Steady-state spectroscopy and time-resolved solvation dynamics have been used to investigate the effects
the addition of alkanol has on the location of coumarin 343 (C343) in cetyltrimethylammonium bromide
(CTAB)/1-pentanol/cyclohexane/water, CTAB/1-heptanol/cyclohexane/water, and sodium dodecyl sulfate/1-heptanol/cyclohexane/water reverse micelles. Steady-state spectroscopy showed that the probe molecule
is not sensitive to alkanol chain lengths or water loading. Instead, C343 is sensitive to the surfactant used
to form the reverse micelles. Solvation dynamics measurements utilizing ultrafast time-resolved fluorescence-upconversion spectroscopy revealed two solvation reorganization times regardless of the micellar system
studied or hydration level. A hundreds of picosecond time component is attributed to collective motion of
the interface. Time-zero analysis reveals a substantial relaxation component occurring on the femtosecond
time scale.