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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

Nadège Ferlin

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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