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Molecules assymetric

Our strategy is to incorporate a prolate redox molecule into the hydrocarbon phase of the organized monolayer. Steric restraints imposed by a dose-packed monolayer would presumably force the redox molecule to adopt an orientation parallel to the hydrocarbon tails. Spacing can then be controlled by a short hydrocarbon chain between the redox center and the metal. A class of molecules fitting these requirements are the assymetric 4,4 -bipyridiniums ... [Pg.431]

With 1,4-disubstituted dienes, more complex stereochemistry is possible in the polymers. In addition to the possibility of geometrical isomerism, there are two types of completely assymetric centre in the molecule and tritactic polymers can... [Pg.104]

Relative to secondary structure, viscosity, sedimentation velocity, ultraviolet difference spectra and optical rotatory dispersion studies (4,24,25) showed that glutenin appears to be an assymetric molecule with a low a-helix content (10-15%). Glutenin contained more a-helix structure in hydrochloric acid solutions and less in urea solutions. The amount of a-helix structure is also influenced by changes in ionic strength (26). [Pg.198]

For any amino acid except the first one, glycine (where R = H), the amines have an assymetric carbon atom in their molecules. Two optical... [Pg.368]

Such, in barest outline, is the Oparin hypothesis as it has been developed over the last thirty years by biochemists in Russia and elsewhere. Obviously, it raises innumerable questions and problems. Some are complex chemical issues, such as that of the origins of the universal existence in living organisms, but not in non-living nature, of6 assymetric molecules like those of the amino acids or sugars (see page 33). Nor are there yet very satisfactory accounts of the polymerization steps which produced proteins, nucleic acids, and so on from their more primitive ancestors. [Pg.283]

The bond and angle functions are modified Hooke s Law functions. The torsional strain for carbon-carbon single bonds is a function containing the usual (1 + cos 30) term but parameterized to provide the known values for butane. The nonhonded strain term is an exponential-six function. The last term of the function has heen added to assure the proper stereochemistry about an assymetric atom. An adaptive pattern search routine is used to minimize the strain energy because it does not require analytical derivatives. The amount of time necessary to obtain good molecular models depends upon the number of atoms in the molecule, the initial strain of the molecule, and the degrees of freedom in the structure. [Pg.148]

Group VI elements like S, Se and Te also form hexahalides (A Sj and molecules (Figure 2.11) with strictly octahedral symmetry about the A atom. Some d hybridization must be postulated in order to form he 6 necessary symmetrically oriented and only half-filled highly assymetrical d sp orbitals. The corresponding crystals are trigonal Se and Te, and a- and jS-monoclinic Se. [Pg.51]

Liou et al., 1981). A preliminary report has announced the crystallization of CRBP from rat liver and presented early X-ray data on these crystals (Newcomer etal., 1981). The crystals were grown from solutions of polyethylene glycol-6,000 and CdCl2. The crystals are orthorhombic, space group P2,2,2> 40.09, b = 47.39, and c = 69.34. An assymetric unit contains one molecule. Diffraction has been observed to Bragg spacings of 1.7-A resolution. [Pg.92]


See other pages where Molecules assymetric is mentioned: [Pg.235]    [Pg.231]    [Pg.152]    [Pg.37]    [Pg.306]    [Pg.137]    [Pg.124]    [Pg.207]    [Pg.192]    [Pg.208]    [Pg.1549]    [Pg.110]   
See also in sourсe #XX -- [ Pg.237 ]




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