In chemistry, a superoxide is a compound that contains the superoxide ion, which has the chemical formula . The systematic name of the anion is dioxide(1−). The reactive oxygen ion superoxide is particularly important as the product of the one-electron redox of dioxygen , which occurs widely in nature.Sawyer, D. T. Superoxide Chemistry, McGraw-Hill, Oxygen (dioxygen) is a diradical containing two unpaired electrons, and superoxide results from the addition of an electron which fills one of the two degenerate molecular orbitals, leaving a charged ionic species with a single unpaired electron and a net negative charge of −1. Both dioxygen and the superoxide anion are free radicals that exhibit paramagnetism. Superoxide was historically also known as " hyperoxide".
The alkali salts of are orange-yellow in color and quite stable, if kept dry. In water, the dissolved disproportionates extremely rapidly (written here for a basic solution):
More generally, the superoxide anion, , is a weak Brønsted base. Its protonated form, hydroperoxyl (), has pKa around 4.8, and superoxide anion predominates at neutral pH:
Potassium superoxide is soluble in dimethyl sulfoxide (facilitated by ) and is stable as long as protons are not available. Superoxide can also be generated in aprotic solvents by cyclic voltammetry.
Superoxide salts also decompose in the solid state, but this process requires heating:
Like hydroperoxyl, superoxide is classified as reactive oxygen species. It is generated by the immune system to kill invading . In , superoxide is produced in large quantities by the enzyme NADPH oxidase for use in oxygen-dependent killing mechanisms of invading pathogens. Mutations in the gene coding for the NADPH oxidase cause an immunodeficiency syndrome called chronic granulomatous disease, characterized by extreme susceptibility to infection, especially catalase-positive organisms. In turn, micro-organisms genetically engineered to lack the superoxide-scavenging enzyme superoxide dismutase (SOD) lose virulence. Superoxide is also deleterious when produced as a byproduct of respiration (most notably by Complex I and Complex III), as well as several other enzymes, for example xanthine oxidase, which can catalyze the transfer of electrons directly to molecular oxygen under strongly reducing conditions. Superoxide has been proposed to mediate long-distance electron transport between Cytochrome c and Complex III through the aqueous solution, which suggests a role for mitochondrial regulation of reactive oxygen species.
Because superoxide is toxic at high concentrations, nearly all aerobic organisms express SOD. SOD efficiently catalyzes the disproportionation of superoxide:
Yeast lacking both mitochondrial and cytosolic SOD grow very poorly in air, but quite well under anaerobic conditions. Absence of cytosolic SOD causes a dramatic increase in mutagenesis and genomic instability. Mice lacking mitochondrial SOD (MnSOD) die around 21 days after birth due to neurodegeneration, cardiomyopathy, and lactic acidosis. Mice lacking cytosolic SOD (CuZnSOD) are viable but suffer from multiple pathologies, including reduced lifespan, liver cancer, muscle atrophy, cataracts, thymic involution, haemolytic anemia, and a very rapid age-dependent decline in female fertility.
Superoxide may contribute to the pathogenesis of many diseases (the evidence is particularly strong for radiation poisoning and hyperoxia injury), and perhaps also to aging via the oxidative damage that it inflicts on cells. While the action of superoxide in the pathogenesis of some conditions is strong (for instance, mice and rats overexpressing CuZnSOD or MnSOD are more resistant to strokes and heart attacks), the role of superoxide in aging must be regarded as unproven, for now. In (yeast, the fruit fly Drosophila, and mice), genetically Gene knockout CuZnSOD shortens lifespan and accelerates certain features of aging: (cataracts, muscle atrophy, macular degeneration, and thymic involution). But the converse, increasing the levels of CuZnSOD, does not seem to consistently increase lifespan (except perhaps in Drosophila). The most widely accepted view is that oxidative damage (resulting from multiple causes, including superoxide) is but one of several factors limiting lifespan.
The binding of by reduced () heme proteins involves formation of Fe(III) superoxide complex.
The derivatives of dioxygen have characteristic O–O distances that correlate with the bond order of the O–O bond.
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