[en] The present work concentrates on prototypical studies of light-induced correlated many-body dynamics in complex systems. In its course a reflective split-and-delay unit (SDU) for phase-resolved one-color pump-probe experiments with gas phase samples using VUV-XUV laser pulses was built. The collinear propagation of pump and probe pulses is ensured by the special geometry of the SDU and allows to perform phase-resolved (coherent) autocorrelation measurements. The control of the pump-probe delay with attosecond precision is established by a specially developed diagnostic tool based on an in-vacuum white light interferometer that allows to monitor the relative displacement of the SDU reflectors with nanometer resolution. Phase-resolved (interferometric) pump-probe experiments with developed SDU require spatially-resolved imaging of the ionization volume. For this an electron-ion coincidence spectrometer was built. The spectrometer enables coincident detection of photoionization products using velocity map imaging (VMI) technique for electrons and VMI or spatial imaging for ions. In first experiments using the developed SDU and the spectrometer in the ion spatial-imaging mode linear field autocorrelation of free-electron laser pulses at the central wavelength of 38 nm was recorded. A further focus of the work were energy- and time-resolved resonant two-photon ionization experiments using short tunable UV laser pulses on C_6_0 fullerene. The experiments demonstrated that dipole-selective excitation on a timescale faster than the characteristic intramolecular energy dissipation limits the number of accessible excitation pathways and thus results in a narrow resonance. Time-dependent one-color pump-probe study showed that nonadiabatic (vibron) coupling is the dominant energy dissipation mechanism for high-lying electronic excited states in C_6_0.