A band of jet-cooled 48Ti2 has been located in the near infrared by resonant two-photon ionization spectroscopy. Rotational analysis has shown the band to be an Ω′=0±←Ω″=1 transition, which is consistent with the 3Δg ground state proposed by Bauschlicher et al. [J. Chem. Phys. 95, 1057 (1991)]. The band is assigned as a 3Π0u ← X 3Δ1g transition, and lower and upper state bond lengths have been determined as r0(X 3Δg)=1.9422±0.0008 Å and r0(3Πu)=1.997±0.009 Å (1σ error limits, corrected for spin–uncoupling effects). Comparisons are made to the TiV and V2 molecules, a rationale for the unusual filling order of the 3d-based molecular orbitals is provided, and molecular orbital assignments are considered for the excited 3Πu state.
The emission spectrum of PtO has been studied between 3800 Å and 8900 Å. In addition to the earlier reported A-X and D-X transitions several new transitions have been analysed. Most of them have either the X state or another state called the x state as their lower state. The X state has the character of a 0+ state, the x state has the character of a 1 state in Hund's coupling case c which together correspond to a 3Σ- state. The X state together with the x state seem to constitute the ground state of PtO.The following molecular constants in cm-1 were obtained:
We report the direct observation of interference effects in a Young's double-slit experiment where the interfering waves are two spatially separated components of the de Broglie wave of single 1.3 MeV hydrogen atoms formed close to either target nucleus in H++H2 electron-transfer collisions. Quantum interference strongly influences the results even though the hydrogen atoms have a de Broglie wavelength, lambda_{dB}, as small as 25 fm.
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