Rotational spectroscopy of 10 (XIIi)-I-2

Citation
Ce. Miller et Ea. Cohen, Rotational spectroscopy of 10 (XIIi)-I-2, J CHEM PHYS, 115(14), 2001, pp. 6459-6470
Citations number
46
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF CHEMICAL PHYSICS
ISSN journal
00219606 → ACNP
Volume
115
Issue
14
Year of publication
2001
Pages
6459 - 6470
Database
ISI
SICI code
0021-9606(20011008)115:14<6459:RSO1(>2.0.ZU;2-S
Abstract
Pure rotational spectra of the IO radical have been observed for vibrationa l levels up to v =13 in the X-1 (2)Pi (3/2) state and up to v =9 in the X-2 (2)Pi (1/2) state. Isotopically enriched (IO)-O-18 rotational spectra have been observed for vibrational levels up to v = 5 in both the X-1 and X-2 s tates. These are the first high-resolution spectra of any kind reported for the X-2 state and greatly extend the available data for the X-1 state. The data for both isotopomers have been fitted simultaneously to a single set of (2)Pi parameters with fixed isotopic ratios. The isotope relations among the parameters have provided a means of decorrelating the electron spin-ro tation constant gamma from the fine-structure centrifugal distortion consta nt, A(D), and have allowed the first determination of an effective value fo r gamma. The rotation-vibration constants correspond to the equilibrium mol ecular properties r(e)(X-1) =186.762 pm, r(e)(X-2)=188.468 pm, omega (e)(X- 1)=681.69 cm(-1), and omega (e)(X-2)=645.29 cm(-1). These constants have be en used to calculate X-1 and X-2 Rydberg-Klein-Rees potentials encompassing energies up to 40% of the dissociation limit. A complete set of hyperfine coupling constants has been determined for the first time and interpreted u sing appropriate relativistic atomic radial integrals. (C) 2001 American In stitute of Physics.