Search

Radiation damage in biological systems by ionizing radiation is predominantly caused by secondary processes such as charge and energy transfer leading to the breaking of bonds in DNA. Here, we study the fragmentation of cytosine (Cyt) and thymine (Thy) molecules, clusters and microhydrated derivatives induced by direct and indirect ionization initiated by extreme-ultraviolet (XUV) irradiation. Photofragmentation mass spectra and photoelectron spectra of free Cyt and Thy molecules are compared with mass and electron spectra of Cyt/Thy clusters and microhydrated Cyt/Thy molecules formed by aggregation in superfluid helium (He) nanodroplets. Penning ionization after resonant excitation of the He droplets is generally found to cause less fragmentation compared to direct photoionization and charge-transfer ionization after photoionization of the He droplets. When Cyt/Thy molecules and oligomers are complexed with water molecules, their fragmentation is efficiently suppressed. However, a similar suppression of fragmentation is observed when homogeneous Cyt/Thy clusters are formed in He nanodroplets, indicating a general trend. Penning ionization electron spectra (PIES) of Cyt/Thy are broad and nearly featureless but PIES of their microhydrated derivatives point at a sequential ionization process ending in unfragmented microsolvated Cyt/Thy cations. [ABSTRACT FROM AUTHOR]

Doped He nanodroplets are ideal model systems to study the dynamics of elementary photophysical processes in heterogeneous nanosystems. Here we present a combined experimental and theoretical investigation of the formation of free RbHe exciplex molecules from laser-excited Rb-doped He nanodroplets. Upon excitation of a droplet-bound Rb atom to the 5p3/22Π3/2-state, a stable RbHe exciplex forms within about 20 ps. Only due to 2Π3/2→2Π1/2 spin-relaxation does the RbHe exciplex detach from the He droplet surface with a half life of about 700 ps, given by the spin-relaxation time and the coupling of spin and translational degrees of freedom. [ABSTRACT FROM AUTHOR]

Phase-modulated wave packet interferometry is combined with mass-resolved photoion detection to investigate rubidium atoms attached to helium nanodroplets in a molecular beam experiment. The spectra of atomic Rb electronic states show a vastly enhanced sensitivity and spectral resolution when compared to conventional pump–probe wave packet interferometry. Furthermore, the formation of Rb*He exciplex molecules is probed and for the first time a fully resolved vibrational spectrum for transitions between the lowest excited 5Π3/2 and the high-lying electronic states 22Π, 42Δ, 62Σ is obtained and compared to theory. The feasibility of applying coherent multidimensional spectroscopy to dilute cold gas phase samples is demonstrated in these experiments. [ABSTRACT FROM AUTHOR]

Homo- and heteronuclear alkali quartet trimers of type K3−nRbn(n= 0,1,2,3) formed on helium nanodroplets are probed by one-color femtosecond (fs) photoionization (PI) spectroscopy. The obtained frequencies are assigned to vibrations in different electronic states in comparison to high level ab initiocalculations of the involved potentials including pronounced Jahn–Teller and spin–orbit couplings. Despite the fact that the resulting complex vibronic structure of the heavy alkali molecules complicates the comparison of experiment and theory we find good agreement for many of the observed lines for all species. [ABSTRACT FROM AUTHOR]