TY - JOUR
T1 - Cationic and perfluorinated polymeric pseudostationary phases for electrokinetic chromatography
AU - Rauk, Erika
AU - Kotzev, Anton
AU - Laschewsky, André
AU - Palmer, Christopher P.
N1 - Funding Information:
The authors thank the Department of Chemistry of the University of Montana and the Montana NSF EPSCoR program for financial support.
PY - 2006/2/17
Y1 - 2006/2/17
N2 - Separation selectivity in electrokinetic chromatography (EKC) is directly affected by the chemistry and solvent characteristics of the pseudostationary phase (PSP). The chemical selectivity of micellar PSPs has been previously demonstrated to vary significantly between anionic and cationic surfactants as well as between hydrocarbon and fluorocarbon surfactants. Polymeric PSPs have also been demonstrated to provide unique selectivity. In the current study, four cationic polymeric pseudo-stationary phases, two of which have perfluorinated pendant groups, are introduced and characterized as PSPs in EKC. Their performance and selectivity is compared to conventional micellar PSPs with similar structure. The solvation characteristics and selectivity of the four polymers most closely resemble those observed for cationic micelles. The polymers are all more cohesive and more polar than their hydrocarbon micellar counterparts. The fluorocarbon PSPs did show preferential interaction with fluorocarbon solutes, were somewhat more cohesive, and were stronger hydrogen bond donors. However, the presence of fluorocarbon moieties did not have as dramatic an effect on selectivity as was observed and published previously for fluorocarbon micelles. This may result from the selectivity being dominated by the presence of the cationic head groups or from the fluorocarbon character of the pendant groups being moderated by the presence of hydrocarbon functionality on the polymer backbones.
AB - Separation selectivity in electrokinetic chromatography (EKC) is directly affected by the chemistry and solvent characteristics of the pseudostationary phase (PSP). The chemical selectivity of micellar PSPs has been previously demonstrated to vary significantly between anionic and cationic surfactants as well as between hydrocarbon and fluorocarbon surfactants. Polymeric PSPs have also been demonstrated to provide unique selectivity. In the current study, four cationic polymeric pseudo-stationary phases, two of which have perfluorinated pendant groups, are introduced and characterized as PSPs in EKC. Their performance and selectivity is compared to conventional micellar PSPs with similar structure. The solvation characteristics and selectivity of the four polymers most closely resemble those observed for cationic micelles. The polymers are all more cohesive and more polar than their hydrocarbon micellar counterparts. The fluorocarbon PSPs did show preferential interaction with fluorocarbon solutes, were somewhat more cohesive, and were stronger hydrogen bond donors. However, the presence of fluorocarbon moieties did not have as dramatic an effect on selectivity as was observed and published previously for fluorocarbon micelles. This may result from the selectivity being dominated by the presence of the cationic head groups or from the fluorocarbon character of the pendant groups being moderated by the presence of hydrocarbon functionality on the polymer backbones.
KW - Cationic polymer
KW - Electrokinetic chromatography
KW - Fluorocarbon
KW - Polymeric pseudostationary phase
UR - http://www.scopus.com/inward/record.url?scp=31344459476&partnerID=8YFLogxK
U2 - 10.1016/j.chroma.2005.07.114
DO - 10.1016/j.chroma.2005.07.114
M3 - Article
C2 - 16443449
AN - SCOPUS:31344459476
SN - 0021-9673
VL - 1106
SP - 29
EP - 35
JO - Journal of Chromatography A
JF - Journal of Chromatography A
IS - 1-2
ER -