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  Molecular dissociation by mid-IR femtosecond pulses

Windhorn, L., Witte, T., Yeston, J. S., Proch, D., Motzkus, M., Kompa, K.-L., et al. (2002). Molecular dissociation by mid-IR femtosecond pulses. Chemical Physics Letters, 357(1-2), 85-90. Retrieved from http://www.sciencedirect.com/science/article/B6TFN-45H0CW0-3/1/0bdf02ce4e4e425bdeecfba910a95f03.

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 Creators:
Windhorn, Lars1, Author           
Witte, Thomas1, Author           
Yeston, Jake S.2, Author
Proch, Detlev1, Author           
Motzkus, Marcus1, Author           
Kompa, Karl-Ludwig1, Author           
Fuß, Werner1, 3, Author           
Affiliations:
1Laser Chemistry, Max Planck Institute of Quantum Optics, Max Planck Society, ou_1445565              
2Max Planck Society, ou_persistent13              
3Laboratory for Attosecond Physics, Max Planck Institute of Quantum Optics, Max Planck Society, ou_1445564              

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 Abstract: By focusing a MIR femtosecond laser in a cell containing gas- phase metal carbonyls, the resonant infrared multiphoton dissociation of molecules was observed, Cr(CO)6, Mo(CO)6,W(CO)6, and Fe(CO)5 could easily be dissociated, which requires an excitation to at least v = 7 or 8 of the CO stretch vibration. After irradiation with ~150 fs pulses at 5 µm the metal carbonyl practically disappears in favor of free CO, as detected by the IR spectrum. By comparing the power dependence of the total conversion with a model, we can infer that only few vibrational degrees of freedom are involved in the excitation process. (C) 2002 Published by Elsevier Science B.V.

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Language(s): eng - English
 Dates: 2002-05-01
 Publication Status: Issued
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 Table of Contents: -
 Rev. Type: Peer
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Title: Chemical Physics Letters
  Alternative Title : Chem. Phys. Lett.
Source Genre: Journal
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Pages: - Volume / Issue: 357 (1-2) Sequence Number: - Start / End Page: 85 - 90 Identifier: ISSN: 0009-2614