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Thiocyanate

From Wikipedia, the free encyclopedia
(Redirected from Sulphocyanide)
For organic derivatives, see Organic thiocyanates. For the binary compound, ScN, see Scandium nitride.
Thiocyanate
Names
Preferred IUPAC name
Thiocyanate[1]
Other names
  • Rhodanide
  • Sulfocyanate
  • Sulphocyanate
  • Thiocyanide
  • Cyanosulfanide
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
UNII
  • InChI=1S/CHNS/c2-1-3/h3H/p-1 checkY
    Key: ZMZDMBWJUHKJPS-UHFFFAOYSA-M checkY
  • InChI=1/CHNS/c2-1-3/h3H/p-1
    Key: ZMZDMBWJUHKJPS-REWHXWOFAX
  • [S-C≡N]-: [S-]C#N
  • [S=C=N]-: S=C=[N-]
Properties
[SCN]−
Molar mass 58.08 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Thiocyanates are salts containing the thiocyanate anion [SCN]− (also known as rhodanide or rhodanate). [SCN]− is the conjugate base of thiocyanic acid. Common salts include the colourless salts potassium thiocyanate and sodium thiocyanate. Mercury(II) thiocyanate was formerly used in pyrotechnics.

Thiocyanate is analogous to the cyanate ion, [OCN]−, wherein oxygen is replaced by sulfur. [SCN]− is one of the pseudohalides, due to the similarity of its reactions to that of halide ions. Thiocyanate used to be known as rhodanide (from a Greek word for rose) because of the red colour of its complexes with iron.

Thiocyanate is produced by the reaction of elemental sulfur or thiosulfate with cyanide: The second reaction is catalyzed by thiosulfate sulfurtransferase, a hepatic mitochondrial enzyme, and by other sulfur transferases, which together are responsible for around 80% of cyanide metabolism in the body.[2]

Oxidation of thiocyanate inevitably produces hydrogen sulfate. The other product depends on pH: in acid, it is hydrogen cyanide, presumably via HOSCN and with a sulfur dicyanide side-product; but in base and neutral solutions, it is cyanate.[3]

Biology

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Occurrences

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Thiocyanate occurs widely in nature, albeit often in low concentrations. It is a component of some sulfur cycles.

Biochemistry

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Thiocyanate hydrolases catalyze the conversion of thiocyanate to carbonyl sulfide[4] and to cyanate:[5]

SCN− + H2O + H+ → SCO + NH3
SCN− + H2O → OCN− + H2S

Medicine

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Thiocyanate[6] is known to be an important part in the biosynthesis of hypothiocyanite by a lactoperoxidase.[7][8][9] Thus the complete absence of thiocyanate or reduced thiocyanate[10] in the human body, (e.g., cystic fibrosis) is damaging to the human host defense system.[11][12]

Thiocyanate is a potent competitive inhibitor of the thyroid sodium-iodide symporter.[13] Iodine is an essential component of thyroxine. Since thiocyanates will decrease iodide transport into the thyroid follicular cell, they will decrease the amount of thyroxine produced by the thyroid gland. As such, foodstuffs containing thiocyanate are best avoided by iodide deficient hypothyroid patients.[14]

In the early 20th century, thiocyanate was used in the treatment of hypertension, but it is no longer used because of associated toxicity.[15] Sodium nitroprusside, a metabolite of which is thiocyanate, is however still used for the treatment of a hypertensive emergency. Rhodanese catalyzes the reaction of sodium nitroprusside (like other cyanides) with thiosulfate to form the metabolite thiocyanate.

Coordination chemistry

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Main article: Transition metal complexes of thiocyanate
Structure of Pd(Me2N(CH2)3PPh2)(SCN)(NCS).[16]
Resonance structures of the thiocyanate ion

Thiocyanate shares its negative charge approximately equally between sulfur and nitrogen. As a consequence, thiocyanate can act as a nucleophile at either sulfur or nitrogen—it is an ambidentate ligand. [SCN]− can also bridge two (M−SCN−M) or even three metals (>SCN− or −SCN<). Experimental evidence leads to the general conclusion that class A metals (hard acids) tend to form N-bonded thiocyanate complexes, whereas class B metals (soft acids) tend to form S-bonded thiocyanate complexes. Other factors, e.g. kinetics and solubility, are sometimes involved, and linkage isomerism can occur, for example [Co(NH3)5(NCS)]Cl2 and [Co(NH3)5(SCN)]Cl2.[17] It [SCN] is considered as a weak ligand. ([NCS] is a strong ligand)[18]

Test for iron(III) and cobalt(II)

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The blood-red colored (up) complex [Fe(NCS)(H2O)5]2+ (left), indicates the presence of Fe3+ in solution.

If [SCN]− is added to a solution with iron(III) ions, a blood-red solution forms mainly due to the formation of [Fe(NCS)(H2O)5]2+, i.e. pentaaqua(thiocyanato-N)iron(III). Lesser amounts of other hydrated compounds also form: e.g. Fe(SCN)3 and [Fe(SCN)4]−.[19]

Similarly, Co2+ gives a blue complex with thiocyanate.[20] Both the iron and cobalt complexes can be extracted into organic solvents like diethyl ether or amyl alcohol. This allows the determination of these ions even in strongly coloured solutions. The determination of Co(II) in the presence of Fe(III) is possible by adding KF to the solution, which forms uncoloured, very stable complexes with Fe(III), which no longer react with SCN−.[21]

Phospholipids or some detergents aid the transfer of thiocyanatoiron into chlorinated solvents like chloroform and can be determined in this fashion.[22]

See also

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References

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  • Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.

Citations

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  1. ^ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. pp. 784, 1069. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
  2. ^ Abraham, Klaus; Buhrke, Thorsten; Lampen, Alfonso (24 February 2015). "Bioavailability of cyanide after consumption of a single meal of foods containing high levels of cyanogenic glycosides: a crossover study in humans". Archives of Toxicology. 90 (3): 559–574. doi:10.1007/s00204-015-1479-8. PMC 4754328. PMID 25708890.
  3. ^ Wilson, I. R.; Harris, G. M. (January 1, 1961). "The oxidation of thiocyanate ion by hydrogen peroxide II: The acid-catalyzed reaction". Journal of the American Chemical Society. 83 (2): 286–289. doi:10.1021/ja01463a007.
  4. ^ Katayama, Yoko; Hashimoto, Kanako; Nakayama, Hiroshi; Mino, Hiroyuki; Nojiri, Masaki; Ono, Taka-aki; Nyunoya, Hiroshi; Yohda, Masafumi; Takio, Koji; Odaka, Masafumi (2006). "Thiocyanate Hydrolase is a Cobalt-Containing Metalloenzyme with a Cysteine-Sulfinic Acid Ligand". Journal of the American Chemical Society. 128 (3): 728–729. doi:10.1021/ja057010q. PMID 16417356.
  5. ^ Tikhonova, Tamara V.; Sorokin, Dimitry Y.; Hagen, Wilfred R.; Khrenova, Maria G.; Muyzer, Gerard; Rakitina, Tatiana V.; Shabalin, Ivan G.; Trofimov, Anton A.; Tsallagov, Stanislav I.; Popov, Vladimir O. (2020). "Trinuclear Copper Biocatalytic Center Forms an Active Site of Thiocyanate Dehydrogenase". Proceedings of the National Academy of Sciences. 117 (10): 5280–5290. Bibcode:2020PNAS..117.5280T. doi:10.1073/pnas.1922133117. PMC 7071890. PMID 32094184.
  6. ^ Pedemonte, N.; Caci, E.; Sondo, E.; Caputo, A.; Rhoden, K.; Pfeffer, U.; di Candia, M.; Bandettini, R.; Ravazzolo, R.; Zegarra-Moran, O.; Galietta, L. J. (2007). "Thiocyanate Transport in Resting and IL-4-Stimulated Human Bronchial Epithelial Cells: Role of Pendrin and Anion Channels". Journal of Immunology. 178 (8): 5144–5153. doi:10.4049/jimmunol.178.8.5144. PMID 17404297.
  7. ^ Conner, G. E.; Wijkstrom-Frei, C.; Randell, S. H.; Fernandez, V. E.; Salathe, M. (2007). "The Lactoperoxidase System Links Anion Transport to Host Defense in Cystic Fibrosis". FEBS Letters. 581 (2): 271–278. doi:10.1016/j.febslet.2006.12.025. PMC 1851694. PMID 17204267.
  8. ^ White, W. E.; Pruitt, K. M.; Mansson-Rahemtulla, B. (1983). "Peroxidase-Thiocyanate-Peroxide Antibacterial System Does not Damage DNA". Antimicrobial Agents and Chemotherapy. 23 (2): 267–272. doi:10.1128/aac.23.2.267. PMC 186035. PMID 6340603.
  9. ^ Thomas, E. L.; Aune, T. M. (1978). "Lactoperoxidase, Peroxide, Thiocyanate Antimicrobial System: Correlation of Sulfhydryl Oxidation with Antimicrobial Action". Infection and Immunity. 20 (2): 456–463. doi:10.1128/IAI.20.2.456-463.1978. PMC 421877. PMID 352945.
  10. ^ Minarowski, Ł.; Sands, D.; Minarowska, A.; Karwowska, A.; Sulewska, A.; Gacko, M.; Chyczewska, E. (2008). "Thiocyanate concentration in saliva of cystic fibrosis patients" (PDF). Folia Histochemica et Cytobiologica. 46 (2): 245–246. doi:10.2478/v10042-008-0037-0. PMID 18519245.[permanent dead link‍]
  11. ^ Moskwa, P.; Lorentzen, D.; Excoffon, K. J.; Zabner, J.; McCray, P. B. Jr.; Nauseef, W. M.; Dupuy, C.; Bánfi, B. (2007). "A Novel Host Defense System of Airways is Defective in Cystic Fibrosis". American Journal of Respiratory and Critical Care Medicine. 175 (2): 174–183. doi:10.1164/rccm.200607-1029OC. PMC 2720149. PMID 17082494.
  12. ^ Xu, Y.; Szép, S.; Lu, Z.; Szep; Lu (2009). "The antioxidant role of thiocyanate in the pathogenesis of cystic fibrosis and other inflammation-related diseases". Proceedings of the National Academy of Sciences of the United States of America. 106 (48): 20515–20519. Bibcode:2009PNAS..10620515X. doi:10.1073/pnas.0911412106. PMC 2777967. PMID 19918082.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  13. ^ Braverman L. E.; He X.; Pino S.; et al. (2005). "The effect of perchlorate, thiocyanate, and nitrate on thyroid function in workers exposed to perchlorate long-term". J Clin Endocrinol Metab. 90 (2): 700–706. doi:10.1210/jc.2004-1821. PMID 15572417.
  14. ^ "Hypothyroidism". umm.edu. University of Maryland Medical Center. Retrieved 3 December 2014.
  15. ^ Warren F. Gorman; Emanuel Messinger; And Morris Herman (1949). "Toxicity of Thiocyanates Used in Treatment of Hypertension". Ann Intern Med. 30 (5): 1054–1059. doi:10.7326/0003-4819-30-5-1054. PMID 18126744.
  16. ^ Palenik, Gus J.; Clark, George Raymond (1970). "Crystal and molecular structure of isothiocyanatothiocyanato-(1-diphenylphosphino-3-dimethylaminopropane)palladium(II)". Inorganic Chemistry. 9 (12): 2754–2760. doi:10.1021/ic50094a028. ISSN 0020-1669.
  17. ^ Greenwood, p. 326
  18. ^ "coordination compounds" (PDF).
  19. ^ Greenwood, p. 1090
  20. ^ Uri, N (1947-01-01). "The stability of the cobaltous thiocyanate complex in ethyl alcohol-water mixtures and the photometric determination of cobalt". Analyst. 72 (860): 478–481. Bibcode:1947Ana....72..478U. doi:10.1039/AN9477200478. PMID 18917685.
  21. ^ Kolthoff, I. M. (1930). "The Cobalt-Thiocyanate Reaction for the Detection of Cobalt and Thiocyanate". Mikrochemie. 8 (S1): 176–181. doi:10.1007/BF02759120. ISSN 0369-0261.
  22. ^ Stewart, J.C. (1980). "Colorimetric determination of phospholipids with ammonium ferrothiocyanate". Anal. Biochem. 104 (1): 10–14. doi:10.1016/0003-2697(80)90269-9. PMID 6892980.
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