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Electronegativity of metal atom

The chemical reactivity of metal alkoxides toward hydrolysis and condensation mainly depends on the positive charge of the metal atom 8m and its ability to increase its coordination number N [2]. As a general rule, the electronegativity of metal atoms decreases and their size increases when going down the periodic table, from the top right to the bottom left (Table 1). The chemical reactivity of the corresponding alkoxides toward hydrolysis and condensation then increases. [Pg.4]

Batsanov SS (2001) Electronegativities of metal atoms in crystalline solids. Inorg Mater 37 23-30... [Pg.152]

In the above discussion the effect of difference in electronegativity of unlike atoms on bond length (usually a decrease) has been ignored. There is the possibility also of a small change in bond length between unlike atoms, such as of a metal and a metalloid, that reflects the difference in the nature of the overlapping orbitals, in addition to the effects of partial ionic character and of electron transfer. I believe that a thorough... [Pg.395]

The binary acids of non-metals exhibit periodic trends in their acid strength, as shown in Figure 8.5. Two factors are responsible for this trend the electronegativity of the atom that is bonded to hydrogen, and the strength of the bond. [Pg.383]

Metal atoms are oxidized on interaction with many compounds containing polar bonds R—X. This effect has already been noted in Section III in reactions of metal atoms with arenes containing electronegative substituents. The products of oxidation that can be isolated are of three types, namely, RMX, RM, and R2 + MX unstable organometallic products can be sometimes stabilized by addition of a ligand, L, at low temperatures to give RM(Ln)X or RML . [Pg.78]

This formula determines the sign of the dipole moment. According to the present assumptions, the sign of the adsorption dipole would be determined by the difference of the work function of the metal and the Mulliken electronegativity of the atom to be adsorbed. [Pg.272]

Variation of bond strength with electronegativities of metal ions and ligand donor atoms. [Pg.293]

In general, for second row atoms, the most electronegative atoms are located at the ends of the molecule, corresponding to a minimized repulsion of negative electric poles. Similarly, metal complexes contain a central electropositive atom surrounded by more electronegative ligands. When the electronegativities of the atoms involved are similar, then isomers may occur. One example is aoa and CICIO. [Pg.238]

The type of bonding found in metals is quite different from that in other crystals. As we compare the various main group and transition metals in the periodic table we see only small differences in electronegativity. So, there is little tendency for ionic bonding in metals. The electronic configurations of metal atoms, even in the transition metals, do not have nearly-filled subshells, so there is little tendency to form covalent bonds by sharing electrons to achieve a stable octet. The familiar classical models of chemical bonding (see Chapter 3) do not extend to metals. [Pg.876]

The spectra of different molecules that are related by substitution of atoms down a group of the periodic table is another common example where ligand replacements can yield significant electronic structure information. For instance, two molecules may be the same except for the replacement of a chlorine atom by a bromine atom, or the replacement of an oxygen by a sulfur. The first effect observed from such a replacement is the altered stability of the ionizations caused by the different stability (electronegativity) of the atomic orbitals. Incorporation of a third row transition metal or heavy... [Pg.272]


See other pages where Electronegativity of metal atom is mentioned: [Pg.85]    [Pg.4501]    [Pg.4500]    [Pg.662]    [Pg.1016]    [Pg.146]    [Pg.136]    [Pg.85]    [Pg.4501]    [Pg.4500]    [Pg.662]    [Pg.1016]    [Pg.146]    [Pg.136]    [Pg.37]    [Pg.206]    [Pg.129]    [Pg.559]    [Pg.15]    [Pg.119]    [Pg.166]    [Pg.502]    [Pg.504]    [Pg.175]    [Pg.279]    [Pg.263]    [Pg.67]    [Pg.337]    [Pg.445]    [Pg.72]    [Pg.58]    [Pg.6235]    [Pg.705]    [Pg.37]    [Pg.184]    [Pg.42]    [Pg.206]    [Pg.38]    [Pg.225]    [Pg.58]    [Pg.663]    [Pg.37]    [Pg.872]    [Pg.42]    [Pg.15]    [Pg.484]   
See also in sourсe #XX -- [ Pg.1016 ]




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