학술논문

Liquefying Flavonoids with Terpenoids through Deep Eutectic Solvent Formation.
Document Type
Article
Source
Molecules. May2022, Vol. 27 Issue 9, p2649-2649. 12p.
Subject
*FLAVONOIDS
*TERPENES
*EUTECTICS
*SOLVENTS
*INTERMOLECULAR interactions
*HYDROGEN bonding
*FLAVONES
*THYMOL
Language
ISSN
1420-3049
Abstract
The formation of deep eutectic solvents (DES) is tied to negative deviations to ideality caused by the establishment of stronger interactions in the mixture than in the pure DES precursors. This work tested thymol and menthol as hydrogen bond donors when combined with different flavonoids. Negative deviations from ideality were observed upon mixing thymol with either flavone or flavanone, two parent flavonoids that only have hydrogen bond acceptor (HBA) groups, thus forming non-ionic DES (Type V). On the other hand, the menthol systems with the same compounds generally showed positive deviations from ideality. That was also the case with the mixtures containing the more complex hydroxylated flavonoid, hesperetin, which resulted in positive deviations when mixed with either thymol or menthol. COSMO-RS successfully predicted the behavior of the solid-liquid phase diagram of the studied systems, allowing for evaluation of the impact of the different contributions to the intermolecular interactions, and proving to be a good tool for the design of DES. [ABSTRACT FROM AUTHOR]