Phosphorous acid: Difference between revisions
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*Holleman, A. F.; Wiberg, E. “Inorganic Chemistry.” Academic Press: San Diego, 2001. ISBN 0-12-352651-5. | *Holleman, A. F.; Wiberg, E. “Inorganic Chemistry.” Academic Press: San Diego, 2001. ISBN 0-12-352651-5. | ||
*D. E. C. Corbridge. “Phosphorus: An Outline of its Chemistry, Biochemistry, and Technology.” 5th ed. Elsevier: Amsterdam. ISBN 0-444-89307-5. | *D. E. C. Corbridge. “Phosphorus: An Outline of its Chemistry, Biochemistry, and Technology.” 5th ed. Elsevier: Amsterdam. ISBN 0-444-89307-5. | ||
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Overview
Phosphorous acid is the compound described by the formula H3PO3. It is one of the oxoacids of phosphorus, other important members being phosphoric acid (H3PO4) and hypophosphorous acid (H3PO2). Note that only the reduced phosphorus compounds are spelled with an "ous" ending. Other names for this acid are orthophosphorous acid and dihydroxyphosphine oxide.
HP(O)(OH)2 is the product of the hydrolysis of its acid anhydride, P4O6:
- P4O6 + 6 H2O → 4 HP(O)(OH)2
An analogous relationship connects H3PO4 and P4O10.
Tautomerization
H3PO3 is better described with the structural formula HP(O)(OH)2. This species exists in equilibrium with a minor tautomer P(OH)3. The latter is called phosphorous acid.[1]
P(OH)3 (IUPAC: phosphorous acid) has CAS number 10294-56-1 and CID: 107909[1]. It is sometimes called phosphorus acid or orthophosphorous acid. It has been shown to be a stable tautomer.[2][3]
The dihydroxy form, HP(O)(OH)2, is called phosphonic acid. Many of the reduced phosphorus acids are subject to similarly complicated equilibria involving shifts of H between O and P. In the solid state, HP(O)(OH)2 is tetrahedral with one shorter P=O bond of 148 pm and two longer P-O(H) bonds of 154 pm.
Preparation
Although commercially available, the acid is most commonly prepared by hydrolysis of phosphorus trichloride with water or steam:
- PCl3 + 3 H2O → HP(O)(OH)2 + 3 HCl
Potassium phosphite is a convenient precursor to phosphorous acid:
- K2HPO3 + 2 HCl → 2 KCl + H3PO3
In practice aqueous potassium phosphite is treated with excess hydrochloric acid. By concentrating the solution and precipitations with alcohols, the pure acid can be separated from the salt.
Polymerization
An oligophosphorous acid of the phosphonic acid tautomer refers to a few molecules of phosphorous acid condensed into a molecule with the loss of water.
A general formula for such oligophosphorous acids is (HPO)nOn-1(OH)2, where n = 2, 3, 4, etc., oligo-. A polyphosphorous acid can have dozens of such phosphorous acid units condensed in a row with the loss of H2O for each unit added on.
Acid-base properties
Phosphorous acid is a diprotic acid, since the hydrogen bonded directly to the central phosphorus atom is not readily ionizable. Chemistry examinations often test students' appreciation of the fact that all three hydrogen atoms are not acidic under aqueous conditions, in contrast with phosphoric acid. HP(O)2(OH)− is a moderately strong acid.
- HP(O)(OH)2 → HP(O)2(OH)− + H+ pKa = 1.3[4]
- HP(O)2(OH)− → HPO32− + H+ pKa = 6.7
The monodeprotonated species, HP(O)2(OH)− is called the phosphite ion.
The IUPAC (mostly organic) name is phosphonic acid. This nomenclature is commonly reserved for substituted derivatives, that is, organic group bonded to phosphorus, not simply an ester. For example, (CH3)PO(OH)2 is "methylphosphonic acid", which may of course form "methylphosphonate" esters.
Both phosphorous acid and its deprotonated forms are good reducing agents, although not necessarily quick to react. They are oxidized to phosphoric acid or its salts. It reduces solutions of noble metal cations to the metals.
Uses
Conversion to phosphine
Phosphine, being a flammable and toxic gas, is inconvenient to store. Fortunately this useful species is readily prepared by thermal decomposition of phosphorous acid, which degrades at about 180°C:
- 4 HP(O)(OH)2 → PH3 + 3 H3PO4
Since phosphoric acid is a syrupy non-volatile liquid, the gaseous PH3 is readily separated.
In agriculture
A large quantity of phosphorous acid is used as phosphatic fertilizer. [5] Pure phosphorous acid is also used for preparing phosphite salts, such as monopotassium phosphite or aluminum phosphonite. These salts, as well as aqueous solutions of pure phosphorous acid, have shown effectiveness in controlling a variety of microbial plant diseases—in particular, treatment using either trunk injection or foliar containing phosphorous acid salts is indicated in response to infections by phytophthora and pythium-type plant pathogens (both within class oomycetes, known as water molds), such as dieback/root rot and downy mildew.[6] Anti-microbial products containing salts of phosphorous acid are marketed in Australia as 'Yates Anti-Rot'; and in the United States of America, for example, aluminum salts of phosphorous acid (known generically as 'Fosetyl-Al') are sold under the trade name 'Aliette'.[7][8]
As a chemical reagent
Phosphorous acid is used in chemical reactions as a reducing agent that is somewhat less vigorous than the related hypophosphorous acid.[9]
References
- ↑ 1.0 1.1 http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=107909&loc=ec_rcs. Missing or empty
|title=(help) - ↑ Xi C, Liu Y, Lai C, Zhou L (2004). "Synthesis of molybdenum complex with novel P(OH)3 ligand based on the one-pot reaction of Mo(CO)6 with HP(O)(OEt)2 and water". Inorgn Chem Commun. 7 (11): 1202–4. doi:10.1016/j.inoche.2004.09.012.
- ↑ Sokolov MN, Chubarova EV, Kovalenko KA, Mironov IV, Virovets1 AV, Peresypkina EV, Fedin VP (2005). "Stabilization of tautomeric forms P(OH)3 and HP(OH)2 and their derivatives by coordination to palladium and nickel atoms in heterometallic clusters with the Mo3MQ44+ core (M = Ni, Pd; Q = S, Se)". Russ Chem Bull. 54, (3): 615–22. doi:10.1007/s11172-005-0296-1.
- ↑ CRC Handbook of Chemistry and Physics, 87th Ed. 8-42
- ↑ Allison E. McDonald; Bruce R. Grant; William C. Plaxton (2001). "Phosphite (Phosphorous acid ): Its Relevance in the Environment and Agriculture and Influence on Plant Phosphate Starvation Respose". Journal of Plant Nutrition. 24 (10): 1505–1519. doi:10.1081/PLN-100106017.
- ↑ Organic Labs. Product label for 'Exel LG,' Retrieved April 9, 2007.
- ↑ Yates, a Division of Orica Australia Pty Ltd. “MSDS ('Yates Anti Rot Phosacid Systemic Fungicide').” Version 1. SH&E Shared Services, Orica. Homebush, NSW (Australia): April 4, 2005 (retrieved from www.orica.com April 9, 2007).
- ↑ US EPA. “Fosetyl-Al (Aliette): Reregistration Eligibility Decision (RED) Fact Sheet.” Office of Pesticide Programs, US EPA. Washington, DC (USA): 1994 (retrieved from www.epa.gov April 9, 2007).
- ↑ “Phosphorous acid.” The American Heritage® Dictionary of the English Language, 4th ed. Boston: Houghton Mifflin, 2000 (retrieved from www.bartleby.com April 9, 2007).
Other references
- Holleman, A. F.; Wiberg, E. “Inorganic Chemistry.” Academic Press: San Diego, 2001. ISBN 0-12-352651-5.
- D. E. C. Corbridge. “Phosphorus: An Outline of its Chemistry, Biochemistry, and Technology.” 5th ed. Elsevier: Amsterdam. ISBN 0-444-89307-5.
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cs:Kyselina fosforitá de:Phosphonsäure eo:Fosfonata acido it:Acido fosforoso