Lima, Emanuel Fernandes de [UNESP]Rosado, E. C.Castelano, L. K.Carvalho, Ricardo Egydio de [UNESP]2015-03-182015-03-182014-07-18Physics Letters A. Amsterdam: Elsevier Science Bv, v. 378, n. 36, p. 2657-2663, 2014.0375-9601http://hdl.handle.net/11449/116695We consider the quantum and classical dissociation dynamics of heteronuclear diatomic molecules induced by infrared laser pulses. The field-molecule interaction is given by the product of the time-dependent electric field and the molecule permanent dipole. We investigate the influence of the dipole function in molecular dissociation. We show that the dissociation can be suppressed at certain external field frequencies for a nonlinear and finite-range dipole function. The correspondence between quantum and classical results is established by relating classical Fourier amplitudes to discrete-continuum quantum matrix elements. (C) 2014 Elsevier B.V. All rights reserved.2657-2663engQuantum-classical correspondenceDipole functionMolecular dissociationMorse oscillatorQuantum-classical correspondence and the role of the dipole function in molecular dissociationArtigo10.1016/j.physleta.2014.07.026WOS:000340989200002Acesso restrito784560589019511574977815566223280000-0002-2684-5058