Abstract
Experimental observations of the gerade (g) states of O2 that exist between the dissociation limit of the B3Σu- state and the X2Πg ground state of O2+ are reexamined. Emphasis is placed on the assignment of electronic structures of the [X2Πg]ndλ1,3∧g Rydberg states for which experimental data can be obtained from the literature: mainly, ndπg- and ndδg-based 1,3∧g states with n = 3-5 and the ndπg 1Σg+ and 3g- series with n = 6-11. In many cases, characterizations of these electronic structures are limited by the quality of existing experimental data and, in cases where rotational band structures were analyzed, by the unavailability of most of the rotational energy level data upon which reported parameterizations were based. Thus, while a general picture of some segments of the ndπg - and ndδg-based structures can be presented, quantitative descriptions of these structures and unique identification of the causes of many apparent structural irregularities will not be possible until a new well-calibrated, rotationally resolved database is developed.
| Original language | English |
|---|---|
| Pages (from-to) | 217-226 |
| Number of pages | 10 |
| Journal | Journal of Molecular Spectroscopy |
| Volume | 219 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Jun 2003 |