Misplaced Pages

Phosphite anion: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editNext edit →Content deleted Content addedVisualWikitext
Revision as of 12:27, 24 February 2011 editLuckas-bot (talk | contribs)929,662 editsm r2.7.1) (robot Adding: ca:Fosfit← Previous edit Revision as of 12:37, 24 February 2011 edit undoCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation (Next edit →
Line 1: Line 1:
{{Chembox {{Chembox
| verifiedrevid = 409318703 | verifiedrevid = 411474802
| ImageFile = | ImageFile =
| IUPACName = phosphite | IUPACName = phosphite

Revision as of 12:37, 24 February 2011

Phosphite anion
Names
IUPAC name phosphite
Identifiers
3D model (JSmol)
CompTox Dashboard (EPA)
SMILES
  • P()()
Properties
Chemical formula PO3
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

A phosphite a salt of phosphorous acid. The phosphite ion (PO3) is a polyatomic ion with a phosphorus central atom where phosphorus has an oxidation state of +3. Its molecular geometry is approximately tetrahedral like ammonia.

Because phosphorous acid exists as an equilibrium tautomeric mixture of P(OH)3 and HP(O)(OH)2, predominantly the latter, there is some confusion in nomenclature. The IUPAC recommends that the trihydroxy form be called phosphorous acid and its salts phosphites, with the dihydroxy form being called phosphonic acid and its salts phosphonates, but despite this, salts of HP(O)(OH)2 are often called phosphites rather than phosphonates.

The term phosphite is also used to mean phosphite ester, an organophosphorus compound with the formula P(OR)3.

Acid phosphites

Acid or hydrogen phosphites (which the IUPAC recommends be called acid or hydrogen phosphonates), such as NH4HP(O)2OH, can be prepared from phosphorous acid, HP(O)(OH)2. Hydrogen bonding between anions leads to polymeric anionic structures. Recently some others, RbHPHO3, CsHPHO3, TlHPHO3 have been prepared by reacting phosphorous acid with the metal carbonate. These compounds contain a layer polymeric anion consisting of HPO3 tetrahedra linked by hydrogen bonds. These layers are interleaved by layers of metal cations.

Pyrophosphites

Pyrophosphites (diphosphites) can be produced by gently heating acid phosphites under reduced pressure. They contain the ion, H2P2O5which can be formulated .

Naming of phosphite ions

The traditional name for HPO3 is phosphite, and for HPO2(OH) is hydrogenphosphite or acid phosphite. However IUPAC recommendations are that HPO3 is to be named hydrogenphosphite or phosphonate, HPO2(OH) is to be named dihydrogenphosphite or hydrogenphosphonate and phosphite is reserved for the hypothetical PO3 ion.

Synthesis of phosphite esters

Organophosphorus compounds called phosphite esters (or sometimes just phosphites) have the formula (RO)3P. They are prepared by reacting phosphorus trichloride (or phosphorus tribromide) with an alcohol and a tertiary amine.

PCl3 + 3 ROH + 3 R'3N → P(OR)3 + 3R'3NHCl

Use in plants

Inorganic phosphites have been applied to crops to combat fungus-like pathogens of the order Oomycetes. The situation is confusing because of the similarity in name between phosphite and phosphate (a major plant nutrient and fertilizer 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. Lemoynie 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.

See also

Further reading

  • A. Earnshaw, Norman Greenwood (1997). The Chemistry of the Elements - Second Edition. pp. 513–514.

References

  1. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  2. ^ Crystal chemistry of inorganic phosphites, J. Loub, Acta Cryst. (1991), B47, 468-473, doi:10.1107/S0108768191002380
  3. ^ International Union of Pure and Applied Chemistry (2005). Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005). Cambridge (UK): RSCIUPAC. ISBN 0-85404-438-8. Electronic version.. Cite error: The named reference "IUPAC inorganic" was defined multiple times with different content (see the help page).
  4. Kosterina, E. V., Troyanov, S. I., Kemnitz, E. & Aslanov, L. A. (2001). "Synthesis and Crystal Structure of Acid Phosphites RbH2PO3, CsH2PO3, and TlH2PO3". Russian Journal of Coordination Chemistry. 27: 458–462. doi:10.1023/A:1011377229855.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. Phosphites and Phosphates: When Distributors and Growers alike could get confused! by Jean-Pierre Leymonie. Courtesy of New Ag International, September 2007 edition.
  6. Thao; Yamakawa (2008). Soil Science and Plant Nutrition. 55: 228–234. {{cite journal}}: Missing or empty |title= (help)
Categories: