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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 116 (2002), S. 5308-5314 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The static structure of solutions of DNA fragments is investigated using integral equation theory. The solution is modeled as a four-component system with DNA molecules, bound counterions, free counterions, and coions, all of which are treated explicitly. Each DNA fragment is modeled as a shish-kebab chain with three kinds of sites, i.e., charged sites, neutralized (protonated) sites, and sites with bound counterions. The partial structure factors are obtained using a generalization of the polymer reference interaction model. The undetermined parameters in the model, namely the fraction of protonated and bound sites, are obtained by fitting theoretical predictions for the polymer–polymer and polymer–counterions structure factors to experimental data. It is found that a large majority of counterions is localized near the DNA molecules due to counterions binding and protonation. The bound counterions make a dominant contribution to the total scattering from counterion species. The best fit is obtained when each DNA molecule contains about 22% protonated sites and 53% counterion occupied sites, i.e., the effective DNA charge fraction is about 0.25. This DNA charge fraction is consistent with electrospray ionization and DNA titration experiments. © 2002 American Institute of Physics.
    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 115 (2001), S. 11325-11332 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We investigate the dynamics of a copolymer molecule in a θ-solvent under a weak alternating field using the Zimm model. We first consider a diblock copolymer with two blocks of same force constant, where the monomers on the two different blocks interact with the applied field differently. The theory predicts that the center-of-mass and the chain conformation of copolymer molecules oscillate in response to the sinusoidal electric field. For the center-of-mass, the oscillation becomes more pronounced as the charge fraction is increased. However, the oscillation of chain conformation is not observed for neutral or fully charged homopolymers, but is enhanced when the fraction of the two blocks becomes equal. In highly viscous solutions, the strength of the oscillation of the center-of-mass and conformation is weakened, and the phase of oscillation is shifted. Moreover, the oscillatory behavior diminishes at higher frequencies. For comparison, we also study a special copolymer model where the two monomers alternate along the polymer backbone. Again the oscillation emerges for the molecular motion and conformation, but the oscillation of chain properties becomes much weaker than diblock copolymers. These results disclose the effect of the chemical architectures of copolymers on their chain dynamic behavior under an alternating field. © 2001 American Institute of Physics.
    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 114 (2001), S. 2830-2838 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The effect of acid-base equilibria on the properties of polyelectrolyte solutions is investigated using the self-consistent polymer reference interaction site model theory with the random phase approximation. In the model, each monomer on the chain consists of charged and protonated sites, which contribute an electrostatic repulsion and a short-ranged attraction, respectively. The proportions of charged and protonated sites are governed by a chemical equilibrium constant. The polymer chains are highly charged and expanded when the strength of attraction is low. As the strength of the attraction is increased, the monomer fractional charge and chain size decrease in a continuous or discontinuous manner, depending on the equilibrium constant. For a fixed value of the strength of the attractive interaction, the monomer charge fraction and chain size display a nonmonotonic dependence on the concentration. The theory could provide a rationalization of some recent experimental measurements of the conformational and structural properties of DNA fragments and synthetic polyelectrolytes. © 2001 American Institute of Physics.
    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 114 (2001), S. 4717-4723 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present theoretical studies for the conformational behavior of isolated polymers under an external field in good solvents. We assume the monomers of the polymer chain are subject to a three-dimensional external field, which is modeled as a spherical harmonic potential, and monomers interact via hard-core repulsions. We begin with Monte Carlo simulations to investigate the effects of the external field. The chain conformation changes insignificantly if the external field is weak. When the strength of the external field is increased, the chain contracts drastically. A first-order perturbation theory (with ideal-chain reference system) is proposed, with the hard-core repulsion modeled as a perturbation. This approach yields good agreement with the simulations, but with the discrepancy between these two approaches becoming pronounced for strong external field. The perturbation theory makes the prediction that the size of a polymer chain contracts approximately one order of magnitude before collapsing to its globular conformation. Further, to account for behavior under strong fields, a theory of mean-field type is developed, which predicts 〈R2〉∼(N/k)2/5 (where k denotes field strength), consistent with the simulations. These studies are of importance in understanding supercoiled long chain DNA in a tiny cellular nucleus, and deformation of polymer materials under external fields. © 2001 American Institute of Physics.
    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 115 (2001), S. 9084-9091 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Monte Carlo simulations are conducted to investigate a model composed of a fluctuating sphere labeled on one chain end of an isolated flexible chain polymer in good solvents. The labeled sphere is to model the instantaneous size of a bound flexible chain segment or a vibrating chromophore on a polymer chain. We assume the vibration of the sphere is governed by a harmoniclike potential, and the sphere size stays positive. We first address the issue regarding the confinement effect induced by a flexible chain. To rationalize the simulation results, we carry out a detailed analysis for a simple case containing a dimer grafted onto a fluctuating sphere. Using the sphere with a large size fluctuation, we find that the fluctuating sphere can be confined within the coiled polymer chain, and even trapped inside the grooves between neighboring monomers. The results imply the confinement effects may influence the properties of chromophores labeled on polymers or drugs bound to biopolymers. Moreover, in a separate study, we show the fluctuating sphere model can be used to fit a bound flexible chain segment, and provides a means to parameterize a polymer chain to a dumbbell, with possible applications in the dynamics of dilute polymer solutions. © 2001 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 114 (2001), S. 4323-4330 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A density functional theory is presented for the pair correlation functions in polymeric liquids. The theory uses the Yethiraj–Woodward free-energy functional for the polymeric liquid, where the ideal gas free-energy functional is treated exactly and the excess free-energy functional is obtained using a weighted density approximation with the simplest choice of the weighting function. Pair correlation functions are obtained using the Percus trick, where the external field is taken to be a single polymer molecule. The minimization of the free energy in the theory requires a two molecule simulation at each iteration. The theory is very accurate for the pair correlation functions in freely jointed tangent-hard-sphere chains and freely rotating fused-hard-sphere chains, especially at low densities and for long chains. In addition, the theory allows the calculation of the virial pressure in these systems and shows a remarkable degree of consistency between the virial and compressibility pressure. © 2001 American Institute of Physics.
    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 113 (2000), S. 8841-8847 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A self-consistent integral equation theory is presented for the conformational behavior and static structure of polyelectrolyte solutions composed of semiflexible chain molecules. The free energy of the solution is expressed as the sum of an elastic, a Coulombic, and a medium-induced contribution, and is minimized with respect to the single chain structure factor. In the flexible limit, the theory is accurate for the chain conformations and static structure factor when compared to Monte Carlo simulations of flexible chains. For semiflexible chains near the flexible limit, the chain conformations are sensitive to the bare persistence length in dilute solutions but not in the semidilute regime. In contrast, the effect of the bare persistence length on the static structure factor is not as significant. The theory predicts that charged flexible chains exhibit more pronounced liquidlike order in solution than their rigid-rod counterparts, and the length scale of these liquidlike correlations is also shorter in flexible chains. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 97 (1993), S. 13824-13830 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 12980-12987 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 99 (1995), S. 12988-12997 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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