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  • 1985-1989  (12)
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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 5011-5020 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A Pt(111) surface saturated with molecular oxygen was irradiated by UV light from a mercury arc lamp with various cutoff filters. High-resolution electron energy-loss spectroscopy (HREELS) and temperature programmed desorption mass spectroscopy (TPD) were used to characterize the products retained on the surface. Upon UV irradiation at 95 K, chemisorbed O2 (peroxo) undergoes dissociation, desorption and rearrangement. Different wavelength dependences were observed for the three processes: dissociation was not observed at wavelengths longer than 295 nm, in agreement with gas phase photodissociation of the O–O bond in hydrogen peroxide; desorption and rearrangement became negligible at wavelengths longer than 420 nm, in agreement with the photolysis of an organometallic peroxoplatinum complex. For wavelengths between 230 and 315 nm, the average cross sections of dissociation and desorption were estimated to be 5.7×10−20 and 1.2×10−19 cm2 , respectively. The possible origins of the three processes are discussed.
    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 88 (1988), S. 441-450 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report the vibrational and electronic spectra for pyridine and benzene adsorbed on the Rh(111) crystal surface obtained by high-resolution electron energy loss spectroscopy (HREELS). Low-energy electron diffraction (LEED), thermal desorption spectroscopy (TDS), and optical second harmonic generation (SHG) have also been used to provide complementary information. Pyridine adsorption on Rh(111) was studied over the 77–450 K temperature range. At 77 K, multilayers of pyridine are observed with a vibrational spectrum similar to that of liquid pyridine. Between 185 and 230 K, HREELS and TDS indicate that both physisorbed and chemisorbed pyridine species are present on the surface. The physisorbed species desorbs at 295 K, while the chemisorbed species is stable until it decomposes on the surface at 400 K. We propose that the chemisorbed species is an α-pyridyl complex as thermal desorption spectroscopy indicates partial dehydrogenation of this pyridine surface species. Electronic energy loss spectra for both benzene and pyridine adsorbed at 310 K show only a weak transition centered at ∼4 eV. The absence of prominent π→π* transitions, which are readily observed for multilayers of benzene adsorbed on Rh(111), implies that the π orbitals are strongly involved in the chemisorption bond of these molecules with the Rh(111) surface.
    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 90 (1989), S. 7442-7447 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report evidence for the coexistence of direct and precursor dynamics in the dissociative chemisorption of H2 on Ni(l00). Hydrogen and deuterium uptakes on Ni(l00) were measured at various surface temperatures by following the secondary ion ratios, Ni2 H+/Ni+ and Ni2 D+/Ni+ , which are proportional to surface hydrogen and deuterium coverage on both clean and carbon-covered Ni(100). Between 100 and 200 K on clean Ni(l00), the initial sticking coefficient of hydrogen decreases, but only slightly, as the surface temperature increases. The decrease is more pronounced both in the presence of predosed carbon and for deuterium adsorption on Ni(100). This is interpreted as due to the involvement at low temperatures of a molecular precursor which mediates dissociative adsorption at low temperatures. The precursor probably involves surface defects and sites formed in the presence of carbon. In addition to the precursor channel, a direct dissociation channel also operates, and dominates for T≥200 K.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 49 (1987), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Two [3H]ketanserin recognition sites are present in the rat striatum. The high-affinity site (Kd, 0.39 nM) is similar to the 5-hydroxytryptamine2 (5-HT2) site previously characterized by various investigators. The low-affinity site (Kd, 21.8 nM) has a unique pharmacologic specificity and is preferentially localized to rat striatum and septum. Conventional 5-HT2 antagonists as well as 5-HT and 5-HT uptake inhibitors are ineffective at inhibiting [3H]ketanserin binding to this low-affinity site. Also, chronic treatment with p-chlorophenylalanine, which depletes brain 5-HT, upregulates only the high-affinity site. Thus, in the striatum and septum, [3H]ketanserin labels a unique recognition site. This site has recently been shown to be associated with dopaminergic nerve endings and may regulate biogenic amine release.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 93 (1989), S. 75-83 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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 84 (1986), S. 6086-6090 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Homodyne depolarized photon-correlation functions of 1,3,5-tri-α-naphthyl benzene (TαNB) have been measured at the 90° scattering angle in the temperature range of 75–110 °C. The correlation functions are analyzed in terms of a fractional exponential function and a modified constrained regularization method originally developed by Provencher. The results from both methods of data analysis are in agreement. The temperature dependence of the mean orientational relaxation time when fitted to the Arrhenius equation, gives an apparent activation energy E=85.3 kcal/mol. The Antoine–WLF equation provides a better fit of the mean reorientational relaxation time data. It is also found that orientational time τ¯ is linearly proportional to η/T, indicating that the Debye–Stokes–Einstein equation is applicable to describe molecular reorientation in the supercooled TαNB liquid.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 92 (1988), S. 3970-3974 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1434-601X
    Keywords: 25.70.Bc
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Deep inelastic collisions in light systems formed with12C,14N and16O projectiles and different target nuclei have been studied at incident energies between 5 and 7 MeV/u. A detailed analysis is presented for the results of the16O+27Al reaction at 80.6 MeV incident energy which is based on trajectory calculations and the transport theory. The questions of angular distributions and the interaction time, the energy dissipation and the fragment deformation as well as the element-distribution and the effect of the nuclear structure are discussed.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 1 (1988), S. 247-254 
    ISSN: 1572-879X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Evidence for ethylidyne formation and decomposition on Ni(111) was found in the thermal decomposition of ethylene and acetylene. The formation of ethylidyne depends critically on the initial acetylene or ethylene coverage: ethylidyne forms in detectable concentrations only when the initial acetylene coverage is above 70% of saturation or when the initial ethylene coverage is above 80% of saturation. This work is related to recent IR evidence for ethylidyne on supported Ni at atmospheric pressure.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Astrophysics and space science 115 (1985), S. 99-106 
    ISSN: 1572-946X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract According to the proposal developed by Fanget al. (1984, referred to as Paper I) on formation of large-scale structure in the Universe, we should expect that: (1) The distributions of quasars should be different from that of galaxies by no strong inhomogeneity on the scale of 10–100 Mpc. (2) The distributions of quasars withZ〉2 andZ〈2 should be different from each other with no large-scale structure in the former, and conversely in the latter. Our various statistical results obtained from quasar distributions are consistent with these predictions. Particularly, the nearest neighbour test for the complete quasar sample given by Savage and Bolton (1979) clearly shows that the distribution ofZ〉2 quasars is rather homogeneous while theZ〈2 quasars have a tendency to cluster.
    Type of Medium: Electronic Resource
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