Conformation conformational stiffness

All of the likely conformations of cellobiose, cellulose, and xylan are explored systematically assuming the ring conformations and IC-D-O-IC-4 ) angle for each pair of residues to be fixed and derivable from known crystal structures. The absolute van der Waals energies, but not the relative energies of different conformations, are sensitive to the choice of energy functions and atomic coordinates. The results lead to possible explanations of the known conformational stiffness of cellulose and Its solubility properties in alkali. The characteristics of xylan conformations are compared with cellulose. 

Generally, the practical difficulties in the SEC fractionation exponentially increase with the polymer molecule s dimension, hydrodynamic volume, hence with the molar mass and the conformation, stiffness, of... 

The standard molecular structural parameters that one would like to control in block copolymer structures, especially in the context of polymeric nanostructures, are the relative size and nature of the blocks. The relative size implies the length of the block (or degree of polymerization, i.e., the number of monomer units contained within the block), while the nature of the block requires a slightly more elaborate description that includes its solubility characteristics, glass transition temperature (Tg), relative chain stiffness, etc. Using standard living polymerization methods, the size of the blocks is readily controlled by the ratio of the monomer concentration to that of the initiator. The relative sizes of the blocks can thus be easily fine-tuned very precisely to date the best control of these parameters in block copolymers is achieved using anionic polymerization. The nature of each block, on the other hand, is controlled by the selection of the monomer for instance, styrene would provide a relatively stiff (hard) block while isoprene would provide a soft one. This is a consequence of the very low Tg of polyisoprene compared to that of polystyrene, which in simplistic terms reflects the relative conformational stiffness of the polymer chain. 

Short-range interactions (knowledge-based or semiemperical) must account for the polypeptide chain s conformational stiffness [20,42]. In other words, protein-like correlations enforced by the potential should extend over several residues. This would considerably narrow the available conformational space. 

Generally, the practical difficulties in the SEC fractionation exponentially increase with the polymer molecule s dimension, hydrodynamic volume, hence with the molar mass and the conformation, stiffness, of the polymer. For many years, SEC has been considered inadequate for the fractionation of UHMM polymers. In the past, there have been many theoretical and experimental studies to elucidate a better knowledge of the degradation of UHMM polymers. Furthermore, there have been notable improvements in the SEC column s performance. At this time. 

The conformational characteristics of PVF are the subject of several studies (53,65). The rotational isomeric state (RIS) model has been used to calculate mean square end-to-end distance, dipole moments, and conformational entropies. C-nmr chemical shifts are in agreement with these predictions (66). The stiffness parameter (5) has been calculated (67) using the relationship between chain stiffness and cross-sectional area (68). In comparison to polyethylene, PVF has greater chain stiffness which decreases melting entropy, ie, (AS ) = 8.58 J/(molK) [2.05 cal/(molK)] versus... 

The conformations adopted by polyelectrolytes under different conditions in aqueous solution have been the subject of much study. It is known, for example, that at low charge densities or at high ionic strengths polyelectrolytes have more or less randomly coiled conformations. As neutralization proceeds, with concomitant increase in charge density, so the polyelectrolyte chain uncoils due to electrostatic repulsion. Eventually at full neutralization such molecules have conformations that are essentially rod-like (Kitano et al., 1980). This rod-like conformation for poly(acrylic acid) neutralized with sodium hydroxide in aqueous solution is not due to an increase in stiffness of the polymer, but to an increase in the so-called excluded volume, i.e. that region around an individual polymer molecule that cannot be entered by another molecule. The excluded volume itself increases due to an increase in electrostatic charge density (Kitano et al., 1980). 

In a study of the transition in conformation from random coil to stiff rod by poly(acrylic acid), it was found that the point of transition depended on a number of factors, including the nature of the solvent, the temperature, the particular counterion used and the degree of dissociation (Klooster, van der Trouw Mandel, 1984). 

The polymer we consider here is a semi-flexible chain which has some bending stiffness (Eq. 3). We first estimated the chain conformation in the melt. The calculated mean-square end-to-end distance R2n between atoms n-bond apart has shown that the chains have an ideal Gaussian conformation R2 is a linear function of n (see Fig. 35 given later). The value of R2 for n = 100... 

Conformational Change and Parallel Orientation of Stiff Segments (PSs). 210... 

The time evolution of the absorption intensity of each component is plotted in Fig. 19. Since the conformation in the iPS crystal is 3/1 helix (TG)3, two GTGT bands at 567 and 586 cm-1 may be assigned to a 3/1 helical conformation, which corresponds to the stiff segments. Here, it should be noted... 

Region I here the molecular chains partly assume helical (stiff) conformation from random coils where the persistence length gradually increases. 

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