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Robert L Sams

Publications and source records attributed to Robert L Sams.

4 recordsLinked to original sources

Quantum tunneling in the midrange vibrational fundamentals of tropolone.

The Fourier transform infrared spectrum of tropolone(OH) vapor in the 1175-1700 cm(-1) region is reported at 0.0025 and 0.10 cm(-1) spectral resolutions. The 12 vibrational fundamentals in this region of rapidly rising vibrational state density are dominated by mixtures of the CC, CO, CCH, and COH internal coordinates. Estimates based on the measurement of sharp Q branch peaks are reported for 11 of the spectral doublet component separations DS(v) = |Delta(v) +/- Delta(0)|. Delta(0) = 0.974 cm(-1) is the known zero-point splitting, and three a(1) modes show tunneling splittings Delta(v) approximately Delta(0), four b(2) modes show splittings Delta(v) approximately 0.90Delta(0), and the remaining four modes show splittings Delta(v) falling 5-14% from Delta(0.) Significantly, the splitting for the nominal COH bending mode nu(8) (a(1)) is small, that is, 10% from Delta(0). Many of the vibrational excited states demonstrate strong anharmonic behavior, but there are only mild perturbations on the tautomerization mechanism driving Delta(0). The data suggest, especially for the higher frequency a(1) fundamentals, the onset of selective intramolecular vibrational energy redistribution processes that are fast on the time scale of the tautomerization process. These appear to delocalize and smooth out the topographical modifications of the zero-point potential energy surface that are anticipated to follow absorption of the nu(v) photon. Further, the spectra show the propensity for the Delta(v) splittings of b(2) and other complex vibrations to be damped relative to Delta(0).

Journal Article↗

18O effects on the infrared spectrum and skeletal tunneling of tropolone.

Infrared-absorption profiles observed for vibrational transitions of gaseous tropolone often show sharp Q branch peaks, some of them ultranarrow spikes, indicative of the band origins for vibrational state-specific spectral tunneling doublets. In this work oxygen isotope effects for two CH wagging fundamentals, the COH torsion fundamental, and the skeletal contortion fundamental are reported. They allow considerations to be given: (1) oxygen isotope effects on the vibrational frequencies and state-specific tunneling splittings; (2) the asymmetry offset of the potential-energy minima for 16O and 18O tropolone; and (3) additional details concerning previously proposed high J rotation-contortion resonances in the contortional fundamental. The new results help to characterize the skeletal contortion fundamental and support the joint participation of skeletal tunneling with H tunneling in the vibrational state-specific tautomerization processes of tropolone in its ground electronic state.

Oxygen Isotopes↗

Gas-phase databases for quantitative infrared spectroscopy.

The National Institute of Standards and Technology (NIST) and the Pacific Northwest National Laboratory (PNNL) are each creating quantitative databases containing the vapor-phase infrared spectra of pure chemicals. The digital databases have been created with both laboratory and remote-sensing applications in mind. A spectral resolution of approximate, equals 0.1 cm(-1) was selected to avoid degrading sharp spectral features, while also realizing that atmospheric broadening typically limits line widths to 0.1 cm(-1). Calculated positional (wave- number, cm(-1)) uncertainty is </=0.005 cm(-1), while the 1sigma statistical uncertainty in absorbance values is <2% for most compounds. The latter was achieved by measuring multiple (typically >/=9) path length-concentration burdens and fitting a weighted Beer's law plot to each wavenumber channel. The two databases include different classes of compounds and were compared using 12 samples. Though these 12 samples span a range of polarities, absorption strengths, and vapor pressures, the data agree to within experimental uncertainties with only one exception.

Calibration↗

Removing aperture-induced artifacts from Fourier transform infrared intensity values.

Two Fourier transform infrared intensity artifacts have been observed at moderately high (0.1 cm(-1)) spectral resolution: Light reflected off the aperture was double modulated by the interferometer, producing a 2f alias, and the warm (approximately 310 K) annulus of the aperture seen by a cooled detector resulted in distorted line shapes and anomalous intensities in the fingerprint region. Although the second artifact has been alluded to previously, we report corrections to remove both of these anomalies and to demonstrate the efficacy of these corrections. Prior to correction, integrated-band intensities were found to be in error by up to 12%.

Journal Article↗