Results of theoretical studies of rotational branching ratios and photoelectron angular distributions for (2 + 1) resonance-enhanced multiphoton ionization (REMPI) of NO via the Qz, ( 13.5) branch of the C \*H(3px) Rydberg state are reported and compared with recent measurements. Both calculated and
Rydberg states of acetylene clusters (C2H2)2 and (C2H2)3 resolved by two-photon resonant ionization spectroscopy
โ Scribed by Y.F. Zhu; S.L. Allman; R.C. Phillips; W.R. Garrett; C.H. Chen
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 812 KB
- Volume
- 224
- Category
- Article
- ISSN
- 0009-2614
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โฆ Synopsis
The Rydberg states of the acetylene clusters ( C2H2)a and (C,H,), have been resolved by the technique of twophoton resonant ionization spectroscopy in the energy region of the monomer gerade Rydberg states. The stability of these cluster Rydberg states has been found to be vibrational mode dependent. The geometry of the clusters, and the mechanism of the dissociative ionization have been discussed.
๐ SIMILAR VOLUMES
Formation of methyl radicals via the consecutive reactions H+C2H,+M+C2H,+M ( I ) and H+CLH,+CH,+CH3 (?a) was initiated by pulse radiolysis of IO-100 mbar Hz in the presence of ethylene. The kinetics of CH, were studied by monitoring the transient infrared absorption at the Q( 3, 3) line of the u,=O+