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Alkali metals ionic charge

Ogihara, W. et al., Ionic conductivity of polymer gels deriving from alkali metal ionic liquids and negatively charged polyelectrolytes, Electrochim. Acta, 49,1797,... [Pg.71]

Essentially covalent compounds such as the lithium alkyls. Derivatives of any alkali metal where charge delocalization can occur over several carbon atoms (e. g. triphenylmethyl-sodium, lithium-benzyl) were also considered to be largely ionic in constitution. [Pg.68]

A series of polymer gels derived from alkali metal ionic liquids and negatively charged polyelectrolytes were studied for their ion transport properties. The conductivity observed was mostly in the range of 10 to 10" S/cm at room temperature. The gels showed a decrease in conductivity with increasing polymer fraction. [Pg.436]

The compounds which most nearly fit the clas-sicial conception of ionic bonding are the alkali metal halides. However, even here, one must ask to what extent it is reasonable to maintain that positively charged cations M+ with favourably... [Pg.80]

Many of the ionic fiuorides of M, M and M dissolve to give highly conducting solutions due to ready dissociation. Some typical values of the solubility of fiuorides in HF are in Table 17.11 the data show the expected trend towards greater solubility with increase in ionic radius within the alkali metals and alkaline earth metals, and the expected decrease in solubility with increase in ionic charge so that MF > MF2 > MF3. This is dramatically illustrated by AgF which is 155 times more soluble than AgF2 and TIF which is over 7000 times more soluble than TIF3. [Pg.817]

The nature of the Debye-Hiickel equation is that the activity coefficient of a salt depends only on the charges and the ionic strength. The effects, at least in the limit of low ionic strengths, are independent of the chemical identities of the constituents. Thus, one could use N(CH3)4C1, FeS04, or any strong electrolyte for this purpose. Actually, the best choices are those that will be inert chemically and least likely to engage in ionic associations. Therefore, monovalent ions are preferred. Anions like CFjSO, CIO, /7-CIC6H4SO3 are usually chosen, accompanied by alkali metal or similar cations. [Pg.209]

If the allyl alkali metal compounds are ionic compounds, then if the allyl ion is delocalized the terminal carbons would be equivalent and contain most of the charge, and all three... [Pg.91]

The electrical conductivity of TTF TCNQ is of the order of 10 S m at room temperature and increases with decreasing temperature until around 80 K when the conductivity drops as the temperature is lowered. TCNQ is a good electron acceptor and, for example, accepts electrons from alkali metal atoms to form ionic salts. In TTF-TCNQ, the columns of each type of molecule interact to form delocalised orbitals. Some electrons from the highest energy filled band of TTF move across to partly fill a band of TCNQ, so that both types of columns have partially occupied bands. The number of electrons transferred corresponds to about 0.69 electrons per molecule. This partial transfer only occurs with molecules such as tetrathiafulvalene whose electron donor ability is neither too small nor too large. With poor electron donors, no charge transfer... [Pg.287]

Notice that the oxidation states for the families such as the alkali metals, alkaline earth metals, and so on correspond to the ionic charges those elements have. [Pg.248]


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See also in sourсe #XX -- [ Pg.153 , Pg.163 ]




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