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Hypobromite

From Wikipedia, the free encyclopedia
Ion, and compounds containing the ion
Hypobromite
Names
IUPAC name
hypobromite
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
1040
  • InChI=1S/BrO/c1-2/q-1 checkY
    Key: JGJLWPGRMCADHB-UHFFFAOYSA-N checkY
  • [O-]Br
Properties
BrO
Molar mass95.904 g/mol
Conjugate acidHypobromous acid
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Chemical compound

Thehypobromiteion, also called alkalinebromine water, is BrO. Bromine is in the +1oxidation state. The Br–O bond length is 1.82 Å.[1] Hypobromite is the bromine compound analogous tohypochlorites found in common bleaches, and in immune cells. In many ways, hypobromite functions in the same manner as hypochlorite, and is also used as a germicide and antiparasitic in both industrial applications, and in the immune system.

Preparation

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Hypobromite salts form upon treating bromine with aqueous alkali, such as sodium or potassium hydroxide. At 20 °C the reaction is rapid.[2]

Br2 + 2 OH(aq) → Br + BrO + H2O

In this reaction the brominedisproportionates (some undergoes reduction and some oxidation) from oxidation state 0 (Br2) to oxidation state −1 (Br) and oxidation state +1 (BrO).Sodium hypobromite can be isolated as an orange solid.

A secondary reaction, where hypobromite spontaneously disproportionates tobromide (bromine oxidation state −1) andbromate (bromine oxidation state +5) takes place rapidly at 20 °C and slowly at 0 °C.

3 BrO → 2 Br +BrO
3

Hence, in reaction 2, the formation and proportions of the −1, +1 and +5 bromine oxidation state products can be controlled by temperature. Hypobromite is not thermodynamically stable at any pH (see Pourbaix diagram for bromine athttp://www.eosremediation.com/download/Chemistry/Chemical%20Properties/Eh_pH_Diagrams.pdf ), but it is kinetically locked toward a further disproportion into bromate and bromide above the pKa of HBrO.

These reactions of bromine are analogous to those of chlorine forminghypochlorite andchlorate. The corresponding chlorine reaction 1 (to form ClO) is fast at 20 °C and reaction 2 (to formClO
3
) is slow at 20 °C and fast at 70 °C.

Compounds

[edit]

A hypobromite is a compound that contains this anion. Examples includesodium hypobromite andpotassium hypobromite.

In nature and industry

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Bromide from the diet, naturally present in the blood, is used byeosinophils, white blood cells of the granulocyte class, specialized for dealing with multi-cellular parasites. These cells react the bromide with peroxide to generate hypobromite by the action ofeosinophil peroxidase, ahaloperoxidase enzyme which preferentially uses bromide over chloride for this purpose.[3]

Simple bromide salts (such as sodium bromide) are also sometimes used inhot tubs and spas as mild germicidal agents, using the action of an added oxidizing agent (such as hydrogen peroxide) to generatein situ hypobromite, in a similar fashion to the action of peroxidase on bromide in eosinophils.

Hypobromite has been proposed to be a reactive intermediate in theHofmann rearrangement.

See also

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Other bromine anions:

Bromine oxidation state−1+1+3+5+7
Namebromidehypobromitebromitebromateperbromate
FormulaBrBrOBrO
2
BrO
3
BrO
4
StructureThe bromide ionThe hypobromite ionThe bromite ionThe bromate ionThe perbromate ion

References

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  1. ^Topić, Filip; Marrett, Joseph M.; Borchers, Tristan H.; Titi, Hatem M.; Barrett, Christopher J.; Friščić, Tomislav (2021). "After 200 Years: The Structure of Bleach and Characterization of Hypohalite Ions by Single-Crystal X-Ray Diffraction".Angew. Chem. Int. Ed.60 (46):24400–24405.doi:10.1002/anie.202108843.
  2. ^Kneen; Rogers; Simpson (1972). "The Halogens".Chemistry. Facts, Patterns and Principles. Addison-Wesley.ISBN 0-201-03779-3.
  3. ^Mayeno, A N; Curran, A J; Roberts, R L; Foote, C S (5 April 1989),"Eosinophils preferentially use bromide to generate halogenating agents",Journal of Biological Chemistry,264 (10):5660–8,doi:10.1016/S0021-9258(18)83599-2,PMID 2538427, archived fromthe original on 26 May 2009, retrieved25 October 2009
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