Optical–Optical Double Resonance Spectroscopy of theA–XandB–XSystems of Na3
✍ Scribed by David T. Vituccio; Oleg Golonzka; Wolfgang E. Ernst
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 445 KB
- Volume
- 184
- Category
- Article
- ISSN
- 0022-2852
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✦ Synopsis
The X and A states of the sodium trimer may be treated as rigid asymmetric rotors of C 2£ symmetry. The B state, however, is a floppy molecule where the three sodium nuclei can perform a pseudorotational motion in the molecular plane. A recently developed model Hamiltonian for the B state is applied to new rotationally resolved optical-optical double resonance measurements of the B-X system of Na 3 . These recorded transitions, in the u Å 1, j Å 0, 1, 2, and 3 bands of that system, are fit to the new Hamiltonian and rotational assignments are made. The double resonance technique utilized one dye laser fixed to a transition in the A-X system while another dye laser was scanned throughout several vibronic bands in the B-X system. In addition to providing a substantially improved signal-to-noise ratio, this method allows for a check of the consistency between previous analyses of both optical systems.
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Infrared optical double resonance (IODR) effects have been observed in ND2\_ The infrared transitions, 505 -5 ,\_, (F1 + Ft) and 212 -22, (Fz + Fz,), in the 2~2 band of ND2 were efficiently pumped with P(10) of '\*C"Oz at 1076.57 Clll -l and R(26) of 12C'602 at 1082.30 cm-', respectively. IODR sigia