Hexaphenylbenzene
Names
Preferred IUPAC name
23,24,25,26-Tetraphenyl-11,21:22,31-terphenyl
Other names
Hexaphenylbenzene
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.012.356
UNII
  • InChI=1S/C42H30/c1-7-19-31(20-8-1)37-38(32-21-9-2-10-22-32)40(34-25-13-4-14-26-34)42(36-29-17-6-18-30-36)41(35-27-15-5-16-28-35)39(37)33-23-11-3-12-24-33/h1-30H checkY
    Key: QBHWPVJPWQGYDS-UHFFFAOYSA-N checkY
  • InChI=1/C42H30/c1-7-19-31(20-8-1)37-38(32-21-9-2-10-22-32)40(34-25-13-4-14-26-34)42(36-29-17-6-18-30-36)41(35-27-15-5-16-28-35)39(37)33-23-11-3-12-24-33/h1-30H
    Key: QBHWPVJPWQGYDS-UHFFFAOYAG
  • c1cc(ccc1)c3c(c(c(c(c3c2ccccc2)c4ccccc4)c5ccccc5)c6ccccc6)c7ccccc7
Properties
C42H30
Molar mass 534.702 g·mol−1
Appearance white solid
Melting point 454 to 456 °C (849 to 853 °F; 727 to 729 K)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Hexaphenylbenzene is an aromatic compound composed of a benzene ring substituted with six phenyl rings. It is a colorless solid. The compound is the parent member of a wider class of hexaarylbenzenes, which are mainly of theoretical interest.[2]

Preparation

It is prepared by heating tetraphenylcyclopentadienone and diphenylacetylene in benzophenone or other high-temperature solvent. The reaction proceeds via a Diels-Alder reaction to give the hexaphenyldienone, which then eliminates carbon monoxide.[1]

Hexaphenylbenzene synthesis

Together with 1,2,3,4-tetraphenylnaphthalene, hexaphenylbenzene forms by the chromium-catalyzed oligomerization of diphenylacetylene.[3] It may also be prepared by the dicobalt octacarbonyl-catalyzed alkyne trimerisation of diphenylacetylene.[2]

Diphenylacetylene cyclotrimerization using dicobalt octacarbonyl

Structure

Perspective view of the crystal structure of hexaphenylbenzene, showing the rotation of the phenyl rings. Hydrogen atoms have been omitted for clarity.[4]

The stable conformation of this molecule has the phenyl rings rotated out of the plane of the central benzene ring. The molecule adopts a propeller-like conformation in which the phenyl rings are rotated about 65°,[4] while in the gas phase, they are perpendicular with some slight oscillations.[5]

References

  1. 1 2 Louis Fieser (1966). "Hexaphenylbenzene". Organic Syntheses. 46: 44. doi:10.15227/orgsyn.046.0044.
  2. 1 2 Varun Vij, Vandana Bhalla, and Manoj Kumar (2016). "Hexaarylbenzene: Evolution of Properties and Applications of Multitalented Scaffold". Chemical Reviews. 116 (16): 9565–9627. doi:10.1021/acs.chemrev.6b00144. PMID 27498592.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ↑ W. Herwig, W. Metlesics, H. Zeiss (1959). "π-Complexes of the Transition Metals. X. Acetylenic π-Complexes of Chromium in Organic Synthesis". J. Am. Chem. Soc. 81 (23): 6203–6207. doi:10.1021/ja01532a024.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. 1 2 Bart, J. C. J. (1968). "The crystal structure of a modification of hexaphenylbenzene" (PDF). Acta Crystallographica Section B. 24 (10): 1277–1287. doi:10.1107/S0567740868004176.
  5. ↑ Gust, D. (1977). "Restricted Rotation in Hexaarylbenzenes". J. Am. Chem. Soc. 99 (21): 6980–6982. doi:10.1021/ja00463a034.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.