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In chemistry, a (redox) non-innocent ligand is a ligand in a metal complex where the oxidation state is not clear. Typically, complexes containing non-innocent ligands are redox active at mild potentials. The concept assumes that redox reactions in metal complexes are either metal or ligand localized, which is a simplification, albeit a useful ...
Illustration of a redox reaction Sodium chloride is formed through the redox reaction of sodium metal and chlorine gas. Redox reactions can be understood in terms of the transfer of electrons from one involved species (reducing agent) to another (oxidizing agent). In this process, the former species is oxidized and the latter is reduced. Though ...
Electron transfer reactions are central to myriad processes and properties in soils, and redox potential, quantified as Eh (platinum electrode potential relative to the standard hydrogen electrode) or pe (analogous to pH as -log electron activity), is a master variable, along with pH, that controls and is governed by chemical reactions and ...
A redox gradient is a series of reduction-oxidation reactions sorted according to redox potential. [ 4 ] [ 5 ] The redox ladder displays the order in which redox reactions occur based on the free energy gained from redox pairs.
True organic redox chemistry can be found in electrochemical organic synthesis or electrosynthesis. Examples of organic reactions that can take place in an electrochemical cell are the Kolbe electrolysis. [3] In disproportionation reactions the reactant is both oxidised and reduced in the same chemical reaction forming two separate compounds.
Reductive elimination is an elementary step in organometallic chemistry in which the oxidation state of the metal center decreases while forming a new covalent bond between two ligands. It is the microscopic reverse of oxidative addition , and is often the product-forming step in many catalytic processes.
In outer sphere redox reactions no bonds are formed or broken; only an electron transfer (ET) takes place. A quite simple example is the Fe 2+ /Fe 3+ redox reaction, the self exchange reaction which is known to be always occurring in an aqueous solution containing the aquo complexes [Fe(H 2 O) 6] 2+ and [Fe(H 2 O)6] 3+.
Although nitrous acid is located above nitrate in the redox scale and so is a stronger oxidant than nitrate, the Gibbs free energy of the half-reaction for nitrate reduction is more important (∆G° < 0 indicates an exothermic reaction releasing energy) because of the larger number (n) of electrons transferred in the half-reaction (10 versus 6).
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