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A phosphite ion in inorganic chemistry usually refers to HPO32โˆ’ but includes H2PO3โˆ’ (HPO2(OH)โˆ’). These anions are the conjugate bases of (H3PO3). The corresponding salts, e.g. (Na2HPO3) are reducing in character.


Nomenclature
The IUPAC recommended name for phosphorous acid is . Correspondingly, the IUPAC-recommended name for the ion is . In the US the IUPAC naming conventions for inorganic compounds are taught at high school, but not as a 'required' part of the curriculum.Physical setting/ chemistry core curriculum, The University of the State of New York, The State Education Department, http://www.p12.nysed.gov/ciai/mst/pub/chemist.pdf A well-known university-level textbook follows the IUPAC recommendations.Egon Wiberg, Arnold Frederick Holleman (2001) Inorganic Chemistry, Elsevier In practice any reference to "phosphite" should be investigated to determine the naming convention being employed.


Salts containing HPO32โˆ’, called phosphonates or phosphites
. The anion has C3v symmetry.]]
From the commercial perspective, the most important phosphite salt is basic lead phosphite. Many salts containing the phosphite ion have been investigated structurally, these include pentahydrate (Na2HPO3ยท5H2O). (NH4)2HPO3ยทH2O, CuHPO3ยทH2O, SnHPO3 and Al2(HPO3)3ยท4H2O."Synthesis and crystal structures of aluminum and iron phosphites", D.M. Poojary, Y. Zhang, D.E. Cox, P.R. Rudolf, S. Cheng & A. Clearfield, J. Chem. Crystallogr. 24 (1994) 155โ€“163 The structure of is approximately tetrahedral.L. E. Gordon, W. T. A. Harrison. "Bis(melaminium) hydrogen phosphite tetrahydrate". Acta Crystallogr. 59 (2): o195โ€“o197. "Crystal chemistry of inorganic phosphites", J. Loub, Acta Crystallogr. (1991), B47, 468โ€“473,

has a number of canonical resonance forms making it isoelectronic with [[bisulfite]] ion, , which has a similar structure.
     


Salts containing HP(O)2OHโˆ’
Acid or hydrogen phosphites are called hydrogenphosphonates or acid phosphites. IUPAC recommends the name hydrogenphosphonates). They are anions HP(O)2OHโˆ’. A typical derivative is the salt NH4HP(O)2OH. Many related salts are known, e.g., RbHPHO3, CsHPHO3, TlHPHO3. These salts are prepared by treating with the metal . These compounds contain a layer polymeric anion consisting of HPO3 tetrahedra linked by hydrogen bonds. These layers are interleaved by layers of metal cations.

Organic esters of hydrogen phosphites are anions with the formula HP(O)2ORโˆ’ (R = organic group). One commercial example is the with the formula C2H5OP(H)O23Al.


Salts containing H2P2O52โˆ’, called diphosphites or pyrophosphites
Pyrophosphites (diphosphites) can be produced by gently heating acid phosphites under reduced pressure. They contain the ion , which can be formulated HP(O)2Oโˆ’P(O)2H2โˆ’.


Parallels in arsenic chemistry
In contrast to the paucity of evidence for , the corresponding arsenic ion, ortho-, is known. An example is Ag3AsO3 as well as the polymeric meta-arsenite . The iso-electronic ion, is known from its salts.


Use as fungicides
Inorganic phosphites (containing ) have been applied to crops to combat fungus-like pathogens of the order (water molds). The situation is confusing because of the similarity in name between phosphite and (a major plant and ingredient), and controversial because phosphites have sometimes been advertised as fertilizers, even though they are converted to phosphate too slowly to serve as a plant's main phosphorus source. In fact, phosphites may cause phytotoxicity when a plant is starved of phosphates. Lemoynie "Phosphites and Phosphates: When Distributors and Growers alike could get confused!" by Jean-Pierre Leymonie. Courtesy of New Ag International, September 2007 edition. and others have described this complicated situation and noted that calling phosphites fertilizers avoided the regulatory complication and negative public perceptions that might have been incurred by registering them as fungicides.

A major form of inorganic phosphite used in agriculture is monopotassium phosphite. This compound does serve as a potassium fertilizer.


See also


Further reading
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