Chemistry:Hydromelonic acid

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Hydromelonic acid
Hydromelonic acid.png
Names
IUPAC name
1,3,4,6,7,9,9b-heptaazaphenalene-2,5,8-tricarbodiimide
Other names
hydromelonic acid;[1] tricyanamido‐s‐heptazine;[2] tricyanomelem;[2] [7,11-bis(cyanoimino)-2,4,6,8,10,12,13-heptazatricyclo[7.3.1.05,13]trideca-1,3,5,8-tetraen-3-yl]cyanamide
Identifiers
3D model (JSmol)
Properties
C9H3N13
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Hydromelonic acid,[1] is an elusive chemical compound with formula C9H3N13 or (HNCN)3(C6N7), whose molecule would consist of a heptazine H3(C6N7) molecule, with three cyanamido groups H–N=C=N– or N≡C–NH– substituted for the hydrogen atoms.

The compound had not been properly isolated as of 2010, due to its tendency to polymerize.[3][4] However, removal of three protons yields the melonate[5] (formerly hydromelonate[1]) anion (NCN)3(C6N7)3−, whose salts are stable and have been known since the 19th century. Removal of only two protons yields the divalent hydrogenmelonate anion H(NCN)3(C6N7)2−.[3][5]

History

In 1834 Justus von Liebig described the compounds that he named melamine, melam, and melon.[6] In 1835 Leopold Gmelin prepared a potassium salt (later identified as K3[(NCN)3(C6N7)]) by heating potassium ferrocyanide with sulfur); recognizing their connection to the compounds described by Liebig, he named the salt "hydromelonate" and the corresponding acid "hydromelonic".[1] In the following years Liebig prepared the same salt by other methods, such as by fusing potassium thiocyanate with antimony trichloride,[7] and eventually determined the formula C9N13H3 for the acid.[8][9]

The correct structure for the cation was published in 1937 by Linus Pauling and J. H. Sturdivant.[9]

Starting in the 1970s, melonates have attracted new interest, motivated by research in cubic carbon nitride c-C3N4.[3] Salts of many cations have been synthesized and studied,[2][10][4][11] including mixed-cation salts[5] and calcium hydrogenmelonate Ca[HC9N13]·7H2O.[3] The structure of potassium melonate pentahydrate K3C9N13·5H2O was elucidated only in 2005.[5]

Preparation

Sodium and potassium melonates are still routinely prepared by variations of one of Liebig's methods,[7] namely by reacting melon with molten potassium thiocyanate, potassium cyanate, or sodium thiocyanate.[2] Other salts can be prepared by double displacement reactions.[3]

Melonates

Melonate anion (NCN)3(C6N7)3−.

Alkali melonates are soluble in water without decomposition.[10] Treatment of melonates with alkali gives salts of cyameluric acid.[12]

Potassium melonate pentahydrate has planar sheets of melonate anions with potassium cations between the layers. The same generals structure is seen in the anhydrous salt (except that the melonate ions are asymmetric due to an NHN– group being turned by 180°) and in the salts Rb3C9N13·3H2O and Cs3C9N13·3H2O.[3][5]

Melonate salts decompose when melted with cyanates to form tricyanomelaminates, the first selective decomposition reaction leading from heptazines to triazines.[2]

Pyrolysis of iron(III) melonate Fe[C9N13] at very high temperature yields carbon in the form of nanotubes.[4]

See also

References

  1. ↑ 1.0 1.1 1.2 1.3 L. Gmelin, Ann. Pharmacie, 15, 252 (1835).
  2. ↑ 2.0 2.1 2.2 2.3 2.4 Andreas Sattler and Wolfgang Schnick (2009): "On the Formation and Decomposition of the Melonate Ion in Cyanate and Thiocyanate Melts and the Crystal Structure of Potassium Melonate,K3[C6N7(NCN)3". European Journal of Inorganic Chemistry, volume 2009, issue 33, pages 4972-4981. doi:10.1002/ejic.200900585
  3. ↑ 3.0 3.1 3.2 3.3 3.4 3.5 Sophia J. Makowski, Daniel Gunzelmann, Jürgen Senker, Wolfgang Schnick (2009): "Protonated Melonate Ca[HC6N7(NCN)3]·7H2O – Synthesis, Crystal Structure, and Thermal Properties". Zeitschrift für anorganische und allgemeine Chemie (ZAAC), volume 635, issue 15, pages 2434-2439. doi:10.1002/zaac.200900231
  4. ↑ 4.0 4.1 4.2 Corinna Clauss, Marcus Schwarz, and Edwin Kroke (2010): "Microwave-induced decomposition of nitrogen-rich iron salts and CNT formation from iron(III)–melonate Fe[C9N13]". Carbon, volume 48, issue 4,pages 1137-1145. doi:10.1016/j.carbon.2009.11.036
  5. ↑ 5.0 5.1 5.2 5.3 5.4 Fabian Karl Keßler (2019), Structure and Reactivity of s-Triazine-Based Compounds in C/N/H Chemistry. Doctoral thesis, Fakultät für Chemie und Pharmazie, Ludwig-Maximilians-Universität München
  6. ↑ J. Liebig, Ibid., 10, 1 (1834).
  7. ↑ 7.0 7.1 J. Liebig, Ann. Chem. Pharm., 50, 337 (1844).
  8. ↑ J. Liebig, Ibid., 95, 257 (1855).
  9. ↑ 9.0 9.1 Linus Pauling and J. H. Sturdivant (1937): "The Structure of Cyameluric Acid, Hydromelonic Acid and Related Substances". Proceedings of the National Academy of Sciences, volume 23, issue 12, page 615–620. doi:10.1073/pnas.23.12.615
  10. ↑ 10.0 10.1 Corinna Clauss, Jörg Wagler, Marcus Schwarz, Anke Schwarzer, and Edwin Kroke (2010): "Lithium Melonate, Li3[C6N7(NCN)3]·6H2O – Synthesis, Crystal Structure and Thermal Properties of a Novel Precursor for Graphitic Carbon Nitrides". 'Zeitschrift für anorganische und allgemeine Chemie (ZAAC), vlume 636, issue 1, pages 196-200. doi:10.1002/zaac.200900326
  11. ↑ Wolfgang Schnick and Sophia Makowski (2010): "Rb3[C6N7(NCN)3]•3H2O and Cs3[C6N7(NCN)3]•3H2O – Synthesis, Crystal Structure and Thermal Behavior of two Novel Alkali Melonates". CSSD HAL, article hal-00511998 version 1 doi:10.1002/zaac.200900232
  12. ↑ W. Henneberg, Ibid., 73, 228 (1850).



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