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Absent reflections tables

It is seen for this structure that (100) is a reflection plane, (010) a glide plane with translation a/2, and (001) a glide plane with translation a/2 + bj2. The space group is accordingly Y h—Pman. The absent reflections required by V h are (hOl), h odd, and (M0), h- -k odd. Hassel and Luzanski report no reflections of the second class. However, they list (102) in Table V as s.s.schw. This reflection, if real, eliminates this space group and the suggested structure I believe, however, in view of the reasonableness of the structure and the simple and direct way in which it has been derived, as well as of the fact that although thirty reflections of the type (hOl), h even, were observed, only one apparently... [Pg.419]

The eombination of the information on the Laue group with the analysis of the systematieally absent reflections allows the determination of the so-called Extinction symbol fES). In the International Tables for Crystallography the list of extinetion symbols is given per erystal system. There are 14 ES for the... [Pg.207]

Ashm. 1403. This contains a table of contents which does not reflect the organization of the MS, and in which sections were listed which are absent from the MS. In particular, it lacks the prefatory p es, which may account for why this text is undated. It seems that at some point Forman partially dismantled this treatise without discarding its remnants it has multiple sets of pagination and foliation, and from these it appears that many pages have been excised. [Pg.112]

Table 9.12 compares partial rate factors for substitution by phenyl radical with those for electrophilic bromination. Selectivity is clearly much lower for the radical substitution furthermore, for attacking phenyl radical, nearly all positions in the substituted benzenes are more reactive than in benzene itself, a finding that reflects the tendency for most substituents to stabilize a radical, and thus to lower transition state energy for formation of the cyclohexadienyl intermediate, when compared with hydrogen. The strong polar effects, which cause the familiar pattern of activation and deactivation in the electrophilic substitutions, are absent. One factor that presumably contributes to the low selectivity in radical attack is an early transition state in the addition step, which is exothermic by roughly 20 kcal mole-1.178... [Pg.515]

In Table 7 the effectiveness and corresponding Thiele modulus for the different support materials is given. The particle size for the ASA, SiC>2 and HT supports was taken equal to the sieve fraction. This is a worst-case scenario, since it is far more likely that the particles in the sieve fraction are constructed of several crystallites which contain the relevant pores and Pt particles. Between those crystallites, the pore radii will be very large compared to the pore radius in the support material. Even in this worst case scenario, the effectiveness is still high, close to unity, for all catalysts. This demonstrates that the observed reaction kinetics reflect the intrinsic catalyst properties, since internal diffusion limitations are absent. [Pg.74]

Table III lists strongly bound dimeric and trimeric structures. A number of structures reported in the literature as dimers have not been included in Table III as distances between the monomeric units would constitute an uncharacteristically long bond. This distinction does not suggest that an important electronic interaction is absent within these excluded structures, but instead reflects ambiguity in distinguishing between a weakly joined dimer and a distorted asymmetric stacking arrangement. For almost all dimeric examples, the central metals have formally d5 through d1 electronic configurations. Table III lists strongly bound dimeric and trimeric structures. A number of structures reported in the literature as dimers have not been included in Table III as distances between the monomeric units would constitute an uncharacteristically long bond. This distinction does not suggest that an important electronic interaction is absent within these excluded structures, but instead reflects ambiguity in distinguishing between a weakly joined dimer and a distorted asymmetric stacking arrangement. For almost all dimeric examples, the central metals have formally d5 through d1 electronic configurations.
In Table 7.1, where real and reciprocal cell dimensions, or other distances are related, an orthogonal system is assumed for the sake of simplicity. For nonorthogonal systems, the relationships are somewhat more complicated and contain trigonometric terms (as we saw in Chapter 3), since the unit cell angles must be taken into account. Rotational symmetry is preserved in going from real to reciprocal space, and translation operations create systematic absences of certain reflections in the diffraction pattern that makes them easily recognized. As already noted, because of Friedel s law a center of symmetry is always present in diffraction space even if it is absent in the crystal. This along with the absence of... [Pg.167]


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See also in sourсe #XX -- [ Pg.257 ]




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Absent reflections

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