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Expanded molecules

The negative charges on these groups at neutral pH lead to electrostatic repulsion which increases the dimensions of the molecule. The large volume of solution occupied by such expanded molecules contributes to high viscosity, and aids in the function of hyaluronic acid as a joint lubricant. [Pg.47]

In 1948, the ring-expanded version of penicillin, cephalosporin C 22, was reported from Cephalosporium sp. by Brotzu its structure was determined in 1961 by the Oxford group.42,43 As with the penicillin nucleus, this ring-expanded molecule, 7-aminocephalosporanic acid 21, also served as the building block for many thousands of cephalosporins with the first orally active molecule, cephalexin 23 being introduced in 1970. Since that time, a multitude of cephalosporins have been synthesised with the aim of producing molecules that are more resistant to (3-lactamases. [Pg.12]

All data by different methods over tbe temperature of 0° to nearly 30°C did not show any changes in properties other than those commonly found with other expanded molecules (Table XII, Fig. 14). [Pg.218]

For studies where the periodicity of the graphite surface plays a role in the determination of properties, (e.g., low-temperature determinations of the structure of layers adsorbed on graphite), the Fourier expanded molecule-surface potential of Steele is commonly used [4—6, 19]. For complex geometries such as heterogeneous surfaces (see Bojan et al., coal pores [20]) and fuUerenes [21] (Martinez-Alonso et al., Ar on C q), a fuU sum of the direct atom—atom potentials is needed. In the recent simulation studies of carbon nanotubes, some studies have used asummed atom-atom potential description (e.g., see the work of Stan et al. [22]) while others use a continuum cylindrical pore model [23, 24]. [Pg.81]

As follows from the recently performed analyses [3] the shape of the v (AH) IR absorption bands results usually from the indirect relaxation of the excited vibrational levels, i.e. through the coupling with the low frequency internal modes which next interact with phonons of the condensed phase. The broad bands are characteristic not only for condensed phases. They are also observed in the gas phase in the case of bulky expanded molecules, which can be treated as a bath. In this case a crucial is the coupling of v (A-H) vibrations with low frequency bridge vibrations. [Pg.392]

Ouibrahim and Fruman (47) in 1980 found dilational flow in three distinct flow situations, which each involve an extensional component capillary tube flow, orifice flow, and pitot tube flow. They examined extensively hydrolyzed polyacrylamide (HPAA) and found that the dilatant effect was greatly reduced in the presence of excess salt. This finding was attributed to the effect of the salt ions in screening the charges on the polyelectrolytic HPAA and thus causing the contraction of the highly expanded molecule. [Pg.226]

If we call the frequency that the master oscillator is locked at, V, then the local oscillator frequency is 30 MHz. The pulse of microwave energy creates a macroscopic polarization in the expanding molecules, which then emit radiation at the rotational transition frequency, v. Both of the frequencies, v and have to be within the bandwidth of the cavity, so that 1 MHz. Usually... [Pg.266]

This framework is too simple, however, to explain the detailed dynamics occurring in the boundary layer. For example, it does not explain during which part of the turbulent motion outside the sublayer the molecules expand, and how the expanded molecules are distributed. Prediction of the bursting period and large eddy sizes have not yet been made. [Pg.21]

The ability of fatty acids to destabilize LHC depends on the length of their hydrocarbon chain. Little destabilizing effect was observed for fatty acids with 12 or less carbon atoms (length of the expanded molecule up to 15 X Ref.5) whereas fatty acids with 14 to 18 carbon atoms (17.6 to 22 8) caused significant destabilization. Two properties of the intact LHC have been used to assay destabilization ... [Pg.1206]

Since the presence of an imide ring in a linear polymer chain 1, stiffens the chain to produce an expanded molecule in solution and 2, introduces a 2-chain, ladder-like unit to withstand shear stress, structures containing this ring system have been synthesized and tested (9). [Pg.31]

If the effective circular cross section of the molecule for collisions has diameter p, two molecules will collide if their centers come within a distance p of each other. If we now imagine that all of the molecules except one (which we will call X) shrink to points, X will still collide with the other molecules when they come within a distance p of each other provided that we artificially expand the diameter of X to 2p. Now, in unit time the expanded molecule X, which has an artificial radius p, will sweep out a volume vrp c, where c is the average speed of a molecule. Therefore, if there are n point molecules per unit volume, and we assume that all of these molecules are stationary, the number of molecules with which X will collide in unit time will be iTfrcn ... [Pg.52]


See other pages where Expanded molecules is mentioned: [Pg.5]    [Pg.160]    [Pg.148]    [Pg.877]    [Pg.95]    [Pg.160]    [Pg.97]    [Pg.243]    [Pg.3]    [Pg.12]    [Pg.260]    [Pg.118]    [Pg.180]    [Pg.288]    [Pg.626]    [Pg.220]    [Pg.318]    [Pg.320]    [Pg.324]    [Pg.498]    [Pg.241]    [Pg.254]    [Pg.299]    [Pg.139]    [Pg.364]    [Pg.363]    [Pg.366]    [Pg.366]    [Pg.367]    [Pg.109]    [Pg.53]    [Pg.388]   


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Expanded Octet in the PF5 Molecule

Valence shells, molecules with expanded

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