Direct Production of CH(A2Δ) Radical from Intense Femtosecond Near-IR Laser Pulses
Author:
Affiliation:
1. ELI-ALPS, ELI-HU Non-Profit Ltd., Wolfgang Sandner u. 3. H-6728 Szeged, Hungary
2. Department of Chemistry, Kansas State University, 213 CBC Building, Manhattan, Kansas 66506-0401, United States
Funder
European Regional Development Fund
European Social Fund
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.0c05206
Reference31 articles.
1. Photodissociation of bromoform cation at 308, 355, and 610 nm by means of time-of-flight mass spectroscopy and ion velocity imaging
2. Ultraviolet photodissociation of bromoform at 234 and 267 nm by means of ion velocity imaging
3. Photodissociation of Bromoform at 248 nm: Single and Multiphoton Processes
4. Tracking dissociation dynamics of strong-field ionized 1,2-dibromoethane with femtosecond XUV transient absorption spectroscopy
5. Concerted elimination of Br2+ resulting from the Coulomb explosion of 1,2-dibromoethane in an intense femtosecond laser field
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