Extended solids

These include cold drawn, high pressure oriented chain-extended, solid slate extruded, die-drawn, and injection moulded polymers. Correlation of hardness to macroscopic properties is also examined. In summary, microhardness is shown to be a useful complementary technique of polymer characterization providing information on microscopic mechanical properties. 

Compounds isotypic with the k phases arc found among intcrmetallics, borides, carbides and oxides and also with silicides, germanides, arsenides, sulfides and sclcnides no nitrides, however, are found. The mode of filling the various voids in the metal host lattice of the k phases follows the schemein Ref. 4 and is presented in Table 1 for all those compounds for which the atom distribution is well known from x-ray or neutron diffraction. Accordingly, B atoms in tc-borides, Zr, Mo, W, Re)4B and Hfy(Mo, W, Re, Os)4B , occupy the trigonal prismatic interstices within the parent metal framework of a Mn, Aln,-type structure (see Table 1 see also ref. 48). Extended solid solutions are found for (Hf, Al)[Pg.140]

Hughbanks T, Hoffmann R (1983) Molybdenum chalcogenides Clusters, chains, and extended solids. The approach to bonding in three dimensions. J Am Chem Soc 105 1150-1162... 

Extended solid state n systems facilitate CT, particularly when doped [4-6]. The analogy between DNA and conductive solid state -stacks therefore establishes that a requisite condition for CT may exist in DNA. DNA contains an array of heterocyclic aromatic base pairs, stacked at a distance of 3.4 A, wrapped within a negatively charged sugar phosphate backbone [7] (Fig. 1). The interactions between the n electrons of the DNA base pairs provide the electronic coupling necessary for CT to occur. 

In the field of porous supramolecular metal complexes, both molecular and extended-solid materials have been extensively studied in recent years. A particularly well-studied class of compounds is the metal-containing molecular squares, that is, square-shaped porous tetrameric structures (30,108). These have been prepared by several approaches, the most common being the reaction of an organic bridging ligand with a metal complex that has available cis-coordination sites (109-113) (Fig. 13). However, the resulting metal centers are usually coordinatively saturated, which makes it difficult for guest molecules to interact directly with the metal atoms. 

Surface catalysis. As the name implies, surface catalysis takes place on the surface atoms of an extended solid. This often involves different properties for the surface atoms and hence different types of sites (unlike molecular catalysis, in which all the sites are equivalent). Because the catalyst is a solid, surface catalysis is by nature heterogeneous (see (6) below). The extended nature of the surface enables reaction mechanisms different from those with molecular catalysts. 

First rule Effect of the size factor. If the atomic sizes of the two components differ more than 15%, extended solid solution formation is not expected. 

A few general remarks about a group of metal-hydrogen phases have been included in 3.8.4.1 where interstitial hydrogen solutions in metallic structures have been described. However, as previously observed, a number of intermediate phases are also formed in several systems. A short summary of these is shown in Table 5.2 where their formulae very often have only an indicative character and several structure types correspond to more or less extended solid solution ranges. 

Remarks on the alloy crystal chemistry of the 4th group metals. Selected groups of isostructural phases, pertaining to simple common structural types have been collected in Table 5.25. A number of them (for instance CsCl, AuCu types, Laves phases, AuCu3 type) correspond to more or less extended solid solution... 

According to the U.S. National Nanotechnology Institute, nanotechnology encompasses research and development to synthesize, control, and manipulate stmctures, devices, and systems of novel properties and functions because of their size at the atomic, molecular, or macromolecular levels in the length scale ranging from approximately 1 to 100 nanometers. Indeed, this length scale is of particular relevance to heterogeneous catalysis, where the active sites are small crystallites or domains of the active phase. The reaction typically involves atom-molecule interactions, and the active sites are placed in or on an extended solid where the access paths to the active sites are tens to hundreds of nanometers. The issue of access path is a familiar territory in... 

The concept of phonons describing vibrations in extended solids is a core topic in solid-state physics. Two classic books for this field are ... 

Metal-metal bonding in transition metal complexes of low nuclearity (i.e., with only a few metal atoms) tends to be more directed and therefore stronger than the bonding in metals discussed in chapter 11. Accordingly, the metal-metal bonds in transition metal complexes are often localized and considerably shorter than those in most extended solids. Charge accumulations are frequently observed in metal-metal bonding regions of deformation density maps. 

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