya, B., Aparicio, S., & Atilhan, M. (2017) · ChemistrySelect · doi:10.1002/slct.201701223 · Cited by 74
Mouden, S., Klinkhamer, P. G. L., Choi, Y. H., & Leiss, K. A. (2017) · Phytochemistry Reviews · doi:10.1007/s11101-017-9502-8 · Cited by 67
Khezeli, T., & Daneshfar, A. (2015) · RSC Advances · doi:10.1039/c5ra08058d · Cited by 66
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Farajzadeh, M. A., Abbaspour, M., Kazemian, R., & Afshar Mogaddam, M. R. (2020) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.10200 · Cited by 41
Wan, Y., Wang, M., Zhang, K., Fu, Q., Wang, L., Gao, M., Xia, Z., & Gao, D. (2019) · Journal of Separation Science · doi:10.1002/jssc.201900031 · Cited by 40
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Tang, B., Park, H. E., & Row, K. H. (2014) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-014-7817-5 · Cited by 37
Metadata
- Authors
- Maugeri, Z., & Domínguez de María, P.
- Venue
- RSC Adv.
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2012
- Volume
- 2
- Issue
- 2
- Pages
- 421-425
- ISSN
- 2046-2069 (ISSN-L)
- OpenAlex
- W1994619041
- Cited by
- 434
- References
- 3
- FWCI
- 6.62
- Type
- journal article
- Language
- en
- Open access
- closed
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