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Oxygen arrangement

Fig. 2.23 Shear operation (250)5[2il] on structure (b) of Fig. 2.19. (a) The oxygen arrangement on the shear plane (250). The oxygens marked are removed, (b) After removing oxygens on the shear plane, each slab is separated by the vector [010] of ReOj for visualization. Note that special consideration is taken in order to form the block structure. The marks 0 and O denote the oxygen vacancies derived from the shear operation and from the separation of the slabs for visualization, respectively, (c) On closing up the slabs by the shear vector 2[211], a new type of block structure is obtained. By supplying oxygen to oxygen vacancies (O), tetrahedral sites for metals (x) are possible. Fig. 2.23 Shear operation (250)5[2il] on structure (b) of Fig. 2.19. (a) The oxygen arrangement on the shear plane (250). The oxygens marked are removed, (b) After removing oxygens on the shear plane, each slab is separated by the vector [010] of ReOj for visualization. Note that special consideration is taken in order to form the block structure. The marks 0 and O denote the oxygen vacancies derived from the shear operation and from the separation of the slabs for visualization, respectively, (c) On closing up the slabs by the shear vector 2[211], a new type of block structure is obtained. By supplying oxygen to oxygen vacancies (O), tetrahedral sites for metals (x) are possible.
The sulfite anion is pyramidal, with the three oxygens arranged around the sulfur apex. In Na2S03 the O-S distance is 1.39 A. Detailed bonding information has been discussed in a review of sulfite spectroscopy by Verma1 which also classifies sulfites according to bonding ionic or covalent. [Pg.68]

Procure all the supplies before attempting to prepare the oxygen. Arrange the apparatus as shown in Fig. 25, and collect the gas ovex... [Pg.24]

Simple ethers are usually assigned common names. To do so, name both alkyl groups bonded to the oxygen, arrange these names alphabetically, and add the word ether. For symmetrical ethers, name the alkyl group and add the prefix di-. [Pg.318]

Layer lattices, which are uncommon among oxides, indicate a predominantly covalent character in the metal-oxygen bonds. SnO and PbO are solids of this type. Each metal atom is joined to four oxygens arranged in a square on one side of it (Fig. 196). [Pg.376]

Fig. 6. Diffraction pattern, at 72 volts or 1.44 A., from the nickel surface covered by atoms of oxygen arranged in the 4-Structure (Fig. 7), the same surface which gave the pattern of Fig. 5. The single spot at the top is a (511) Laue diffraction beam from the nickel lattice. Fig. 6. Diffraction pattern, at 72 volts or 1.44 A., from the nickel surface covered by atoms of oxygen arranged in the 4-Structure (Fig. 7), the same surface which gave the pattern of Fig. 5. The single spot at the top is a (511) Laue diffraction beam from the nickel lattice.
By reference to degradative work of Horii and collaborators (Section II, A, 2) these spectral data were only compatible with a cis C-lla— C-llb —OH structure, 154. On this basis phyllanthine should possess a securinine-type (trans C-2-H-C-9-lactone oxygen) arrangement as indicated and not the allosecurinine (cis C-2-H-C-9 lactone oxygen) structure. It was also observed that the relative rate of methiodide formation of allosecurinine is about 8 times faster than that for phyllanthine (41a) but previous discussion (Section II, G) deems tenuous any stereochemical significance which would be placed on this result. [Pg.483]

Another new series of oxyhalides, M M6Xi303, is based on an isomeric M6X 90 3X6 unit.f The three oxygens, arranged in inner position, are now adjacent around the cluster, one located on the twofold axis and the two others related to one another by this axis. In these compounds, the units are linked together by four apical apical halogen bridges to form helices of units this series is not covered by this review. These oxyhalides also have a VEC of 14. [Pg.1573]

In contrast to rutile, anatase [145] and brookite [146] are derived from distorted cubic close-packed oxygen arrangements in which again half the octahedral voids are filled by titanium atoms. The voids are filled in such a way, that the octahedra... [Pg.34]

Fig. 2. Oxygen arrangement around the thorium atom in Th(N03)4- SHjO as viewed in the b direction. Fig. 2. Oxygen arrangement around the thorium atom in Th(N03)4- SHjO as viewed in the b direction.
In YBCO, Co substitutes predominantly at the chain (Cu( I)) site. Despite this restriction, Mossbauer spectra appear to be very complicated, mainly due to variable local oxygen arrangements around Co (and therefore the nucleogenic Fe) atoms situated at Cu( I). Furthermore, it is not only one particular spectrum that is complicated, but thermal treatments changing the oxygen stoichiometry of the compound make it even more complex. [Pg.395]

Stereoscopic drawing of the oxygen arrangement around thorium in Th(N03)4 5H20 as viewed along the Th-0(1) bond [19]. [Pg.76]


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Oxygen atoms, spatial arrangement

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