Contact Ion Pair Formation Is Not Necessarily Stronger than Solvent Shared Ion Pairing.

Vibrational sum frequency spectroscopy (VSFS) and pressure-area Langmuir trough measurements were used to investigate the binding of alkali metal cations to eicosyl sulfate (ESO 4 ) surfactants in monolayers at the air/water interface. The number density of sulfate groups could be tuned by mixing the anionic surfactant with eicosanol. The equilibrium dissociation constant for K + to the fatty sulfate interface showed 10 times greater affinity than for Li + and approximately 3 times greater than for Na + . All three cations formed solvent shared ion pairs when the mole fraction of ESO 4 was 0.33 or lower. Above this threshold charge density, Li + formed contact ion pairs with the sulfate headgroups, presumably via bridging structures. By contrast, K + only bound to the sulfate moieties in solvent shared ion pairing configurations. The behavior for Na + was intermediate. These results demonstrate that there is not necessarily a correlation between contact ion pair formation and stronger binding affinity.