High-resolution infrared studies of the v₁₀, v₁₁, v₁₄, and v₁₈ levels of [1.1.1]propellane

Journal Article · Thu Nov 15 00:00:00 EST 2012 · Journal of Molecular Spectroscopy

DOI:https://doi.org/10.1016/j.jms.2012.09.001· OSTI ID:1059615

Kirkpatrick, Robynne W. ^[1]; Masiello, Tony ^[2]; Martin, Matthew A. ^[1]; Nibler, Joseph W. ^[1]; Maki, Arthur ^[3]; Weber, Alfons ^[4]; Blake, Thomas A. ^[5]

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1. Oregon State Univ., Corvallis, OR (United States)
2. California State Univ., Hayward, CA (United States)
3. 14012 24th Ave., Mill Creek, WA (United States)
4. National Inst. of Standards and Technology, Gaithersburg, MD (United States)
5. Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

This paper is a continuation of earlier work for which the high resolution infrared spectrum of [1.1.1]propellane was measured and its k and l structure resolved for the first time. Here we present results from an analysis of more than 16,000 transitions involving three fundamental bands v₁₀ (E'-A1'), v₁₁ (E'-A1'), v₁₄ (A2''-A1') and two difference bands (v₁₀- v₁₈) (E'-E'') and (v₁₁-v₁₈) (E'-E"). Additional information about v18 was also obtained from the difference band (v₁₅+v₁8)-v₁₈ (E'-E") and the binary combination band (v₁₅+v₁₈) (E'-A1'). Through the use of the ground state constants reported in an earlier paper [1], rovibrational constants have been determined for all the vibrational states involved in these bands. The rovibrational parameters for the v₁₈(E'') state were obtained from combination-differences and showed no need to include interactions with other states. The v₁₀(E') state analysis was also straight-forward, with only a weak Coriolis interaction with the levels of the v₁₄(A2'') state. The latter levels are much more affected by a strong Coriolis interaction with the levels of the nearby v₁₁(E') state and also by a small but significant interaction with another state, presumably the v16(E'') state, that is not directly observed. Gaussian calculations (B3LYP/cc-pVTZ) computed at the anharmonic level aided the analyses by providing initial values for many of the parameters. These theoretical results generally compare favorably with the final parameter values deduced from the spectral analyses. Finally, evidence was obtained for several level crossings between the rotational levels of the v₁₁ and v₁₄ states and, using a weak coupling term corresponding to a Δk = ±5, Δl = ∓1 matrix element, it was possible to find transitions from the ground state that, combined with transitions to the same upper state, give a value of C₀ = 0.1936519(4) cm^-1. This result, combined with the value of B₀ = 0.28755833(14) cm-1 reported earlier [1], yields a value of 1.586282(3) Å for the length of the novel axial CC bond in propellane.

• Research Organization: Pacific Northwest National Lab. (PNNL), Richland, WA (United States). Environmental Molecular Sciences Lab. (EMSL)
• Sponsoring Organization: USDOE
• DOE Contract Number: AC05-76RL01830
• OSTI ID: 1059615
• Report Number(s): PNNL-SA-89494; 20907; KP1704020
• Journal Information: Journal of Molecular Spectroscopy, Vol. 281; ISSN 0022-2852
• Publisher: Elsevier
• Country of Publication: United States
• Language: English

Related Subjects

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GENERAL PHYSICS
Environmental Molecular Sciences Laboratory