4.7 Article

Strong ortho/para effects in the vibrational spectrum of Cl-(H2)

Journal

JOURNAL OF CHEMICAL PHYSICS
Volume 155, Issue 24, Pages -

Publisher

AIP Publishing
DOI: 10.1063/5.0073749

Keywords

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Funding

  1. Austrian Science Fund (FWF) [I2920-N27]
  2. Doctoral Program Atoms, Light and Molecules [W1259-N27]
  3. project CALIPSOplus from the EU Framework Program for Research and Innovation HORIZON 2020 [730872]
  4. Agence Nationale de la Recherche project COLD HMINUS
  5. DFG via the DFG Geratezentrum Cologne Center for Terahertz Spectroscopy [DFG SCHL 341/15-1]
  6. Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO)

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The predissociation spectrum of the Cl-35(-)(H-2) complex was measured in a multipole radiofrequency ion trap at different temperatures using the FELIX infrared free electron laser. Removal of the Cl-(p-H-2) para nuclear spin isomer by ligand exchange to the Cl-(o-H-2) ortho isomer above a certain temperature allows for detecting the spectrum of the more weakly bound complex. Two vibrational bands of Cl-(p-H-2) at 510(1) and 606(1) cm(-1) were detected at trap temperatures of 30.5 and 41.5 K.
The predissociation spectrum of the Cl-35(-)(H-2) complex is measured between 450 and 800 cm(-1) in a multipole radiofrequency ion trap at different temperatures using the FELIX infrared free electron laser. Above a certain temperature, the removal of the Cl-(p-H-2) para nuclear spin isomer by ligand exchange to the Cl-(o-H-2) ortho isomer is suppressed effectively, thereby making it possible to detect the spectrum of this more weakly bound complex. At trap temperatures of 30.5 and 41.5 K, we detect two vibrational bands of Cl-(p-H-2) at 510(1) and 606(1) cm(-1). Using accurate quantum calculations, these bands are assigned to transitions to the inter-monomer vibrational modes (v(1),v(2)(l2)) = (0, 2(0)) and (1, 2(0)), respectively. (C) 2021 Author(s).

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