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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 9979-9985 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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 101 (1994), S. 7230-7240 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Microwave spectra of CH4– –H2O, CH4– –H218O, CH4– –H217O, CH4– –D2O, and CH4– –DOH have been measured using a pulsed-nozzle Fourier-transform microwave spectrometer. The spectra were recorded to aid the assignment of the high-resolution far-infrared spectrum of CH4– –H2O reported recently [L. Dore, R. C. Cohen, C. A. Schmuttenmaer, K. L. Busarow, M. J. Elrod, J. G. Loeser, and R. J. Saykally, J. Chem. Phys. 100, 863 (1994)]. Spectral assignments were guided by Stark-effect and nuclear-spin hyperfine measurements. For the primary isotopic species, CH4– –H2O, four K=0 (Σ) and six K=1 (Π) rotational progressions were observed at the ∼1 K rotational temperature of the supersonic expansion. The internal-rotor state of the complex correlating to j=0 H2O+j=0 CH4 is found to have a rotational constant B=4346.7202(7) MHz and centrifugal distortion constant DJ=119.72(9) kHz, where the numbers in parentheses represent one standard deviation of the fit. These constants imply a zero-point center-of-mass separation of 3.7024 A(ring) between the two subunits and a pseudodiatomic weak-bond stretching force constant of 1.53 N/m and stretching frequency of 55 cm−1. Stark-effect measurements reveal that two of the K=1 progressions originate from degenerate states while the other four K=1 transitions arise from two Π states which are K (or l) doubled. The effective electric dipole moments vary from 1.95×10−30 to 2.67×10−30 C m (0.58–0.83 D) for the states studied. The isotopic results are consistent with a CH4– –H2O structure in which one of the hydrogens of H2O proton donates to CH4, analogous to structures previously reported for CH4 with HCN and HCl. A combined analysis of the microwave and far-infrared data allow estimates of the barriers to internal rotation of the H2O and CH4 units. The H2O internal rotation potential is found to be much more anisotropic than that of Ar– –H2O.
    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 100 (1994), S. 831-839 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Microwave/radio-frequency-infrared multiple resonance has been used with an electric-resonance optothermal spectrometer to characterize a weak 21.6 MHz perturbation in the infrared spectrum of the ν14 C–O stretching vibration of 2-fluoroethanol. The infrared spectrum of 2-fluoroethanol was recorded at a resolution of ∼2 MHz using a tunable microwave-sideband CO2 laser. The spectrum is fit by an asymmetric-rotor Hamiltonian to a precision of 0.6 MHz, except for the transitions to the 413 upper state which are split into doublets by an interaction between the 413 level and a rotational level of a nearby background, or dark, vibrational state. Microwave/radio-frequency-infrared double and triple resonance reveals that the 413 level of the C–O stretching vibration is interacting with the 431 level of the dark state. The rotational constants determined for the dark state allow us to assign the perturbing state to the ν18+4ν21 combination vibration of the lowest energy conformer, where ν18 is the CCO bending vibration and ν21 is the C–C torsional vibration. From the weak ΔKa=2 matrix element between ν14 and ν18+4ν21 it is possible to derive a J=0 anharmonic interaction between these states of ∼3.5 GHz.
    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 99 (1993), S. 2396-2404 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A tunable microwave-sideband CO2 laser is used with an electric-resonance optothermal spectrometer to investigate the infrared spectrum of CF3CH3 near 970 cm−1. A Fermi-coupled triad of states is observed, resulting from the interactions of 2ν6+ν11 and ν5+ν12 with the fundamental vibration, ν10, which is assumed to carry the oscillator strength in this region. The high resolution (∼3 MHz) of the spectrometer allows the observation of tunneling splittings associated with the ν6 torsional vibration. These splittings are used to identify the torsional character of the states observed. At the normal-mode level the ν10 and ν5+ν12 states are found to be nearly degenerate and interacting by an anharmonic matrix element of ∼3 cm−1. The lower-energy component of this diad exhibits torsional splittings of up to 400 MHz due to an anharmonic coupling of 0.70 cm−1 with the lower energy 2ν6+ν11 state which has an intrinsic tunneling splitting of ∼800 MHz. A fourth state, 3ν6+ν12, which has a still larger zeroth-order tunneling splitting, may also be affecting the torsional splittings of the observed states. The present investigation illustrates the utility of using resolved torsional splittings to unravel complex vibrational couplings in molecules.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 4724-4733 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The rotational spectra of YO, LaO, ZrO, and HfO have been measured using a Fourier-transform microwave spectrometer in combination with a laser-ablation source. Here, a Q-switched Nd:YAG laser (532 nm) was used to vaporize the metal oxides from a target source rod located in the throat of a pulsed-molecular-beam valve. A description of the instrument is given. The electric dipole moments of the four species have been measured and compared to ab initio results, where available. The experimental values are μYO =4.524(7), μLaO =3.207(11), μZrO =2.551(11), and μHfO =3.431(5) D. Of special note are the extremely large nuclear quadrupole coupling constants, eQq, determined for the 177HfO and 179HfO isotopic species, with values of −5952.649(35) MHz and −6726.981(39) MHz, respectively. This is the first determination of nuclear quadrupole coupling constants for a molecule containing the Hf atom.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 793-803 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Microwave and submillimeter transitions for Ar–NH3 have been observed and assigned for the ∑ and Π states correlating asymptotically with Ar+NH3 (j=1,||k||=1). The ∑ states are found to lie below the Π states and are separated by approximately the inversion splitting of free NH3. For the Π states the NH3 inversion tunneling is nearly quenched, being only weakly allowed through Coriolis interactions with the nearby ∑ states. The observed microwave and submillimeter spectra also allow the determination of 14N quadrupole coupling constants and relative submillimeter absorption intensities. All the above results are interpreted using a model internal–rotation inversion Hamiltonian, leading to detailed information about the anisotropy of the intermolecular potential.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 5306-5312 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The microwave spectrum of the weakly bound complex Ar–CH3CN has been observed using a pulsed-nozzle Fourier-transform microwave spectrometer. The spectrum is characteristic of an asymmetric rotor with nearly free internal rotation of the methyl group. Spectroscopic constants for the ground internal rotor state, in megaHertz, are 3:[RW3:A=9323.7769(22),:B+C=3439.5578(15),:B–C=326.6860(12)].
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 7287-7297 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A tunable microwave-sideband CO2 laser has been used with a molecular-beam electric-resonance optothermal spectrometer to observe the infrared spectrum of the NH3 umbrella fundamental vibration (ν5 in Cs ) of HOH––NH3 at a resolution of ∼3 MHz. Ground- and excited-state assignments were verified and extended using microwave–infrared double-resonance spectroscopy, with microwave transitions observed in both the ground and the excited states. The spectrum exhibits numerous perturbations, as evidenced by the observation of a minimum of 13 subbands originating from the (K,m)=(0,0) ground NH3 internal-rotor state and the (K,m)=(±1,±1) first excited NH3 internal-rotor state. For an unperturbed spectrum, only four such subbands are expected, two for the symmetric H2O tunneling state and two for the antisymmetric H2O tunneling state. The rotational progressions within the excited states are poorly fit to polynomial series in J(J+1), in contrast to the ground-state progressions which are well characterized by such series. The B rotational constants in the excited states are smaller than in the ground state, indicating an extension of the hydrogen-bonding interaction distance upon vibrational excitation. This is consistent with the observed infrared band origin for the (K,m)=(0,0) state of ∼1021 cm−1, which is blue shifted by 71 cm−1 from the hypothetical inversion-free 950 cm−1 ν2 band origin of uncomplexed NH3. The observed ν5 band origin is also in good agreement with matrix-isolation results scaled to correct for the matrix shift of the NH3 umbrella frequency found in the recently studied NH3–HCN complex. The complex does not dissociate upon vibrational excitation, implying that the binding energy is greater than the laser frequency of ∼1021 cm−1.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 7061-7067 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A microwave-sideband CO2-laser optothermal spectrometer with a resolution better than 1 MHz has been used to record the infrared spectrum of Ar–NH3 in the vicinity of the aR(0,0) line of the ν2 vibration of free NH3. A Π←∑ type band is observed, giving a positive l-type doubling constant q, of 90.9 MHz for the upper state. The positive q indicates that the j=1, k=0, ∑ state is above the j=1, k=0, Π state in the v2=1 excited state, where j and k specify the correlation of the internal-rotor state of the Ar–NH3 complex to the NH3 monomer rotational state j,k. The ν2 vibrationally excited complex is found to predissociate in less than the 0.9 ms transit time between the bolometer detector and laser-excitation region. A lower limit to the upper-state lifetime can be obtained from the observed linewidths, which range from 1.5 to 3 MHz (FWHM). The present results agree with and extend the previous free-jet diode-laser absorption measurements on this band.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 2992-3004 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The HF stretching band of the NO–HF open-shell complex has been recorded using a molecular-beam optothermal spectrometer. The spectrum exhibits P-type doubling indicative of an unpaired electron spin coupled to the rotational angular momentum of a bent complex with substantially quenched electron orbital angular momentum. From B¯‘=0.111 320(17) cm−1, and an off-axis angle for the NO of 30°, the zero-point center-of-mass separation is estimated to be 3.4396(3) A(ring). The HF frequency shift of 84 cm−1 indicates that the complex is hydrogen bonded, and the spectral intensities imply that the HF axis is aligned closely to the center-of-mass axis and the NO is off axis by 30±15°. The Renner–Teller-like orbital quenching parameter is somewhat larger than the spin–orbit constant in the free NO molecule and increases substantially upon vibrational excitation. The transitions in this band exhibit vibrational predissociation broadening of 200±40 MHz (FWHM), similar to that observed for a number of closed-shell hydrogen-bonded HF complexes.
    Type of Medium: Electronic Resource
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