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  Relaxation dynamics of deuterated formyl and isoformyl cations

Wester, R., Hechtfischer, U., Knoll, L., Lange, M., Levin, J., Scheffel, M., et al. (2002). Relaxation dynamics of deuterated formyl and isoformyl cations. Journal of Chemical Physics, 116(16), 7000-7011.

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 Creators:
Wester, R.1, Author           
Hechtfischer, U.1, Author           
Knoll, L.1, Author           
Lange, M.2, Author           
Levin, J.1, Author           
Scheffel, M.1, Author           
Schwalm, D.1, Author           
Wolf, A.2, Author           
Baer, A.3, Author
Vager, Z.3, Author
Zajfman, D.1, Author           
Mladenovic, M.3, Author
Schmatz, S.3, Author
Affiliations:
1Prof. Dirk Schwalm, Emeriti, MPI for Nuclear Physics, Max Planck Society, ou_907546              
2Division Prof. Dr. Klaus Blaum, MPI for Nuclear Physics, Max Planck Society, ou_904548              
3Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA; Weizmann Inst Sci, IL-79100 Rehovot, Israel; Univ Gottingen, Inst Phys Chem, D-37077 Gottingen, Germany, ou_persistent22              

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 Abstract: Vibrational relaxation and isomerization of internally excited deuterated formyl and isoformyl cations has been investigated on the time scale of 2 ms to 12 s using the nearly interaction- free environment of an ion storage ring. De-excitation of the v(2) bending modes of DCO+ and DOC+ due to spontaneous radiative transitions was observed as a function of the storage time by measuring their foil-induced Coulomb explosion using three-dimensional coincident fragment imaging. No isomerization of low-lying vibrational levels of DOC+ ions was observed on the time scales considered. By comparing the Coulomb explosion data to molecular bond angle distributions obtained from vibrational wave function calculations, the time evolution of the mean v(2) population is deduced for both isomers. The stored DOC+ ions are found to thermalize with the 300 K black- body radiation, while relaxation of the DCO+ bending vibrations was found to require considerably longer times, in agreement with a predicted very small transition moment of the v(2)=1 level. (C) 2002 American Institute of Physics.

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Language(s): eng - English
 Dates: 2002-04-22
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 31850
ISI: 000174973600017
 Degree: -

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Title: Journal of Chemical Physics
  Alternative Title : J. Chem. Phys.
Source Genre: Journal
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Pages: - Volume / Issue: 116 (16) Sequence Number: - Start / End Page: 7000 - 7011 Identifier: ISSN: 0021-9606