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Oxygen polyhedra

The oxygen polyhedra (strnctnral nnits) share corners with each other, not edges or faces. [Pg.69]

Fig. 2.5 Shear operation of (130)i[li0] on ReOj-type structure, (a) Arrangement of the oxygen polyhedra of both slabs after the elimination of one sheet of A plane (oxygen only plane). For visualization the two slabs are separated by vector [110]. The mark denotes the point defects of oxygen on plane A, which are produced by operation (2), and the mark x denotes the point defects produced by the separation of the slabs, (b) New structure formed by shear operation (3). By this operation the point defects are annihilated, which results in the occurrence of edge-sharing octahedra near the shear plane. Fig. 2.5 Shear operation of (130)i[li0] on ReOj-type structure, (a) Arrangement of the oxygen polyhedra of both slabs after the elimination of one sheet of A plane (oxygen only plane). For visualization the two slabs are separated by vector [110]. The mark denotes the point defects of oxygen on plane A, which are produced by operation (2), and the mark x denotes the point defects produced by the separation of the slabs, (b) New structure formed by shear operation (3). By this operation the point defects are annihilated, which results in the occurrence of edge-sharing octahedra near the shear plane.
In summary, oxygen associated with Bi is responsible for allylic hydrogen abstraction, whereas oxygen polyhedra around Mo are inserted into the allylic intermediate.962-964 Nitrogen insertion in ammoxidation takes place in a similar way965 on an active site containing Mo=NH instead of Mo=0. [Pg.512]

Fig. 4. Schematic phospholipid membrane cross-section composed of double aggregates of hydrocarbons and oxygen polyhedra. Glycerol is presented schematically the PC -residues have been omitted. The molecular dimensions are based on the Na+0 octahedron (after Matheja and Degens48))... Fig. 4. Schematic phospholipid membrane cross-section composed of double aggregates of hydrocarbons and oxygen polyhedra. Glycerol is presented schematically the PC -residues have been omitted. The molecular dimensions are based on the Na+0 octahedron (after Matheja and Degens48))...
The literature on inorganic open-framework materials abounds in the synthesis and characterization of metal silicates, phosphates and carboxylates. Most of these materials have an organic amine as the template. In the last few years, it has been shown that anions such as sulfate, selenite and selenate can also be employed to obtain organically templated open-framework materials. This tutorial review provides an up-to-date survey of organically templated metal sulfates, selenites and selenates, prepared under hydrothermal conditions. The discussion includes one-, two-, and three-dimensional structures of these materials, many of which possess open architectures, The article should be useful to practitioners of inorganic and materials chemistry, besides students and teachers. The article serves to demonstrate how most oxy-anions can be used to build complex structures with metal-oxygen polyhedra. [Pg.369]

Thorium sulfate. In [HN(CH2)6NH]2[Th2(S04)<,(H20)2]-2H20, XVIII,13 two crystallographically distinct metal-oxygen polyhedra are capped by four sulfate ions in Q2 connectivity to form the Th2S4 unit. The Th(2)09 polyhedra share edges with the S(2)04 tetrahedra to form a sinusoidal chain along the... [Pg.374]

The two-dimensional structures are extended networks formed by the linking of the metal-oxygen polyhedra and the phosphate tetrahedra. These are sheet structures and often resemble those of naturally occurring clay minerals. The sheets are usually anionic and the protonated (cationic) amine molecules, located between the two sheets, render the framework neutral. The two-dimensional structures are intermediates between the one-dimensional chains and the three-dimensional structures, and the literature on phosphate networks contains descriptions of several layered materials, owing to the wide compositional diversity exhibited by them [22-24]. The layered materials are of interest because they act as precursors for the three-dimensional structures. [Pg.220]

The spectra of mixtures 3 and 4 differ from those of mixtures 1 and 2. They practically do not contain bands of Bs, polyhedra at 918 cm . Consequently, silicon atoms in mixtures 3 and 4 are surrounded by oxygen polyhedra of As, type only. The range of the Zr-0 frequencies is dominated by a broad band of Bzr polyhedra at 500 cm", with the absorption bands of Azr polyhedra being weak. The spectmm of mixture 4 differs significantly from the spectrum of mixture 3. The peak of the broad absorption band v(Zr-O) is shifted to lower frequencies by 50 cm". This means that a part of zirconium atoms in mixture 4 has a different composition of the first coordination sphere a number of oxygen atoms in it increases. Only H2O molecules, present in a large excess in mixture 4, can serve as a source of these O atoms. [Pg.94]

Therefore, RE(III)-polycarboxylic acid complexes can be considered as polymeric structures made by edge-sharing rare earth-oxygen polyhedra REOm (m = l- 0) linked together by carbon chains [71],... [Pg.107]

The oxygen polyhedra must share corners, not edges or faces, to form a three-dimensional network. [Pg.210]

The oxygen polyhedra share only comers with each other, neither edges nor faces. [Pg.23]


See other pages where Oxygen polyhedra is mentioned: [Pg.285]    [Pg.291]    [Pg.289]    [Pg.34]    [Pg.34]    [Pg.119]    [Pg.74]    [Pg.148]    [Pg.130]    [Pg.118]    [Pg.155]    [Pg.285]    [Pg.240]    [Pg.190]    [Pg.334]    [Pg.369]    [Pg.420]    [Pg.72]    [Pg.94]    [Pg.95]    [Pg.1524]    [Pg.6430]    [Pg.12]    [Pg.387]    [Pg.106]    [Pg.1102]    [Pg.90]    [Pg.23]    [Pg.24]    [Pg.24]    [Pg.26]    [Pg.121]    [Pg.13]    [Pg.402]    [Pg.1]    [Pg.11]   
See also in sourсe #XX -- [ Pg.9 , Pg.120 , Pg.123 , Pg.125 ]




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Polyhedra

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