Selective vibrational excitations in the OX (X=F, Cl, Br, I) molecules
Author(s) -
Ce ́line Le ́onard,
Fre ́de ́ric Le Que ́re ́,
P. Rosmus,
Cristina Puzzarini,
María Pilar de LaraCastells
Publication year - 2000
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/a908993d
Subject(s) - dipole , wave packet , electric dipole moment , atomic physics , transition dipole moment , moment (physics) , molecule , ab initio , chemistry , ab initio quantum chemistry methods , physics , diatomic molecule , molecular vibration , molecular physics , quantum mechanics
International audienceUsing ab initio calculated potential energy and electric dipole moment functions for the X(2)Pi states of OF, OCl, OBr and OI, two models have been tested to selectively populate their vibrational modes by ultrashort coherent light pulses. For a given form of the pulses either a perturbative approach using discrete vibrational eigenstates and electric dipole transition moment matrix elements or a wavepacket propagation technique were used. The optimisation of the pulse parameters and the mechanisms of the multiphoton processes are discussed. For the target level v=10 populations of more than 60% have been achieved in all four molecules. For OCl it was possible to populate selectively all target levels between v=2 and v=15 using chirped pulses
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