Stark-selected beam of ground-state OCS molecules characterized by revivals of impulsive alignment

We make use of an inhomogeneous electrostatic dipole field to impart a quantum-state-dependent deflection to a pulsed beam of OCS molecules, and show that those molecules residing in the absolute ground state, X(1)Σ(+), |00(0)0>, J = 0, can be separated out by selecting the most deflected part of the molecular beam. Past the deflector, we irradiate the molecular beam by a linearly polarized pulsed nonresonant laser beam that impulsively aligns the OCS molecules. Their alignment, monitored via velocity-map imaging, is measured as a function of time, and the time dependence of the alignment is used to determine the quantum state composition of the beam. We find significant enhancements of the alignment ( = 0.84) and of state purity (>92%) for a state-selected, deflected beam compared with an undeflected beam.     

Differentielle Pulsinversvoltammetrie für die Schwermetallanalytik von Trinkwasser

Analytical and Bioanalytical Chemistry - Die Betriebserfahrungen mit dem Gerät PAR 384A —mit zwei Elektrodenständen PAR 303 —haben gezeigt, daß die Inversvoltammetrie...     

Quantum state tomography of dissociating molecules

Using tomographic reconstruction we determine the complete internuclear quantum state, represented by the Wigner function, of a dissociating I2 molecule based on femtosecond time resolved position and momentum distributions of the atomic fragments. The experimental data are recorded by timed ionization of the photofragments with an intense 20 fs laser pulse. Our reconstruction method, which relies on Jaynes's maximum entropy principle, will also be applicable to time resolved position or momentum data obtained with other experimental techniques.     

Observation of enhanced field-free molecular alignment by two laser pulses

We show experimentally that field-free alignment of iodobenzene molecules, induced by a single, intense, linearly polarized 1.4-ps-long laser pulse, can be strongly enhanced by dividing the pulse into two optimally synchronized pulses of the same duration. For a given total energy of the two-pulse sequence the degree of alignment is maximized with an intensity ratio of 1:3 and by sending the second pulse near the time where the alignment created by the first pulse peaks.     

Holding and spinning molecules in space

We illustrate, experimentally and theoretically, a laser-based method to control the rotations of polyatomic molecules in 3D space. A linearly polarized nanosecond pulse strongly aligns the most polarizable axis of an asymmetric top molecule along its polarization axis while an orthogonally polarized, femtosecond pulse sets the molecules into controlled rotation about the aligned axis. As a result, strong three-dimensional (3D) alignment occurs shortly after the femtosecond pulse and is repeated periodically, reflecting coherent revolution about the molecular axis. Our method opens new directions for research in orientationally confined complex molecules.     

Vectorization hierarchies of some graph quantifiers

We give a sufficient condition for the inexpressibility of the k-th extended vectorization of a generalized quantifier in , the extension of first-order logic by all k-ary quantifiers. The condition is based on a model construction which, given two -equivalent models with certain additional structure, yields a pair of -equivalent models. We also consider some applications of this condition to quantifiers that correspond to graph properties, such as connectivity and planarity. Received: 15 October 1996