15min:
ULTRAFAST SPECTROSCOPY OF METHYL VIOLOGEN: EFFECTS OF ZEOLITE ENTRAPMENT.

JOSEPH HENRICH, BERN KOHLER, HAOYU ZHANG, JEREMY WHITE AND PRABIR DUTTA, Department of Chemistry, The Ohio State University, Columbus, OH 43210.

Bipyridinium compounds are attractive electron relay agents that can be easily incorporated into zeolite voids by ion

exchange. By preparing zeolite particles of colloidal size, we have been able to suppress light scattering and greatly

improve the optical properties of zeolite nanoparticles suspended in various solvents. With these systems, femtosecond

transient absorption signals can be recorded in a conventional transmission geometry with high signal-to-noise ratios. The

extreme sensitivity of methyl viologen (1,1\'-dimethyl-4,4\'-bipyridinium) excited-state dynamics to the solvent in

homogeneous solution makes this molecule an excellent probe of the microenvironment within zeolite cavities. Steady-state

excitation and emission spectra of zeolite-entrapped viologens exhibit spectral shifts. Additionally, time-resolved

measurements reveal how impediments to molecular motion by the viologen and entrapped solvent molecules affect radiative and

nonradiative decay. We report that the entrapped viologens experience lifetimes similar to those in bulk solvent in addition

to a new decay pathway that is indicative of a direct effect of the zeolite on the excited viologen. These results are

helping to explain the static and dynamical factors that modulate charge separation, propagation, and recombination within

zeolite membranes.