Selective excitation of the vibrational-rotational states and dissociation of diatomic molecules by picosecond infrared laser pulses: Modeling for HF in the ground electronic state

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Inst. F. Phys. und Theor. Chemie, Freie Universität Berlin, WE 3, Takustrasse 3, D-14195 Berlin, Germany ^{[1
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Phys Rev A | / 3卷 / 2134-2138期

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2134

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[21] Picosecond laser control of bond-selective dissociation and clockwise and anticlockwise rotation of the dissociation fragments:: applications to a three-dimensional model of HONO2 in the ground electronic state
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[22] MANY-PHOTON EXCITATION OF SPHERICALLY SYMMETRIC MOLECULES IN AN INFRARED LASER FIELD BY WEAKLY FORBIDDEN DELTA R does not equal O, DELTA n does not equal O VIBRATIONAL-ROTATIONAL TRANSITIONS.
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[23] THE INFLUENCE OF GROUND-STATE VIBRATIONALLY EXCITED N-2 MOLECULES ON THE VIBRATIONAL-EXCITATION OF N2, N2+ ELECTRONIC STATES
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[24] MECHANISM OF STATE-SELECTIVE VIBRATIONAL-EXCITATION BY AN INFRARED PICOSECOND LASER-PULSE STUDIED BY 2 TECHNIQUES - FAST FOURIER-TRANSFORM PROPAGATION OF A MOLECULAR WAVE PACKET AND ANALYSIS OF THE CORRESPONDING VIBRATIONAL TRANSITIONS
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[25] Ultrafast laser control of vibrational dynamics for a two-dimensional model of HONO2 in the ground electronic state:: separation of conformers, control of the bond length, selective preparation of the discrete and the continuum states
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