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  • American Institute of Physics (AIP)  (130)
  • 1990-1994  (130)
  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 3192-3199 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Molecular dynamics calculations are performed that simulate the diffusion of penetrant molecules through an amorphous polymer. For the polymer and the penetrant molecules, model potentials are chosen that approximate polyethylene and methane, respectively. The simulations extend over several hundred picoseconds. The results indicate that permeation proceeds by a hopping mechanism: The penetrants dwell in voids in the polymer matrix for a considerable time and perform fast jumps between neighboring voids. A potential scaling technique based on the fact that individual jump events are activated processes is presented by which the calculation of penetrant self-diffusion coefficients is speeded up.
    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. 4796-4803 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The proton spin–lattice relaxation rate has been investigated as a function of pressure (p≤250 MPa), temperature (180 K≤T≤300 K), and oxygen-17 enrichment (25.7 atom-%, 50.7 atom-%) in metastable water. Intramolecular proton–oxygen 17 dipolar interactions in light water in relation to deuterium electric quadrupole interactions in heavy water carry similar dynamic information and allow the complicated dynamic isotope effect in liquid water to be investigated in the whole metastable range. Under hydrostatic pressure the proton relaxation rate curve R1 (T, p, ωH) has been investigated at five different Larmor frequencies (100 MHz≤ω≤500 MHz). These experiments unequivocally prove the isotropy of reorientational motions of water molecules on a nanosecond time scale and demonstrate the necessity to include fast quasilattice vibrations into a consistent interpretation of the relaxation rates in the dispersion regime.
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 6432-6440 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Molecular motions in solids cover a broad dynamic range, extending from the fast rotational to the ultraslow motional regime. Two dimensional (2D) NMR relaxation spectroscopy is designed to follow these motions and to differentiate the various motional modes. The method employs the pronounced anisotropy of the nuclear spin relaxation times, observed for polycrystalline or multidomain samples. Generally, 2D NMR relaxation spectra are obtained by recording the time signals S(t2) after the last pulse as a function of successive incremented time intervals t1, corresponding to the relaxation period of the particular sequence. A Fourier transformation in both time domains transforms S(t1,t2) into a 2D representation S(ω1,ω2) of the relevant relaxation experiment.The normalized contour plot then displays the change of the corresponding relaxation rate 1/Ti along the frequency spectrum. It turns out that this variation is very dependent upon the character of the molecular motion. Model calculations for deuterons, involved in planar motions, demonstrate the potential of 2D NMR relaxation techniques. Generally, the type of motion can reliably be deduced from the shape of the contour plots. A model independent analysis provides the geometrical parameters of the dynamic process, including the jump angle ΔψK and the orientation cursive-thetaK of the rotation axis in the magnetic frame. In addition, from the separation of the contour lines the motional correlation times can be determined. The techniques are employed in the dynamical characterization of L-alanine, specifically deuteriated at the methyl group. From an analysis of 2D quadrupole echo spectra geometrical parameters of ΔψK=(120±1)° and cursive-thetaK=(70.5±1)° have been determined. Apparently, methyl group reorientation in L-alanine occurs via three-site jumps about a rotation axis, tilted by an angle of cursive-thetaK=70.5° relative to the C–2H bond direction. Computer simulations of 2D quadrupole echo and inversion recovery experiments provide the correlation times for this motion. The values range from τJ=5×10−10 s at T=353 K to τJ=3×10−5 s at T=140 K. An Arrhenius plot for these correlation times is linear over the entire dynamic range. From the slope of the straight line an activation of Ea=20 kJ/mol has been determined.
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    Journal of Mathematical Physics 33 (1992), S. 2265-2268 
    ISSN: 1089-7658
    Source: AIP Digital Archive
    Topics: Mathematics , Physics
    Notes: It is shown that the entropy principle provides a unique specific form of the radiative momentum flux. Also the nonequilibrium entropy and entropy flux of radiation thermodynamics are calculated explicitly. Waves are discussed in two limiting cases.
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 3399-3402 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A new scheme for the detection of ions produced by delayed pulsed field ionization of long-lived high-n Rydberg states (ZEKE Rydberg states) is presented. The equivalence of this new ion detection scheme with high resolution zero kinetic energy photoelectron (ZEKE) spectroscopy is proven by the simultaneous measurement of electrons and ions originating from the same ZEKE Rydberg states, taking into account the effects of pulsed and static low electric fields on the ZEKE Rydberg states. Using this ion detection, a rotationally resolved mass analyzed threshold ionization (MATI) spectrum of benzene with the same resolution (the rotational structure of the benzene cation) as the simultaneously recorded ZEKE photoelectron spectrum has been obtained.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 10263-10273 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Three-dimensional calculations of the nuclear dynamics of the ozone cation have been performed involving the vibronically coupled 2A1–2B2 electronic states and using the results of large-scale ab initio computations of Schmelz et al. [Chem. Phys. Lett. 183, 209 (1991)]. Anharmonic (diabatic) potential surfaces are employed and the vibronic coupling term is taken to be a linear function of the asymmetric stretch coordinate. These calculations are compared to the first and second bands of the experimental photoelectron spectrum. Most features of its peculiar shape can be correctly reproduced and interpreted in this way. The band maximum for zero temperature is assigned to the fourth peak and the first peak of the experimental spectrum is interpreted as a hot band (vibronic temperature ≈275 K). In addition the properties of a quadratic model Hamiltonian are investigated and compared to the afore mentioned calculations. It is found that the model Hamiltonian is suitable to reproduce the full three-dimensional computations. As a by-product of this work the vertical ionization potentials (IP) of the interacting states are determined to be IP(2A1)=12.78 eV and IP(2B2)=13.02 eV. © 1994 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 100 (1994), S. 719-724 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We are presenting a new method to measure the chemical potential of polymer chains in computer simulations which has virtually no limitations in chain length. The method uses a thermodynamic integration over the excluded volume interaction of a ghost chain to determine its excess chemical potential. It is exemplified with a Monte Carlo simulation of the athermal bondflucutation model for various densities and the chain lengths N=20,50,80. Furthermore, the osmotic equation of state and the entropy density are determined.
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 7154-7160 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Collision experiments between two different molecules both oriented with their axis are presented: The kinetics of the CO desorption and NO sticking probability by oriented NO has been investigated using supersonic molecular beam and work function techniques. The work function measurements exhibit mainly molecular adsorption of NO on a CO precovered Ni(100) surface at T=300 K. The desorption and the sticking depend strongly on the initial orientation of the NO molecules in the gas phase. The sticking probability is higher for preferential N-end collisions and the sticking asymmetry is constant, whereas the desorption asymmetry changes its sign from initially negative to positive values, depending on the exposure time or NO coverage. We explain the asymmetries by two different mechanisms, namely direct and indirect molecular exchange. N-end collisions lead preferentially to NO sticking and NO induced CO desorption, whereas O-end collisions enhance the direct CO displacement.
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 974-989 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Two-photon, two-color (1+1') zero-kinetic-energy (ZEKE) photoelectron spectra are presented for the 1:1 phenol-water complex, a prototype system for hydrogen bonding between an aromatic molecule and a simple solvent. ZEKE spectra via different (intermolecular) vibrational intermediate S1 levels of the fully protonated complex (C6H5OH–H2O, h3) as well as the ZEKE spectrum via the vibrationless S1 state of the threefold deuterated complex (C6H5OD–D2O, d3) have been recorded. The spectra are rich in structure, which is mainly attributable to intermolecular vibrations of the ionic complex. Progressions of the intermolecular stretch vibration (240 cm−1) in combination with different intermolecular and intramolecular vibrational levels are the dominant feature of all ZEKE spectra obtained and indicate a large change in the complex geometry along the hydrogen-bond coordinate on ionization. Comparison between the spectrum of the d3 complex and the spectra via different intermediate intermolecular levels of the h3 complex has allowed a more detailed analysis of the intermolecular features compared to previously reported results. Finally, the vibrational assignments obtained are compared with ab initio results for the phenol-water cation reported in the following paper in this issue.
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 101 (1994), S. 990-997 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The phenol-water cation radical has been investigated by ab initio theory using the spin-restricted open-shell Hartree–Fock and spin-restricted open-shell second-order Møller–Plesset theories with 3-21G*(O) and 6-31G* basis sets. The full geometrical optimization was performed for several hydrogen-bonded structures and one hemibonded structure. Clearly, the most stable structure has been found for Cs symmetry with the linear hydrogen bond between the proton of the OH group of the phenol cation radical and the oxygen of the water, and the water hydrogens pointing away from the phenyl ring. For this structure harmonic (and for some intermolecular modes anharmonic) vibrational frequencies have been computed for various isotopic complexes. The computed shifts of phenol-localized intramolecular modes on complexation and on deuteration as well as the calculated intermolecular frequencies of the different isotopic complexes allow for an assignment of vibrational frequencies observed in the experimental zero-kinetic-energy (ZEKE) photoelectron spectra. Five out of a possible six intermolecular vibrations and several intramolecular modes have been assigned, including the 18b vibration which shows a strong blue shift in frequency upon complexation. Structure and properties of the phenol-water cation radical are compared with those of the corresponding neutral complex.
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