Correlating proton transfer dynamics to probe location in confined environments.

The dramatic impact of differing environments on proton transfer dynamics of the photoacid HPTS prompted us to investigate these systems with two highly complementary methods: ultrafast time-resolved transient absorption and two-dimensional NMR spectroscopies. Both ultrafast time-resolved transient absorption spectroscopy and time-resolved anisotropy decays demonstrate the proton transfer dynamics depend intimately on the specific reverse micellar system. For w(0) = 10 reverse micelles formed with anionic AOT surfactant, the HPTS proton transfer dynamics are similar to dynamics in bulk aqueous solution, and the corresponding (1)H 2D NOESY NMR spectra display no cross peaks between HPTS and AOT consistent with the HPTS residing well hydrated by water in the interior of the reverse micelle water pool.

Logarithmic based optical delay for time-resolved data collection.

A method has been established that generates values spaced according to a mathematical function, specifically the logarithm function that can be applied to a stepper motor. Here, it is applied to yield logarithmically spaced time delay points for subnanosecond interferometric time-resolved experiments using a stepper motor controlled translation stage. Application of this method is discussed in terms of three input parameters: the optical delay stage time resolution, dt; the time of maximum delay, d(stop); and the desired number of data points, N.