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  • Artikel  (332)
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  • 1
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 4483-4484 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 7534-7534 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 2284-2298 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Six of the 14 unidentified bands in the stimulated emission pumping (SEP) spectrum of HCN are shown to be forbidden transitions to l‘=1 e parity levels of the ground state. The band origins agree with predictions within the error of the anharmonic expansion; the rotational constants, when corrected for rotational-l doubling, agree within experimental error. Rotational-l resonance between l‘=0 and l‘=2 is found in highly excited bending levels, confirming the extrapolation of the rotational-l resonance and doubling constant q2 from microwave and infrared measurements to 17 000 cm−1. The rotational intensity of the l‘=1 bands due to the axis-switching mechanism of Hougen and Watson [Can. J. Phys. 43, 298 (1965)] is shown to be greater than some of the observed allowed rotational transitions to l‘=2 when laser polarization effects are taken into account. A qualitative Franck–Condon analysis of the SEP spectrum provides unusually strong evidence for the axis-switching mechanism. The eight remaining unassigned bands are evidently perturbed and are assigned based on agreement between sums of observed rotational constants and sums of zero-order (unperturbed) rotational constants predicted by the anharmonic expansion, the magnitude of the rotational-l resonance, and the expected Franck–Condon factors.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 5111-5122 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The dependence of vibrational energy transfer on vibrational excitation has been studied using the stimulated emission pumping technique to efficiently prepare a large range of specific vibrational states of the nitric oxide molecule in its ground electronic state. Laser induced fluorescence was used to detect collisionally relaxed NO. The self-relaxation rate constants of NO(v(very-much-greater-than)1) were up to 200 times larger than that of NO(v=1). Multiquantum relaxation was found to be important at high energy and was quantified at 3.8 eV. Self-relaxation rate constants of 15N18O as well as 14N16O were measured and a large isotope effect was observed. Relaxation of NO(v‘=22) with H2 was also investigated. Theoretical explanations of our experimental results were attempted and it is shown that at vibrational energy up to ≈3 eV the qualitative trends observed in these experiments such as the mass effect and the multiquantum relaxation can be explained by Schwartz–Slawsky–Herzfeld theory. A simple explanation of the anomalously high NO self-relaxation rate is given. The large acceleration of the vibrational relaxation rate above 3.0 eV is coincident with the energetic onset of high energy (NO)2 isomer complexes. More theoretical and experimental work is needed to explain the quantitative aspects of these observations.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 3723-3724 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 2111-2113 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 7
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 5123-5128 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: PUMP–DUMP–PROBE experiments were performed on nitric oxide (NO) in order to study the rotational and spin–orbit energy transfer in a highly vibrationally excited diatomic. Total depopulation as well as state-to-state rotational and spin–orbit energy transfer rate constants were measured for v=8 and 19 of the ground electronic state. By comparing this new set of results with previously measured results for v=2 [Aa. Sudbo and M. M. T. Loy, J. Chem. Phys. 76, 3646 (1982)] the vibrational influence on the rotational and spin–orbit energy transfer dynamics could be evaluated. Total depopulation rate constants for individual rovibrational states were found to be very similar for v=2, 8, and 19. State-to-state rotational energy transfer rate constants could be compared for v=8 and 19, and again only small differences were found. It appears that vibrational energy does not have a significant impact on the rotational and spin–orbit energy transfer dynamics for NO–NO collisions.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 98 (1993), S. 1748-1749 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The high resolution spectrum of the fundamental C–H stretch in (CF3)3C–C≡C–H has been measured using optothermal detection of a collimated molecular beam. Only the Q branch was resolvable and was fit to a Lorentzian with a full width at half maximum of 2.76 GHz, corresponding to an IVR lifetime of 60 ps. The decrease in lifetime in comparison to (CH3)3C–C≡C–H is thought to be due to strong mixing between the C–F stretches and bends and the backbone C–C stretches and bends.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 66 (1995), S. 4841-4844 
    ISSN: 1089-7623
    Quelle: AIP Digital Archive
    Thema: Physik , Elektrotechnik, Elektronik, Nachrichtentechnik
    Notizen: A differentially pumped rare gas cell has been developed to suppress undulator harmonics on the Chemical Dynamics Beamline at the Advanced Light Source. Greater than 104 suppression of the harmonics has been demonstrated with no measurable (〈5%) attenuation of the fundamental. The overall design is presented, and vacuum and optical performance are reported. © 1995 American Institute of Physics.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 6067-6077 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The photodissociation of ozone has been studied at 193 nm using high resolution photofragment translational spectroscopy. The results show six distinct peaks in the time-of-flight spectra for the O2 product and its momentum-matched O atom counterpart. The translational energy distributions determined from the time-of-flight spectra reveal the production of a range of electronic states of the photofragments. The product electronic states were identified based on the translational energy distributions, with the aid of state-resolved imaging experiments by Houston and co-workers. The results reveal the production of a substantial yield of highly excited triplet states of O2, recently suggested to play an important role in the stratospheric ozone balance. In addition, peaks corresponding to O2(a 1Δg) and O2(b 1Σg+) were observed, the latter confirming a previous report [A. A. Turnipseed et al., J. Chem. Phys. 95, 3244 (1991)]. Evidence was seen for a small contribution from the triple dissociation O3→3O(3P), and insight into the dissociation dynamics for this process was inferred from the translational energy distributions. Branching fractions and angular distributions were measured for all channels. The latter were found in general to yield negative β parameters, in contrast to what is seen at longer wavelengths. © 1995 American Institute of Physics.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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