• Author: Kollipost, F.

    Institut für Physikalische Chemie, Universität Göttingen, Germany

  • Author: Larsen, René Wugt

    X-ray Crystallography, Department of Chemistry, Technical University of Denmark, Kemitorvet, 2800, Kgs. Lyngby, Denmark

  • Author: Domanskaya, A.V.

    Institut für Physikalische Chemie, Universität Göttingen, Germany

  • Author: Nörenberg, M.

    Institut für Physikalische Chemie, Universität Göttingen, Germany

  • Author: Suhm, M.A.

    Institut für Physikalische Chemie, Universität Göttingen, Germany

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The highest frequency hydrogen bond fundamental of formic acid dimer, ν24 (Bu), is experimentally located at 264 cm−1. FTIR spectra of this in-plane bending mode of (HCOOH)2 and band centers of its symmetric D isotopologues (isotopomers) recorded in a supersonic slit jet expansion are presented. Comparison to earlier studies at room temperature reveals the large influence of thermal excitation on the band maximum. Together with three Bu combination states involving hydrogen bond fundamentals and with recent progress for the Raman-active modes, this brings into reach an accurate statistical thermodynamics treatment of the dimerization process up to room temperature. We obtain D0 = 59.5(5) kJ/mol as the best experimental estimate for the dimer dissociation energy at
0 K. Further improvements have to wait for a more consistent determination of the room temperature equilibrium constant.

Original languageEnglish
JournalJournal of Chemical Physics
Publication date2012
Volume136
Pages151101
Number of pages4
ISSN0021-9606
DOIs
StatePublished

Bibliographical note

© 2012 American Institute of Physics.

CitationsWeb of Science® Times Cited: 11
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