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borate

 
Dictionary: bo·rate   (bôr'āt', bōr'-) pronunciation
n.
A salt or an ester of boric acid.


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Any of a wide range of ionic compounds that have negative ions containing boron and oxygen (see formulae). Lithium borate, for example, contains the simple anion B(OH)4. Most borates, however, are inorganic polymers with rings, chains, or other networks based on the planar BO3 group or the tetrahedral BO3(OH) group. 'Hydrated' borates are ones containing –OH groups; many examples occur naturally. Anhydrous borates, which contain BO3 groups, can be made by melting together boric acid and metal oxides.




borate



Any salt of boric acid.

Wikipedia: Borate
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Borates in chemistry are chemical compounds containing boron oxoanions, with boron in oxidation state +3. The simplest borate ion is the trigonal planar, BO33−, although many others are known.[1] BO33− forms salts with metallic elements. Boron found in nature is commonly as a borate mineral. Boron is also found combined with silicate to form complex borosilicate minerals such as the tourmalines. Many borates are readily hydrated and contain structural hydroxide groups and should formally be considered as hydroxoborates.

Contents

Aqueous chemistry

In aqueous solution borate exists in many forms. In acid and near-neutral conditions, it is boric acid, commonly written as H3BO3 but more correctly B(OH)3. The pKa of boric acid is 9.14 at 25C. Boric acid does not dissociate in aqueous solution, but is acidic due to its interaction with water molecules, forming tetrahydroxyborate:

B(OH)3 + H2O is in equilibrium with B(OH)4 + H+
Ka = 5.8x10−10 mol/l; pKa = 9.24.

Polymeric anions containing structural OH units (polyhydroxoborates) are formed at pH 7–10 if the boron concentration is higher than about 0.025 mol/L. The best known of these is the ion found in the mineral borax:

4 B(OH)4 + 2 H+ is in equilibrium with B4O5(OH)2−4 + 7 H2O

Even though boric acid adds hydroxide to form B(OH)4, the fictitious ions are easier to use for pKa values and other calculations. Thus for a typical polyprotic acid, the deprotonation series dihydrogen borate [H2BO3], hydrogen borate [HBO2−3], and borate [BO3−3] may be written as pH increases.

Polymeric ions

A number of polymeric borate ions are known in anhydrous compounds, which are made by reacting B(OH)3 or B2O3 with metal oxides, for example[1]:-

  • diborate B2O54− e.g. in Mg2B2O5 (suanite)
  • triborate B3O75- in CaAlB3O7 (johachidolite)
  • tetraborate B4O96− in e.g. Li6B4O9
  • metaborates containing the linear [BO2]n with three coordinate boron e.g. in LiBO2, CaB2O4
  • metaborates containing 3 and four coordinate boron, often these are high pressure modifications.

Common borate salts

Common borate salts include sodium metaborate, NaBO2, and sodium tetraborate, Na2B4O7, which is usually encountered as borax the so-called decahydrate, and actually contains the hydroxoborate ion, B4O5(OH)4 2− and is formulated Na2[B4O5(OH)4]·8H2O.
Boron, California contains large borax deposits and is used extensively for borate mining. The Atacama Desert in Chile also contains mineable borate concentrations. Gerry, New York has been described by Agapito Associates Inc. as a "very nice place to mine for [borate]" although it is uncertain how much damage that might do to the surrounding area.

Various forms of borate are used as wood preservatives or fungicides such as disodium octaborate tetrahydrate.

Borate esters

Borate esters are organic compounds of the type B(OR)3 where R is an organic residue (for example alkyl or aryl). Borate esters include trimethyl borate, B(OCH3)3, which is used as a precursor to boronic esters for Suzuki couplings.

External links

References

  1. ^ a b Egon Wiberg, Arnold Frederick Holleman (2001) Inorganic Chemistry, Elsevier ISBN 0123526515

 
 
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