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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 95 (1991), S. 9404-9407 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The high resolution spectrum of the fundamental band of deuterium impurity embedded in solid parahydrogen has been studied using a difference frequency laser spectrometer. This observation represents the first case of high resolution matrix spectroscopy in solid hydrogen. Both the Q1←0(0) and Q1←0(1) transitions were resolved into sharp features with a typical linewidth of (approximately-less-than) 10 MHz, while both the S1←0(0) and S1←0(1) transitions appeared to be much broader with widths of ∼0.07 cm−1. A discussion of the linewidths based on homogeneous broadening is presented.
    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 93 (1990), S. 6210-6215 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The overtone band of 2ν2(l=2)←0 of H+3 in the 2 μm infrared region has been observed in absorption by using a difference frequency laser spectrometer. The LiIO3 nonlinear optical system assembled by Bawendi and the bidirectional multiple path optical arrangement with velocity modulation have enabled us to observe 34 vibrational–rotation transitions from 5094 to 4557 cm−1. Liquid-N2 cooled plasmas were used for transitions involving low rotational levels, while gaseous-N2 cooled plasmas were used for high rotational levels, up to J,K=(9,9). From the relative intensities of the transitions, rotational temperature has been estimated to be ∼270 K for the former and ∼1300 K for the latter. The Δ||k−l||=±3 selection rule of the overtone band allows us to determine the absolute energy level values by combining the frequencies of the overtone band with those of the fundamental and hot bands.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The infrared spectra of the band of the 2Π–2Π asymmetric hydrogen stretching vibration in the three isotopic acetylene ions C2H2+ (ν3), 13C2H2+ (ν3), and DCCH+ (ν1) have been observed and analyzed. The high resolution infrared spectra were recorded using a difference-frequency laser spectrometer as the tunable coherent infrared source probing an ac glow discharge. Velocity modulation, noise subtraction, and unidirectional multipassing of the infrared beam through the discharge cell provided high sensitivity. C2H2+ was produced in a gas mixture of H2, He, and either CH4 or C2H2, with a total pressure of ≈7 Torr in multiple-inlet–outlet air-, water-, and liquid-nitrogen-cooled discharge tubes; C2H2 freezing precluded its use in liquid-N2-cooled discharges. Complicated by a strong perturbation whose maximum occurred at N'=15 for F1 and N'=14 for F2, the assignment of the spectrum of normal C2H2+ was made possible by (1) fortuitous discharge conditions which provided unambiguous discrimination of C2H2+ lines from among concurrent CH3+ and C2H3+ lines, and (2) fitting the ground state combination differences. Sufficiently high N transitions were observed where Λ doubling was evident. The average bond lengths rz(CH)=1.077 (5) A(ring) and rz(CC)=1.257 (8) A(ring) were calculated from the spectroscopic constants determined from nonlinear least-squares fitting. Vibration–rotation interactions, the Renner–Teller interaction of perturbing states, plasma chemistry, and the relevance of the work in astrophysics are discussed.
    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 100 (1994), S. 6267-6274 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Infrared spectrum of the ν2 fundamental band of H+3 in high rotational levels has been studied. Three motives for this study were (i) to provide laboratory data for the observation of astronomical objects in which a large abundance of H+3 exists at high temperature, (ii) to study kinetic energy distribution of H+3 in plasmas and to determine its rotational and translational temperatures, and (iii) to provide information on high rovibrational states for the variational calculations on the intramolecular dynamic of H+3. In order to increase the kinetic temperature, water-cooled plasmas with helium dominated gas mixtures with He/H2∼5/0.6 torr were used. The observed rotational level in the ground state with the highest rotational quantum numbers was J=K=15 which has the rotational energy of 5091.6 cm−1. It was found from the observed relative intensities of the rovibrational transitions and linewidths that H+3 in the plasmas were in approximate thermal equilibrium with both rotational and translational temperature of ∼1000 K. On the contrary, an analysis of the relative intensities of the H+3 spectral lines observed in our previous study of carbocation spectroscopy showed nonthermal rotational distribution. A semiquantitative discussion is given on the observed results.
    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 100 (1994), S. 7840-7843 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A sharp spectral line has been observed in γ-ray irradiated para-H2 crystals and assigned to the pure vibrational Q1(0)(v=1←0, J=0←0) transition induced via the Condon effect by charges distributed in the crystal. The remarkable sharpness and stability of the signal is reported and discussed.
    Type of Medium: Electronic Resource
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