Zobrazeno 1 - 10
of 217
pro vyhledávání: '"H.-H. Ritze"'
Publikováno v:
Chemical Physics Letters. 398:526-531
Applying femtosecond pump–probe spectroscopy at different wavelengths we demonstrate that for the indole molecule an efficient coupling does not exist between the initially excited ππ* state and the adjacent higher lying π σ * state. This resul
Publikováno v:
The Journal of Chemical Physics. 121:1765-1770
Two-photon excitation with femtosecond laser pulses in the spectral range 240-250 nm was used to prepare vapor phase H(2)O and D(2)O in the C (1)B(1) and D (1)A(1) states. Both states are predissociated via the B (1)A(1) state, forming excited OH/OD(
Publikováno v:
Chemical Physics Letters. 388:144-149
The ultrafast dynamics of the electronically excited ethylene molecule has been studied in pump–probe experiments with the pump wavelength of 198 nm and the probe wavelength of 790 nm. The lifetime measured for the initially excited ππ ∗ state
Publikováno v:
The Journal of Chemical Physics. 120:3619-3629
Ab initio calculations on the heterodimer C8H6NH...NH3 are carried out for its ground, the excited pisigma*, and the ground cationic electronic states, enabling the description of hydrogen or proton transfer, respectively. Two-dimensional quantum-dyn
Publikováno v:
The European Physical Journal D. 19:193-209
Neutral ammonia clusters (NH3)m are photo-excited to the electronic \(\) state by a deep UV femtosecond laser pump pulse. Within a few hundred femtoseconds a significant fraction of the clusters rearrange to form an H-transfer state (NH3)m-2NH4(3s)NH
Publikováno v:
Chemical Physics Letters. 355:449-456
We studied the time evolution of the wave packet formed by the excitation of the Ba⋯FCH 3 complex with a 120 fs laser pulse at 745 nm to its electronic A ′ state which is repulsive at the ground state geometry and decays to Ba and CH 3 F fragment
Publikováno v:
The Journal of Chemical Physics. 116:1443-1456
The energetics and ultrafast dynamics in the H atom transfer configuration of ammonia dimer and trimer clusters have been studied. The clusters are first excited to the electronic A state with a 208 nm femtosecond laser pump pulse. This state is allo
Publikováno v:
Chemical Physics. 272:99-110
Applying the coincident detection of photoions and photoelectrons with femtosecond time resolution we have analyzed the energetics and the dynamics of the ultrafast processes initiated by excitation of OClO molecules with 50 fs laser pulses at 398 nm
Publikováno v:
The Journal of Chemical Physics. 115:277-284
Applying photoion and coincident photoelectron detection in femtosecond pump–probe experiments, we have studied the change of the fragmentation behavior of ammonia clusters excited by femtosecond (fs) laser pulses at 200 nm to the electronic A stat
Publikováno v:
Chemical Physics Letters. 337:299-305
Applying femtosecond pump–probe spectroscopy combined with the coincidence detection of photoelectrons and photoions, we have analyzed the energetics of the photoinitiated intracluster reaction in Ba⋯FCH 3 on the femtosecond time scale. The rate-