Intramolecular photoelectron diffraction in the gas phase
Entity
UAM. Departamento de QuímicaPublisher
AIP Publishing LLCDate
2013-10-18Citation
10.1063/1.4820814
Journal of Chemical Physics 139.12 (2013): 124306
ISSN
0021-9606 (print); 1089-7690 (online)DOI
10.1063/1.4820814Funded 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 FinlandEditor's Version
http://dx.doi.org/10.1063/1.4820814Subjects
QuímicaNote
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/139/12/10.1063/1.4820814Rights
© 2013 AIP Publishing LLCAbstract
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
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Miron, Catalin
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Plésiat, Etienne
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Argenti, Luca
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Patanen, Minna
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Kooser, Kuno
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Ayuso, D.
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Mondal, Subhendu
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Kimura, Miku
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Sakai, Kazuma
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Travnikova, Oksana
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Palacios Cañas, Alicia
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Decleva, Piero
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Kukk, Edwin
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Martín García, Fernando
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