Fluorescence Studies in a Pyrrolidinium Ionic Liquid: Polarity of the Medium and Solvation Dynamics

Abstract

While the imidazolium ionic liquids have been studied for some time, little is known about the pyrrolidinium ionic liquids. In this work, steady-state and picosecond time-resolved fluorescence behavior of three electron donor-acceptor molecules, coumarin-153 (C153), 4-aminophthalimide (AP), and 6-propionyl-2-dimethylaminonaphthalene (PRODAN), has been studied in a pyrrolidinium ionic liquid, N-butyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide, abbreviated here as [bmpy][Tf2N]. The steady-state fluorescence data of the systems suggest that the microenvironment around these probe molecules, which is measured in terms of the solvent polarity parameter, E(T)(30), is similar to that in 1-decanol and that the polarity of this ionic liquid is comparable to that of the imidazolium ionic liquids. All three systems exhibit wavelength-dependent fluorescence decay behavior, and the time-resolved fluorescence spectra show a progressive shift of the fluorescence maximum toward the longer wavelength with time. This behavior is attributed to solvent-mediated relaxation of the fluorescent state of these systems. The dynamics of solvation, which is studied from the time-dependent shift of the fluorescence spectra, suggests that approximately 45% of the relaxation is too rapid to be measured in the present setup having a time resolution of 25 ps. The remaining observable components of the dynamics consist of a short component of 115-440 ps (with smaller amplitude) and a long component of 610-1395 ps (with higher amplitude). The average solvation time is consistent with the viscosity of this ionic liquid. The dynamics of solvation is dependent on the probe molecule, and nearly 2-fold variation of the solvation time depending on the probe molecule could be observed. No correlation of the solvation time with the probe molecule could, however, be observed.