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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 7049-7053 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The Fourier-transform spectrum of the CH3OH overtone C–O stretching band (vCO=2←0) has been recorded in the range 1950–2060 cm−1, at a resolution of 0.004 cm−1. The spectrum is resolved into J multiplets, each displaying complicated substructure due to strong torsion–vibration–rotation effects. Within this structure, it has been possible so far to identify R and P branch transitions for K=0 and K=1 for both A and E torsional symmetry species for J≤24. The assignments are supported by combination differences derived from known ground-state frequencies. The identified branches have been analyzed in terms of effective state-dependent series-expansion parameters, and the leading terms in the torsion–rotation Hamiltonian have been derived for the second excited C–O stretching state. The vCO=2 torsional barrier height is obtained as 395.5±0.2 cm−1, and the effective B value as 23 671.9±1.3 MHz. In addition, the 34.946 cm−1 far-infrared laser line pumped by the 10R(48) CO2 laser line has been tentatively identified as the (nτK,J)v=(031+,16)2→(010+,15)2 transition, and its parent IR pump absorption as the P(031+,17) vCO=2←1 hot-band line.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 6444-6455 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The Fourier transform spectrum of the CO-stretching fundamental band of 13CH3OH has been investigated at 0.002 cm−1 resolution. For the n=0 torsional ground state, 35 subbands containing some 2300 lines have been identified for K values from 0 to 10 for the three torsional symmetries A, E1, and E2 up to J values typically well over 30. The assigned transitions have been fitted to J(J+1) power-series expansions to obtain subband origins and sets of phenomenological state-specific parameters describing the J dependence of the subbands. These parameters reproduce the observed wave numbers to within the experimental uncertainty of ±0.0005 cm−1 for unblended lines, except when particularly large asymmetry shifts or perturbations due to Fermi or Coriolis resonances are present. The subband origins have been fitted to effective molecular constants for the excited CO-stretching state and a torsional barrier of 378.7(8) cm−1 is found, representing a 1.3% increase over the ground state value. A wide variety of global or J-localized perturbations has been seen, and most of the interacting states have been identified. New assignments have been obtained for far-infrared laser lines optically pumped by the 10R(2) and 9P(12) CO2 laser lines. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 107 (1997), S. 1765-1778 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The Fourier transform infrared spectrum of the in-plane CH3-rocking fundamental of 13CH3OH has been investigated at 0.002 cm−1 resolution. The rocking band is principally of parallel character and has a double-peaked Q branch and relatively wide spread subbands indicative of a substantial change in torsional barrier height. All A subbands from K=0 to 11 and all but one E subband from K=0 to 9 have been assigned in the n=0 torsional state and fitted to J(J+1) power-series expansions to obtain the subband origins and excited-state energy structure. The effects of vibrational interactions between the CH3-rocking and CO-stretching modes are prominent in the spectrum. Coriolis coupling between rocking (K−1) and CO-stretching K levels is observable for K≥6, and makes significant contributions to the subband origins and effective B values. Several J-localized perturbations due to level-crossing resonances with CO-stretch states have been observed and characterized. Two reported strong far-infrared laser lines optically pumped by the 10R(26) CO2 laser line have been found to arise through such a ΔK=3 level-crossing resonance. Modeling of the rocking-state torsion-K-rotation energies yields a height of V3r=469.2(38) cm−1 for the torsional potential barrier, a 26% increase over the ground state. The asymmetry K-doubling pattern in the excited state is qualitatively consistent with this barrier for K=2 to 4, but the K=5 rocking substate displays strongly enhanced splitting. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 3406-3418 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Torsionally excited n=1 and n=2 subbands of the CO-stretching fundamental have been assigned in the Fourier transform infrared spectrum of 13CH3OH recorded at a resolution of 0.002 cm−1. For the n=1 torsional state, subbands with K values up to 7 have been identified for A torsional symmetry and up to 5 for E symmetry. For n=2, four subbands have so far been assigned. Subband origins have been obtained by fitting the observed wave numbers to J(J+1) power-series expansions. The expansion parameters represent the data compactly to close to the experimental uncertainty in the absence of line blending or perturbations. Significant downshifting of the n=1 origins is observed, correlated closely with proximity to the n=0 OH-bending state. J-localized perturbations have been observed and characterized for several subbands. Two of the far-infrared laser lines optically pumped by the 10R(14) CO2 laser line have been assigned. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
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    Unknown
    Harlow, etc. : Periodicals Archive Online (PAO)
    English Historical Review. 54 (1939) 38 
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  • 6
    ISSN: 1432-0649
    Keywords: 33.20E ; 42.55H
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract High-resolution Fourier transform spectroscopy has been applied to confirm previously proposed assignments for nine far infrared (FIR) laser lines from the CH3-deformation state of CH3OH and one line from the CH3-rocking state. Accurate frequencies are deduced for the observed and other predicted FIR laser transitions. FIR torsional branch frequencies in the ground state which were used in the confirmation are presented. Comments are also made on the OH-bending mode of CH3OH.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    International journal of infrared and millimeter waves 11 (1990), S. 505-517 
    ISSN: 1572-9559
    Keywords: CD3OH ; 13CH3OH ; Stark spectroscopy ; HCN laser ; Stark coefficient
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Laser Stark spectra have been observed for CD3OH and13CH3OH using the 311 μm line of the HCN laser. The spectra were taken for both parallel and perpendicular polarizations up to 60,000 Volts/cm. For CD3OH, the two characteristic structures in the spectra have been identified as the JK=144←133, A± doublet in the vt=0 torsional state. For13CH3OH, the low field structure observed is assigned as JK=153←142, A− in the vt=0 torsional state.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    International journal of infrared and millimeter waves 14 (1993), S. 2569-2582 
    ISSN: 1572-9559
    Keywords: Microwave ; spectra ; methanol ; CD3OH ; torsion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The microwave spectrum of CD3OH has been studied over the 8 to 58 GHz region, and numerousb-type transitions have been assigned. Many of these belong toP subbranches which descend to the microwave region from subband origins lying much higher in the far-infrared, pass through zero frequency, and return upward again. Others are members ofb-typeQ branches which extend across the region. As well, variousa-typeK-doublet lines arising as transitions directly across the split levels of asymmetry doublets have been identified.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    International journal of infrared and millimeter waves 3 (1982), S. 517-527 
    ISSN: 1572-9559
    Keywords: laser-Stark spectra ; methyl alcohol ; farinfrared spectroscopy ; internal rotation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Laser-Stark spectra have been observed for methyl alcohol using the 311 μm line of the HCN laser. Partial assignments are presented for the three most distinctive structures in the spectra. The low field structure is clearly associated with a member of the J=20↭19qRa-type multiplet, and is tentatively identified as the k=13 A vt=0 transition. The other two structures originate from the 93↭82 E vt=0 transition, and from a member of the k= 6↭5 A vt=1 Q branch, tentatively assigned as the J=32 member.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    International journal of infrared and millimeter waves 9 (1988), S. 545-553 
    ISSN: 1572-9559
    Keywords: far-infrared (FIR) lasers ; FIR spectroscopy ; methanol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract An assignment is proposed for the strong 127.0 μm far-infrared (FIR) line of13CD3OH known to be pumped with very high efficiency by the 10P(8) CO2 laser line. On the basis of spectroscopic clues derived from calculated molecular parameters and energies for13CD3OH, the 127 μm line is identified as the (nτK,J)=(116,17)→(125, 16) transition, and its companion 462.8 μm line as the (116,17)→(116,16) transition. Proposed partial assignments and predictions are also discussed for a number of other FIR laser lines in13CD3OH, CD3OH, CD3OD, CH3OD, CH3OH and13CH3OH.
    Type of Medium: Electronic Resource
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