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Half shell structure models

Figure 3. Half-shell structure model for organosilicon compounds with different spacers along the C3 symmetric substituent axis and dihedral angles go(X3Y-YX3) determined for the molecular skeletons. Figure 3. Half-shell structure model for organosilicon compounds with different spacers along the C3 symmetric substituent axis and dihedral angles go(X3Y-YX3) determined for the molecular skeletons.
The structural comparison (Fig. 3) with both the twofold tris(trimethylsilyl)methyl substituted acetylene and 1,4-benzene derivatives (Fig. 1) as well as with the literature data [6a] for hexa-kis(rm.butyl)disilane [6b] containing a SiSi bond elongated to 270 pm ( ), for the linear ( ) hexa-kis(rm.butyl)disiloxane [6c] or for di(tris(trimethylsilyl)silyl)zinc [6d] is based advantageously on a model in which the two substituent half-shells are separated along their central C3 axes by spacers of different lengths. [Pg.353]

An ideal study of support effects requires model catalysts with metal particles that are identical in size and shape (so that only the support oxide varies). This is difficult to achieve for impregnated catalysts, but identical metal particles can be prepared via epitaxial model catalysts [36]. Well-faceted Rh nanocrystals were grown on a 100-cm area NaCl(OOl) thin film at 598 K. One half of a Rh/NaCl sample was covered with Al Oj, and the other half with TiO. The preparation of Rh particles for both Al Oj- and TiO -supported model catalysts in a single step prevents any differences in particle size, shape, and surface structure which could occur if the samples were prepared in separate experiments. Three model catalysts were prepared, with a mean Rh particle size of 7.8, 13.3, and 16.7 mn (the films were finally removed from the NaCl substrate by flotation in water). Activation was performed by O /H treatments, with the structural changes followed by TEM (Fig. 15.6). Oxidation was carried out in 1 bar O at 723 K prodncing an epitaxially grown rhodium oxide shell on a Rh core (cf Fig. 15.5e), whereas the hydrogen reduction temperature was varied. [Pg.326]

In O Fig. 19.11 the partial fission half-lives of the doubly even isotopes of uranium and beyond are plotted on a logarithmic time scale versus the fissility parameter. In accordance with the expectation from the liquid drop model the dashed line labeled Bld, describing the fission half-life calculated with only the liquid drop barrier Bid, crosses the 2. line at nobeKum. The time Te. is needed for the formation of the electron shell of the atom, the lower time limit considered beyond which a chemical element cannot be formed (Barber et al. 1992). The experimental half-lives follow this general trend. They decrease from uranium to nobelium over more than 20 orders of magnitude, from the age of the solar system down to fractions of seconds. The structure of the isotopic chains of elements from curium to nobelium is caused by a subshell closure at M = 152. [Pg.900]

Abstract Water ice consists about a half of mass and therefore about 0.75 of volume of most of the icy satellites. Differentiated, with water ice forming outer shells, and undifferentiated models of internal structure of the icy satellites of the giant planets are mentioned. It is stressed that the modelling of the evolution of satellites structure should be supported by laboratory experiments (i) concerning rheology of compaction of icy/mineral granular porous media, and (ii) concerning kinetics of phase transitions of water ice in these media. [Pg.315]


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