Ion Pairing
Posted: Sat Sep 11, 2004 12:16 am
could anyone please suggest useful references, or explain the change in retention mechanism when ion pairing a basic analyte with a TFA mobile phase?
we observed changing RT and elution order for an impure methyl ether-substited pyridine (NMR indicates imp is positional isomer) when reversed phase chromatographing with 0.1% HCOOH in H2O/ACN then 0.1% TFA.
1) H2O/ACN/0.1% HCOOH. prod 6.0 min, imp 7.0 min
2) H2O/ACN/0.1% TFA. imp 12.5 min, prod 13.0 min
does TFA travel down the column paired with the analyte or equilibrate with the stationary phase?
what is it about TFA which makes it suitable for selectivity changes via ion pairing? is it strong acids which will form ion pairs with basic analytes but ion pairs of other strong acid salts (HCl, HBr etc) dont change RT as the anion isn't retained and this is what makes TFA unique?
we observed changing RT and elution order for an impure methyl ether-substited pyridine (NMR indicates imp is positional isomer) when reversed phase chromatographing with 0.1% HCOOH in H2O/ACN then 0.1% TFA.
1) H2O/ACN/0.1% HCOOH. prod 6.0 min, imp 7.0 min
2) H2O/ACN/0.1% TFA. imp 12.5 min, prod 13.0 min
does TFA travel down the column paired with the analyte or equilibrate with the stationary phase?
what is it about TFA which makes it suitable for selectivity changes via ion pairing? is it strong acids which will form ion pairs with basic analytes but ion pairs of other strong acid salts (HCl, HBr etc) dont change RT as the anion isn't retained and this is what makes TFA unique?