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Particular stoichiometry, effect

Gross stoichiometry variations in these modular systems are often acconunodated by the formation of other series members or the incorporation of planar faults, often equivalent to isolated lamellae of other series members, into the structure. However, many individual phases also show composition variation which is sometimes accommodated by random populations of point defects and in other phases by ordering and the generation of new structures. In both cases composition flexibility is important in influencing the physical and chemical properties of these materials. In particular this effect has been well studied in the cuprate superconductors, where changes in composition have repercussions for the superconducting transition temperature, r, of the phase. [Pg.146]

Strained set of lattice parameters and calculating the stress from the peak shifts, taking into account the angle of the detected sets of planes relative to the surface (see discussion above). If the assumed unstrained lattice parameters are incorrect not all peaks will give the same values. It should be borne in mind that, because of stoichiometry or impurity effects, modified surface films often have unstrained lattice parameters that are different from the same materials in the bulk form. In addition, thin film mechanical properties (Young s modulus and Poisson ratio) can differ from those of bulk materials. Where pronounced texture and stress are present simultaneously analysis can be particularly difficult. [Pg.217]

Numerous investigators have attempted to control the precursor structure and related solution chemistry effects with varying degrees of success, to influence subsequent processing behavior, such as crystallization tempera-ture.40-42,78,109 110 Particular attention has been given to precursor characteristics such as structural similarity to the desired product and the chemical homogeneity of the precursor species. For multicomponent films, this latter factor is believed to influence the interdiffusional distances associated with the formation of complex crystal structures, such as perovskite compounds. Synthetic approaches have been geared toward the preparation of multimetal species with cation stoichiometry identical to that of the desired crystalline phase.40 42 83 84... [Pg.57]

Unfortunately, OH and O concentrations in flames are determined by detailed chemical kinetics and cannot be accurately predicted from simple equilibrium at the local temperature and stoichiometry. This is particularly true when active soot oxidation is occurring and the local temperature is decreasing with flame residence time [59], As a consequence, most attempts to model soot oxidation in flames have by necessity used a relation based on oxidation by 02 and then applied a correction factor to augment the rate to approximate the effect of oxidation by radicals. The two most commonly applied rate equations for soot oxidation by 02 are those developed by Lee el al. [61] and Nagle and Strickland-Constable [62],... [Pg.547]

The consequences of histone HI elimination in Tetrahymena and in the three species of fungi are consistent with the interpretation that linker histones do not have a role which is essential for the normal life-cycle of these organisms including sexual reproduction. Indeed, it has been reported that in yeast the HI occurs with a stoichiometry of about one molecule per 37 nucleosomes showing a preferential association with rDNA sequences [126]. The analyses of the effects of HI loss on transcription, particularly in Tetrahymena and yeast, provide strong... [Pg.92]

ID-ROESY studies performed on the complex between (+)-BrPh and /3-CD in solution did not allow one to explain the NOE effect observed on the protons of the maleate counteranion (70). X-ray crystallographic studies performed on the monocrystals obtained from a 1 1 aqueous solution of (+)-BrPh maleate and /3-CD (Fig. 8) provide a plausible explanation for the contradiction maintained in Ref. 70. In particular, as shown in Fig. 8, (+)-BrPh forms with /3-CD, at least in the solid state, not a 1 1 complex but a complex with 1 2 stoichiometry. In this complex the (+)-BrPh molecule is sandwiched between two molecules of /3-CD. The 4-bromophenyl moiety of (+)-BrPh enters the cavity of one of the /3-CD molecules, whereas the cavity of another /3-CD molecule is occupied by the maleate counteranion. Thus, X-ray crystallography may provide useful information on the supra-molecular structure of the selector-selectand complexes and in this way complement well ID-ROESY data. However, the aforementioned possible differences between the structure of the complexes in solution and in the solid phase must be considered. [Pg.214]


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See also in sourсe #XX -- [ Pg.393 , Pg.394 , Pg.395 ]




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