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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 48 (1983), S. 4629-4634 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 49 (1984), S. 4009-4011 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 86 (1982), S. 3223-3231 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 88 (1984), S. 243-248 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 47 (1982), S. 1215-1220 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 71 (1992), S. 4693-4708 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The present paper is the first of a series reporting on a comprehensive study of the hydrodynamics, kinetics, and spectroscopy of the transient species formed following the detonation of lead azide (LA). The spatial and temporal behavior of the detonation products expanding into vacuum is obtained via high-speed framing photography, transmission of a HeNe laser beam, and chemiluminescence from excited Pb atoms. The photography reveals that following the initiation of LA the products form an expanding, bell-shaped cloud. The HeNe beam is attenuated when the cloud of products traverses its route. The attenuation starts 4–15 μs after initiation and depends on the height of the beam above the LA sample. The chemiluminescence consists of two components: the first, appearing 1–2 μs after initiation, is obtained from excited products formed by the detonation near the surface of the sample, while the second, starting 2–14 μs after initiation, originates from the expanding cloud of products.The intensity and the temporal behavior of the second component of chemiluminescence depend on the distance to a barrier placed above the LA sample. The cloud contains gaseous products and solid particles which propagate perpendicular to the LA surface with a maximum velocity of 4.48±0.10 km/s and 3.78±0.18 km/s, respectively. To reproduce the experimental results, two alternative hydrodynamic models are applied: Stanyukovich's model [K. P. Stanyukovich, Unsteady Motion of Continuous Media (Pergamon, London, 1960), pp. 498–501] for isentropic expansion and London and Rosen's model [R. A. London and M. D. Rosen, Phys. Fluids 29, 3813 (1986)] for exploding foil. The latter model is preferred and when incorporating Beer's law and Mie's theory [C. F. Bohren and D. R. Huffman, Absorption and Scattering of Light in Small Particles (Wiley, New York, 1983), p. 77] it reproduces very well both the temporal behavior of the second component of chemiluminescence and the attenuation of the HeNe beam and suggests that lead particles with radius of 0.05–0.15 μm are involved in the attenuation. The model also provides an estimate of the composition of the product cloud and of the density of the gaseous and solid species as a function of time and distance from the LA sample.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 74 (1993), S. 45-52 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The cloud of products formed following the detonation of lead azide (LA) contains solid particles. Utilizing a pulsed beam of a neodymium: yttrium aluminum garnet (Nd:YAG) laser, the particles are evaporated and hole burning through the opaque cloud is demonstrated. The characteristics of the hole and of the expanding cloud are monitored in real time by a HeNe beam, high-speed framing photography and emission of excited Pb atoms. The hole is carried with the cloud and propagates at a constant velocity of 0.5–2.8 km/s, depending on the time and location of burning and given by d(h)/t(h), where d(h) is the distance from the LA sample to the center of the Nd:YAG beam and t(h) is the time from detonation to hole burning. The reduction in the number and size of the particles is monitored by scanning electron microscopy of the deposits formed on a substrate following the detonation. The propagation of the Nd:YAG laser pulse through the cloud is numerically modeled and provides an estimate of the increase in the temperature and the decrease of the size of the particles as a result of the interaction with the laser beam.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 73 (1993), S. 2138-2144 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The formation and temporal behavior of charged particles ensuing from the detonation of lead azide (LA) is studied. An ion probe tailored for measurements in the hostile environment produced following the detonation is described. The positive ions (most probably singly ionized lead atoms) and the electrons, which are simultaneously collected on separate electrodes, are embedded in the outer half of the expanding product cloud resulting from the detonation. They show similar temporal behavior and their maximum velocity is ∼4.5 km/s. The density of each of them at a distance of 2.5 cm from the LA sample is 4.3×1011–1.3×1012 cm−3 for detonation of 5–15 mg of LA, respectively. From the hydrodynamics of the expanding cloud and the density of the electrons, their temperature is estimated to be in the range 2600–3000 K. The results of the measurements are discussed in view of the mechanisms believed to govern the expansion of the product cloud following the detonation.
    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 93 (1990), S. 2146-2148 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The 193 nm photodissociation of individual rotational levels of HOD molecules excited with one quantum of O–H stretching vibrational energy is described. Stimulated Raman excitation and coherent anti-Stokes Raman scattering are used to prepare and detect, respectively, the (0,0,1) vibrationally excited HOD. The OD and OH fragments are detected by laser induced fluorescence. The photodissociation of the HOD (0,0,1) molecules yields at least three times more OD than OH.
    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 95 (1991), S. 3341-3346 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The 193 nm photodissociation of individual rotational levels of HOD molecules excited with one quantum of O–H or O–D stretching vibrational energy is described. Stimulated Raman excitation and coherent anti-Stokes Raman scattering are used to prepare and detect, respectively, the (0,0,1) (O–H stretch) or (1,0,0) (O–D stretch) vibrationally excited HOD. The OD and OH fragments are detected by laser-induced fluorescence. In the photodissociation of HOD (0,0,1), the yield of both fragments is enhanced [relative to HOD (0,0,0)], but the yield of OD is increased 2.5±0.5 times more than that of OH. In the photodissociation of HOD (1,0,0), no enhancement of the yield of the fragments is obtained. Our results show that even the very lowest possible level of vibrational excitation can be "leveraged'' to effect selective bond breaking. Also, these results demonstrate that bond cleavage does not necessarily occur on the weakened bond and they agree with theoretical calculations indicating that the yield of OD and OH fragments depends on the Franck–Condon overlap of the vibrational wave function with the repulsive surface of the upper state.
    Type of Medium: Electronic Resource
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