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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 4364-4367 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We investigate by molecular dynamics computer simulation the distribution of ground- and excited-state energies and the degree of correlation between them for a chomophore dissolved in an amorphous solid. The system studied is resorufin in amorphous glycerol. We find that there is considerable but not complete correlation between the absolute energy of the chromophore in the ground electronic state and its energy in the first excited electronic state. This is shown to be reasonable in view of the microscopic model of inhomogeneous broadening introduced by Laird and Skinner [J. Chem. Phys. 90, 3880 (1989)].
    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 95 (1991), S. 8390-8397 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Nonlinear integral equations are commonly used as a basis for determining radial distribution functions in equilibrium fluids. We show that a solution to such an equation does not provide sufficient information to fix a unique equilibrium state because no explicit external field is prescribed. It follows that many physically distinct interpretations may be associated with each numerically generated solution. This is illustrated by showing that a family of physically distinct external fields can be associated with the same integral equation. In this context the occurrence of multiple solutions and the occurrence of solutions with long-range oscillations—both formally impossible events in the context of a well-posed problem—can be given a reasonable interpretation, for external fields in which these solutions are in fact appropriate can be identified. This shows, however, that the physical interpretation of numerically generated radial distribution functions is nontrivial. The problems are illustrated explicitly with a simple model integral equation which does exhibit multiple solutions and long-range solutions even though these are absent in the system the integral equation is intended to model.
    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 89 (1988), S. 5081-5095 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The measurable properties of supercooled liquids and amorphous solids reflect the short-range packing geometry of the contituent particles. This paper is devoted to the description of that short-range order by the Born–Green–Yvon (BGY) local stress equation which relates pair and triplet distribution functions to the pair potential. Since metastable (but long-lived) phases are at issue, it has been necessary to identify an appropriate class of ensembles for which the BGY relation can be justified. In particular, low-temperature amorphous solids have preparation-method-dependent properties, and we propose to classify their representative ensembles by the choice of a triplet superposition correction function K. As background for such choice, we have reexamined and extended Alder's lattice enumeration method for K in regular structures. The Kirkwood superposition approximation K≡1 has disastrous consequences for the BGY equation at low temperature; numerical pair correlation functions for the cases of hard spheres and of repelling Gaussian particles display long-range ordering that is impossible for the amorphous solid state. This failure is partially relieved by choosing a K that enhances the concentration of compact pentagonal particle groupings. Study of the inverse problem of determining K from physically reasonable pair correlation functions suggests that K must possess relatively long-ranged fluctuations about unity. These considerations highlight the desirability of accurate simulation studies of K for amorphous deposits at absolute zero.
    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. 1200-1208 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A molecular model has been constructed for glycerol and has been applied to a study of clusters and condensed phases by molecular dynamics simulation. Each molecule is regarded as a flexible polar complex of nine mass points (CH and CH2 groups are treated as "united atoms''). Periodic arrays stabilize in a close approximation to the observed glycerol crystal structure, with identical extended molecules connected by infinite chains of hydrogen bonds. By contrast the stable and supercooled liquids display a variety of asymmetrical molecular conformations and an irregular network of hydrogen bonds. Detailed examination of the various atomic pair correlation functions reveals considerable overlap of intramolecular and intermolecular features, implying intrinsic ambiguity in the interpretation of x-ray and neutron diffraction measurements designed to determine the short-range order of liquid glycerol.
    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〉 88 (1984), S. 5919-5923 
    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 88 (1988), S. 7791-7798 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Many integral equations for numerically predicting pair correlation functions g(2) in classical fluids have been proposed, each based on its own "closure approximation.'' We have investigated a procedure for evaluating such closures, particularly their capacity to describe clustering under the influence of attractive interparticle forces. Our approach utilizes the Gaussian core model in a large closed system which, under sign change of the coupling constant λ, undergoes a collapse to form a single compact aggregate with known properties. In the infinite system limit this phenomenon causes inverse temperature (β) expansions, such as that for g(2), to diverge. By contrast available closures lead to convergent expansions for the Gaussian core model, but with a "critical point'' on the negative real βλ axis. Specific calculations have been performed illustrating this behavior for the BGYK and the PY integral equations. We suggest that the proximity of the artifactual negative-axis critical point to the origin (where the collapse singularity should actually appear) provides a measure of accuracy of closure approximations.
    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 107 (1997), S. 4350-4357 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We report results of a molecular dynamics study of liquid glycerol at the experimental density and at a series of elevated densities corresponding in our model to pressures of up to 0.7 GPa. We find that the degree of hydrogen bonding increases with increasing pressure over the range studied, and that the width of the hydrogen bond angle distribution increases with increasing pressure. The relevance to the experimental finding by Cook et al. [R. L. Cook, H. E. King, C. A. Herbst, and D. R. Herschbach, J. Chem. Phys. 100, 5178 (1994)] that the fragility of glycerol increases with increasing pressure is discussed. © 1997 American Institute of Physics.
    Type of Medium: Electronic Resource
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