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Flexibility structural

The apocamphyl structure is particularly rigid, and bridgehead caibocationa become accessible in more flexible structures. The relative solvolysis rates of the bridgehead bromides 1-bromoadamantane, l-bromobicyclo[2.2.2]octane, and l-bromobicyclo[2.2,l]-... [Pg.288]

Aromatic polyesters that do not contain any flexible structural units are often nonmeltable or extremely high melting polymers that cannot be processed. Copolymerization is a way to obtain processable wholly aromatic polyesters The Tm versus copolyester composition curve is a U-shaped curve exhibiting a minimum that is generally well below the Tm of corresponding homopolymers. Liquid crystalline aromatic polyesters, for instance, are usually copolymers.72 An example is Ticona s Vectra, a random copolyester containing 4-oxybenzoyl and 6-oxy-2-naphthoyl units in ca. 70 30 mol ratio. This copolymer melts at ca. [Pg.35]

The sedimentation coefficient provides a useful indicator of polysaccharide conformation and flexibility in solution, particiflarly if the dependence of on Mw is known [62]. There are two levels of approach (i) a general level in which we are delineating between overall conformation types (coil, rod, sphere) (ii) a more detailed representation where we are trying to specify particle aspect ratios in the case of rigid structures or persistence lengths for linear, flexible structures. [Pg.236]

Photodiode arrays have been used as retinal implants [684]. These arrays of p-i-n diodes are fabricated on a thin titanium layer bonded to a glass plate. The total thickness of this flexible structure is 1.5 yum. The microphotodiode array (MPDA) is used to replace photoreceptors (rods and cones) that have become defective due to disease. [Pg.188]

Table II shows Tgs obtained from DSC traces. (Footnotes a and b in Table II show T s values of three reference polymers two PIBs, whose Mns are similar to the Mns of MA-PIB-MA used in the network synthesis, and a PDMAAm the difference in the Tg for the Mn=4,000 and 9,300 PIBs is due to the dependence of Tg on Mn(72)). The DSC traces of the networks exhibited two Tgs, one in the range of -63 to -52 °C (PIB domains) and another in the range of 90 to 115 °C (PDMAAm domains) indicating microphase separated structures. The Tgs associated with the PIB phase in the PDMAAm-1-PIB networks were higher than those of the reference homoPIBs which may be due to PIB chain-ends embedded in the glassy PDMAAm phase restricting segmental mobility. The Tg of the PIB phase in the PDMAAm-1-PIB increases by increasing the PIB content which may be due to an increase in crosslink density. In contrast, the Tg for the PDMAAm phase in the network decreases upon increasing the PIB content. Interaction of the (-CH2-CH-) moiety of the PDMAAm with the flexible PIB and thus the formation of a more flexible structure may explain this phenomenon. Table II shows Tgs obtained from DSC traces. (Footnotes a and b in Table II show T s values of three reference polymers two PIBs, whose Mns are similar to the Mns of MA-PIB-MA used in the network synthesis, and a PDMAAm the difference in the Tg for the Mn=4,000 and 9,300 PIBs is due to the dependence of Tg on Mn(72)). The DSC traces of the networks exhibited two Tgs, one in the range of -63 to -52 °C (PIB domains) and another in the range of 90 to 115 °C (PDMAAm domains) indicating microphase separated structures. The Tgs associated with the PIB phase in the PDMAAm-1-PIB networks were higher than those of the reference homoPIBs which may be due to PIB chain-ends embedded in the glassy PDMAAm phase restricting segmental mobility. The Tg of the PIB phase in the PDMAAm-1-PIB increases by increasing the PIB content which may be due to an increase in crosslink density. In contrast, the Tg for the PDMAAm phase in the network decreases upon increasing the PIB content. Interaction of the (-CH2-CH-) moiety of the PDMAAm with the flexible PIB and thus the formation of a more flexible structure may explain this phenomenon.
In general, dendrimers of size G-0 through G-3 have open, asymmetric, and flexible structures with effectively no protected internal areas, due to a large freedom of motion in their branches, and they can readily accommodate additional covalent attachments to their surfaces. See Figures 73-7.5 for illustrations of the two-dimension and three-dimension structure of a... [Pg.352]

Biopolymers e.g., polysaccharides, polynucleotides, unfolded protein molecules, that all attain expanded flexible structures in solution adsorb more or less according to the principles discussed above. [Pg.103]

The spin-spin coupling constants [2-4] of the enkephalins in solution can be interpreted in terms of folded conformations resembling that of morphine in the placement of the residues which appear important for biological activity. X-ray crystallography and theoretical calculations (4-9) have also shown that methionine and leucine enkephalin adopt conformations similar to those concluded from NMR studies. Hence it would appear that opioid peptides can topographically resemble the opiates by assuming preferred, folded, conformations. However, earlier studies from this laboratory (TO) have shown that NMR data can be interpreted in terms of a conformationally flexible structure for methionine enkephalin. [Pg.159]


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See also in sourсe #XX -- [ Pg.17 , Pg.18 ]




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Advanced molecular structure, consisting of rigid and flexible segments

Crystal structure prediction molecular flexibility

Dynamic structure factors flexible polymers

Experimental Results for Polymer Chain Flexibility and Correlation with Structure

Flexibility in 3D Structure Searching

Flexible Structures for Mechanical Sensors

Flexible Structures in DNA-binding Proteins

Flexible continuum structure

Flexible continuum structure solar collectors support

Flexible foams crosslinked structure

Flexible molecules, structure determination

Flexible structural bonding

Flexible structures

Flexible structures

Folded flexible structure

HMGA proteins flexible players in a structured world

Host Structural Flexibility

Molecular Structure and Flexibility

Polyelectrolytes flexible structures

Protein Flexibility in Structure-Based Virtual Screening From Models to Algorithms

Protein structural flexibility

Proteins flexible structure

Reinforcement structure, mechanical flexibility

Rigidised inflatable flexible continuum structure

Seeking structural flexibility

Structural Flexibility Can Increase the Specificity of Enzymes

Structure flexibility

Structure flexibility

Structure prediction flexible molecules

Structure searching conformational flexibility

Structure small flexible ligands

Structure-Direction by Flexible, Hydrophilic OSDAs

Three-dimensional structure searching conformational flexibility

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