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Study of the Interactions of Ionic Liquids in IC by QSRR

The nature of ionic liquids (ILs) facilitates their analysis by ion chromatography which, unlike conventional high-performance liquid chromatography, enables analysis both of cations and anions. This paper describes a pioneering ion-chromatographic investigation of IL cations and statistical evaluat...

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Detalles Bibliográficos
Autores principales: Studzińska, S., Molíková, M., Kosobucki, P., Jandera, P., Buszewski, B.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098970/
https://www.ncbi.nlm.nih.gov/pubmed/21765535
http://dx.doi.org/10.1007/s10337-011-1960-3
Descripción
Sumario:The nature of ionic liquids (ILs) facilitates their analysis by ion chromatography which, unlike conventional high-performance liquid chromatography, enables analysis both of cations and anions. This paper describes a pioneering ion-chromatographic investigation of IL cations and statistical evaluation of quantitative structure–retention relationships with the objective of predicting the molecular mechanism responsible for retention. Eleven ionic liquid imidazolium and pyridinium cations were analyzed on a CS15 cation-exchange column by isocratic elution with acetonitrile–methanesulfonic acid mixtures. Structural descriptors of the cations obtained from molecular modeling were used to describe their hydrophobicity as determined by chromatography. The most statistically significant were three-term QSRR regression equations relating log k (w) to analyte n-octanol–water partition coefficient (log P), dipole moment (μ), solvent accessible surface area (A (SAS)), and hydration energy (HE). They indicate the important role of both hydrophobic and polar the retention of ILs on the CS15 column.