High Oxidation State Anion Group

Reactive electrodes refer mostly to metals from the alkaline (e.g., lithium, sodium) and the alkaline earth (e.g., calcium, magnesium) groups. These metals may react spontaneously with most of the nonaqueous polar solvents, salt anions containing elements in a high oxidation state (e.g., C104 , AsF6 , PF6 , SO CF ) and atmospheric components (02, C02, H20, N2). Note that ah the polar solvents have groups that may contain C—O, C—S, C—N, C—Cl, C—F, S—O, S—Cl, etc. These bonds can be attacked by active metals to form ionic species, and thus the electrode-solution reactions may produce reduction products that are more stable thermodynamically than the mother solution components. Consequently, active metals in nonaqueous systems are always covered by surface films [46], When introduced to the solutions, active metals are usually already covered by native films (formed by reactions with atmospheric species), and then these initial layers are substituted by surface species formed by the reduction of solution components [47], In most of these cases, the open circuit potentials of these metals reflect the potential of the M/MX/MZ+ half-cell, where MX refers to the metal salts/oxide/hydroxide/carbonates which comprise the surface films. The potential of this half-cell may be close to that of the M/Mz+ couple [48],... 

This group of compounds includes those containing comer-sharing actinyl polyhedra (Table 11). It is important to remember that coordination polyhedra of actinides in high oxidation states possess two different t es of anions (i) apical anions that are part of the actinyl [An 02] ions and (ii) equatorial anions. If an apical anion of one polyhedron is shared with the other, we deal with the so-called cation-cation interactions. 

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