TY  - UNPB
ID  - pittir38241
UR  - http://d-scholarship-dev.library.pitt.edu/38241/
A1  - Horner, Anthony
Y1  - 2020/06/08/
N2  - In reversed-phase liquid chromatography, temperature significantly affects analyte retention factor. The dependence of analyte retention can be expressed either simply being 1) dependent on temperature alone, or more complex being dependent on 2) mobile phase pH, buffer, and temperature, or 3) mobile phase composition and temperature. Analyte retention commonly increases with decreasing temperature. Temperature assisted solute focusing (TASF) takes advantage of this effect by decreasing the temperature of the head of the column to focus analytes. Temperature is increased to release the concentrated analyte bands, improving method limits of detection. Simple expressions for the temperature dependence of retention allowed capillary scale TASF to be extended to the analytical scale. Understanding more complex dependencies of analyte retention on experimental conditions allows for the optimization of chromatographic separations. We explored the effect of pH and buffer selection on the retention of ionizable analytes when mobile phase pH is near analyte pKa. Buffer ionization enthalpy affects pH change with temperature. Thus, when mobile phase pH is near analyte pKa, buffer selection can be used to modify the temperature dependence of retention. We also compared the ability of mobile phase composition and temperature dependent retention expressions to predict retention for 101 compounds. To extend predictions of the effect of experimental conditions on retention, we explored functional group contributions to thermodynamic parameters. We demonstrated that the temperature dependence of retention, enthalpy, is additive for 39 functional groups, where each functional group?s contribution is temperature and mobile phase composition dependent. Predicted enthalpies show reasonable agreement with literature but demonstrate that different functional groups behave differently on columns with different chemistries and ligand densities. However, functional group contributions accurately predict enthalpy on the same column.
Separately, we studied the complex equilibrium of a molecular receptor extraction. This extraction enhances selectivity by using a fluorous solvent, which is simultaneously hydrophobic and oleophobic, in combination with a fluorous carboxylic acid molecular receptor, which complexes with pyridine. This approach of using a poor solvent in combination with a selective molecular receptor could enhance partitioning of pyridine from aqueous or organic solvent into a fluorous phase.
KW  - Functional group contributions
Liquid chromatography
Mobile phase composition dependence
Selective separations
Solute focusing
Temperature dependence
TI  - The effect of temperature in chemical separations: 1) reversed-phase liquid chromatography and 2) molecular-receptor interactions
EP  - 524
AV  - restricted
ER  -