Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 18 (1985), S. 821-823 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 21 (1988), S. 3204-3216 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 19 (1986), S. 2770-2778 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 22 (1989), S. 1853-1862 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 20 (1987), S. 1345-1353 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 18 (1985), S. 2455-2463 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 822-836 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A theory for long time random coil peptide dynamics is developed based on a generalization of the optimized Rouse–Zimm model of Perico et al. [J. Chem. Phys. 87, 3677 (1987)] and Perico [J. Chem. Phys. 88, 3996 (1988) and Biopolymers 28, 1527 (1989)]. The generalized model employs the rotational potential energy for specific amino acid residues and amino acid friction coefficients to compute all input parameters in the model. Calculations of the fluorescence depolarization correlation function P2(t ) and of the local persistence length are found to be sensitive to the amino acid sequence, the length of the polypeptide chain, and the location of the probe. Model computations of P2(t ) are compared with new experimentally determined rotational correlation times (of the order of nanoseconds) from fluorescence depolarization measurements of three different synthetic 17-residue peptides, each containing a single tryptophan (TRP) residue as a probe. In addition, the previous anisotropy measurements on ACTH, glucagon, and their fragments are discussed and compared with the model calculations. Our results indicate that the theory gives a reasonable prediction for the fluorescence depolarization correlation times of random coil polypeptides, but the calculated rotational correlation function predicts a much faster initial decay and a slower final decay than is observed. Possible theoretical improvements are discussed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 7448-7460 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A theoretical description of the critical point of a polymer solution is formulated directly from the Edwards continuum model of polymers with two- and three-body excluded-volume interactions. A Hubbard–Stratonovich transformation analogous to that used in recent work on the liquid–vapor critical point of simple fluids is used to recast the grand partition function of the polymer solution as a functional integral over continuous fields. The resulting Landau–Ginzburg–Wilson (LGW) Hamiltonian is of the form of a generalized nonsymmetric n=1 component vector model, with operators directly related to certain connected correlation functions of a reference system. The latter is taken to be an ensemble of Gaussian chains with three-body excluded-volume repulsions, and the operators are computed in three dimensions by means of a perturbation theory that is rapidly convergent for long chains. A mean field theory of the functional integral yields a description of the critical point in which the power-law variations of the critical polymer volume fraction φc, critical temperature Tc, and critical amplitudes on polymerization index N are essentially identical to those found in the Flory–Huggins theory. In particular, we find φc ∼N−1/2, Tθ−Tc∼N−1/2 with (Tθ the theta temperature), and that the composition difference between coexisting phases varies with reduced temperature t as N−1/4t1/2. The mean field theory of the interfacial tension σ between coexisting phases near the critical point, developed by considering the LGW Hamiltonian for a weakly inhomogeneous solution, yields σ∼N−1/4t3/2, with the correlation length diverging as ξ∼N1/4t−1/2 within the same approximation, consistent with the mean field limit of de Gennes' scaling form. Generalizations to polydisperse systems are discussed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 87 (1987), S. 3089-3098 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The three-parameter model of excluded volume is employed to calculate both the moments 〈R2n〉{n=2,3,...} of the end-to-end vector distance of a linear homopolymer and the average square moment 〈R2〉 for a single branch of an f-armed star. These results complement the calculations of 〈R2〉, the radius of gyration RG, the Kirkwood approximation to the hydrodynamic radius RH, and the second virial coefficient A2 for linear chains given in paper I. These calculations are intended to check the self-consistency of the ternary interaction theory against recent simulation data for lattice chains under theta conditions (A2=0) using the fact that higher moments and properties of branched polymers are more sensitive to the presence of ternary interactions. No free parameters are involved in the comparison, and the agreement between theory and numerical data is quite satisfactory. In addition, a general discussion is provided of differences in values of various polymer properties that can result from different methods of regularizing the continuum theory.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 86 (1987), S. 7204-7217 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Renormalization group methods are developed for describing the osmotic pressure of semidilute polymers in the theta region, where large binary polymer interactions may become screened. The analysis requires a combination of renormalization group methods as they are applied, on the one hand, to semidilute polymer solutions in marginal-to-good solvents, and, on the other hand, to single polymers in theta solutions. Ternary interactions are shown to contribute to the screening of binary interactions in these semidilute theta solutions, and an effective binary interaction is introduced that is defined to vanish at the theta point along with the second virial coefficient, leaving residual ternary interactions. Screening of the effective binary interactions is described through an Edwards decoupling scheme, and perturbation expansions are developed in the presumed small screened effective binary and the residual ternary interactions. Formal divergences in the osmotic pressure are absorbed into phenomenologically defined second and third virial coefficients. The renormalized osmotic pressure, which is written solely in terms of direct observables, is found to be a simple generalization of the results obtained for semidilute polymer solutions in good-to-marginal solvents. It is also found to agree with experimental results on semidilute polymer solutions that cover the temperature domain between theta and good solvents. The present work is carried to lowest order in both the effective binary interaction and the residual ternary interaction, but the general method of treating higher order corrections is outlined. A recent result for the special limit of semidilute solutions at the theta point with three-body fixed point interactions is recovered as a limit of our more general formulation.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...