Borate
You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.
Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
Borates in chemistry are chemical compounds containing boron bonded to three oxygen atoms written as B(OR)3. In B(OR)4− anions, this number increases to four.
The borate ion is BO33−. it 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.
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 ⇌ B(OH)4− + H+
- Ka = 5.8x10−10 mol/l; pKa = 9.24.
- B(OH)3 + H2O ⇌ B(OH)4− + H+
Polyborate anions 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 tetraborate ion, found in the mineral borax:
- 4B(OH)4− + 2H+ ⇌ B4O72− + 9H2O
Even though boric acid adds hydroxide to form B(OH)4−, you may find for pKa values and other calculations, the fictitious ions are easier to use. Thus for a typical polyprotic acid, the deprotonation series dihydrogen borate [H2BO3−;], hydrogen borate [HBO32−] and borate [BO33−] may be written as pH increases.
Boric acid can be used to form many polymeric ions. The tetraborate ion, B4O72−, is very common; the hydrogen tetraborate ion, HB4O7−, as well as triborate and pentaborate, are also seen. The various metaborate ions have an empirical formula of BO2−, and form metaborate compounds. Formation of these complicated, potentially infinite network structures is extensive, perhaps surpassed only by the silicates.
Common borate salts include sodium metaborate, NaBO2, and sodium tetraborate, Na2B4O7. The latter also occurs naturally as the hydrous mineral borax, Na2B4O7·10H2O. Boron, California contains large borax deposits and is used extensively for borate mining. The Atacama Desert in Chile also contains mineable borate concentrations.
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
- Non-CCA Wood Preservatives: Guide to Selected Resources - National Pesticide Information Centerbn:বোরেট
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

