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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 5517-5526 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Inelastic neutron scattering spectra of the mixed system (CH4)1−c(CD4)c, c=0.05, 0.15, 0.20, and 0.96, were measured with high energy resolution (δE〉9μeV). For c=0.05 and 0.15 weakly disturbed tunnel transitions and almost free-rotor lines, both characteristic of phase II of methane, are observed. The line shifts and broadenings in this concentration range are almost quantitatively described by a statistical model, which assumes a linear decrease of the tunnel splitting with the number of ordered CD4 neighbors. The decrease of the tunnel splitting is compatible with an octopole moment of the CD4 molecules increased by about 20% compared to CH4 molecules at ordered sites. Changes of the lattice parameter are incorporated into the model. The model also accounts for a part of the linewidth. Additionally a splitting of T states occurs as a consequence of the symmetry reduction. The systems show strong relaxation effects. The shift of the free-rotor lines is described by a quadratic dependence on the potential strength. At c=0.2 the mixed compound undergoes a phase transition into a more ordered phase at Tc≈12.9 K. It is not certain that this phase is identical with the formerly established phase III, characteristic of pure CD4 and CH4 under pressure. A three-site model not very different from that used for CD4 III describes the spectra rather well, including that obtained for c=0.96. The spectra are incompatible with a proposed crystal structure P42/mbc [Maki et al., J. Chem. Phys. 70, 655 (1979)].
    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 86 (1987), S. 6465-6473 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The perturbation of the partial orientational order in CH4II caused by dilution with Kr(xKr≤0.20) has been studied with inelastic incoherent neutron scattering. Both, the lines assigned as rotational tunneling and almost free molecular rotation, display a characteristic asymmetric broadening which gets more pronounced with increasing Kr concentration. At low Kr concentrations (xKr≤0.05) the tunneling spectra are well explained by a model which is based on a statistical distribution of local rotational potentials. In this model only the number of Kr atoms replacing orientationally ordered CH4 nearest neighbors is relevant for the local potential at the sites of tunneling molecules. The different local symmetries are not considered in the model. It was not possible to formulate a quantitative model for the scattering from molecules at nearly free rotor sites.
    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 91 (1989), S. 1167-1172 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The bcc structure of Ca(ND3)5.7 is found to be stable down to He temperatures. The crystal is characterized by frozen-in orientational disorder and also positional disorder of the ND3 molecules. The latter may be explained by a distribution of octahedrally coordinated and tetrahedrally coordinated Ca ions. The relation of occupation numbers with stoichiometry cannot be made quantitatively, however. There are no indications of a significant departure from the geometry of a free ammonia molecule in the solid.
    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 90 (1989), S. 400-405 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Rotational excitations of CH4 molecules, matrix isolated in solid argon, are observed with inelastic neutron scattering (INS). In the argon matrix the orientational crystalline field Vc(Ω) leads to weakly hindered rotation. Experimental data are compared with the predictions of the "Extended James–Keenan model'' for solid CH4 II. Deviations from complete orientational disorder are studied via the Q dependence of the scattered intensities. The transition energies for CH4 in Ar differ considerably from the corresponding transition energies in solid CH4 II due to the stronger crystalline field, while the transition matrix elements seem to be rather similar. The parameters β4=7.5 and β6=−25 of the expansion of the crystalline field into octahedral rotor functions are estimated from the experimental data and compared with predictions, based on different empirical potentials between nonbonding atoms.
    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 113 (2000), S. 3219-3225 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The hydrogen dynamics in the metalhexahydrateperchlorates with Mg, Mn, Fe, Ni, and Zn as metal ions has been investigated with quasielastic neutron scattering. The water molecules perform 180°-flip motions on a picosecond time scale through a series of solid–solid phase transitions. In the highest temperature phase I and the subsequent phase II, rotational barriers of typically Ea=50 meV are found. These values are surprisingly small in view of the low symmetry of H2O molecules. The I → II phase transition has only very small effects on the hydrogen dynamics. At the transition into phase III an increase of the rotational barriers to typically Ea=250 meV is found. This is interpreted as the formation of weak hydrogen bonds. In phase I 180°-flip motions provide a complete description of the observed data. In phases II and III an extension of the dynamical model toward a stronger localization of hydrogen is required. A preference is given to a mechanism leading to a temporary blockade of the flip motions. In phase III of the Fe compound, the existence of crystallographically different sites for water molecules is inferred. © 2000 American Institute of 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 113 (2000), S. 4713-4721 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present the results of a high-resolution neutron diffraction experiment with a fully deuterated methane hydrate type I at temperatures of 2, 100, and 150 K. Precise crystallographic parameters of the ice-like D2O lattice and the thermal parameters of the encaged methane molecules have been obtained. The parameters of the host lattice differ only slightly from values found for hydrates with asymmetric guests included, which leads to the conclusion that the host lattice of structure I is only a little adaptive. At low temperatures (2 K) the methane molecules in both types of cages present in structure I occupy positions in the center of the cages. At higher temperatures the thermal parameters in both types of cages reflect the surrounding cage geometries or more precisely the translational potentials of the cages. The orientational scattering length density of the CD4 molecules has been analyzed in terms of a multipole expansion with symmetry adapted functions [Press and Hüller, Acta Crystallogr., Sect. A: Cryst. Phys., Diffr., Theor. Gen. Crystallogr. A29, 252 (1972); Press, ibid. A29, 257 (1972)]. In both types of cages we found only small modulations of a spherically symmetric scattering density accounting for almost free rotations of the methane molecules. The large and asymmetric cage leads to a somewhat more pronounced modulation of the orientational density than in the small dodecahedral cage. The orientational probability distribution function (PDF) remains nearly unchanged from 2 to 150 K. At 200 K we observed the time-resolved decomposition of the hydrate structure I into hexagonal ice Ih. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 32 (1976), S. 170-170 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Corrections are given to Press [Acta Cryst. (1973). A29, 257-263]. Two misprints in Table 2 should be corrected to cT61 = \sqrt{26}, {{4}\over{9}} and cT71 = - \sqrt{455/9}. In the 3rd line of equation (2.1) js(QQ) should be changed to j6(QQ).
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 35 (1979), S. 881-885 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The concept of a 'rotational form factor' analysis of molecular crystalline structures is generalized by allowing correlations between the orientation of a molecule and its centre-of-mass position. This coupling results in correction terms to the well known rotational form factor. The method is illustrated with the example of (i) tetrahedral molecules and (ii) dumbells at a site of cubic symmetry (m3m) and the rô1e of the site symmetry as well as the magnitude of the mean-squared amplitude (u2) of the centre-of-mass motion are investigated.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 35 (1979), S. 876-880 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: In previous publications [Press & Hüller (1973). Acta Cryst. A29, 252-256; Press (1973). Acta Cryst. A29, 257-263], the analysis of molecular crystalline structures by symmetry-adapted surface harmonics has been discussed. Implications of both molecular and site symmetry have been emphasized. Here the question is raised whether the magnitude of symmetry-allowed expansion coefficients is subject to constraints or not. Obvious restrictions result from the requirement that the density distribution at a molecular site has to be positive definite. Even stronger conditions are imposed by the requirement that the orientational distribution function g(τ) has to be positive definite, too. The area in parameter space for parameter values which are in agreement with the strong conditions is shown. Physically meaningful expansion coefficients are guaranteed by starting from a symmetry-allowed rotational potential V(τ).
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 29 (1973), S. 252-256 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A new method of analyzing the orientational structure of molecular solids is proposed. It is based on an expansion of the coherent scattering-length density of a molecule into a complete set of orthonormal functions. Explicit expressions for the structure factor are given in the three-dimensional case with use of symmetry-adapted cubic harmonics and for planar molecules with use of trigonometric functions. The method is especially well suited for analysis of plastic crystalline phases, orientationally disordered phases and ordered phases with molecules performing large librational motions. The treatment reveals a close analogy between orientationally ordered or disordered systems and magnetic systems.
    Type of Medium: Electronic Resource
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