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We present experimental results for the ionization of aniline and benzene molecules subjected to intense ultrashort laser pulses. Measured parent molecular ions yields were obtained using a recently developed technique capable of three-dimensional imaging of ion distributions within the focus of a laser beam. By selecting ions originating from the central region of the focus, where the spatial intensity distribution is nearly uniform, volumetric-free intensity-dependent ionization yields were obtained. The measured data revealed a previously unseen resonant-like multiphoton ionization process. Comparison of benzene, aniline and Xe ion yields demonstrate that the observed intensity dependent structures are not due to geometric artifacts in the focus. Finally we attribute the ionization of aniline to a stepwise process going through the pi-sigma^star state which sits 3 photons above the ground state and 2 photons below the continuum.
A theoretical study of the intense-field single ionization of molecular hydrogen or deuterium oriented either parallel or perpendicular to a linear polarized laser pulse (400 nm) is performed for different internuclear separations and pulse lengths i
Triple-differential cross sections for two-photon double ionization of molecular hydrogen are presented for a central photon energy of 30 eV. The calculations are based on a fully {it ab initio}, nonperturbative, approach to the time-dependent Schroe
We investigate the carrier-envelope phase and intensity dependence of the longitudinal momentum distribution of photoelectrons resulting from above-threshold ionization of argon by few-cycle laser pulses. The intensity of the pulses with a center wav
Multiphoton ionization of sodium by femtosecond laser pulses of 800 nm wavelength in the range of laser peak intensities entering over-the-barrier ionization domain is studied. Photoelectron momentum distributions and the energy spectra are determine
We investigate molecular dynamics of multiple ionization in N2 through multiple core-level photoabsorption and subsequent Auger decay processes induced by intense, short X-ray free electron laser pulses. The timing dynamics of the photoabsorption and