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Threshold photoelectron spectroscopy of the methyl radical isotopomers, CH3, CH2D, CHD2 and CD3: synergy between VUV synchrotron radiation experiments and explicitly correlated coupled cluster calculations

Authors :
Peter Botschwina
Stéphane Douin
Bastian Noller
Bérenger Gans
Gustavo A. Garcia
Jan Zabka
Patrick Hemberger
Christian Alcaraz
Luiz A. Vieira Mendes
Héloïse Soldi-Lose
Mohamed Elhanine
Barbara Cunha de Miranda
Ingo Fischer
Séverine Boyé-Péronne
Laboratoire de Chimie Physique D'Orsay (LCPO)
Université Paris-Sud - Paris 11 (UP11)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Paul Scherrer Institut (PSI)
Paul Scherrer Institute (PSI)
Department of Applied Physics and Photonics [Brussels] (TONA)
Vrije Universiteit Brussel (VUB)
Synchrotron SOLEIL (SSOLEIL)
Centre National de la Recherche Scientifique (CNRS)
Institut des Sciences Moléculaires d'Orsay (ISMO)
Université Paris-Sud - Paris 11 (UP11)-Centre National de la Recherche Scientifique (CNRS)
Universidade Federal Fluminense [Rio de Janeiro] (UFF)
J. Heyrovský Institute of Physical Chemistry
J. Heyrovsky Institute of Physical Chemistry
Institute of Physical Chemistry
University of Göttingen - Georg-August-Universität Göttingen
Georg-August-University [Göttingen]
Source :
Journal of Physical Chemistry A, Journal of Physical Chemistry A, American Chemical Society, 2010, 114 (14), pp.4818-4830. ⟨10.1021/jp909422q⟩
Publication Year :
2010

Abstract

Threshold photoelectron spectra (TPES) of the isotopomers of the methyl radical (CH(3), CH(2)D, CHD(2), and CD(3)) have been recorded in the 9.5-10.5 eV VUV photon energy range using third generation synchrotron radiation to investigate the vibrational spectroscopy of the corresponding cations at a 7-11 meV resolution. A threshold photoelectron-photoion coincidence (TPEPICO) spectrometer based on velocity map imaging and Wiley-McLaren time-of-flight has been used to simultaneously record the TPES of several radical species produced in a Ar-seeded beam by dc flash-pyrolysis of nitromethane (CH(x)D(y)NO(2), x + y = 3). Vibrational bands belonging to the symmetric stretching and out-of-plane bending modes have been observed and P, Q, and R branches have been identified in the analysis of the rotational profiles. Vibrational configuration interaction (VCI), in conjunction with near-equilibrium potential energy surfaces calculated by the explicitly correlated coupled cluster method CCSD(T*)-F12a, is used to calculate vibrational frequencies for the four radical isotopomers and the corresponding cations. Agreement with data from high-resolution IR spectroscopy is very good and a large number of predictions is made. In particular, the calculated wavenumbers for the out-of-plane bending vibrations, nu(2)(CH(3)(+)) = 1404 cm(-1), nu(4)(CH(2)D(+)) = 1308 cm(-1), nu(4)(CHD(2)(+)) = 1205 cm(-1), and nu(2)(CD(3)(+)) = 1090 cm(-1), should be accurate to ca. 2 cm(-1). Additionally, computed Franck-Condon factors are used to estimate the importance of autoionization relative to direct ionization. The chosen models globally account for the observed transitions, but in contrast to PES spectroscopy, evidence for rotational and vibrational autoionization is found. It is shown that state-selected methyl cations can be produced by TPEPICO spectroscopy for ion-molecule reaction studies, which are very important for the understanding of the planetary ionosphere chemistry.

Details

ISSN :
15205215 and 10895639
Volume :
114
Issue :
14
Database :
OpenAIRE
Journal :
The journal of physical chemistry. A
Accession number :
edsair.doi.dedup.....437ac270d81867e1d3fb95e4751cda6b
Full Text :
https://doi.org/10.1021/jp909422q⟩