Thiophosphate

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Template:Short description Thiophosphates (or phosphorothioates, PS) are chemical compounds and anions with the general chemical formula Template:Chem/link (x = 0, 1, 2, or 3) and related derivatives where organic groups are attached to one or more O or S. Thiophosphates feature tetrahedral phosphorus(V) centers.[1]

Organic

Script error: No such module "Labelled list hatnote". Organothiophosphates are a subclass of organophosphorus compounds that are structurally related to the inorganic thiophosphates. Common members have formulas of the type (RO)3−x(RS)xPS and related compounds where RO is replaced by RS. Many of these compounds are used as insecticides, some have medical applications, and some have been used as oil additives.[1]

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Oligonucleotide phosphorothioates (OPS) are modified oligonucleotides where one of the oxygen atoms in the phosphate moiety is replaced by sulfur. They are the basis of antisense therapy, e.g., the drugs fomivirsen (Vitravene), oblimersen, alicaforsen, and mipomersen (Kynamro).[2]

Inorganic

File:ThiophosphateVarietyPack.png
Structures of selected thiophosphates.

The simplest thiophosphates have the formula [PS4−xOx]3−. These trianions are only observed at very high pH, instead they exist in protonated form with the formula [HnPS4−xOx](3−n)− (x = 0, 1, 2, or 3 and (n = 1, 2, or 3).

Monothiophosphate

File:Thiophosphate-ion-3D-balls.png
Ball-and-stick model of the hypothetical monothiophosphate trianion.

Monothiophosphate is the anion [PO3S]3−, which has C3v symmetry. A common salt is sodium monothiophosphate (Na3PO3S). Monothiophosphate is used in research as an analogue of phosphate in biochemistry. Monothiophosphate esters are biochemical reagents used in the study of transcription,[3] substitution interference assays. Sometimes, "monothiophosphate" refers to esters such as (CH3O)2POS−.[4]

Dithiophosphates

Dithiophosphate has the formula [PO2S2]3−, which has C2v symmetry. Sodium dithiophosphate, which is colorless, is the major product from the reaction of phosphorus pentasulfide with NaOH:[5]

P2S5 + 6 NaOH → 2 Na3PO2S2 + H2S + 2 H2O

Dithiophosphoric acid is obtained by treatment of barium dithiophosphate with sulfuric acid:

Ba3(PO2S2)2 + 3 H2SO4 → 3 BaSO4 + 2 H3PO2S2

Both Na3PO2S2 and especially H3PO2S2 are prone toward hydrolysis to their monothio derivatives.

Tri- and tetrathiophosphates

Trithiophosphate is the anion [POS3]3−, which has C3v symmetry. Tetrathiophosphate is the anion [PS4]3−, which has Td symmetry.

PxSy: binary thiophosphates and polyphosphates

File:PS3-dimerization.png
Dimerization equilibrium observed for PS3−.[6]

A number of these anions known. Some have attracted interest as components in fast ion conductors for use in solid state batteries. The binary thiophosphates do not exhibit the extensive diversity of the analogous oxyanions but contain similar structural features, for example P is 4 coordinate, P−S−P links form and there are P−P bonds. One difference is that ions may include polysulfide fragments of 2 or more S atoms whereas in the P−O anions there is only the reactive −O−O−, peroxo, unit.

References

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  1. ↑ a b J. Svara, N. Weferling, T. Hofmann "Phosphorus Compounds, Organic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2006. Script error: No such module "CS1 identifiers".
  2. ↑ Kurreck, J., "Antisense technologies. Improvement through novel chemical modifications", European Journal of Biochemistry 2003, 270, 1628-1644.Script error: No such module "CS1 identifiers".
  3. ↑ Script error: No such module "Citation/CS1".
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  5. ↑ R. Klement "Phosphorus" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1., p. 571.
  6. ↑ Script error: No such module "Citation/CS1".
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  8. ↑ a b Phosphorus: Chemistry, Biochemistry and Technology, Sixth Edition, 2013, D.E.C. Corbridge, CRC Pres, Taylor Francis Group, Template:ISBN
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