English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  The v4 = 1 and v4 = 2 rovibrational levels of PF3 revisited: New solutions for old topics

Ceausu-Velcescu, A., Pracna, P., Breidung, J., Thiel, W., & Badaoui, M. (2015). The v4 = 1 and v4 = 2 rovibrational levels of PF3 revisited: New solutions for old topics. Journal of Molecular Spectroscopy, 316, 11-21. doi:10.1016/j.jms.2015.07.004.

Item is

Files

show Files

Locators

show

Creators

show
hide
 Creators:
Ceausu-Velcescu, Adina1, Author
Pracna, Petr2, Author
Breidung, Jürgen3, Author              
Thiel, Walter3, Author              
Badaoui, Mohamed4, Author
Affiliations:
1Université de Perpignan, Laboratoire de Mathématiques et Physique, 52 Avenue Paul Alduy, 66860 Perpignan Cedex, France, ou_persistent22              
2J. Heyrovský Institute of Physical Chemistry, v.v.i., Academy of Sciences of the Czech Republic, Dolejškova 3, 18223 Prague, Czech Republic, ou_persistent22              
3Research Department Thiel, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445590              
4Institut Agronomique et Vétérinaire Hassan II, B.P. 6202, Rabat-Instituts, 10101 Rabat, Morocco, ou_persistent22              

Content

show
hide
Free keywords: Phosphorus trifluoride; High-resolution IR spectroscopy; Hot bands; Ab initio equilibrium structure; Anharmonic force fields;
 Abstract: The high-resolution infrared spectra of trifluorophosphine (PF3) were reinvestigated in the ν4 fundamental region near 350 cm−1, and around 690 cm−1, with the aim to provide a necessary reassignment of the 2±2 sublevel of the v4 = 2 overtone level. The present paper reports on the first complete study of both sublevels of v4 = 2 (of A1 and E symmetry, corresponding to l4 = 0 and ±2, respectively), through the high-resolution analysis of the overtone 2V40 band and the V4±2 – V4±1hot band. The assignments of the latter were corrected and extended, spanning the rotational states J ⩽ 82 and −80 ⩽ K″ · ΔK ⩽ 48. These new infrared assignments in the v4 = 2 state were combined with accurate infrared, radiofrequency, centimeter-, millimeter- and submillimeter-wave data of the v4 = 1 level (Thiessen et al., 2000), together with rotational data in the ground vibrational state (Cotti et al., 1995), in a simultaneous fit. The existence of resonance crossings due to a Δk = ±1, Δl = ∓2 l-type resonance in the v4 = 1 state, which generated perturbation-allowed transitions, provided independent values of the C4 and Cζ4 constants. Combining these rotational transitions with the wavenumbers of the ν4 fundamental band enabled us to determine accurately the C0 axial ground state constant. Moreover, the assignment of a few, very weak rRK transitions 2ν4−2 overtone band and their inclusion in the global least-squares fit allowed also the first accurate experimental determination of DK0. The obtained results are (in cm−1): C0 = 0.159970241(29) and DK0=1.80457(49) × 10−7. Quadratic, cubic, and semidiagonal quartic force fields of PF3 have been calculated at the CCSD(T) level of theory employing a variety of large correlation-consistent basis sets. These force fields have been used to evaluate spectroscopic constants which are generally found to be in very good agreement with experiment. The present best estimate of the re structure of PF3 based on an explicitly correlated coupled-cluster approach (CCSD(T)-F12b) is almost identical with its latest experimental counterpart.

Details

show
hide
Language(s): eng - English
 Dates: 2015-07-162015-06-082015-07-262015-10-01
 Publication Status: Published in print
 Pages: 11
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.jms.2015.07.004
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Journal of Molecular Spectroscopy
  Other : J. Mol. Spectrosc.
  Abbreviation : JMS
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Elsevier B. V.
Pages: - Volume / Issue: 316 Sequence Number: - Start / End Page: 11 - 21 Identifier: ISSN: 0022-2852
CoNE: https://pure.mpg.de/cone/journals/resource/954922646043