## Abstract The original article to which this Erratum refers was published in Journal of Chemical Technology and Biotechnology (**81**: 1441β1446).
Analysis of solvation in ionic liquids using a new linear solvation energy relationship
β Scribed by Sun Bok Lee
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2005
- Tongue
- English
- Weight
- 101 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0268-2575
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
A new linear solvation energy relationship (LSER) equation, where the solute internal energy term has been incorporated into the traditional LSER equation, is used for the analysis of solvation in ionic liquids. Modeling results obtained using the new LSER equation indicate that all solute parameters (dispersion, polarity, hydrogen bonding, cavity formation, and solute internal energy) have approximately equal importance in the solvation of organic solutes in ionic liquids. The magnitude of dispersion interaction is stronger in ionic liquids than in aqueous solution, whereas hydrogenβbonding interactions are stronger in water than in ionic liquids. This indicates that the solubility of polar compounds that contain bulky and aromatic groups can be enhanced in ionic liquids due to higher dispersion interactions in ionic liquids than in aqueous solution. On the other hand, the LSER equation without the solute internal energy term does not yield the meaningful soluteβsolvent interaction terms, indicating that the inclusion of a solute internal energy term is necessary to properly describe the solvation of organic solutes in liquid solvents. Copyright Β© 2004 Society of Chemical Industry
π SIMILAR VOLUMES
## Abstract The contentions made in an earlier paper [__J Chem Technol Biotechnol__ **80**: 133β137 (2005)] that the coefficients of the Abraham solvation equation do not provide meaningful information on the molecular properties of ionic liquid solvents is refuted. The objections noted in the earl
## Abstract Supercritical fluid chromatography was utilized in combination with the Abraham model of linear solvation energy relationship to characterize 11 different HPLC stationary phases. System constants were determined at one supercritical fluid chromatography condition for each stationary pha