Crystal axial

The ambiguity involved in assigning the absolute configuration of a chiral molecule in a chiral crystal is presented in Scheme 1. Scheme la depicts a chiral molecule of, say, configuration S, with individual atomic coordinates — x — y - z, (i = 1,. . . , n, for n atoms) in a crystal axial system a,b,c. Scheme 1 b represents the enantiomeric crystal structure containing a molecule of configuration... 

Finally, reference should be made to copolymerization in this series. The diacetylene 142 is (homo)-polymerizable by high-energy radiation, whereas 143, though structurally very similar, is not. This difference in reactivity is apparently due to the difference between the crystal axial lengths in the direction in which polymerization would be expected to proceed this length is 4.37 A for 142 and 4.55 A for 143 (216). The two monomers are miscible in all proportions in the... 

Hydrite Properties well-crystallized, axial ratio 10 1, narrow particle size distribution, equivalent spherical particle size 550 nm [2263],... 

FIGURE 10 Variation of measured crystal axial growth rates with temperature over a period of 3 min following ice crystal nucle-ation. [Adapted from Ryan, B. F., Wishart, E. R., and Shaw, D. E. (1976). J. Atm. Sci. 33, 842-851. Courtesy of the American Meteorological Society and the lead author.]... 

FIGURE 12 Variation of calculated crystal axial growth rates with temperature over a period of --3 min following ice crystal nucleation. 

This is because on one hand, heav wave is weaker and on the other hand, photoelastic testing method is unfavorable for observing the sound field of axial symmetry. The sound field (see Fig.4) excited by strip ciystal in solid is observed with photoelastic testing method. The wavefront of head wave can be see in Fig.4, which is a circumstantial evidence of wavefront of head wave excited just by point-shape crystal. We can calculate... 

A dense-bed center-fed column (Fig. 22-li) having provision for internal crystal formation and variable reflux was tested by Moyers et al. (op. cit.). In the theoretical development (ibid.) a nonadiabatic, plug-flow axial-dispersion model was employed to describe the performance of the entire column. Terms describing interphase transport of impurity between adhering and free liquid are not considered. 

Compounds in which conformational, rather than configurational, equilibria are influenced by the anomeric effect are depicted in entries 4—6. Single-crystal X-ray dilfiaction studies have unambiguously established that all the chlorine atoms of trans, cis, ira j-2,3,5,6-tetrachloro-l,4-dioxane occupy axial sites in the crystal. Each chlorine in die molecule is bonded to an anomeric carbon and is subject to the anomeric effect. Equally striking is the observation that all the substituents of the tri-0-acetyl-/ -D-xylopyranosyl chloride shown in entry 5 are in the axial orientation in solution. Here, no special crystal packing forces can be invoked to rationalize the preferred conformation. The anomeric effect of a single chlorine is sufficient to drive the equilibrium in favor of the conformation that puts the three acetoxy groups in axial positions. 

Y. Y. Khine, J. S. Walker. Thermoelectric magnetohydrodynamic effects during Bridgman semiconductor crystal growth with a uniform axial magnetic field. J Cryst Growth 7 5 150, 1998. 

Conversely, when A-alkyl tryptophan methyl esters were condensed with aldehydes, the trans diastereomers were observed as the major products." X-ray-crystal structures of 1,2,3-trisubstituted tetrahydro-P-carbolines revealed that the Cl substituent preferentially adopted a pseudo-axial position, forcing the C3 substituent into a pseudo-equatorial orientation to give the kinetically and thermodynamically preferred trans isomer." As the steric size of the Cl and N2 substituents increased, the selectivity for the trans isomer became greater. A-alkyl-L-tryptophan methyl ester 42 was condensed with various aliphatic aldehydes in the presence of trifluoroacetic acid to give predominantly the trans isomers. ... 

On the other hand, in the single crystals prepared from equivalent amounts of heterochiral 1 1 complexes, a pair of two heterochiral 1 1 complexes are incorporated in a unit cell to form a layered structure with alternate layer distances of 7.33 and 7.6 A. Two perchlorate ions stay in the narrower gap, and two additional acetone molecules as crystallization solvent occupy the wider gap. The perchlorate ions interact with two axial water ligands by hydrogen bonds (3.71 and 3.77 A) to construct a layered structure. The adjacent two molecules of heterochiral 1 1 com-... 

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