A compact hexapole state-selector for NO radicals.

Focusing of molecular beams using an electrostatic hexapole is a mature technique to produce samples of state-selected molecules. The ability to efficiently focus molecules depends on the properties of the molecular species of interest, the length of the hexapole state selector, as well as on the maximum electric field strength that can be achieved in these devices. In particular for species with a small effective dipole moment such as nitric oxide (NO), hexapole state selectors of several meters in length are required to focus the beam.

Quantum-state resolved bimolecular collisions of velocity-controlled OH with NO radicals.

Whereas atom-molecule collisions have been studied with complete quantum-state resolution, interactions between two state-selected molecules have proven much harder to probe. Here, we report the measurement of state-resolved inelastic scattering cross sections for collisions between two open-shell molecules that are both prepared in a single quantum state. Stark-decelerated hydroxyl (OH) radicals were scattered with hexapole-focused nitric oxide (NO) radicals in a crossed-beam configuration.

Communication: Magnetic dipole transitions in the OH A 2Σ+ ← X 2Π system.

We report on the observation of magnetic dipole allowed transitions in the well-characterized A (2)Σ(+) - X (2)Π band system of the OH radical. A Stark decelerator in combination with microwave Rabi spectroscopy is used to control the populations in selected hyperfine levels of both Λ-doublet components of the X (2)Π(3/2), v = 0, J = 3/2 ground state. Theoretical calculations presented in this Communication predict that the magnetic dipole transitions in the A (2)Σ(+), v = 1 ← X (2)Π, v = 0 band are weaker than the electric dipole transitions by a factor of 2.