A theory of the helix-coil transition in solutions containing a denaturing agent is proposed. It is shown that, if the transition is induced by an increase in the concentration of the denaturant, the range of the conformational transition narrows with a growing activity of the agent. In contrast, if the transition is induced by temperature variation, addition of a denaturant makes the transition broader, the more so for a higher activity of the agent. The results of the computation agree with published experimental data. 相似文献
Physics of the Solid State - X-ray diffraction patterns of a photocurable epoxy acryl-based polymer composite with addition of ZnO nanocrystals are analyzed. We recover the size distribution... 相似文献
The free volume (voids) distribution in the lamellae of the conventional symmetric and amphiphilic diblock copolymers is studied via Monte–Carlo simulation based on the standard bond fluctuation model. Both in the conventional and amphiphilic block copolymers the voids are found to concentrate on the interfaces between the incompatible units, the magnitude of the effect being unexpectedly significant. A crystalline‐like ordering of voids with increase of the incompatibility between the different repeated units in amphiphilic copolymers is first reported and implications of this peculiarity for the morphology and mechanical properties of the amphiphilic copolymers are discussed.
We report optical studies of the new material – Cr3+-doped lithium–germanate glass, containing Li2Ge7O15 (LGO) nanocrystalline particles. While only broadband 4T2–4A2 fluorescence from the low-field octahedral Cr3+ sites was observed from Cr3+ ions in the glass, in LGO nanocrystals high-field Cr3+ centers emit 2E–4A2 (R–lines) fluorescence. The process of crystallization in the course of isothermal annealing of glasses was monitored spectroscopically and the nucleation of LGO crystallites was observed starting from the smallest clusters. Using the 2E–4A2 fluorescence spectra it is possible to detect the ferroelectric phase transition in LGO:Cr3+ nanocrystals, whose critical temperature was found to be similar to that of the bulk crystals. Long-lived spectral holes were burned in the inhomogeneously broadened R-lines of Cr3+ in LGO nanocrystals at low temperatures. The linear temperature dependence of hole widths shows that the homogeneous broadening of 4A2–2E transitions of Cr3+ in nanocrystals is due to interaction of Cr3+ electronic levels with the two-level systems (TLS) of the surrounding glass. The range of the Cr3+-TLS elastic dipole–dipole interaction is estimated. 相似文献
A coarse-grained model is used to study the conformational properties of semiflexible polymers with amphiphilic monomer units containing both hydrophilic and hydrophobic interaction sites. The hydrophobically driven conformational transitions are studied using molecular dynamics simulations for the chains of varying stiffness, as characterized by intrinsic Kuhn segment lengths that vary over a decade. It is shown that the energy of hydrophobic attraction required for the realization of the coil-to-globule transition increases with increasing chain stiffness. For rather stiff backbone, the coil-to-globule transition corresponds to a first order phase transition. We find that depending on the chain stiffness, a variety of thermodynamically stable anisometric chain morphologies are possible in a solvent selectively poor for hydrophobic sites of amphiphilic monomer units. For flexible chains, the amphiphilic polymer forms a cylindrical globule having blob structure with nearly spherical blobs. With increasing stiffness, the number of blobs composing the globule decreases and the shape of blobs transforms into elongated cylinder. Further increase in stiffness leads to compaction of macromolecules into a collagenlike structure when the chain folds itself several times and different strands wind round each other. In this state, the collagenlike structures coexist with toroidal globules, both conformations having approximately equal energies. 相似文献
The precession dynamics of the magnetization of a film with an in-plane uniaxial anisotropy is analyzed in the spectrum of
ferromagnetic resonance corresponding to magnetic biasing along the hard axis of the film. An additional resonance peak is
revealed near magnetic anisotropy field Hu. This peak is related to the appearance of angular bistability due to the presence of two symmetric angular equilibrium positions
in field H < Hu. 相似文献