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Radii compounds

Apart from the well-known donor (or ligand) atoms such as C, N, O, F, and Cl, an increasing number of higher-coordinated silicon compounds with hydrogen, on the one hand, and heavy nonmetal as well as main group and transition metal donor atoms, on the other hand, have been reported. The latter may be separated into species without any bonding or donor-acceptor interaction (but distances below the sum of the van der Waals radii), compounds containing silicon atoms which act as electron pair acceptors as well as species where the Si is the Lewis donor. [Pg.94]

Radius-edged Double radius Bevel and radius (compound cup) (convex with bevel... [Pg.3790]

The co-ordination number in ionic compounds is determined by the radius ratio - a measure of the necessity to minimize cationic contacts. More subtle effects are the Jahn-Teller effect (distortions due to incomplete occupancy of degenerate orbitals) and metal-metal bonding. [Pg.416]

The small lithium Li" and beryllium Be ions have high charge-radius ratios and consequently exert particularly strong attractions on other ions and on polar molecules. These attractions result in both high lattice and hydration energies and it is these high energies which account for many of the abnormal properties of the ionic compounds of lithium and beryllium. [Pg.134]

CompoundShrinka.g e. In its simplest form (Fig. 8a) compound shrinkage consists of machining the inner radius of an outer component I, (Qp so that it is smaller than the outer radius of an inner component II, The difference between the two is known as the radial interference 5. To assemble the cylinders, outer component I is heated and/or inner component II cooled so that the outer component can be sHpped over the inner as shown in Figure 8b. When the temperature of the assembly returns to ambient, a compressive stress (pressure) is generated across the interface which simultaneously compresses the inner and expands the outer component and, in so doing, displaces radius (r/j by Uj and radius ( jj by U, Unfortunately, it is difficult to carry out this operation without setting up stresses in the axial direction (32). [Pg.82]

The residual shear stress distribution in the assembled cylinders, prior to the appHcation of internal pressure, may be calculated, from pressure P, generated across the interface. The resulting shear stress distribution in the compound cylinder, when subjected to an internal pressure may be calculated from the sum of the residual stress distribution and that which would have been generated elastically in a simple cylinder of the same overall radius ratio as that of the compound cylinder. [Pg.82]

In practice compound shrinkage is often used to prestress a high strength or corrosion-resistant liner. The optimum radius ratios of components of different yield strengths have been shown (37,38) to be... [Pg.83]

Physical Properties. The absorption of x-rays by iodine has been studied and the iodine crystal stmcture deterrnined (12,13). Iodine crystallizes in the orthorhombic system and has a unit cell of eight atoms arranged as a symmetrical bipyramid. The cell constants at 18°C (14) are given in Table 1, along with other physical properties. Prom the interatomic distances of many iodine compounds, the calculated effective radius of the covalently bound iodine atom is 184 pm (15). [Pg.358]

The most common oxidation state of niobium is +5, although many anhydrous compounds have been made with lower oxidation states, notably +4 and +3, and Nb can be reduced in aqueous solution to Nb by zinc. The aqueous chemistry primarily involves halo- and organic acid anionic complexes. Virtually no cationic chemistry exists because of the irreversible hydrolysis of the cation in dilute solutions. Metal—metal bonding is common. Extensive polymeric anions form. Niobium resembles tantalum and titanium in its chemistry, and separation from these elements is difficult. In the soHd state, niobium has the same atomic radius as tantalum and essentially the same ionic radius as well, ie, Nb Ta = 68 pm. This is the same size as Ti ... [Pg.20]

For halides the cation should have a charge of 2+ rather than 4+ for tetrahedral coordination. The only fluoride compound capable of containing two-coordinate F and four-coordinate cations is Bep2. For ZrF, the radius ratio rule predicts that Zr" " is eight-coordinate if all fluorine atoms are two - c o o rdinate. [Pg.331]

In addition to the Zachariasen and radius ratio rules, for oxides the electronegativity of the predominant cation should be between 1.7 and 2.1 (7). If the cation electronegativity is too high, the compound tends to form molecules or discrete polyatomic ions rather than a connected network. For example, CrO satisfies the radius ratio rule, but the highly electronegative Cr ions promote the formation of discrete dichromate(VI) ions, Cr202 , in the presence of other oxides. [Pg.331]

Modifiers in glass are compounds that tend to donate anions to the network, whereas the cations occupy "holes" in the disordered stmcture. These conditions cause the formation of nonbridging anions, or anions that are connected to only one network-forming cation, as shown in Figure 2. Modifier compounds usually contain cations with low charge-to-radius ratios (Z/r), such as alkali or alkaline-earth ions. [Pg.331]

The strain energies of these five-membered heterocycles are relatively small with values of 23.5, 24.8 and S.SkJmoF estimated for tetrahydrofuran, pyrrolidine and tetrahy-drothiophene respectively (74PMH(6)199). The closeness of the values for the two former compounds reflects the almost identical covalent radii of oxygen (0.66 A) and nitrogen (0.70 A) atoms. The sulfur atom with a much larger covalent radius of 1.04 A causes a... [Pg.27]

Umesi-Danner They developed an equation for nonaqueous solvents with nonpolar and polar solutes. In all, 258 points were involved in the regression. Rj is the radius of gyration in A of the component molecule, which has been tabulated by Passut and Danner for 250 compounds. The average absolute deviation was 16 percent, compared with 26 percent for the Wilke-Chang equation. [Pg.597]

Radium, the last element in the group, was isolated in trace amounts as the chloride by P. and M. Curie in 1898 after their historic processing of tonnes of pitchblende. It was named by Mme Curie in allusion to its radioactivity, a word also coined by her (Latin radius, a ray) the element itself was isolated electrolytically via an amalgam by M. Curie and A. Debieme in 1910 and its compounds give a carmine-red flame test. [Pg.108]

Table 5.1 lists some of the atomic properties of the Group 2 elements. Comparison with the data for Group 1 elements (p. 75) shows the substantial increase in the ionization energies this is related to their smaller size and higher nuclear charge, and is particularly notable for Be. Indeed, the ionic radius of Be is purely a notional figure since no compounds are known in which uncoordinated Be has a 2- - charge. In aqueous solutions the reduction potential of... [Pg.111]

As a result of these effects, anions in general are larger than cations. Compare, for example, the Cl- ion (radius = 0.181 nm) with the Na+ ion (radius = 0.095 nm). This means that in sodium chloride, and indeed in the vast majority of all ionic compounds, most of the space in the crystal lattice is taken up by anions. [Pg.154]

Since hydrofluoride synthesis is based on thermal treatment at relatively high temperatures, the possibility of obtaining certain fluorotantalates can be predicted according to thermal stability of the compounds. In the case of compounds whose crystal structure is made up of an octahedral complex of ions, the most important parameter is the anion-cation ratio. Therefore, it is very important to take in to account the ionic radius of the second cation in relation to the ionic radius of tantalum. Large cations, are not included in the... [Pg.46]

The space group of LnNbF7 compounds is most probably P2j, and the volume of the elementary cell increases linearly with the increase in the Ln3+ ionic radius as reported by Bizot et al. [149]. [Pg.65]


See other pages where Radii compounds is mentioned: [Pg.37]    [Pg.75]    [Pg.366]    [Pg.1446]    [Pg.30]    [Pg.79]    [Pg.121]    [Pg.160]    [Pg.568]    [Pg.242]    [Pg.224]    [Pg.540]    [Pg.21]    [Pg.475]    [Pg.331]    [Pg.158]    [Pg.224]    [Pg.127]    [Pg.55]    [Pg.16]    [Pg.568]    [Pg.299]    [Pg.80]    [Pg.113]    [Pg.114]    [Pg.338]    [Pg.375]    [Pg.382]    [Pg.417]    [Pg.948]    [Pg.961]    [Pg.981]    [Pg.213]    [Pg.34]   
See also in sourсe #XX -- [ Pg.39 , Pg.40 ]




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Compounds, ionic radii

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