| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 170584 | Comptes Rendus Chimie | 2015 | 8 Pages |
Abstract
Pentose-derived surfactants were easily synthesized and fully characterized through classical analytical methods. The interfacial behaviors revealed the importance of both the length of the hydrophobic chain and the nature of the anomeric form. Finally, the spatial conformation of four xylosides was obtained by molecular modeling with software Hyperchem® 4 using the semi-empirical method PM3, which demonstrated the role of hydrophobic interactions in the stability of the compounds.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Nadia Klai, Chahra Bidjou-Haiour, Sandrine Bouquillon,