Using a high-resolution (R = 0.0025 cm-1) Fourier transform spectrum of nitric acid recorded at room temperature in the 1100-1240 cm-1 region, it has been possible to perform a more extended analysis of the nu8 + nu9 band of HNO3 centered at 1205.7075 cm-1. As in a recent analysis of this band [W. F. Wang, P. P. Ong, T. L. Tan, E. C. Looi, and H. H. Teo, J. Mol. Spectrosc. 183, 407-413 (1997)], the Hamiltonian used for the line positions calculation takes into account, for the upper state, the DeltaK = +/-2 anharmonic resonance linking the rotational levels of the v8 = v9 = 1 "bright" vibrational state and those of the "dark" v6 = v7 = 1 vibrational state. More than 4800 lines were assigned in the nu8 + nu9 band, which involve significantly higher rotational quantum numbers than in previous works. On the other hand, and surprisingly as compared to previous studies, the nu8 + nu9 band appears to be a hybrid band. In fact, nonnegligible B-type transitions could be clearly identified among the much stronger A-type lines. Accordingly, a set of individual line intensities were measured for lines of both types and were introduced in a least-squares fit to get the A- and B-type components of the transition moment operator. Finally, a synthetic spectrum of the 8.3-µm region of HNO3 has been generated, using for the line positions and line intensities the Hamiltonian constants and the expansion of the transition moment operator which were determined in this work. In this way, the B-type and the A-type components of the nu8 + nu9 band appear to contribute for about (1/4) and (3/4), respectively, to the total band intensity. Copyright 1999 Academic Press.

Download full-text PDF

Source
http://dx.doi.org/10.1006/jmsp.1998.7765DOI Listing

Publication Analysis

Top Keywords

nu8 nu9
20
nu9 band
20
analysis nu8
8
band
8
band hno3
8
positions intensities
8
vibrational state
8
transition moment
8
moment operator
8
nu9
5

Similar Publications

Curvilinear kinetic energy models are developed for variational nuclear motion computations including the inter- and the low-frequency intra-molecular degrees of freedom of the formic acid dimer. The coupling of the inter- and intra-molecular modes is studied by solving the vibrational Schrödinger equation for a series of vibrational models, from two up to ten active vibrational degrees of freedom by selecting various combinations of active modes and constrained coordinate values. Vibrational states, nodal assignment, and infrared vibrational intensity information is computed using the full-dimensional potential energy surface (PES) and electric dipole moment surface developed by Qu and Bowman [Phys.

View Article and Find Full Text PDF

Matrix-Isolated Infrared Absorption Spectrum of CH2IOO Radical.

J Phys Chem A

January 2016

Jet Propulsion Laboratory, California Institute of Technology, 4800 Oak Grove Drive, Pasadena, California 91109-8099, United States.

The peroxyiodomethyl radical, CH2IOO, was generated in cryogenic matrices using tandem supersonic nozzles. One hyperthermal nozzle decomposes diiodomethane (CH2I2) to generate intense beams of CH2I radicals, while the second nozzle continuously deposits O2/argon (Ar) on the matrix at 10 K. The CH2I and O2 in the Ar matrix react to produce the target peroxy radical (CH2IOO).

View Article and Find Full Text PDF

Spectroscopy and Dynamics of Jet-Cooled Polyynes in a Slit Supersonic Discharge: Sub-Doppler Infrared Studies of Diacetylene HCCCCH.

J Phys Chem A

July 2015

JILA, National Institute of Standards and Technology University of Colorado, and Department of Chemistry and Biochemistry, University of Colorado at Boulder, Boulder, Colorado 80309, United States.

Fundamental, bending (ν6, ν7, ν8, ν9), and CC-stretch (ν2, ν3) hot band spectra in the antisymmetric CH stretch (ν4) region near 3330 cm(-1) have been observed and analyzed for jet cooled diacetylene (HC≡C-C≡CH) under sub-Doppler conditions. Diacetylene is generated in situ in the throat of a pulsed supersonic slit expansion by discharge dissociation of acetylene to form ethynyl (C≡CH) + H, followed by radical attack (HC≡CH + C≡C-H) to form HC≡C-C≡CH + H. The combination of (i) sub-Doppler line widths and (ii) absence of spectral congestion permits rotational structure and Coriolis interactions in the ν4 CH stretch fundamental to be observed and analyzed with improved precision.

View Article and Find Full Text PDF

Bimolecular reaction of CH3 + CO in solid p-H2: infrared absorption of acetyl radical (CH3CO) and CH3-CO complex.

J Chem Phys

June 2014

Department of Applied Chemistry and Institute of Molecular Science, National Chiao Tung University, Hsinchu 30010, Taiwan.

We have recorded infrared spectra of acetyl radical (CH3CO) and CH3-CO complex in solid para-hydrogen (p-H2). Upon irradiation at 248 nm of CH3C(O)Cl/p-H2 matrices, CH3CO was identified as the major product; characteristic intense IR absorption features at 2990.3 (ν9), 2989.

View Article and Find Full Text PDF

The IR spectrum of dichlorodifluoromethane (i.e., R12 or Freon-12) is central to its role as a major greenhouse contributor.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!