Electronic spectroscopy and excited state mixing of OThF.

Electronic spectra for OThF have been recorded using fluorescence excitation and two-photon resonantly enhanced ionization techniques. Multiple vibronic bands were observed in the 340-460 nm range. Dispersed fluorescence spectra provided ground state vibrational constants and evidence of extensive vibronic state mixing at higher excitation energies.

Photoelectron Velocity Map Imaging Spectroscopy of the Beryllium Trimer and Tetramer.

Computational studies of small beryllium clusters (Be) predict dramatic, nonmonotonic changes in the bonding mechanisms and per-atom cohesion energies with increasing . To date, experimental tests of these quantum chemistry models are lacking for all but the Be molecule. In the present study, we report spectroscopic data for Be and Be obtained via anion photodetachment spectroscopy.

High resolution electronic spectroscopy of uranium mononitride, UN.

The isoelectronic molecules UN and UO+ are known to have Ω = 3.5 and Ω = 4.5 ground states, respectively (where Ω is the unsigned projection of the electronic angular momentum along the internuclear axis).

Kinetics of O with Ca and Its Higher Oxides CaO ( = 1-3) and Updates to a Model of Meteoric Calcium in the Mesosphere and Lower Thermosphere.

The room-temperature rate constants and product branching fractions of CaO ( = 0-3) + O are measured using a selected ion flow tube apparatus. Ca + O produces CaO + O with = 9 ± 4 × 10 cm s, within uncertainty equal to the Langevin capture rate constant. This value is significantly larger than several literature values.

Near-thermo-neutral electron recombination of titanium oxide ions.

While the dissociative recombination (DR) of ground-state molecular ions with low-energy free electrons is generally known to be exothermic, it has been predicted to be endothermic for a class of transition-metal oxide ions. To understand this unusual case, the electron recombination of titanium oxide ions (TiO) with electrons has been experimentally investigated using the Cryogenic Storage Ring. In its low radiation field, the TiO ions relax internally to low rotational excitation (≲100 K).