Hexazine
Kekulé and aromatic, skeletal formulae of hexazine
Ball and stick, and spacefill models of hexazine
Names
Preferred IUPAC name
Hexazine (preselected name)
Systematic IUPAC name
Hexaazabenzene
Other names
Hexazabenzene[1]
Hexaazabenzene
Azabenzene
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
1819
  • InChI=1S/N6/c1-2-4-6-5-3-1 ☒N
    Key: YRBKSJIXFZPPGF-UHFFFAOYSA-N ☒N
  • n1nnnnn1
  • N1=NN=NN=N1
Properties
N6
Molar mass 84.042 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 ?)

Hexazine (also known as hexaazabenzene) is a hypothetical allotrope of nitrogen composed of 6 nitrogen atoms arranged in a ring-like structure analogous to that of benzene. As a neutrally charged species, it would be the final member of the azabenzene (azine) series, in which all of the methine groups of the benzene molecule have been replaced with nitrogen atoms. The two last members of this series, hexazine and pentazine, have not been observed, although all other members of the azine series have (such as pyridine, pyrimidine, pyridazine, pyrazine, triazines, and tetrazines).

While a neutrally charged hexazine species has not yet been synthesized, two negatively charged variants, [N6]2-[2] and [N6]4-,[3] have been produced in potassium-nitrogen compounds under very high pressures (> 40 GPa) and temperatures (> 2000 K). In particular, [N6]4- is aromatic, respecting Hückel's rule, while [N6]2- is anti-aromatic.

Stability

The hexazine molecule bears a structural similarity to the very stable benzene molecule. Like benzene, it has been calculated that hexazine is likely an aromatic molecule. Despite this, it has yet to be synthesized. Additionally, it has been predicted computationally that the hexazine molecule is highly unstable, possibly due to the lone pairs on the nitrogen atoms, which may repel each other electrostatically and/or cause electron-donation to sigma antibonding orbitals. A figure-8-shaped isomer is predicted to be metastable.[4]

See also

References

  1. ^ "Hexazine - PubChem Public Chemical Database". The PubChem Project. USA: National Center for Biotechnology Information.
  2. ^ Wang, Yu; Bykov, Maxim; Chepkasov, Ilya; Samtsevich, Artem; Bykova, Elena; Zhang, Xiao; Jiang, Shu-qing; Greenberg, Eran; Chariton, Stella; Prakapenka, Vitali B.; Oganov, Artem R.; Goncharov, Alexander F. (July 2022). "Stabilization of hexazine rings in potassium polynitride at high pressure". Nature Chemistry. 14 (7): 794–800. arXiv:2010.15995. Bibcode:2022NatCh..14..794W. doi:10.1038/s41557-022-00925-0. ISSN 1755-4330. PMID 35449217. S2CID 226222305.
  3. ^ Laniel, Dominique; Trybel, Florian; Yin, Yuqing; Fedotenko, Timofey; Khandarkhaeva, Saiana; Aslandukov, Andrey; Aprilis, Georgios; Abrikosov, Alexei I.; Bin Masood, Talha; Giacobbe, Carlotta; Bright, Eleanor Lawrence; Glazyrin, Konstantin; Hanfland, Michael; Wright, Jonathan; Hotz, Ingrid (2023-03-06). "Aromatic hexazine [N6]4− anion featured in the complex structure of the high-pressure potassium nitrogen compound K9N56". Nature Chemistry. 15 (5): 641–646. Bibcode:2023NatCh..15..641L. doi:10.1038/s41557-023-01148-7. ISSN 1755-4349. PMID 36879075. S2CID 257377020.
  4. ^ J. Fabian and E. Lewars (2004). "Azabenzenes (azines) — The nitrogen derivatives of benzene with one to six N atoms: Stability, homodesmotic stabilization energy, electron distribution, and magnetic ring current; a computational study" (PDF). Canadian Journal of Chemistry. 82 (1): 50–69. doi:10.1139/v03-178. Archived from the original (PDF) on 2005-03-29.

Further reading

External links

Categories