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Intramolecular photoelectron diffraction in the gas phase

Author
Ueda, Kiyoshi; Miron, Catalin; Plésiat, Etienne; Argenti, Luca; Patanen, Minna; Kooser, Kuno; Ayuso, D.; Mondal, Subhendu; Kimura, Miku; Sakai, Kazuma; Travnikova, Oksana; Palacios Cañas, Aliciauntranslated; Decleva, Piero; Kukk, Edwin; Martín García, Fernandountranslated
Entity
UAM. Departamento de Química
Publisher
AIP Publishing LLC
Date
2013-10-18
Citation
10.1063/1.4820814
Journal of Chemical Physics 139.12 (2013): 124306
 
 
 
ISSN
0021-9606 (print); 1089-7690 (online)
DOI
10.1063/1.4820814
Funded by
Work supported by the Advanced Grant of the European Research Council XCHEM 290853, the MICINN Project Nos. FIS2010-15127, ACI2008-0777, and CSD 2007-00010 (Spain), the ERAChemistry Project No. PIM2010EEC-00751, the European GrantNos. MC-ITN CORINF and MC-RG ATTOTREND, the European COST Action CM0702, the MC-IEF CHICROCSX under Grant Agreement No. 252781 (OT) and I3 program, the MEXT and JSPS agencies (Japan), and the Academy of Finland
Editor's Version
http://dx.doi.org/10.1063/1.4820814
Subjects
Química
URI
http://hdl.handle.net/10486/664602
Note
The following article appeared in Journal of Chemical Physics 139.12 (2013): 124306 and may be found at http://scitation.aip.org/content/aip/journal/jcp/139/12/10.1063/1.4820814
Rights
© 2013 AIP Publishing LLC

Abstract

We report unambiguous experimental and theoretical evidence of intramolecular photoelectron diffraction in the collective vibrational excitation that accompanies high-energy photoionization of gas-phase CF4, BF3, and CH4 from the 1s orbital of the central atom. We show that the ratios between vibrationally resolved photoionization cross sections (v-ratios) exhibit pronounced oscillations as a function of photon energy, which is the fingerprint of electron diffraction by the surrounding atomic centers. This interpretation is supported by the excellent agreement between first-principles static-exchange and time-dependent density functional theory calculations and high resolution measurements, as well as by qualitative agreement at high energies with a model in which atomic displacements are treated to first order of perturbation theory. The latter model allows us to rationalize the results for all the v-ratios in terms of a generalized v-ratio, which contains information on the structure of the above three molecules and the corresponding molecular cations. A fit of the measured v-ratios to a simple formula based on this model suggests that the method could be used to obtain structural information of both neutral and ionic molecular species
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Google™ Scholar:Ueda, Kiyoshi - Miron, Catalin - Plésiat, Etienne - Argenti, Luca - Patanen, Minna - Kooser, Kuno - Ayuso, D. - Mondal, Subhendu - Kimura, Miku - Sakai, Kazuma - Travnikova, Oksana - Palacios Cañas, Alicia - Decleva, Piero - Kukk, Edwin - Martín García, Fernando

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  • Producción científica en acceso abierto de la UAM [16865]

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