The levels with \(v\) from 1 to 9 in the \((8 d)^{\prime} \Delta_{8}\) state of \(\mathrm{Na}_{2}\) have been observed by means of optical-optical double-resonance (OODR) fluorescence excitation spectroscopy. The intermediate levels in the \(B^{1} \Pi_{u}\) state are justified by numerical calculati
Optical-optical double-resonance spectroscopy of high vibrational levels of the Na2 A 1Σu+ state in a molecular beam
✍ Scribed by G. Gerber; R. Möller
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 606 KB
- Volume
- 113
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
We report the analysis of the H1 u ( 3 P 1 ) state of I 2 by optical-optical double resonance. This state lies in the second tier of ion-pair states and its observation was achieved by using the (1 ϩ 2) photoexcitation sequence using the A 3 ⌸ 1u state as an intermediate. The molecular parameters we
We describe the results of optical-optical double-resonance spectroscopy of Cl2 on the 1,(3Pt)+-(hvl)-A%( 1,) + (hu, )-X 'Zi transition. The state-selective transition from the ground state of Cl2 to the A 'lI( I,) state was observed by scanning the pump laser ( hu, ) frequency, while furing the pro
Optical-optical double resonance spectroscopy was used to study the 1 g ( 3 P 1 ) ion-pair state of I 2 correlating to I -( 1 S) + I + ( 3 P 1 ) at the dissociation limit. We gained access to the 1 g ( 3 P 1 ) state though the A 3 (1 u ) state in the (1 + 1) photon-excitation scheme. The pump laser
## Microwave -optical double resonance experiments have been camed out on the 4; band of the A 'AZ-R 'At system of thioformaldehyde &CS). More than 100 microwave and radiofrequency transitions have been observed in the ii ' A2 excited state. Many of these transitions are magnetically sensitive. So
In a molecular-beam laser-induced fIuorescence experiment on SH, the hyperfine and spin-rotation structure in the A++ \_1/z, u = 0 state has been determined. From Iinewidth measurements. a rotationally dependent predissociation is shown to be present. A natural Lifetime of 3.2 k 0.3 ns is obtained f