Nadège Ferlin
Click Reactions as a Key Step for an Efficient and Selective Synthesis of D-Xylose-Based ILs
Ferlin, Nadège; Gatard, Sylvain; Van Nhien, Albert; Courty, Matthieu; Bouquillon, Sandrine
Authors
Sylvain Gatard
Albert Van Nhien
Matthieu Courty
Sandrine Bouquillon
Abstract
d-Xylose-based ionic liquids have been prepared from d-xylose following a five steps reaction sequence, the key step being a click cycloaddition. These ionic liquids (ILs) have been characterized through classical analytical methods (IR, NMR, mass spectroscopy, elemental analysis) and their stability constants, Tg and Tdec, were also determined. Considering their properties and their hydrophilicity, these compounds could be alternative solvents for chemical applications under mild conditions.
Citation
Ferlin, N., Gatard, S., Van Nhien, A., Courty, M., & Bouquillon, S. (2013). Click Reactions as a Key Step for an Efficient and Selective Synthesis of D-Xylose-Based ILs. Molecules, 18(9), 11512-11525. https://doi.org/10.3390/molecules180911512
| Journal Article Type | Article |
|---|---|
| Acceptance Date | Sep 10, 2023 |
| Online Publication Date | Sep 17, 2013 |
| Publication Date | 2013 |
| Deposit Date | Apr 3, 2014 |
| Publicly Available Date | Apr 3, 2014 |
| Electronic ISSN | 1420-3049 |
| Publisher | MDPI |
| Peer Reviewed | Peer Reviewed |
| Volume | 18 |
| Issue | 9 |
| Pages | 11512-11525 |
| DOI | https://doi.org/10.3390/molecules180911512 |
| Keywords | ionic liquids, D-xylose, click chemistry |
| Public URL | http://researchrepository.napier.ac.uk/id/eprint/6739 |
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Click Reactions as a Key Step for an Efficient and Selective Synthesis of D-Xylose-Based ILs
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Copyright Statement
© 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).