Vibrational energy relaxation of benzene dimer and trimer in the CH stretching region studied by picosecond time-resolved IR-UV pump-probe spectroscopy J. Chem. Phys. 136, 044304 (2012) Influence of the cluster dimensionality on the binding behavior of CO and O2 on Au13 J. Chem. Phys. 136, 024312 (2012) Core-to-Rydberg band shift and broadening of hydrogen bonded ammonia clusters studied with nitrogen K-edge excitation spectroscopy J. Chem. Phys. 136, 014308 (2012) Theoretical characterization of intermolecular vibrational states through the multi-configuration time dependent Hartree approach: The He2,3ICl clusters J. Chem. Phys. 135, 244309 (2011) Studies on the structure, stability, and spectral signatures of hydride ion-water clusters J. Chem. Phys. 135, 214308 (2011) Additional information on J. Chem. Phys. High resolution IR spectra of aniline, styrene, and 1,1-diphenylethylene cations embedded in superfluid helium nanodroplets have been recorded in the 300-1700 cm −1 range using a free-electron laser as radiation source. Comparison of the spectra with available gas phase data reveals that the helium environment induces no significant matrix shift nor leads to an observable line broadening of the resonances. In addition, the IR spectra have provided new and improved vibrational transition frequencies for the cations investigated, as well as for neutral aniline and styrene. Indications have been found that the ions desolvate from the droplets after excitation by a non-evaporative process in which they are ejected from the helium droplets. The kinetic energy of the ejected ions is found to be ion specific and to depend only weakly on the excitation energy.