Triazine

Not to be confused with triazene or triazane.

A triazine is class of nitrogen-containing heterocycles. The parent molecules' molecular formula is C3H3N3. They exist in three isomeric forms, 1,3,5-triazines being common.

Structure

The triazines have planar six-membered benzene-like ring but with three carbons replaced by nitrogens. The three isomers of triazine are distinguished by the positions of their nitrogen atoms, and are referred to as 1,2,3-triazine, 1,2,4-triazine, and 1,3,5-triazine. Other aromatic nitrogen heterocycles are pyridines with one ring nitrogen atom, diazines with 2 nitrogen atoms in the ring and tetrazines with 4 ring nitrogen atoms.

Uses

The best known triazines are derivatives of the 1,3,5-triazine derivatives melamine and cyanuric chloride (2,4,6-trichloro-1,3,5-triazine). With three amino substituents melamine is a precursor to commercial resins. Another triazine extensively used in resins is benzoguanamine. Chlorine-substituted triazines are components of reactive dyes.[1] These compounds react through a chlorine group with hydroxyl groups present in cellulose fibres in nucleophilic substitution, the other triazine positions contain chromophores. Triazine compounds are often used as the basis for various herbicides.

Triazines also have wide use in the oil and gas and petroleum processing industries as a non-regenerating sulfide removal agent; they are applied to fluid streams to remove hydrogen sulfide gas and mercaptan species, which can decrease the quality of the processed hydrocarbon and be harmful to pipeline and facility infrastructure if not removed.

Synthesis

Main article: 1,3,5-Triazine

The more common 1,3,5-isomers are prepared by trimerization of nitrile and cyanide compounds, although more specialized methods are known.

The 1,2,3- and 1,2,4-Triazines are more specialized methods. The former family of triazines can be synthesized by thermal rearrangement of 2-azidocyclopropenes. Also mainly of specialized interest, the 1,2,4-isomer is prepared from condensation of 1,2-dicarbonyl compounds with amidrazones. A classical synthesis is also the Bamberger triazine synthesis.

Reactions

Although triazines are aromatic compounds, their resonance energy is much lower than in benzene. Electrophilic aromatic substitution is difficult but nucleophilic aromatic substitution easier than typical chlorinated benzenes. 2,4,6-Trichloro-1,3,5-triazine is easily hydrolyzed to cyanuric acid by heating with water. 2,4,6-Tris(phenoxy)-1,3,5-triazine results when the trichloride is treated with phenol. With amines, one or more chloride is displaced. The remaining chlorides are reactive, and this theme is the basis of the large field of reactive dyes.

Cyanuric chloride assists in the amidation of carboxylic acids.[2]

The 1,2,4-triazines can react with electron-rich dienophiles in an inverse electron demand Diels-Alder reaction. This forms a bicyclic intermediate which normally then extrudes a molecule of nitrogen gas to form an aromatic ring again. In this way the 1,2,4-triazines can be reacted with alkynes to form pyridine rings. An alternative to using an alkyne is to use norbornadiene which can be thought of as a masked alkyne.[3]

In 2007, triazines were found to be crucial synthons in the design of new functional materials for applications in sustainable growth.[4][5]

Ligands

A series of 1,2,4-triazine derivatives known as bis-triazinyl bipyridines (BTPs) have been considered as possible extractants for use in the advanced nuclear reprocessing.[6][7][8] BTPs are molecules containing a pyridine ring bonded to two 1,2,4-triazin-3-yl groups.

Triazine-based ligands have been used to bind three dinuclear arene ruthenium (or osmium) compounds to form metallaprisms.[9]

References

  1. ↑ Horst Tappe, Walter Helmling, Peter Mischke, Karl Rebsamen, Uwe Reiher, Werner Russ, Ludwig Schläfer and Petra Vermehren "Reactive Dyes"in Ullmann's Encyclopedia of Industrial Chemistry 2000, Wiley-VCH, Weinheim. doi:10.1002/14356007.a22_651
  2. ↑ Triazine-Promoted Amidation of Various Carboxylic Acids Jeremy Schlarb 1999 Article
  3. ↑ Shi, B.; Lewis, W.; Campbell, I. B.; Moody, C. J. Org. Lett., 2009, 3686-3688 doi:10.1021/ol901502u
  4. ↑ https://worldwide.espacenet.com/publicationDetails/biblio;jsessionid=XU+H4ZRvzVIvNFl9IQOmRhmA.espacenet_levelx_prod_0?FT=D&date=20101104&DB=EPODOC&locale=fr_EP&CC=US&NR=2010280216A1&KC=A1&ND=4
  5. ↑ http://cordis.europa.eu/result/rcn/179610_en.html
  6. ↑ Geist, Andreas; Michael Weigl; Udo Müllich; Klaus Gompper (2000). "ACTINIDE(III)/LANTHANIDE(III) PARTITIONING USING n-Pr-BTP AS EXTRACTANT: EXTRACTION KINETICS AND EXTRACTION TEST IN A HOLLOW FIBER MODULE" (PDF). 6th Information Exchange Meeting on Actinide and Fission Product Partitioning and Transmutation: 641–647. Retrieved 30 April 2013.
  7. ↑ Hill, C.; D. Guillaneux; X. Hérès; N. Boubals; L. Ramain. "SANEX-BTP PROCESS DEVELOPMENT STUDIES" (PDF). Retrieved 30 April 2013.
  8. ↑ Development Of Electrochemical Separations Of Uranium And Re Elements From Fluoride Melts
  9. ↑ Hudson, Michael J.; Michael G. B. Drew; Mark R. StJ. Foreman; Clément Hill; Nathalie Huet; Charles Madic; Tristan G. A. Youngs (2003). "The coordination chemistry of 1,2,4-triazinyl bipyridines with lanthanide(III) elements – implications for the partitioning of americium(III)". Dalton Transactions (9): 1675–1685. doi:10.1039/B301178J. Retrieved 30 April 2013.

See also

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