We study the intensity-dependent behavior of laser-induced vibrational quasi-energy (VQE) resonance structure and photodissociation rates of H: molecular ions in intense laser fields at 775 nm and report a novel new high-intensity phenomenon. At strong fields, the vibrational levels are shifted and
Chemical bond hardening and molecular stabilization of D+2 in one- and two-color laser fields
✍ Scribed by Jingyan Wang; Shih-I Chu
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 471 KB
- Volume
- 227
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
We report the first theoretical study of the structure of laser-induced vibrational quasi-energy (VQE) resonance states of D: in intense one-and two-color (fundamental and its third harmonic) laser fields by means of the complex-scaling generalized Fourier-grid Floquet Hamiltonian technique. Stabilization and chemical bond hardening for high-lying VQE resonances are observed. It is shown that by tuning the relative phase between the fundamental and the third harmonic fields, the electronicfield potential surface and the multiphoton dissociation rates can be modified significantly, suggesting some degree of 'coherent control' of multiphoton dynamics may be feasible.
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The influence of solvent polarity on the properties of hydrogen-bonded 1 : 1 complexes of 2,4,6trimethylpyridine-15 N with HF and DF, labeled below as FHN and FDN, has been studied by multinuclear magnetic resonance spectroscopy in the slow hydrogen bond exchange regime reached below 190 K. Mixtures