PHOTODISSOCIATION SPECTROSCOPY OF MG2-1(2)SIGMA(G)(+))( (1(2)SIGMA(U)(+))

Citation
Ln. Ding et al., PHOTODISSOCIATION SPECTROSCOPY OF MG2-1(2)SIGMA(G)(+))( (1(2)SIGMA(U)(+)), Physical review. A, 48(3), 1993, pp. 2024-2030
Citations number
19
Categorie Soggetti
Physics
Journal title
ISSN journal
10502947
Volume
48
Issue
3
Year of publication
1993
Pages
2024 - 2030
Database
ISI
SICI code
1050-2947(1993)48:3<2024:PSOM(>2.0.ZU;2-3
Abstract
We have observed the photodissociation of Mg2+ via the repulsive 1 2SI GMA(g)+ state in a reflection time-of-flight mass spectrometer. The ph otodissociation spectrum consists of a broad structureless continuum r anging from almost-equal-to 580 to almost-equal-to 690 nm and peaking near 640 nm. A spectral simulation based on theoretical ab initio pote ntial-energy curves agrees well with the experimental profile. We have observed a triple-vector (E-mu-v) correlation in the photofragment ti me-of-flight spectrum. Analysis of the correlation allows a determinat ion of the anisotropy parameter beta and the recoil velocity as a func tion of the laser wavelength. In the long- and short-wavelength limits of the photodissociation spectrum, the anisotropy parameter attains i ts maximum value, beta = 2, characterizing the process as a parallel ( 1 2SIGMA(u)+ --> 1 2SIGMA(g)+) transition followed by a rapid, recoil- like fragmentation. However, excitation in the middle of the spectrum (almost-equal-to 620-660 nm) results in an anisotropy parameter that v aries smoothly and significantly from the maximum value, indicating a second dissociation pathway for excitation in this region. Several alt ernatives for the competing channel are discussed. The measured recoil energy varies from E almost-equal-to 4100 to 7100 cm-1 as the dissoci ating wavelength is tuned from lambda=680 to 590 nm. This allows us to obtain an estimate for the ground-state binding energy D0'' almost-eq ual-to 10 200 +/- 300 cm - 1, a result in very good agreement with rec ent theoretical predictions [G. Durand, J.-P. Daudey, and J.-P. Malrie u, J. Phys. (Paris) 47, 1335 (1986); M. Sodupe, C. W. Bauschlicher, Jr ., and H. Partridge, Chem. Phys. Lett. 192,185 (1992)].