Article ID Journal Published Year Pages File Type
5387843 Chemical Physics Letters 2008 5 Pages PDF
Abstract
Nonadiabatic rotational excitation of benzene induced by intense nonresonant femtosecond laser fields (820 nm, up to 2.2 TW/cm2, 700 fs) is studied with a quantum-state resolved manner employing the REMPI technique. The excitation spectra of the S1-S0601 band after the interaction with the intense femtosecond pulse show the drastic change in the rotational-state distribution.
Related Topics
Physical Sciences and Engineering Chemistry Physical and Theoretical Chemistry
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Nonadiabatic rotational excitation of benzene by nonresonant intense femtosecond laser fields
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