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  • 1
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    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 84 (1986), S. 5131-5142 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The distribution of population in the internal energy levels of nitric oxide thermally desorbed from Pt(111) has been probed using laser excited fluorescence. The observed rotational distributions have been found to follow the Boltzmann distribution function, independent of NO coverage or the presence of pre- or post-adsorbed CO. Under all conditions of NO desorption, the observed NO was characterized by a temperature (0.95±0.05) times the surface temperature. No evidence of a preferred alignment of the rotational angular momentum vectors was observed, nor was there any difference between the two spin-orbit multiplets beyond that associated with the rotational temperature.
    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 85 (1986), S. 2333-2334 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Rotational, spin-orbit, lambda doublet, and kinetic energy distributions were measured by laser-excited fluorescence techniques for the nitric oxide fragments formed from the vibrational predissociation of nitric oxide dimers in a free jet expansion. The NO fragments, produced following excitation in the dimer ν1 fundamental, were described by a rotational "temperature'' of TR(approximately-equal-to)100 K, with full equilibration of lambda doublet states, and approximately equal populations in the two spin-orbit states. The velocity distributions were isotropic with an average fragment kinetic energy of 400 cm−1. Time-resolved measurements placed a 15 ns upper limit on the predissociation lifetime.
    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 82 (1985), S. 5286-5288 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The rotational level distribution of the NO fragments formed as a result of the predissociation of the vibrationally excited NO–C2H4 (ν7) van der Waals molecule was measured by laser excited fluorescence techniques. The distribution was found to be Boltzmann in character, described by the rotational temperature 75±15 K. An average kinetic energy release of ≈105 cm−1 per fragment, in an isotropic flux distribution, was determined from Doppler profiles of the NO fragments in selected rotational levels.
    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 82 (1985), S. 2236-2239 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The rotational-, spin-, and lambda doublet-state distributions for nitric oxide (NO) formed in the CO2 laser multiphoton dissociation of methyl nitrite, CH3ONO, in a pulsed molecular beam are reported. Upon methyl nitrite photolysis by temporal square wave infrared laser pulses at 983 cm−1 of 50 ns duration and 800 MW/cm2 intensity, the low-lying rotational levels of the nitric oxide fragments formed in the 2Π1/2 (F1) and 2Π3/2 (F2) spin-orbit states exhibited Boltzmann-like population distributions, characterizable by the rotational temperatures TR (F1)=400±10 K and TR (F2)=530±100 K; the integrated populations for J〈30.5 of the two spin components were in the ratio F1/F2=2.7 : 1. For those highly rotationally excited levels with J(approximately-greater-than)24.5 there is no measurable spin preference, the level population depending solely on total internal energy Eint. There is no apparent preference for formation of either lambda doublet component and there is no observable fragment alignment, the nascent NO species exhibiting an isotropic distribution of angular momentum vectors.
    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 82 (1985), S. 1046-1048 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Internal state distributions were obtained by laser-excited fluorescence for NO desorbing from a saturation coverage on Pt(111). Two major peaks are observed in the thermal desorption spectrum at crystal temperatures Ts=200 and 340 K. The rotational state distributions for each desorption feature were Boltzmann, described by the rotational temperatures TR=195±10 K and 305±10 K, respectively. The two spin-orbit states were occupied to a degree consistent with equilibration between spin and rotational degrees of freedom, both Lambda doublet species were statistically populated and no molecular alignment was observed.
    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 85 (1986), S. 6235-6237 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Direct picosecond measurements of the vibrational predissociation rates of the nitric oxide dimer excited to v=1 levels of the symmetric (ν1=1870 cm−1) and antisymmetric (ν4=1789 cm−1) N–O stretching fundamentals are reported. Lifetimes obtained are 880±260 ps for ν1 and 39±8 ps for ν4 excitations.
    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 82 (1985), S. 3629-3633 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The internal state and kinetic energy distributions of the X˜ NO fragments formed from the ultraviolet photodissociation of the NO–Ar van der Waals species were obtained by laser-excited fluorescence techniques. The initially excited A˜ NO–Ar rapidly dissociates to form X˜ NO with little rotational excitation, with vibrational excitation determined by a Franck–Condon process, with a cos2 θ angular flux distribution (θ defined relative to the direction of polarization of the pump laser), and with a speed v∼4.4×105 cm/s.
    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 96 (1992), S. 2324-2338 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The results of a quantum-state-resolved study of the laser-induced desorption (LID) of NO from Si(111) 7×7 at a surface temperature of 100 K are reported. All aspects of the LID are found to be sensitive to the initial coverage. The coverage dependence indicates that there are two desorption mechanisms, one operative at low coverages that is quenched with increasing NO exposure, and one operative at high coverage. This report characterizes the low coverage channel. Most of the energy in the desorbed NO occurs as vibration and translation, with the rotations substantially cooler. The desorption is selective for production of the ground spin–orbit state. The energy partitioning shows strikingly little change as the desorption-laser wavelength was varied from 1907 to 355 nm. This, coupled with a quantitative study of the yield over the same photon energy range and selective coadsorption experiments, establishes that the desorption is specifically due to an interaction involving photogenerated holes in the rest-atom localized, intrinsic surface state of the 7×7 reconstructed surface. It is suggested that the surface state hole drives the desorption by neutralization of a NO−δ adsorbate.
    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 94 (1991), S. 250-261 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: NH stretching overtone and combination states in HN3 X˜ 1A' were excited by IR–visible double resonance pumping and by direct overtone pumping in the range 6ν1 (17 670 cm−1) to 7ν1 (20 070 cm−1). NH fragments in the a 1Δ and X 3Σ− states were detected by laser induced fluorescence with sub-Doppler resolution to determine branching ratios, correlated fragment rotational state and kinetic energy distributions, and fragment vector correlations. The spin-forbidden triplet channel was accessible to all states excited, while the threshold for the singlet channel was determined to lie in the range 18 190 to 18 755 cm−1. The measured energy release places limits on the HN–NN bond energy, and the heights of barriers to reaction. The barrier in the singlet exit channel is at least 540 cm−1. The singlet channel accessed by 7ν1 dissociation is characterized by a Boltzmann-like NH rotational distribution (〈J NH〉≈3.5), highly excited N2 rotations (〈JN2〉 ≥ 20), and total translational energy release peaked away from zero (〈ET〉≈1350 cm−1). Vector correlations and Λ-doublet propensities indicate that nonplanar dissociation processes influence the NH rotations, but become less important for higher NH rotational states. The principal correlations are a strong positive recoil anisotropy (β≈0.6), a weak positive v–J correlation (βvJ≈0.17), and a JNH-dependent Λ-doublet propensity. A model using parent vibrational motion projected onto fragment rotation is suggested to explain these observations. The triplet channel exhibits similar NH and N2 rotational state distributions, with most of the available energy (substantially greater than in the singlet channel) appearing as fragment kinetic energy.
    Type of Medium: Electronic Resource
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