Aniodate is the polyatomic anion with the formula IO−3. It is the most common form of iodine in nature, as it comprises the major iodine-containing ores.[1] Iodate salts are often colorless. They are the salts of iodic acid.
The iodate anion, IO−3 | |
Space-filling model of the iodate anion | |
Identifiers | |
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3D model (JSmol) |
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ChEBI |
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ChemSpider | |
1676 | |
PubChem CID |
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UNII | |
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Properties | |
IO3− | |
Molar mass | 174.902 g·mol−1 |
Related compounds | |
Related compounds |
Periodate, Fluoroiodate, Bromate, Chlorate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Iodate is pyramidal in structure. The O–I–O angles range from 97° to 105°, somewhat smaller than the O–Cl–O angles in chlorate.[2]
Iodate is one of several oxyanions of iodine, and has an oxidation number of +5. It participates in several redox reactions, such as the iodine clock reaction. Iodate shows no tendency to disproportionate to periodate and iodide, in contrast to the situation for chlorate.
Iodate is reducedbysulfite:[1]
Iodate oxidizes iodide:
Similarly, chlorate oxidizes iodide to iodate:
Iodate is also obtained by reducing a periodate with a sulfide. The byproduct of the reaction is a sulfoxide.[3]
Iodate is unusual in that it forms a strong hydrogen bond with its parent acid:[2]
The anion H(IO3)−2 is referred to as biiodate.
Minerals containing iodate are found in the caliche deposits of Chile. The most important iodate minerals are lautarite and brüggenite, but also copper-bearing iodates such as salesite are known.[7]
Natural waters contain iodine in the form of iodide and iodate, their ratio being dependent on redox conditions and pH. Iodate is the second most abundant form in water. It is mostly associated with alkaline waters and oxidizing conditions.[8]
Thioethers can be oxidized to sulfoxides by periodate, and periodate is reduced to iodate