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Oxidation states, metal ions

A chain mechanism is proposed for this reaction. The first step is oxidation of a carboxylate ion coordinated to Pb(IV), with formation of alkyl radical, carbon dioxide, and Pb(III). The alkyl radical then abstracts halogen from a Pb(IV) complex, generating a Pb(IIl) species that decomposes to Pb(II) and an alkyl radical. This alkyl radical can continue the chain process. The step involving abstraction of halide from a complex with a change in metal-ion oxidation state is a ligand-transfer type reaction. [Pg.726]

Electron transport in cytochromes occurs by direct electron transfer between Fe2+ and Cu+ in cytochromes a and a3. These changes in metal-ion oxidation state lead to changes in the visible absorption spectra of the cytochromes spectrophotometric measurement of these changes allows quantification of the electron flow. [Pg.405]

Actinide complexes rarely follow the conventional rules, for example, 18-electron rule, typically found in inorganic and coordination chemistry of the transition metals. A prime example of the difference in actinide chemistry is the pervasiveness of the linear dioxo rmit, which is immatched in transition metal chemistry. For the actinides, the trans dioxo structure is maintained through different metal ions, oxidation states, and valence electron cormts, for example,... [Pg.10]

Further, oxides that are characterized by the possibility of metal ion reduction without oxide state modification have the greatest ability to promote oxidizing dehydrogenation processes. Oxide such as Iu203 is inclined to the changing of the metal ion oxidizing state In(III) In(II), while the oxide phase remains original. Due to this fact, sensors based on heterojunction oxide composites show considerable response to alcohol vapors (methanol, ethanol). The heterojunction between an oxide and solid solution phases appears to be very active in both adsorption and oxidation of alcohol. [Pg.250]

The magnitude of Aq is dependent on three factors such as the nature of the ligands, the charge on the metal ion (oxidation state), and from what row the transition metal comes from (first, second, or third). [Pg.216]

The contribution from each reaction varies with acidity but the major product is [CrS2HFe] + in which the metal-ion oxidation states are ambiguous. A dependence on IH+] in the experimental rate law... [Pg.70]


See other pages where Oxidation states, metal ions is mentioned: [Pg.193]    [Pg.465]    [Pg.760]    [Pg.81]    [Pg.452]    [Pg.27]    [Pg.121]    [Pg.740]    [Pg.38]    [Pg.471]    [Pg.479]    [Pg.531]    [Pg.446]    [Pg.43]    [Pg.244]    [Pg.440]    [Pg.51]   
See also in sourсe #XX -- [ Pg.4 ]




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Low oxidation state metal ion

Metal ions oxidation

Metal oxidation state

Metal states

Metallic state

Oxidation states of transition metal ions

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